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58857-02-6

58857-02-6 Structure

58857-02-6 Structure
IdentificationBack Directory
[Name]

Ambruticin
[CAS]

58857-02-6
[Synonyms]

W7783
W-7783
W 7783
Ambruticin
(+)-ambruticin S
L-gluco-Non-8-enonic acid, 3,7-anhydro-2,4,8,9-tetradeoxy-9-[(1S,2S,3R)-2-[(1E,3R,4E)-5-[(2R,6R)-6-ethyl-3,6-dihydro-5-methyl-2H-pyran-2-yl]-3-methyl-1,4-hexadien-1-yl]-3-methylcyclopropyl]-, (8E)-
[Molecular Formula]

C28H42O6
[MDL Number]

MFCD00865607
[MOL File]

58857-02-6.mol
[Molecular Weight]

474.634
Hazard InformationBack Directory
[Originator]

Ambruticin,Universitet Karlsruhe (TH)
[Uses]

Antifungal.
[Therapeutic Function]

Antifungal
[in vivo]

The acute LD50 values for the sodium salt of Ambruticin in mice were: intravenous 315 mg/kg, oral > 1000 mg/kg[1].
Ambruticin is rapidly absorbed by the oral route in mice. Ambruticin (75 mg/kg, gavage) produces a peak serum level of 46 μg/mL with a serum half-life of 3.1 h[2].
Ambruticin (40 mg/kg, oral, twice daily for a total of 10 days) shows protective activity in Guinea pigs infected with a severe T. mentagrophytes challenge[2].
Ambruticin shows protective activity in mice acutely infected with a severe C. albicans challenge[2].

Animal Model:Guinea pigs (infected with a strain of T. mentagrophytes)[2]
Dosage:40 mg/kg
Administration:Oral, starting on day 3 postinfection, twice daily for a total of 10 days
Result:On postinfection day 15, the guinea pig mean lesion score was approximately 1.3; by postinfection day 27, all the lesions were essentially healed.
Safety DataBack Directory
[Toxicity]

LD50 intravenous in mouse: 315mg/kg
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