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| Product | Description | |
|---|---|---|
| Cytidyl-3'-5'-adenosine ammonium salt | Cytidyl-3'-5'-adenosine ammonium salt. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg, 2mg, 5mg. US Biological Life Sciences. |  Worldwide |
| Cytidyl-3'-5'-uridine ammonium salt | Cytidyl-3'-5'-uridine ammonium salt. Group: Biochemicals. Grades: Highly Purified. CAS No. 27552-97-2. Pack Sizes: 1mg, 2mg, 5mg. Molecular Formula: C18H24N5O13P·NH3. US Biological Life Sciences. | Worldwide |
| cytidylate cyclase | This enzyme belongs to the family of lyases, specifically the class of phosphorus-oxygen lyases. Group: Enzymes. Synonyms: 3',5'-cyclic-CMP synthase; cytidylyl cyclase; cytidyl cyclase; CTP diphosphate-lyase (cyclizing). Enzyme Commission Number: EC 4.6.1.6. CAS No. 65357-82-6. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-5356; cytidylate cyclase; EC 4.6.1.6; 65357-82-6; 3',5'-cyclic-CMP synthase; cytidylyl cyclase; cytidyl cyclase; CTP diphosphate-lyase (cyclizing). Cat No: EXWM-5356. |  |
| CYTIDYLYL(25)GUANOSINE AMMONIUM | CYTIDYLYL(25)GUANOSINE AMMONIUM. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 102601-47-8, Cytidylyl(2 inverted exclamation marka inverted exclamation marku5 inverted exclamation marka)guanosine ammonium salt. Product Category: Heterocyclic Organic Compound. CAS No. 102601-47-8. Molecular formula: C19H28N9O12P. Mole weight: 605.452482 [g/mol]. Purity: 0.96. IUPACName: [5-(2-amino-6-oxo-3H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methyl [2-(4-amino-2-oxopyrimidin-1-yl)-4-hydroxy-5-(hydroxymethyl)oxolan-3-yl] hydrogen phosphate;azane. Canonical SMILES: C1=CN(C(=O)N=C1N)C2C(C(C(O2)CO)O)OP(=O)(O)OCC3C(C(C(O3)N4C=NC5=C4NC(=NC5=O)N)O)O.N. Product ID: ACM102601478. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Cytidylyl(3',5')adenosine | Cytidylyl(3',5')adenosine, a vital molecule in RNA metabolism, assumes an indispensable role in regulating gene expression. The compound doubles as an elite research instrument, enabling a detailed study of diverse biological processes, such as transcription and translation. Some studies intimate that the molecule's paucity may underpin multiple diseases, like neurological disorders and cancer. Concomitantly, its healing potential warrants considerable investigation. Synonyms: Cytidylyl-3',5'-adenosine phosphate; Cytidylyl adenosine; CpA RNA Dinucleotide (5'-3'). Grades: ≥95% by AX-HPLC. Molecular formula: C19H25N8O11P. Mole weight: 572.40. |  |
| Cytidylyl-(3'-5')-cytidine | Cytidylyl-(3'-5')-cytidine is a biochemical utilized in the production of RNA. It also plays a crucial role in signaling pathways. In the biomedical field, it is being researched as a potential treatment for certain cancers, such as pancreatic cancer. Synonyms: CpC RNA Dinucleotide (5'-3'). Grades: ≥95% by AX-HPLC. CAS No. 2536-99-4. Molecular formula: C18H25N6O12P. Mole weight: 548.40. | |
| Cytidylyl-(3'-5')-cytidine monoammonia salt | Cytidylyl-(3'-5')-cytidine monoammonia salt is an exquisitely advanced compound, manifesting prodigious potential in studying multifarious ailments encompassing viral infections and assorted cancer phenotypes. Synonyms: [5-(4-amino-2-oxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methyl [5-(4-amino-2-oxopyrimidin-1-yl)-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl] hydrogen phosphate; azane. CAS No. 27552-98-3. Molecular formula: C18H25N6O12P.NH3. Mole weight: 565.48. | |
| Cytidylyl-(3'-5')-guanosine | Cytidylyl-(3'-5')-guanosine is a pivotal compound entity, assuming a pivotal role in the intricacies of RNA synthesand serves as a potent catalyst for RNA-dependent protein kinase. Synonyms: Cytidylyl-3'-5'-guanosine; CpG RNA Dinucleotide (5'-3'). Grades: 95%. CAS No. 2382-65-2. Molecular formula: C19H25N8O12P. Mole weight: 588.4. | |
