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Cas号索引 1

• 158663-69-5 | (S)-Piperazine-2-carboxylic acid dihydrochloride (Catalog# : 81718)Coming soon!
• 1613028-81-1 | SR9243 (Catalog# : 80701)SR9243 is a LXR inverse agonist that induces LXR-corepressor interaction, which shows
• 1052532-15-6 | SBE13 Hydrochloride (Catalog# : 52751)SBE13 Hcl is a potent and selective PLK1 with IC50 of 0.2 nM; no inhibition om Aurora
• 1020149-73-8 | SGI-1027 (Catalog# : 52737)SGI-1027 is a potent and selective inhibitor of DNA methyltransferase (DNMT) with IC5
• 182498-32-4 | SB225002 (Catalog# : 52714)SB225002 is a potent and selective non-peptide inhibitor of CXCR2 with IC50 of 22 nM;
• 147817-50-3 | Siramesine (Catalog# : 52548)Siramesine(Lu 28-179) is a selective sigma-2 receptor agonist, which has been shown t
• 1125780-41-7 | SKLB610 (Catalog# : 52536)SKLB610, a novel multi-targeted inhibitor, inhibits angiogenesis-related tyrosine kin
• 1227633-49-9 | StemRegenin 1 (Catalog# : 52531)StemRegenin 1(SR1) is an antagonist of the aryl hydrocarbon receptor.SR1 is the first
• 1019331-10-2 | S0859 (Catalog# : 52507)S0859, an N-cyanosulphonamide compound, reversibly inhibit NBC-mediated pH(i) recover
• 1415238-77-5 | 5S rRNA modificator (Catalog# : 52243)5S rRNA modificator is a suitable electrophile for 2-hydroxyl acylation on structured
• 162520-00-5 | Salirasib (Catalog# : 52106)Salirasib(S-Farnesylthiosalicylic aci) is an S-farnesyl cysteine analog that interfer
• 1057249-41-8 | SNS-314 Mesylate (Catalog# : 52102)SNS-314 Mesylate is a potent and selective inhibitor ofAurora A,Aurora BandAurora Cwi
• 1001645-58-4 | SRT1720 (Catalog# : 52007)SRT1720 is a selectiveSIRT1activator withEC50of 0.16 M, but is >230-fold less pote
• 149682-77-9 | Talabostat (Catalog# : 24102)Talabostat, also known as PT-100 and BXCL701, is dipeptidyl peptidase inhibitor with
• 1622204-21-0 | Tasurgratinib (Catalog# : 24099)Tasurgratinib, also known as E-7090, is a fibroblast growth factor receptor inhibitor
• 1801756-06-8 | tunlametinibum (Catalog# : 24085)tunlametinibum is a tyrosine kinase inhibitor and antineoplastic
• 1613200-51-3 | Tuvusertib (Catalog# : 24069)Tuvusertib, also known as M-1774 and ATR inhibitor 1, is a ATR inhibitor. M1774 selec
• 1849590-02-8 | Tomivosertib HCl (Catalog# : 20673)Tomivosertib, also known as eFT508 is a MNK1/2 inhibitor. Tomivosertib binds to and i
• 1164471-33-3 | TT-012 (Catalog# : 20660)TT-012 specifically binds to dynamic MITF and destroys the latter's dimer formati
• 1821327-95-0 | Tinlarebant ( LBS-008 ) (Catalog# : 20474)Tinlarebant (LBS-008) 是一种视黄醇结合蛋白 4 (RBP4) 的小分子抑制剂。
• 1597403-47-8 | trans-ISRIB (Catalog# : 20465)trans-ISRIB is an Integrated Stress Response Inhibitor. trans-ISRIB inhibits the eIF2
• 163089-34-7 | 2-(叔丁基二甲硅氧基)-N-甲氧基-N-甲基乙酰胺 (Catalog# : 20409)
• 1784751-19-4 | TA-02 (Catalog# : G20380)TA-02 is a p38 MAPK inhibitor with IC50 of 20 nM.
• 16544-67-5 | 6-(三氟甲基)-4(3H)-喹唑啉酮 (Catalog# : 20311)
• 1200443-21-5 | Targocil (Catalog# : 21239)Targocil is a antibiotic, inhibiting a late step in wall teichoic acid biosynthesis a
• 1597403-47-8 | trans-ISRIB (Catalog# : 2112801)trans-ISRIB is an Integrated Stress Response Inhibitor. trans-ISRIB inhibits the eIF2
• 1971920-73-6 | Tolebrutinib (Catalog# : 20736)Tolebrutinib, also known as SAR442168, is a Bruton tyrosine kinase inhibitor.
• 1977495-97-8 | Trilaciclib hydrochloride (G1T28 hydrochloride) (Catalog# : 2073107)Trilaciclib是一种小分子竞争性细胞周期蛋白依赖性激酶4和6（CDK4 /
• 1422535-52-1 | T-3775440 HCl (Catalog# : 2071541)T-3775440 HCl is a potent, selecitve, irreversible LSD1 inhibitor.
• 1476799-74-2 | 2-(tert-butoxycarbonylamino)pyrazolo[1,5-a]pyridine-3-carboxylic acid (Catalog# : 262322)