ChemicalBook--->CAS DataBase List--->33538-72-6

33538-72-6

33538-72-6 Structure

33538-72-6 Structure
IdentificationBack Directory
[Name]

Venturicidin
[CAS]

33538-72-6
[Synonyms]

AaboMycin A2
Venturicidin
4,21-Dioxabicyclo[15.3.1]heneicosa-9,15,18-trien-3-one, 11-[(2,6-dideoxy-β-D-arabino-hexopyranosyl)oxy]-1-hydroxy-5-[(1R,3R,4S,5S)-4-hydroxy-1,3,5-trimethyl-6-oxooctyl]-6,8,16,18-tetramethyl-, (1R,5S,6R,8R,9E,11R,15E,17R)-
(1R,2E,7R,8E,10R,12R,13S,17R)-7-[(2R,4R,6R)-4,5-dihydroxy-6-methyloxan-2-yl]oxy-17-hydroxy-13-[(2R,4R,5S,6S)-5-hydroxy-4,6-dimethyl-7-oxononan-2-yl]-2,10,12,20-tetramethyl-14,21-dioxabicyclo[15.3.1]henicosa-2,8,19-trien-15-one
[Molecular Formula]

C40H66O10
[MOL File]

33538-72-6.mol
[Molecular Weight]

706.95
Chemical PropertiesBack Directory
[Melting point ]

168-170°; mp 145-149° (ethyl acetate-petr ether)
[alpha ]

D +100° (c = 0.847 in chloroform)
[Boiling point ]

823.4±65.0 °C(Predicted)
[density ]

1.14±0.1 g/cm3(Predicted)
[solubility ]

DMF: Soluble; DMSO: Soluble; Ethanol: Soluble; Methanol: Soluble
[form ]

White to off-white solid.
[pka]

11.80±0.70(Predicted)
Hazard InformationBack Directory
[Description]

Venturicidin B is a macrolide bacterial metabolite that has been found in Streptomyces.
[Uses]

The macrolide antibiotic Venturicidin B, isolated from a Streptomyces sp., is a potent inhibitor of mitochondrial ATP synthase complex acting on the F0 membrane sector. Venturicidin A was originally isolated as an antifungal agent.
[Uses]

Venturicidin B is a potent inhibitor of mitochondrial ATP synthase complex acting on the F0 membrane sector.
[IC 50]

Macrolide
[References]

[1] H AKITA. Identity of aabomycin A with venturicidins.[J]. Agricultural and biological chemistry, 1990, 54 9: 2465-2466.
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