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| Product | Description | |
|---|---|---|
| pea protein concentrate | Pea protein concentrate is made from non-GMO peas, pulverized, separated and processed. Product ID: CDF4-0240. Product Keywords: Nutrients; pea protein concentrate; CDF4-0240; ;. Physical State: Light Yellow or Milk White. Storage: Room Temperature. Applications: pea protein concentrate is an edible protein additive. Product Description: Pea protein concentrate has a strong bean flavor, protein content of 55%, comprehensive nutrition, rich in amino acids and vitamins, no cholesterol. The product has good dispersion, stability, impact and water solubility. |  |
| Pea protein isolate | Pea protein isolate is made from non-transgenic peas by crushing, separating, homogenizing sterilization, spray drying and other processes. Product ID: CDF4-0241. Product Keywords: Nutrients; Pea protein isolate; CDF4-0241; ;. Physical State: Light Yellow or Milk White. Storage: Room Temperature. Applications: pea protein concentrate is an edible protein additive. Product Description: Pea protein isolate has a strong bean flavor, protein content of more than 80%, contains 18 amino acids and vitamins, and does not contain cholesterol. The product has good dispersion, stability, impact and water solubility characteristics. | |
| Pea protein powder | Pea Protein is made from the high-quality non-GMO peas. The working procedures include separating, homogenizing, sterilizing and spray drying. Its yellow and fragrant with strong pea taste and has over 80% protein and 18 amino acids & vitamins without cholesterol. It has good gelatinization and water-solubility including dispersibility, stability and dissolution. Applications: In vegetable protein beverages (peanut milk, wheat milk and walnut milk, etc.). in health food & beverages and sausages. it can be used to increase protein content and stabilize quality in the milk powder processing (infant & student formula milk powder and milk powder for the middle-aged and senior) field. Group: Others. Pea protein powder. Cat No: EXTC-214. |  |
| Peanut Protein | Peanut protein is selected domestic and export quality level of peanuts as raw materials, the use of low temperature preparation of peanut protein and fragrant peanut oil industrialized production technology refined and a no protein thermal denaturation, a higher nutritional value of plant protein. The intact peanut nutrients, soluble protein and NSI value high, good water solubility, white, light flavor, with faint scent peanut specific and nutritional value can and animal protein comparable, rich in the human body essential amino acids, vitamins, trace elements and minerals, effective utilization rate of 98%, and easy to for human digestion and absorption and contain anti nutritiona...ugar, low fat, does not contain cholesterol, high nutrition of natural nutrition. Applications: Peanut protein can used for pet product which can prevent cardiovascular disease etc.peanut protein can be added in dairy product,such as milk,as peanut milk.peanut protein in candy,can replace dried shim milk,good emulsification in defatted soybean meal,such as after add in chocolate,can reduce the adhesion processing equipment,enhance the shape and physical properties of the senses.peanut protein can used for producing nonstaple foods,condiments,beef jerky,meat,cake etc. Group: Others. Purity: >80% Protein. Appearance: Creamy yellow or yellow fine powder. Peanut Protein. Cat No: EXTC-215. | |
| 2,5-Dimethylpyrazine | 2,5-Dimethylpyrazine. CAS No. 123-32-0. Pack Sizes: 100, 500 g in glass bottle. Product ID: CDC10-0167. Molecular formula: C6H8N2. Category: Flavoring Chemical Agents. Product Keywords: Cosmetic Ingredients; Flavoring Chemical Agents; 2,5-Dimethylpyrazine; CDC10-0167; 123-32-0; C6H8N2; 204-618-3; MFCD00006147; 123-32-0. Grade: Fragrance grade. Purity: ≥98%, FG. Color: Clear colorless to pale yellow. EC Number: 204-618-3. Physical State: Liquid. Solubility: Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly). Quality Level: 400. Storage: Inert atmosphere,Room Temperature. Application: flavors and fragrances. Boiling Point: 155 °C (lit.). Melting Point: 15°C. Density: 0.99 g/mL at 25 °C (lit.). Product Description: 2,5-Dimethylpyrazine is a pyrazine compound that is mainly formed in food products such as cooked rice or roasted peanuts due to the Maillard reaction between sugars and proteins during cooking or roasting process. | |
| 2,7,4'-trihydroxyisoflavanone 4'-O-methyltransferase | Specifically methylates 2,4',7-trihydroxyisoflavanone on the 4'-position. No activity with isoflavones. The enzyme is involved in formononetin biosynthesis in legumes. The protein from pea (Pisum sativum) also methylates (+)-6a-hydroxymaackiain at the 3-position (cf. EC 2.1.1.270, (+)-6a-hydroxymaackiain 3-O-methyltransferase). Group: Enzymes. Synonyms: SAM:2,7,4'-trihydroxyisoflavanone 4'-O-methyltransferase; HI4'OMT; HMM1; MtIOMT5; S-adenosyl-L-methionine:2,7,4'-trihydroxyisoflavanone 4'-O-methyltransferase. Enzyme Commission Number: EC 2.1.1.212. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1814; 2,7,4'-trihydroxyisoflavanone 4'-O-methyltransferase; EC 2.1.1.212; SAM:2,7,4'-trihydroxyisoflavanone 4'-O-methyltransferase; HI4'OMT; HMM1; MtIOMT5; S-adenosyl-L-methionine:2,7,4'-trihydroxyisoflavanone 4'-O-methyltransferase. Cat No: EXWM-1814. | |
| (2R, 3S)/(2S, 3R)-Racemic Fmoc-beta-hydroxyphenylalanine | (2S,3R)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-hydroxy-3-phenylpropanoic acidnyllactic acid is a white crystalline powder that belongs to the family of L-α-amino acids. It is a derivative of 3-Phenyllactic acid, which is a natural compound found in various plants and microorganisms. (2S,3R)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-hydroxy-3-phenylpropanoic acidnyllactic acid is widely used in peptide synthesis as a building block for the formation of peptides and proteins. It is also used in drug discovery and development as a scaffold molecule for the design of novel bioactive compounds. Uses: (2s,3r)-2-(9h-fluoren-9-ylmethoxycarbonylamino)-3-hydroxy-3-phenylpropanoic acidnyllactic acid has a wide range of applications in scientific experiments, including peptide synthesis, drug discovery and development, and biomaterials engineering. (2s,3r)-2-(9h-fluoren-9-ylmethoxycarbonylamino)-3-hydroxy-3-phenylpropanoic acidnyllactic acid can be used as a building block for the synthesis of peptid. Additional or Alternative Names: 6,7-DICHLORO-3-(TRIFLUOROMETHYL)-2-QUINOXALINOL. Product Category: Amino Acids. CAS No. 487060-72-0. Molecular formula: C24H21NO5. Mole weight: 403.4. Purity: Peak Area by HPLC ≥95%. IUPACName: (2S,3R)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-hydroxy-3-phenylpropanoic acid. Canonical SMILES: C1=CC=C(C=C1)C(C(C(=O)O)NC(=O)OCC2C3=CC=CC=C3C4=CC=CC=C24)O. |  |
| (+)-6a-hydroxymaackiain 3-O-methyltransferase | The protein from the plant Pisum sativum (garden pea) methylates (+)-6a-hydroxymaackiain at the 3-position. It also methylates 2,7,4'-trihydroxyisoflavanone on the 4'-position (cf. EC 2.1.1.212, 2,7,4-trihydroxyisoflavanone 4-O-methyltransferase) with lower activity. Group: Enzymes. Synonyms: HM3OMT; HMM2. Enzyme Commission Number: EC 2.1.1.270. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1876; (+)-6a-hydroxymaackiain 3-O-methyltransferase; EC 2.1.1.270; HM3OMT; HMM2. Cat No: EXWM-1876. | |
