Find where to buy products from suppliers in the USA, including: distributors, industrial manufacturers in America, bulk supplies and wholesalers of raw ingredients & finished goods.
Search for products or services, then visit the American suppliers website for prices, SDS or more information. You can also view suppliers in Australia, NZ or the UK.
| Product | Description | |
|---|---|---|
| Ro 51 | Ro 51 is a potent and selective dual antagonist of purinoceptor subtypes P2X3 and P2X2/3 (IC50 values are 2 and 5 nM for rP2X3 and hP2X2/3 respectively), without significant activity on other P2X receptors (IC50 values are > 10 μM for P2X1, P2X2, P2X4, P2X5, and P2X7). P2X3 and P2X2/3 have been shown to play a pivotal role in models of various pain conditions making Ro 51 a potential option in the treatment of pain. Synonyms: 2-[[4-Amino-5-[5-iodo-4-methoxy-2-(1-methylethyl)phenoxy]-2,4-pyrimidinyl]amino]-1,3-propanediol; Ro51; Ro-51; CHEMBL494161; 1050670-85-3; SCHEMBL4970553. Grades: ≥98% by HPLC. CAS No. 1050670-85-3. Molecular formula: C17H23IN4O4. Mole weight: 474.29. |  |
| Ro 51 | Ro 51 is a potent and selective dual antagonist of purinoceptor subtypes P2X3 and P2X2/3. P2X3 and P2X2/3 have been shown to play a pivotal role in models of various pain conditions making Ro 51 a potential option in the treatment of pain. Group: Biochemicals. Alternative Names: 2-[[4-Amino-5-[5-iodo-4-methoxy-2-(1-methylethyl)phenoxy]-2-pyrimidinyl]amino]-1,3-propanediol; RO-51. Grades: Highly Purified. CAS No. 1050670-85-3. Pack Sizes: 10mg. US Biological Life Sciences. |  Worldwide |
| Arabinofuranosidase 51A from Clostridium thermocellum, Recombinant | Alpha-N-arabinofuranosidase is an enzyme with system name alpha-L-arabinofuranoside arabinofuranohydrolase. This enzyme catalyses the following chemical reaction: Hydrolysis of terminal non-reducing alpha-L-arabinofuranoside residues in alpha-L-arabinosides. The enzyme acts on alpha-L-arabinofuranosides, alpha-L-arabinans containing (1,3)- and/or (1,5)-linkages, arabinoxylans and arabinogalactans. Group: Enzymes. Synonyms: non-reducing end alpha-L-arabinofuranosidase; alp. Enzyme Commission Number: EC 3.2.1.55. CAS No. 9067-74-7. Purity: >90% by SDS-PAGE. α-L-Arabinofuranosidase. Mole weight: 58.7 kDa. Activity: 125 U/mg. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Clostridium thermocellum. non-reducing end alpha-L-arabinofuranosidase; alpha-L-arabinofuranoside non-reducing end alpha-L-arabinofuranosidase; EC 3.2.1.55; arabinosidase; alpha-arabinosidase; alpha-L-arabinosidase; alpha-arabinofuranosidase; polysaccharide alpha-L-arabinofuranosidase; alpha-L-arabinofuranoside hydrolase; L-arabinosidase; alpha-L-arabinanase; Alpha-N-arabinofuranosidase; α-L-Arabinofuranosidase; Arabinofuranosidase 51A. Cat No: NATE-1324. |  |
| Arabinofuranosidase 51A from Podospora anserina, Recombinant | Alpha-N-arabinofuranosidase is an enzyme with system name alpha-L-arabinofuranoside arabinofuranohydrolase. This enzyme catalyses the following chemical reaction: Hydrolysis of terminal non-reducing alpha-L-arabinofuranoside residues in alpha-L-arabinosides. The enzyme acts on alpha-L-arabinofuranosides, alpha-L-arabinans containing (1,3)- and/or (1,5)-linkages, arabinoxylans and arabinogalactans. Group: Enzymes. Synonyms: non-reducing end alpha-L-arabinofuranosidase; alpha-L-arabinofuranoside non-reducin. Enzyme Commission Number: EC 3.2.1.55. CAS No. 9067-74-7. Purity: >90% by SDS-PAGE. α-L-Arabinofuranosidase. Mole weight: 86 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Podospora anserina. non-reducing end alpha-L-arabinofuranosidase; alpha-L-arabinofuranoside non-reducing end alpha-L-arabinofuranosidase; EC 3.2.1.55; arabinosidase; alpha-arabinosidase; alpha-L-arabinosidase; alpha-arabinofuranosidase; polysaccharide alpha-L-arabinofuranosidase; alpha-L-arabinofuranoside hydrolase; L-arabinosidase; alpha-L-arabinanase; Alpha-N-arabinofuranosidase; α-L-Arabinofuranosidase; Arabinofuranosidase 51A. Cat No: NATE-1317. | |
| RO5126766 | RO5126766, also known as CH5126766, is a protein kinase inhibitor specific for the Raf and MEK mitogen-activated protein kinases (MAPKs) with potential anti-neoplastic activity. Raf/MEK dual kinase Inhibitor RO5126766 specifically inhibits the kinase activities of Raf and MEK, resulting in the inhibition of of target gene transcription that promotes malignant transformation of cells. Both Raf and MEK are serine/threonine-specific kinases that respond to extracellular stimuli, such as mitogens, and are involved in the regulation of cellular processes, such as gene expression, mitosis, differentiation, and apoptosis. Synonyms: RO5126766; RO 5126766; RO-5126766; CH5126766; CH-5126766; CH 5126766. Grades: >98%. CAS No. 946128-88-7. Molecular formula: C21H18FN5O5S. Mole weight: 471.463. | |
| RO5166017 | RO5166017 is a highly potent, selective, and orally active agonist for the trace amine-associated receptor 1(TAAR1) with no significant activity at other targets. It is weak and rapidly metabolized (endogenous ligands). It has strong pharmacological activity at other targets. Uses: Ro5166017 has strong pharmacological activity. Synonyms: RO5166017; RO 5166017; RO-5166017; (4S)-4-[(N-ethylanilino)methyl]-4,5-dihydro-1,3-oxazol-2-amine;RO-5166017;(S)-4-[(ethyl-phenyl-amino)-methyl]-4,5-dihydro-oxazol-2-ylamine. Grades: >98 %. CAS No. 1048346-74-2. Molecular formula: C12H17N3O. Mole weight: 219.29. | |
| 1, 10-Phenanthroline monohydrate | 1,10-Phenanthroline is a classic chelating bidentate ligand for transition metal ions that has played an important role in the development of coordination chemistry. It is an inhibitor of metallopeptidases. Uses: Chelating agents. Synonyms: Phenanthroline monohydrate; 1,10-phenanthroline hydrate. Grades: ≥98%. CAS No. 5144-89-8. Molecular formula: C12H8N2·H2O. Mole weight: 198.22. | |
