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Cat. No. Product Name Information
PC-23729

JN-KI3

PI3Kγ inhibitor

JN-KI3 is a potent, selective inhibitor of phosphoinositide 3-kinase gamma (PI3Kγ) with IC50 of 3.87 uM, with no actiivity against PI3Kα, PI3Kβ and PI3Kδ (IC50>20 uM).
PC-23245

Menadione sodium bisulfite

Vps34 inhibitor

Menadione sodium bisulfite (MSB) is a water-soluble form of vitamin K precursor menadione, suppresses prostate cancer growth by targeting the kinase VPS34 (phosphatidylinositol 3-kinase catalytic subunit type 3).
PC-23119

AS041164

PI3Kγ inhibitor

AS041164 is a potent, selective and orally bioavailable PI3Kγ inhibitor with IC50 of 70 nM, blocks RANTES-induced chemotaxis and reduces the level of AKT phosphorylation.
PC-23007

PITCOIN1

PI3KC2α inhibitor

PITCOIN1 is a potent, highly selective inhibitor of class II alpha PI3K (PI3K-C2α) with IC50 of 100 nM, with no activity against class I and III PI3Ks.
PC-23006

PI-701

PI3KC2β inhibitor

PI-701 (YM185453) is a selective inhibitor of class II PI3KC2β isoform with IC50 of 528 nM, does not display activity toward PI3K class I isoforms.
PC-23005

PI3K-C2γ inhibitor 26

PI3K-C2γ inhibitor

PI3K-C2γ inhibitor 26 is a potent, isoform-selective inhibitor of PI3K-C2γ with IC50 of 340 nM, with no activity against class I and III PI3Ks or a panel of 60 other protein kinases.
PC-23004

MIPS-21335

PI3KC2α inhibitor

MIPS-19416 is a potent selective inhibitor of class II alpha PI3K (PI3K-C2α) with IC50 of 7 nM, six-fold selective over PI3K-C2β, 20-fold over PI3K-p110α.
PC-23003

MIPS-19416

PI3K inhibitor

MIPS-19416 is a potent dual class I and class II PI3Ks inhibitor with IC50 of 13 nM (PI3KC2α), equal to or more potent than against class I isoforms or against PI3KC2β (IC50=12-94 nM).
PC-23002

PITCOIN4

PI3KC2α inhibitor

PITCOIN4 is a potent, highly selective inhibitor of class II alpha PI3K (PI3K-C2α) with IC50 of 56 nM, >100-fold selectivity over PI3K-C2β.
PC-22536

TYM-3-98

PI3Kδ inhibitor

TYM-3-98 is a potent, selective inhibitor of PI3Kδ (PI3Kdelta) with IC50 of 7.1 nM, highly selective over other PI3K isoforms at both molecular and cellular levels.
PC-22488

Taselisib

PI3Kα inhibitor

Taselisib (GDC-0032) is a potent, selective inhibitor of PIK3CA (PI3Kα) with Ki of 0.29 nM and pAkt IC50 of 4 nM, 31-fold selective over PI3Kβ.
PC-22090

QR-7909

PI3Kα H1047R inhibitor

QR-7909 is a potent, specific and allosteric PI3Kα H1047R inhibitor with IC50 of 51 nM, 27-fold selective over WT PI3Kα in biochemical assays.

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