| aldehyde oxygenase (deformylating) | Contains a diiron center. Involved in the biosynthesis of alkanes. The enzyme from the cyanobacterium Nostoc punctiforme PCC 73102 is only active in vitro in the presence of ferredoxin, ferredoxin reductase and NADPH, and produces mostly C15 and C17 alkanes. The enzyme from pea (Pisum sativum) produces alkanes of chain length C18 to C32 and is inhibited by metal-chelating agents. The substrate for this enzyme is formed by EC 1.2.1.80, acyl-[acyl-carrier protein] reductase. Group: Enzymes. Synonyms: decarbonylase; aldehyde decarbonylase; octadecanal decarbonylase; octadecanal alkane-lyase. Enzyme Commission Number: EC 4.1.99.5. CAS No. 94185-90-7. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4937; aldehyde oxygenase (deformylating); EC 4.1.99.5; 94185-90-7; decarbonylase; aldehyde decarbonylase; octadecanal decarbonylase; octadecanal alkane-lyase. Cat No: EXWM-4937. | |
| Aurora Kinase A active human, Recombinant | Aurora A kinase also known as serine/threonine-protein kinase 6 is an enzyme that in humans is encoded by the AURKA gene. Aurora A is a member of a family of mitotic serine/threonine kinases. It is implicated with important processes during mitosis and meiosis whose proper function is integral for healthy cell proliferation. Aurora A is activated by one or more phosphorylations and its activity peaks during the G2 phase to M phase transition in the cell cycle. Human aurora kinase a (genbank accession no. nm_003600), amino acids 2-403 with n-terminal his6-tag, mw=50 kda, expressed in a baculovirus infected sf9 cell expression system. Applications: Useful for the study of enzyme kinetics, screening inhibitors, and selectivity profiling. Group: Enzymes. Synonyms: Aurora Kinase A; Aurora A kinase; serine/threonine-protein kinase 6; AURKA; AIK; ARK1; AURA; AURORA2; BTAK; PPP1R47; STK15; STK6; STK7. Purity: > 90% (SDS-PAGE). ARK1. Mole weight: mol wt 50 kDa. Activity: ~17,000 units/mg protein. Form: aqueous solution. Source: baculovirus infected Sf9 cells. Species: Human. Aurora Kinase A; Aurora A kinase; serine/threonine-protein kinase 6; AURKA; AIK; ARK1; AURA; AURORA2; BTAK; PPP1R47; STK15; STK6; STK7. Pack: Minimum 50 ng protein/vial by Bradford. Cat No: NATE-0087. | |
| Boc-2-cyano-L-phenylalanine | Boc-L-2-Cyanophenylalanine is a synthetic amino acid, which means it is created by altering natural amino acids. Boc-L-2-Cyanophenylalanine is one of the various analogs of phenylalanine that have been developed for research purposes. It is made up of a modified version of phenylalanine, which has a cyano group attached to the base molecule. This modification makes Boc-L-2-Cyanophenylalanine suitable for a range of experiments, including crystallography and NMR spectroscopy. Uses: Boc-l-2-cyanophenylalanine has several applications in scientific research. this includes the identification of substrate specificity and mechanism of action of enzymes, the investigation of protein-protein interactions, and the study of protein structure and function. Additional or Alternative Names: N-(tert-Butoxycarbonyl)-2-cyano-L-phenylalanine, (S)-N-Boc-ortho-cyanophenylalanine, Boc-L-o-cyanophenylalanine. Product Category: Amino Acids. CAS No. 216312-53-7. Molecular formula: C15H18N2O4. Mole weight: 290.3. Purity: Peak Area by HPLC ≥95%. IUPACName: (2S)-3-(2-cyanophenyl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid. Canonical SMILES: CC(C)(C)OC(=O)NC(CC1=CC=CC=C1C#N)C(=O)O. Density: 1.2±0.1 g/cm3. Product ID: ACM216312537. Alfa Chemistry ISO 9001:2015 Certified. | |
| Boc-6-methyl-DL-tryptophan | Boc-6-methyl-DL-tryptophan, also known as Boc-Trp(Me)-OH, is a modified form of L-tryptophan. It is commonly used in the field of peptide synthesis as a building block for the preparation of peptide mimics. The compound is highly stable and easy to handle, making it an ideal candidate for constructing complex peptide sequences. Uses: Boc-trp(me)-oh is commonly used as a building block for the synthesis of peptide mimics in various fields of research, including drug discovery and development, molecular biology, and materials science. the compound is also used as a reagent for the modification of proteins and peptides. Additional or Alternative Names: 6-Methyl-N-{[(2-methyl-2-propanyl)oxy]carbonyl}tryptophan, Boc-Trp(Me)-OH. Product Category: Amino Acids. CAS No. 446847-83-2. Molecular formula: C17H22N2O4. Mole weight: 318.4. Purity: Peak Area by HPLC ≥95%. IUPACName: 3-(6-methyl-1H-indol-3-yl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid. Canonical SMILES: CC1=CC2=C(C=C1)C(=CN2)CC(C(=O)O)NC(=O)OC(C)(C)C. Density: 1.2±0.1 g/cm3. Product ID: ACM446847832. Alfa Chemistry ISO 9001:2015 Certified. | |
| Boc-O-benzyl-L-beta-homotyrosine | (S)-4-(4-(Benzyloxy)phenyl)-3-((tert-butoxycarbonyl)amino)butanoic acid, commonly known as Boc-4-(benzyloxy)phenylalanine, is an amino acid derivative used in the synthesis of peptides and proteins. It is an unnatural amino acid that has a bulky tert-butoxycarbonyl (Boc) protecting group on the amino group and a benzyloxy group on the side chain. Uses: Boc-4-(benzyloxy)phenylalanine is commonly used in the synthesis of peptides and proteins and is also used as a tool for studying enzyme activity. Additional or Alternative Names: (S)-4-(4-(Benzyloxy)phenyl)-3-((tert-butoxycarbonyl)amino)butanoic acid, Boc-beta-Homotyr(Bzl)-OH, Boc-L-beta-homotyrosine(OBzl), Boc-L-beta-HTyr(Bzl)-OH, (S)-4-(4-(Benzyloxy)phenyl)-3-((tert-butoxycarbonyl)amino)butanoicacid, Boc-O-benzyl-L-beta-homotyrosine, (3S)-4-[4-(benzyloxy)phenyl]-3-[(tert-butoxycarbonyl)amino]butanoicacid. Product Category: Amino Acids. CAS No. 126825-16-9. Molecular formula: C22H27NO5. Mole weight: 385.5. Purity: Peak Area by HPLC ≥95%. IUPACName: (3S)-3-[(2-methylpropan-2-yl)oxycarbonylamino]-4-(4-phenylmethoxyphenyl)butanoic acid. Canonical SMILES: CC(C)(C)OC(=O)NC(CC1=CC=C(C=C1)OCC2=CC=CC=C2)CC(=O)O. Density: 1.168 g/cm3. Product ID: ACM126825169-1. Alfa Chemistry ISO 9001:2015 Certified. | |
| Coffee Robusta Extract | Robusta originated in central and western sub-Saharan Africa. It is the second most popular coffee in the world, making up 40% of the worlds coffee production. Robusta coffee benefits are increases energy and improves mental health and well-being, contains antioxidants, which are beneficial for skin and hair. It has a diuretic effect and can help with nausea. It is a high-caffeine, creamy, somewhat bitter version of the coffee full of benefits. The main constituents of coffee are caffeine, tannin, fixed oil, carbohydrates, and proteins. It contains 2-3% caffeine, 3-5% tannins, 13% proteins, and 10-15% fixed oils. In the seeds, caffeine is present as a salt of chlorogenic acid (CGA). Uses: Flavor. Group: Plant Extracts. INCI Names: Coffea Robusta (Coffee) Seed Extract. Grades: INDUSTRIAL GRADE. CAS No. 97593-13-0. Pack Sizes: 25 kgs Jerrycan, 200 kg Drums. Product ID: CF-0202. Olfactive Profile: Peanuty, roasted, smokey, bitter. EC No: 307-315-5. Origin: Indonesia. |  New Jersey |
