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| Product | Description | |
|---|---|---|
| CHIR 98014 | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. |  |
| CHIR-98014 | CHIR-98014 is a potent, cell-permeable GSK-3 inhibitor with IC50s of 0.65 and 0.58 nM for GSK-3? and GSK-3?, respectively; it shows less potent activities against cdc2 and erk2. Uses: Scientific research. Group: Signaling pathways. CAS No. 252935-94-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-13076. |  |
| CHIR-98014 | A glycogen synthase kinase-3 (GSK-3). Group: Biochemicals. Alternative Names: N6- [2- [ [4- (2, 4-Dichlorophenyl) -5- (1H-imidazol-2-yl) -2-pyrimidinyl] amino] ethyl] -3-nitro-2, 6-pyridinediamine. Grades: Highly Purified. CAS No. 556813-39-9. Pack Sizes: 5mg. US Biological Life Sciences. |  Worldwide |
| CHIR-98014 | CHIR-98014 is a GSK3 inhibitor with IC50 values of 0.65 nM and 0.58 nM for GSK-3α and GSK-3β respectively. It can activate Wnt/β-catenin pathway in mouse embryonic stem cells (mESCs). Synonyms: CHIR98014; 6-N-[2-[[4-(2,4-dichlorophenyl)-5-imidazol-1-ylpyrimidin-2-yl]amino]ethyl]-3-nitropyridine-2,6-diamine. Grades: >98%. CAS No. 252935-94-7. Molecular formula: C20H17Cl2N9O2. Mole weight: 486.31. |  |
| CHIR-98023 | CHIR-98023 is a glycogen synthase kinase 3 inhibitor developed for the treatment of Type 2 diabetes mellitus. Synonyms: N'-[4-(2,4-dichlorophenyl)-5-(1H-imidazol-2-yl)pyrimidin-2-yl]-N-(5-nitropyridin-2-yl)ethane-1,2-diamine; CHIR-98023; CHIR98023; CHIR 98023; CT-98023; UNII-CMQ1L0E91Y; CHIR-837. Grades: >98%. CAS No. 252916-76-0. Molecular formula: C20H16Cl2N8O2. Mole weight: 471.3. | |
| CHIR-98024 | CHIR98014 is a reversible, cell-permeable inhibitor of GSK3α and GSK3β (IC50 = 0.65 and 0.58 nM, respectively). It is inactive against a series of other serine/threonine or tyrosine kinases. Synonyms: CHIR98014; CHIR-98014; CHIR 98014; CT 98024; CT-98024; CT98024. Grades: 98%. CAS No. 556813-39-9. Molecular formula: C20H17Cl2N9O2. Mole weight: 486.31. | |
| CHIR99021 | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| CHIR-99021 | CHIR-99021 (CT99021) is a glycogen synthase kinase 3β (GSK3β) inhibitor that has antiproliferative activity in vitro and in vivo. It enhances reprogramming of mouse embryonic fibroblasts, transduced by Oct4 and Klf4 only, into iPSCs in combination with tranylcypromine. It also induces cardiomyocyte differentiation from human embryonic stem (ES). Uses: Potential antineoplastic agent. Synonyms: CHIR-99021; CT99021; 6-[2-[[4-(2,4-dichlorophenyl)-5-(5-methyl-1H-imidazol-2-yl)pyrimidin-2-yl]amino]ethylamino]pyridine-3-carbonitrile. Grades: >98%. CAS No. 252917-06-9. Molecular formula: C22H18Cl2N8. Mole weight: 465.342. | |
| CHIR-99021 | A potent and highly selective inhibitor of glycogen synthase kinase-3beta (GSK-3b) (IC50 = 6.7nM). CHIR99021 has been shown to allow for long-term expansion of murine embryonic stem cells in a chemically-defined medium in conjunction with MEK/MAPK inhibitor PD184352 and fibroblast growth factor receptor (FGFR) inhibitor SU5402. Group: Biochemicals. Alternative Names: 6-((2-((4-(2,4-Dichlorophenyl)-5-(4-methyl-1H-imidazol-2- yl) pyrimidin-2-yl) amino) ethyl) amino) nicotinonitrile; CT99021; CHIR 911. Grades: Highly Purified. CAS No. 252917-06-9. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| CHIR 99021 dihydrochloride | CHIR 99021 is a potent glycogen synthase kinase GSK-3 inhibitor. Synonyms: CHIR-99021 dihydrochloride; CHIR99021 dihydrochloride; CT-99021 dihydrochloride; CT 99021 dihydrochloride; CT99021 dihydrochloride; GSK-3 Inhibitor XVI dihydrochloride; 6-[2-[[4-(2,4-dichlorophenyl)-5-(5-methyl-1H-imidazol-2-yl)pyrimidin-2-yl]amino]ethylamino]pyridine-3-carbonitrile dihydrochloride. Grades: 99%. CAS No. 2109414-84-6. Molecular formula: C22H18Cl2N8.2HCl. Mole weight: 538.26. | |