| cytidylyl(3'-5')uridine | Cytidylyl(3'-5')uridine, a critical biochemical intermediate imperative in nucleotide metabolism, presents as a promising therapeutic agent for various ailments. Such ailments involve, but are not limited to, viral infections and certain cancerous illnesses. Moreover, this novel product provides researchers with an advantageous tool in understanding the molecular mechanisms that facilitate nucleotide biosynthesis and metabolism. Synonyms: Cytidylyl-(3',5')-uridine; CpU RNA Dinucleotide (5'-3'). Grades: ≥95% by AX-HPLC. CAS No. 2382-64-1. Molecular formula: C18H24N5O13P. Mole weight: 549.40. | |
| Cytisine | Cytisine. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Sophorine. Product Category: Heterocyclic Organic Compound. Appearance: powder. CAS No. 485-35-8. Molecular formula: C11H14N2O. Mole weight: 190.24. Purity: 98%+. Product ID: ACM485358. Alfa Chemistry ISO 9001:2015 Certified. | |
| Cytisine | Toxic priniciple in seed of Laburnum anagyroides and other Leguminosae. A neuronal nicotinic acetylcholine agonist. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 50mg. US Biological Life Sciences. | Worldwide |
| Cytisine | Cytisine is a nicotinic acetylcholine receptor (nAChR) agonist. It has been used medically to help with smoking cessation. Cytisine can be used in health products. Uses: Smoking cessation. Synonyms: Baptitoxin; Citizin; HSDB 3560; HSDB3560; HSDB-3560; Laburnin; NSC 407282; NSC407282; NSC-407282; Sophorin; Cytisine; Cytisinicline; Baptitoxine; Sophorine; (-)-Cytisine; Laburnin. Grades: ≥ 98%. CAS No. 485-35-8. Molecular formula: C11H14N2O. Mole weight: 190.246. | |
| Cytisine-d4 | Cytisine-d4. Group: Biochemicals. Alternative Names: (1R,5S)-. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Cytisinicline | Cytisinicline (Cytisine) is an alkaloid. Cytisinicline (Cytisine) is a partial agonist of α4β2 nAChRs [1] , and partial to full agonist at β4 containing receptors and α7 receptors [2]. Has been used medically to help with smoking cessation [3]. Uses: Scientific research. Group: Natural products. Alternative Names: Cytisine; Sophorine; Baptitoxine. CAS No. 485-35-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg. Product ID: HY-N0175. |  |
| Cytochalasin A | Cytochalasin A is a cell-permeable fungal toxin that is an oxidized derivative of cytochalasin B. Cytochalasin A is an inhibitor of HIV-1 protease ( IC 50 =3 μM) and inhibits actin polymerization and interferes with microtubule assembly by reacting with sulfhydryl groups. Antibiotic and fungicidal activitives [1] [2]. Uses: Scientific research. Group: Natural products. CAS No. 14110-64-6. Pack Sizes: 5 mg; 10 mg. Product ID: HY-N6773. | |
| Cytochalasin A | Cytochalasin A is one of a family of potent mycotoxins produced by several species of fungi. All members of the class exhibit profound effects on cytoskeletal proteins which give rise to pronounced morphogenic activity in animals and plants. Like most cytochalsins, cytochalasin A exhibits potent inhibition of actin filament function leading to cell death by apoptosis and displays a broad range of resultant cellular actions. Despite the common mode of action, there is evidence that individual members of this class display diverse selectivity. Specifically, cytochalasin A was shown to be one of the few cytochalasins exhibiting activity against HIV-1 protease. Group: Biochemicals. Grades: Highly Purified. CAS No. 14110-64-6. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Cytochalasin A | 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. Cytochalasin A is an HIV protease inhibitor. Synonyms: NSC174119; Dehydrophomin; 5-Dehydrophomin; 5,5-Didehydrophomin; 2H-Oxacyclotetradecino(2,3-d)isoindole-2,5,18-trione, 6,7,8,9,10,12a,13,14,15,15a,16,17-dodecahydro-13-hydroxy-9,15-dimethyl-14-methylene-16-(phenylmethyl)-, (3E, 9R, 11E, 12aS, 13S, 15S, 15aS, 16S, 18aS)-; (7S,13E,16R,21E)-7-Hydroxy-16-methyl-10-phenyl-24-Oxa[14]cytochalasa-6(12),13,21-triene-1,20,23-trione; 16-Benzyl-6,7,8,9,10,12a,13,14,15,15a,16,17-dodecahydro-13-hydroxy-9,15-dimethyl-14-methylene-2H-Oxacyclotetradecino[2,3-d]isoindole-2,5,18-trione. Grades: >98% by HPLC. CAS No. 14110-64-6. Molecular formula: C29H35NO5. Mole weight: 477.59. | |
