Cas号索引 9

905854-02-6 | Tivantinib (Catalog# : 16070802)Tivantinib (ARQ-197) is an orally bioavailable small molecule inhibitor of c-Met with
918633-87-1 | TH-302 (Catalog# : 011812)TH-302 is selective hypoxia-activated prodrug targeting hypoxic regions of solid tumo
916141-36-1 | TCS 1102 (Catalog# : 121408)TCS 1102 is a potent, dual orexin receptor antagonist (Ki values are 0.2 and 3 nM for
941685-27-4 | trimethyl-[2-[[4-(1H-pyrazol-4-yl)pyrrolo[2,3-d]pyrimidin-7-yl]methoxy]ethyl]silane (Catalog# : 91701)Coming soon!
928025-61-0 | tert-butyl (3R)-3-(2-methylpropyl)piperazine-1-carboxylate (Catalog# : 81907)Coming soon!
928025-57-4 | tert-butyl (3R)-3-propylpiperazine-1-carboxylate (Catalog# : 81906)Coming soon!
928025-58-5 | tert-butyl (3S)-3-propylpiperazine-1-carboxylate (Catalog# : 81905)Coming soon!
960283-58-3 | tert-butyl (2S)-2-methylpiperazine-1-carboxylate,hydrochloride (Catalog# : 81034)Coming soon!
91131-72-5 | 4-tert-butyl-3-iodobenzoic acid (Catalog# : 80315)Coming soon!
937270-47-8 | TG02 ( SB1317 ) (Catalog# : 62502)SB1317 (TG02) is a novel small molecule potent CDK/JAK2/FLT3 inhibitor. SB1317 was so
948304-40-3 | UC-1728 (Catalog# : 1812292)UC-1728，又称t-TUCB，是一种可溶性环氧化物水解酶抑制剂。
903564-48-7 | UM-164 (Catalog# : 186282)UM-164是一种抗癌抑制剂。CAS号为903564-48-7。
956590-23-1 | UNBS-5162 (Catalog# : 101907)UNBS5162 is a novel naphthalimide that binds to DNA by intercalation and suppresses C
934826-68-3 | Visomitin (Synonyms: SKQ1) (Catalog# : 171423)Visomitin（别名：SKQ1）是一种线粒体靶向抗氧化剂。
934493-76-2 | Voxtalisib ( XL-765) (Catalog# : 160926001)PI3K/mTOR dual kinase inhibitor XL765 inhibits both PI3K kinase and mTOR kinase, whic
936727-05-8 | VX-809(Lumacaftor) (Catalog# : 92219)From Wikipedia, the free encyclopediaLumacaftor (USAN, codenamed VX-809) is an experi
960203-27-4 | Vortioxetine hydrobromide (Catalog# : 52716)Vortioxetine Hcl (Lu AA21004 Hcl) is a multimodal serotonergic agent, inhibits 5-HT1A
918504-65-1 | Vemurafenib (PLX4032, RG7204) (Catalog# : 52589)Vemurafenib (PLX4032, RG7204) is a novel and potent inhibitor ofB-RafV600EwithIC50of
947669-91-2 | WWL70 (Catalog# : 16122847)WWL70是选择性ABHD6抑制剂，在创伤性脑损伤和多发性硬化症的动物
90332-66-4 | 7-xylosyltaxol (Catalog# : 611947)7-xylosyltaxol(Taxol-7-xyloside) is a taxol (Paclitaxel) derivative; Paclitaxel binds
912656-34-9 | XEN907 (Catalog# : 112006)XEN907 is a spirooxindole blocker of NaV1.7 for the treatment of pain.
956958-53-5 | XL147 (Catalog# : 51506)XL147 (SAR245408) is a potent and highly selective inhibitor of class I PI3Ks (, , ,
912287-56-0 | YHO-13177 (Catalog# : 6111511)YHO-13177 is a potent and specific inhibitor of BCRP; potentiated the cytotoxicity of

667411-04-3 | TRPM4-IN-2 (Catalog# : 24147)TRPM4-IN-2 (NBA) is a potent transient receptor potential melastatin 4 (TRPM4) inhibi
1534-35-6 | Isolithocholic Acid (Catalog# : 24146)Isolithocholic acid is a bile acid that is formed via microbial metabolism of lithoch
877768-84-8 | H2-Gamendazole (Catalog# : 24145)H2-Gamendazole is a derivative of Lonidamine that reduces cyst formation in polycysti
2095432-28-1 | CPI-455 HCl (Catalog# : 24144)CPI-455 is a potent and selective inhibitor of KDM5 demethylases which reduces surviv
1215115-03-9 | KH-3 (Catalog# : 24143)KH-3 is a potent RNA-binding protein Hu antigen R (HuR) inhibitor with an IC50 value
2097938-74-2 | Stafib-2 (Catalog# : 24142)Stafib-2 is a potent and selctive inhibitor of the transcription factor STAT5b, with
2032123-28-5 | TCRS-417 (Catalog# : 24141)TCRS-417 (T417) is a small molecule compound capable of docking to the interface betw
1096144-06-7 | PST3 1a (Catalog# : 24140)PST3 1a is a Novel selective inhibitor of the N-acetylglucosamine glycosyltransferase
2225824-53-1 | YTX-465 (Catalog# : 24139)YTX-465 is a SCD inhibitor. YTX-465 strongly reduced fatty desaturation in a concentr
944808-88-2 | CAY10566 (Catalog# : 10403)Coming soon!

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