| CHIR99021 HCl | CHIR99021, also known as CT99021, is a GSK-3α/β inhibitor (IC50= 10 nM/6.7 nM) with antiproliferative activity in vitro and in vivo. CHIR-99021 has also been shown to induce the reprogramming of murine and human somatic cells into stem cells. Synonyms: 6-((2-((4-(2,4-dichlorophenyl)-5-(4-methyl-1H-imidazol-2-yl)pyrimidin-2-yl)amino)ethyl)amino)nicotinonitrile hydrochloride; CHIR99021 HCl; CHIR99021 hydrochloride; CHIR99021; CHIR-99021; CHIR 99021; CT99021; CT-99021; CT 99021. CAS No. 1797989-42-4. Molecular formula: C22H19Cl3N8. Mole weight: 501.8. | |
| CHIR-99021 Hydrochloride | CHIR-99021 is a potent and highly selective inhibitor of glycogen synthase kinase 3 (GSK-3). CHIR-99021 activates glycogen synthesis in CHO-IR cells and in isolated type 1 diabetic rat skeletal muscle. CHIR-99021 has also been shown to induce the reprogramming of murine and human somatic cells into stem cells. Group: Biochemicals. Alternative Names: 6- [ [2- [ [4- (2, 4-Dichlorophenyl) -5- (5-methyl-1H-imidazol-2-yl) -2-pyrimidinyl] amino] ethyl] amino] -3-pyridinecarbonitrile Hydrochloride; CHIR 911 Hydrochloride; CT 99021 Hydrochloride. Grades: Highly Purified. CAS No. 1797989-42-4. Pack Sizes: 10mg. Molecular Formula: C22H19Cl3N8, Molecular Weight: 501.8. US Biological Life Sciences. | Worldwide |
| CHIR 99021 trihydrochloride | CHIR 99021 is a highly selective GSK-3 inhibitor. CHIR 99021 is used in the treatment of parkinsonism. Uses: The treatment of parkinsonism. Synonyms: CHIR-99021 trihydrochloride; CHIR 99021 trihydrochloride; CHIR99021 trihydrochloride; 6-[[2-[[4-(2,4-Dichlorophenyl)-5-(5-methyl-1H-imidazol-2-yl)-2-pyrimidinyl]amino]ethyl]amino]-3-pyridinecarbonitrile trihydrochloride. Grades: ≥98% by HPLC. CAS No. 1782235-14-6. Molecular formula: C22H18Cl2N8.3HCl. Mole weight: 574.72. | |
| CHIR 99021 trihydrochloride | CHIR 99021 trihydrochloride. Group: Biochemicals. Grades: Purified. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| Chirabite-ar | Chirabite-ar. Uses: Designed for use in research and industrial production. Additional or Alternative Names: C2184. Product Category: Heterocyclic Organic Compound. CAS No. 909254-56-4. Molecular formula: C42H29N7O8. Mole weight: 759.72. Purity: 0.96. IUPACName: Chirabite-AR. Canonical SMILES: C1C(=O)NC2=CC=CC(=N2)NC(=O)C3=CC(=CC(=C3)[N+](=O)[O-])C(=O)NC4=NC(=CC=C4)NC(=O)COC5=C(C6=CC=CC=C6C=C5)C7=C(O1)C=CC8=CC=CC=C87. Product ID: ACM909254564. Alfa Chemistry ISO 9001:2015 Certified. |  |
| CHITEMPO | [4-N-(4-amino-2,2,6,6-tetramethylpiperidine-1-oxyl)] chitosan. Product ID: 9-00247. Properties: water soluble starch. Reference: Can. J. Chem., 59, 3105, 1981; Can. J. Chem., 59, 2934, 1981. |  |
| CHITEMPO B | [4-N-(4-amino-2,2,6,6-tetramethylpiperidine-1-oxyl)] N,O-carboxymethyl chitosan. apoptosis probe. Product ID: 9-00248. Properties: water soluble xanthan. Reference: J. Physiol., 506, 109, 1998; Biophys. J., 69, 2112, 1995. | |
| Chitin | Poly(N-Acetylglucosamine). from crab shells. Grades: High purity powder. CAS No. 1398-61-4. Product ID: 4-00019. Properties: flakes, technical. Source : from crab shells. | |
