A directory of where to buy chemicals in the USA, including: distributors, industrial manufacturers, bulk supplies and wholesalers of raw ingredients & finished goods.
Search for products or services, then visit the suppliers website for prices or more information.
| Product | Description | |
|---|---|---|
| Chebulagic | Chebulagic Inhibitor. Uses: Scientific use. Product Category: TQ0180. CAS No. 23094-71-5. |  |
| Chebulagic acid | Chebulagic acid is a COX-LOX dual inhibitor isolated from the fruits of Terminalia chebula Retz, on angiogenesis. Chebulagic acid is a M2 serine to asparagine 31 mutation (S31N) inhibitor and influenza antiviral. Chebulagic acid also against SARS-CoV-2 viral replication with an EC50 of 9.76 μM. Uses: Scientific research. Category: Signaling pathways. CAS No. 23094-71-5. Pack Sizes: 10 mM * 1 mL in DMSO; 2 mg; 5 mg; 10 mg. Product ID: HY-N1996. |  |
| Chebulagic acid | Chebulagic acid. Group: Biochemicals. Grades: Plant Grade. CAS No. 23094-71-5. Pack Sizes: 10mg. Molecular Formula: C41H30O27, Molecular Weight: 954.66. US Biological Life Sciences. |  Worldwide |
| Chebulic acid | Chebulic acid. Alternative Names: (2S) -[(3S, 4S) - 3- Carboxy- 3, 4- dihydro- 5, 6, 7- trihydroxy- 1- oxo- 1H- 2- benzopyran- 4- yl] -butanedioic Acid. CAS No. 23725-05-5. Purity: 95%. Product ID: ACM23725055. Molecular formula: C14H12O11. Mole weight: 356.24. IUPAC Name: (2S)-2-[(3S,4S)-3-carboxy-5,6,7-trihydroxy-1-oxo-3,4-dihydroisochromen-4-yl]butanedioic acid. Canonical SMILES: C1=C2C(=C(C(=C1O)O)O)[C@@H]([C@H](OC2=O)C(=O)O)[C@H](CC(=O)O)C(=O)O. Alfa Chemistry - ISO 9001:32057 Certified. |  |
| Chebulic acid | Chebulic acid is a phenolic acid compound isolated from Terminalia chebula with strong antioxidant activity, which breaks protein cross-links induced by advanced glycation end products (AGEs) and inhibits the formation of AGEs. Chebulic acid is effective in controlling elevated metabolic parameters, oxidative stress, and liver damage, supporting its beneficial role in asthma, diabetes, and liver protection[1][2][3][4][5]. Uses: Scientific research. Category: Signaling pathways. CAS No. 23725-05-5. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-N4170. | |
| Chebulic acid | Chebulic acid is a phenol isolated from Terminalia chebula with potent anti-oxidant activity. Synonyms: (2S)-2-[(3S)-3,4-Dihydro-3α-carboxy-5,6,7-trihydroxy-1-oxo-1H-2-benzopyran-4β-yl]butanedioic acid; Butanedioic acid,[(3S,4S)-3-carboxy-3,4-dihydro-5,6,7-trihydroxy-1-oxo-1H-2-benzopyran-4-yl]-,(2S)-; Chebulic acid; Split acid; CHEBULIC ACID(SH); (2S)-[(3S,4S)-3-Carboxy-3,4-dihydro-5,6,7-trihydroxy-1-oxo-1H-2-benzopyran-4-yl]butanedioic acid. Grade: 98%. CAS No. 23725-05-5. Molecular formula: C14H12O11. Mole weight: 356.2. |  |
| Chebulinic acid | Chebulinic acid is a potent natural inhibitor of M. tuberculosis DNA gyrase, also can inhibit SMAD-3 phosphorylation, inhibit H+ K+-ATPase activity. Uses: Scientific research. Category: Signaling pathways. CAS No. 18942-26-2. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-N2033. | |
| Chebulinic acid | Chebulinic acid. Group: Biochemicals. Alternative Names: Eutannin. Grades: Plant Grade. CAS No. 18942-26-2. Pack Sizes: 10mg. Molecular Formula: C41H32O27, Molecular Weight: 956.677. US Biological Life Sciences. | Worldwide |
| Chebulinic Acid | Chebulinic Acid. Alternative Names: CHEBULINIC ACID;NSC69862;CHEBULINIC ACID(SH);Eutannin. CAS No. 18942-26-2. Purity: 98%. Product ID: ACM18942262. Molecular formula: C41H32O27. Mole weight: 956.7. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Checkpoint Kinase 2, Active Human, Recombinant | CHEK2 is the official symbol for the human gene Checkpoint kinase 2. CHEK2 is located on the the long (q) arm of chromosome 22. CHEK2 is tumor suppressor gene that encodes the protein CHK2, a serine threonine kinase. CHK2 operates in an intricate network of proteins to elicit DNA repair, cell cycle arrest or apoptosis in response to DNA damage. Mutations to the CHEK2 gene have been linked to a wide range of cancers including breast cancer. Buffered aqueous glycerol solution, recombinant, expressed in e. coli, > 85% (sds-page). Applications: Kinase activity is measured as the molar amount of phosphate incorporated into the chktide per minute per mg protein at 30°c using a final concentration of 50 μm [32p] atp. Group: Enzymes. Synonyms: Checkpoint Kinase 2; CHEK2; CDS1; CHK2; HuCds1; LFS2; PP1425; RAD53; hCds1; Chek2; Chk2. Purity: > 85% (SDS-PAGE). CHEK2. Mole weight: protein apparent mol wt ~88 kDa. Stability: -70°C. Form: buffered aqueous glycerol solution. Source: E. coli. Species: Human. Checkpoint Kinase 2; CHEK2; CDS1; CHK2; HuCds1; LFS2; PP1425; RAD53; hCds1; Chek2; Chk2. Cat No: NATE-0122. |  |
