Products

Catalog No	Chemical Name	CAS Number	Purity
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%
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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	≧98.0%
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
17011713	Sugammadex sodium	343306-79-6	98%
Sugammadex soidum is an agent for reversal of neuromuscular blockade by the agent roc
17011712	Streptozocin	18883-66-4	98%
Streptozocin is a methylnitrosourea antineoplastic antibiotic isolated from the bacte
17011711	Sotagliflozin	1018899-04-1	98%
Sotagliflozin, also known as LX4211, is an orally active and a dual SGLT1/SGLT2 inhib
17011710	Solithromycin	760981-83-7	98%
Solithromycin, also known as CEM-101 and OP-1068, is a ketolide antibiotic undergoing
17011709	SMER28	307538-42-7	98%
SMER28 is a small molecule modulator of autophagy, inducing autophagy independently o
17011707	SKF-38393 hydrochloride	62717-42-4	98%
SKF-38393, aslo known as (+/-)-SKF-38393, is a synthetic compound of the benzazepine