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标准品 麦可酚酸/霉酚酸/麦考酚酸/Mycophenolic acid

产品信息
麦可酚酸/霉酚酸/麦考酚酸/Mycophenolic acid

Source: Wortmanin is produced by the fungus  Talaromyces (Penicillium) wortmannii
Synonyms BRN 0067676
NSC 627609
Antibiotic SL-2052
Wartmannin
Wortmannin
KY 12420
Systematic Name
(1alpha,11alpha)-11-(Acetyloxy)-1-(methoxymethyl)-2-oxaandrosta-5,8-dieno(6,5,4-bc)furan-3,7,17-trione
 
Description: Wortmannin is an antifungal antibiotic, similar to viridin.
CAS number: 19545-26-7
Merck index: 12, 10188
Molecular weight: 428.44
Structure:
Molecular Formula: C23H24O8
Solubility
information:
DMSO, Methanol. Unstable in aqueous and ethanolic solutions.
Specifications  
Appearance: Off-white to pale yellow powder
Purity: At least 97.5% by TLC, HPLC
λmax: 210-220, 256, 293 (not a part of specification)
Melting point 240oC +- 2oC. not a part of specification
Solubility Clear colorless solution at 5 mg/ml Methanol.
Storage -20°C .Hygroscopic. Protect from light and moisture.
Applications Wortmannin is an inhibitor of phosphatidyl-inositol 3-kinase
Wortmannin inhibits the growth of mammary tumors despite the existence of a novel wortmannin-insensitive phosphatidylinositol-3-kinase.
Wortmannin inhibits repair of DNA double-strand breaks in irradiated normal human cells. Wortmannin was shown to have enhancing influence on memory and impair learning abilities.
Warnings
POTENTIALLY FATAL IF SWALLOWED, INHALLED OR ABSORBED THROUGH SKIN.
Classification chemical class:Androstadiene
phospholipase D inhibitor. Immunosupressor. Antifungal.
Related products  
  For Research use only. Not for Human or Drug use
GMP/API grade



No genetically modified organisms are used.
 Publications Yuan H, Luo J, Weissleder R, Cantley L, Josephson L.
Wortmannin-C20 conjugates generate wortmannin.
J Med Chem. 2006 Jan 26;49(2):740-7.
  Nakipova OV, Andreeva LA, Zakharova NM, Semenova TP, Solomonov NG.
Influence of wortmannin on the inotropic effect of insulin in papillary muscles of Siberian ground squirrel heart.
Dokl Biochem Biophys. 2006 Mar-Apr;407:91-3
  Zhu T, Gu J, Yu K, Lucas J, Cai P, Tsao R, Gong Y, Li F, Chaudhary I, Desai P, Ruppen M, Fawzi M, Gibbons J, Ayral-Kaloustian S, Skotnicki J, Mansour T, Zask A.
Pegylated wortmannin and 17-hydroxywortmannin conjugates as phosphoinositide 3-kinase inhibitors active in human tumor xenograft models.
J Med Chem. 2006 Feb 23;49(4):1373-8.
  Hazeki K, Kinoshita S, Matsumura T, Nigorikawa K, Kubo H, Hazeki O.
Opposite effects of wortmannin and 2-(4-morpholinyl)-8-phenyl-1(4H)-benzopyran-4-one hydrochloride on toll-like receptor-mediated nitric oxide production: negative regulation of nuclear factor-{kappa}B by phosphoinositide 3-kinase.
Mol Pharmacol. 2006 May;69(5):1717-24.
  Giner JL, Kehbein KA, Cook JA, Smith MC, Vlahos CJ, Badwey JA.
Synthesis of fluorescent derivatives of wortmannin and demethoxyviridin as probes for phosphatidylinositol 3-kinase.
Bioorg Med Chem Lett. 2006 May 1;16(9):2518-21.
  Sullivan JA, Grummer MA, Yi FX, Bird IM.
Pregnancy-enhanced endothelial nitric oxide synthase (eNOS) activation in uterine artery endothelial cells shows altered sensitivity to Ca2+, U0126, and wortmannin but not LY294002--evidence that pregnancy adaptation of eNOS activation occurs at multiple levels of cell signaling.
Endocrinology. 2006 May;147(5):2442-57
 
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