| Chitin | . also available in pharma grade. CAS No. 1398-61-4. Product ID: 4-00020. | |
| Chitin | The monomers are identified as N-Acetyl-Amnioglucose. Chitin is a polysaccharide containing nitrogen in which monomers occur with the glycosidically linked components beta 1,4. It is the same coupling as glucose with cellulose, however in chitin the hydroxyl group of the monomer is replaced with an acetyl amine group. The resulting, stronger hydrogen bond between the bordering polymers makes chitin harder and more stabile than cellulose. Group: Polymers. Alternative Names: (1,4)-N-acetyl-D-glucos-2-amine. CAS No. 1398-61-4. Pack Sizes: 1 ton. Product ID: N-[(2R)-2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]acetamide. Molecular formula: 161.16. Mole weight: (C8H13NO5)n. CC(=O)NC1[C@@H](OC(C(C1O)O)CO)O. OVRNDRQMDRJTHS-WTZNIHQSSA-N. InChI=1S/C8H15NO6/c1-3 (11)9-5-7 (13)6 (12)4 (2-10)15-8 (5)14/h4-8, 10, 12-14H, 2H2, 1H3, (H, 9, 11)/t4?, 5?, 6?, 7?, 8-/m1/s1. 96%. |  |
| Chitin | Chitin. Synonyms: Poly-(1→4)-β-N-acetyl-D-glucosamine. CAS No. 1398-61-4. Pack Sizes: 100 g, 1 kg. Product ID: CDC10-0010. Molecular formula: C8H15NO6. Category: Cosmetic Chemical Abrasives. Product Keywords: Cosmetic Ingredients; Cosmetic Chemical Abrasives; Chitin; CDC10-0010; 1398-61-4; C8H15NO6; Poly-(1→4)-β-N-acetyl-D-glucosamine; 215-744-3; MFCD00466914; 1398-61-4. Grade: practical grade. EC Number: 215-744-3. Physical State: Powder. Solubility: Dilute aqueous acid (pH <6.5).: soluble. Quality Level: 200. Boiling Point: 522.4ºC at 760 mmHg. Melting Point:>300°C (dec.). Density: 1.37 g/cm3. |  |
| Chitin | Chitin. We stock inventory in warehouses throughout the United States, allowing us to serve customers in all regions in a timely and cost effective manner. |  California |
| Chitin | Chitin. Group: Molecular Biology. CAS No. 1398-61-4. Pack Sizes: 25g, 250g. Molecular Formula: C30H50N4O19. US Biological Life Sciences. | Worldwide |
| Chitin | It is produced by the strain of Fungi, yeasts, Marine vertebrates and arthropods. Chitin is often used as a trauma therapy and its product of the Chitosan can be used for water treatment and the preparation of photographic emulsion fluid. Uses: Occurs naturally in fungi, yeasts, marine invertebrates, and exoskeletons of arthropods; the second most abundant biopolymer on earth; used to make chitosan; used to control nematodes in various field crops, ornamentals, turf grown in fields, home gardens, and nurseries. Synonyms: Poly-(b1-4)-N-acetyl glucosamine; Poly-(a1-4)-N-acetyl glucosamine. CAS No. 1398-61-4. Molecular formula: (C8H13NO5)n. | |
| chitinase | Some chitinases also display the activity defined in EC 3.2.1.17 lysozyme. Group: Enzymes. Synonyms: chitodextrinase; 1,4-β-poly-N-acetylglucosaminidase; poly-β-glucosaminidase; β-1,4-poly-N-acetyl glucosamidinase; poly[1,4-(N-acetyl-β-D-glucosaminide)] glycanohydrolase. Enzyme Commission Number: EC 3.2.1.14. CAS No. 9001-6-3. Chitinase. 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-3822; chitinase; EC 3.2.1.14; 9001-06-3; chitodextrinase; 1,4-β-poly-N-acetylglucosaminidase; poly-β-glucosaminidase; β-1,4-poly-N-acetyl glucosamidinase; poly[1,4-(N-acetyl-β-D-glucosaminide)] glycanohydrolase. Cat No: EXWM-3822. |  |
| CHITINASE | HGAPDH is an antifungal peptide isolated from Streptomyces violaceus. Synonyms: Glu-Gln-Pro-Gly-Gly-Asp-Lys-Val-Asn-Leu-Gly-Tyr-Phe-Thr-Asn. Grades: 96.9%. CAS No. 9001-6-3. Molecular formula: C72H107N19O25. Mole weight: 1638.75. | |
