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| Product | Description | |
|---|---|---|
| Cytochalasin C from Metarrhizium anisopliae | ?97.0% (TLC). Group: Fluorescence/luminescence spectroscopy. |  |
| Cytochalasin D | It is produced by the strain of Metarrhizium anisopliae, Coriolus vernicipes. It has many biological activities, such as inhibiting cytokinesis reversibly, inhibiting megasophil endocytosis and exocytosis. Uses: Anti-hypertensive. Synonyms: (3S, 3aR, 4S, 6S, 6aR, 7E, 10S, 12R, 13E, 15R, 15aR)-15-(Acetyloxy)-3, 3a, 4, 5, 6, 6a, 9, 10, 12, 15-decahydro-6, 12-dihydroxy-4, 10, 12-trimethyl-5-methylene-3-(phenylmethyl)-1H-cycloundec[d]isoindole-1, 11(2H)-dione; (7S,13E,16S,18R,19E,21R)-[11]21-(Acetyloxy)-7,18-dihydroxy-16,18-dimethyl-10-phenylcytochalasa-6(12),13,19-triene-1,17-dione; (-)-Cytochalasin D; 1H-Cycloundec[d]isoindole-1,11(2H)-dione, 15-(acetyloxy)-3,3a,4,5,6,6a,9,10,12,15-decahydro-6,12-dihydroxy-4,10,12-trimethyl-5-methylene-3-(phenylmethyl)-, [3S-(3R*, 3aS*, 4R*, 6R*, 6aS*, 7E, 10R*, 12S*, 13E, 15S*, 15aS*)]-; NSC 209835; Zygosporin A; Cytohalasin D; Lygosporin A. Grades: >98%. CAS No. 22144-77-0. Molecular formula: C30H37NO6. Mole weight: 507.62. |  |
| Cytochalasin D | from Zygosporium mansonii, ?98% (TLC and HPLC), powder. Group: Fluorescence/luminescence spectroscopy. | |
| Cytochalasin D | Cytochalasin D (Zygosporin A) is a potent actin polymerization inhibitor, could be derived from fungus. Cytochalasin D has cell-permeable activity. Cytochalasin D inhibits the G-actin - cofilin interaction by binding to G-actin. Cytochalasin D also inhibits the binding of cofilin to F-actin and decreases the rate of both actin polymerization and depolymerization in living cells. Cytochalasin D can reduce exosome release, in turn reducing the amount of survivin present in the tumour environment. Cytochalasin D induces phosphorylation and cytoplasmic retention of Yap [1] [2] [3] [4]. Uses: Scientific research. Group: Natural products. Alternative Names: Zygosporin A; NSC 209835. CAS No. 22144-77-0. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg. Product ID: HY-N6682. |  |
| Cytochalasin e | Cytochalasin E, an epoxide containing Aspergillus-derived fungal metabolite, inhibits angiogenesis and tumor growth. Cytochalasin E is a potent actin depolymerization agent, and it binds and caps the barbed end of actin filaments to prevent actin elongation. Uses: Designed for use in research and industrial production. Additional or Alternative Names: (7s,13e,16s,18r,19e)-18-dimethyl-10-phenyl;21,23-dioxa(13)cytochalasa-13,19-diene-1,17,22-trione,6,7-epoxy-18-hydroxy-16,;6,7-epoxy-10-phenyl-5,6,16,18-tetramethyl-21,23-dioxa-[13]cytochalas-13,19-die;CYTOCHALASIN 3;CYTOCHALASIN E;CYTOCHALASIN E, ASPERGI. Product Category: Inhibitors. Appearance: white powder. CAS No. 36011-19-5. Molecular formula: C28H33NO7. Mole weight: 495.56. Purity: >98%. IUPACName: CYTOCHALASIN E. Canonical SMILES: CC1CC=CC2C3C(O3)(C(C4C2(C(=O)NC4CC5=CC=CC=C5)OC(=O)OC=CC(C1=O)(C)O)C)C. Density: 1.3 g/cm³. ECNumber: 252-835-7. Product ID: ACM36011195. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Cytochalasin E | It is produced by the strain of Rosellina necatrix. It has many biological activities, such as inhibiting cytokinesis reversibly, inhibiting megasophil endocytosis and exocytosis. Synonyms: (7S,13E,16S,18R,19E)-6,7-Epoxy-18-hydroxy-16,18-dimethyl-10-phenyl-21,23-Dioxa[13]cytochalasa-13,19-diene-1,17,22-trione; NSC 175151; [4S-(1E, 4R*, 6S*, 7E, 11aR*, 14R*, 14aR*, 15R*, 15aS*, 16aR*, 16bR*)]-3, 13, 14, 14a, 15, 15a, 16a, 16b-Octahydro-6-hydroxy-4, 6, 15, 15a-tetramethyl-14-(phenylmethyl)-[1, 3]Dioxacyclotridecino[4, 5-d]oxireno[f]isoindole-5, 10, 12(4H, 6H)-trione. Grades: >99% by HPLC. CAS No. 36011-19-5. Molecular formula: C28H33NO7. Mole weight: 495.56. | |
