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| Product | Description | |
|---|---|---|
| Channel sediment (trace elements) | certified Reference Material. Group: Pharmacopeia & metrological institutes standards. |  |
| chanoclavine-I aldehyde reductase | Contains FMN. The enzyme participates in the biosynthesis of fumigaclavine C, an ergot alkaloid produced by some fungi of the Trichocomaceae family. The enzyme catalyses the reduction of chanoclavine-I aldehyde to dihydrochanoclavine-I aldehyde. This hydrolyses spontaneously to form 6,8-dimethyl-6,7-didehydroergoline, which is converted to festuclavine by EC 1.5.1.44, festuclavine dehydrogenase. Group: Enzymes. Synonyms: FgaOx3; easA (gene name). Enzyme Commission Number: EC 1.3.1.100. 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-1272; chanoclavine-I aldehyde reductase; EC 1.3.1.100; FgaOx3; easA (gene name). Cat No: EXWM-1272. |  |
| chanoclavine-I dehydrogenase | The enzyme catalyses a step in the pathway of ergot alkaloid biosynthesis in certain fungi. Group: Enzymes. Synonyms: easD (gene name); fgaDH (gene name). Enzyme Commission Number: EC 1.1.1.332. 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-0246; chanoclavine-I dehydrogenase; EC 1.1.1.332; easD (gene name); fgaDH (gene name). Cat No: EXWM-0246. | |
| Chaperonin 10 from Escherichia coli | ?95.0% (SDS-PAGE), recombinant, expressed in E. coli overproducing strain, lyophilized powder. Group: Fluorescence/luminescence spectroscopy. | |
| Chaperonin 60 from Escherichia coli | >95% (SDS-PAGE), recombinant, expressed in E. coli overproducing strain, lyophilized powder. Group: Fluorescence/luminescence spectroscopy. | |
| chaperonin ATPase | Multisubunit proteins with 2x7 (Type I, in most cells) or 2x8 (Type II, in Archaea) ATP-binding sites involved in maintaining an unfolded polypeptide structure before folding or entry into mitochondria and chloroplasts. Molecular masses of subunits ranges from 10-90 kDa. They are a subclass of molecular chaperones that are related to EC 3.6.4.8 (proteasome ATPase). Group: Enzymes. Synonyms: chaperonin. Enzyme Commission Number: EC 3.6.4.9. 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-4711; chaperonin ATPase; EC 3.6.4.9; chaperonin. Cat No: EXWM-4711. | |
| CHAPS | CHAPS. CAS No. 75621-03-3. Pack Sizes: Gram Quantities: 5 gm , 1 gm. Order Number: S112. |  www.prochemonline.com |
| CHAPS | CHAPS, a derivative of Cholic acid, is a zwitterionic detergent for solubilizing membrane proteins. CHAPS is used for stabilization of various protein-DNA complexes and can retain biochemical activity of proteins in solution [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 75621-03-3. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g; 5 g. Product ID: HY-15435. |  |
| CHAPS ( (3-[ (3-Cholamidopropyl) dimethylammonio]-1-propanesulfonate) ) | Non-denaturing zwitterionic detergent with cholic acid and sulfobetaine moieties, used to dissolve biological membranes, useful for protein extraction methods due to its ease of removal by dialysis or gel filtration. Low background UV absorption for protein detection.Designed by Good, et al., and typically referred to as Goods buffer useful in cell culture media formulations. Selection of biological buffer systems should include the following criteria: exclusion by biological membranes, low absorption between 240 and 700nm, chemically stable, and stable to temperature and concentration changes. Group: Biochemicals. Alternative Names: (3-[ (3-Cholamidopropyl) dimethylammonio]-1-propanesulfonate) ; N,N-Dimethyl-N-(3-sulfopropyl)-3-[[(3α,5 β, 7α, 12α)-3, 7, 12-trihydroxy-24-oxocholan-24-yl]amino]-1-propanaminium Inner Salt; CHAPS. Grades: Molecular Biology Grade. CAS No. 75621-03-3. Pack Sizes: 5g, 25g, 100g. Molecular Formula: C32H58N2O7S, Molecular Weight: 614.88. US Biological Life Sciences. |  Worldwide |
