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Cas Index 1

• 1037210-93-7 | Saridegib (Catalog# : 1812251)Saridegib, also known as IPI-926, is an orally bioavailable, cyclopamine-derived inhi
• 1260612-13-2 | SAR260301 (Catalog# : 1812134)SAR260301 is potent and selective Class I phosphatidylinositol-3-kinase (PI3K)β spec
• 1613695-14-9 | SGC-CBP30 (Catalog# : 1810244)SGC-CBP30 is a potent and selective inhibitor of CREBBP (CBP) and EP300; which are ge
• 1362850-20-1 | Seletalisib (Catalog# : 1810221)Seletalisib, also known as UCB-5857, is a potent and selective PI3 kinase inhibitor,
• 188817-13-2 | SC-560 (Catalog# : 185113)SC-560 is a potent, orally active and selective inhibitor of COX-1.
• 1609452-30-3 | SEL120-34A HCl (Catalog# : 18574)SEL120-34A is a potent and selective CDK8 inhibitor active in AML cells with high lev
• 1816294-67-3 | SR-4370 (Catalog# : 1842814)SR-4370 is an HDAC inhibitor.
• 1821908-49-9 | SGC2085 HCl (Catalog# : 184287)SGC2085 is a Potent and Selective Coactivator Associated Arginine Methyltransferase 1
• 1222097-72-4 | S38093 HCl (Catalog# : 184176)S38093 is an inverse agonist at histamine H3 receptors.
• 1173022-21-3 | STO-609 acetate (Catalog# : 184123)STO-609 is a cell-permeable inhibitor of calcium/calmodulin-dependent kinase kinases
• 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