| 1,2,3,6-Tetra-O-pivaloyl-a-D-galactofuranoside | 1,2,3,6-Tetra-O-pivaloyl-α-D-galactofuranoside, a pivotal compound widely utilized in the biomedical industry, plays a crucial role as a synthetic intermediary for the advancement of groundbreaking pharmaceuticals aiming at diverse ailments. Boasting remarkable versatility, this compound exhibits promise in combating cancer, neurodegenerative afflictions, and inflammation-induced maladies. Synonyms: 1,2,3,6-TETRA-O-PIVALOYL-ALPHA-D-GALACTOFURANOSIDE; 3W6JGY33Z7; 1,2,3,6-Tetra-O-pivaloyl-a-D-galactofuranoside; alpha-D-Galactofuranose, 1,2,3,6-tetrakis(2,2-dimethylpropanoate); (2R,3R,4S,5S)-5-((R)-1-Hydroxy-2-(pivaloyloxy)ethyl)tetrahydrofuran-2,3,4-triyl tris(2,2-dimethylpropanoate); [(2R)-2-hydroxy-2-[(2S,3S,4R,5R)-3,4,5-tris(2,2-dimethylpropanoyloxy)oxolan-2-yl]ethyl] 2,2-dimethylpropanoate; ((2R)-2-Hydroxy-2-((2S,3S,4R)-3,4,5-tris(2,2-dimethylpropanoyloxy)oxolan-2-yl)ethyl)2,2-dimethylpropanoate; [(2R)-2-hydroxy-2-[(2S,3S,4R)-3,4,5-tris(2,2-dimethylpropanoyloxy)oxolan-2-yl]ethyl]2,2-dimethylpropanoate; UNII-3W6JGY33Z7; SCHEMBL4618517. CAS No. 220017-49-2. Molecular formula: C26H44O10. Mole weight: 516.62. | |
| 1,2-Di-O-tert-butyldimethylsilyl-3,4:5,6-di-O-isopropylidene-D-glycero-a-D-talopyranoside | 1,2-Di-O-tert-butyldimethylsilyl-3,4:5,6-di-O-isopropylidene-D-glycero-a-D-talopyranoside is a significant entity in the field of biomedicine, playing a role in the research of disease-targeting pharmaceuticals. Molecular formula: C25H51O7Si2. Mole weight: 519.85. | |
| 1,3-Dimethylparabanic Acid | Chronic exposure to 1,3-Dimethylparabanic Acid can cause inhibition of growth population on rotifers while algae seems to be unaffected. Furthermore, 1,3-Dimethylparabanic Acid is a derivative of Caffeine (C080100). Group: Biochemicals. Grades: Highly Purified. CAS No. 5176-82-9. Pack Sizes: 40mg, 80mg. Molecular Formula: C5H6N2O3, Molecular Weight: 142.11. US Biological Life Sciences. | Worldwide |
| 1-Chloro-2-deoxy-3,5-di-O-p-nitrobenzoyl-D-ribofuranose | 1-Chloro-2-deoxy-3,5-di-O-p-nitrobenzoyl-D-ribofuranose, an indispensable compound in the field of biomedicine, emerges as a cornerstone. Its paramount significance lies in its involvement in the formulation of therapeutics targeting a myriad of ailments. By participating in the synthesis of nucleosides and nucleotides, integral to antiviral and anticancer treatments, this compound assumes a pivotal role. CAS No. 51841-98-6. Molecular formula: C19H15ClN2O9. Mole weight: 450.78. | |
| 1-Deoxy-D-ribose | 1-Deoxy-D-ribose is a vital product extensively utilized in the biomedicine industry. It plays a significant role in the synthesis of nucleotides, DNA, and RNA, thus contributing to genetic material integrity and stability. Furthermore, it is involved in various physiological processes and is utilized as a therapeutic agent in the treatment of certain rare genetic disorders and diseases related to nucleotide metabolism. Synonyms: 1,4-Anhydro-L-ribitol. CAS No. 51607-76-2. Molecular formula: C5H10O4. Mole weight: 134.2. | |
| (1R,2S)-anti-Nicotine N'-Oxide Hydrate | (1R,2S)-anti-Nicotine N'-Oxide Hydrate is the hydrate form of (1R,2S)-anti-Nicotine N'-Oxide (CAS 51020-67-8) which is a Nicotine derivative (N412420), found in the leaves, stems, and roots of N. tabacum, N. affinis and N. sylvestris. Nicotine-1-N-oxide has also been identified as a metabolite of nicotine in animals and in man. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg, 2.5mg. Molecular Formula: C10H14N2O; H2O. US Biological Life Sciences. | Worldwide |
| 2,3-Butanediol | 2,3-Butanediol, is occurring naturally in cocoa butter, in the roots of Ruta graveolens, sweet corn, and in rotten mussels. It is used in the resolution of carbonyl compounds in gas chromatography. Group: Biochemicals. Grades: Highly Purified. CAS No. 513-85-9. Pack Sizes: 10g, 25g. Molecular Formula: C4H10O2. US Biological Life Sciences. | Worldwide |
| 2',3'-Dideoxyinosine-5'-monophosphate triethylammonium salt | 2',3'-dideoxyinosine-5'-monophosphate triethylammonium salt (DDI 5'-MP-TEA) serves a pivotal role in combating pervasive viral infections like HIV. Functioning as a potent nucleoside analog, it orchestrates an orchestrated inhibition of viral replication, consequently achieving a substantial reduction in viral load. Synonyms: Didanosine 5'-monophosphate sodium salt. Molecular formula: C22H43N6O6P. Mole weight: 518.60. | |
| 2,4,7,8,9-Penta-O-acetyl N-acetylneuraminic acid | 2,4,7,8,9-Penta-O-acetyl N-acetylneuraminic acid, also known as the vital compound in the biomedical sector, plays a pivotal role. This compound finds widespread application in crafting anti-influenza medications and therapeutically addressing specific illnesses. Its exceptional antiviral attributes make it a potent inhibitor of influenza virus replication within host cells. Synonyms: N-Acetylneuraminic acid 2,4,7,8,9-pentaacetate. CAS No. 4887-11-0. Molecular formula: C21H29NO14. Mole weight: 519.45. | |
| 2,4,7,8-Tetra-O-acetyl-9-azido-9-deoxy-N-acetylneuraminic acid methyl ester | 2,4,7,8-Tetra-O-acetyl-9-azido-9-deoxy-N-acetylneuraminic acid methyl ester is a novel synthetic analog of sialic acid. Primarily used in biomedical research, it aids in investigating the role of sialic acid in various diseases including cancer and neurodegenerative disorders. CAS No. 219814-64-9. Molecular formula: C20H28N4O12. Mole weight: 516.46. | |
| 2',7'-Dichlorofluorescein | 2',7'-Dichlorofluorescein. CAS No. 76-54-0. Product ID: CDC10-0131. Molecular formula: C20H10O5Cl2. Category: Cosmetic Color Additives. Product Keywords: Cosmetic Ingredients; Cosmetic Color Additives; 2',7'-Dichlorofluorescein; CDC10-0131; 76-54-0; C20H10O5Cl2; 200-968-6; MFCD00005047; 76-54-0. Purity: ~90% (TLC). Color: Orange to red-brown, Powder. EC Number: 200-968-6. Physical State: Crystalline. Solubility: ethanol: 25 mg/mL. Quality Level: 200. Storage: room temp. Application: 2',7'-Dichlorofluorescein has been used as an oxidation-sensitive fluorescent probe to measure ROS (reactive oxygen species) formation in cells. Boiling Point: 514.77°C (rough estimate). Melting Point: 280 °C (dec.) (lit.). Density: 0.79 g/cm3. Product Description: 2',7'-Dichlorofluorescein is an oxidation-sensitive fluorescent probe. 2'7'-dichlorofluorescein diacetate is oxidized to 2'7'-dichlorofluorescein in the presence of ROS (reactive oxygen species).citation. |  |
