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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.
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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.

VENTURICIDIN A Preparation Products And Raw materials

Raw materials

Preparation Products

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VENTURICIDIN A Suppliers

China 13 India 1 Switzerland 1 United Kingdom 2 United States 5 Global 22
Novachemistry
Tel
44-20819178-90 02081917890
Fax
(0)2080432064
Email
info@novachemistry.com
Country
United Kingdom
ProdList
4381
Advantage
58

33538-71-5, VENTURICIDIN ARelated Search:

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

  • 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