| Checkpoint Protein Hus1 (213-232) (human) | HDAC1 plays an important role in regulating eukaryotic chromatin structure and specifically interacts with human Hus1 gene products in yeast, mammalian cells, and in vitro. S. Pombe's Hus1 protein is associated with G2/M checkpoint control and is a member of the cell cycle checkpoint Rad protein, which is involved in the mitotic checkpoint induced by DNA damage or DNA replication arrest. Synonyms: H-Leu-Ala-Ser-Glu-Ser-Thr-His-Glu-Asp-Arg-Asn-Val-Glu-His-Met-Ala-Glu-Val-His-Ile-OH. Grade: ≥95%. Molecular formula: C95H150N30O35S. Mole weight: 2304.48. | |
| Cheimonophyllal | It is produced by the strain of Cheimonophyllum candidissiumun sing. It has nematode killing, cytotoxicity (L1210, HL60, BHK21) and weak antifungal bacterial activity. CAS No. 160299-95-6. Molecular formula: C14H20O5. Mole weight: 268.30. | |
| Cheimonophyllon A | It is produced by the strain of Cheimonophyllum candidissiumun sing. It has nematode killing, cytotoxicity (L1210, HL60, BHK21) and weak antifungal bacterial activity. Molecular formula: C15H22O4. Mole weight: 266.33. | |
| Cheimonophyllon E | It is produced by the strain of Cheimonophyllum candidissiumun sing. It has nematode killing, cytotoxicity (L1210, HL60, BHK21) and weak antifungal bacterial activity. CAS No. 160299-94-5. Molecular formula: C15H24O4. Mole weight: 268.30. | |
| Cheirolin | Cheirolin is a glucosinolate from plants of the Brassicaceae family which has shown to be a potent inducer of phase II detoxification enzymes. Applications: A phase ii detoxification enzyme activator. Group: Coenzymes. Synonyms: 1-Isothiocyanato-3-(methylsulfonyl)-propane. CAS No. 505-34-0. Mole weight: 179.26. Form: Solid. 1-Isothiocyanato-3-(methylsulfonyl)-propane; Cheirolin; 505-34-0. Cat No: COEC-110. | |
| Chelates (Extensive Range) | Chelates (Extensive Range) - Agriculture Chemicals. SUPPLIERS TO BUSINESS CUSTOMERS ONLY. |  North America & APAC |
| Chelerythrine | Chelerythrine Inhibitor. Uses: Scientific use. Product Category: T3419. CAS No. 3895-92-9. | |
| Chelerythrine | Chelerythrine is a benzophenanthridine alkaloid extracted from the plant Greater celandine (Chelidonium majus). It is a potent, selective, and cell-permeable protein kinase C inhibitor. It is also the major active natural product found in the plant Zanthoxylum clava-herculis, exhibiting anti-bacterial activity against Staphylococcus aureus. Chelerythrine inhibits the BclXL-Bak BH3 peptide binding with IC50 of 1.5 μM and displaces Bax from BclXL. Chelerythrine triggers apoptosis and autophagy. Uses: Antibacterial agent. Synonyms: Toddalin; cheleritrine; broussonpapyrine; Toddaline; [1,3]Benzodioxolo[5,6-c]phenanthridinium, 1,2-dimethoxy-12-methyl-; NSC646662; 1,2-Dimethoxy-N-methyl(1,3)benzodioxolo(5,6-c)phenanthridinium chloride. Grade: 98%. CAS No. 34316-15-9. Molecular formula: C21H18NO4+. Mole weight: 348.37. | |
| Chelerythrine | Chelerythrine. Group: Biochemicals. Alternative Names: Toddaline; Broussonpapyrine. Grades: Plant Grade. CAS No. 34316-15-9. Pack Sizes: 20mg. Molecular Formula: C21H18NO4+, Molecular Weight: 348.370999999999. US Biological Life Sciences. | Worldwide |
| Chelerythrine chloride | Cell permeable potent inhibitor of protein kinase C. Does not inhibit tyrosine protein kinases, cAMP-dependent protein kinase or calcium/calmodulin-dependent protein kinase. Antiplatelet, anti-inflammatory, antibacterial and antitumor compound. Apoptosis inducer in cancer cells in vitro and in vivo. Activates MAPK and JUNK signaling pathways. Affects translocation of PKC from cytosol to plasma membrane. Neurite outgrowth stimulator. Inhibits binding of BclXL to Bak (IC50 =1.5uM) or Bad proteins and stimulates apoptosis in several cancer cell lines. Blocks human P2X7 receptor. Induces cell cycle arrest in G1 phase. Specific cyclooxygenase-2 inhibitor. Group: Biochemicals. Alternative Names: NSC 36405, 1,2-Dimethoxy-N-methyl-[1,3]benzodioxolo[5,6-c]phenanthridinium chloride. Grades: Highly Purified. CAS No. 3895-92-9. Pack Sizes: 1mg, 5mg, 25mg. Molecular Formula: C21H18ClNO4. US Biological Life Sciences. | Worldwide |