| Cytochalasin E | Cytochalasin E is one of a family of potent mycotoxins produced by a range of fungi. All members of the class exhibit profound effects on cytoskeletal proteins resulting in pronounced morphogenic changes in animals and plants. Despite this common mode of action, within the class there is evidence that individual members display diverse selectivity. Specifically, cytochalasin E acts as an angiogenesis inhibitor and, unlike other cytochalasins, is unable to inhibit glucose transport. Group: Biochemicals. Grades: Highly Purified. CAS No. 36011-19-5. Pack Sizes: 1mg. US Biological Life Sciences. |  Worldwide |
| Cytochalasin F | It is produced by the strain of Helminthosporium dematioideum, Coriolus vernicipes. It has many biological activities, such as inhibiting cytokinesis reversibly, inhibiting megasophil endocytosis and exocytosis. Synonyms: (7S,13E,16R,20R,21E)-6,7-Epoxy-20-hydroxy-16-methyl-10-phenyl-24-oxa[14]cytochalasa-13,21-diene-1,23-dione; 24-Oxa(14)cytochalasa-13,21-diene-1,23-dione,6,7-epoxy-20-hydroxy-16-methyl-10-phenyl-, (7S,13E,16R,20R,21E)-. CAS No. 36084-18-1. Molecular formula: C29H37NO5. Mole weight: 479.61. | |
| Cytochalasin G | It is produced by the strain of Curvularia lunata, Drechslera dematioidea. It has many biological activities, such as inhibiting cytokinesis reversibly, inhibiting megasophil endocytosis and exocytosis. CAS No. 54874-57-6. Molecular formula: C29H34N2O4. Mole weight: 474.59. | |
| Cytochalasin h | Cytochalasin h. Uses: Designed for use in research and industrial production. Additional or Alternative Names: (11)cytochalasa-6(12),13,19-trien-1-one,21-(acetyloxy)-7,18-dihydroxy-16,18-di;(7s,13e,16s,18s,19e,21r)-methyl-10-phenyl;19-triene-1-one;21-acetoxy-7,18-dihydroxy-16,18-dimethyl-10-phenyl-(11)cytochalasa-6(12),13,;cytochalasinhfromphomopsissp.;kodocytoch. Product Category: Heterocyclic Organic Compound. CAS No. 53760-19-3. Molecular formula: C30H39NO5. Mole weight: 493.63. Purity: 0.96. IUPACName: CYTOCHALASIN H. Density: 1.19g/cm³. Product ID: ACM53760193. Alfa Chemistry ISO 9001:2015 Certified. Categories: Cytochalasin B. | |
| Cytochalasin H | It is produced by the strain of Pestalotia sp. AB 1942R-114. It has many biological activities, such as inhibiting cytokinesis reversibly, inhibiting megasophil endocytosis and exocytosis. Cytosine H has immunosuppressive effects. Synonyms: (7S,13E,16S,18R,19E,21R)-21-(Acetyloxy)-7,18-dihydroxy-16,18-dimethyl-10-phenyl-[11]Cytochalasa-6(12),13,19-trien-1-one; (3S, 3aR, 4S, 6S, 6aR, 7E, 10S, 12R, 13E, 15R, 15aR)-15-(Acetyloxy)-2, 3, 3a, 4, 5, 6, 6a, 9, 10, 11, 12, 15-dodecahydro-6, 12-dihydroxy-4, 10, 12-trimethyl-5-methylene-3-(phenylmethyl)-1H-cycloundec[d]isoindol-1-one; Cytochalasin H; Kodocytochalasin 1; Paspalin P I; [3S-(3R*, 3aS*, 4R*, 6R*, 6aS*, 7E, 10R*, 12S*, 13E, 15S*, 15aS*)]-15-(Acetyloxy)-2, 3, 3a, 4, 5, 6, 6a, 9, 10, 11, 12, 15-dodecahydro-6, 12-dihydroxy-4, 10, 12-trimethyl-5-methylene-3-(phenylmethyl)-1H-cycloundec[d]isoindol-1-one; Paspalin; SC 305222; NSC305222; NSC-305222; (11)Cytochalasa-6(12),13,19-trien-1-one; phenyl-(11)cytochalasa-6(12),13,19-triene-1-one. Grades: >95% by HPLC. CAS No. 53760-19-3. Molecular formula: C30H39NO5. Mole weight: 493.63. | |
| Cytochalasin H (Kodocytochalasin 1, Paspalin P1, 17-Deoxo-21-acetyl-zygosporin D) | Cytochalasin H is one of a family of potent mycotoxins produced by a range of fungi. All members of the class exhibit profound effects on cytoskeletal proteins resulting in pronounced morphogenic changes in animals and plants. In vitro, cytochalasin H exhibits antibacterial, antifungal, nematocidal and antitumor activity. Group: Biochemicals. Alternative Names: Kodocytochalasin 1, Paspalin P1, 17-Deoxo-21-acetyl-zygosporin D. Grades: Highly Purified. CAS No. 53760-19-3. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Cytochalasin J | It is produced by the strain of Pestalotia sp. AB 1942R-114. It has many biological activities, such as inhibiting cytokinesis reversibly, inhibiting megasophil endocytosis and exocytosis. Cytosine J has immunosuppressive effects. Synonyms: Deacetylcytochalasin H; Kodocytochalasin 2; Paspalin P II; [3S-(3R*, 3aS*, 4R*, 6R*, 6aS*, 7E, 10R*, 12S*, 13E, 15S*, 15aS*)]-2, 3, 3a, 4, 5, 6, 6a, 9, 10, 11, 12, 15-Dodecahydro-6, 12, 15-trihydroxy-4, 10, 12-trimethyl-5-methylene-3-(phenylmethyl)-1H-cycloundec[d]isoindol-1-one; (7S,13E,16S,18R,19E,21R)-7,18,21-Trihydroxy-16,18-dimethyl-10-phenyl-[[11]cytochalasa-6(12),13,19-trien-1-one. Grades: ≥ 95%. CAS No. 56144-22-0. Molecular formula: C28H37NO4. Mole weight: 451.60. | |
