C0889
细胞松驰素 H 来源于拟茎点霉 属
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经验公式（希尔记法）:
C30H39NO5
化学文摘社编号:
分子量:
493.63
UNSPSC Code:
12352103
NACRES:
NA.77
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1632647
Form:
crystals
InChI
1S/C30H39NO5/c1-18-10-9-13-23-27(33)20(3)19(2)26-24(16-22-11-7-6-8-12-22)31-28(34)30(23,26)25(36-21(4)32)14-15-29(5,35)17-18/h6-9,11-15,18-19,23-27,33,35H,3,10,16-17H2,1-2,4-5H3,(H,31,34)/b13-9+,15-14+/t18-,19+,23?,24-,25+,26?,27+,29-,30+/m0/s1
SMILES string
C[C@H]1C\C=C\C2[C@H](O)C(=C)[C@@H](C)C3[C@H](Cc4ccccc4)NC(=O)[C@@]23C(OC(C)=O)\C=C\[C@](C)(O)C1
InChI key
NAEWXXDGBKTIMN-QHDZSFFESA-N
form
crystals
storage temp.
2-8°C
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Biochem/physiol Actions
Cytochalasin reported to have CNS activity
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 1 Inhalation - Acute Tox. 2 Dermal - Acute Tox. 2 Oral - Repr. 2
存储类别
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 3
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
法规信息
新产品
此项目有
S Ghaskadbi et al.
Experimental cell biology, 50(3), 155-161 (1982-01-01)
Cytochalasin H (CH) has been shown to inhibit the reaggregation of dissociated cells of a fresh water sponge. The effect is dose-dependent and reversible. Even after 24 h of CH treatment, the cells show the formation of pseudopodia suggesting that
Scott M Stoeger et al.
Cancer chemotherapy and pharmacology, 63(5), 807-818 (2008-07-29)
Previous studies have indicated that the ERK1/2 MAP kinase signaling pathway plays an important role not only in cell growth, cell cycle regulation, and differentiation, but also in determining the sensitivity of cells to anticancer agents as well. Furthermore, expression
S Ghaskadbi et al.
Toxicology, 33(3-4), 323-330 (1984-12-01)
Effects of the mould metabolite, cytochalasin H (CH) were studied in chick embryos explanted at stages 4, 5 and 8 and cultured in vitro. Morphological and histological observations revealed that the major effects of CH are inhibition of primary morphogenesis
Effect of cytochalasins B & H on isoelectric focusing of chick embryonic neural retina cells.
S Ghaskadbi et al.
Indian journal of experimental biology, 20(12), 869-871 (1982-12-01)
J Ondeyka et al.
The Journal of antibiotics, 45(5), 679-685 (1992-05-01)
A novel HIV-1 protease inhibitor, L-696,474 (C30H39NO4, 477), was isolated from the fermentations of the fungus Hypoxylon fragiforme (ATCC 20995, MF5511) and purified by silica gel chromatography followed by crystallization. Spectroscopic studies have shown the competitive inhibitor L-696,474 to be
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