| Chelerythrine chloride | Chelerythrine chloride. Alternative Names: 1,2-Dimethoxy-N-methyl(1,3)benzodioxolo(5,6-c)phenanthridinium chloride. CAS No. 3895-92-9. Purity: >98.0%. Product ID: FFC-AR-3895929. Molecular formula: C21H18ClNO4. Mole weight: 383.82. IUPAC Name: 1,2-dimethoxy-12-methyl-[1,3]benzodioxolo[5,6-c]phenanthridin-12-ium chloride. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Chelerythrine chloride | Chelerythrine chloride is a potent, cell-permeable inhibitor of protein kinase C, with an IC50 of 660 nM. Chelerythrine chloride inhibits the Bcl-XL-Bak BH3 peptide binding with IC50 of 1.5 μM and displaces Bax from Bcl-XL. Chelerythrine chloride induces apoptosis and autophagy. Uses: Scientific research. Category: Signaling pathways. CAS No. 3895-92-9. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-12048. | |
| Chelerythrine chloride | Chelerythrine is a cell-permeable inhibitor of protein kinase C (IC50 = 660 nM) with a wide range of biological activities. Synonyms: Broussonpapyrine Chloride. Grade: >98%. CAS No. 3895-92-9. Molecular formula: C21H19NO4. Mole weight: 383.82. | |
| Chelidamic Acid | Chelidamic Acid is considered as one of the most potent "conformationally restricted glutamate analogs" as an inhibitor of glutamate decarboxylase. Group: Biochemicals. Alternative Names: 1,4-Dihydro-4-oxo-2,6-pyridinedicarboxylic Acid; 4-Oxo-1,4-dihydropyridine-2,6-dicarboxylic Acid; NSC 3983; Chelidamic Acid; 4-Hydroxypyridine-2,6-dicarboxylic acid, Hydrate. Grades: Highly Purified. CAS No. 138-60-3. Pack Sizes: 10g, 25g, 50g. Molecular Formula: C?H?NO?, Molecular Weight: 183.12 (anhy). US Biological Life Sciences. | Worldwide |
| Chelidamic acid monohydrate | Chelidamic acid monohydrate. CAS No. 138-60-3. Purity: >95.0%(T). Product ID: ACM138603. Molecular formula: C7H5NO5. Mole weight: 183.12. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Chelidonic acid | Chelidonic acid. Alternative Names: 4-oxo-4H-pyran-2,6-dicarboxylic acid. CAS No. 99-32-1. Purity: >95.0%. Product ID: FFC-AR-99321. Molecular formula: C7H4O6. Mole weight: 184.1. IUPAC Name: 4-oxopyran-2,6-dicarboxylic acid. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Chelidonic acid monohydrate | Chelidonic acid monohydrate. CAS No. 6003-94-7. Molecular formula: C7H6O7. Mole weight: 202.12g/mol. Purity: technical. IUPAC Name: 4-oxopyran-2,6-dicarboxylic acid;hydrate. SMILES: C1=C(OC(=CC1=O)C(=O)O)C(=O)O.O. InChI: InChI=1S/C7H4O6.H2O/c8-3-1-4(6(9)10)13-5(2-3)7(11)12;/h1-2H,(H,9,10)(H,11,12);1H2. |  |
| Chelidonic Acid Monohydrate | Chelidonic Acid Monohydrate. Alternative Names: 4-Oxo-4H-pyran-2,6-dicarboxylic Acid Monohydrate. CAS No. 6003-94-7. Purity: 95.0%(T). Product ID: ACM-MO-6003947. Molecular formula: C7H4O6·H2O. Mole weight: 202.12 g/mol. IUPAC Name: 4-oxopyran-2,6-dicarboxylic acid;hydrate. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Chelidonic Acid Monohydrate, ≥95% | Chelidonic Acid Monohydrate, ≥95%. CAS No. 6003-94-7. Molecular formula: C7H6O7. Mole weight: 202.12g/mol. IUPAC Name: 4-oxopyran-2,6-dicarboxylic acid;hydrate. SMILES: C1=C(OC(=CC1=O)C(=O)O)C(=O)O.O. InChI: InChI=1S/C7H4O6.H2O/c8-3-1-4(6(9)10)13-5(2-3)7(11)12;/h1-2H,(H,9,10)(H,11,12);1H2. | |
| Chelidonine | Chelidonine, an isoquinoline alkaloid, can be isolated from Chelidonium majus L. Chelidonine causes G2/M arrest and induces caspase-dependent and caspase-independent apoptosis, and prevents cell cycle progression of stem cells in Dugesia japonica. Chelidonine has cytotoxic activity against melanoma cell lines. with anticancer and antiviral activity[1][2][3]. Uses: Scientific research. Category: Signaling pathways. CAS No. 476-32-4. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg. Product ID: HY-N2369. | |
| Chelidonine | Chelidonine. Group: Biochemicals. Alternative Names: Stylophorine. Grades: Plant Grade. CAS No. 476-32-4. Pack Sizes: 10mg. Molecular Formula: C20H19NO5, Molecular Weight: 353.369. US Biological Life Sciences. | Worldwide |