| 2-Acetamido-2-deoxy-6-a-O-sialyl-D-galactopyranose | 2-Acetamido-2-deoxy-6-a-O-sialyl-D-galactopyranose, a compound utilized in the realm of biomedical research and pharmaceutical advancement, assumes a pivotal role in the exhaustive investigation of the intricate nature and performance of sialylated glycoproteins. Synonyms: 6-O-a-Sialyl-2-acetamido-2-deoxy-D-galactopyranose. CAS No. 72506-87-7. Molecular formula: C19H32N2O14. Mole weight: 512.46. | |
| 2-Amino-6-chloro-[(4-methylphenyl)thio]-9-(2',3',5'-tri-O-acetyl-β-D-ribofuranosyl)purine | 2-Amino-6-chloro-[(4-methylphenyl)thio]-9-(2',3',5'-tri-O-acetyl-β-D-ribofuranosyl)purine is an immensely robust biomedicine, frequently harnessed to delve into the intricacies of adenosine receptors, purine metabolism is as well as antiviral treatment modalities. Synonyms: 6-S-(4-Methylphenyl)-6-thio-guanosine 2',3',5'-Triacetate. Grades: 95%. CAS No. 135041-23-5. Molecular formula: C23H25N5O7S. Mole weight: 515.54. | |
| (2 β, 3α, 5α, 16 β,17 β)-2,16-di-1-Pyrrolidinylandrostane-3,17-diol 3,17-Diacetate | (2 β, 3α, 5α, 16 β,17 β)-2,16-di-1-Pyrrolidinylandrostane-3,17-diol 3,17-Diacetate is an impuritiy of Rocuronium bromide (R639500), an aminosteroid and a competitive neuromuscular blocker. Group: Biochemicals. Grades: Highly Purified. CAS No. 1190105-62-4. Pack Sizes: 5mg, 25mg. Molecular Formula: C31H50N2O4, Molecular Weight: 514.74. US Biological Life Sciences. | Worldwide |
| 2'-Deoxyxanthosine 5'-monophosphate | 2'-Deoxyxanthosine 5'-monophosphate is a pivotal compound within the biomedical sector, holds immense value in examining nucleotide metabolism and the enzymatic reactions fundamental to DNA research and development. With an inherent significance in investigations concerning cancer and genetic disorders, this compound assuming the role of a precursor in the creation of nucleosides and nucleotides, hence facilitating nucleic acid analysis and the advancement of pharmaceuticals. Synonyms: [(2R,3S,5R)-5-(2,6-dioxo-3H-purin-9-yl)-3-hydroxyoxolan-2-yl]methyl dihydrogen phosphate; 5'-Xanthylic acid,2'-deoxy. CAS No. 5187-90-6. Molecular formula: C10H13N4O8P. Mole weight: 348.21. | |
| 2'-O-Methyl-5-methyluridine 5'-triphosphate | 2'-O-Methyl-5-methyluridine 5'-triphosphate is a pivotal element for studying the captivating realm of RNA modifications. Profoundly influencing diverse cellular processes, this exquisite modified nucleotide assuming a paramount role in unraveling the enigmatic function of methylated RNA. As a versatile substrate for RNA-modifying enzymes, it unleashes unprecedented opportunities to scrutinize mesmeric methyltransferase activities and decode the multifaceted impact of this modification on the intricate structure and myriad functions of RNA. Synonyms: (((2R,3R,4R,5R)-3-Hydroxy-4-methoxy-5-(5-methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)tetrahydrofuran-2-yl)methyl)triphosphoric acid. CAS No. 444789-41-7. Molecular formula: C11H19N2O15P3. Mole weight: 512.19. | |
| (2R,3R,4S)-2-(Acetoxymethyl)-5-((2-amino-7-benzyl-6-hydroxy-7H-purin-9(8H)-yl)methyl)tetrahydrofuran-3,4-diyl diacetate | (2R,3R,4S)-2-(Acetoxymethyl)-5-((2-amino-7-benzyl-6-hydroxy-7H-purin-9(8H)-yl)methyl)tetrahydrofuran-3,4-diyl diacetate is an intricate chemical compound, harboring potential for combating viral afflictions. Originating from the vast purine family, this derivative plays frequent roles in antiviral therapeutics research, particularly aiming its molecular machinery towards RNA viruses. Synonyms: (2R,3R,4S)-2-(acetoxymethyl)-5-((2-amino-7-benzyl-6-hydroxy-7H-purin-9(8H)-yl)methyl)tetrahydrofuran-3,4-Diyl sodium diacetate. Molecular formula: C24H29N5O8. Mole weight: 515.52. | |
| 3,3',5-Triiodo Thyroacetic Acid | 3,3',5-Triiodo Thyroacetic Acid. Uses: For analytical and research use. Group: Impurity standards. CAS No. 51-24-1. Pack Sizes: 1G. IUPAC Name: 2-[4-(4-hydroxy-3-iodophenoxy)-3,5-diiodophenyl]acetic acid. Molecular formula: C14H9I3O4. Mole weight: 621.93. Catalog: APS51241A. SMILES: OC(=O)Cc1cc(I)c(Oc2ccc(O)c(I)c2)c(I)c1. Format: Neat. Shipping: Room Temperature. |  |
| 3-Methyladenine | 3-Methyladenine is an autophagy inhibitor that protects cerebellar granule cells (CGCs) from apoptosis following serum/potassium deprivation. 3-Methyladenine inhibits phosphoinositide 3-kinase (PI3K) activity, which plays a key role in autophagy process. Synonyms: NSC 66389; NSC-66389; NSC66389; 6-Amino-3-methylpurine; 3-MA; 3H-Purin-6-amine, 3-methyl-; 3-Methyl Adenine; 3-Methyl-6-aminopurine; N3-Methyladenine. Grades: ≥98% by HPLC. CAS No. 5142-23-4. Molecular formula: C6H7N5. Mole weight: 149.15. | |
| 4,7,8,9-Tetra-O-acetyl-N-acetyl-2-deoxy-2-fluoro-b-D-neuraminic acid allyl ester | 4,7,8,9-Tetra-O-acetyl-N-acetyl-2-deoxy-2-fluoro-b-D-neuraminic acid allyl ester is an imperative compound widely employed in the development of pharmaceuticals, specifically those targeting neuraminidase enzymes and associated molecular pathways. This compound plays a crucial role in drug development for diverse diseases pertaining to neuraminic acid metabolism. CAS No. 98712-63-1. Molecular formula: C22H30FNO12. Mole weight: 519.47. | |
| 4-Cyano-4-pentylbiphenyl | 4-Cyano-4-pentylbiphenyl. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 1'-biphenyl]-4-carbonitrile,4'-pentyl-[;1'-Biphenyl]-4-carbonitrile,4'-pentyl-[1;4'-pentyl-biphenyl-4-carbonitrile;4-cyano-4'-pentyldiphenyl;4-Pentyl[1,1-biphenyl]-4-carbonitrile;CB5;p-Cyano-p'-pentylbiphenyl;RO-CM-5115. Product Category: Organic & Printed Electronics. Appearance: liquid crystal (nematic). CAS No. 40817-08-1. Molecular formula: C18H19N. Mole weight: 249.35. Density: 1.008g/mL at 25°C(lit.). Product ID: ACM40817081. Alfa Chemistry ISO 9001:2015 Certified. Categories: 4-Cyano-4'-pentylbiphenyl. |  |
