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Name Index P

• Pamiparib (Catalog# : 512195, Cas# : 1446261-44-4)Pamiparib is an antineoplastic drug candidate. Pamiparib (BGB-290) is an investigational small molecule inhibitor of PARP1 and PARP2. Pamiparib is being evaluated as a monothera
• PAC 14028 (Catalog# : 185223, Cas# : 1005168-10-4)PAC 14028, also known as Asivatrep, is a vanilloid VR1 receptor (TRPV1) antagonist potentially.
• PE859 (Catalog# : 185157, Cas# : 1402727-29-0)PE859 is a potent inhibitor of both tau and Aβ aggregation with IC50 values of 0.66 and 1.2 μM, respectively.
• PD 168 077 (Catalog# : 185156, Cas# : 190383-31-4)PD168077 is a dopamine D4 receptor agonist which has a facilitatory effect on memory consolidation.
• PF-06462894 (Catalog# : 185155, Cas# : 1622291-66-0)PF-06462894 is a morpholinopyrimidone mGlu5 (mGlu5 Ki = 6 nM).
• PF-06291874 (Catalog# : 185154, Cas# : 1393124-08-7)PF-06291874 is a glucagon receptor antagonist and potentially usefully for patients with type 2 diabetes mellitus.
• Poseltinib (Catalog# : 185153, Cas# : 1353552-97-2)Poseltinib, also known HM-71224 and LY3337641, is a tyrosine kinase inhibitor.
• Pibrentasvir (Catalog# : 185148, Cas# : 1353900-92-1)Pibrentasvir, also known as ABT-530, is a protease inhibitor potentially for the treatment of HCV infection.
• PP2 Analog (Catalog# : 185147, Cas# : 309739-67-1)PP2 Analog is an analog of PP2 that acts as a protein trafficking modulator.
• PP2 (Catalog# : 185146, Cas# : 172889-27-9)PP2, also known as AG 1879, is a substance that has frequently been used in cancer research as a "selective" inhibitor for Src-family kinases.
• PP1 (Catalog# : 185145, Cas# : 172889-26-8)PP1 is a potent and selective Src family protein tyrosine kinase inhibitor.
• Pocapavir (Catalog# : 185144, Cas# : 146949-21-5)Pocapavir, also known as SCH-48973 and V-073, is a potent, selective, antienterovirus agent.
• PSMA617 TFA (Catalog# : 185143, Cas# : 1702967-37-0)PSMA-617 is a ligand used to make 177Lu-PSMA-617, which is a radioactive molecule to fight cancer.
• Pyridostatin TFA salt (Catalog# : 185142, Cas# : 1472611-44-1)Pyridostatin stabilizes G-quadruplexes (G4s) in cells and elicits a DNA damage response by causing the formation of DNA double strand breaks (DSB).
• PF-06260933 (Catalog# : 18544, Cas# : 1811510-56-1)PF-06260933 is a potent and highly selective inhibitor of MAP4K4.
• PHA-767491 HCl (Catalog# : 184286, Cas# : 942425-68-5)PHA-767491, also known as CAY10572, is a potent, ATP-competitive dual cdc7/cdk9 inhibitor (IC50 values are 10 and 34 nM respectively) that prevents initiation of DNA replication.
• PLX51107 (Catalog# : 184285, Cas# : 1627929-55-8)PLX51107 is a potent and selective BRD4 inhibitor or BET inhibitor with novel in vitro and in vivo pharmacologic properties that emulates or exceeds the efficacy of BCR signaling
• PD 158780 (Catalog# : 184284, Cas# : 171179-06-9)PD 158780 is a potent in vitro inhibitor of the tyrosine kinase activity of the epidermal growth factor receptor (EGFR) (IC50 0.08 nM).
• PZM21 (Catalog# : 184162, Cas# : 1997387-43-5)PZM21 is a potent Gi activator with exceptional selectivity for μOR and minimal β-arrestin-2 recruitment.
• PF-9366 (Catalog# : 184107, Cas# : 72882-78-1)PF-9366 is a novel inhibitor of human methionine adenosyltransferase 2A (Mat2A), the extrahepatic isoform.
• PFI-2 hydrochloride (Catalog# : 184106, Cas# : 1627607-87-7)PFI-2 is a potent inhibitor of SETD7 with IC50 2 nM and 1000-fold selectivity over other methyltransferases and other non-epigenetic targets.
• PCI-29732 (Catalog# : 184101, Cas# : 330786-25-9)PCI-29732 is a BTK inhibitor. It acts by blocking B cell antigen receptor (BCR)-mediated gene expression in CD20+ B cells.
• PF-0684000 (Catalog# : 184318, Cas# : 198474-05-4)PF-0684000, also known as EOS200271, is potent IDO-1 inhibitor (IC50 0.15 μM). PF-0684000 has moderate hIDO1 enzyme inhibition (IC50 0.41 μM).
• PF-06651600 (Catalog# : 18435, Cas# : 1792180-81-4)PF-06651600 is a potent and selective JAK3 inhibitor. PF-06651600, a potent and low clearance compound with demonstrated in vivo efficacy.
• PF-06409577 (Catalog# : 18434, Cas# : 1467057-23-3)PF-06409577 is a potent and selective activator of 5′ adenosine monophosphate-activated protein kinase (AMPK) for the Potential Treatment of diabetic nephropathy.
• PhTx-74 HCl (Catalog# : 18429, Cas# : 1227301-51-0)Philanthotoxin-74, also known as PhTx-74, is a synthetic analog of the naturally-occurring wasp venom toxin philanthotoxin-4,3,3. PhTX-74 may be of potential use in studies of th
• PRN-1371 (Catalog# : 17101614, Cas# : 1802929-43-6)PRN-1371 is a covalent, irreversible, highly selective FGFR1, 2, 3 and 4 inhibitor. PRN1371 inhibits all four FGFR isoforms and blocks aberrant FGFR kinase signaling.
• PF-5006739 (Catalog# : 17101612, Cas# : 1293395-67-1)PF-5006739 is a Potent CK1δ/ε inhibitor. PF-5006739 attenuates opioid drug-seeking behavior.
• PF-04628935 (Catalog# : 17101611, Cas# : 1383719-97-8)PF-04628935 is a potent antagonist/inverse agonist of the ghrelin receptor, growth hormone secretagogue receptor 1a (GHS-R1a) with an IC50 of 4.6 nM.
• PIM447 (Catalog# : 1710134, Cas# : 1210608-43-7)PIM447, also known as LGH447, is a potent Moloney murine leukemia (PIM) 1, 2, and 3 kinase inhibitor. Pan proviral insertion site of Moloney murine leukemia (PIM) 1, 2, and 3 kin