| Chelidonine hydrochloride | Chelidonine hydrochloride. Alternative Names: Chelidonine chloride. CAS No. 4312-31-6. Product ID: FFC-AR-4312316. Molecular formula: C20H20ClNO5. Mole weight: 389.83. IUPAC Name: (1S,12S,13R)-24-methyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.02,10.04,8.014,22.017,21]tetracosa-2,4(8),9,14(22),15,17(21)-hexaen-12-ol;hydrochloride. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Chelocardin | Chelocardin is produced by the strain of Nocardia sulphurea M-319. It has anti-gram-positive and negative bacterial activity, and is partially cross-resistant to tetracycline. Synonyms: Cetocycline; 2-Decarboxamido-2-acetyl-4-desdimethylamino-4-amino-9-methyl-5a,6-anhydrotetracycline. Grade: 95%. CAS No. 29144-42-1. Molecular formula: C22H21NO7. Mole weight: 411.41. | |
| CHEMBL2426474 | CHEMBL2426474, also called as UNC1079, the piperidine analog of UNC1021 that has binding affinity to L3MBTL3 in human G401 cells by Western blot based pulldown assay. Synonyms: CHEMBL2426474UNC1079; UNC-1079; UNC 1079.1,4-Phenylenebis(1,4'-bipiperidin-1'-ylmethanone)1418741-86-2BDBM50440571AKOS025405429CS-5532; AK-185224; HY-18373; CS 5532; AK 185224; HY 18373; CS5532; AK185224; HY183731,4-Bis(4-(piperidinyl)piperidinyl)benzamide. CAS No. 1418741-86-2. Molecular formula: C28H42N4O2. Mole weight: 466.67. | |
| CHEMBL333994 | CHEMBL333994 is a potent and orally active antagonist of cholecystokinin A (CCK-A), with an IC50 of 0.67 nM. Synonyms: FK-480; N-[(3R)-1-(2-Fluorophenyl)-4-oxo-3,4,6,7-tetrahydro[1,4]diazepino[6,7,1-hi]indol-3-yl]-1H-indole-2-carboxamide; 1H-Indole-2-carboxamide, N-[(3R)-1-(2-fluorophenyl)-3,4,6,7-tetrahydro-4-oxo[1,4]diazepino[6,7,1-hi]indol-3-yl]-. Grade: ≥95%. CAS No. 167820-10-2. Molecular formula: C26H19FN4O2. Mole weight: 438.45. | |
| CHEMBRDG-BB 7118966 | CHEMBRDG-BB 7118966 is a Bromodomain-containing protein 4 (human) inhibitor. Synonyms: 2(1H)-Quinazolinone, 6-bromo-3,4-dihydro-3-methyl-; 6-Bromo-3,4-dihydro-3-methyl-2(1H)-quinazolinone; 6-Bromo-3-methyl-3,4-dihydroquinazolin-2(1H)-one; CHEMBRDG-BB7118966; CHEMBRDG-BB-7118966; 6-bromo-3-methyl-1,2,3,4-tetrahydroquinazolin-2-one. Grade: 95%. CAS No. 328956-24-7. Molecular formula: C9H9BrN2O. Mole weight: 241.08. | |
| Chemerin15 | Chemerin15 is an anti-inflammatory peptide derived from Chemerin. Chemerin15 binds to ChemR23. Chemerin15 inhibits TNFα-induced activation of Syk, ERK and Src kinases. Chemerin15 increases the expression of p-p38 mRNA and protein. Chemerin15 mediates phagocytosis, resolution of inflammation, CD62L shedding and downregulation of PSGL-1 expression in macrophages and microglia. Chemerin15 inhibits neutrophil-mediated vascular inflammation and myocardial ischemia-reperfusion injury via ChemR23. Chemerin15 enhances microglial phagocytosis, thereby alleviating cerebral ischemia-reperfusion injury[1][2][3]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1020407-90-2. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg. Product ID: HY-P6442. | |
| Chemerin-9 149-157 | Chemerin-9 (149-157), the 149-157 amino acid fragment of Chemerin-9, corresponding to the C-terminal of processed Chemerin, retains most of the activity of the full-size protein, with regard to agonism toward the chemerin R. Synonyms: Tyr-Phe-Pro-Gly-Gln-Phe-Ala-Phe-Ser; chemerin 9; L-tyrosyl-L-phenylalanyl-L-prolyl-glycyl-L-glutaminyl-L-phenylalanyl-L-alanyl-L-phenylalanyl-L-serine. Grade: ≥95%. CAS No. 676367-27-4. Molecular formula: C54H66N10O13. Mole weight: 1063.16. | |
| Chemerin-9 (149-157) acetate | Chemerin-9 (149-157) acetate, the 149-157 amino acid fragment of Chemerin-9, corresponding to the C-terminal of processed Chemerin, retains most of the activity of the full-size protein, with regard to agonism toward the chemerin R. It is the natural ligand of ChemR23 (chemerinR23). Synonyms: Chemerin-9 (human) (acetate); L-Tyrosyl-L-phenylalanyl-L-prolylglycyl-L-glutaminyl-L-phenylalanyl-L-alanyl-L-phenylalanyl-L-serine acetate; Human chemerin-9 acetate; H-Tyr-Phe-Pro-Gly-Gln-Phe-Ala-Phe-Ser-OH.CH3CO2H. Grade: ≥95%. Molecular formula: C56H70N10O15. Mole weight: 1123.23. | |
| Chemerin-9 (149-157) (TFA) | Chemerin-9 (149-157) (TFA) is a potent CMKLR1 (chemokine-like receptor 1) agonist with anti-inflammatory properties. Chemerin-9 (149-157) (TFA) stimulates phosphorylation of Akt and ERK as well as ROS production. Synonyms: H-Tyr-Phe-Pro-Gly-Gln-Phe-Ala-Phe-Ser-OH.TFA. Molecular formula: C56H67F3N10O15. Mole weight: 1177.18. | |