| 4-Hexyl-4-biphenylcarbonitrile | 4-Hexyl-4-biphenylcarbonitrile. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 1,1-Biphenyl, 4-cyano-4-hexyl-;1'-Biphenyl)-4-carbonitrile,4'-hexyl-(1;1'-biphenyl]-4-carbonitrile,4'-hexyl-[;4-Hexyl[1,1-biphenyl]-4-carbonitrile;4-n-hexyl-4'-cyanobiphenyl;K18;RO-CM-5118;TIMTEC-BB SBB008608. Product Category: Organic & Printed Electronics. CAS No. 41122-70-7. Molecular formula: C19H21N. Mole weight: 263.38. Purity: 0.96. IUPACName: 4-(4-hexylphenyl)benzonitrile. Canonical SMILES: CCCCCCC1=CC=C(C=C1)C2=CC=C(C=C2)C#N. Density: 1.02g/cm³. ECNumber: 255-228-5. Product ID: ACM41122707. Alfa Chemistry ISO 9001:2015 Certified. | |
| 4-Thio-methyl-UTP | 4-Thio-methyl-UTP is an intricate compound commonly employed in the realm of investigative research and diagnostics. This distinctive altered nucleotide analog effortlessly integrates into RNA throughout transcription, bestowing itself as a paramount instrument for scrutinizing DNA research and development and RNA alterations. Notably, it showcases exceptional utility in delving into the significant role that precise nucleotides play in influencing the intricate facets of RNA's structural composition and functional behavior. Synonyms: 4-Thio-methyl-uridine-5'-triphosphate, Sodium salt. Grades: ≥ 95% by HPLC. Molecular formula: C10H17N2O14P3S (free acid). Mole weight: 514.23 (free acid). | |
| 5-Carboxy-2'-deoxyuridine-5'-Triphosphate | 5-Carboxy-2'-deoxyuridine-5'-Triphosphate is a potent and versatile nucleotide analog employed in meticulous research and extensive investigations related to DNA sequencing and labeling. Its phenomenal attributes enable seamless integration into the genomic structure with the aid of polymerase chain reaction (PCR) or DNA synthesis processes, subsequently opening a plethora of detection techniques. The robust and dynamic properties of this nucleotide analog have been pivotal in unravelling complex and critical mechanisms behind cancer and viral diseases. Synonyms: 5-Carboxy-dUTP; 5-cadUTP. Grades: ≥95% by AX-HPLC. Molecular formula: C10H15N2O16P3. Mole weight: 512.15. | |
| 5-hme-CTP | 5-hme-CTP, a nucleotide analog, has been found to selectively activate purinergic P2Y1 receptors, thereby enhancing biomedical research efforts aimed at uncovering cellular signaling pathways relevant to diverse biological phenomena such as platelet activation. Given its multifaceted role, it comes as no surprise that beyond being a great tool for scientific inquiry, 5-hme-CTP holds great potential for therapeutic interventions in diseases associated with compromised cellular function, such as stroke, multiple sclerosis, and Alzheimer's disease. Synonyms: 5-Hydroxymethylcytidine-5'-Triphosphate; 5-hm-CTP; 5-HmCTP; 5-Hydroxymethyl-CTP; 5-(Hydroxymethyl)cytidine 5'-triphosphoric acid. Grades: ≥90% by AX-HPLC. Molecular formula: C10H18N3O15P3. Mole weight: 513.18. | |
| 5-Methoxy-CTP | 5-Methoxy-CTP is a pharmaceutical compound that plays a crucial role in treating certain cancers through chemotherapy. As a derivative of CTP, it targets the replication process of cancer cells, ultimately leading to their destruction. Its potent anti-cancer properties make it a vital component of many chemotherapy treatments. Synonyms: 5-Methoxycytidine-5'-Triphosphate; 5-moCTP. Grades: ≥95% by AX-HPLC. Molecular formula: C10H18N3O15P3. Mole weight: 513.18. | |
| 5-Methoxyuridine 5'-triphosphate | 5-Methoxyuridine 5'-triphosphate is a vital component used in the biomedical industry for various applications serving as a key building block in the research and development of RNA molecules for research purposes. Additionally, it plays a significant role in studying RNA post-transcriptional modifications and RNA labeling techniques. Its incorporation supports investigations related to drug discovery, gene expression profiling and disease understanding. Synonyms: 5-Methoxy-UTP; 5-OMe-UTP; [[(2R,3S,4R,5R)-3,4-dihydroxy-5-(5-methoxy-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl] phosphono hydrogen phosphate. CAS No. 847649-65-4. Molecular formula: C10H17N2O16P3. Mole weight: 514.17. | |
| 5'-O-TBDMS-2'-deoxyadenosine | 5'-O-TBDMS-2'-deoxyadenosine, a synthetic nucleoside derivative, utilized in the manufacturing of anti-cancer agents and antiviral drugs. It also plays a crucial role in gene therapy research and gene expression analyses as an oligonucleotide synthesizing agent. Moreover, this exceptional compound boasts of its remarkable metabolic stability, and is renowned for its potent DNA polymerase and reverse transcriptase inhibitory effects. Synonyms: 5'-O-TBDMS-dA; Adenosine, 2'-deoxy-5'-O-[(1,1-dimethylethyl)dimethylsilyl]-; 5'-O-(tert-Butyldimethylsilyl)-2'-deoxyadenosine; (2R, 3S, 5R) -5- (6-Amino-9H-purin-9-yl) -2- ( ( (tert-butyldimethylsilyl) oxy) methyl) tetrahydrofuran-3-ol; 2'-Deoxy-5'-O-[dimethyl(2-methyl-2-propanyl)silyl]adenosine. Grades: ≥97% by HPLC. CAS No. 51549-30-5. Molecular formula: C16H27N5O3Si. Mole weight: 365.51. | |
| 6Beta-Hydroxy Norethindrone | 6Beta-Hydroxy Norethindrone. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: Norethisterone Imp. H (EP), 6beta-Hydroxynorethisterone,6beta,17-Dihydroxy-19-nor-17alpha-pregn-4-en-20-yn-3-one. CAS No. 51724-44-8. Pack Sizes: 10MG. IUPAC Name: (6R,8R,9S,10R,13S,14S,17R)-17-ethynyl-6,17-dihydroxy-13-methyl-1,2,6,7,8,9,10,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthren-3-one. Molecular formula: C20H26O3. Mole weight: 314.42. Catalog: APS51724448A. SMILES: C[C@]12CC[C@H]3[C@@H](C[C@@H](O)C4=CC(=O)CC[C@H]34)[C@@H]1CC[C@@]2(O)C#C. Format: Neat. Shipping: Room Temperature. | |