| CHAPS(3-((3-Cholamidopropyl)dimethylammonio)propanesulfonate) | 5g Pack Size. Group: Buffers. Formula: C32H58N2O7S. CAS No. 75621-03-3. Prepack ID 90005195-5g. Molecular Weight 614.88. See USA prepack pricing. |  |
| CHAPS(3-((3-Cholamidopropyl)dimethylammonio)propanesulfonate) | 25g Pack Size. Group: Buffers. Formula: C32H58N2O7S. CAS No. 75621-03-3. Prepack ID 90005195-25g. Molecular Weight 614.88. See USA prepack pricing. | |
| CHAPS hydrate | CHAPS hydrate, a derivative of Cholic acid, is a zwitterionic detergent for solubilizing membrane proteins. CHAPS hydrate is used for stabilization of various protein-DNA complexes and can retain biochemical activity of proteins in solution [1] [2]. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 331717-45-4. Pack Sizes: 500 mg; 1 g. Product ID: HY-15435A. | |
| CHAPSO | CHAPSO. CAS No. 82473-24-3. Pack Sizes: Gram Quantities: 1 gm. Order Number: S113. | www.prochemonline.com |
| CHAPSO | CHAPSO is a zwitterionic detergent that is thermally stable. CHAPSO is able to broaden the particle orientation distribution, enabling single-particle cryo-electron microscopy (cryo-EM) to produce isotropically uniform maps. CHAPSO can eliminate the directional bias of bacterial transcription complexes and help determine the structure of bacterial transcription complexes under cryo-electron microscopy [1] [2]. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: 3-[3- (Cholamidopropyl)dimethylammonio]-2-hydroxy-1-propanesulfonate. CAS No. 82473-24-3. Pack Sizes: 100 mg; 500 mg. Product ID: HY-W040201. | |
| CHAPSO | Non-denaturing zwitterionic detergent with cholic acid and sulfobetaine moieties, used to dissolve biological membranes, useful for protein extraction methods due to its ease of removal by dialysis or gel filtration. Low background UV absorption for protein detection. Group: Biochemicals. Alternative Names: (3-[ (3-Cholamidopropyl) dimethylammonio]-2-hydroxy-1-propanesulfonate) . Grades: Molecular Biology Grade. CAS No. 82473-24-3. Pack Sizes: 5g, 25g. US Biological Life Sciences. | Worldwide |
| Characteristic MSH-Tetrapeptide | Synonyms: His-DPhe-Arg-Trp; ACTH (6-9). CAS No. 4289-2-5. Molecular formula: C32H40N10O5. Mole weight: 644.72. |  |
| Charantin,Bitter Melon P.E | Charantin,Bitter Melon P.E. Uses: Designed for use in research and industrial production. Appearance: Yellowish brown powder. CAS No. 57126-62-2. Molecular formula: C70H118O12. Mole weight: 1151.68. Purity: 10%-20%. Product ID: ACM57126622. Alfa Chemistry ISO 9001:2015 Certified. |  |
| CHARANTIN(NEW)(P) | Charantin is a potent natural compound derived from bitter melon primarily used in the biomedical industry for the research of diabetes mellitus and related conditions. Synonyms: CHARANTIN(NEW)(P); Monordica Charantia. Grades: 98%. CAS No. 57126-62-2. Molecular formula: A - C35H58O6; B - C35H60O6. | |
| Charantoside | | |
| Charcoal | This ingredient is key to detoxifying skin thats been pummeled by aging and acne-inducing environmental toxins, debris, and pollution. Charcoal is commonly derived from wood, and can hit the reset button on your skin. Pack Sizes: 1 kg. Product ID: CDC10-0558. Category: Anti-Acne Ingredients. Product Keywords: Cosmetic Ingredients; Active Ingredients; Anti-Acne Ingredients; Charcoal; CDC10-0558. |  |