| Chemerin-9, mouse | Chemerin-9, mouse, a ligand for ChemR23, is a potent CMKLR1 agonist. Synonyms: Phe-Leu-Pro-Gly-Gln-Phe-Ala-Phe-Ser. CAS No. 686324-96-9. Molecular formula: C51H68N10O12. Mole weight: 1013.15. | |
| Chemerin peptide 4 | Chemerin peptide 4 is an antibacterial peptide isolated from Homo sapiens. Synonyms: Val-Arg-Leu-Glu-Phe-Lys-Leu-Gln-Gln-Thr-Ser-Cys-Arg-Lys-Arg-Asp-Trp-Lys-Lys-Pro. Grade: 95.4%. Molecular formula: C113H188N36O29S. Mole weight: 2547.03. | |
| Chemically Functionalized Carbon Nanotubes | Chemically Functionalized Carbon Nanotubes. CAS No. 308068-56-6. Purity: >95wt% (MWNT). | |
| Chemically modified Aspergillus niger Glucose Oxidase | Oxidoreductase that catalyzes the conversion of D-glucose to D-glucono-1,5-lactone which hydrolyzes spontanously to gluconate. Take advantage of the enhanced liquid stability. Rely on the proven diagnostic quality of this product. Applications: Use glucose oxidase (god), chemically modified for the determination of α-amylase and d-glucose or o2. Group: Enzymes. Synonyms: glucose oxyhydrase; corylophyline; penatin; glucose aerodehydrogenase; microcid; β-D-glucose oxidase; D-glucose oxidase; D-glucose-1-oxidase; β-D-glucose:quinone oxidoreductase; glucose oxyhydrase; deoxin-1; GOD; GOx; notatin; glucose oxidase. GOD. Mole weight: 79 kD. Activity: >20 U/mg lyophilizate. Stability: At +2 to +8°C within specification range for 12 months. Store dry. Appearance: Yellowish white lyophilizate. Source: Aspergillus niger. EC 1.1.3.4; glucose oxyhydrase; corylophyline; penatin; glucose aerodehydrogenase; microcid; β-D-glucose oxidase; D-glucose oxidase; D-glucose-1-oxidase; β-D-glucose:quinone oxidoreductase; glucose oxyhydrase; deoxin-1; GOD; 9001-37-0; glucose oxidase enzyme; GOx; notatin; glucose oxidase. Cat No: DIA-285. | |
| Chemically modified Cholesterol Oxidase from Brevibacterium species | Oxidoreductase that catalyzes the interconversion of cholesterol to cholest-4-en-3-one. Rely on the proven diagnostic quality of this product. Applications: Use cholesterol oxidase in diagnostic tests for the determination of cholesterol in combination with cholesterol esterase. Group: Enzymes. Synonyms: Cholesterol-O2 oxidoreductase; 3 beta-Hydroxy steroid oxidoreductase; 3β-hydroxysteroid: oxygen oxidoreductase; cholesterol: oxygen oxidoreductase; cholesterol oxidase. CHOD. Mole weight: 60 kD (native and SDS). Activity: 10-20 U/mg lyophilizate. Stability: At -15 to -25°C within specification range for 12 months. Store dry. Protect from light. Appearance: Yellow lyophilizate. Storage: No decrease in activity over 6 weeks at +35°C. Source: Brevibacterium species. Cholesterol-O2 oxidoreductase; 3 beta-Hydroxy steroid oxidoreductase; 3β-hydroxysteroid: oxygen oxidoreductase; cholesterol: oxygen oxidoreductase; cholesterol oxidase; EC 1.1.3.6. Cat No: DIA-284. | |
| Chemically modified Cucurbita species Ascorbate Oxidase | Oxidoreductase that oxidizes ascorbic acid to dehydroascorbate. Take advantage of the improved stability in liquid reagents. Rely on the proven diagnostic quality of this product. Applications: Use ascorbate oxidase, chemically modified, in a variety of diagnostic tests to eliminate the interference of ascorbic acid, since ascorbic acid interferes with the trinder reaction that is widely used for the colorimetric determination of analytes. it is useful in liquid as well as dry chemistry test, e.g., for the determination of uric acid, lactate or creatinine. Group: Enzymes. Synonyms: ascorbase; ascorbic acid oxidase; ascorbate oxidase; ascorbic oxidase; ascorbate dehydrogenase; L-ascorbic acid oxidase; AAO; L-ascorbate: O2 oxidoreductase; AA oxidase; L-ascorbate oxidase. AAO. Mole weight: Approximately 140 kD. Activity: >180 U/mg lyophilizate (+37°C, L-ascorbate); Specific activity (+37°C): >1,800 U/mg protein. Stability: At -15 to -25°C within specification range for 12 months. Store dry. Keep tightly sealed. Appearance: Turquoise lyophilizate. Source: Cucurbita species. ascorbase; ascorbic acid oxidase; ascorbate oxidase; ascorbic oxidase; ascorbate dehydrogenase; L-ascorbic acid oxidase; AAO; L-ascorbate: O2 oxidoreductase; AA oxidase; EC 1.10.3.3; 9029-44-1; L-ascorbate oxidase. Cat No: DIA-283. | |
| Chemically Modified Fullerenes | Chemically Modified Fullerenes. Purity: >99%. | |