| 6-Chloropurine-2'-deoxyriboside-5'-Triphosphate | 6-Chloropurine-2'-deoxyriboside-5'-Triphosphate is a crucial recompound, serving as a substrate for DNA polymerases aiding in the research and development of modified nucleotides. This compound plays a vital role in studying DNA and RNA structure, replication and repair mechanisms. Its utility extends to investigating various diseases like cancer, genetic disorders and viral infections, providing insights into their molecular mechanisms. Synonyms: 6-Cl-purine-drTP. Grades: ≥95% by AX-HPLC. Molecular formula: C10H14N4O12P3Cl. Mole weight: 510.60. | |
| 7-b,17-a-Dimethyl-5-b-androstane-3-a,17-b-diol glucuronide | 7-b,17-a-Dimethyl-5-b-androstane-3-a,17-b-diol glucuronide is a vital compound playing a crucial role in the research of hormone-related disorders, particularly those involving impaired androgen metabolism. Molecular formula: C27H43O8.Na. Mole weight: 518.62. | |
| 9-cis-Retinal | 9-cis-Retinal is a natural retinoid. Dietary 9-cis-β-carotene generates 9-cis-retinoids via cleavage into 9-cis-retinal. 9-cis Retinal binds to cellular retinol-binding protein-I (CRBP-I) and CRBP-II with K d s of 8 nM and 5 nM, respectively. 9-cis-Retinal expedites differentiation and maturation of rod photoreceptors in retinal organoids [1] [2] [3]. Uses: Scientific research. Group: Natural products. CAS No. 514-85-2. Pack Sizes: 1 mg; 5 mg. Product ID: HY-W009310. |  |
| Abietic | Abietic. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Rosin Acid. Product Category: Chlorinated Phenol and Resin Acids Standards. CAS No. 514-10-3. Molecular formula: C20H30O2. Mole weight: 302.45. Purity: 90-95%. Product ID: ACM514103-1. Alfa Chemistry ISO 9001:2015 Certified. Categories: Abietic acid. | |
| Abietic Acid | Abietic Acid is the primary component of resin acid found commonly in rosin. Abietic Acid exhibited potent testosterone 5α-reductase inhibitory activity in vitro. Group: Biochemicals. Alternative Names: (1R, 4aR, 4bR, 10aR)-1, 2, 3, 4, 4a, 4b, 5, 6, 10, 10a-Decahydro-1, 4a-dimethyl-7-(1-methylethyl)-1-phenanthrenecarboxylic Acid; 13-Isopropylpodocarpa-7,13-dien-15-oic Acid; (-)-Abietic Acid; 7,13-Abietadien-18-oic Acid; Abietic Acid; NSC 25149; Odomit B 10; Sylvic Acid; ZAO; l-Abietic Acid. Grades: Highly Purified. CAS No. 514-10-3. Pack Sizes: 25g. US Biological Life Sciences. | Worldwide |
| Abietic Acid, >95% | Abietic Acid is the primary component of resin acid found commonly in rosin. Abietic Acid exhibited potent testosterone 5α-reductase inhibitory activity in vitro. Group: Biochemicals. Grades: Highly Purified. CAS No. 514-10-3. Pack Sizes: 10mg, 25mg. Molecular Formula: C20H30O2. US Biological Life Sciences. | Worldwide |
| α-Galactosidase 4A from Bacillus halodurans, Recombinant | Alpha-galactosidase is a glycoside hydrolase enzyme that hydrolyses the terminal alpha-galactosyl moieties from glycolipids and glycoproteins. It is encoded by the GLA gene. Two recombinant forms of alpha-galactosidase are called agalsidase alfa (INN) and agalsidase beta (INN). Group: Enzymes. Synonyms: Alpha-Galactosidase; Galactosidase; EC 3.2.1.22; GLA; GALA; melibiase; α-D-galactosidase; α-galactosidase A; α-galactoside galactohydrolase. Enzyme Commission Number: EC 3.2.1.22. CAS No. 9025-35-8. Purity: >90% by SDS-PAGE. GLA. Mole weight: 51.8 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Bacillus halodurans. Alpha-Galactosidase; Galactosidase; EC 3.2.1.22; GLA; GALA; melibiase; α-D-galactosidase; α-galactosidase A; α-galactoside galactohydrolase; α-Galactosidase 27A. Cat No: NATE-1404. | |
| α-Mannosidase 125A from Clostridium perfringens, Recombinant | α-Mannosidase is an acid hydrolase which is located in plant vacuoles and is thought to be involved with the turnover of N-linked glycoproteins. α-Mannosidase has been shown to inhibit the proliferation of B-lymphocytes. Group: Enzymes. Synonyms: alpha-D-mannosidase; alpha-mannosidase; alpha-D-mannoside mannohydrolase; α-D-Mannosidase; EC 3.2.1.24; 9025-42-7. Enzyme Commission Number: EC 3.2.1-. Purity: >90% by SDS-PAGE. Mannosidase. Mole weight: 51.8 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Clostridium perfringens. alpha-D-mannosidase; alpha-mannosidase; alpha-D-mannoside mannohydrolase; α-D-Mannosidase; EC 3.2.1.-; α-Mannosidase 125A. Cat No: NATE-1472. | |
| α-Mannosidase 125A from Streptococcus pneumoniae, Recombinant | α-Mannosidase is an acid hydrolase which is located in plant vacuoles and is thought to be involved with the turnover of N-linked glycoproteins. α-Mannosidase has been shown to inhibit the proliferation of B-lymphocytes. Group: Enzymes. Synonyms: alpha-D-mannosidase; alpha-mannosidase; alpha-D-mannoside mannohydrolase; α-D-Mannosidase; EC 3.2.1.24; 9025-42-7. Enzyme Commission Number: EC 3.2.1-. Purity: >90% by SDS-PAGE. Mannosidase. Mole weight: 51.1 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Streptococcus pneumoniae. alpha-D-mannosidase; alpha-mannosidase; alpha-D-mannoside mannohydrolase; α-D-Mannosidase; EC 3.2.1.-; α-Mannosidase 125A. Cat No: NATE-1473. | |
| Angiotensin A | Angiotensin A is a potent endogenous vasoconstrictor octapeptide. It is a derivative of angiotensin II (Ang II) that differs from Ang II in having alanine instead of aspartic acid as the first amino acid. It shows similar affinity for AT1 and AT2 receptors as angiotensin II with Ki values of 1.6 and 2.3 nM in vitro. It causes pressor and renal vasoconstrictor effects in rodents by the AT1 receptor. It is inhibited by Candesartan but not by AT2 receptor ligands in vivo. It also increases inositol phosphate accumulation with a similar potency to Ang II with EC50 value of 6.7 nM. Synonyms: Ala-Angiotensin III; H-Ala-Arg-Val-Tyr-Ile-His-Pro-Phe-OH; Ang A; Angiotensin II, 1-L-alanine-5-L-isoleucine-; L-alanyl-L-arginyl-L-valyl-L-tyrosyl-L-isoleucyl-L-histidyl-L-prolyl-L-phenylalanine. Grades: ≥95%. CAS No. 51833-76-2. Molecular formula: C49H71N13O10. Mole weight: 1002.18. | |
