Search By Initial

Cas Index 9

• 900510-03-4 | PF-3274167 (Catalog# : 020101)PF-3274167 is a high-affinity nonpeptide oxytocin receptor (OTR) antagonist, with Ki
• 942487-16-3 | PF-03814735 (Catalog# : 011105)PF-03814735 is an orally bioavailable, ATP-competitive, reversible small-molecule Aur
• 956905-27-4 | PF-04217903 (Catalog# : 010807)PF-04217903 is a selective ATP-competitive c-Met inhibitor with IC50 of 4.8 nM, susce
• 92623-83-1 | Pravadoline (Catalog# : 010415)Coming soon!
• 937272-79-2 | Pacritinib ( SB1518 ) (Catalog# : 122941)Pacritinib(SB1518) is a highly selective kinaseinhibitorwith specificity for JAK2, FL
• 955977-50-1 | PI-3065 (Catalog# : 122908)PI-3065 is a novel potent and selective PI3K p110 inhibitor with IC50 of 15 nM; exhib
• 939791-38-5 | PF-562271 benzenesulfonate salt (Catalog# : 101919)PF-562271 is an orally bioavailable small molecule and ATP-competitive focal adhesion
• 900305-37-5 | PFI-4 (Catalog# : 82406)PFI-4 is a potent and selective BRPF1 bromodomain inhibitor (IC50 = 80 nM). Exhibits
• 918505-84-7 | PLX-4720 (Catalog# : 52592)PLX 4720 is a potent and selective inhibitor of B-RafV600E(IC50=13 nM) and c-Raf-1Y34
• 914913-88-5 | Palomid 529 (Catalog# : 52591)Palomid 529 (P529) is a novel potent inhibitor of both the mTORC1 and mTORC2 complexe
• 929016-96-6 | Pracinostat (Catalog# : 52552)Pracinostat(SB939) is a potent pan-HDAC inhibitor with IC50 of 40-140 nM with excepti
• 931706-15-9 | PPQ-102 (Catalog# : 52233)PPQ-102 is a potent CFTR inhibitor which can completely inhibited CFTR chloride curre
• 943319-70-8 | Ponatinib (AP24534) (Catalog# : 52107)Ponatinib (AP24534) is a novel, potent multi-target inhibitor ofAbl, PDGFR, VEGFR2, F
• 950769-58-1 | Quizartinib (Catalog# : 82703)Quizartinib is a second-generation FLT3 inhibitor for Flt3(ITD/WT) with IC50 of 1.1 n
• 93265-81-7 | Ropidoxuridine (Catalog# : 20595)Ropidoxuridine is a novel, orally available, thymidine analogue and prodrug for IUdR,
• 925206-65-1 | RRX-001 (Catalog# : 233901)RRx-001 is a highly selective NLRP3 inhibitor with vascular normalization and tumor a
• 946150-57-8 | Remetinostat (Catalog# : 193111)Remetinostat, also known as SHP-141, is a topical formulation containing the histone
• 920113-03-7 | Riviciclib HCl (Catalog# : 179131)Riviciclib, also known as P276-00 , is a flavone and cyclin dependent kinase (CDK) in
• 947620-48-6 | RVT-501 (Catalog# : 17917)RVT-501, also known as E-6005, is a phosphodiesterase 4 (PDE-4) inhibitor potentially
• 914462-92-3 | Rolapitant HCl (Catalog# : 17030609)Rolapitant, also known as SCH-619734, is an orally bioavailable, centrally-acting, se
• 939981-39-2 | RO5045337 (Catalog# : 16071112)RO5045337, also known as R7112, RG7112, is a MDM2 antagonist with potential antineopl
• 926037-48-1 | Radotinib (Catalog# : 011307)Radotinib is an orally available, a second-generation tyrosine kinase inhibitor of Bc
• 941678-49-5 | Ruxolitinib (Catalog# : 01118)Ruxolitinib is the first potent, selective, JAK1/2 inhibitor to enter the clinic with
• 946128-88-7 | Ro 5126766 (Catalog# : 010812)Ro 5126766 is a potent and selective dual RAF/MEK inhibitor. For SK-MEL-28, SK-MEL-2,
• 923032-37-5 | Refametinib (Catalog# : 010810)Refametinib is an orally bioavailable selective MEK inhibitor with potential antineop
• 901119-35-5 | R788 (Catalog# : 122928)Fostamatinib is a small molecule Syk kinase inhibitor with potential anti-inflammator
• 927880-90-8 | RAF265 (Catalog# : 122202)RAF265 is a potent selective inhibitor of C-Raf/B-Raf/B-Raf V600E with IC50 of 3-60 n
• 928025-63-2 | (R)-1-Boc-3-Isopropylpiperazine (Catalog# : 81908)Coming soon!
• 955979-06-3 | (R)-tert-Butyl 2-isopropylpiperazine-1-carboxylate hydrochloride (Catalog# : 81903)Coming soon!
• 911222-45-2 | Rabusertib(LY2603618) (Catalog# : 52807)LY2603618(IC-83) is a potent and selective small molecule inhibitor of Chk1 protein k