| Charcoal, Activated Carbon, Reagent Grade, 500 g | Formula: C. Formula Wt: 12. 01. Storage Code: Green; general chemical storage. Grades: chem-grade reagent. CAS No. 7440-44-0. Product ID: 853740. -- SOLD FOR EDUCATIONAL USE ONLY -- |  |
| Charcoal, Wood, Lump, Laboratory Grade, 500 g | Formula: C. F. W: 12. 01. Characteristics: Black lumps Notes: Insoluble in water and/or organic solvents Storage Code: Green; general chemical storage. Grades: chem-grade laboratory. CAS No. 7440-44-0. Product ID: 853780. -- SOLD FOR EDUCATIONAL USE ONLY -- | |
| Chartreusin | It is produced by the strain of Streptomyces chartreusis. It has the activity of anti-gram-positive bacteria and mycobacterium. Chartreusin is an antitumour antibiotic that binds to GC-rich tracts in DNA, with a clear preference for B-DNA over Z-DNA; inhibits RNA synthesis and causes single-strand scission of DNA via the formation of free radicals; a potent inhibitor of topoisomerase II. Synonyms: Lambdamycin; Antibiotic X-465A; NSC 5159; (1R,2R,3aS,8aR)-1-[(Z)-5-hydroxy-3-(hydroxymethyl)pent-3-enyl]-1-(hydroxymethyl)-2,5-dimethyl-2,3,4,7,8,8a-hexahydroazulene-3a-carbaldehyde; 10-[[6-Deoxy-2-O-(6-deoxy-3-O-methyl-α-D-galactopyranosyl)-β-D-galactopyranosyl]oxy]-6-hydroxy-1-methylbenzo[h][1]benzopyrano[5,4,3-cde][1]benzopyran-5,12-dione. Grades: >99% by HPLC. CAS No. 6377-18-0. Molecular formula: C32H32O14. Mole weight: 640.59. | |
| Chartreusin (Lambdamycin) | Antibiotic. Antitumor compound. Topoisomerase II inhibitor. Induces single-strand scission in DNA in the presence of reducing agents. Group: Biochemicals. Grades: Highly Purified. CAS No. 6377-18-0. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Chartreusin (Lambdamycin, NSC 5159, Antibiotic 747, Antibiotic 1293, Antibiotic X465A, Antibiotic G 261A) | Chartreusin is an antitumor antibiotic that binds to GC-rich tracts in DNA, with a clear preference for B-DNA over Z-DNA. It inhibits RNA synthesis and causes single-strand scission of DNA via the formation of free radicals. Chartreusin is also potent inhibitor of topoisomerase II. Group: Biochemicals. Alternative Names: Lambdamycin, NSC 5159, Antibiotic 747, Antibiotic 1293, Antibiotic X465A, Antibiotic G 261A. Grades: Highly Purified. CAS No. 6377-18-0. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Charybdotoxin | Charybdotoxin is a Ca2+-activated K+ channel blocker used as an ADC Cytotoxin. Synonyms: CTX Toxin; Quinquestriatus Toxin. Grades: 95%. CAS No. 95751-30-7. Molecular formula: C176H277N57O55S7. Mole weight: 4295.88. | |
| Charybdotoxin | ?90% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| Charybdotoxin, recombinant from Leiurus quinquestriatus hebraeus | recombinant, expressed in E. coli, lyophilized powder. Group: Fluorescence/luminescence spectroscopy. | |
| Charybdotoxin trifluoroacetate salt | Charybdotoxin is a specific inhibitor of the big conductance Ca2+-activated K+ channel which is originally isolated from the scorpion L. quinquestriatus. It blocks large-conductance Ca2+-activated K+ channels (BKCas) in GH3 rat pituitary tumor cells and primary bovine aortic smooth muscle cells (Kds = 2.1 and ~2.1 nM, respectively). Synonyms: ChTX. Grades: ≥95%. Molecular formula: C176H277N57O55S7·xCF3COOH. Mole weight: 4295.90. | |