| Avapritinib | BLU-285 is a potent and selective inhibitor of exon 17 mutant KIT (IC50 = 0.27 nM for KIT D816V). BLU-285 showed dose-dependent, robust anti-tumor efficacy in a TKI-resistant KIT exon 11/17 mutant GIST PDX model through inhibition of tumor growth, proliferation, KIT signaling and induction of apoptosis. Synonyms: (1S)-1-(4-fluorophenyl)-1-[2-[4-[6-(1-methylpyrazol-4-yl)pyrrolo[2,1-f][1,2,4]triazin-4-yl]piperazin-1-yl]pyrimidin-5-yl]ethanamine; BLU-285; BLU 285; BLU285; UNII-513P80B4YJ; SCHEMBL16652297. CAS No. 1703793-34-3. Molecular formula: C26H27FN10. Mole weight: 498.56. | |
| Avutometinib | Avutometinib (Ro 5126766) is a first-in-class dual MEK / RAF inhibitor that allosterically inhibits BRAF V600E , CRAF , MEK , and BRAF (IC 50 : 8.2, 56, 160 nM, and 190 nM, respectively). Uses: Scientific research. Group: Signaling pathways. Alternative Names: Ro 5126766; CH5126766. CAS No. 946128-88-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-18652. | |
| Basmisanil | Basmisanil is a highly selective inverse agonist/negative allosteric modulator GABAAα5 receptors. It was developed by Roche to treat cognitive impairment associated with Down syndrome. In Apr 2016, Roche completed the phase II in Down syndrome (In adolescents, In adults) in USA, Argentina, Canada, France, Italy, Mexico, New Zealand, Singapore, Spain and the UK. In Sep 2016, Phase-II clinical trials in Neurological disorders (In adults, In the elderly) in Spain was on going. Uses: Down syndrome; neurological disorders. Synonyms: (1,1-dioxidothiomorpholino)(6-((3-(4-fluorophenyl)-5-methylisoxazol-4-yl)methoxy)pyridin-3-yl)methanone; RG 1662; RG-1662; RG1662; RO5186582; RO-5186582; RO 5186582. Grades: 98%. CAS No. 1159600-41-5. Molecular formula: C21H20FN3O5S. Mole weight: 445.47. | |
| Batatasin I | Batatasin I is a natural product that can be isolated from tuberous roots of Dioscorea batatas, with antifungal activity and anti-inflammatory effects. Uses: Designed for use in research and industrial production. Product Category: Inhibitors. Appearance: Powder. CAS No. 51415-00-0. Molecular formula: C17H16O4. Mole weight: 284.31. Purity: 0.98. IUPACName: 2,5,7-trimethoxyphenanthren-3-ol. Canonical SMILES: COC1=CC(=C2C(=C1)C=CC3=CC(=C(C=C32)O)OC)OC. Product ID: ACM51415000-1. Alfa Chemistry ISO 9001:2015 Certified. | |
| Benzyl 2-acetamido-3,6-di-O-benzoyl-2-deoxy-a-D-galactopyranoside | Benzyl 2-acetamido-3,6-di-O-benzoyl-2-deoxy-a-D-galactopyranoside is a valuable compound used in biomedicine. It is commonly utilized in the synthesis of glycolipids and glycosaminoglycans, playing a crucial role in various pharmaceutical applications. This compound exhibits potential antiviral and anticancer activities, making it a promising candidate for drug development to treat viral infections and certain types of cancer. Synonyms: [(2R,3R,4R,5R,6S)-5-Acetamido-4-benzoyloxy-3-hydroxy-6-phenylmethoxyoxan-2-yl]methyl benzoate; alpha-D-Galactopyranoside, phenylmethyl 2-(acetylamino)-2-deoxy-, 3,6-dibenzoate;Benzyl 2-Acetamido-3,6-di-O-benzoyl-2-deoxy-?-D-galactopyranoside; Benzyl 2-Acetamido-3,6-di-O-benzoyl-2-deoxy- alpha -D-galactopyranoside; Benzyl 2-acetamido-3,6-di-O-benzoyl-2-deoxy-alpha-D-galactopyranoside?. CAS No. 141019-70-7. Molecular formula: C29H29NO8. Mole weight: 519.54. | |
| beta-Lac-TEG-Alkyne | beta-Lac-TEG-Alkyne is a valuable tool in biomedicine for studying the role of beta-lactamase enzymes in drug resistance. It is widely used in drug discovery and development to identify and characterize new inhibitors for treating antibiotic-resistant bacterial infections. This compound serves as a crucial link in the design and synthesis of potential novel antibiotics, ultimately combating drug resistance and improving patient outcomes. Molecular formula: C21H36O14. Mole weight: 512.5. | |
| BMS 903452 | G-protein-coupled receptor 119 agonists can stimulate glucose-dependent insulin release by direct action in the pancreas and promote secretion of the incretin GLP-1 by action in the gastrointestinal tract. BMS-903452 is a selective G-protein-coupled receptor 119 (GRP119) agonist and it is efficacious in both acute and chronic in vivo rodent models of diabetes. Till now, no development was reported for the treatment of Type 2 diabetes mellitus using BMS-903452. Uses: Type 2 diabetes mellitus. Synonyms: BMS-903452; BMS 903452; BMS903452; 5-chloro-4-((1-(5-chloropyrimidin-2-yl)piperidin-4-yl)oxy)-1-(2-fluoro-4-(methylsulfonyl)phenyl)pyridin-2(1H)-one. Grades: 98%. CAS No. 1339944-47-6. Molecular formula: C21H19Cl2FN4O4S. Mole weight: 513.37. | |
| Briciclib sodium | Briciclib, also known as ON 013105 or ON 014185, is a benzyl styryl sulfone analog, and a disodium phosphate ester prodrug of ON 013100, with potential antineoplastic activity. Upon hydrolysis, cyclin D modulator ON 013105 is converted to ON 013100, which blocks cyclin D mRNA translation and decreases protein expression of cyclin D. This may induce cell cycle arrest and apoptosis in cancer cells overexpressing cyclin D and eventually decrease tumor cell proliferation. This agent may exhibit synergistic antitumor activity in combination with other chemotherapeutic agents. Cyclin D, a member of the cyclin family of cell cycle regulators, plays a key role in cell cycle division and is often overexpressed in a variety of hematologic and solid tumors and is correlated with poor prognosis. Synonyms: ON-013105; ON013105; ON 013105; ON 014185; ON014185; ON-014185. Grades: >98%. CAS No. 865784-01-6. Molecular formula: C19H21Na2O10PS. Mole weight: 518.38. | |
| Calcium Saccharin | Calcium Saccharin. Synonyms: Calcium benzosulphimide; Saccharin Calcium; Calcium o-benzosulfimide; Calciumo-benzosulphimide; Calcium 2-benzosulphimide. CAS No. 6485-34-3. Product ID: PE-0500. Molecular formula: C14H8CaN2O6S·3(1/2)H2O. Mole weight: 467.48. Category: Sweetening agent. Product Keywords: Pharmaceutical Excipients; Excipients for Solid Dosage Form; Calcium Saccharin; Sweeteners Excipients; Sweetening agent; C14H8CaN2O6S·3(1/2)H2O; 6485-34-3; 6485-34-3. UNII: 5101OP7P2I. Administration route: Oral. Dosage Form: Syrups and solutions. Source and Preparation: Saccharin reacts with half equivalent calcium hydroxide in water medium to form calcium salt, concentrates the reaction liquid to crystallization, and then dries. Safety: Limit: FDA and USDA rules, same as "saccharin". Toxicity: ADI 0-5 (Total ADI of saccharin and its salts; FAO/WHO, 2001). | |
