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VENTURICIDIN A

Product Name
VENTURICIDIN A
CAS No.
33538-71-5
Chemical 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)-
CBNumber
CB7505296
Molecular Formula
C41H67NO11
Formula Weight
749.97
MOL File
33538-71-5.mol
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VENTURICIDIN A Property

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
pka
11.80±0.70(Predicted)
form 
White to off-white solid.
color 
White to off-white
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Safety

RTECS 
YX4556000
HS Code 
2941900000
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P271Use only outdoors or in a well-ventilated area.

P280Wear protective gloves/protective clothing/eye protection/face protection.

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N-Bromosuccinimide Price

Cayman Chemical
Product number
15377
Product name
Venturicidin A
Purity
≥95%
Packaging
1mg
Price
$125
Updated
2024/03/01
Cayman Chemical
Product number
15377
Product name
Venturicidin A
Purity
≥95%
Packaging
5mg
Price
$500
Updated
2024/03/01
TRC
Product number
V121003
Product name
VenturicidinA
Packaging
1mg
Price
$635
Updated
2021/12/16
ApexBio Technology
Product number
C4641
Product name
VenturicidinA
Packaging
5mg
Price
$1005
Updated
2021/12/16
Adipogen Life Sciences
Product number
BVT-0454-M001
Product name
VenturicidinA
Purity
≥98%(1H-NMR,HPLC)
Packaging
1mg
Price
$120
Updated
2021/12/16
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VENTURICIDIN A Chemical Properties,Usage,Production

Description

Venturicidin 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.

Uses

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.

Uses

Venturicidin A is an antibiotic and potent inhibitor of mitochondrial ATP synthase.

Definition

ChEBI: Venturicidin a is a diterpene lactone.

IC 50

Aminoglycoside

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

Raw materials

Preparation Products

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VENTURICIDIN A Suppliers

Shanghai EFE Biological Technology Co., Ltd.
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China
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Lynnchem
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86-(0)29-85992781 17792393971
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Shenzhen Polymeri Biochemical Technology Co., Ltd.
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+86-400-002-6226 +86-13028896684;
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ChemeGen(Shanghai) Biotechnology Co.,Ltd.
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Nanjing Shizhou Biology Technology Co.,Ltd
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Cayman Chemical Company
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Guangzhou WeiBo Chemical Co., Ltd.
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33538-71-5, VENTURICIDIN ARelated Search:


  • 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)-
  • 33538-71-5
  • C41H67NO11
  • Antibiotic