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Cas Index 1

• 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
• 149400-88-4 | Sardomozide (Catalog# : 17011607)Sardomozide , also known as SAM486A or CGP48664, is a second-generation polyamine syn
• 1092539-44-0 | SAR131675 (Catalog# : 17011605)SAR131675 is a potent and selective VEGFR-3 inhibitor. It inhibited VEGFR-3 tyrosine
• 127373-66-4 | Sivelestat (ONO-5046) (Catalog# : 16122760)Sivelestat is a potent and selective inhibitor of neutrophil elastase with IC50 of 44
• 17318-31-9 | SQ22536 (Catalog# : 16122726)SQ22536 is an inhibitor of adenylyl cyclase with an IC50 of 1.4 M. It can inhibit PGE
• 111540-00-2 | STA-21 (Catalog# : 16122706)STA-21 is a selective STAT3 inhibitor.In cells, STA-21 inhibits Stat3 DNA binding act
• 1335106-03-0 | SR1001 (Catalog# : 6111522)SR1001 is a selective ROR and ROR inverse agonist; suppresses TH17 cell differentiati
• 1324003-64-6 | S1P1 Agonist III (Catalog# : 61119)S1P1 Agonist III is a potent and orally active S1P1 agonist with EC50 of 18 nM; no ac
• 1186222-89-8 | 4SC-202 (Catalog# : 611937)4SC-202 is an orally available potent HDACi specific for class I HDAC isoenzymes(NO H
• 1454585-06-8 | SR-3029 (Catalog# : 611915)SR 3029 is a potent and highly specific CK1/CK1 inhibitor with the IC50 of 97 nM.SR-3
• 1456632-40-8 | SH-4-54 (Catalog# : 16071406)SH-4-54 is a potent STAT inhibitor with KD of 300 nM and 464 nM for STAT3 and STAT5,
• 1230487-00-9 | Siponimod (Catalog# : 16071404)Siponimod, also known as BAF-312, is a a potent and orally selective S1P Receptor Mod