| Cellulose propionate | Cellulose propionate. Group: Natural polymers and biopolymers. Alternative Names: Cellulose,acetatepropanoate; CELLULOSE PROPIONATE; CELLULOSE ACETATE PROPIONATE; CELLULOSE ACETATE PROPIONATE, 42.5 WT. %PROPIONYL CONTENT, AVE. MN CA. 15,000; CELLULOSE ACETATE PROPIONATE, 46 WT. % P ROPIONYL CONTENT, AVE. MN CA. 75,000; CELLULOSE ACETATE PRO. CAS No. 9004-39-1. Product ID: 2-(hydroxymethyl)-6-[4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxyoxane-3,4,5-triol; [4,5,6-triacetyloxy-3-[3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxyoxan-2-yl]methyl acetate; [4,5,6-tri(propanoyloxy)-3-[3,4,5-tri(propanoyloxy)-6-(propanoyloxymethyl)oxan-2-yl]oxyoxan-2-yl]methyl propanoate. Molecular formula: 1811.7g/mol. Mole weight: C76H114O49. CCC (=O)OCC1C (C (C (C (O1)OC (=O)CC)OC (=O)CC)OC (=O)CC)OC2C (C (C (C (O2)COC (=O)CC)OC (=O)CC)OC (=O)CC)OC (=O)CC. CC (=O)OCC1C (C (C (C (O1)OC (=O)C)OC (=O)C)OC (=O)C)OC2C (C (C (C (O2)COC (=O)C)OC (=O)C)OC (=O)C)OC (=O)C. C (C1C (C (C (C (O1)OC2C (OC (C (C2O)O)O)CO)O)O)O)O. InChI=1S/C36H54O19. C28H38O19. C12H22O11/c1-9-21 (37)45-17-19-29 (49-23 (39)11-3)31 (50-24 (40)12-4)34 (53-27 (43)15-7)36 (48-19)55-30-20 (18-46-22 (38)10-2)47-35 (54-28 (44)16-8)33 (52-26 (42)14-6)32 (30)51-25 (41)13-5; 1-11 (29)37-9-19-21 (39-13 (3)31)23 (40-14 (4)32)26 (43-17 (7)35)28 (46-19)47-22-20 (10-38-12 (2)30)45-27 (44-18 (8)36)25 (42-16 (6)34)24 (22)41-15 (5)33; 13-1-3-5 (15)6 (16)9 (19)12 (22-3)23-10-4 (2-14)21 |  |
| CH5424802 Hydrochloride | CH5424802 Hcl (AF 802 Hcl; Alectinib Hcl) is a potent ALK inhibitor with IC50 of 1.9 nM, sensitive to L1196M mutation. Synonyms: Alectinib Hydrochloride; AF-802 Hydrochloride; CH-5424802 Hydrochloride; RG-7853 Hydrochloride; RO-5424802 Hydrochloride; AF 802 Hydrochloride; CH 5424802 Hydrochloride; RG 7853 Hydrochloride; RO 5424802 Hydrochloride; AF802 Hydrochloride; CH5424802 Hydrochloride; RG7853 Hydrochloride; RO5424802 Hydrochloride. Grades: >98%. CAS No. 1256589-74-8. Molecular formula: C30H35ClN4O2. Mole weight: 519.08. | |
| Chitinase 18A from Bacillus cereus, Recombinant | Chitosanase catalyzes the endohydrolysis of β (1,4) linkages between N-acetyl-D-glucosamine and D-glucosamine residues in partially deacetylated chitosan. Chitosanase from Streptomyces griseus is capable of hydrolyzing both chitosan and carboxymethyl cellulose. It is used for the lysis of cell walls of fungi belonging to the group Mucorales. It is found in several types of microorganisms. Group: Enzymes. Synonyms: Chitosanase; EC 3.2.1.132; 51570-20-8; Chitosan N-acetylglucosaminohydrolase. Enzyme Commission Number: EC 3.2.1.14. Purity: >90% by SDS-PAGE. Chitosanase. Mole weight: 38.3 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Bacillus cereus. Chitosanase; EC 3.2.1.132; 51570-20-8; Chitosan N-acetylglucosaminohydrolase; Chitosanase 18A. Cat No: NATE-1377. | |
| Chitinase 18A from Bacillus licheniformis, Recombinant | Chitosanase catalyzes the endohydrolysis of β (1,4) linkages between N-acetyl-D-glucosamine and D-glucosamine residues in partially deacetylated chitosan. Chitosanase from Streptomyces griseus is capable of hydrolyzing both chitosan and carboxymethyl cellulose. It is used for the lysis of cell walls of fungi belonging to the group Mucorales. It is found in several types of microorganisms. Group: Enzymes. Synonyms: Chitosanase; EC 3.2.1.132; 51570-20-8; Chitosan N-acetylglucosaminohydrolase. Enzyme Commission Number: EC 3.2.1.14. Purity: >90% by SDS-PAGE. Chitosanase. Mole weight: 49.2 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Bacillus licheniformis. Chitosanase; EC 3.2.1.132; 51570-20-8; Chitosan N-acetylglucosaminohydrolase; Chitosanase 18A. Cat No: NATE-1378. | |
| Chitinase 18A from Clostridium thermocellum, Recombinant | Chitosanase catalyzes the endohydrolysis of β (1,4) linkages between N-acetyl-D-glucosamine and D-glucosamine residues in partially deacetylated chitosan. Chitosanase from Streptomyces griseus is capable of hydrolyzing both chitosan and carboxymethyl cellulose. It is used for the lysis of cell walls of fungi belonging to the group Mucorales. It is found in several types of microorganisms. Group: Enzymes. Synonyms: Chitosanase; EC 3.2.1.132; 51570-20-8; Chitosan N-acetylglucosaminohydrolase. Enzyme Commission Number: EC 3.2.1.14. Purity: >90% by SDS-PAGE. Chitosanase. Mole weight: 43.9 kDa. Activity: 25 U/mg. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Clostridium thermocellum. Chitosanase; EC 3.2.1.132; 51570-20-8; Chitosan N-acetylglucosaminohydrolase; Chitosanase 18A. Cat No: NATE-1379. | |
| Chitosanase 46A from Bacillus subtilis, Recombinant | Chitosanase catalyzes the endohydrolysis of β (1,4) linkages between N-acetyl-D-glucosamine and D-glucosamine residues in partially deacetylated chitosan. Chitosanase from Streptomyces griseus is capable of hydrolyzing both chitosan and carboxymethyl cellulose. It is used for the lysis of cell walls of fungi belonging to the group Mucorales. It is found in several types of microorganisms. Group: Enzymes. Synonyms: Chitosanase; EC 3.2.1.132; 51570-20-8; Chitosan N-acetylglucosaminohydrolase. Enzyme Commission Number: EC 3.2.1.132. CAS No. 51570-20-8. Purity: >90% by SDS-PAGE. Chitosanase. Mole weight: 29.5 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Bacillus subtilis. Chitosanase; EC 3.2.1.132; 51570-20-8; Chitosan N-acetylglucosaminohydrolase; Chitosanase 46A. Cat No: NATE-1376. | |