| 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. | |
| Chitinase from Aspergillus niger (food grade) | Chitinase is an extracellular enzyme complex that degrades chitin. Chitin is degraded to N-acetyl-D-glucosamine in 2 enzymatic reactions. Group: Enzymes. Synonyms: Chitinase; chitodextrinase; 1,4-β-poly-N-acetylglucosaminidase; poly-β-glucosaminidase; β-1,4-poly-N-acetyl glucosamidinase; poly[1,4-(N-acetyl-β-D-glucosaminide)] glycanohydrolase; (1->4)-2-acetamido-2-deoxy-beta-D-glucan glycanohydrolase; EC 3.2.1.14. Enzyme Commission Number: EC 3.2.1.14. CAS No. 9001-6-3. Chitinase. Activity: 200U/g min. Stability: 1 year when properly stored. Storage: STORED HUMIDITY PROTECTED (RH LESS THAN 60) AT TEMPERATURE BELOW 25°C. Form: Light-brown Powder. Source: Aspergillus niger. Chitinase; chitodextrinase; 1,4-β-poly-N-acetylglucosaminidase; poly-β-glucosaminidase; β-1,4-poly-N-acetyl glucosamidinase; poly[1,4-(N-acetyl-β-D-glucosaminide)] glycanohydrolase; (1->4)-2-acetamido-2-deoxy-beta-D-glucan glycanohydrolase; EC 3.2.1.14. Cat No: DIS-1010. | |
| Chitinase from Clostridium thermocellum, Recombinant | Chitinase is an extracellular enzyme complex that degrades chitin and has a molecular mass of approximately 30 kDa. Chitin is degraded to N-acetyl-D-glucosamine in 2 enzymatic reactions. Firstly, chitobiose units are removed from chitin by chitodextrinase-chitinase. The second reaction involves N-acetyl-glucosaminidase-chitobiase, which cleaves the disaccharide to its monomer subunits (that comprise of N-acetyl-D-glucosamine). Group: Enzymes. Synonyms: Chitinase; chitodextrinase; 1,4-β-poly-N-acetylglucosaminidase; poly-β-glucosaminidase; β-1,4-poly-N-acetyl glucosamidinase; poly[1,4-(N-acetyl-β-D-glucosaminide)] glycanohydrolase; (1->4)-2-acetamido-2-deoxy-beta-D-glucan glycanohydrolase; EC 3.2.1.14. Enzyme Commission Number: EC 3.2.1.14. Purity: > 80 % as judged by SDS-PAGE. Chitinase. Mole weight: 43927.1 Da. Activity: 25 U/mg. Storage: Store at -20°C (shipped at room temperature). Form: Glycerol/buffer solution. Source: Clostridium thermocellum ATCC 27405. Chitinase; chitodextrinase; 1,4-β-poly-N-acetylglucosaminidase; poly-β-glucosaminidase; β-1,4-poly-N-acetyl glucosamidinase; poly[1,4-(N-acetyl-β-D-glucosaminide)] glycanohydrolase; (1->4)-2-acetamido-2-deoxy-beta-D-glucan glycanohydrolase; EC 3.2.1.14. Cat No: NATE-1201. | |
| Chitinase-IN-1 | Chitinase-IN-1 is a insect chitinase and N- acetyl hexosaminidase inhibitor and pesticide; 50 uM/20uM compound concentration's inhibitory percentage are 75%/67% for chitinase/N- acetyl-hexosaminidase respectively. Synonyms: Chitinase-IN-1. Grades: >98%. CAS No. 1579991-61-9. Molecular formula: C18H16N4O2S. Mole weight: 352.41. | |
| Chitinase-IN-2 | Chitinase-IN-2 is a insect chitinase and N- acetyl hexosaminidase inhibitor and pesticide; 50 uM/20uM compound concentration's inhibitory percentage are 98%/92% for chitinase/N- acetyl-hexosaminidase respectively. Synonyms: Chitinase-IN-2. Grades: >98%. CAS No. 1579991-63-1. Molecular formula: C20H21N5O2S. Mole weight: 395.48. | |
| Chitinase, Serratia marcescens | Chitinase, Serratia marcescens (EC 3.2.1.14) has partial lysozyme activity and is widely found in bacteria, fungi, animals and some plants. Chitinase belongs to the glycosyl hydrolase family. Chitinase catalyzes chito-oligosaccharide hydrolysis. Chitinases also can serve as prognostic biomarkers of disease progression. Chitinase can be used in the research of pathogenesis of various human fibrotic and inflammatory disorders, particularly those of the lung (idiopathic pulmonary fibrosis, chronic obstructive pulmonary disease, sarcoidosis, and asthma) and the gastrointestinal tract (inflammatory bowel diseases (IBDs) and colon cancer) [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: AMCase, Serratia marcescens. CAS No. 9001-6-3. Pack Sizes: 5 U. Product ID: HY-P2797. | |
