ChemicalBook--->CAS DataBase List--->113204-43-6

113204-43-6

113204-43-6 Structure

113204-43-6 Structure
IdentificationBack Directory
[Name]

17-Hydroxyventuricidin A
[CAS]

113204-43-6
[Synonyms]

YP 02259L-C
17-Hydroxyventuricidin A
17-Hydroxyventuricidin B 3'-carbamate
4,21-Dioxabicyclo[15.3.1]heneicosa-9,15,18-trien-3-one, 11-[[3-O-(aminocarbonyl)-2,6-dideoxy-β-D-arabino-hexopyranosyl]oxy]-1,7-dihydroxy-5-[(1R,3R,4S,5S)-4-hydroxy-1,3,5-trimethyl-6-oxooctyl]-6,8,16,18-tetramethyl-, (1R,5R,6R,8S,9E,11R,15E,17R)-
[Molecular Formula]

C41H67NO12
[MOL File]

113204-43-6.mol
[Molecular Weight]

765.97
Chemical PropertiesBack Directory
[storage temp. ]

Store at -20°C
[solubility ]

DMSO: Soluble; Ethanol: 1 mg/ml; Methanol: Soluble
[form ]

A solid
[color ]

White
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302+H312+H332
[Precautionary statements ]

P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P321-P330-P362+P364-P501
Hazard InformationBack Directory
[Description]

17-hydroxy Venturicidin A is a macrolide fungal metabolite originally isolated from Streptomyces. It has antibiotic activity against M. luteus, B. subtilis, and S. aureus and antifungal activity against V. dahlia, Fusarium, and C. tropicalis in a disc assay.
[Uses]

17-Hydroxyventuricidin A is has antibacterial activity against gram-positive bacteria.
[storage]

+4°C
[References]

[1] LILIA FOURATI-BEN FGUIRA . Purification and structure elucidation of antifungal and antibacterial activities of newly isolated Streptomyces sp. strain US80[J]. Research in microbiology, 2005, 156 3: Pages 341-347. DOI: 10.1016/j.resmic.2004.10.006
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