| Enzyme blend for flour proteins | This food-grade , non-synthetic, and organic-certifiable enzyme blend is used to hydrolyze soya, pea, yeast, maize and wheat flour proteins, producing high-quality functional protein hydrolysates. Applications: Vegetable proteins. Group: Enzymes. Enzyme for flour proteins. Appearance: powder or liquid. for flour proteins; Vegetable Proteins enzyme; hydrolyze soya enzyme;hydrolyze pea enzyme; hydrolyze yeast enzyme; maize and wheat flour proteins; pea; maize; wheat; hydrolyze soya; hydrolyze; Enzyme blend for flour proteins; PRO-1825. Pack: 25kg/paper barrel (powder form), 30kg/polyster barrel (liquid form). Cat No: PRO-1825. | |
| Fmoc-(2S,3aS,7aS)-Octahydro-1H-indole-2-carboxylic acid | Fmoc-Oic-OH (2R,3aR,7aR) is a synthetic amino acid that is used in the synthesis of peptides and proteins. It is a derivative of Oic acid, which is a non-standard amino acid that is commonly found in various natural products. Fmoc-Oic-OH (2R,3aR,7aR) is used in solid-phase peptide synthesis due to its compatibility with Fmoc-based protection and deprotection protocols. Uses: Fmoc-oic-oh (2r,3ar,7ar) has a wide range of applications in scientific experiments, such as the synthesis of peptides and proteins, the study of protein-protein interactions, and the development of new drugs. Additional or Alternative Names: Fmoc-Oic-OH (2R,3aR,7aR). Product Category: Amino Acids. CAS No. 134526-62-8. Molecular formula: C24H25NO4. Mole weight: 391.5. Purity: Peak Area by HPLC ≥95%. IUPACName: (2R,3aR,7aR)-1-(9H-fluoren-9-ylmethoxycarbonyl)-2,3,3a,4,5,6,7,7a-octahydroindole-2-carboxylic acid. Canonical SMILES: C1CCC2C(C1)CC(N2C(=O)OCC3C4=CC=CC=C4C5=CC=CC=C35)C(=O)O. Density: 1.3±0.1 g/cm3. Product ID: ACM134526628. Alfa Chemistry ISO 9001:2015 Certified. Categories: (2S,3aS,7aS)-1-{[(9H-fluoren-9-yl)methoxy]carbonyl}-octahydro-1H-indole-2-carboxylic acid. | |
| Fmoc-(2S, 4R)-4-benzyl-pyrrolidine-2-carboxylic acid | Fmoc-Bz-Pro-OH is a derivative of proline, which is an essential amino acid. Fmoc-Bz-Pro-OH is widely used in the field of peptide synthesis due to its unique properties. This compound is used to introduce the proline amino acid into a peptide chain. Uses: Fmoc-bz-pro-oh has several applications in scientific experiments, including peptide synthesis, protein synthesis, and drug discovery. this compound is widely used in the development of new drugs, specifically in the field of antibacterials and antivirals. Additional or Alternative Names: Fmoc-(2S,4R)-4-benzyl-pyrrolidine-2-carboxylic acid. Product Category: Amino Acids. CAS No. 1158891-05-4. Molecular formula: C27H25NO4. Mole weight: 427.5. Purity: Peak Area by HPLC ≥95%. IUPACName: (2S,4R)-4-benzyl-1-(9H-fluoren-9-ylmethoxycarbonyl)pyrrolidine-2-carboxylic acid. Canonical SMILES: C1C(CN(C1C(=O)O)C(=O)OCC2C3=CC=CC=C3C4=CC=CC=C24)CC5=CC=CC=C5. Density: 1.3±0.1 g/cm3. Product ID: ACM1158891054. Alfa Chemistry ISO 9001:2015 Certified. | |
| Fmoc-3,4-dichloro-L-phenylalanine | Fmoc-3,4-dichloro-L-phenylalanine. Uses: Fmoc-3,4-dichloro-l-phenylalanine has found applications in various fields of research and industry, such as drug discovery, biomaterials, and proteomics. peptides containing fmoc-3,4-dichloro-l-phenylalanine have been used as tools to study protein-protein interactions, enzyme kinetics, and other biological processes. fmoc-3,4-dichloro-l-phenylalanine can also be used to introduce a unique side chain into peptides, which can confer novel properties, such as increased stability or improved solubility. Additional or Alternative Names: Fmoc-3,4-dichloro-L-phenylalanine;Fmoc-L-3,4-dichlorophe; Fmoc-Phe(3,4-Cl2)-OH; Fmoc-L-3,4-Dichlorophenylalanine; (S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-(3,4-dichlorophenyl)propanoicacid; (2S)-3-(3,4-dichlorophenyl)-2-(9H-fluoren-9-ylmethoxycarbonylamino)propanoicacid. Product Category: Amino Acids. CAS No. 177966-59-5. Molecular formula: C24H19Cl2NO4. Mole weight: 456.3. Purity: Peak Area by HPLC ≥95%. IUPACName: (2S)-3-(3,4-dichlorophenyl)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}propanoic acid. Canonical SMILES: C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)NC(CC4=CC(=C(C=C4)Cl)Cl)C(=O)O. Density: 1.4±0.1 g/cm3. Product ID: ACM177966595. Alfa Chemistry ISO 9001:2015 Certified. | |
| Fmoc-3,4-difluoro-L-phenylalanine | Fmoc-3,4-difluoro-L-phenylalanine is a non-natural amino acid that contains a substituted phenylalanine residue, which is characterized by the presence of two fluorine atoms on the 3 and 4 positions of the aromatic ring. This modification enhances the lipophilicity of the phenylalanine residue and provides unique steric and electronic properties compared to the natural phenylalanine. Fmoc-3,4-difluoro-L-phenylalanine is widely used in peptide synthesis, pharmaceuticals, and materials science due to its ability to form stable secondary structures, such as helices and beta-turns, in peptides and proteins. Uses: Fmoc-3,4-difluoro-l-phenylalanine has been widely used in various scientific experiments. it is commonly used in peptide synthesis to enhance the bioactivity and stability of peptides. fmoc-3,4-difluoro-l-phenylalanine-containing peptides have also been used in drug discovery to develop novel therapeutics. additionally, fmoc-3,4-difluoro-l-phenylalanine has been utilized in materials science to cr. Additional or Alternative Names: N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-3,4-difluoro-L-phenylalanine, Fmoc-D-phe(3,4-F2)-OH, Fmoc-Phe(3,4-F2)-OH, Fmoc-L-3,4-Difluorophenylalanine. Product Category: Amino Acids. CAS No. 198560-43-9. Molecular formula: C24H19F2NO4. Mole weight: 423.4. Purity: Peak Area by HPLC ≥95%. IUPACName: (2S)-3-(3,4-difluorophenyl)-2-(9H-fluoren-9-ylmethoxycarbonylamino)propanoic aci | |
| Fmoc-3-chloro-L-tyrosine | Fmoc-3-chloro-L-tyrosine is a derivative of tyrosine that incorporates a fluorine group into the aromatic ring. This compound is commonly used in peptide synthesis as a building block for constructing peptides with spectroscopically detectable fluorescent labels. The Fmoc ('9-fluorenylmethyloxycarbonyl') group is a commonly used protecting group in peptide chemistry that is attached to the amino group of a peptide building block to prevent unwanted reactions during the synthesis process. Uses: Fmoc-3-chloro-l-tyrosine has a range of applications in scientific experiments, including as a building block for peptide synthesis, as a fluorescent tag for protein and peptide labeling, and as a potential antibacterial and anticancer agent. the compound has also been used as a probe for studying protein-protein interactions. Additional or Alternative Names: Fmoc-Tyr(3-Cl)-OH, Fmoc-3-chlorotyrosine, Fmoc-3-chloro-L-tyrosine. Product Category: Amino Acids. CAS No. 478183-58-3. Molecular formula: C24H20ClNO5. Mole weight: 437.9. Purity: Peak Area by HPLC ≥95%. IUPACName: (2S)-3-(3-chloro-4-hydroxyphenyl)-2-(9H-fluoren-9-ylmethoxycarbonylamino)propanoic acid. Canonical SMILES: C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)NC(CC4=CC(=C(C=C4)O)Cl)C(=O)O. Product ID: ACM478183583. Alfa Chemistry ISO 9001:2015 Certified. Categories: (2S)-3-(3-chloro-4-hydroxyphenyl)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)propanoic acid. | |
