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Cas Index 1

• 1005168-10-4 | PAC 14028 (Catalog# : 185223)PAC 14028, also known as Asivatrep, is a vanilloid VR1 receptor (TRPV1) antagonist po
• 1402727-29-0 | PE859 (Catalog# : 185157)PE859 is a potent inhibitor of both tau and Aβ aggregation with IC50 values of 0.66
• 190383-31-4 | PD 168 077 (Catalog# : 185156)PD168077 is a dopamine D4 receptor agonist which has a facilitatory effect on memory
• 1622291-66-0 | PF-06462894 (Catalog# : 185155)PF-06462894 is a morpholinopyrimidone mGlu5 (mGlu5 Ki = 6 nM).
• 1393124-08-7 | PF-06291874 (Catalog# : 185154)PF-06291874 is a glucagon receptor antagonist and potentially usefully for patients w
• 1353552-97-2 | Poseltinib (Catalog# : 185153)Poseltinib, also known HM-71224 and LY3337641, is a tyrosine kinase inhibitor.
• 1353900-92-1 | Pibrentasvir (Catalog# : 185148)Pibrentasvir, also known as ABT-530, is a protease inhibitor potentially for the trea
• 172889-27-9 | PP2 (Catalog# : 185146)PP2, also known as AG 1879, is a substance that has frequently been used in cancer re
• 172889-26-8 | PP1 (Catalog# : 185145)PP1 is a potent and selective Src family protein tyrosine kinase inhibitor.
• 146949-21-5 | Pocapavir (Catalog# : 185144)Pocapavir, also known as SCH-48973 and V-073, is a potent, selective, antienterovirus
• 1702967-37-0 | PSMA617 TFA (Catalog# : 185143)PSMA-617 is a ligand used to make 177Lu-PSMA-617, which is a radioactive molecule to
• 1472611-44-1 | Pyridostatin TFA salt (Catalog# : 185142)Pyridostatin stabilizes G-quadruplexes (G4s) in cells and elicits a DNA damage respon
• 1811510-56-1 | PF-06260933 (Catalog# : 18544)PF-06260933 is a potent and highly selective inhibitor of MAP4K4.
• 1627929-55-8 | PLX51107 (Catalog# : 184285)PLX51107 is a potent and selective BRD4 inhibitor or BET inhibitor with novel in vitr
• 171179-06-9 | PD 158780 (Catalog# : 184284)PD 158780 is a potent in vitro inhibitor of the tyrosine kinase activity of the epide
• 1997387-43-5 | PZM21 (Catalog# : 184162)PZM21 is a potent Gi activator with exceptional selectivity for μOR and minimal β-a
• 1627607-87-7 | PFI-2 hydrochloride (Catalog# : 184106)PFI-2 is a potent inhibitor of SETD7 with IC50 2 nM and 1000-fold selectivity over ot
• 198474-05-4 | PF-0684000 (Catalog# : 184318)PF-0684000, also known as EOS200271, is potent IDO-1 inhibitor (IC50 0.15 μM). PF-06
• 1467057-23-3 | PF-06409577 (Catalog# : 18434)PF-06409577 is a potent and selective activator of 5′ adenosine monophosphate-activ
• 1802929-43-6 | PRN-1371 (Catalog# : 17101614)PRN-1371 is a covalent, irreversible, highly selective FGFR1, 2, 3 and 4 inhibitor. P
• 1293395-67-1 | PF-5006739 (Catalog# : 17101612)PF-5006739 is a Potent CK1δ/ε inhibitor. PF-5006739 attenuates opioid drug-seeking
• 1383719-97-8 | PF-04628935 (Catalog# : 17101611)PF-04628935 is a potent antagonist/inverse agonist of the ghrelin receptor, growth ho
• 1210608-43-7 | PIM447 (Catalog# : 1710134)PIM447, also known as LGH447, is a potent Moloney murine leukemia (PIM) 1, 2, and 3 k
• 179474-81-8 | Pyridostatin TFA salt (Catalog# : 1791517)Pyridostatin stabilizes G-quadruplexes (G4s) in cells and elicits a DNA damage respon
• 179474-85-2 | Prucalopride Succinate (Catalog# : 1791516)Prucalopride, also known as R-108512, is a selective, high affinity serotonin (5-HT4)
• 104632-25-9 | Pramipexole HCl (Catalog# : 1791510)Pramipexole Dihydrochloride is an agonist of the Gαi-linked dopamine receptors D2, D
• 1435467-38-1 | PF-06281355 (Catalog# : 1791312)PF-06281355, also known as PF-1355, is an orally available, selective and potent mech
• 1235481-43-2 | P7C3-OMe (Catalog# : 179116)P7C3-OMe, also known as (R)-P7C3-OMe, is an analogue of P7C3 and P3C3-A20. P7C3 Atten
• 1962928-21-7 | PF-CBP1 free base (Catalog# : 179113)PF-CBP1, also known as PF-06670910, is potent and highly-selective inhibitor of the b
• 1817626-54-2 | PF-06650833 (Catalog# : 17988)PF-06650833 is an inhibitor of Interleukin-1 receptor associated kinase 4 (IRAK4). RA