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Merck
CN

C0889

Cytochalasin H from Phomopsis sp.

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About This Item

Empirical Formula (Hill Notation):
C30H39NO5
CAS Number:
53760-19-3
Molecular Weight:
493.63
UNSPSC Code:
12352103
NACRES:
NA.77
PubChem Substance ID:
24892283
MDL number:
MFCD00010539
Beilstein/REAXYS Number:
1632647
Form:
crystals

Key Documents

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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

pictograms

Skull and crossbonesHealth hazard
GHS06,GHS08

signalword

Danger

Hazard Classifications

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

Storage Class

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

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
113H4017
084H0024
016H0282
125H0923
050K0776

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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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