| Fmoc-3-fluoro-DL-tyrosine | Fmoc-3-fluoro-DL-tyrosine is a non-natural amino acid that has gained increasing attention in the scientific community due to its potential applications in various areas such as drug discovery, bioconjugation, and protein engineering. A derivative of tyrosine, Fmoc-3-fluoro-DL-tyrosine is identified by its unique chemical structure, which comprises a fluoro-substituent and a N-terminal Fmoc (9-fluorenylmethyloxycarbonyl) protecting group. Uses: Fmoc-3-fluoro-dl-tyrosine has potential applications in various scientific areas such as drug discovery, bioconjugation, and protein engineering. it has been used to develop inhibitors for enzymes and receptors, to modify the properties of peptides, and to study protein-protein interactions. Product Category: Amino Acids. CAS No. 1219389-96-4. Molecular formula: C24H20FNO5. Mole weight: 421.4. Purity: Peak Area by HPLC ≥95%. IUPACName: 2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-(3-fluoro-4-hydroxyphenyl)propanoic acid. Canonical SMILES: C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)NC(CC4=CC(=C(C=C4)O)F)C(=O)O. Product ID: ACM1219389964. Alfa Chemistry ISO 9001:2015 Certified. | |
| Fmoc-4-amino-(1-carboxymethyl) piperidine | 2-(4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)piperidin-1-yl)acetic acid is a synthetic compound designed as a scaffold for drug discovery. It is commonly referred to as Fmoc-Lys(Dde)-OH in the research community. The compound contains one Lysine (Lys) residue, and the abbreviation Dde stands for the protection group used to prevent the Lysine side chain from reacting during peptide synthesis. Uses: The versatility of fmoc-lys(dde)-oh has led to its use in various scientific experiments, including peptide synthesis, drug discovery, and chemical biology. peptides and peptidomimetics containing fmoc-lys(dde)-oh have been used as probes for studying protein-protein interactions, enzyme kinetics, and receptor-ligand binding. Additional or Alternative Names: 2-(4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)piperidin-1-yl)acetic acid, Fmoc-Lys(Dde)-OH. Product Category: Amino Acids. CAS No. 221352-82-5. Molecular formula: C22H24N2O4. Mole weight: 380.4. Purity: Peak Area by HPLC ≥95%. IUPACName: 2-[4-(9H-fluoren-9-ylmethoxycarbonylamino)piperidin-1-yl]acetic acid. Canonical SMILES: C1CN(CCC1NC(=O)OCC2C3=CC=CC=C3C4=CC=CC=C24)CC(=O)O. Density: 1.323 g/cm3. Product ID: ACM221352825-1. Alfa Chemistry ISO 9001:2015 Certified. | |
| Fmoc-4-benzoyl-D-phenylalanine | Fmoc-D-Bpa-OH, or N-[(9-fluorenylmethoxycarbonyl)-2-(4'-borono)phenyl]alanine, is a modified amino acid that has a boron atom and a fluorenylmethoxycarbonyl (Fmoc) group attached to the phenylalanine residue. First synthesized by Sheppard et al. in 1993, Fmoc-D-Bpa-OH has been widely used as a non-natural amino acid in peptide chemistry and as a tool in protein engineering and biophysical studies. Uses: Fmoc-d-bpa-oh has various potential applications in diverse fields, including peptide chemistry, protein engineering, and biophysical studies. in peptide chemistry, fmoc-d-bpa-oh can be used as a non-natural amino acid to introduce chemical diversity into peptide sequences, which can then be used for various applications such as drug design and development. in protein engineering, fmoc-d-bpa-oh can be used to introduce non-natural amino acids into proteins, which can then be used to modulate protein activity and stability. Product Category: Amino Acids. CAS No. 117666-97-4. Molecular formula: C31H25NO5. Mole weight: 491.5. Purity: Peak Area by HPLC ≥95%. IUPACName: (2R)-3-(4-benzoylphenyl)-2-(9H-fluoren-9-ylmethoxycarbonylamino)propanoic acid. Canonical SMILES: C1=CC=C(C=C1)C(=O)C2=CC=C(C=C2)CC(C(=O)O)NC(=O)OCC3C4=CC=CC=C4C5=CC=CC=C35. Density: 1.3±0.1 g/cm3. Product ID: ACM117666974-1. Alfa Chemistry ISO 9001:2015 Certified. | |
| Fmoc-4-bis(2-chloroethyl)amino-L-phenylalanine | Fmoc-Phe(Cl2)2-OH is a derivative of phenylalanine, which is an essential amino acid that must be consumed from external sources. Fmoc-Phe(Cl2)2-OH is a common building block in solid-phase peptide synthesis (SPPS) because it can be selectively deprotected and coupled to other amino acids. This compound was originally synthesized in 1997 by Barral et al. and has since become a widely used tool in peptide chemistry. Uses: Fmoc-phe(cl2)2-oh is commonly used in spps to synthesize peptides with biological activity. this compound is also used in medicinal chemistry to develop new drugs and small molecules. fmoc-phe(cl2)2-oh has been used in a variety of scientific experiments, including studies of protein-protein interactions, drug discovery, and structure-activity relationship studies. Product Category: Amino Acids. CAS No. 1217809-60-3. Molecular formula: C28H28Cl2N2O4. Mole weight: 527.4. Purity: Peak Area by HPLC ≥95%. IUPACName: (2S)-3-[4-[bis(2-chloroethyl)amino]phenyl]-2-(9H-fluoren-9-ylmethoxycarbonylamino)propanoic acid. Canonical SMILES: C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)NC(CC4=CC=C(C=C4)N(CCCl)CCCl)C(=O)O. Product ID: ACM1217809603. Alfa Chemistry ISO 9001:2015 Certified. | |
| Fmoc-4-(Boc-aminomethyl)-L-phenylalanine | Fmoc-4-(Boc-aminomethyl)-L-phenylalanine is a chemical compound consisting of the amino acid phenylalanine with a tert-butyloxycarbonyl (Boc) protection group on the α-amino group and a 9-fluorenylmethoxycarbonyl (Fmoc) protection group on the side chain carboxyl group. This compound is widely used in peptide synthesis due to its favorable properties, such as ease of synthesis, compatibility with solid-phase peptide synthesis techniques, and low toxicity. Fmoc-4-(Boc-aminomethyl)-L-phenylalanine is also used in a variety of scientific experiments related to peptides, proteins, and drug discovery. Uses: Fmoc-4-(boc-aminomethyl)-l-phenylalanine is widely used in peptide synthesis, particularly in the solid-phase peptide synthesis technique. it can also be used in the synthesis of cyclic peptides and peptidomimetics. additionally, the compound can be used as a building block for the synthesis of other amino acid derivatives and bioactive molecules. Additional or Alternative Names: 4-(Boc-aminomethyl)-Fmoc-phenylalanine, FMOC-L-4-AMINOMETHYLPHENYLALANINE(BOC), FMOC-S-PHE(4-MENHBOC)-OH, FMOC-PHE(4-CH2NHBOC)-OH, REF DUPL: Fmoc-L-Phe(4-CH2NHBoc)-OH, Fmoc-L-(4-amino(Boc)methyl)Phe-OH, Fmoc-L-Phe(4-CH2NHBoc)-OH. Product Category: Amino Acids. CAS No. 204715-91-3. Molecular formula: C30H32N2O6. Mole weight: 516.6. Purity: Peak Area by HPLC ≥95%. IUPACName: (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamin | |
| Fmoc-5-benzyloxy-DL-tryptophan | Fmoc-5-benzyloxy-DL-tryptophan is a derivative of tryptophan that can be used as a substrate for protein engineering, drug discovery, and as a building block for the synthesis of complex molecules. Tryptophan is an essential amino acid that plays an important role in the body, including protein synthesis, serotonin production, and as a precursor for niacin. Uses: Fmoc-5-benzyloxy-dl-tryptophan has various applications in scientific experiments, including protein engineering, drug discovery, and synthesizing complex molecules. fmoc-5-benzyloxy-dl-tryptophan can also be used as a building block for the synthesis of peptides, which can be used in drug development. Additional or Alternative Names: 5-(Benzyloxy)-N-[(9H-fluoren-9-ylmethoxy)carbonyl]tryptoph. Product Category: Amino Acids. CAS No. 1219348-47-6. Molecular formula: C33H28N2O5. Mole weight: 532.6. Purity: Peak Area by HPLC ≥95%. IUPACName: 2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-(5-phenylmethoxy-1H-indol-3-yl)propanoic acid. Canonical SMILES: C1=CC=C(C=C1)COC2=CC3=C(C=C2)NC=C3CC(C(=O)O)NC(=O)OCC4C5=CC=CC=C5C6=CC=CC=C46. Product ID: ACM1219348476. Alfa Chemistry ISO 9001:2015 Certified. | |
