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Search Results for " pi4k "

20

Compounds

Cat No. Product Name Synonyms Targets
T61971 CHMFL-PI4K-127
CHMFL-PI4K-127 (compound 15g) is a highly selective inhibitor of PfPI4K (Plasmodium falciparum PI4K kinase) with oral activity (IC50=0.9 nM). CHMFL-PI4K-127 shows strong inhibitory activity against Plasmodium falciparum ...
T16530 BF738735 Antiviral , PI4K
BF738735 is a selective inhibitor of phosphatidylinositol 4-kinase III beta (PI4KIIIβ, IC50 = 5.7 nM) showing higher activity over α(IC50 = 1.7 μM). BF738735 exhibits a broad spectrum of antiviral activity.
TQ0009 UCB9608 PI4K
UCB9608 is a selective and orally active PI4KIIIβ inhibitor (IC50: 11 nM), selective over PI3KC2 α, β, and γ lipid kinases.
T16125 MMV390048 Parasite , PI4K
MMV390048 is an antimalarial agent and is a representative of a new chemical class of Plasmodium PI4K inhibitor (Kdapp=0.3 μM). MMV390048 binds to the ATP binding site of Plasmodium PI4K and does not bind to other P. fal...
T16967 T-00127_HEV1 PI4K
T-00127_HEV1 is an inhibitor of phosphatidylinositol 4-kinase III beta (IC50: 60 nM).
T12454 PI-273 Apoptosis , PI4K
PI-273, a Substrate-Competitive, Specific Small-Molecule Inhibitor of PI4KIIα, Inhibits the Growth of Breast Cancer Cells
T12468 PI4KIIIbeta-IN-10 PI3K , PI4K
PI4KIIIbeta-IN-10 is a potent inhibitor of PI4KIIIβ (IC50 of 3.6 nM).
T2616 PIK-93 PIK 93 ATM/ATR , DNA-PK , Virus Protease , PI3K , Carbonic Anhydrase , PI4K , mTOR , HSV
PIK-93 is the first potent, synthetic PI4K inhibitor with IC50 of 19 nM; inhibits PI3Kα with IC50 of 39 nM.
T12469 PI4KIIIbeta-IN-9 PI3K , PI4K
PI4KIIIbeta-IN-9 is a potent inhibitor of PI4KIIIβ(IC50 of 7 nM). .
T5421 KDU691 Parasite , PI4K
KDU691 is a PI4K inhibitor.
T4220 BQR-695 BQR695,NVP-BQR695 PI3K , Parasite , PI4K
BQR-695 (NVP-BQR695) is a phosphatidylinositol 4-kinase (PI4K) inhibitor with IC50s of 80 and 3.5 nM for human PI4KIIIβ and Plasmodium variant of PI4KIIIβ, respectively.
T27499 GSK-A1 HCV Protease , PI4K
GSK-A1 is a specific inhibitor of PI4KA, also inhibited calcium-driven PRL secretion without affecting calcium signaling and Prl expression. GSK-A1 has anti-hepatitis C virus (HCV) potential.
T19840 GSK-F1 PI4KA inhibitor-F1 PI4K
GSK-F1 (PI4KA inhibitor-F1) is a novel potent PI4KA inhibitor.
T64106 PI4KIIIbeta-IN-11
PI4KIIIbeta-IN-11 is a PI4KIIIβ inhibitor (mean pIC50=9.1) that can be used to study diseases caused by RNA viruses and Plasmodium falciparum.
T12467 PI4KIII beta inhibitor 3 PI3K
PI4KIII beta inhibitor 3 is a novel and high effective inhibitor of PI4KIIIβ (IC50 of 5.7 nM).
T13246 UCT943 Parasite , PI4K
UCT943 is an inhibitor of Plasmodium falciparum PI4K (IC50 = 23 nM).
T2685 KU-55933 ATM Kinase Inhibitor ATM/ATR , DNA-PK , PI3K , mTOR , Autophagy
KU-55933 (ATM Kinase Inhibitor) is a potent and specific ATM inhibitor.
T71694 BRD73842
BRD73842 is an inhibitor of Plasmodium PI4K.
T25826 MMV024101 MMV-024101,TCMDC 134293,TCMDC134293,TCMDC-134293,MMV 024101
MMV024101 is a PI4K inhibitor. MMV024101 exhibits submicromolar potency against P. falciparum NF54 (IC50 =543 nM), low aqueous solubility (<5 μM), and rapid clearance by mouse liver microsomes with only 2% of parent comp...
T79876 EDI048 PI4K
EDI048, also known as compound 1.16, is an orally active inhibitor of Cryptosporidium PI4K, utilized in the study of cryptosporidiosis [1].
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TargetMol