| Chasmanine | Chasmanine. Group: Biochemicals. Alternative Names: Tokoro-base II. Grades: Plant Grade. CAS No. 5066-78-4. Pack Sizes: 10mg. Molecular Formula: C25H41NO6, Molecular Weight: 451.596. US Biological Life Sciences. | Worldwide |
| Chasteberry Extract (Ratio) | Chasteberry Extract (Ratio). Group: Others. Purity: 4:1~20:1. Chasteberry Extract (Ratio). Cat No: EXTW-064. | |
| Chaste Tree Berry P.E. 0.5% Angusides HPLC | Chaste Tree Berry P.E. 0.5% Angusides HPLC. |  CA, FL & NJ |
| Chaste Tree Extract (Ratio) | Chaste Tree Extract (Ratio). Group: Others. Purity: 4:1~20:1. Chaste Tree Extract (Ratio). Cat No: EXTW-030. | |
| Chaulmoogric acid | Chaulmoogric acid. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Chaulmoogrinsaeure; hydnocarpylacetic acid; (-)-(S)-13-(cyclopent-2-en-1-yl)tridecanoic acid; 2-Cyclopentene-1-tridecanoic acid; 13-(Cyclopent-2-enyl)tridecanoic acid; chaulmoogric acid; 13-cyclopent-2-en-1-yltridecanoic acid; 2-Cyclopentene-1-tridecanoic acid,(S); (S)-2-Cyclopentene-1-tridecanoic acid. CAS No. 29106-32-9. Molecular formula: C18H32O2. Mole weight: 280.45. Purity: 0.96. IUPACName: (S)-chaulmoogric acid. Density: 0.948g/cm³. Product ID: ACM29106329. Alfa Chemistry ISO 9001:2015 Certified. | |
| Chavicol | Chavicol (p-Hydroxyallylbenzene, compound 6) can inhibit acetylcholinesterase ( Cholinesterase (ChE) ), with an IC 50 of 7.42 μM. Chavicol has anti-cancer activity and can suppress the growth, survival, migration, and invasion of cancer cells. Chavicol cytotoxic effect is significant, approximately 31 μg/mL in A-549 cells [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: p-Hydroxyallylbenzene. CAS No. 501-92-8. Pack Sizes: 10 mM * 1 mL; 100 mg; 250 mg; 500 mg; 1 g. Product ID: HY-W159754. | |
| ChBac5 | ChBac5 is an antibacterial peptide isolated from Capra hircus (Goat). It has activity against gram-positive bacteria and gram-negative bacteria. Synonyms: Cathelicidin-2; Bactenecin-5; Bac5; Arg-Phe-Arg-Pro-Pro-Ile-Arg-Arg-Pro-Pro-Ile-Arg-Pro-Pro-Phe-Asn-Pro-Pro-Phe-Arg-Pro-Pro-Val-Arg-Pro-Pro-Phe-Arg-Pro-Pro-Phe-Arg-Pro-Pro-Phe-Arg-Pro-Pro-Ile-Gly-Pro-Phe-Pro. Molecular formula: C252H376N74O45. Mole weight: 5162.23. | |
| CHC | CHC. Group: Biochemicals. Grades: Purified. CAS No. 28166-41-8. Pack Sizes: 50mg. US Biological Life Sciences. | Worldwide |
| CHD-5 | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| CHD-5 | CHD-5 is a potent AhR (aryl hydrocarbon receptor) antagonist [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 289494-16-2. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-118780. | |
| 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 EC 50 of 9.76 μM. Uses: Scientific research. Group: Natural products. CAS No. 23094-71-5. Pack Sizes: 10 mM * 1 mL; 2 mg; 5 mg; 10 mg. Product ID: HY-N1996. | |
| Chebulagic acid | Chebulagic acid is a polyphenol and tannin that has been found in T. chebula and has diverse biological activities. It is an inhibitor of COX-1, COX-2, and 5-lipoxygenase (5-LO; IC50s = 15, 0.92, and 2.1 μM, respectively) as well as α-glucosidase and 15-LO (IC50s = 0.05 and 24.9 μM, respectively). Chebulagic acid inhibit the LPS-induced upregulation of TNF-α and IL-1β in a dose- and time-dependent manner. And it can also inhibit the production of NO, prostaglandin E2 (PGE2), and reactive oxygen species (ROS), and nuclear translocation of NF-κB in RAW 264.7 macrophages in a concentration-dependent manner. Chebulagic acid also show a protective effect against 1-methyl-4-phenylpyridinium (MPP+) - induce cytotoxicity which mimics the pathological symptom of Parkinson's disease. Uses: Topoisomerase i inhibitors. Synonyms: β-D-glucopyranose; Cyclic 3,6-[(1R)-4,4',5,5',6,6'-hexahydroxy[1,1'-biphenyl]-2,2'-dicarboxylate] 1-(3,4,5-trihydroxybenzoate); Cyclic 2?2:4?1-ester with (2S)-2-[(3S,4S)-5-carboxy-3,4-dihydro-3,7,8-trihydroxy-2-oxo-2H-1-benzopyran-4-yl]butanedioic acid. Grades: ≥98%. CAS No. 23094-71-5. Molecular formula: C41H30O27. Mole weight: 954.66. | |