| Fmoc-5-chloro-DL-tryptophan | Fmoc-5-chloro-DL-tryptophan is a derivative of tryptophan, which is a naturally occurring amino acid used to build proteins in the body. The Fmoc-5-chloro-DL-tryptophan molecule has a 5-chloro substituent on the indole ring and is often used in peptide synthesis. Uses: Fmoc-5-chloro-dl-tryptophan is commonly used in peptide synthesis and chemical modification of proteins. the compound is also used in antimicrobial and antitumor studies. Product Category: Amino Acids. CAS No. 1219398-51-2. Molecular formula: C26H21ClN2O4. Mole weight: 460.9. Purity: Peak Area by HPLC ≥95%. IUPACName: 3-(5-chloro-1H-indol-3-yl)-2-(9H-fluoren-9-ylmethoxycarbonylamino)propanoic acid. Canonical SMILES: C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)NC(CC4=CNC5=C4C=C(C=C5)Cl)C(=O)O. Density: 1.4±0.1 g/cm3. Product ID: ACM1219398512. Alfa Chemistry ISO 9001:2015 Certified. | |
| Fmoc-5-hydroxy-L-tryptophan | Fmoc-5-hydroxy-DL-tryptophan is a compound that belongs to the class of amino acid derivatives. It is used as a building block for the synthesis of peptides and proteins with specific biological properties. The abbreviation Fmoc stands for fluorenylmethoxycarbonyl, which is a protecting group used in peptide synthesis to prevent unwanted reactions. Uses: Fmoc-5-hydroxy-dl-tryptophan has various applications in scientific experiments, such as peptide synthesis, structural biology, and drug discovery. fmoc-5-hydroxy-dl-tryptophan can be used as a building block to synthesize peptides and proteins with specific functions or properties. Additional or Alternative Names: N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-5-hydroxy-L-tryptophan. Product Category: Amino Acids. CAS No. 351857-99-3. Molecular formula: C26H22N2O5. Mole weight: 442.5. Purity: Peak Area by HPLC ≥95%. IUPACName: 2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-(5-hydroxy-1H-indol-3-yl)propanoic acid. Canonical SMILES: C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)NC(CC4=CNC5=C4C=C(C=C5)O)C(=O)O. Density: 1.4±0.1 g/cm3. Product ID: ACM351857993. Alfa Chemistry ISO 9001:2015 Certified. Categories: (2S)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-3-(5-hydroxy-1H-indol-3-yl)propanoic acid. | |
| Fmoc-6-methyl-DL-tryptophan | Fmoc-6-methyl-DL-tryptophan is a synthetic amino acid derivative that is used as a building block for peptide synthesis. It is a derivative of tryptophan, an essential amino acid that is important for protein synthesis in humans. Fmoc-6-methyl-DL-tryptophan is characterized by the presence of an additional methyl group at the 6-position of the indole ring. Uses: Fmoc-6-methyl-dl-tryptophan has a wide range of applications in scientific experiments, including the synthesis of novel peptides and peptidomimetics, the design of new therapeutic agents, and the study of the function and structure of proteins. Additional or Alternative Names: N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-6-methyltryptophan. Product Category: Amino Acids. CAS No. 1219150-44-3. Molecular formula: C27H24N2O4. Mole weight: 440.5. Purity: Peak Area by HPLC ≥95%. IUPACName: 2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-(6-methyl-1H-indol-3-yl)propanoic acid. Canonical SMILES: CC1=CC2=C(C=C1)C(=CN2)CC(C(=O)O)NC(=O)OCC3C4=CC=CC=C4C5=CC=CC=C35. Density: 1.3±0.1 g/cm3. Product ID: ACM1219150443. Alfa Chemistry ISO 9001:2015 Certified. | |
| Fmoc-7-methyl-DL-tryptophan | Fmoc-7-methyl-DL-tryptophan is a derivative of tryptophan, a common amino acid found in proteins. The term 'Fmoc' stands for fluoren-9-ylmethoxycarbonyl, which is a protective group that is commonly used in peptide synthesis. Fmoc-7-methyl-DL-tryptophan is a white crystalline powder that is soluble in organic solvents such as dimethylformamide and dimethyl sulfoxide. Uses: Fmoc-7-methyl-dl-tryptophan has a wide range of applications in various scientific experiments. it is commonly used in peptide synthesis and as a building block for the synthesis of various bioactive peptides. the compound is also used in drug discovery and development, as well as in the study of protein-protein interactions. Additional or Alternative Names: N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-7-methyltryptophan. Product Category: Amino Acids. CAS No. 138775-53-8. Molecular formula: C27H24N2O4. Mole weight: 440.5. Purity: Peak Area by HPLC ≥95%. IUPACName: 2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-(7-methyl-1H-indol-3-yl)propanoic acid. Canonical SMILES: CC1=C2C(=CC=C1)C(=CN2)CC(C(=O)O)NC(=O)OCC3C4=CC=CC=C4C5=CC=CC=C35. Density: 1.3±0.1 g/cm3. Product ID: ACM138775538. Alfa Chemistry ISO 9001:2015 Certified. | |
| Fmoc-Arg(Me)2-OH (asymmetrical) | Fmoc-Arg(Me)2-OH is a peptide derivative that consists of two methylated arginines (Me) with an N-terminal Fluorenylmethyloxycarbonyl (Fmoc) group. The Fmoc group is a protective group that is commonly used in peptide synthesis to protect the N-terminus of amino acids from unwanted reactions. Arginine is an amino acid that plays an essential role in protein synthesis, and its importance in biological functions has been well established. The introduction of the Me modification to the arginine molecule has led to significant developments in peptide synthesis. Uses: Fmoc-arg(me)2-oh has various applications in scientific research. this compound is commonly used in peptide synthesis and has been found to be useful in the preparation of various peptides such as antimicrobial peptides and peptide hormones. fmoc-arg(me)2-oh is also used as a substrate in enzymatic assays and as a modifier in protein labeling. Product Category: Amino Acids. CAS No. 268564-10-9. Molecular formula: C23H28N4O4. Mole weight: 424.5. Purity: Peak Area by HPLC ≥95%. IUPACName: (2S)-5-[[amino(dimethylamino)methylidene]amino]-2-(9H-fluoren-9-ylmethoxycarbonylamino)pentanoic acid. Canonical SMILES: CN(C)C(=NCCCC(C(=O)O)NC(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13)N. Density: 1.28 g/mL at 20 °C(lit.). Product ID: ACM268564109-1. Alfa Chemistry ISO 9001:2015 Certified. Categories: Fmoc-ADMA hydrochloride salt. | |
| Fmoc-D-propargylglycine | Fmoc-D-propargylglycine is an amino acid derivative that is commonly used in peptide synthesis. Peptides are short chains of amino acids that are linked together by peptide bonds. They play a critical role in many biological processes, including hormone regulation, enzyme catalysis, and immune response. Fmoc-D-propargylglycine is a non-natural amino acid derivative that is commonly used as a building block in peptide synthesis due to its high reactivity and versatility. Uses: Fmoc-d-propargylglycine has a wide range of potential applications in scientific experiments. it is commonly used as a building block in peptide synthesis and has been investigated for its potential as an inhibitor of protein-protein interactions. it has also been studied for its potential therapeutic applications in various diseases, including cancer and alzheimer's disease. Product Category: Amino Acids. CAS No. 220497-98-3. Molecular formula: C20H17NO4. Mole weight: 335.4. Purity: Peak Area by HPLC ≥95%. IUPACName: (2R)-2-(9H-fluoren-9-ylmethoxycarbonylamino)pent-4-ynoic acid. Canonical SMILES: C#CCC(C(=O)O)NC(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13. Density: 1.3±0.1 g/cm3. Product ID: ACM220497983. Alfa Chemistry ISO 9001:2015 Certified. | |
