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Cas Index 1

• 1144035-53-9 | PF-8380 (Catalog# : 17030115)PF-8380 is a potent autotaxin inhibitor with an IC(50) of 2.8 nM in isolated enzyme a
• 153168-05-9 | Pleconaril (Catalog# : 17030111)Pleconaril is an antiviral drug potentially for the treatment of enterovirus infectio
• 1235481-90-9 | P7C3-A20 (Catalog# : 16122838)P7C3-A20 is an analogue of P7C3, and is a proneurogenic, neuroprotective agent. P7C3-
• 13309-08-5 | 3PO (Catalog# : 161227109)3PO is a PFKFB3 (6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase) inhibitor. 3PO
• 1393465-84-3 | PLX7904 (Catalog# : 16122777)PLX7904, also known as PB04, is a potent and selective paradox-breaker RAF inhibitor.
• 1452-77-3 | Picolinamide (Catalog# : 16122714)Picolinamide is found to be a strong inhibitor of poly (ADP-ribose) synthetase of nuc
• 185039-89-8 | PD0166285 (Catalog# : 16122710)PD0166285 is a potent Wee1 and Chk1 inhibitor with activity at nanomolar concentratio
• 1415562-83-2 | PF-543 Citrate (Catalog# : 6111525)PF-543 Citrate is a novel cell-permeant inhibitor of SphK1 with a K(i) of 3.6 nM, PF-
• 1819363-80-8 | PFI-3 (Catalog# : 6111020)PFI-3
• 1173111-67-5 | PF-04929113 Mesylate (Catalog# : 611939)PF-04929113 Mesylate is a potent and selective Hsp90 inhibitor with an IC50 of median
• 1429624-84-9 | PI4KIIIbeta-IN-9 (Catalog# : 611908)PI4KIII-IN-9 is a potent PI4KIII inhibitor (IC50 of 7 nM) and is >140-fold selecti
• 1881233-39-1 | PI4KIIIbeta-IN-10 (Catalog# : 611907)PI4KIIIbeta-IN-10 is the most potent PI4KIII inhibitor currently reported, with very
• 1235449-52-1 | PI3Kα inhibitor 1 (Catalog# : 611903)PI3Kα inhibitor 1 is a PI3Kα inhibitor extracted from patent US/20120088764A1, comp
• 1220699-06-8 | PF-04979064 (Catalog# : 611902)PF-04979064 is a potent and selective PI3K/mTOR dual kinase inhibitor with an IC(50)
• 1927857-56-4 | PQR620 (Catalog# : 611821)PRQ620 is a highly potent and selective mTORC1/2 inhibitor, shows anti-tumor effects
• 1092788-83-4 | PP121 (Catalog# : 161009011)PP121 blocks the proliferation of tumor cells by direct inhibition of oncogenic tyros
• 1276553-09-3 | PF-4989216 (Catalog# : 161009002)PF-4989216 inhibits the phosphorylation of PI3K downstream molecules and subsequently
• 1180676-32-7 | PS 48 (Catalog# : 16071111)PS 48 has been shown to be a PKB Kinase (phosphoinositide-dependent protein kinase-1,
• 1356033-60-7 | Panulisib (Catalog# : 16071030)Panulisib, also known as AK151761, is a potent and selective imidazoquinoline based P
• 152918-18-8 | Piclidenoson (Catalog# : 16071028)Piclidenoson, also known as CF101, is a specific agonist to the A3 adenosine receptor
• 1180676-33-8 | PS47 (Catalog# : 16070703)PS47
• 1477-24-3 | 5-pyridin-4-yl-2,4-dihydro-3H-1,2,4-triazole-3-thione (Catalog# : 16062108)5-PYRIDIN-4-YL-4H-[1,2,4]TRIAZOLE-3-THIOL
• 1216941-48-8 | Paritaprevir (Catalog# : 16060702)Paritaprevir, also known as ABT-450, is an acylsulfonamide inhibitor of the NS3-4A se
• 1388712-98-8 | 2-Pyridinemethanamine, N-[2-(diphenylphosphino)ethyl]- (Catalog# : 032407)Coming soon!
• 1469284-78-3 | PF-06424439 (Catalog# : 020202)PF-06424439 is a potent and selective Diacylglycerol Acyltransferase 2 ( DGAT2) inhib
• 1808094-07-6 | PF-06471553 (Catalog# : 020201)PF-06471553 is a potent and selective Monoacylglycerol acyltransferase 3 (MGAT3) inhi
• 1435467-37-0 | PF-06282999 (Catalog# : 020102)PF-06282999 is an irreversible inactivator of myeloperoxidase, and currently in clini
• 1111636-35-1 | PF-04880594 (Catalog# : 012008)PF-04880594 is a RAF inhibitor, which induces ERK phosphorylation and RAF dimerizatio
• 1061353-68-1 | PND-1186 (Catalog# : 010821)PND-1186 is a potent FAK inhibitor with a 50% inhibitory concentration of 1.5 nM in v
• 1373615-35-0 | PF-5274857 (Catalog# : 010423)PF-5274857 is a potent and selective Smoothened (Smo) antagonist, inhibits Hedgehog (