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Name Index P

• PP2 (Catalog# : 185146, Cas# : 172889-27-9)PP2, also known as AG 1879, is a substance that has frequently been used in cancer re
• 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
• 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
• Pyridostatin TFA salt (Catalog# : 185142, Cas# : 1472611-44-1)Pyridostatin stabilizes G-quadruplexes (G4s) in cells and elicits a DNA damage respon
• 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 inhib
• PLX51107 (Catalog# : 184285, Cas# : 1627929-55-8)PLX51107 is a potent and selective BRD4 inhibitor or BET inhibitor with novel in vitr
• PD 158780 (Catalog# : 184284, Cas# : 171179-06-9)PD 158780 is a potent in vitro inhibitor of the tyrosine kinase activity of the epide
• PZM21 (Catalog# : 184162, Cas# : 1997387-43-5)PZM21 is a potent Gi activator with exceptional selectivity for μOR and minimal β-a
• PF-9366 (Catalog# : 184107, Cas# : 72882-78-1)PF-9366 is a novel inhibitor of human methionine adenosyltransferase 2A (Mat2A), the
• 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 ot
• PCI-29732 (Catalog# : 184101, Cas# : 330786-25-9)PCI-29732 is a BTK inhibitor. It acts by blocking B cell antigen receptor (BCR)-media
• PF-0684000 (Catalog# : 184318, Cas# : 198474-05-4)PF-0684000, also known as EOS200271, is potent IDO-1 inhibitor (IC50 0.15 μM). PF-06
• PF-06409577 (Catalog# : 18434, Cas# : 1467057-23-3)PF-06409577 is a potent and selective activator of 5′ adenosine monophosphate-activ
• PRN-1371 (Catalog# : 17101614, Cas# : 1802929-43-6)PRN-1371 is a covalent, irreversible, highly selective FGFR1, 2, 3 and 4 inhibitor. P
• PF-5006739 (Catalog# : 17101612, Cas# : 1293395-67-1)PF-5006739 is a Potent CK1δ/ε inhibitor. PF-5006739 attenuates opioid drug-seeking
• PF-04628935 (Catalog# : 17101611, Cas# : 1383719-97-8)PF-04628935 is a potent antagonist/inverse agonist of the ghrelin receptor, growth ho
• PIM447 (Catalog# : 1710134, Cas# : 1210608-43-7)PIM447, also known as LGH447, is a potent Moloney murine leukemia (PIM) 1, 2, and 3 k
• PF-562271 HCl (Catalog# : 179302, Cas# : 939791-41-0)PF-562271, also known as PF-562,271 and PF-271, is an orally bioavailable small molec
• Pemafibrate (Catalog# : 179221, Cas# : 848259-27-8)(1)Pemafibrate, also known as K-877 and (R)-K 13675, is a PPAR alpha agonist. (R)-K-1
• Pyridostatin TFA salt (Catalog# : 1791517, Cas# : 179474-81-8)Pyridostatin stabilizes G-quadruplexes (G4s) in cells and elicits a DNA damage respon
• Prucalopride Succinate (Catalog# : 1791516, Cas# : 179474-85-2)Prucalopride, also known as R-108512, is a selective, high affinity serotonin (5-HT4)
• PRT4165 (Catalog# : 1791515, Cas# : 31083-55-3)PRT4165 is a small molecule inhibitor of polycomb repressive complex 1, which inhibit
• Pramipexole HCl (Catalog# : 1791510, Cas# : 104632-25-9)Pramipexole Dihydrochloride is an agonist of the Gαi-linked dopamine receptors D2, D
• PF-06281355 (Catalog# : 1791312, Cas# : 1435467-38-1)PF-06281355, also known as PF-1355, is an orally available, selective and potent mech
• Puromycin Aminonucleoside (Catalog# : 1791310, Cas# : 58-60-6)Puromycin Aminonucleoside, also known as PAN, NSC3056, is useful in the study of huma
• P7C3-OMe (Catalog# : 179116, Cas# : 1235481-43-2)P7C3-OMe, also known as (R)-P7C3-OMe, is an analogue of P7C3 and P3C3-A20. P7C3 Atten
• PF-CBP1 free base (Catalog# : 179113, Cas# : 1962928-21-7)PF-CBP1, also known as PF-06670910, is potent and highly-selective inhibitor of the b
• PF-CBP1 HCl (Catalog# : 179112, Cas# : 2070014-93-4)PF-CBP1, also known as PF-06670910, is potent and highly-selective inhibitor of the b