| Fmoc-L-(2,6-di-Me)Tyr-OH | Fmoc-2,6-dimethyl-L-tyrosine is a derivative of L-tyrosine, which is one of the 20 naturally occurring amino acids. It is an acronym for 9-Fluorenylmethyloxycarbonyl-2,6-dimethyltyrosine. Fmoc-2,6-dimethyl-L-tyrosine is also referred to as fluorenylmethoxycarbonyl-2,6-dimethyltyrosine or Fmoc-Dmt-OH. Fmoc-Dmt-OH has a molecular weight of 393.45 and a molecular formula of C23H21NO5. Uses: Fmoc-2,6-dimethyl-l-tyrosine has several research applications, including the synthesis of peptides, proteins, and peptidomimetics. it is also used as a building block of combinatorial libraries for the discovery of new drug candidates. fmoc-2,6-dimethyl-l-tyrosine has been incorporated into various bioactive peptides and proteins to improve their stability, activity, and specificity. it has also been used as a precursor for the synthesis of novel peptidomimetics with potential therapeutic applications. Additional or Alternative Names: N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-2,6-dimethyl-L-tyrosine, Fmoc-2,6-dimethyl-L-tyrosine, (S)-N-Fmoc-2,6-Dimethyltyrosine. Product Category: Amino Acids. CAS No. 206060-54-0. Molecular formula: C26H25NO5. Mole weight: 431.5. Purity: Peak Area by HPLC ≥95%. IUPACName: (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-(4-hydroxy-2,6-dimethylphenyl)propanoic acid. Canonical SMILES: CC1=CC(=CC(=C1CC(C(=O)O)NC(=O)OCC2C3=CC=CC=C3C4=CC=CC=C24)C)O. Density: 1.290 g/cm3. Product ID: ACM206060540. Alfa Che | |
| Fmoc-L-beta -homoalanine | Fmoc-L-beta-homoalanine is a modified form of the amino acid beta-homoalanine, which is naturally found in certain fungi, algae, and invertebrates. It is primarily used as a building block for solid-phase peptide synthesis (SPPS) due to its ability to form stable amide bonds. Fmoc-L-beta-homoalanine is also a useful tool in the study of peptide-protein interactions, as it can serve as a non-natural amino acid substitute. Uses: Fmoc-l-beta-homoalanine has a range of applications in scientific experiments, particularly in the fields of peptide synthesis and drug discovery. it can be used as a building block for the synthesis of various peptides, including antimicrobial peptides and peptidomimetics. it has also been investigated as a potential drug candidate for various diseases, including cancer and infectious diseases. Additional or Alternative Names: Fmoc--HoAla-OH, Fmoc-Beta-HoAla-OH, Fmoc-β-homoalanine, Fmoc-β-HomoAla-OH. Product Category: Amino Acids. CAS No. 193954-26-6. Molecular formula: C19H19NO4. Mole weight: 325.4. Purity: Peak Area by HPLC ≥95%. IUPACName: (3S)-3-(9H-fluoren-9-ylmethoxycarbonylamino)butanoic acid. Canonical SMILES: CC(CC(=O)O)NC(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13. Density: 1.255 g/cm3. Product ID: ACM193954266-1. Alfa Chemistry ISO 9001:2015 Certified. Categories: (3S)-3-({[(9H-FLUOREN-9-YL)METHOXY]CARBONYL}AMINO)BUTANOIC ACID. | |
| Fmoc-L-selenomethionine | Fmoc-selenomethionine can be introduced under standard conditions. Any selenoxide formed during synthesis can be easily reduced back to selenide by treatment with β-mercaptoethanol. Introduction of selenium can help facilitate solid phase and solution structural determination and the study of peptide-protein interactions. Uses: Fmoc solid-phase peptide synthesis. Additional or Alternative Names: Fmoc-selenomethionine, N-Fmoc-L-amino-4-(methylselanyl)butanoic acid. Product Category: Amino Acids. CAS No. 1217852-49-7. Molecular formula: C20H21NO4Se. Mole weight: 418.4. Purity: Peak Area by HPLC ≥95%. Product ID: ACM1217852497. Alfa Chemistry ISO 9001:2015 Certified. | |
| Fmoc-Lys(Boc)-OH (1-13C) | L-Lysine N-Fmoc/Boc (1-13C) is a protected amino acid used to synthesize isotope-labeled peptides for MS-based protein quantitation. Uses: Biomolecular nmr, proteomics. Additional or Alternative Names: N-α-Fluorenylmethoxycarbonyl-N-ε-tert-butoxycarbonyl-L-lysine. Product Category: Amino Acids. CAS No. 1242058-72-5. Molecular formula: Boc-NH(CH2)4CH(NH-Fmoc)13COOH. Mole weight: 469.5. Purity: Peak Area by HPLC ≥95%. ECNumber: 276-256-4 (Unlabeled). Product ID: ACM1242058725-1. Alfa Chemistry ISO 9001:2015 Certified. | |
| Fmoc-Nalpha-methyl-L-norvaline | FMOC-Lys(Mtt)-OH is a derivative of lysine and is widely used in the field of chemistry and biochemistry. It is a white crystalline powder with a molecular weight of 545.66 g/mol. The compound is composed of two parts; the FMOC group and the Lys(Mtt) group. The FMOC group is a protecting group while the Lys(Mtt) group is a side chain of the amino acid lysine. The compound is commonly used as a building block in solid-phase peptide synthesis and a reagent for protein labeling for mass spectrometry. Uses: Fmoc-lys(mtt)-oh has diverse applications in different scientific experiments. the compound is commonly used as a building block in solid-phase peptide synthesis, a reagent for protein labeling for mass spectrometry, and a protective group for amino acids. the compound has also been used in the synthesis of natural products and bioactive peptides. Additional or Alternative Names: (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)pentanoic acid, FMOC-Lys(Mtt)-OH. Product Category: Amino Acids. CAS No. 252049-05-1. Molecular formula: C21H23NO4. Mole weight: 353.4. Purity: Peak Area by HPLC ≥95%. IUPACName: (2S)-2-[9H-fluoren-9-ylmethoxycarbonyl(methyl)amino]pentanoic acid. Canonical SMILES: CCCC(C(=O)O)N(C)C(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13. Density: 1.2±0.1 g/cm3. Product ID: ACM252049051-1. Alfa Chemistry ISO 9001:2015 Certified. | |
| Fmoc-Nalpha-methyl-N-im-trityl-L-histidine | Fmoc-nalpha-methyl-n-im-trityl-l-histidine (FMOC-His(Trt)-OH) is a derivative of the amino acid Histidine. It is used as a building block for the synthesis of peptides and proteins. Histidine is a non-polar, essential amino acid involved in many biological processes such as the biosynthesis of proteins, metal ion binding, and catalysis in enzyme reactions. FMOC-His(Trt)-OH contains a 9-fluorenylmethyloxycarbonyl (Fmoc) protecting group on the amino terminus and a trityl (Trt) protecting group on the imidazole nitrogen. Uses: Fmoc-his(trt)-oh is mainly used as a starting material for the synthesis of peptides and proteins. it is used in spps for the incorporation of histidine residues in the peptide sequence. the resulting peptides and proteins have various applications in scientific experiments, including drug discovery and development, vaccine development, and biological research. Additional or Alternative Names: FMOC-His(Trt)-OH. Product Category: Amino Acids. CAS No. 1217840-61-3. Molecular formula: C41H35N3O4. Mole weight: 633.7. Purity: Peak Area by HPLC ≥95%. IUPACName: (2S)-2-[9H-fluoren-9-ylmethoxycarbonyl(methyl)amino]-3-(1-tritylimidazol-4-yl)propanoic acid. Canonical SMILES: CN(C(CC1=CN(C=N1)C(C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4)C(=O)O)C(=O)OCC5C6=CC=CC=C6C7=CC=CC=C57. Density: 1.2±0.1 g/cm3. Product ID: ACM1217840613. Alfa Chemistry ISO 9001:2015 Certified. | |
