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Wortmannin (Standard)

CAT: 0804-HY-10197R-01Size: 1 mgDry Ice: NoHazardous: No
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CAT#:0804-HY-10197R-01Size:1 mg
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Description
Wortmannin (Standard) is the analytical standard of Wortmannin. This product is intended for research and analytical applications. Wortmannin (SL-2052; KY-12420) is a potent, selective and irreversible PI3K inhibitor with an IC50 of 3 nM. Wortmannin also blocks autophagy formation, and potently inhibits Polo-like kinase 1 (PlK1) and Plk3 with IC50s of 5.8 and 48 nM, respectively[1][2][3].
CAS Number
19545-26-7
Product Name Alternative
SL-2052 (Standard) ; KY-12420 (Standard)
UNSPSC
12352005
Target
Antibiotic; Autophagy; Organoid; PI3K; Polo-like Kinase (PLK) ; Reference Standards
Type
Reference Standards
Related Pathways
Anti-infection; Autophagy; Cell Cycle/DNA Damage; Others; PI3K/Akt/mTOR; Stem Cell/Wnt
Field of Research
Cancer
Assay Protocol
https://www.medchemexpress.com/wortmannin-standard.html
Smiles
O=C1C([C@@](CC2)([H])[C@@]3(C)C2=O)=C([C@H](OC(C)=O)C3)[C@]4(C)C5=C1OC=C5C(O[C@@H]4COC)=O
Molecular Formula
C23H24O8
Molecular Weight
428.43
References & Citations
[1]Yano H, et al. Inhibition of histamine secretion by wortmannin through the blockade of phosphatidylinositol 3-kinase in RBL-2H3 cells. J Biol Chem. 1993 Dec 5;268 (34) :25846-56.|[2]Moon EK, et al. Autophagy inhibitors as a potential antiamoebic treatment for Acanthamoeba keratitis. Antimicrob Agents Chemother. 2015 Jul;59 (7) :4020-5.|[3]Liu Y, et al. Polo-like kinases inhibited by wortmannin. Labeling site and downstream effects. J Biol Chem. 2007 Jan 26;282 (4) :2505-11.|[4]Wu Q, et al. Wortmannin inhibits K562 leukemic cells by regulating PI3k/Akt channel in vitro. J Huazhong Univ Sci Technolog Med Sci. 2009 Aug;29 (4) :451-6.|[5]Lemke LE, et al. Wortmannin inhibits the growth of mammary tumors despite the existence of a novel wortmannin-insensitive phosphatidylinositol-3-kinase. Cancer Chemother Pharmacol. 1999;44 (6) :491-7.|[6]Liu Y, et al. Wortmannin, a widely used phosphoinositide 3-kinase inhibitor, also potently inhibits mammalianpolo-like kinase. Chem Biol. 2005 Jan;12 (1) :99-107.|[7]Pobbati AV, et al. A combat with the YAP/TAZ-TEAD oncoproteins for cancer therapy. Theranostics. 2020 Feb 18;10 (8) :3622-3635.
Shipping Conditions
Room temperature
Scientific Category
Reference Standards

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