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NVP-BAG956

NVP-BAG956

NVP-BAG956 is a cell-permeable imidazoquinoline compound that acts as a potent, reversible, and ATP-competitive PI 3-K/PDK1 dual kinase inhibitor (IC5...
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BX 912

BX 912

BX912 prevents ChcK1, PKA, c-kit, and KDR with IC50 of 0.83, 0.11, 0.85, and 0.41 μM, resepectively. BX912 blocks PDK1/Akt signaling in tumor cells...
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AZD 8055

AZD 8055

AZD 8055 is a potent, selective, and orally bioavailable ATP-competitive mTOR kinase inhibitor with an IC50 of 0.8 nM. mTOR kinase inhibitor AZD8055 i...
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WYE 125132 (WYE 132)

WYE 125132 (WYE 132)

WYE-125132 (WYE-132), is a highly potent, ATP-competitive, and specific mTOR kinase inhibitor (IC50: 0.19 ± 0.07 nmol/L; >5,000-fold selecti...
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OSI 027

OSI 027

OSI 027 is an orally bioavailable mammalian target of rapamycin (mTOR) kinase inhibitor with potential antineoplastic activity. mTOR kinase inhibitor ...
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CAL101

CAL101

CAL-101 (GS 1101) is a potent PI3K p110δ inhibitor with an IC50 of 65 nM. PI3K-delta inhibitor CAL-101 inhibits the production of the second mes...
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A 66

A 66

A66 is a novel small molecule inhibitor of PI3K p110α with IC50 values of 32, 30 and 43 nM for p110α, p110α/E545K and p110α/H1...
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PIK 75

PIK 75

PIK-75 Hydrochloride is a hydrochloride salt form of PIK-75, which is a preferential p110α/γ forms of PI3K inhibitor with IC50 of 6, 1300,...
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GDC 0941

GDC 0941

GDC 0941 against p110a IC50=0.003μM, U87MG IC50=0.95μM, A2780 IC50=0.14 μM, and in vitro metabolic stability in mouse and human is 91.96%. Th...
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XL 147

XL 147

XL147 reversibly binds to class 1 PI3Ks in an ATP-competitive manner, inhibiting the production of the secondary messenger phosphatidylinositol-3,4,5-...
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PIK 90

PIK 90

PIK 90 is a cell-permeable imidazoquinazoline compound that acts as a potent, reversible, and ATP-competitive inhibitor against all three classes of P...
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XL 765 (SAR 245409)

XL 765 (SAR 245409)

XL 765(SAR 245409) is a mixed mTOR/PI3k inhibitor with IC50 of 157, 39, 113, 9 and 43 nM for mTOR, p110α, β, γ and δ, respectiv...
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PP 121

PP 121

PP 121 is a dual inhibitor of receptor tyrosine kinases (RTKs) (IC50 < 0.02 μM for Abl, Src, VEGFR-2 and PDGFR) and PI 3-K family kinases (IC50 ...
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PKI 402

PKI 402

PKI-402 is a selective, reversible, ATP-competitive, equipotent class I phosphatidylinositol 3-kinases (PI3K) inhibitor with IC50 of 1, 7, 16 and 14 n...
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PKI 587 (PF-05212384)

PKI 587 (PF-05212384)

PKI 587 (PF-05212384) is highly potent dual PI3K/mTOR kinase inhibitor with IC50 of 0.4 nM and < 0.1 μM for PI3K-α and mTOR, respectively....
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AZD 6482

AZD 6482

AZD 6482 is a PI3Kβ inhibitor (IC50=0.021μM) used in antithrombotic therapy. This agent targets a process that is critical to pathological thr...
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