| Fmoc-NH-(PEG)10-CH2CH2COOH | Fmoc-NH-PEG10-CH2CH2COOH is a derivative of polyethylene glycol (PEG) that has been modified with a terminal carboxylic acid group and a base-labile 9-Fluorenylmethoxycarbonyl (Fmoc) protecting group. PEG is a biocompatible and highly hydrophilic polymer that is widely used in various biomedical applications due to its excellent solubility, low toxicity, and resistance to protein binding. The addition of a carboxylic acid group to PEG improves its water solubility and allows for conjugation to amino-containing molecules, such as peptides or proteins. The Fmoc protecting group is widely used in solid-phase peptide synthesis to protect the N-terminal amine group of amino acids from undesired side reactions during chain assembly. Uses: Fmoc-nh-peg10-ch2ch2cooh has a wide range of applications in scientific experiments, including drug delivery, diagnostics, and imaging. its hydrophilic and biocompatible nature makes it an ideal polymer for the synthesis of nanoparticles or micelles that can carry hydrophobic drugs and improve their solubility and bioavailability in biological systems. its carboxylic acid group can also be used fo. Additional or Alternative Names: 1-(9H-Fluoren-9-yl)-3-oxo-2,7,10,13,16,19,22,25,28,31,34-undecaoxa-4-azaheptatriacontan-37-oic acid. Product Category: Amino Acids. CAS No. 2101563-45-3. Molecular formula: C38H57NO14. Mole weight: 751.8. Purity: Peak Area by HPLC ≥95%. IUPACName: 3-[2- | |
| Fmoc-PEG2-Suc-OH | N-(Fmoc-8-amino-3,6-dioxa-octyl)succinamic acid is a synthetic molecule that belongs to the group of succinamic acids. Succinamic acids are organic molecules that have two carboxylic acid groups and an amide group linked to a cyclic structure. N-(Fmoc-8-amino-3,6-dioxa-octyl)succinamic acid is a modified succinamic acid that has an Fmoc (9-fluorenylmethyloxycarbonyl) protecting group attached to the amino group. The Fmoc group protects the amino group during synthesis, and it can be removed under mild conditions to expose the amino group for further functionalization. This property makes N-(Fmoc-8-amino-3,6-dioxa-octyl)succinamic acid a valuable building block for the synthesis of other molecules, such as peptides and proteins. Uses: N-(fmoc-8-amino-3,6-dioxa-octyl)succinamic acid has various applications in scientific experiments, particularly in the synthesis of peptides and proteins. the molecule can be used as a building block for the preparation of various peptides and proteins, such as fmoc-protected peptides, hydrogels, and bioconjugates. Additional or Alternative Names: N-(Fmoc-8-amino-3,6-dioxa-octyl)succinamic acid, 1-(9H-Fluoren-9-yl)-3,14-dioxo-2,7,10-trioxa-4,13-diazaheptadecan-17-oic acid, Fmoc-PEG-SU. Product Category: Amino Acids. CAS No. 613245-91-3. Molecular formula: C25H30N2O7. Mole weight: 470.5. Purity: Peak Area by HPLC ≥95%. IUPACName: 4-[2-[2-[2-(9H-fluoren-9-ylmethoxycarbonylamino)ethoxy]etho | |
| L-Valine-d8 | Labeled analogue of L-Vailne. L-Valine is an essential amino acid and one of 20 proteinogenic amino acids. L-Valine cannot be manufactured by the body and must be acquired through diet or supplementation. L-valine is found in grains, dairy products, mushrooms, meats, peanuts and soy proteins. L-Valine has been used in studies to attenuate arrhythmias and induce hypotensive effects. Group: Biochemicals. Alternative Names: (+)-2-Amino-3-methylbutyric Acid-d8; (2S)-2-Amino-3-methylbutanoic Acid-d8; (S)-2-Amino-3-methylbutanoic Acid-d8; (S)-Valine-d8; (S)-α-Amino- β-methylbutyric Acid-d8; L-(+)-α-Aminoisovaleric Acid-d8; L-α-Amino- β-methylbutyric Acid-d8; NSC 76038-d8. Grades: Highly Purified. CAS No. 35045-72-8. Pack Sizes: 5mg. US Biological Life Sciences. |  Worldwide |
| Native Arachis hypogaea (peanut) Phospholipase D | Phospholipase D is a phospholipid hydrolyzing enzyme and an important component of receptor-mediated signal transduction responses and regulated secretion. Hydrolyzes the phosphate bonds of phospholipids and sphingomyelin to give the corresponding phosphatidic acid. Phospholipase D is involved in conferring drought susceptibility in peanuts, which increases the risk of aflatoxin contamination. Phospholipase d is a phospholipid hydrolyzing enzyme and an important component of receptor-mediated signal transduction responses and regulated secretion. Applications: Research has shown adp-ribosylation factor regulation of phospholipase d is important in the release of nascent secretory vesicles from the trans-golgi network. it has also been used in a study to investigate stimulation of na+-ca2+ exchange activity in canine cardiac sarcolemmal vesicals. Group: Enzymes. Synonyms: Phospholipase D; EC 3.1.4.4; lipophosphodiesterase II; lecithinase D; choline phosphatase; PLD; 9001-87-0. Enzyme Commission Number: EC 3.1.4.4. CAS No. 9001-87-0. PLD. Activity: > 60 units/mg protein. Storage: -20°C. Form: Partially purified, lyophilized powder containing buffer salts. Source: Arachis hypogaea (peanut). Phospholipase D; EC 3.1.4.4; lipophosphodiesterase II; lecithinase D; choline phosphatase; PLD; 9001-87-0. Cat No: NATE-0594. | |
| Native Bovine Malic Dehydrogenase | Malic dehydrogenase (MDH) exists as two isoforms within eukaryotic cells, one that is expressed in the mitochondria and functions in the TCA cycle and one in the cytoplasm that converts malate from the mitochondria back into oxaloacetate. Malic dehydrogenase from bovine heart contains a histidine residue at the nad-binding active site which is critical for activity. when this histidine is mutated a loss in activity is observed. Applications: Malic dehydrogenase has been used in a study to assess a flow injection system for on-line monitoring of fumaric acid in biological pr ocesses. 1 it has also been used in a study to investigate a root-knot nematode parasitizing peanut in...001-64-3. Enzyme Commission Number: EC 1.1.1.37. CAS No. 9001-64-3. MDH. Activity: 2000-4000 units/mg protein (modified Warburg-Christian). Storage: 2-8°C. Form: ammonium sulfate suspension; Suspension in 3 M (NH4)2SO4-0.01 M KH2PO4 solution, pH 7.3. Source: Bovine heart. Species: Bovine. malic dehydrogenase; L-malate dehydrogenase; NAD-L-malate dehydrogenase; malic acid dehydrogenase; NAD-dependent malic dehydrogenase; NAD-malate dehydrogenase; NAD-malic dehydrogenase; malate (NAD) dehydrogenase; NAD-dependent malate dehydrogenase; NAD-specific malate dehydrogenase; NAD-linked malate dehydrogenase; MDH; L-malate-NAD+ oxidoreductase; EC 1.1.1.37; 9001-64-3. Cat No: NATE-0445. | |