| Cytochalasin J (Kodocytochalasin 2, Paspalin P11, Deacetylcytochalasin H, 17-Deoxo-zygosporin D) | Cytochalasin J is one of a family of potent mycotoxins produced by a range of fungi. All members of the class exhibit profound effects on cytoskeletal proteins which give rise to pronounced morphogenic activity in animals and plants. Cytochalasin J is the deacetyl analogue of cytochalasin H and exhibits similar, though less potent, antibacterial, antifungal, nematocidal and antitumor activities. Group: Biochemicals. Alternative Names: Kodocytochalasin 2, Paspalin P11, Deacetylcytochalasin H, 17-Deoxo-zygosporin D. Grades: Highly Purified. CAS No. 56144-22-0. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Cytochalasin K | It is produced by the strain of Curvularia lunata, Drechslera dematioidea. It has many biological activities, such as inhibiting cytokinesis reversibly, inhibiting megasophil endocytosis and exocytosis. Synonyms: 3H-Cyclotridec(d)oxireno(f)isoindole-8,11,12(13H)-trione, 7-(acetyloxy)-4,7,14,14a,15,15a,16a,16b-octahydro-4,6,15,15a-tetramethyl-14-(phenylmethyl)-, (1E, 4S, 5E, 7R, 9E, 11aR, 14S, 14aR, 15S, 15aR, 16aS, 16bR)-. CAS No. 79648-72-9. Molecular formula: C32H37NO6. Mole weight: 531.64. | |
| Cytochalasin L | It is produced by the strain of Curvularia lunata, Drechslera dematioidea. It has many biological activities, such as inhibiting cytokinesis reversibly, inhibiting megasophil endocytosis and exocytosis. Synonyms: 24-Oxa(14)cytochalasa-13,17,21-triene-1,20,23-trione, 19-(acetyloxy)-6,7-epoxy-16,18-dimethyl-10-phenyl-, (7S,13E,16S,17E,19R,21E)-; 3H-Oxacyclotetradecino(2,3-d)oxireno(f)isoindole-8,11,13(14H)-trione, 7-(acetyloxy)-4,7,15,15a,16,16a,17a,17b-octahydro-4,6,16,16a-tetramethyl-15-(phenylmethyl)-, (1E, 4S, 5E, 7R, 9E, 12aS, 15S, 15aS, 16S, 16aR, 17aS, 17bS)-. CAS No. 79637-87-9. Molecular formula: C32H37NO7. Mole weight: 547.64. | |
| Cytochalasin M | It is produced by the strain of Curvularia lunata, Drechslera dematioidea. It has many biological activities, such as inhibiting cytokinesis reversibly, inhibiting megasophil endocytosis and exocytosis. Synonyms: 24-Oxa(14)cytochalasa-13,17-diene-1,19,23-trione, 6,7-epoxy-20-hydroxy-16,18-dimethyl-10-phenyl-, (7S,13E,16S,17E,20S)-; 3H-Oxacyclotetradecino(2,3-d)oxireno(f)isoindole-7,11,13(4H,8H,14H)-trione,9,10,15,15a,16,16a,17a,17b-octahydro-8-hydroxy-4,6,16,16a-tetramethyl-15-(phenylmethyl)-, (4S-(1E, 4R*, 5E, 8R*, 12ar*, 15R*, 15ar*, 16R*, 16as*, 17ar*, 17br*))-. CAS No. 79648-73-0. Molecular formula: C30H37NO6. Mole weight: 507.62. | |
| Cytochlor | Cytochlor is a radio-sensitizing pyrimidine nucleoside with potential antineoplastic activity. Cytochlor is metabolized first to a phosphate derivative, CldCMP, by the enzyme deoxycytidine kinase and then to the active uracyl derivative, CldUMP, by the enzyme dCMP deaminase; deoxycytidine kinase and dCMP deaminase have been found in abnormally high concentrations in most cancers. CldUMP, the active metabolite, incorporates into DNA and, upon exposure to radiation, induces the formation of uracil radicals and double-strand DNA breaks. Synonyms: 5-Chloro-2'-deoxycytidine; 5-Chlorodeoxycytidine; 2'-Deoxy-5-chlorocytidine; NSC-371331; NSC 371331. Grades: ≥ 97%. CAS No. 32387-56-7. Molecular formula: C9H12ClN3O5. Mole weight: 261.66. | |
| Cytochrome b5 human | recombinant, expressed in E. coli (histidine-tagged), ?90% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy. | |
