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Merck
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C0889

Sigma-Aldrich

Cytochalasin H from Phomopsis sp.

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About This Item

Formula empirica (notazione di Hill):
C30H39NO5
Numero CAS:
53760-19-3
Peso molecolare:
493.63
Beilstein:
1632647
Numero MDL:
MFCD00010539
Codice UNSPSC:
12352103
ID PubChem:
24892283
NACRES:
NA.77

Stato

crystals

Temperatura di conservazione

2-8°C

Stringa SMILE

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
NAEWXXDGBKTIMN-QHDZSFFESA-N

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Azioni biochim/fisiol

Cytochalasin reported to have CNS activity

Pittogrammi

Skull and crossbonesHealth hazard
GHS06,GHS08

Avvertenze

Danger

Indicazioni di pericolo

H300 + H310 + H330,H361

Classi di pericolo

Acute Tox. 1 Inhalation - Acute Tox. 2 Dermal - Acute Tox. 2 Oral - Repr. 2

Codice della classe di stoccaggio

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

Classe di pericolosità dell'acqua (WGK)

WGK 3

Dispositivi di protezione individuale

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

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Certificati d'analisi (COA)

Lot/Batch Number
125H0923
050K0776
048H1153
113H4017
084H0024

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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.
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
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
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
Visualizza tutti i documenti correlati

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