VENTURICIDIN A

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CAS:33538-71-5
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CAS:33538-71-5
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CAS:33538-71-5
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CAS:33538-71-5
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Products Intro: Product Name:VENTURICIDIN A
CAS:33538-71-5
Purity:>95% by HPLC Package:1mg;5mg

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  • Venturicidin A
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  • 2026-01-04
  • CAS:33538-71-5
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VENTURICIDIN A Basic information
Product Name:VENTURICIDIN A
Synonyms:a-130;aa-0368;venturicidinb,3’-carbamate;HHQKNFDAEDTRJK-WLJINWSWSA-N;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)-
CAS:33538-71-5
MF:C41H67NO11
MW:749.97
EINECS:251-568-3
Product Categories:Antibiotic
Mol File:33538-71-5.mol
VENTURICIDIN A Structure
VENTURICIDIN A Chemical Properties
Melting point 145-147°; mp 140-142°
alpha D +119° (c = 0.5 in chloroform)
Boiling point 874.9±65.0 °C(Predicted)
density 1.16±0.1 g/cm3(Predicted)
storage temp. 2-8°C
solubility DMF: Soluble; DMSO: Soluble; Ethanol: Soluble; Methanol: Soluble
pka11.80±0.70(Predicted)
form White to off-white solid.
color White to off-white
Safety Information
RTECS YX4556000
HS Code 2941900000
MSDS Information
VENTURICIDIN A Usage And Synthesis
DescriptionVenturicidin A is a macrolide antibiotic isolated from strains of Streptomyces. It is active against fungi in the genus Venturia which cause apple scab, as well as other fungi, but not against higher plants. Venturicidin A is also cytotoxic against trypanosomes (IC50 = 120-540 ng/ml) while being more than 25,000 times less effective against mammalian cells. It inhibits bacterial and mitochondrial ATP synthases.
UsesThe 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.
UsesVenturicidin A is an antibiotic and potent inhibitor of mitochondrial ATP synthase.
DefinitionChEBI: Venturicidin a is a diterpene lactone.
IC 50Aminoglycoside
References[1] A. RHODES. Venturicidin: A New Antifungal Antibiotic of Potential Use in Agriculture[J]. Nature, 1961, 192 4806: 952-954. DOI: 10.1038/192952a0
[2] DAVID S. PERLIN  Alan E S  Lisa R Latchney. Inhibition of Escherichia coli H+-ATPase by venturicidin, oligomycin and ossamycin[J]. Biochimica et Biophysica Acta-Bioenergetics, 1985, 807 3: Pages 238-244. DOI: 10.1016/0005-2728(85)90254-3
[3] A MATSUNO-YAGI  Y H. Studies on the mechanism of oxidative phosphorylation. ATP synthesis by submitochondrial particles inhibited at F0 by venturicidin and organotin compounds.[J]. The Journal of Biological Chemistry, 1993, 268 9: 6168-6173.
VENTURICIDIN A Preparation Products And Raw materials
Tag:VENTURICIDIN A(33538-71-5) Related Product Information
Venturicidin Methyl (S)-(+)-3-hydroxybutyrate Isobutyl butyrate 1,4-Pentadien-3-ol 2-METHYL-1-PENTEN-3-OL TRANS-5-DECEN-1-OL n-Butyl carbamate 4-METHYL-4-HEPTEN-3-OL 2-HEXEN-4-OL (+)-METHYL (S)-3-HYDROXYPENTANOATE N-PROPYLCARBAMATE 2-OCTEN-4-OL Ethyl (S)-3-hydroxybutyrate Methyl (R)-(-)-3-hydroxybutyrate TRANS-2-DODECEN-1-OL 2-HEPTEN-4-OL TRANS-2-UNDECEN-1-OL 2-(ALLYLOXY)TETRAHYDROPYRAN

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