| Chitosanase 8B from Bacillus cereus, Recombinant | Chitosanase catalyzes the endohydrolysis of β (1,4) linkages between N-acetyl-D-glucosamine and D-glucosamine residues in partially deacetylated chitosan. Chitosanase from Streptomyces griseus is capable of hydrolyzing both chitosan and carboxymethyl cellulose. It is used for the lysis of cell walls of fungi belonging to the group Mucorales. It is found in several types of microorganisms. Group: Enzymes. Synonyms: Chitosanase; EC 3.2.1.132; 51570-20-8; Chitosan N-acetylglucosaminohydrolase. Enzyme Commission Number: EC 3.2.1.132. CAS No. 51570-20-8. Purity: >90% by SDS-PAGE. Chitosanase. Mole weight: 47.8 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Bacillus cereus. Chitosanase; EC 3.2.1.132; 51570-20-8; Chitosan N-acetylglucosaminohydrolase; Chitosanase 8B. Cat No: NATE-1375. | |
| Citicoline sodium | Citicoline sodium. Uses: For analytical and research use. Group: Pharma & vet compounds & metabolites; pharma & vet compounds & metabolites. Alternative Names: Gerolin, Strolin, Cytidine 5'-(trihydrogen diphosphate), P'-[2-(trimethylammonio)ethyl] ester, inner salt, monosodium salt (9CI), CerAxon, IP 302 sodium, Cebroton, Sinkron, Cidifos, Cytidine 5'-(trihydrogen diphosphate), P'-[2-(trimethylammonio)ethyl] ester, hydroxide, inner salt, monosodium salt, Flussorex, Neurotron, Citicoline sodium, Acticolin,Cytidine 5'-(trihydrogen diphosphate), P'-[2-(trimethylammonio)ethyl] ester, inner salt, sodium salt (1:1), Choline, hydroxide, monoester with cytidine 5'-(trihydrogen pyrophosphate), inner salt, monosodium salt (8CI), Brassel, Logan. CAS No. 33818-15-4. IUPAC Name: sodium;[[(2R,3S,4R,5R)-5-(4-amino-2-oxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-oxidophosphoryl] 2-(trimethylazaniumyl)ethyl phosphate. Molecular formula: C14H25N4O11P2.Na. Mole weight: 510.31. Catalog: APS33818154. SMILES: [Na+].C[N+](C)(C)CCOP(=O)([O-])OP(=O)([O-])OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N2C=CC(=NC2=O)N. Format: Neat. Shipping: Room Temperature. | |
| Danoprevir | Danoprevir(ITMN-191;R7227; RO5190591;RG7227) is a peptidomimetic inhibitor of the NS3/4A protease of hepatitis C virus (HCV) with IC50 of 0.2-3.5 nM, inhibition effect for HCV genotypes 1A/1B/4/5/6 is ~10-fold higher than 2B/3A. Synonyms: RG7227; RG 7227; RG-7227; ITMN191; ITMN-191; ITMN 191; RO5190591; RO-5190591; RO 5190591. Grades: 0.98. CAS No. 850876-88-9. Molecular formula: C35H46FN5O9S. Mole weight: 731.837. | |
| DB-cGMP | DB-cGMP, an exceedingly compelling analogue of cyclic guanosine monophosphate (cGMP), a pivotal secondary messenger in myriad biological processes, serves as an invaluable tool in biomedical research. With a primary focus on unraveling the intricate role of cGMP in signal transduction pathways, cellular proliferation, and apoptosis, it facilitates the understanding of diseases stemming from aberrant cGMP signaling. Synonyms: N2, 2'- O- Dibutyrylguanosine- 3', 5'- cyclic monophosphate, sodium salt. Grades: ≥ 97% by HPLC. CAS No. 51116-00-8. Molecular formula: C18H23N5O9P · Na. Mole weight: 507.4. | |
| Decitabine Impurity 1 (alpha-Isomer) | Decitabine Impurity 1 (alpha-Isomer) is a pharmacological compound serving as an impurity reference standard for decitabine, a compound primarily employed for the research of myelodysplastic syndrome (MDS) and acute myeloid leukemia (AML). It plays a crucial role in facilitating the identification and quantification of impurities present in decitabine formulations. Synonyms: Decitabine Impurity 1. Grades: > 95%. CAS No. 51255-17-5. Molecular formula: C6H12O4. Mole weight: 148.16. | |
| Diclofop-methyl | Diclofop-methyl, a common post-emergence herbicide, is widely used in agriculture production. Diclofop-methyl increases the proton permeability of isolated oat-root tonoplast [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 51338-27-3. Pack Sizes: 5 mg; 10 mg. Product ID: HY-136367. | |
| Diethylenetriaminepentaacetic acid | Diethylenetriaminepentaacetic acid. Synonyms: (Carboxymethylimino)bis (ethylenenitrilo)tetraacetic acid, N, N-Bis (2-[bis (carboxymethyl)amino]ethyl)glycine, DETAPAC, DTPA, Penta (carboxymethyl)diethylenetriamine, Pentetic acid. CAS No. 67-43-6. Pack Sizes: 5, 10, 50, 100 g in glass bottle. Product ID: CDC10-0103. Molecular formula: [(HOOCCH2)2NCH2CH2]2NCH2COOH. Category: Cosmetic Chelating Chemicals. Product Keywords: Cosmetic Ingredients; Cosmetic Chelating Chemicals; Diethylenetriaminepentaacetic acid; CDC10-0103; 67-43-6; [(HOOCCH2)2NCH2CH2]2NCH2COOH; Carboxymethylimino)bis (ethylenenitrilo)tetraacetic acid, N, N-Bis (2-[bis (carboxymethyl)amino]ethyl)glycine, DETAPAC, DTPA, Penta (carboxymethyl)diethylenetriamine, Pentetic acid; 200-652-8; MFCD00004289; 67-43-6. Purity: ≥99% (titration). Color: White to almost white. EC Number: 200-652-8. Physical State: Powder. Solubility: 1 M HCl: 50 mg/mL, clear, colorless. Quality Level: 200. Storage: room temp. Boiling Point: 517.84°C (rough estimate). Melting Point: 219-220 °C (lit.). Density: 1.56 g/cm3. Product Description: Diethylenetriaminepentaacetic acid is a diethylenetriaminepentaacetic anhydride, which is a bifunctional chelating agent. It is used for the treatment of poisoning. | |
| DL-threo-PPMP hydrochloride | DL-threo-PPMP is a ceramide analog that inhibits glucosylceramide synthase. It has been used to study the role of glucosylceramide synthase in cell growth, apoptosis, and autophagy. Synonyms: DL-threo-1-Phenyl-2-palmitoylamino-3-morpholino-1-propanol; DL-PPMP; BML3-D12; CTK8E7792. Grades: ≥98%. CAS No. 139974-41-7. Molecular formula: C29H50N2O3·HCl. Mole weight: 511.2. | |
| Dopamine | Dopamine is a catecholamine neurotransmitter that is produced in the substantia nigra, ventral tegmental area, and hypothalamus of the brain. Dopamine plays several important roles in the brain and body [1]. Dopamine acts through D2 dopamine receptor s to induce endocytosis of VEGFR2, which is critical for promoting angiogenesis [1]. Uses: Scientific research. Group: Natural products. Alternative Names: ASL279 free base. CAS No. 51-61-6. Pack Sizes: 10 mM * 1 mL; 10 mg. Product ID: HY-B0451. | |
Our database is helping our users find suppliers everyday.
