Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
---|---|---|---|---|
17101610 | SAR-7334 HCl | 1333207-63-8 | >98% | |
SAR7334 is a novel, highly potent and bioavailable inhibitor of TRPC6 channels that o | ||||
1710168 | SEN-826 | 1160833-51-1 | >98% | |
SEN-826 is a potential anticancer agent. | ||||
17101310 | SRT3025 HCl | 2070015-26-6 | >98% | |
SRT3025 is an orally available small molecule activator of the SIRT1 enzyme. | ||||
1710136 | Senexin A | 1366002-50-7 | >98% | |
Senexin A is a potent and selective CDK8 inhibitor (IC50 = 280 nM). Senexin A binds t | ||||
171071 | S63845 | 1799633-27-4 | >98% | |
S63845 is a small molecule that specifically binds with high affinity to the BH3-bind | ||||
1791511 | Salermide | 1105698-15-4 | 98.0% | |
Salermide is a Sirtuin inhibitor with a strong cancer-specific proapoptotic effect. S | ||||
1791320 | SD-06 | 271576-80-8 | 98.0% | |
SD-06 is a MAPK p38 alpha inhibitor for the treatment of arthritis. | ||||
179135 | Sulfatinib | 1308672-74-3 | 98.0% | |
Sulfatinib is an orally bioavailable, small molecule inhibitor of vascular endothelia | ||||
1791111 | S107 HCl | 927871-76-9 | 98.0% | |
S107 is a Type 1 ryanodine receptor (RyR1) stabilizer; binds RyR1 and enhances the bi | ||||
179830 | Sematilide hydrochloride | 101526-62-9 | 98.0% | |
Sematilide, also known as CK-1752, is a class III antiarrhythmic. It is a selective d | ||||
179815 | SNX-2112 | 908112-43-6 | 98.0% | |
SNX-2112, also known as PF 04928473, is an Hsp90 inhibitor which is currently undergo | ||||
17984 | SU-1498 | 168835-82-3 | 98.0% | |
SU 1498 is a selective inhibitor of the receptor tyrosine kinase VEGF receptor 2 (VEG | ||||
17918 | SF2523 | 1174428-47-7 | 98.0% | |
SF2523 is a highly selective and potent dual pan-PI3K/BRD4 inhibitor. SF2523 exhibits | ||||
1781101 | SAR-20347 | 1450881-55-6 | 98.0% | |
SAR-20347 is a potent dual inhibitor of JAK1 and tyrosine kinase 2 (TYK2). | ||||
20178811 | SB756050 | 447410-57-3 | 98.0% | |
SB-756050 is a G protein-coupled bile acid receptor 1 (GPBAR1) agonist potentially fo | ||||
2017882 | SAR-405 | 1523406-39-4 | 98.0% | |
<span style="color:#34495E;font-family:" font-size:14px;background-color | ||||
20177313 | Seco Rapamycin (sodium salt) | 148554-65-8 | 98.0% | |
Seco-rapamycin is the first in vivo open-ring metabolite of rapamycin that does not a | ||||
174191 | SU5402 | 215543-92-3 | 98% by HNMR/HPLC | |
SU5402 is a fibroblast growth factor receptor (FGFR)-specific tyrosine kinase inhibit | ||||
17031004 | SAR-020106 | 1184843-57-9 | 98% | |
SAR-020106 is an ATP-competitive, potent, and selective CHK1 inhibitor with an IC50 | ||||
17031002 | SH5-07 | 1456632-41-9 | 98% | |
SH5-07 is a robust hydroxamic acid-based STAT3 inhibitor, which induce antitumor ce | ||||
17030603 | SUN11602 | 704869-38-5 | 98% | |
SUN11602 is a novel aniline compound, which mimics the neuroprotective mechanisms of | ||||
17030306 | Sardomozide HCl | 138794-73-7 | 98% | |
Sardomozide , also known as SAM486A or CGP48664, is a second-generation polyamine syn | ||||
17030108 | Sacubitril sodium | 149690-05-1 | 98% | |
Sacubitril, also known as AHU377, is angiotensin receptor neprilysin inhibitor being | ||||
17030107 | SHP099 free base | 1801747-42-1 | 98% | |
SHP099 is a potent, selective, orally bioavailable, and efficacious SHP2 inhibitor wi | ||||
17022802 | Semagacestat | 425386-60-3 | 98% | |
Semagacestat (LY450139) is a -secretase blocker for A42, A40 and A38 with IC50 of 10. | ||||
17021402 | (S)-Tedizolid | 1431699-67-0 | 98% | |
Tedizolid is the active moiety of the prodrug tedizolid phosphate, with high potency | ||||
17021319 | STO-609 | 52029-86-4 | 98% | |
STO-609 is a specific inhibitor of the Ca2+/Calmodulin-dependent protein kinase kina | ||||
17021309 | S49076 | 1265965-22-7 | 98% | |
S49076 is a novel, potent inhibitor of MET, AXL/MER, and FGFR1/2/3 with IC50 valu | ||||
17021306 | SRT2183 | 1001908-89-9 | 98% | |
SRT2183 is a small-molecule activator of the sirtuin subtype SIRT1, currently being | ||||
17011714 | SW044248 | 522650-83-5 | 98% | |
SW044248 is a potent and selective Topoisomerase I inhibitor. SW044248 killed approxi |
Overnight Delivery
Fast & Safe Delivery Worldwide
Safety and Security
Intimate Service
Copyright 2015-2022 武汉永璨生物科技有限公司 版权所有 | 鄂ICP备17005301号-1