| cytochrome-b5 reductase | A flavoprotein (FAD). Group: Enzymes. Synonyms: cytochrome b5 reductase; dihydronicotinamide adenine dinucleotide-cytochrome b5 reductase; reduced nicotinamide adeninedinucleotide-cytochrome b5 reductase; NADH-ferricytochrome b5 oxidoreductase; NADH-cytochrome b5 reductase; NADH 5α-reductase NADH-cytochrome-b5 reductase. Enzyme Commission Number: EC 1.6.2.2. CAS No. 9032-25-1. 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-1579; cytochrome-b5 reductase; EC 1.6.2.2; 9032-25-1; cytochrome b5 reductase; dihydronicotinamide adenine dinucleotide-cytochrome b5 reductase; reduced nicotinamide adeninedinucleotide-cytochrome b5 reductase; NADH-ferricytochrome b5 oxidoreductase; NADH-cytochrome b5 reductase; NADH 5α-reductase NADH-cytochrome-b5 reductase. Cat No: EXWM-1579. |  |
| Cytochrome C | 500mg Pack Size. Group: Biochemicals, Organics, Research Organics & Inorganics. Formula: C42H54FeN8O6S2. CAS No. 9007-43-6. Prepack ID 46874650-500mg. Molecular Weight 886.91. See USA prepack pricing. |  |
| Cytochrome C | Cytochrome C is a multi-functional enzyme involving in life and death decisions of the cell. Cytochrome C is essential in mitochondrial electron transport and intrinsic type II apoptosis [1]. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 9007-43-6. Pack Sizes: 10 mg; 25 mg; 50 mg. Product ID: HY-125857. | |
| cytochrome-c3 hydrogenase | An iron-sulfur protein. Some forms of the enzyme contain nickel ([NiFe]-hydrogenases) and, of these, some contain selenocysteine ([NiFeSe]-hydrogenases). Methylene blue and other acceptors can also be reduced. Group: Enzymes. Synonyms: H2:ferricytochrome c3 oxidoreductase; cytochrome c3 reductase; cytochrome hydrogenase; hydrogenase [ambiguous]. Enzyme Commission Number: EC 1.12.2.1. CAS No. 9027-5-8. 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-0521; cytochrome-c3 hydrogenase; EC 1.12.2.1; 9027-05-8; H2:ferricytochrome c3 oxidoreductase; cytochrome c3 reductase; cytochrome hydrogenase; hydrogenase [ambiguous]. Cat No: EXWM-0521. | |
| Cytochrome c(88-104)(domestic pigeon) | Cytochrome c(88-104)(domestic pigeon). Uses: Designed for use in research and industrial production. Additional or Alternative Names: H2N-KAERADLIAYLKQATAK-OH;KAERADLIAYLKQATAK;H-LYS-ALA-GLU-ARG-ALA-ASP-LEU-ILE-ALA-TYR-LEU-LYS-GLN-ALA-THR-ALA-LYS-OH;CYTOCHROME C - PIGEON (88-104);CYTOCHROME C (88-104) (DOMESTIC PIGEON);PCC (88-104). Product Category: Heterocyclic Organic Compound. CAS No. 86579-06-8. Molecular formula: C84H144N24O25. Mole weight: 1890.19. Purity: 0.96. IUPACName: Cytochrome c - pigeon (88-104). Canonical SMILES: CCC(C)C(C(=O)NC(C)C(=O)NC(CC1=CC=C(C=C1)O)C(=O)NC(CC(C)C)C(=O)NC(CCCCN)C(=O)NC(CCC(=O)N)C(=O)NC(C)C(=O)NC(C(C)O)C(=O)NC(C)C(=O)NC(CCCCN)C(=O)O)NC(=O)C(CC(C)C)NC(=O)C(CC(=O)O)NC(=O)C(C)NC(=O)C(CCCNC(=N)N)NC(=O)C(CCC(=O)O)NC(=O)C(C)NC(=O)C(CCCCN)N. Product ID: ACM86579068. Alfa Chemistry ISO 9001:2015 Certified. Categories: DTXSID20856122. | |
| Cytochrome C (88-104) (domestic pigeon) | Cytochrome C (88-104) (domestic pigeon) is specific for a peptide within the COOH-terminal sequence 88-104. Synonyms: Cytochrome c-pigeon (88-104); L-Lysine, L-lysyl-L-alanyl-L-α-glutamyl-L-arginyl-L-alanyl-L-α-aspartyl-L-leucyl-L-isoleucyl-L-alanyl-L-tyrosyl-L-leucyl-L-lysyl-L-glutaminyl-L-alanyl-L-threonyl-L-alanyl-; L-Lysyl-L-alanyl-L-α-glutamyl-L-arginyl-L-alanyl-L-α-aspartyl-L-leucyl-L-isoleucyl-L-alanyl-L-tyrosyl-L-leucyl-L-lysyl-L-glutaminyl-L-alanyl-L-threonyl-L-alanyl-L-lysine; H-Lys-Ala-Glu-Arg-Ala-Asp-Leu-Ile-Ala-Tyr-Leu-Lys-Gln-Ala-Thr-Ala-Lys-OH. Grades: ≥95%. CAS No. 86579-06-8. Molecular formula: C84H144N24O25. Mole weight: 1890.19. | |
| Cytochrome c equine | recombinant, expressed in E. coli. Group: Fluorescence/luminescence spectroscopy. | |
| Cytochrome c from human heart | ?95% (SDS-PAGE), lyophilized powder. Group: Fluorescence/luminescence spectroscopy. | |
| Cytochrome c from pigeon breast muscle | ?95% based on Mol. Wt. 12,173 basis. Group: Fluorescence/luminescence spectroscopy. | |
| Cytochrome c from Saccharomyces cerevisiae | ?85% based on Mol. Wt. 12,588 basis. Group: Fluorescence/luminescence spectroscopy. | |
