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Cas Index 1

• 1995889-48-9 | Parsaclisib HCl (Catalog# : L20333)Parsaclisib, also known as INCB050465, is a novel PI3Kδ inhibitor which synergizes w
• 1426698-88-5 | Parsaclisib free base (Catalog# : L20332)Parsaclisib, also known as INCB050465, is a novel PI3Kδ inhibitor which synergizes w
• 1221962-86-2 | PS210 (Catalog# : 20282)PS210 is a substrate-selective inhibitor of protein kinase PDK1. It acts by binding t
• 171744-42-6 | PD-159206 (Catalog# : 20278)PD-159206 is a nucleocapsid inhibitor. It exhibits good antiviral activity against HI
• 18550-98-6 | 3PO (Catalog# : 21227)3PO is a PFKFB3 (6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase) inhibitor. 3PO
• 1034189-82-6 | PF-06802861 ( ARRY 371797 ; ARRY-797 ) (Catalog# : 2073108)ARRY 797 (also known as ARRY 371797 or PF 06802861) is an orally active, selective p3
• 1917294-46-2 | PF-04745637 (Catalog# : 2071623)PF-04745637 is a TRPV1 antagonist.
• 1629869-44-8 | Pimodivir ( VX-787 ) (Catalog# : 2071401)Pimodivir, also known as VX-787, JNJ-872, is a novel inhibitor of influenza virus rep
• 1454619-14-7 | PU-WS13 (Catalog# : 206701)PU-WS13 is a potent, Grp94-specific Hsp90 inhibitor of the purine scaffold class. PU-
• 1953130-87-4 | PTI-428(PTI428) (Catalog# : 31619)PTI-428 is a type of CFTR modulator called an amplifier. Amplifiers increase the amou
• 1415637-72-7 | PF-05085727 (Catalog# : 1932011)PF-05085727 is a Potent, Selective, and Brain Penetrant Phosphodiesterase 2A Inhibito
• 1252637-35-6 | Petesicatib (Catalog# : 193206)Petesicatib is a cathepsin inhibitor drug candidate.
• 187235-37-6 | Pretomanid (Catalog# : 193110)Pretomanid, aslo known as PA-824, a bioreductive drug. PA-824 has potent in vitro act
• 1341224-83-6 | PF-4136309 (Catalog# : 192282)PF-4136309, also known as INCB8761, is an orally available human chemokine receptor 2
• 1078166-57-0 | PF04418948 (Catalog# : 191141)PF-04418948 is a novel, potent and selective prostaglandin EP2 receptor antagonist.
• 1352879-65-2 | PF74 (Catalog# : 1812253)PF-3450074, also known as PF74, is a HIV-1 inhibitor that targets HIV capsid protein.
• 1672665-49-4 | PT2385 (Catalog# : 1812135)PT2385 is an orally active, small molecule inhibitor of hypoxia inducible factor (HIF
• 133413-70-4 | PF 1022A (Catalog# : 1811232)PF1022A is a novel anthelmintic that binds to the latrophilin-like transmembrane rece
• 146464-95-1 | Pralatrexate (Catalog# : 1811221)Pralatrexate is a folate analogue inhibitor of dihydrofolate reductase (DHFR) exhibit
• 1037589-69-7 | PF-05231023 (Catalog# : 1811162)PF-05231023 is a long-acting FGF21 mimetic. PF-05231023 decreases body weight and imp
• 1311174-68-1 | PH-002 (Catalog# : 1810234)PH-002 is a novel inhibitor of apolipoprotein (apo) E4 intramolecular domain interact
• 1513857-77-6 | Pemigatinib (INCB054828) (Catalog# : 1810164)Pemigatinib (INCB054828) is an orally active, selectiveFGFRinhibitor withIC50s of 0.4
• 1022899-36-0 | PCI-33380 (Catalog# : 18943)PCI-33380 was designed based on the ibrutinib scaffold and has been used in both cell
• 1613373-33-3 | PCO371 (Catalog# : 187125)PCO371 is a potent and selective PTHR1 agonist for the treatment of hypoparathyroidis
• 1927857-61-1 | PQR530 (Catalog# : 18756)PQR530 is a highly potent dual pan-PI3K/mTORC1/2 inhibitor.
• 1269662-73-8 | Pyrotinib (Catalog# : 18731)Pyrotinibm, also known as SHR-1258, is an orally bioavailable, dual kinase inhibitor
• 1268244-85-4 | PX20606 trans-isomer (Catalog# : 186274)PX20606, also known as PX-102, is a FXR agonist.
• 1394033-54-5 | PF-05180999 (Catalog# : 186153)PF-05180999 is a potent and selective PDE2a inhibitor (PDE2a IC50 = 0.001 μM, 2000-f
• 1428333-96-3 | Pritelivir mesylate (Catalog# : 186152)Pritelivir, also known as AIC-316 and BAY 57-1293, is a potent helicase primase inhib
• 1446261-44-4 | Pamiparib (Catalog# : 185233)Pamiparib is an antineoplastic drug candidate.Pamiparib (BGB-290) is an investigation