| 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 |
| Chebulagic acid | analytical standard. Group: Herbal medicinal products standards. | |
| 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: Designed for use in research and industrial production. Product Category: Inhibitors. Appearance: Beige powder. CAS No. 23094-71-5. Molecular formula: C41H30O27. Mole weight: 954.7. Purity: 0.98. Canonical SMILES: C1C2C3C(C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C6=C5C(C(C(=O)O3)CC(=O)O)C(C(=O)O6)O)O)O)OC(=O)C7=CC(=C(C(=C7C8=C(C(=C(C=C8C(=O)O1)O)O)O)O)O)O. Product ID: ACM23094715. Alfa Chemistry ISO 9001:2015 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. Group: Natural products. CAS No. 23725-05-5. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg. Product ID: HY-N4170. | |
| Chebulic acid | Chebulic acid. Uses: Designed for use in research and industrial production. Additional or Alternative Names: (2S) -[(3S, 4S) - 3- Carboxy- 3, 4- dihydro- 5, 6, 7- trihydroxy- 1- oxo- 1H- 2- benzopyran- 4- yl] -butanedioic Acid. Appearance: Solid. CAS No. 23725-05-5. Molecular formula: C14H12O11. Mole weight: 356.24. Purity: 0.95. IUPACName: (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. Product ID: ACM23725055. Alfa Chemistry ISO 9001:2015 Certified. | |
| 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. Group: Natural products. CAS No. 18942-26-2. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 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 is a potent natural inhibitor of M. tuberculosis DNA gyrase, also can inhibit SMAD-3 phosphorylation, inhibit H+ K+-ATPase activity. Uses: Designed for use in research and industrial production. Additional or Alternative Names: CHEBULINIC ACID;NSC69862;CHEBULINIC ACID(SH);Eutannin. Product Category: Inhibitors. Appearance: Beige powder. CAS No. 18942-26-2. Molecular formula: C41H32O27. Mole weight: 956.7. Purity: 0.98. Canonical SMILES: C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C3C(C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C6=C5C(C(C(=O)O3)CC(=O)O)C(C(=O)O6)O)O)O)OC(=O)C7=CC(=C(C(=C7)O)O)O. Density: 2.04. Product ID: ACM18942262. Alfa Chemistry ISO 9001:2015 Certified. | |
| Checkpoint Kinase 2, Active human | buffered aqueous glycerol solution, recombinant, expressed in E. coli, ?85% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy. | |
| 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. Grades: ≥95%. Molecular formula: C95H150N30O35S. Mole weight: 2304.48. | |
| Cheilanthifoline | Cheilanthifoline is an alkaloid isolated from rhizomes of Sinomenium acutum with anti-osteoclastogenic property. Synonyms: (S)-Cheilanthifoline; (6aS)-6,6a,11,14-Tetrahydro-8-methoxy-12H-benzo[a]-1,3-benzodioxolo[4,5-g]quinolizim-9-ol; (6aS)-9-methoxy-6,11,12,14-tetrahydro-2H,6aH-[1,3]dioxolo[4,5-h]isoquino[2,1-b]isoquinolin-8-ol. Grades: >98%. CAS No. 483-44-3. Molecular formula: C19H19NO4. Mole weight: 325.264. | |
