Venturicidin A
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Venturicidin A
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CAS No:
33538-71-5
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Formula:
C41H67NO11
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Chemical Name:
Venturicidin A
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Synonyms:
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-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)-;Venturicidin A;Venturicidin B,3′-carbamate;(1R,5S,6R,8R,9E,11R,15E,17R)-11-[[3-O-(Aminocarbonyl)-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-4,21-dioxabicyclo[15.3.1]heneicosa-9,15,18-trien-3-one;Aabomycin A1;11076-79-2;39405-78-2
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CAS No:
Venturicidin A Use and Manufacturing
The macrolide antibiotic, Venturicidin A, 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.
Computed Properties
Molecular Weight:750.0
XLogP3:5
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:11
Rotatable Bond Count:11
Exact Mass:749.47141195
Monoisotopic Mass:749.47141195
Topological Polar Surface Area:184
Heavy Atom Count:53
Complexity:1310
Defined Atom Stereocenter Count:14
Defined Bond Stereocenter Count:2
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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