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Cas Index 1

• 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
• 1234015-55-4 | Prexasertib mesylate (Catalog# : 17986)Prexasertib, also known as LY2606368, is a potent and selective Chk1/Chk2 inhibitor.
• 192705-79-6 | PD166866 (Catalog# : 178814)PD166866 has clear antiproliferative effects. 
• 135729-61-2 | Palonosetron (Catalog# : 2017080119)Palonosetron is a 5-HT3 antagonist used in the prevention and treatment of chemothera
• 1776112-90-3 | PF-06747775 (Catalog# : 175161)PF-06747775(PF06747775;CAS 1776112-90-3) is an orally available inhibitor of the epid
• 1331782-27-4 | PF-04995274 (Catalog# : 17031017)PF-04995274 is a 5-HT4 receptor partial agonist. It thought to act centrally as a pro
• 113906-27-7 | PNU-74654 (Catalog# : 17031011)PNU-75654 disrupts the Wnt signaling pathway via inhibition of the interaction (KD5
• 127317-03-7 | PACAP 1-27 (Catalog# : 17031005)Pituitary adenylate cyclase activating polypeptide (PACAP 1-27) is a potent PACAP re
• 1462249-75-7 | PFK-158 (Catalog# : 17030915)PFK-158, also known as ACT-PFK-158, is an inhibitor of 6-phosphofructo-2-kinase/fruct
• 1235403-62-9 | PF-05089771 (Catalog# : 17030912)PF-05089771 is a Selective Nav1.7 Inhibitor (IC50 = 11 nM) that interacts with the vo
• 135-87-5 | Piperoxan HCl (Catalog# : 17030708)Piperoxan, also known as benodaine, is a drug which was the very first antihistamine
• 1403764-72-6 | PFI-1 (Catalog# : 17030704)PFI-1 is a potent and highly selective protein interaction Inhibitor, which targets B
• 1114544-31-8 | Ponatinib HCl (Catalog# : 17030607)Ponatinib, also known as AP24534 is an oral drug for the treatment of chronic myeloid
• 192705-80-9 | PD-161570 (Catalog# : 17030304)PD-161570 is a selective FGFR inhibitor (IC50 values are 40, 262 and 3700 nM for FGFR