| Chemically modified Glucose-6-phosphate Dehydrogenase from Leuconostoc mesenteroides | Glucose-6-phosphate dehydrogenase (G6PD or G6PDH) (EC 1.1.1.49) is a cytosolic enzyme that catalyzes the chemical reaction:D-glucose 6-phosphate + NADP+ <-> 6-phospho-D-glucono-1,5-lactone + NADPH + H+. This enzyme is in the pentose phosphate pathway, a metabolic pathway that supplies reducing energy to cells (such as erythrocytes) by maintaining the level of the co-enzyme nicotinamide adenine dinucleotide phosphate (NADPH). Applications: Use glucose-6-phosphate dehydrogenase for the determination of blood glucose or creatine kinase. Group: Enzymes. Synonyms: D-glucose 6-phosphate dehydrogenase; glucose 6-phosphate dehydrogenase (NADP); NADP-dependent glu. Glucose-6-phosphate dehydrogenase. Mole weight: 110 kD (2 identical subunits 55,000 D). Activity: >30 U/mg lyophilizate. Stability: At +2 to +8°C within specification range for 18 months. Store dry. Appearance: White lyophilizate. Source: E. coli. Species: Leuconostoc mesenteroides. EC 1.1.1.49; NADP-glucose-6-phosphate dehydrogenase; Zwischenferment; D-glucose 6-phosphate dehydrogenase; glucose 6-phosphate dehydrogenase (NADP); NADP-dependent glucose 6-phosphate dehydrogenase; 6-phosphoglucose dehydrogenase; Entner-Doudoroff enzyme; glucose-6-phosphate 1-dehydrogenase; G6PDH; GPD; glucose-6-phosphate dehydrogenase; 9001-40-5. Cat No: DIA-280. | |
| Chemically modified Glycerol-3-phosphate Oxidase from E. coli | Recombinant oxidoreductase that catalyzes the interconversion of glycerol 3-phosphate to dihydroxyacetone phosphate. Take advantage of the enhanced liquid stability of this enzyme. Rely on the proven diagnostic quality of this product. Applications: Use glycerol-3-phosphate oxidase in diagnostic tests for the determination of triglycerides together with glycerol kinase and lipoprotein lipase. Group: Enzymes. Synonyms: glycerol-3-phosphate oxidase; sn-glycerol-3-phosphate: oxygen 2-oxidoreductase; glycerol phosphate oxidase; glycerol-1-phosphate oxidase; glycerol phosphate oxidase; L-alpha-glycerophosphate oxidase; alpha-glycerophosphate oxidase; L-alpha-glycerol-3-phos. Glycerol-3-phosphate oxidase. Mole weight: 75 kD (SDS-PAGE); 74 kD (gel filtration, Sephadex G 150). Activity: >10 U/mg lyophilizate (+37°C, L-α-glycerol phosphate); Specific activity (+25°C): >40 U/mg protein. Stability: At +2 to +8°C within specification range for 12 months. Store dry. Appearance: Green yellow amorphous lyophilizate. Source: E. coli. glycerol-3-phosphate oxidase; EC 1.1.3.21; sn-glycerol-3-phosphate: oxygen 2-oxidoreductase; glycerol phosphate oxidase; glycerol-1-phosphate oxidase; glycerol phosphate oxidase; L-alpha-glycerophosphate oxidase; alpha-glycerophosphate oxidase; L-alpha-glycerol-3-phosphate oxidase. Cat No: DIA-287. | |
| Chemically modified Porcine L-Lactate Dehydrogenase | Dehydrogenase that catalyzes the interconversion of L(+)-lactate to pyruvate. Take advantage of the enhanced liquid stability of this enzyme. Rely on the proven diagnostic quality of this product. Applications: Use l-lactate dehydrogenase (l-ldh), chemically modified, in a variety of diagnostic tests for the removal of pyruvate in determinations working with nadh (i.e., triglycerides, lipase, aldolase, aminotransferases, glutamate dehydrogenase). Group: Enzymes. Synonyms: lactic acid dehydrogenase; L-lactic dehydrogenase; L-lactic acid dehydrogenase; lactate dehydrogenase; L-lactate dehydrogenase; L-LDH; LAD; LD; Lactate. LDH. Activity: >25 U/mg lyophilizate; >150 U/mg protein. Stability: At +2 to +8°C within specification range for 12 months. Appearance: White lyophilizate. Source: Porcine heart. Species: Porcine. EC 1.1.1.27; 9001-60-9; lactic acid dehydrogenase; L (+)-nLDH; L-(+)-lactate dehydrogenase; L-lactic dehydrogenase; L-lactic acid dehydrogenase; lactate dehydrogenase; lactate dehydrogenase NAD-dependent; lactic dehydrogenase; NAD-lactate dehydrogenase; L-lactate dehydrogenase; (S)-Lactate:NAD+ oxidoreductase; L-LDH; LAD; LD; Lactate. Cat No: DIA-279. | |