| Chitinase, Streptomyces griseus | Chitinase, Streptomyces griseus is a chitinase mainly found in Bacillus species and uses colloidal chitin as a substrate. The Km and Vmax of Chitinase are 4.28 mg/mL and 14.29 μg/(Min·mL) respectively. The final enzymatic hydrolysis product is N-acetylglucosamine, and the monomer and dimer contents are 14.33% and 85.67% respectively [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: AMCase, Streptomyces griseus. CAS No. 9001-6-3. Pack Sizes: 1 g; 5 g. Product ID: HY-P2797A. | |
| Chitin azure | chitinase substrate. Group: Natural polymers and biopolymers. | |
| Chitin azure | Chitin azure. Group: Natural polymers and biopolymers. | |
| Chitin azure | Chitin azure has been used as a substrate to determine chitinase activity. | |
| Chitin Azure | suitable for determining polygalacturonase activity. Product ID: 9-01082. Purity: 'dye content ~5-7 mol%. Properties: Reference: J Biol Chem.,,279, 21888, 2004; Cancer Res., 54, 4516, 1994. | |
| Chitin-binding protein 3 | Chitin-binding protein 3 is an antifungal peptide isolated from Moringa oleifera. It has activity against gram-negative bacteria and fungi. Synonyms: Mo-CBP3; Cys-Pro-Ala-Ile-Gln-Arg-Cys-Cys-Gln-Gln-Leu-Arg-Asn-Ile-Gln-Pro-Pro-Cys-Arg-Cys-Cys-Gln. | |
| chitin deacetylase | Hydrolyses the N-acetamido groups of N-acetyl-D-glucosamine residues in chitin. Group: Enzymes. Enzyme Commission Number: EC 3.5.1.41. CAS No. 56379-60-3. 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-4430; chitin deacetylase; EC 3.5.1.41; 56379-60-3. Cat No: EXWM-4430. | |
| chitin disaccharide deacetylase | Chitin oligosaccharide deacetylase is a key enzyme in the chitin catabolic cascade of chitinolytic Vibrio strains. Besides being a nutrient, the heterodisaccharide product 4-O-(N-acetyl-β-D-glucosaminyl)-D-glucosamine is a unique inducer of chitinase production in Vibrio parahemolyticus. In contrast to EC 3.5.1.41 (chitin deacetylase) this enzyme is specific for the chitin disaccharide. It also deacetylates the chitin trisaccharide with lower efficiency. No activity with higher polymers of GlcNAc. Group: Enzymes. Synonyms: chitobiose amidohydolase; COD; chitin oligosaccharide deacetylase; chitin oligosaccharide amidohydolase; 2-(acetylamino)-4-O-[2-(acetylamino)-2-deoxy-β-D-glucopyranosyl]-2-deoxy-D-glucopyranose acetylhydrolase. Enzyme Commission Number: EC 3.5.1.105. 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-4384; chitin disaccharide deacetylase; EC 3.5.1.105; chitobiose amidohydolase; COD; chitin oligosaccharide deacetylase; chitin oligosaccharide amidohydolase; 2-(acetylamino)-4-O-[2-(acetylamino)-2-deoxy-β-D-glucopyranosyl]-2-deoxy-D-glucopyranose acetylhydrolase. Cat No: EXWM-4384. | |
| Chitin, ethylene glycol | also available in pharma grade. CAS No. 9056-32-0. Product ID: 4-00021. Properties: granule size <0.2 mm. Source : from crab shells. | |