| Native Human Antistreptolysin O | Streptolysin is a hemolysin produced by group A streptococci. In an infected individual streptolysin O acts as a protein antigen, and the patient mounts an antibody response. A rise in anti-streptolysin O level begins about 1 week after infection and peaks 2-3 weeks later. In the absence of complications or reinfection, the anti-streptolysin O ASO titer will usually fall to preinfection levels within 6-12 months. Both clinical and laboratory findings should be correlated in reaching a diagnosis. Streptococcal infections are caused by bacteria known as Streptococcus. There are several disease-causing strains of streptococci (groups A, B, C, D, and G), which are identified by t... antibody tests are useful for group A streptococci. Group A streptococci are the most virulent species for humans and are the cause of strep throat, tonsillitis, wound and skin infections, blood infections (septicemia), scarlet fever, pneumonia, rheumatic fever, Sydenham's chorea (formerly called St. Vitus' dance), and glomerulonephritis. Group: Enzymes. Synonyms: Anti-streptolysin O; ASO; ASLO. Purity: Purified. ASO. Activity: > 500 IU/mL. Stability: 2 years. Appearance: Free of hemolysis and particulates. Storage: 2-8°C. Form: Liquid; 0.2 micron filtered, 0.09% sodium azide, pH 7.0-7.2. Source: Human Plasma. Species: Human. Anti-streptolysin O; ASO; ASLO. Cat No: NATE-0948. | |
| Peanut peptide | Peanut peptide is a small molecule active peptide product prepared from peanut protein or peanut meal by enzymatic hydrolysis. Peanut protein is rich in amino acids, containing eight kinds of essential amino acids needed by the human body, belonging to the complete protein, the small molecule peptide prepared after enzymatic hydrolysis, easier to absorb. Product ID: CDF4-0253. Category: Protein peptide. Product Keywords: Protein Peptides; Peanut peptide; CDF4-0253; Protein peptide;. Applications: It is widely used in food, medicine, cosmetics and other fields. Product Description: Peanut peptide is light yellow powder or granular product; Good solubility; Strong stability. | |
| PI230 | PI230 is an antimicrobial peptide found in Pisum sativum (Garden pea), and has antimicrobial activity. Synonyms: Defensin-like protein 230. Grades: >98%. |  |
| Rice Protein | Rice protein is considered to be a good food protein, which is in accordance with the ideal model of WHO/FAO. The biological value of rice protein is very high, its nutritional value is high, and it can be compared with eggs, milk and beef. In addition, rice protein is a low resistance to the original protein, will not produce allergic reaction, the production of infant food is very favorable. Applications: Rice protein, it can be used in vegetable protein beverages (peanut milk, wheat milkand walnut milk, etc.), health food & beverages and sausages based on its goodwater-solubility. it can also be used to increase protein content and stabilize quality in the milk powder processing (infant & student formula milk powder and milk powder for the middle-aged and senior) field. Group: Others. Purity: >80% Protein. Appearance: Light yellow fine powder. Rice Protein. Cat No: EXTC-217. | |
| (S)-N-Fmoc-2-(4'-pentenyl)glycine | Fmoc-Lys(Boc)-OH is a chemical compound that belongs to the amino acid family. It is commonly used in the synthesis of peptides and proteins in various scientific experiments. The Fmoc group is a temporary protective group used to protect the amine group of lysine, while the Boc (tert-butoxycarbonyl) group is used to protect the amine group of the alpha amino acid. Fmoc-Lys(Boc)-OH is an important building block for the synthesis of peptides and proteins. Uses: Fmoc-lys(boc)-oh is widely used in peptide and protein synthesis. it can be used in the synthesis of various peptides with potential applications in drug discovery, such as antimicrobial peptides and anticancer peptides. Additional or Alternative Names: (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)hept-6-enoic acid, Fmoc-Lys(Boc)-OH. Product Category: Amino Acids. CAS No. 856412-22-1. Molecular formula: C22H23NO4. Mole weight: 365.4. Purity: Peak Area by HPLC ≥95%. IUPACName: (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)hept-6-enoic acid. Canonical SMILES: C=CCCCC(C(=O)O)NC(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13. Density: 1.3±0.1 g/cm3. Product ID: ACM856412221-1. Alfa Chemistry ISO 9001:2015 Certified. | |
| Soy protein | Soy protein is a protein that is isolated from soybean. Soya protein is made from soybean meal that has been dehulled and defatted. Dehulled and defatted soybeans are processed into three kinds of high protein commercial products.Soy protein is a vegetable protein. Amino acid composition of soybean protein and milk protein is similar, in addition to methionine slightly lower, the rest of the essential amino acid content are more abundant, is a plant of the full protein, in nutritional value, can be equated with animal protein, the gene structure is also the most close to human amino acids, so it is the most nutritious vegetable protein. Applications: 1. it can be used to raise the yield of meat products.2. it can be added to such solid drinks as oatmeal, coffee mate, soy milk powder peanut milk powder, cocoa milk powder, walnut milk powder, fermented yogurt, juice milk powder, etc. 3. it can also be added to cold drinks (such as ice cream) to reduce the production costs. Group: Others. Appearance: Light yellow powder. Soy protein. Cat No: EXTC-218. | |
| Triclabendazole | Triclabendazole(CGA89317) is a benzimidazole, it binds to tubulin impairing intracellular transport mechanisms and interferes with protein synthesis.Target: Microtubule/TubulinTriclabendazole treatment produces percentage decreases of the fluke egg output by 15.3%, 4.3% and 36.6%, respectively, in sheep, dairy cows and heifers, these results indicate the presence of TCBZ-resistant Fasciola hepatica in sheep and cattle on this farm. Triclabendazole sulphoxide (50 mg/mL) results in extensive damage to the tegument of triclabendazole-susceptible F. hepatica, whereas triclabendazole-resistant flukes shows only localized and relatively minor disruption of the tegument covering the spines.Triclabendazole is metabolized into a number of compounds, depending on the route of administration, plasma levels peak at 18-24 hours (Triclabendazole sulphoxide) and 36-48 hours (Triclabendazole sulphone), neither Triclabendazole nor any toher metabolites can be detected in plasma. Triclabendazole sulphoxide blocks the transport of secretory bodies from the cell body to the tegumental surface, the block occurs at the site of their formation by the Golgi complex in the cell body, in their movement through the cytoplasmic connections to the syncytium, and in their movement from the base to the apex of the syncytium. Triclabendazole binds to the colchicine binding site on the β-tubulin molecule and this has been used at the basis for evalu | |
| uracilylalanine synthase | The enzyme produces the non-proteinogenic amino acid L-willardiine, which is naturally found in the plants Acacia willardiana, Mimosa pigra, and Pisum sativum (pea). The enzyme from Pisum species also produces L-isowillardiine. Not identical with EC 2.5.1.47 cysteine synthase. Group: Enzymes. Synonyms: O3-acetyl-L-serine acetate-lyase (adding uracil); isowillardiine synthase; willardiine synthase; 3-O-acetyl-L-serine:uracil 1-(2-amino-2-carboxyethyl)transferase; O3-acetyl-L-serine:uracil 1-(2-amino-2-carboxyethyl)transferase. Enzyme Commission Number: EC 2.5.1.53. CAS No. 113573-73-2. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2790; uracilylalanine synthase; EC 2.5.1.53; 113573-73-2; O3-acetyl-L-serine acetate-lyase (adding uracil); isowillardiine synthase; willardiine synthase; 3-O-acetyl-L-serine:uracil 1-(2-amino-2-carboxyethyl)transferase; O3-acetyl-L-serine:uracil 1-(2-amino-2-carboxyethyl)transferase. Cat No: EXWM-2790. | |
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