| cytochrome-c oxidase | A cytochrome of the a type containing copper. The reduction of O2 to water is accompanied by the extrusion of four protons from the intramitochondrial compartment. Several bacteria appear to contain analogous oxidases. Group: Enzymes. Synonyms: cytochrome oxidase; cytochrome a3; cytochrome aa3; Warburg's respiratory enzyme; indophenol oxidase; indophenolase; complex IV (mitochondrial electron transport); ferrocytochrome c oxidase; NADH cytochrome c oxidase. Enzyme Commission Number: EC 1.9.3.1. CAS No. 9001-16-5. 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-1687; cytochrome-c oxidase; EC 1.9.3.1; 9001-16-5; cytochrome oxidase; cytochrome a3; cytochrome aa3; Warburg's respiratory enzyme; indophenol oxidase; indophenolase; complex IV (mitochondrial electron transport); ferrocytochrome c oxidase; NADH cytochrome c oxidase. Cat No: EXWM-1687. | |
| Cytochrome c Oxidase from bovine heart | 5 mg protein/mL. Group: Fluorescence/luminescence spectroscopy. | |
| Cytochrome c partially acetylated from equine heart | lyophilized powder. Group: Fluorescence/luminescence spectroscopy. | |
| cytochrome-c peroxidase | A hemoprotein. Group: Enzymes. Synonyms: cytochrome peroxidase; cytochrome c-551 peroxidase; apocytochrome c peroxidase; mesocytochrome c peroxidase azide; mesocytochrome c peroxidase cyanide; mesocytochrome c peroxidase cyanate; cytochrome c-H2O oxidoreductase; cytochrome c peroxidase. Enzyme Commission Number: EC 1.11.1.5. CAS No. 9029-53-2. 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-0507; cytochrome-c peroxidase; EC 1.11.1.5; 9029-53-2; cytochrome peroxidase; cytochrome c-551 peroxidase; apocytochrome c peroxidase; mesocytochrome c peroxidase azide; mesocytochrome c peroxidase cyanide; mesocytochrome c peroxidase cyanate; cytochrome c-H2O oxidoreductase; cytochrome c peroxidase. Cat No: EXWM-0507. | |
| Cytochrome c-pigeon (88-104) acetate | Cytochrome c-pigeon (88-104) acetate is specific for a peptide within the COOH-terminal sequence 88-104. Synonyms: Cytochrome C (88-104) (domestic pigeon) acetate; H-Lys-Ala-Glu-Arg-Ala-Asp-Leu-Ile-Ala-Tyr-Leu-Lys-Gln-Ala-Thr-Ala-Lys-OH.CH3CO2H; L-lysyl-L-alanyl-L-alpha-glutamyl-L-arginyl-L-alanyl-L-alpha-aspartyl-L-leucyl-L-isoleucyl-L-alanyl-L-tyrosyl-L-leucyl-L-lysyl-L-glutaminyl-L-alanyl-L-threonyl-L-alanyl-L-lysine acetic acid. Grades: ≥95%. CAS No. 2763584-05-8. Molecular formula: C86H148N24O27. Mole weight: 1950.24. | |
| Cytochrome c Reductase from porcine heart | Type I, lyophilized powder, ?1.0 units/mg protein. Group: Fluorescence/luminescence spectroscopy. | |
| Cytochrome p450 14a-demethylase inhibitor 1d | Cytochrome p450 14a-demethylase inhibitor 1d. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Cytochrome P450 14a-demethylase inhibitor 1d, 1155361-02-6, S2138_Selleck, CHEMBL561816, Cytochrome P450 14a-demethylase inhibitor 1d-Supplied by Selleck Chemicals, 2-(2,4-difluorophenyl)-1-{[(4-fluorophenyl)methyl](prop-2-en-1-yl)amino}-3-(1,2,4-triazol-1-yl)propan-2-ol. Product Category: Heterocyclic Organic Compound. CAS No. 1155361-02-6. Molecular formula: 402.41. Mole weight: C21H21F3N4O. Purity: >99%. IUPACName: 2-(2,4-difluorophenyl)-1-[(4-fluorophenyl)methyl-prop-2-enylamino]-3-(1,2,4-triazol-1-yl)propan-2-ol. Product ID: ACM1155361026. Alfa Chemistry ISO 9001:2015 Certified. | |
| Cytochrome p450 14a-demethylase inhibitor 1i | Cytochrome p450 14a-demethylase inhibitor 1i. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Cytochrome P450 14a-demethylase inhibitor 1i, 1155361-07-1, S2143_Selleck, CHEMBL551756, Cytochrome P450 14a-demethylase inhibitor 1i-Supplied by Selleck Chemicals, 1-{[(4-bromophenyl)methyl](prop-2-en-1-yl)amino}-2-(2,4-difluorophenyl)-3-(1,2,4-triazol-1-yl)propan-2-ol. Product Category: Heterocyclic Organic Compound. CAS No. 1155361-07-1. Molecular formula: 463.32. Mole weight: C21H21BrF2N4O. Purity: >99%. IUPACName: 1-[(4-bromophenyl)methyl-prop-2-enylamino]-2-(2,4-difluorophenyl)-3-(1,2,4-triazol-1-yl)propan-2-ol. Canonical SMILES: C=CCN(CC1=CC=C(C=C1)Br)CC(CN2C=NC=N2)(C3=C(C=C(C=C3)F)F)O. Product ID: ACM1155361071. Alfa Chemistry ISO 9001:2015 Certified. | |