| Chitin, from crab carapace (powder) | Chitin, from crab carapace is a long-chain polymer of N-acetylglucosamine with ?-(1-4) linkages. Chitin, from crab carapace is found in the exoskeleton of crabs. Chitin, from crab carapace inhibits the activation of NF-?B p65, alters the translocation of NF-?B p65 to the nucleus, and interacts with the cell wall of Candida species. Chitin, from crab carapace exerts antifungal and anti-inflammatory effects. Chitin, from crab carapace can be used in the research of gastric ulcer and candidiasis[1][2]. Uses: Scientific research. Group: Natural products. CAS No. 1398-61-4. Pack Sizes: 25 g; 100 g. Product ID: HY-126389. | |
| Chitin from shrimp shells | Chitin from shrimp shells. Group: Natural polymers and biopolymerspolysaccharide. Alternative Names: (1,4)-N-acetyl-D-glucos-2-amine. CAS No. 1398-61-4. CC (=O)N[C@@H]1[C@H] (O)O[C@@H] (CO)[C@H] (O)[C@H]1O. 1S/C8H15NO6/c1-3 (11)9-5-7 (13)6 (12)4 (2-10)15-8 (5)14/h4-8, 10, 12-14H, 2H2, 1H3, (H, 9, 11)/t4?, 5?, 6?, 7?, 8-/m1/s1. OVRNDRQMDRJTHS-WTZNIHQSSA-N. | |
| Chitin Nanoparticles | Chitin Nanoparticles. Group: Clay nanopowders. CAS No. 1398-61-4. Molecular formula: 770.8g/mol. Mole weight: C30H50N4O19. >99%. | |
| Chitin Oligosaccharides | Chitin Oligosaccharides. CAS No. 1398-61-4. Product ID: 4-00647. | |
| Chitinovorin A | Chitinovorin A is produced by the strain of Flavobacerium chitinovorum PB-5016 and PB-5246. Molecular formula: C26H41N9O11S. Mole weight: 687.73. | |
| Chitinovorin B | Chitinovorin B is produced by the strain of Flavobacerium chitinovorum PB-5016 and PB-5246. Synonyms: L-Alaninamide, L-alanyl-N-(4-((7-((5-amino-5-carboxy-1-oxopentyl)amino)-2-carboxy-7-(formylamino)-8-oxo-5-thia-1-azabicyclo(4.2.0)oct-2-en-3-yl)methoxy)-1-(3-((aminoiminomethyl)amino)propyl)-2-hydroxy-4-oxobutyl)-, (6R-(3(1S*,2R*),6alpha,7beta(R*)))-. Grades: >98%. CAS No. 95722-76-2. Molecular formula: C29H46N10O12S. Mole weight: 758.80. | |
| Chitinovorin C | Chitinovorin C is produced by the strain of Flavobacerium chitinovorum PB-5016 and PB-5246. It has weak anti-gram-negative bacterial activity. Synonyms: 5-Thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid, 7-((5-amino-5-carboxy-1-oxopentyl)amino)-7-(formylamino)-3-(hydroxymethyl)-8-oxo-, (6R-(6alpha,7beta(R*)))-; 7-[(5-Amino-5-carboxy-1-hydroxypentylidene)amino]-3-(hydroxymethyl)-7-[(hydroxymethylidene)amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid. CAS No. 95230-98-1. Molecular formula: C15H20N4O8S. Mole weight: 416.41. | |
| Chitin phosphate | Chitin phosphate. Product ID: 5-02283. Purity: highly phosphorylated chitin (P 5-7%). Properties: water insoluble. | |
| Chitin phosphate sulphate | phosphorylated and sulfated chitin. Product ID: 5-02284. Properties: Water soluble, salt free sulfated with potential biological activity. | |
| Chitin sulphate | Chitin sulphate. Product ID: 5-02537. Properties: Water soluble, salt free anionic polysaccharide with potential biological activity. | |
| chitin synthase | Converts UDP-N-acetyl-α-D-glucosamine into chitin and UDP. Group: Enzymes. Synonyms: chitin-UDP N-acetylglucosaminyltransferase; chitin-uridine diphosphate acetylglucosaminyltransferase; chitin synthetase; trans-N-acetylglucosaminosylase; UDP-N-acetyl-D-glucosamine:chitin 4-β-N-acetylglucosaminyl-transferase. Enzyme Commission Number: EC 2.4.1.16. CAS No. 9030-18-6. 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-2384; chitin synthase; EC 2.4.1.16; 9030-18-6; chitin-UDP N-acetylglucosaminyltransferase; chitin-uridine diphosphate acetylglucosaminyltransferase; chitin synthetase; trans-N-acetylglucosaminosylase; UDP-N-acetyl-D-glucosamine:chitin 4-β-N-acetylglucosaminyl-transferase. Cat No: EXWM-2384. | |
