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Cas Index 1

• 1599441-71-0 | Super-TDU (Catalog# : 18495)Super-TDU is an inhibitory polypeptide targeting yap-teads interaction.
• 1253955-19-9 | (S)-(4-(3-(tert-butoxycarbonyl)-1-(isoquinolin-6-ylamino)-1-oxopropan-2-yl)phenyl)methyl 2,4-dimethylbenzoate (Catalog# : 183219)(S)-(4-(3-(tert-butoxycarbonyl)-1-(isoquinolin-6-ylamino)-1-oxopropan-2-yl)phenyl)met
• 132513-51-0 | (S)-Butyl 2-hydroxybutanoate (Catalog# : 1712291)butyl (2S)-2-hydroxybutanoate is building blocks.
• 14892-97-8 | SCR7 pyrazine (Catalog# : 1712261)SCR7 pyrazine is a small molecule inhibitor of DNA ligase IV that prevents nonhomolog
• 1333207-63-8 | SAR-7334 HCl (Catalog# : 17101610)SAR7334 is a novel, highly potent and bioavailable inhibitor of TRPC6 channels that o
• 1160833-51-1 | SEN-826 (Catalog# : 1710168)SEN-826 is a potential anticancer agent.
• 1366002-50-7 | Senexin A (Catalog# : 1710136)Senexin A is a potent and selective CDK8 inhibitor (IC50 = 280 nM). Senexin A binds t
• 1799633-27-4 | S63845 (Catalog# : 171071)S63845 is a small molecule that specifically binds with high affinity to the BH3-bind
• 1105698-15-4 | Salermide (Catalog# : 1791511)Salermide is a Sirtuin inhibitor with a strong cancer-specific proapoptotic effect. S
• 1308672-74-3 | Sulfatinib (Catalog# : 179135)Sulfatinib is an orally bioavailable, small molecule inhibitor of vascular endothelia
• 101526-62-9 | Sematilide hydrochloride (Catalog# : 179830)Sematilide, also known as CK-1752, is a class III antiarrhythmic. It is a selective d
• 168835-82-3 | SU-1498 (Catalog# : 17984)SU 1498 is a selective inhibitor of the receptor tyrosine kinase VEGF receptor 2 (VEG
• 1174428-47-7 | SF2523 (Catalog# : 17918)SF2523 is a highly selective and potent dual pan-PI3K/BRD4 inhibitor. SF2523 exhibits
• 1450881-55-6 | SAR-20347 (Catalog# : 1781101)SAR-20347 is a potent dual inhibitor of JAK1 and tyrosine kinase 2 (TYK2). 
• 1523406-39-4 | SAR-405 (Catalog# : 2017882)<span style="color:#34495E;font-family:" font-size:14px;background-color
• 148554-65-8 | Seco Rapamycin (sodium salt) (Catalog# : 20177313)Seco-rapamycin is the first in vivo open-ring metabolite of rapamycin that does not a
• 1184843-57-9 | SAR-020106 (Catalog# : 17031004)SAR-020106 is an ATP-competitive, potent, and selective CHK1 inhibitor with an IC50
• 1456632-41-9 | SH5-07 (Catalog# : 17031002)SH5-07 is a robust hydroxamic acid-based STAT3 inhibitor, which induce antitumor ce
• 138794-73-7 | Sardomozide HCl (Catalog# : 17030306)Sardomozide , also known as SAM486A or CGP48664, is a second-generation polyamine syn
• 149690-05-1 | Sacubitril sodium (Catalog# : 17030108)Sacubitril, also known as AHU377, is angiotensin receptor neprilysin inhibitor being
• 1801747-42-1 | SHP099 free base (Catalog# : 17030107)SHP099 is a potent, selective, orally bioavailable, and efficacious SHP2 inhibitor wi
• 1431699-67-0 | (S)-Tedizolid (Catalog# : 17021402)Tedizolid is the active moiety of the prodrug tedizolid phosphate, with high potency
• 1265965-22-7 | S49076 (Catalog# : 17021309)S49076 is a novel, potent inhibitor of MET, AXL/MER, and FGFR1/2/3 with IC50 valu
• 1001908-89-9 | SRT2183 (Catalog# : 17021306)SRT2183 is a small-molecule activator of the sirtuin subtype SIRT1, currently being
• 18883-66-4 | Streptozocin (Catalog# : 17011712)Streptozocin is a methylnitrosourea antineoplastic antibiotic isolated from the bacte
• 1018899-04-1 | Sotagliflozin (Catalog# : 17011711)Sotagliflozin, also known as LX4211, is an orally active and a dual SGLT1/SGLT2 inhib
• 127254-12-0 | Sitafloxacin anhydrous (Catalog# : 17011706)Sitafloxacin is a new-generation, broad-spectrum oral fluoroquinolone that is very ac
• 1801747-11-4 | SHP099 HCl (Catalog# : 17011704)SHP099 is a potent, selective, orally bioavailable, and efficacious SHP2 inhibitor wi
• 1687736-54-4 | SGC707 (Catalog# : 17011702)SGC707 is a potent, selective and cell-active allosteric inhibitor of protein arginin
• 1884220-36-3 | SBI0206965 (Catalog# : 71161)SBI0206965 is a potent and selective autophagy Kinase ULK1 Inhibitor. Many tumors bec