| Cytochrome P450 2C19, human | recombinant, expressed in E. coli. Group: Fluorescence/luminescence spectroscopy. | |
| Cytochrome P450 2C19 I331V, human | recombinant, expressed in E. coli. Group: Fluorescence/luminescence spectroscopy. | |
| Cytochrome P450 2C9*1 (Wild type allele), human | recombinant, expressed in E. coli. Group: Fluorescence/luminescence spectroscopy. | |
| Cytochrome P450 2C9*2 (R144C), human | recombinant, expressed in E. coli. Group: Fluorescence/luminescence spectroscopy. | |
| Cytochrome P450 2C9*3 (I359L), human | recombinant, expressed in E. coli. Group: Fluorescence/luminescence spectroscopy. | |
| Cytochrome P450 2E1 human | recombinant, expressed in Saccharomyces cerevisiae. Group: Fluorescence/luminescence spectroscopy. | |
| Cytochrome P450 3A4 human | recombinant, expressed in E. coli. Group: Fluorescence/luminescence spectroscopy. | |
| Cytochrome P450 3A5 human | recombinant, expressed in E. coli. Group: Fluorescence/luminescence spectroscopy. | |
| Cytochrome P450 4A1, Rat, primers, 902bp amplimer, Downstream Primer | Cytochrome P450 4A1, Rat, primers, 902bp amplimer, Downstream Primer. Group: Molecular Biology. Pack Sizes: 1x50ul. US Biological Life Sciences. | Worldwide |
| Cytochrome P450 4A1, Rat, primers, 902bp amplimer, Upstream Primer | Cytochrome P450 4A1, Rat, primers, 902bp amplimer, Upstream Primer. Group: Molecular Biology. Pack Sizes: 1x50ul. US Biological Life Sciences. | Worldwide |
| Cytochrome P450 4A2, Rat, primers, 302bp amplimer, Downstream Primer | Cytochrome P450 4A2, Rat, primers, 302bp amplimer, Downstream Primer. Group: Molecular Biology. Pack Sizes: 1x50ul. US Biological Life Sciences. | Worldwide |
| Cytochrome P450 4A2, Rat, primers, 302bp amplimer, Upstream Primer | Cytochrome P450 4A2, Rat, primers, 302bp amplimer, Upstream Primer. Group: Molecular Biology. Pack Sizes: 1x50ul. US Biological Life Sciences. | Worldwide |
| Cytochrome P450 4A3, Rat, primers, 302bp amplimer, Downstream Primer | Cytochrome P450 4A3, Rat, primers, 302bp amplimer, Downstream Primer. Group: Molecular Biology. Pack Sizes: 1x50ul. US Biological Life Sciences. | Worldwide |
| Cytochrome P450 4A3, Rat, primers, 302bp amplimer, Upstream Primer | Cytochrome P450 4A3, Rat, primers, 302bp amplimer, Upstream Primer. Group: Molecular Biology. Pack Sizes: 1x50ul. US Biological Life Sciences. | Worldwide |
| Cytochrome P450 4A8, Rat, primers, 1956bp amplimer, Downstream Primer | Cytochrome P450 4A8, Rat, primers, 1956bp amplimer, Downstream Primer. Group: Molecular Biology. Pack Sizes: 1x50ul. US Biological Life Sciences. | Worldwide |
| Cytochrome P450 4A8, Rat, primers, 1956bp amplimer, Upstream Primer | Cytochrome P450 4A8, Rat, primers, 1956bp amplimer, Upstream Primer. Group: Molecular Biology. Pack Sizes: 1x50ul. US Biological Life Sciences. | Worldwide |
| Cytochrome P450 Monooxygenase | hydroxylation (C-H activation) and oxidation of heteroatoms. Group: Enzymes. Synonyms: Cytochrome P450 Monooxygenase; CYP. Form: 1. Enzyme Powder: 8 items*50mg / item, or other quantity2. Screening Kit: 8 items*1mg / item. Cytochrome P450 Monooxygenase; CYP; Screening Kit; library of enzyme; enzyme library. Cat No: ENLC-010. | |
| Cytochrome P450 Reductase from Human, Recombinant | Cytochrome P450 reductase is a membrane bound enzyme required for electron transfer from NADP to cytochrome P450 in microsomes. It can also provide electron transfer to heme oxygenase and cytochrome B5. The cytochrome P450 enzyme system is mainly involved in the detoxification of xenobiotics in the liver. It also participates in the activation of procarcinogens and the metabolism of endogeneous substrates such as steroids. Applications: Human cytochrome p450 reductase has been used in a study to assess the biocatalytic synthesis and structure elucidation of cyclized metabolites of the