| Cytochalasin B | Cytochalasin B is a cell-permeable mycotoxin binding to the barbed end of actin filaments, disrupting the formation of actin polymers, with K d value of 1.4-2.2 nM for F-actin. Cytochalasin B blocks cell migration. Uses: Scientific research. Group: Natural products. Alternative Names: Phomin. CAS No. 14930-96-2. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg. Product ID: HY-16928. | |
| Cytochalasin B | 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. Cytosine B has immunosuppressive effects. Synonyms: (7S,13E,16R,20R,21E)-7,20-Dihydroxy-16-methyl-10-phenyl-24-oxa[14]cytochalasa-6(12),13,21-triene-1,23-dione; (E,E)-(5R,9R,12aS,13S,15S,15aS,16S,18aS)-16-Benzyl-6,7,8,9,10,12a,13,14,15,15a,16,17-dodecahydro-5,13-dihydroxy-9,15-dimethyl-14-methylene-2H-Oxacyclotetradecino[2,3-d]isoindole-2,18(5H)-dione; NSC 107658; Phomin. Grades: >99% by HPLC. CAS No. 14930-96-2. Molecular formula: C29H37NO5. Mole weight: 479.61. | |
| Cytochalasin B | Cytochalasin B is one of the most extensively studied members of a family of potent mycotoxins produced by several species of fungi. All members of the class exhibit profound effects on cytoskeletal proteins which give rise to pronounced morphogenic activity in animals and plants. Like most cytochalsins, cytochalasin B exhibits potent inhibition of actin filament function leading to cell death by apoptosis and displays a broad range of resultant cellular actions. Despite the common mode of action, class there is evidence that individual members of this class display diverse selectivity. However, lack of comparative co-metabolite analysis has restricted a more complete understanding of their individual selectivity. Group: Biochemicals. Grades: Highly Purified. CAS No. 14930-96-2. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Cytochalasin C | Cytochalasin C 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. The cytochalasins act by disrupting actin microfilaments and these effects are most noticeable by the inhibition of cell division. Group: Biochemicals. Grades: Highly Purified. CAS No. 22144-76-9. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Cytochalasin C | 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. Synonyms: 3-Benzyl-3,3a,6,6a,9,10,12,15-octahydro-6,12,15-trihydroxy-4,5,10,12-tetramethyl-1H-cycloundec[d]isoindole-1,11(2H)-dione 15-Acetate; (7S,13E,16S,18R,19E,21R)-21-(acetyloxy)-7,18-dihydroxy-16,18-dimethyl-10-phenyl-[11]Cytochalasa-5,13,19-triene-1,17-dione; [3S-(3R*, 3aS*, 6R*, 6aS*, 7E, 10R*, 12S*, 13E, 15S*, 15aS*)]-15-(Acetyloxy)-3, 3a, 6, 6a, 9, 10, 12, 15-octahydro-6, 12-dihydroxy-4, 5, 10, 12-tetramethyl-3-(phenylmethyl)-1H-Cycloundec[d]isoindole-1, 11(2H)-dione. Grades: >99% by HPLC. CAS No. 22144-76-9. Molecular formula: C30H37NO6. Mole weight: 507.62. | |
| Cytochalasin C | Cytochalasin C is a cell-permeable fungal toxin and induces the formation of nuclear rodlets. Cytochalasin C is 10 times less toxic in mice than is cytochalasin D [1] [2] [3]. Uses: Scientific research. Group: Natural products. CAS No. 22144-76-9. Pack Sizes: 1 mg. Product ID: HY-N6774. | |
| Cytochalasin C from Metarrhizium anisopliae | ?97.0% (TLC). Group: Fluorescence/luminescence spectroscopy. |  |
| Cytochalasin D | from Zygosporium mansonii, ?98% (TLC and HPLC), powder. 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 | 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 |
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