Identification | Back Directory | [Name]
CYTOCHALASIN C | [CAS]
22144-76-9 | [Synonyms]
CYTOCHALASIN C CYTOCHALASIN C(RG) NAIODHJWOHMDJX-VBWDGLFXSA-N (7s,13e,16s,18r,19e,21r)-methyl-10-phenyl cytochalasin C from metarrhizium anisopliae cytochalasin-C from metarrhizium*anisopliae CYTOCHALASIN C FROM METARRHIRIUM ANISOPL IAE Cytochalasin C, 97%, from Metarrhizium anisopliae (11)cytochalasa-5,13,19-triene-1,17-dione,21-(acetoxy)-7,18-dihydroxy-16,18-di 7(S),18-dihydroxy-16(S),18(R)-dimethyl-10-phenyl[11]cytochalasa-5,13(E),19(E)-triene-1,17-dione 21(R)-acetate 1H-Cycloundec[d]isoindole-1,11(2H)-dione, 15-(acetyloxy)-3,3a,6,6a,9,10,12,15-octahydro-6,12-dihydroxy-4,5,10,12-tetramethyl-3-(phenylmethyl)-, (3S,3aR,6S,6aR,7E,10S,12R,13E,15R,15aR)- | [EINECS(EC#)]
244-803-6 | [Molecular Formula]
C30H37NO6 | [MDL Number]
MFCD00066080 | [MOL File]
22144-76-9.mol | [Molecular Weight]
507.62 |
Chemical Properties | Back Directory | [Melting point ]
260-264°C | [Boiling point ]
595.84°C (rough estimate) | [density ]
1.1764 (rough estimate) | [refractive index ]
1.6310 (estimate) | [storage temp. ]
−20°C
| [solubility ]
methylene chloride: 5 mg/mL, clear, colorless
| [form ]
White to off-white powder. | [pka]
11.95±0.70(Predicted) | [color ]
White to off-white | [BRN ]
1613194 | [LogP]
3.250 (est) |
Safety Data | Back Directory | [Hazard Codes ]
T+,T | [Risk Statements ]
26/27/28-63 | [Safety Statements ]
28-36/37-45 | [RIDADR ]
UN 1544 6.1/PG 2
| [WGK Germany ]
3
| [RTECS ]
HA5300500
| [F ]
10 | [HazardClass ]
6.1(a) | [PackingGroup ]
I | [HS Code ]
29337900 | [Toxicity]
mouse,LD,intraperitoneal,> 100mg/kg (100mg/kg),Chemical and Pharmaceutical Bulletin. Vol. 21, Pg. 2268, 1973. |
Hazard Information | Back Directory | [Chemical Properties]
White solid | [Uses]
Cytochalasin C is one of a family of potent mycotoxins produced by a range of fungi. All members of the class exhibit profound effects on cytoskeletal proteins, resulting in pronounced morphogenic changes in animals and plants. The cytochalasins act by disrupting actin microfilaments and these effects are most noticeable by the inhibition of cell division. |
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