deacetylase inhibitor panobinostat. human cytochrome p450 reductase has also been u...AD-cytochrome c reductase; NADPH-dependent cytochrome c reductase; NADPH:P-450 reductase. Enzyme Commission Number: EC 1.6.2.4. CAS No. 9023-3-4. Purity: >90% (SDS-PAGE). CPR. Mole weight: 76.5 kDa. Activity: >30 U/mg. Storage: Store at -70°C. Form: Supplied in a solution containing 10 mM potassium phosphate, pH 7.4, 0.1 mM EDTA, 0.5 mM DTT, 20% (v/v) glycerol. Source: Baculovirus infected insect cells. Species: Human. EC 1.6.2.4; NADPH:ferrihemoprotein oxidoreductase; NADPH:hemoprotein oxidoreductase; NADPH:P450 oxidoreductase; P450 reductase; CPR; 9039-06-9; FAD-cytochrome c reductase; NADPH-dependent cytochrome c reductase; NADPH:P-450 reductase. Cat No: NATE-1586. | |
| Cytochrome P450 Reductase from rabbit liver induced with phenobarbital | buffered aqueous glycerol solution. Group: Fluorescence/luminescence spectroscopy. | |
| Cytochrome P450 Reductase human | recombinant, expressed in baculovirus infected insect cells. Group: Fluorescence/luminescence spectroscopy. | |
| Cytogenin | It is produced by the strain of Streptoverticillium eurocidicum. It has weak cytotoxicity. Synonyms: Antibiotic MI 43-37F 11; 8-Hydroxy-3-(hydroxymethyl)-6-methoxy-1H-2-benzopyran-1-one; 1H-2-Benzopyran-1-one,8-hydroxy-3-(hydroxymethyl)-6-methoxy-. CAS No. 132971-59-6. Molecular formula: C11H10O5. Mole weight: 222.19. | |
| Cytohelicase from Helix pomatia | lyophilized powder. Group: Fluorescence/luminescence spectroscopy. | |
| Cytokine-Induced Neutrophil Chemoattractant-3 from rat | >97% (SDS-PAGE), recombinant, expressed in E. coli, lyophilized powder, suitable for cell culture. Group: Fluorescence/luminescence spectroscopy. | |
| Cytokine Inhibitor Library | A unique collection of 613 compounds targeting cytokine signaling for high throughput screening and high content screening for drug discovery; - Bioactivity and safety confirmed by pre-clinical research and clinical trials, and most of them are approved to be marketed; - Targets cover various cytokines including IL, CSF, IFN, TNF, TGF-beta family, growth factors, chemokine family, etc; - 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: L3600. Categories: Cytokine Inhibitor Libraries. |  |
| cytokinin 7-β-glucosyltransferase | Acts on a range of N6-substituted adenines, including zeatin and N6-benzylaminopurine, but not N6-benzyladenine. With some acceptors, 9-β-D-glucosides are also formed. Group: Enzymes. Synonyms: uridine diphosphoglucose-zeatin 7-glucosyltransferase; cytokinin 7-glucosyltransferase; UDP-glucose:zeatin 7-glucosyltransferase. Enzyme Commission Number: EC 2.4.1.118. CAS No. 72103-03-8. 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-2344; cytokinin 7-β-glucosyltransferase; EC 2.4.1.118; 72103-03-8; uridine diphosphoglucose-zeatin 7-glucosyltransferase; cytokinin 7-glucosyltransferase; UDP-glucose:zeatin 7-glucosyltransferase. Cat No: EXWM-2344. | |
| cytokinin dehydrogenase | A flavoprotein(FAD). Catalyses the oxidation of cytokinins, a family of N6-substituted adenine derivatives that are plant hormones, where the substituent is a dimethylallyl or other prenyl group. Although this activity was previously thought to be catalysed by a hydrogen-peroxide-forming oxidase, this enzyme does not require oxygen for activity and does not form hydrogen peroxide. 2,6-Dichloroindophenol, methylene blue, nitroblue tetrazolium, phenazine methosulfate and Cu(II) in the presence of imidazole can act as acceptors. This enzyme plays a part in regulating rice-grain production, with lower levels of the enzyme resulting in enhanced grain production. Group: Enzymes. Synonyms: N6-dimethylallyladenine:(acceptor) oxidoreductase; 6-N-dimethylallyladenine:acceptor oxidoreductase; OsCKX2; CKX; cytokinin oxidase/dehydrogenase. Enzyme Commission Number: EC 1.5.99.12. CAS No. 55326-39-1. 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-1566; cytokinin dehydrogenase; EC 1.5.99.12; 55326-39-1; N6-dimethylallyladenine:(acceptor) oxidoreductase; 6-N-dimethylallyladenine:acceptor oxidoreductase; OsCKX2; CKX; cytokinin oxidase/dehydrogenase. Cat No: EXWM-1566. | |
