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Principaux documents

30382

Sigma-Aldrich

Cytochalasin C from Metarrhizium anisopliae

≥97.0% (TLC)

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About This Item

Formule empirique (notation de Hill):
C30H37NO6
Numéro CAS:
Poids moléculaire :
507.62
Numéro Beilstein :
1613194
Numéro CE :
Numéro MDL:
Code UNSPSC :
12352202
ID de substance PubChem :
Nomenclature NACRES :
NA.77

Source biologique

Metarrhizium anisopliae

Pureté

≥97.0% (TLC)

Forme

fibers
powder

Solubilité

methylene chloride: 5 mg/mL, clear, colorless

Température de stockage

−20°C

Chaîne SMILES 

C[C@@H]1C\C=C\[C@H]2[C@H](O)C(C)=C(C)C3[C@H](Cc4ccccc4)NC(=O)[C@@]23C(OC(C)=O)\C=C\[C@@](C)(O)C1=O

InChI

1S/C30H37NO6/c1-17-10-9-13-22-26(33)19(3)18(2)25-23(16-21-11-7-6-8-12-21)31-28(35)30(22,25)24(37-20(4)32)14-15-29(5,36)27(17)34/h6-9,11-15,17,22-26,33,36H,10,16H2,1-5H3,(H,31,35)/b13-9+,15-14+/t17-,22+,23+,24-,25?,26-,29-,30-/m1/s1

Clé InChI

NAIODHJWOHMDJX-QMTXKCDBSA-N

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Autres remarques

Structure of cytochalasins and cytochalasin B binding sites in human erythrocyte membranes

Pictogrammes

Skull and crossbonesHealth hazard

Mention d'avertissement

Danger

Mentions de danger

Classification des risques

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

Code de la classe de stockage

6.1B - Non-combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

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


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Consulter la Bibliothèque de documents

Yong-Xiang Song et al.
Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials, 33(6), 901-903 (2010-11-06)
To study the secondary metabolites of mangrove endophytic fungus BL321. The compounds were isolated by chromatographic technique. The structures were identified by comprehensive physico-chemical properties and spectral methods. Five compounds were isolated and identified as 3,4a-dimethyl-2-oxo-2,4,4a,5,6,7-hexahydronaphtho[2,3-b]furan-5-carboxylic acid(1), cytochalasin C(2), cytochalasin
T Glinsukon et al.
Research communications in chemical pathology and pharmacology, 51(2), 265-268 (1986-02-01)
Cytochalasins A, B, C, D and E at a concentration of 5.0 microgram/ml significantly inhibited the motility of spermatozoa collected from the cauda epididymidis of rats when diluted in Hank's solution containing BSA by 21.6-38.1% within a few min incubation.
H Haimoto et al.
The American journal of pathology, 121(2), 185-191 (1985-11-01)
To elucidate the changes of ultrastructural localization of S-100 protein during lipolysis in adipocytes, an immunoelectron-microscopic study was performed. Epididymal fat pads from Wistar rats were incubated in the buffer with or without 10 microM epinephrine. Before incubation with epinephrine
M Varedi et al.
Journal of cellular physiology, 172(2), 192-199 (1997-08-01)
Cytoskeleton not only controls cell morphology but also regulates cell growth, migration, differentiation, and gene expression, events which are fundamental to embryogenesis, carcinogenesis, and wound healing. We have recently reported that reorganization of cytoskeleton induces expression of mRNA for transforming
B H Patwardhan et al.
Journal of medicinal chemistry, 25(6), 663-666 (1982-06-01)
A series of halogenated and related analogues of cytochalasin C (CC) and D (CD) has been synthesized, and the biological activities of the analogues as inhibitors in a cell-free contractility model system obtained from Ehrlich ascites tumor cells were evaluated.

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