| Chitobiose 2HCl | Chitobiose 2HCl is a highly significant compound extensively employed in the compound sector, serving as a fundamental component facilitating chitosan research, an environmentally friendly polymer derived from crustacean exoskeletons. With its pivotal involvement, Chitobiose 2HCl plays a fundamental role in the progression of targeted therapeutic drug delivery systems. Synonyms: Chitosan dimer dihydrochloride; 4-O-(b-D-Glucosamine)-D-glucosamine. CAS No. 577-76-4. Molecular formula: C12H24N2O9 2HCl. Mole weight: 413.25. | |
| Chitobiose dihydrochloride | Chitobiose dihydrochloride, a chitosan oligosaccharide, is a dimer of β-1,4-linked glucosamine units [1]. Uses: Scientific research. Group: Natural products. CAS No. 115350-24-8. Pack Sizes: 5 mg; 10 mg. Product ID: HY-N7697B. | |
| Chitobiose dihydrochloride | Chitobiose dihydrochloride. CAS No. 577-76-4. Product ID: 5-02409. Molecular formula: GlcNb1-4GlcNb. Mole weight: 413.25. Purity: >98% (HPLC). | |
| Chitobiose GEL | | |
| Chitobiose Hydrochloride | Chitobiose Hydrochloride is an exceptional biomedical compound, exhibiting profound versatility in research of numerous ailments encompassing cancer and diabetes. Its indispensable role as a pivotal intermediate in chitin research and development imparts promising prospects to the realms of pharmaceutical conveyance platforms and tissue engineering. Synonyms: Chitobiose 2HCl. Grades: ≥97% by HPLC. Molecular formula: C12H24N2O9·2HCL. Mole weight: 413.25. | |
| Chitobiose octaacetate | Chitobiose octaacetate. Uses: Designed for use in research and industrial production. Additional or Alternative Names: N,N'-Diacetylchitobiose hexaacetate. Product Category: Heterocyclic Organic Compound. Appearance: White Crystalline Solid. CAS No. 41670-99-9. Molecular formula: C28H40N2O17. Mole weight: 676.6. Purity: 96%+. IUPACName: [(2R,3S,4R,5R)-5-Acetamido-3-[(2S,3R,4R,5S,6R)-3-acetamido-4,5-diacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-4,6-diacetyloxyoxan-2-yl]methyl acetate. Canonical SMILES: CC(=O)NC1C(C(C(OC1OC2C(OC(C(C2OC(=O)C)NC(=O)C)OC(=O)C)COC(=O)C)COC(=O)C)OC(=O)C)OC(=O)C. Product ID: ACM41670999. Alfa Chemistry ISO 9001:2015 Certified. | |
| Chitobiose octaacetate | Chitobiose octaacetate, a carbohydrate derivative, is a promising candidate for the treatment of osteoarthritis. Studies demonstrate that it inhibits cartilage-degrading enzymes, the primary culprits of joint degradation in the disease. Furthermore, it attenuates inflammation and pain associated with osteoarthritis. Experts are currently examining its potential as a therapeutic agent, while the manifold intricacies of its pharmacological workings prompt ongoing investigation. Synonyms: 2-acetamido-4-O-(2-acetamido-2-deoxy-beta-D-glucopyranosyl)-2-deoxy-alpha-D-glucose 1,3,3',4',6,6'-hexaacetate; 1-O,3-O,6-O-Triacetyl-4-O-[3-O,4-O,6-O-triacetyl-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl]-2-(acetylamino)-2-deoxy-α-D-glucopyranose; N,N'-Diacetylchitobiose hexaacetate; α-D-Glucopyranose, 2-(acetylamino)-2-deoxy-4-O-[3,4,6-tri-O-acetyl-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl]-, 1,3,6-triacetate; octaacetylchitobiose. Grades: ≥95%. CAS No. 7284-18-6. Molecular formula: C28H40N2O17. Mole weight: 676.62. | |
