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Products

Catalog NoChemical NameCAS NumberPurityChemical Structure
17101610SAR-7334 HCl1333207-63-8>98%
SAR7334 is a novel, highly potent and bioavailable inhibitor of TRPC6 channels that o
1710168SEN-8261160833-51-1>98%
SEN-826 is a potential anticancer agent.
17101310SRT3025 HCl2070015-26-6>98%
SRT3025 is an orally available small molecule activator of the SIRT1 enzyme.
1710136Senexin A1366002-50-7>98%
Senexin A is a potent and selective CDK8 inhibitor (IC50 = 280 nM). Senexin A binds t
171071S638451799633-27-4>98%
S63845 is a small molecule that specifically binds with high affinity to the BH3-bind
1791511Salermide1105698-15-498.0%
Salermide is a Sirtuin inhibitor with a strong cancer-specific proapoptotic effect. S
1791320SD-06271576-80-898.0%
SD-06 is a MAPK p38 alpha inhibitor for the treatment of arthritis.
179135Sulfatinib1308672-74-398.0%
Sulfatinib is an orally bioavailable, small molecule inhibitor of vascular endothelia
1791111S107 HCl927871-76-998.0%
S107 is a Type 1 ryanodine receptor (RyR1) stabilizer; binds RyR1 and enhances the bi
179830Sematilide hydrochloride101526-62-998.0%
Sematilide, also known as CK-1752, is a class III antiarrhythmic. It is a selective d
179815SNX-2112908112-43-698.0%
SNX-2112, also known as PF 04928473, is an Hsp90 inhibitor which is currently undergo
17984SU-1498168835-82-398.0%
SU 1498 is a selective inhibitor of the receptor tyrosine kinase VEGF receptor 2 (VEG
17918SF25231174428-47-798.0%
SF2523 is a highly selective and potent dual pan-PI3K/BRD4 inhibitor. SF2523 exhibits
1781101SAR-203471450881-55-698.0% 
SAR-20347 is a potent dual inhibitor of JAK1 and tyrosine kinase 2 (TYK2). 
20178811SB756050447410-57-398.0% 
SB-756050 is a G protein-coupled bile acid receptor 1 (GPBAR1) agonist potentially fo
2017882SAR-4051523406-39-498.0% 
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20177313Seco Rapamycin (sodium salt)148554-65-898.0% 
Seco-rapamycin is the first in vivo open-ring metabolite of rapamycin that does not a
174191SU5402215543-92-398% by HNMR/HPLC
SU5402 is a fibroblast growth factor receptor (FGFR)-specific tyrosine kinase inhibit
17031004SAR-0201061184843-57-998% 
SAR-020106 is an ATP-competitive, potent, and selective CHK1 inhibitor with an IC50
17031002SH5-071456632-41-998% 
SH5-07 is a robust hydroxamic acid-based STAT3 inhibitor, which induce antitumor ce
17030603SUN11602704869-38-598% 
SUN11602 is a novel aniline compound, which mimics the neuroprotective mechanisms of
17030306Sardomozide HCl138794-73-798% 
Sardomozide , also known as SAM486A or CGP48664, is a second-generation polyamine syn
17030108Sacubitril sodium149690-05-198% 
Sacubitril, also known as AHU377, is angiotensin receptor neprilysin inhibitor being
17030107SHP099 free base1801747-42-198% 
SHP099 is a potent, selective, orally bioavailable, and efficacious SHP2 inhibitor wi
17022802Semagacestat425386-60-398% 
Semagacestat (LY450139) is a -secretase blocker for A42, A40 and A38 with IC50 of 10.
17021402(S)-Tedizolid1431699-67-098% 
Tedizolid is the active moiety of the prodrug tedizolid phosphate, with high potency
17021319STO-60952029-86-498% 
STO-609 is a specific inhibitor of the Ca2+/Calmodulin-dependent protein kinase kina
17021309S490761265965-22-798% 
S49076 is a novel, potent inhibitor of MET, AXL/MER, and FGFR1/2/3 with IC50 valu
17021306SRT21831001908-89-998% 
SRT2183 is a small-molecule activator of the sirtuin subtype SIRT1, currently being
17011714SW044248522650-83-598% 
SW044248 is a potent and selective Topoisomerase I inhibitor. SW044248 killed approxi