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About This Item
经验公式（希尔记法）:
C30H39NO5
CAS号:
分子量:
493.63
Beilstein:
1632647
MDL编号:
UNSPSC代码:
12352103
PubChem化学物质编号:
NACRES:
NA.77
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表单
crystals
储存温度
2-8°C
SMILES字符串
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
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
InChI key
NAEWXXDGBKTIMN-QHDZSFFESA-N
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生化/生理作用
Cytochalasin reported to have CNS activity
警示用语：
Danger
危险分类
Acute Tox. 1 Inhalation - Acute Tox. 2 Dermal - Acute Tox. 2 Oral - Repr. 2
储存分类代码
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
WGK
WGK 3
个人防护装备
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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
P Natarajan et al.
Platelets, 11(8), 467-476 (2001-02-15)
Platelets contain a well-developed and dynamic cytoskeleton composed mainly of actin and actin-associated proteins. Upon platelet activation there is rapid polymerisation of actin and a marked reorganisation of the platelet cytoskeleton. Cytochalasins are agents that interfere with the polymerisation of
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
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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