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Biological Data
Biological description
Potent, selective, non-compettive and irreversible PI3-K inhibitor (IC50 = 2-4 nM). Also inhibits PI3-K related kinases and PLK1. Cell permeable. Shows variety of biological actions.
Solubility & Handling
Storage instructions
-20°C (desiccate)
Solubility overview
DMSO (50mM) and Ethanol (5mM)
Important
This product is for RESEARCH USE ONLY and is not intended for therapeutic or diagnostic use. Not for human or veterinary use.
Chemical Data
Chemical name
(1S ,6bR ,9aS ,11R ,11bR ) 11-(Acetyloxy)-1,6b,7,8,9a,10,11,11 b-octahydro-1-(methoxymethyl)-9a,11b-dimethyl-3H -f uro[4,3,2-de ]indeno[4,5,-h ]-2-h ]-2-benzopyran-3,6, 9-trione
Molecular Formula
C23 H24 O8
PubChem identifier
3003565
SMILES
O=C(C4=CO5)O[C@H](COC)[C@@]1(C)C4=C5C(C2=C1[C@H](OC(C)=O)C[C@@]3(C)C2CCC3=O)=O
InChiKey
QDLHCMPXEPAAMD-ZGSWIPFCSA-N
References for Wortmannin
References are publications that support the biological activity of the product
Wortmannin, a widely used phosphoinositide 3-kinase inhibitor, also potently inhibits mammalian polo-like kinase.
Liu et al (2005)
Chem Biol 12(1) : 99-107
Wortmannin as a unique probe for an intracellular signalling protein, phosphoinositide 3-kinase.
Ui et al (1995)
Trends Biochem Sci 20(8) : 303-7
Wortmannin, a potent and selective inhibitor of phosphatidylinositol-3-kinase.
Powis et al (1994)
Cancer Res 54(9) : 2419-23
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Potent, selective, irreversible PI3-K inhibitor