| Cytolysin | Cytolysin belongs to class I bacteriocins in lantibiotics. Cytolysin is isolated from Enterococcus faecalis and has antibacterial activity. Synonyms: Thr-Thr-Pro-Ala-Cys-Phe-Thr-Ile-Gly-Leu-Gly-Val-Gly-Ala-Leu-Phe-Ser-Ala-Lys-Phe-Cys. Grades: 95.8%. | |
| Cytoplasmic Dynein Inhibitor, Ciliobrevin D (2- (7-chloro-4-oxo-3, 4-dihydroquinazolin-2 (1H)-ylidene)-3- (2, 4-dichlorophenyl)-3-oxopropanenitrile) (AAA+ ATPase Motor Cytoplasmic Dynein Inhibitor) | A cell-permeable benzoyl dihydroquinazolinone derivative that acts as a reversible and specific blocker of AAA+ ATPase motor cytoplasmic dynein and disrupts spindle pole focusing, cold-stable microtubule formation, kinetochore-microtubule attachment, and melanosome aggregation in a dose-dependent manner (~10-40uM). Shown to perturb protein trafficking within the primary cilia and cause a significant increase in intraflagellar transport protein 88 (IFT88) levels at the distal tip of primary cilia. Reported to disrupt primary cilium-dependent Gli regulation and block Hedgehog signaling. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Cytorhodin A | It is an anthracycline antibiotic produced by the strain of Streptomyces cyaneus (A-447). It can inhibit the growth of P388 murine lymphocytic leukemia cells with IC50 of 2.9 ng/mL. Synonyms: 1-Deoxyobelmycin B; A-447C; Antibiotic A-447C; 5,12-Naphthacenedione, 8-ethyl-7,8,9,10-tetrahydro-1,6,8,11-tetrahydroxy-7,10-bis[[2,3,6-trideoxy-3-(dimethylamino)-4-O-[(2S,5S,6S)-tetrahydro-6-methyl-5-[[(2S,5S,6S)-tetrahydro-5-hydroxy-6-methyl-2H-pyran-2-yl]oxy]-2H-pyran-2-yl]-a-L-lyxo-hexopyranosyl]oxy]-, (7R,8R,10S)-; [7R-(7a,8b,10b)]-8-Ethyl-7,8,9,10-tetrahydro-1,6,8,11-tetrahydroxy-7,10-bis[[2,3,6-trideoxy-3-(dimethylamino)-4-O-[[2S-[2a,5b(2R*,5R*,6R*),6b]]-tetrahydro-6-methyl-5-[(tetrahydro-5-hydroxy-6-methyl-2H-pyran-2-yl)oxy]-2H-pyran-2-yl]-a-L-lyxo-hexopyranosyl]oxy]-5,12-naphthacenedione. CAS No. 95599-38-5. Molecular formula: C60H88N2O20. Mole weight: 1157.34. | |
| Cytorhodin X | It is produced by the strain of Streptomyces sp. HPLY-11472 (DSM 2658). It belongs to Rhodimycin group antibiotic. The ED50 of L1210 cell is 0.36 μmol/L (The ED50 of adriamycin in the control group is 0.036 μmol/L). Synonyms: Cytorhodin A, 7-de((2,3,6-trideoxy-3-(dimethylamino)-4-O-((2S-(2-alpha,5-beta(2R*,5R*,6R*),6-beta))-tetrahydro-6-methyl-5-((tetrahydro-5-hydroxy-6-methyl-2H-pyran-2-yl)oxy)-2H-pyran-2-yl)-alpha-L-lyxo-hexopyranosyl)oxy)-9-O-(2,3,6-trideoxy-3-(dimethylamino)-alpha-L-lyxo-hexopyranosyl)-. CAS No. 133914-58-6. Molecular formula: C48H68N2O15. Mole weight: 913.06. | |
| Cytosaminomycin A | It is produced by the strain of Streptomyces sp. KO-8119. It has anti-eimeria Tenella activity. The concentration of Cytosaminomycin A without cleavage in chicken embryo cells is 0.3-0.6 μg/mL. Synonyms: N-[3-(Methylthio)acryloyl]-1-[4-O-[4-(dimethylamino)-4,6-dideoxy-alpha-D-glucopyranosyl]-2,6-dideoxy-beta-D-arabino-hexopyranosyl]cytosine. CAS No. 157878-02-9. Molecular formula: C22H34N4O8S. Mole weight: 514.59. | |
| Cytosaminomycin B | It is produced by the strain of Streptomyces sp. KO-8119. It has anti-eimeria Tenella activity. The concentration of Cytosaminomycin B without cleavage in chicken embryo cells is 0.3-0.6 μg/mL. Synonyms: 2(1H)-pyrimidinone, 1-[2,6-dideoxy-4-o-[4,6-dideoxy-4-(dimethylamino)-alpha-D-glucopyranosyl]-beta-L-arabino-hexopyranosyl]-4-[[4-(methylamino)benzoyl]amino]-. CAS No. 157878-03-0. Molecular formula: C26H37N5O8. Mole weight: 547.60. | |
| Cytosaminomycin C | It is produced by the strain of Streptomyces sp. KO-8119. It has anti-eimeria Tenella activity. The concentration of Cytosaminomycin C without cleavage in chicken embryo cells is 0.3-0.6 μg/mL. CAS No. 157878-04-1. Molecular formula: C23H36N4O8. Mole weight: 496.55. | |
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