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Product Name:Cytochalasin A, 98% CAS:14110-64-6 Purity:98% Package:10MG;5MG
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| CYTOCHALASIN A Basic information |
Product Name: | CYTOCHALASIN A | Synonyms: | (7S,13E,16R,21E)-7-Hydroxy-16-methyl-10-phenyl-24-oxa[14]cytochalasa-6(12),13,21-triene-1,20,23-trione;5,5-Didehydrophomin;Dehydrophomin;Cytochalasin dreschslera dematioidea;Cytochalasin A 5-Dehydrophomin Dehydrophomin;7(S)-hydroxy-16(R)-methyl-10-phenyl-24-oxa[14]cytochalasa-6(12),13(E),21(E)-triene-1,20,23-trione;2H-Oxacyclotetradecino2,3-disoindole-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)-;CYTOCHALASIN A FROM DRESCHSLERA DEMATIOIDEA | CAS: | 14110-64-6 | MF: | C29H35NO5 | MW: | 477.59 | EINECS: | 237-964-9 | Product Categories: | Actin Inhibitors and ProbesCell Signaling and Neuroscience;Cell Signaling and Neuroscience;antibiotic;Cytoskeleton and Extracellular Matrix;Mold;Toxins and Venoms | Mol File: | 14110-64-6.mol | ![CYTOCHALASIN A Structure](CAS/GIF/14110-64-6.gif) |
| CYTOCHALASIN A Chemical Properties |
Melting point | 190-191 °C | Boiling point | 725.1±60.0 °C(Predicted) | density | 1.20±0.1 g/cm3(Predicted) | storage temp. | -20°C | solubility | ethanol: 20 mg/mL, clear, colorless | pka | 13.54±0.70(Predicted) | form | Powder | color | White | Water Solubility | Soluble in DMF, DMSO, ethanol and acetone. Insoluble in water. | Sensitive | Light Sensitive | BRN | 949521 | LogP | 1.849 (est) | EPA Substance Registry System | Cytochalasin A (14110-64-6) |
Hazard Codes | T+,T | Risk Statements | 26/27/28-63 | Safety Statements | 28-36/37-45 | RIDADR | UN 1544 6.1/PG 2 | WGK Germany | 3 | F | 10 | HazardClass | 6.1(a) | PackingGroup | I | HS Code | 29349990 |
| CYTOCHALASIN A Usage And Synthesis |
Description | The cytochalasins are cell-permeable fungal metabolites which inhibit actin polymerization. This interferes with such diverse processes as cell movement, growth, phagocytosis, degranulation, and secretion. Cytochalasin A is an oxidized analog of cytochalasin B which uniquely inhibits HIV-1 protease (IC50 = 3 μM). Cytochalasins A and B differ from other cytochalasins in being able to rapidly and reversibly inhibit glucose transport by competitively binding glucose transporters (Ki = 4.0 and 0.6 μM, respectively). Cytochalasin A also induces the phosphorylation of the tyrosine phosphatase PTP3 of Dictyostelium, activating STATc. | Chemical Properties | white powder | Uses | Cytochalasin A binds to the glucose transporter and inhibit monosaccharide transport across the plasma membrane. Preventing growth and sugar uptake in a Saccharomyces strain. | Uses | 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, giving 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 the class display diverse selectivity. Specifically, cytochalasin A is one of the few cytochalasins exhibiting activity against HIV-1 protease. | Definition | ChEBI: Cytochalasin A is a cytochalasin. | Biochem/physiol Actions | Cytochalasin A reacts with sulfhydryls, and inhibits growth and glucose transport in Saccharomyces. Cytochalasin A is an oxidizing analog of cytochalsin B. |
| CYTOCHALASIN A Preparation Products And Raw materials |
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