| chitobiosyldiphosphodolichol β-mannosyltransferase | This enzyme belongs to the family of glycosyltransferases, specifically the hexosyltransferases. Group: Enzymes. Synonyms: guanosine diphosphomannose-dolichol diphosphochitobiose mannosyltransferase; GDP-mannose-dolichol diphosphochitobiose mannosyltransferase; GDP-mannose:chitobiosyldiphosphodolichol β-D-mannosyltransferase. Enzyme Commission Number: EC 2.4.1.142. CAS No. 83380-85-2. 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-2368; chitobiosyldiphosphodolichol β-mannosyltransferase; EC 2.4.1.142; 83380-85-2; guanosine diphosphomannose-dolichol diphosphochitobiose mannosyltransferase; GDP-mannose-dolichol diphosphochitobiose mannosyltransferase; GDP-mannose:chitobiosyldiphosphodolichol β-D-mannosyltransferase. Cat No: EXWM-2368. | |
| Chitodecaose 10HCl | Chitodecaose 10HCl is an exceptional biomedical agent, widely employed as an efficacious measure for targeting and impeding the activity of pivotal enzymes implicated in the intricate pathogenesis of ailments like cancer and neurodegenerative maladies. Synonyms: Chitodecaose Hydrochloride; Chitosan Decamer. Molecular formula: C60H112N10O41 10HCl. Mole weight: 1994.18. | |
| Chitodecaose Hydrochloride | Chitodecaose Hydrochloride is an innovative and groundbreaking pharmaceutical compound derived from the polymer Chitodecaose, exhibiting a touch of uniqueness stemming from chitosan. Its multifaceted nature encompasses remarkable antiviral and antibacterial attributes that have garnered substantial attention. Synonyms: Chitodecaose 10HCl. Grades: ≥93% by HPLC. Molecular formula: C60H112N10O41·10HCL. Mole weight: 1994.17. | |
| Chitoheptaose 7HCl | Chitoheptaose 7HCl, a versatile compound extensively employed in the biomedicine sector, exhibits tremendous promise for addressing diverse ailments, encompassing cancer and inflammatory disorders. Functioning as an immunomodulator, this product effectively regulates immune responses and fortifies the body's defense mechanisms. Synonyms: Chitoheptaose 7-hydrochloride; 68232-35-9. CAS No. 68232-35-9. Molecular formula: C42H79N7O29 7HCl. Mole weight: 1401.34. | |
| Chitoheptaose heptahydrochloride | Chitoheptaose heptahydrochloride. CAS No. 68232-35-9. Product ID: 5-02443. Molecular formula: (GlcNb1-4)7. Mole weight: 1,401.34. Purity: >98% (HPLC). Properties: liquid. | |
| Chitoheptaose Hydrochloride | Chitoheptaose Hydrochloride is a remarkable compound, unveiling unrivaled potential in personalized researchs by selectively modulating distinct molecular pathways. Its multifaceted utility spans across research of malignant neoplasms, inflammatory conditions and bacterial afflictions. Synonyms: Chitoheptaose 7HCl. Grades: ≥96% by HPLC. Molecular formula: C42H79N7O29·7HCL. Mole weight: 1401.33. | |
| Chitohexaose 6HCl | Cas No. 41708-95-6. | |
| Chitohexaose hexahydrochloride | Chitohexaose hexahydrochloride. CAS No. 41708-95-6. Product ID: 5-02410. Molecular formula: (GlcNb1-4GlcNb)3. Mole weight: 1,203.73. Purity: >98% (HPLC). Reference: J. Microbiol. Biotechnol., 4, 343-348, 1994; Am. J. Clin. Nutr., 67, 445-51, 1998. | |
| Chitohexaose Hydrochloride | Chitohexaose Hydrochloride is an extraordinary biomedical compound, an inherently-occurring oligosaccharide obtained from chitin. Profoundly endowed with anti-inflammatory and immunostimulating prowess, Chitohexaose Hydrochloride unveiling immense promise in the research of allergies, asthma and the augmentation of wound healing. Synonyms: Chitohexaose 6HCl. Grades: ≥96% by HPLC. Molecular formula: C36H68N6O25·6HCL. Mole weight: 1203.72. | |
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