| Chemically modified Pseudomonas species Cholesterol Esterase | Hydrolase that splits fatty acids from sterols. Take advantage of the enhanced stability of this enzyme in liquid reagents. Rely on the proven diagnostic quality of this product. Applications: Use cholesterol esterase, chemically modified in diagnostic tests for the determination of cholesterol in combination with cholesterol oxidase. Group: Enzymes. Synonyms: cholesterol esterase; cholesteryl ester synthase; triterpenol esterase; cholesteryl esterase; cholesteryl ester hydrolase; sterol ester hydrolase; cholesterol ester hydrolase; cholesterase; acylcholesterol lipase; sterol esterase; CE. Cholesterol Esterase. Mole weight: ~129 kD. Activity: >10 U/mg lyophilizate; >100 U/mg protein. Stability: At +2 to +8°C within specification range for 12 months. Store dry. Appearance: Brownish lyophilizate. Source: Pseudomonas species. cholesterol esterase; cholesteryl ester synthase; triterpenol esterase; cholesteryl esterase; cholesteryl ester hydrolase; sterol ester hydrolase; cholesterol ester hydrolase; cholesterase; acylcholesterol lipase; EC 3.1.1.13; 9026-00-0; sterol esterase; CE. Cat No: DIA-281. | |
| Chemically modified Pseudomonas species Lipoprotein Lipase | Enzyme that hydrolyzes triglycerides into three free fatty acids and glycerol. Take advantage of the enhanced liquid stability of this enzyme. Rely on the proven diagnostic quality of this product. Applications: Use lipoprotein lipase in diagnostic tests for the determination of triglycerides together with glycerol kinase and glycerol-3-phosphate dehydrogenase. Group: Enzymes. Synonyms: Lipoprotein lipase; LPL; Clearing factor lipase; Diacylglycerol lipase; Diglyceride lipase. LPL. Mole weight: 47 kD. Activity: >10 U/mg lyophilizate. Stability: At +2 to +8°C within specification range for 12 months. Store dry. Appearance: Brownish lyophilizate. Source: Pseudomonas species. Lipoprotein lipase; LPL; EC 3.1.1.34; Clearing factor lipase; Diacylglycerol lipase; Diglyceride lipase. Cat No: DIA-282. | |
| Chemical phosphorylation reagent II | Chemical phosphorylation recompound II is a potent instrument utilized within the realm of biomedical industry, serving as a pivotal component for the intricate phosphorylation reactions. This indispensable recompound orchestrates the modification and activation of select biomolecules encompassing proteins, peptides and nucleotides. Its versatility extends to diverse fields including drug development, signal transduction research and researchs targeting anomalous phosphorylation processes underlying numerous pathologies. Synonyms: 2-[(4,4'-Dimethoxytrityloxy)methyl]-2-[[(diisopropylamino)(2-cyanoethoxy)phosphinooxy]methyl]malonic acid diethyl ester. Grade: >95% by HPLC. Molecular formula: C39H51N2O9P. Mole weight: 722.82. | |
| Chemical Properties of 2,6-Dimethyldecane | Chemical Properties of 2,6-Dimethyldecane. Alternative Names: 2,6-Dimethyldecane. CAS No. 13150-81-7. Product ID: ACM13150817. Molecular formula: C12H26. Mole weight: 170.33. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Chemical Properties of 2-Ethyl-1-dodecanol | Chemical Properties of 2-Ethyl-1-dodecanol. Alternative Names: 2-Ethyl-1-dodecanol 2-ethyldodecan-1-ol 1-Dodecanol, 2-ethyl-. CAS No. 19780-33-7. Product ID: ACM19780337. Molecular formula: C14H30O. Mole weight: 214.39. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Chemical Services |  | |
| Chemical Storage & Handling | | |
| Chemokine Inhibitor Library | A unique collection of 59 chemokines or chemokine receptors targeted compounds for high throughput and high content screening; - Targets include chemokines and their receptors, such as CCR, CXCR, CR, CX3CR, etc. ; - Bioactivity and safety confirmed by pre-clinical research and clinical trials, and some of them are approved by FDA; - Detailed compound information with structure, target, activity, IC50 value, and biological activity description; - Structurally diverse, medicinally active, and cell permeable; - NMR and HPLC validated to ensure high purity and quality. Uses: Scientific use. Product Category: L7600. Categories: Chemokine Inhibitor Libraries. | |
| Chemotactic Domain of Elastin | Chemotactic Domain of Elastin stimulated human skin fibroblast proliferation and was chemotactic for fibroblasts and monocytes. The palmitoylated form is marketed as a cosmetic ingredient. Synonyms: Valyl-glycyl-valyl-alanyl-prolyl-glycine; N-[(1-{N-[2-({2-[(2-Amino-1-hydroxy-3-methylbutylidene)amino]-1-hydroxyethylidene}amino)-1-hydroxy-3-methylbutylidene]alanyl}pyrrolidin-2-yl)(hydroxy)methylidene]glycine. CAS No. 92899-39-3. Molecular formula: C22H38N6O7. Mole weight: 498.57. | |
