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Cas Index 2

• 259793-96-9 | T 705 (Catalog# : 52717)There is no brief introduction to the product
• 2076-91-7 | TPT-260 Dihydrochloride (Catalog# : 52235)TPT-260 2Hcl (TPU260 2Hcl) is a thiophene thiourea derivative with molecule weight 26
• 252916-29-3 | TSU-68(SU6668,Orantinib) (Catalog# : 51916)TSU-68 (SU6668, Orantinib) has greatest potency againstPDGFRautophosphorylation withK
• 2226789-82-6 | UNC5293 (Catalog# : 24094)UNC5293 is a MERTK -selective and potent inhibitor ( Ki=190 pM).
• 2414349-93-0 | UJN49930 ( UGT8-IN-1 ) (Catalog# : 20677)UJN49930 ( UGT8-IN-1 ) is an inhibitor of UDP-galactose ceramide galactosyltransferas
• 2455519-86-3 | Usnoflast (Catalog# : 20629)Usnoflast is a non-steroidal anti-inflammatory (NSAID).
• 2244989-34-0 | UCB9608 (Catalog# : 2071516)UCB9608 is a Potent, Orally Bioavailable PI4KIIIβ Inhibitor. UCB9608 showed the impr
• 256477-09-5 | UK-371804 (Catalog# : 1791114)UK-371804 is a potent and selective uPA inhibitor with excellent enzyme potency (Ki 1
• 256476-36-5 | UK-371804 HCl (Catalog# : 17031008)UK-371804 is a potent and selective urokinase-type plasmogen activator (uPA) inhibi
• 2590556-80-0 | Velzatinib (IDRX-42, M-4205) (Catalog# : 26A009)Velzatinib is an orally bioavailable small molecule inhibitor of multiple mutated for
• 2506273-81-8 | VT-3989 (Catalog# : 25200)VT3989, a first-in-class potent oral TEAD palmitoylation inhibitor, disrupts YAP tran
• 2129515-96-2 | Vepafestinib ( Synonyms: TAS0953 ; HM06) (Catalog# : 25166)Vepafestinib, also known as HM06 and TAS0953, is a RET-selective inhibitor with enhan
• 2647442-33-7 | VV116 (Catalog# : 20536)VV116, also known as JT001, is an oral drug candidate of nucleoside analog against SA
• 2649467-58-1 | VX-548 (Catalog# : 20525)
• 2169916-18-9 | VTP-50469 (Catalog# : 20111202)VTP-50469 is a novel, potent, selective, orally-available MeninMLL1 inhibitor, being
• 2173134-00-2 | VUN34002 (Catalog# : 2071534)VUN34002, also known as Vanin-1-IN-1 is an inhibitor of vanin-1 enzyme which is a cel
• 23261-20-3 | VAL-083 (Catalog# : 112091)VAL-083 is a bi-functional alkylating agent, with potential antineoplastic activity.
• 2097381-85-4 | VH298 (Catalog# : 18581)VH-298 is a potent VHL inhibitor that stabilizes HIF-α and elicits a hypoxic respons
• 2095432-65-6 | Verubecestat TFA (Catalog# : 18417)Verubecestat, also known as MK-8931 or SCH 900931, is a potent and selective beta-sec
• 235106-62-4 | VP 14637 (Catalog# : 011112)Coming soon!
• 212141-54-3 | Vatalanib (Catalog# : 010434)Vatalanib free base is an inhibitor of VEGFR2/KDR with IC50 of 37 nM, less potent aga
• 2630378-05-9 | Wu-5 (Catalog# : 24160)Wu-5 is a USP10 inhibitor that can inhibit FLT3 and AMPK pathways, induce FLT3-ITD de
• 2229025-70-9 | WM 3835 (Catalog# : 20504)WM 3835 is a lysine acetyltransferase HBO1 (KAT7) inhibitor. It reduces H3K14ac level
• 2253985-29-2 | WK500B (Catalog# : 20491)WK500B is a BCL6 inhibitor. WK500B engaged BCL6 inside cells, blocked BCL6 repression
• 2055397-28-7 | WM-1119 (Catalog# : 181181)WM-1119 is a highly potent, selective inhibitor of lysine acetyltransferase KAT6A wit
• 211555-05-4 | WHI-P97 (Catalog# : 185710)WHI-P97 is a JAK3 inhibitor.
• 214358-33-5 | 1400W (Catalog# : 17021321)1400W is a slow, tight binding, and highly selective inhibitor ofinducible nitric-oxi
• 2012607-27-9 | WNK463 (Catalog# : 6111509)WNK463 is a pan-WNK-kinase inhibitor. It potently inhibits the in vitro kinase activi
• 211555-04-3 | WHI-P154 (Catalog# : 73107)WHI-P 154 is a JAK3 inhibitor (IC50 = 1.8 M) that displays no activity at JAK1 or JAK
• 211555-08-7 | WHI-P180 (Catalog# : 52221)WHI-P180 is a potent EGFR and Cdk2 inhibitors with IC50 of 4.0 and 1.0 uM, respective