按首字母搜索

Cas号索引 1

• 1269440-17-6 | Encorafenib(LGX-818) (Catalog# : 179308)Encorafenib，即LGX818LGX818 是一种可口服的突变体 B-Raf V600E 酶的抑制
• 177834-92-3 | Eletriptan hydrobromide (Catalog# : 52784)This product is no information for the time being
• 1186486-62-3 | Evacetrapib (Catalog# : 52758)Evacetrapib (LY2484595) is a potent and selective inhibitor of CETP with IC50 of 5.5
• 1291074-87-7 | ENMD-2076 Tartrate (Catalog# : 52637)ENMD-2076 tartrate has selective activity against Aurora A and Flt3 with IC50 of 14 n
• 1396772-26-1 | EPZ005687 (Catalog# : 52303)EPZ-005687 is a potent and selective inhibitor of EZH2 with Ki of 24 nM, 50-fold sele
• 1233948-35-0 | ELR510444 (Catalog# : 52503)ELR510444 is a novel microtubule disruptor; inhibits MDA-MB-231 cell proliferation wi
• 1403254-99-8 | EPZ-6438 (Catalog# : 52302)EPZ-6438 is a potent, and selectiveEZH2inhibitor withKiandIC50of 2.5 nM and 11 nM, ex
• 1614235-14-1 | AAG-1 ( FLAG-003 ) (Catalog# : 20640)FLAG-003 是一种多效水溶性小分子治疗药物，旨在通过两种成熟的作
• 146426-40-6 | Flavopiridol ( 夫拉平度 ) (Catalog# : 237071)Alvocidib is a synthetic dihydroxyflavone that is 5,7-dihydroxyflavone which is subst
• 192570-33-5 | 5-氟喹唑啉-2,4(1H,3H)-二酮 (Catalog# : 20420)
• 1070790-89-4 | Fadraciclib free base (Catalog# : L20347)Fadraciclib, also known as CYC065, is an orally bioavailable inhibitor of cyclin depe
• 1980023-94-6 | 1-[6-(4-fluoro-1H-pyrazol-1-yl)-3-pyridinyl]Ethanone (Catalog# : 20262)
• 1630808-89-7 | FT113 (Catalog# : 2071557)FT113 is a novel potent inhibitor of fatty acid synthase (fasn)
• 1488354-15-9 | Fulacimstat (Catalog# : 2071514)Fulacimstat, also known as BAY1142524, is a chymase inhibitor and antifibrotic drug c
• 1350426-06-0 | 2-(3-Fluoro-4-isopropoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (Catalog# : 262324)
• 1629229-37-3 | Fezolinetant (Catalog# : 18722)Fezolinetant，也被称为ESN-364，是一种神经kinin-3 (NK-3)受体拮抗剂，已
• 1232030-35-1 | FRAX486 (Catalog# : 18721)FRAX486是一种有效的p21激活激酶(PAK)抑制剂(PAK1、PAK2、PAK3和PAK4的IC
• 1394238-91-5 | Fmoc-Val-Ala-PAB (Catalog# : 18431)Fmoc-Val-Ala-PAB, also known as Fmoc-Val-Ala-PAB-OH, is a useful linker for making An
• 1432908-05-8 | FRAX1036 (Catalog# : 1791315)frax1036是强有力的和有选择性的激酶抑制剂。
• 1075705-01-9 | 4-氟-2-甲氧基-5-硝基苯胺 (Catalog# : 521191)AZD9291中间体1
• 125802-18-8 | 1-(3-Fluorophenyl)-cyclohexanamine HCl (Catalog# : 178221)1-(3-Fluorophenyl)-cyclohexanamine HCl
• 13311-84-7 | Flutamide (Catalog# : 16123001)Flutamide, also known as SCH13521, is a toluidine derivative and nonsteroidal antiand
• 1637735-84-2 | FIIN-3 (Catalog# : 16122945)FIIN-3 is a potent, selective, irreversible and the next-generation covalent FGFR inh
• 1708971-72-5 | FGFR4-IN-1 (Catalog# : 16122813)FGFR4-IN-1 is a potent and selective FGFR4 inhibitor. FGFR4 may be a novel therapeuti
• 108409-83-2 | FH535 (Catalog# : 16122788)FH535 is a Wnt/-catenin signaling inhibitor and also a dual PPAR and PPAR antagonist.
• 1226895-15-3 | FLLL32 (Catalog# : 16122709)FLLL32 is a potent JAK2/STAT3 inhibitor with IC50 of <5 M.In MDA-MB-231 breast and
• 1633044-56-0 | FIIN-2 (Catalog# : 16062117)FIIN-2 is a potent, selective, irreversible and the next-generation covalent FGFR inh
• 196612-93-8 | Falnidamol (Catalog# : 122807)Falnidamol is a pyrimido-pyrimidine with antitumor activity.
• 154540-49-5 | Fluoroclebopride (Catalog# : 120811)Coming soon!
• 167933-07-5 | Flibanserin (Catalog# : 101906)Flibanserin is a full agonist of the 5-HT1A receptor (Ki = 1 nM) and, with lower affi