| Chemotactic Domain of Elastin | Chemotactic Domain of Elastin is an elastin-derived peptide with chemotactic effects on certain tumor cells, such as M27 tumor cells. Chemotactic Domain of Elastin can be used in cancer research[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 92899-39-3. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P4998. | |
| Chemotherapy Drug Library | 51 Chemotherapeutic drugs that can be used for high-throughput and high-content screening. - Includes common chemotherapy drugs such as paclitaxel, cyclophosphamide, cytarabine, doxorubicin, etc. - Detailed instructions, compound structures, target information, IC50 values, activity descriptions, etc. - Various detection techniques such as NMR, HPLC/LCMS to ensure correct structure, high purity and reduce the false-positive rates. Uses: Scientific use. Product Category: L2151. Categories: Chemotherapy Drug Libraries. | |
| ChemR23-IN-1 | ChemR23-IN-1 (compound 2) is a ChemR23 inhibitor with IC50s of 38 nM and 100 nM for human and mouse ChemR23, respectively. ChemR23-IN-1 inhibits chemotaxis of CAL-1 triggered by Chemerin in vitro[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2378640-10-7. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg. Product ID: HY-126536. | |
| ChemR23-IN-1 | ChemR23-IN-1 is a ChemR23 inhibitor that acts on human and mouse ChemR23 with IC50 values of 38 nM and 100 nM, respectively. It blocks Chemerin-triggered CAL-1 chemotaxis in vitro. CAS No. 2378640-10-7. Molecular formula: C28H29N7O2. Mole weight: 495.58. | |
| Chenodeoxycholic acid | Chenodeoxycholic acid. Alternative Names: (3α,5β,7α)-3,7-dihydroxy-cholan-24-oic acid. CAS No. 474-25-9. Purity: >95.0%. Product ID: FFC-AR-474259. Molecular formula: C24H40O4. Mole weight: 392.57. IUPAC Name: (4R)-4-[(3R,5S,7R,8R,9S,10S,13R,14S,17R)-3,7-dihydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]pentanoic acid. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Chenodeoxycholic acid | 5g Pack Size. Group: Biochemicals, Detergents. Formula: C24H40O4. CAS No. 474-25-9. Prepack ID 31295558-5g. Molecular Weight 392.57. See USA prepack pricing. |  |
| Chenodeoxycholic Acid | Chenodeoxycholic Acid is a hydrophobic primary bile acid that activates nuclear receptors (FXR) involved in cholesterol metabolism. Uses: Scientific research. Category: Signaling pathways. Alternative Names: CDCA. CAS No. 474-25-9. Pack Sizes: 10 mM * 1 mL in DMSO; 100 mg; 500 mg; 1 g; 5 g; 10 g; 25 g; 50 g; 100 g. Product ID: HY-76847. | |
| Chenodeoxycholic Acid-[13C] | Chenodeoxycholic Acid-[24-13C], is the labelled analogue of Chenodeoxycholic acid, Chenodeoxycholic acid has been used as medical therapy to dissolve gallstones. Synonyms: Chenodeoxycholic Acid-13C; Chenodeoxycholic-24-13C Acid; (3α,5β,7α)-3,7-Dihydroxycholan-24-oic-13C Acid; (+)-Chenodeoxycholic-13C Acid; 17β-(1-Methyl-3-carboxypropyl)etiocholane-3α,7α-diol-13C; Chenodiol-13C; Chendol-13C; Chenocol-13C; Fluibil-13C; Chenodeoxycholic-13C Acid. Grade: 98%; 99% atom 13C. CAS No. 52918-92-0. Molecular formula: C23[13C]H40O4. Mole weight: 393.57. | |
| Chenodeoxycholic acid-(2,2,4,4-d4) | Chenodeoxycholic acid-(2,2,4,4-d4). Alternative Names: 5β-cholanic acid-3α,7α-diol (2,2,4,4-d4). CAS No. 99102-69-9. Purity: >99%. Product ID: ALCFA99102699. Molecular formula: C24H36D4O4. Mole weight: 396.6. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Chenodeoxycholic acid 24-acyl-b-D-glucuronide | Chenodeoxycholic acid 24-acyl-β-D-glucuronide is an indispensable constituent within the biomedical domain predominantly employed for the therapeutic research of hepatic ailments including cholestasand biliary cirrhosis. This compound exerts formidable hepatoprotective attributes and ensures the homeostasis of bile acid metabolism. Synonyms: 1-[(3a,5b,7a)-3,7-Dihydroxycholan-24-oate] b-D-glucopyranuronic acid. CAS No. 208038-27-1. Molecular formula: C30H48O10. Mole weight: 568.70. | |
| Chenodeoxycholic acid 24-acyl-β-D-glucuronide | Chenodeoxycholic acid 24-acyl-β-D-glucuronide is a metabolite of Chenodeoxycholic Acid (HY-76847)[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 208038-27-1. Pack Sizes: 1 mg; 5 mg. Product ID: HY-W585920. | |
Our database is helping our users find suppliers everyday.
