Venturicidin A

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Venturicidin A

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Cat No: 15377

Venturicidin A is a macrolide antibiotic isolated from strains of Streptomyces.{24920} It is active against fungi in the genus Venturia which cause apple scab, as well as other fungi, but not against higher plants.{24920} Venturicidin A is also cytoto...

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Territorial Availability: Available through Bertin Technologies only in France

Synonyms:

(1R,5S,6R,8R,9E,11R,15E,17R)-11-[[3-O-(aminocarbonyl)-2,6-dideoxy-?-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

Correlated keywords:

11076-?79-?2 39405-?78-?2 natural products inhibitors antibiotics mitochondria infectious diseases inhibits inhibitions Streptomyces fungi genus venturia apples scabs plants cytotoxic mitochondrial ATP bacterial bacterias antifungal anti-fungal anti fungal antitrypanosomal trypanosomal anti-trypanosomal macrolides 1076-79-2 39405-78-2 3-carbamate B trypanosomes synthases

Product Overview:
Venturicidin A is a macrolide antibiotic isolated from strains of Streptomyces.{24920} It is active against fungi in the genus Venturia which cause apple scab, as well as other fungi, but not against higher plants.{24920} Venturicidin A is also cytotoxic against trypanosomes (IC50 = 120-540 ng/ml) while being more than 25,000 times less effective against mammalian cells.{24919} It inhibits bacterial and mitochondrial ATP synthases.{24921,24918}

Size	1 mg
Shipping	dry ice
CAS Number	33538-71-5
Molecular Formula	C₄₁H₆₇NO₁₁
SMILES	CC1=CC[C@](CC(O[C@]([H])([C@@H](C[C@H]([C@@H]([C@@H](C(CC)=O)C)O)C)C)[C@@H]2C)=O)(O[C@@]1(/C(C)=C\CCC[C@@]([H])(O[C@@]([H])(C[C@H]3OC(N)=O)O[C@@H]([C@H]3O)C)/C=C/[C@@H](C2)C)[H])O
Molecular Weight	750
Formulation	A lyophilisate
Purity	≥95%
Custom Code	2922.19
UNSPSC code	12352100

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Cayman Chemical's mission is to help make research possible by supplying scientists worldwide with the basic research tools necessary for advancing human and animal health. Our utmost commitment to healthcare researchers is to offer the highest quality products with an affordable pricing policy.

Our scientists are experts in the synthesis, purification, and characterization of biochemicals ranging from small drug-like heterocycles to complex biolipids, fatty acids, and many others. We are also highly skilled in all aspects of assay and antibody development, protein expression, crystallization, and structure determination.

Over the past thirty years, Cayman developed a deep knowledge base in lipid biochemistry, including research involving the arachidonic acid cascade, inositol phosphates, and cannabinoids. This knowledge enabled the production of reagents of exceptional quality for cancer, oxidative injury, epigenetics, neuroscience, inflammation, metabolism, and many additional lines of research.

Our organic and analytical chemists specialize in the rapid development of manufacturing processes and analytical methods to carry out clinical and commercial GMP-API production. Pre-clinical drug discovery efforts are currently underway in the areas of bone restoration and repair, muscular dystrophy, oncology, and inflammation. A separate group of Ph.D.-level scientists are dedicated to offering Hit-to-Lead Discovery and Profiling Services for epigenetic targets. Our knowledgeable chemists can be contracted to perform complete sample analysis for analytes measured by the majority of our assays. We also offer a wide range of analytical services using LC-MS/MS, HPLC, GC, and many other techniques.

Accreditations
ISO/IEC 17025:2005
ISO Guide 34:2009

Cayman is a leader in the field of emerging drugs of abuse, providing high-purity Schedule I-V Controlled Substances to federally-licensed laboratories and qualified academic research institutions for forensic analyses. We are certified by ACLASS Accreditation Services with dual accreditation to ISO/IEC 17025:2005 and ISO Guide 34:2009.