| 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. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 1-isothiocyanato-3-(methylsulfonyl)propane;cheiroline;isothiocyanicacid,3-(methylsulfonyl)propylester;methylpropylsulfonemustardoil;CHEIROLIN;3-(METHYLSULPHONYL)PROPYLISOTHIOCYANATE;3-Methylsulfonylpropyl isothiocyanate;γ-Isothiocyanopropyl methyl sulfone. Product Category: Heterocyclic Organic Compound. CAS No. 505-34-0. Molecular formula: C5H9NO2S2. Mole weight: 179.26. Purity: 0.96. IUPACName: 1-isothiocyanato-3-methylsulfonylpropane. Canonical SMILES: CS(=O)(=O)CCCN=C=S. Density: 1.23g/cm³. Product ID: ACM505340. Alfa Chemistry ISO 9001:2015 Certified. | |
| 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. | |
| Chelants | Our wide distribution network, with locations coast-to-coast, helps guarantee fast, reliable service to Univar's customers. |  |
| Chelates (Extensive Range) | Chelates (Extensive Range) - Agriculture Chemicals. SUPPLIERS TO BUSINESS CUSTOMERS ONLY. |  North America & APAC |
| Chelerythrine | Chelerythrine is a natural alkaloid, acts as a potent and selective Ca2+/phospholopid-dependent PKC antagonist, with an IC50 of 0.7 μM. Chelerythrine has antitumor, antidiabetic and anti-inflammatory activity. 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: Designed for use in research and industrial production. Additional or Alternative Names: Broussonpapyrine; Cheleritrine; Chelerythrin; Chelerythrine chloride; Chelerythrin-Kation; Chelerythrine; Chelerythrin chlorid. Product Category: Inhibitors. CAS No. 34316-15-9. Molecular formula: C21H18ClNO4. Mole weight: 348.83. Purity: 95%-99%. IUPACName: 1,2-dimethoxy-12-methyl-[1,3]benzodioxolo[5,6-c]phenanthridin-12-ium. Canonical SMILES: C[N+]1=C2C(=C3C=CC(=C(C3=C1)OC)OC)C=CC4=CC5=C(C=C42)OCO5. ECNumber: 251-930-0. Product ID: ACM34316159. Alfa Chemistry ISO 9001:2015 Certified. | |
| Chelerythrine | Chelerythrine Inhibitor. Uses: Scientific use. Product Category: T3419. CAS No. 3895-92-9. | |
| 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 is a potent, cell-permeable inhibitor of protein kinase C , with an IC 50 of 660 nM. Chelerythrine chloride inhibits the Bcl-XL-Bak BH3 peptide binding with IC 50 of 1.5 μM and displaces Bax from Bcl-XL. Chelerythrine chloride induces apoptosis and autophagy. Uses: Scientific research. Group: Natural products. CAS No. 3895-92-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-12048. | |
| 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: Designed for use in research and industrial production. Additional or Alternative Names: 1,2-Dimethoxy-12-methyl-[1,3]dioxolo[4',5':4,5]benzo[1,2-c]phenanthridin-12-ium chloride. Product Category: Inhibitors. CAS No. 3895-92-9. Mole weight: 383.8. Purity: 95%+. Product ID: ACM3895929. Alfa Chemistry ISO 9001:2015 Certified. | |
| Chelerythrine Chloride | ?95% (TLC), powder. Group: Fluorescence/luminescence spectroscopyenzyme activators, inhibitors & substrates. | |
| Chelerythrine Chloride - CAS 3895-92-9 | Naturally-occurring alkaloid. Group: Fluorescence/luminescence spectroscopy. | |
| Chelidamic acid | Chelidamic acid is a heterocyclic organic acid with a pyran skeleton. Chelidamic acid has good coordination ability with noble metal ions. Chelidamic acid is also one of the most potent inhibitors of glutamate decarboxylase, with a K i of 33 μM. Uses: Scientific research. Group: Signaling pathways. CAS No. 138-60-3. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg. Product ID: HY-W016349. | |
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