CAS 14110-64-6
:cytochalasin A
Description:
Cytochalasin A is a naturally occurring compound classified as a cytochalasins, which are a group of fungal metabolites known for their ability to disrupt cytoskeletal functions. It is primarily derived from the fungus *Helminthosporium* and exhibits a complex structure characterized by a lactone ring and a polycyclic backbone. Cytochalasin A is recognized for its potent ability to inhibit actin polymerization, which affects cell motility, division, and various cellular processes. This compound has been extensively studied in cell biology and pharmacology for its effects on the cytoskeleton, making it a valuable tool in research. Additionally, cytochalasin A has shown potential in various therapeutic applications, including cancer research, due to its ability to induce apoptosis in certain cell types. However, its use is often limited by its cytotoxicity and the need for careful handling in laboratory settings. Overall, cytochalasin A serves as an important compound for understanding cellular dynamics and exploring new therapeutic avenues.
Formula:C29H35NO5
InChI:InChI=1/C29H35NO5/c1-18-9-7-13-22(31)15-16-25(32)35-29-23(14-8-10-18)27(33)20(3)19(2)26(29)24(30-28(29)34)17-21-11-5-4-6-12-21/h4-6,8,11-12,14-16,18-19,23-24,26-27,33H,3,7,9-10,13,17H2,1-2H3,(H,30,34)/b14-8+,16-15u/t18-,19-,23-,24-,26+,27+,29-/m0/s1
InChI key:InChIKey=ZMAODHOXRBLOQO-TZVKRXPSSA-N
SMILES:O=C1[C@]23[C@]([C@H](CC4=CC=CC=C4)N1)([C@H](C)C(=C)[C@@H](O)[C@@]2(/C=C/C[C@H](C)CCCC(=O)\C=C\C(=O)O3)[H])[H]
Synonyms:- (3E,9R,11E,12aS,13S,15S,15aS,16S,18aS)-6,7,8,9,10,12a,13,14,15,15a,16,17-Dodecahydro-13-hydroxy-9,15-dimethyl-14-methylene-16-(phenylmethyl)-2H-oxacyclotetradecino[2,3-d]isoindole-2,5,18-trione
- (9R,11E,12aS,13S,15R,15aR,16S,18aR)-16-benzyl-13-hydroxy-9,15-dimethyl-14-methylidene-6,7,8,9,10,12a,13,14,15,15a,16,17-dodecahydro-2H-oxacyclotetradecino[2,3-d]isoindole-2,5,18-trione
- (9S,11E,12aS,13S,15R,15aR,16S,18aR)-16-benzyl-13-hydroxy-9,15-dimethyl-14-methylidene-6,7,8,9,10,12a,13,14,15,15a,16,17-dodecahydro-2H-oxacyclotetradecino[2,3-d]isoindole-2,5,18-trione
- 16-benzyl-13-hydroxy-9,15-dimethyl-14-methylidene-6,7,8,9,10,12a,13,14,15,15a,16,17-dodecahydro-2H-oxacyclotetradecino[2,3-d]isoindole-2,5,18-trione
- 24-Oxa(14)cytochalasa-6(12),13,21-triene-1,20,23-trione, 7-hydroxy-16-methyl-10-phenyl-, (7S,13E,16R,21E)-
- 2H-Oxacyclotetradecino(2,3-d)isoindole-2,5,18-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, 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)-
- 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)-, (9R-(3E,9R*,11E,12aS*,13S*,15S*,15aS*,16S*,18aS*))-
- 5,5-Didehydrophomin
- 5-Dehydrophomin
- 7(S)-Hydroxy-16(R)-methyl-10-phenyl-24-oxa(14)cytochalasa-6(12),13(E),21(E)-triene-1,20,23-trione
- Dehydrophomin
- Nsc 174119
- Phomin, 5,5-didehydro-
- Cytochalasin A
- CYTOCHALASIN A FROM DRESCHSLERA DEMATIOIDEA
- cytochalasin a from helminthosporium dematioideum
- Cytochalasin A 5-Dehydrophomin Dehydrophomin
- CytochalasinA from Drechslera dematioidea
- CYTOCHALASIN A FROM DRESCHSLERA DEMATIOIDEA, BIOCHEMIKA, >= 99.0% (TLC)
- CYTOCHALASIN A(RG)
- Cytochalasin dreschslera dematioidea
- (7S,13E,16R,21E)-7-Hydroxy-16-methyl-10-phenyl-24-oxa[14]cytochalasa-6(12),13,21-triene-1,20,23-trione
- See more synonyms
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Found 4 products.
Cytochalasin A
CAS:<p>Cytochalasin A</p>Formula:C29H35NO5Purity:By hplc: 100% (Typical Value in Batch COA)Color and Shape: white powderMolecular weight:477.59g/molCytochalasin A
CAS:<p>Cytochalasin A, a cell-penetrating fungal toxin, blocks HIV-1 protease (IC50 = 3 μM) and hinders actin and microtubule assembly. It's an antibiotic.</p>Formula:C29H35NO5Purity:98%Color and Shape:White Crystalline PowderMolecular weight:477.59Cytochalasin A
CAS:<p>Applications Cytochalasin A binds to the glucose transporter and inhibit monosaccharide transport across the plasma membrane. Preventing growth and sugar uptake in a Saccharomyces strain.<br>References Griffin, J. et al.: Proc. Natl. Acad. Sci., 79, 3759 (1982);<br></p>Formula:C29H35NO5Color and Shape:NeatMolecular weight:477.59



