武汉永璨生物科技有限公司
+86-17702719238 sales@sun-shinechem.com

产品目录

编号化学名称Cas号纯度化学结构
011901SDZ 220-581174575-17-898% 
SDZ 220-581 is a potent, competitive antagonist at the NMDA glutamate receptor subtyp
011815SB-649868380899-24-198% 
Coming soon!
011806SGI-110929901-49-598% 
SGI-110 is a small molecule, DNMT inhibitor with demonstrated activity in restoring s
011313SC144895158-95-998% 
SC144 is the first-in-class orally active small-molecule gp130 inhibitor.
011308SKF-8600272873-74-698% 
SKF-86002 is a potent inhibitor of p38 MAP kinase wit IC50 of 0.5-1 uM.
011304SD-208627536-09-898% 
SD-208 is a potent, orally active ATP-competitive transforming growth factor- recepto
11106SCH772984942183-80-498% 
SCH772984 is a novel, specific inhibitor of ERK1/2 with IC50 of 4 nM and 1 nM, respec
010805Savolitinib(Volitinib)1313725-88-098% 
Savolitinib is an orally bioavailable inhibitor of the c-Met receptor tyrosine kinase
010804SF1126936487-67-198% 
SF1126 is a water soluble, small-molecule prodrug containing the pan-PI3K/mTOR inhibi
010601Staurosporine62996-74-198% 
Staurosporine is a prototypical potent ATP-competitive kinase inhibitor with IC50 of
010438SCH900776 S-isomer891494-64-798% 
SCH900776 (S-isomer) is the S-isomer form of SCH900776(HY-15532), which is a potent,
010427SB 242084181632-25-798% 
SB 242084 is a 5-HT2C receptor antagonist(pKi=9.0) that displays 158- and 100-fold se
010425SB 415286264218-23-798% 
SB 415286 is a potent and selective cell-permeable, ATP-competitive inhibitor of GSK3
122945SGI-17761025065-69-398% 
SGI-1776 is a novel ATP competitive inhibitor of Pim1 with IC50 of 7 nM; 50- and 10-f
122944Sonolisib502632-66-898% 
Sonolisib is a small-molecule wortmannin analogue inhibitor of the alpha, gamma, and
122922Soraphen A122547-72-298% 
Coming soon!
122921Sembragiline676479-06-498% 
Coming soon!
122913Saracatinib379231-04-698% 
Saracatinib is an orally available 5-, 7-substituted anilinoquinazoline with anti-inv
122912SU11274658084-23-298% 
SU11274 is a selective Met inhibitor with IC50 of 10 nM, no effects on PGDFR, EGFR or
122831STF31724741-75-798% 
STF31 is a potent glucose transporter 1 (GLUT1).
122802SM-164957135-43-298% 
SM-164 is a potent cell-permeable and bivalent Smac mimetic which bind to a XIAP prot
122518SB-742457 ( Intepirdine )607742-69-898% 
SB-742457(Intepirdine) is a highly selective 5-HT6 receptor antagonist with pKi of 9.
122516SNG-115398% 
Coming soon!
122504SGC09461561178-17-398% 
SGC0946 is a highly potent and selective DOT1L methyltransferase inhibitor with IC50
122503(S)-2-Ethylpiperazine dihydrochloride128427-05-498% 
Coming soon!
122502SB-505124694433-59-598% 
SB-505124 is a selective inhibitor of TGFR for ALK4, ALK5 with IC50 of 129 nM and 47
122304SP-4201221411-72-898% 
SP-420 is an orally active small molecule that selectively binds iron and removes it
120804(3S)-3-aminooxolan-2-one,hydrochloride2185-03-798% 
Coming soon!
111304Salinosporamide A437742-34-298% 
Salinosporamide A is a novel marine derived proteasome inhibitor which inhibits CT-L,
178906Sitravatinib (MGCD516)1123837-84-298% by HPLC/HNMR
Sitravatinib, also known as MGCD516 or MG516, is a novel small molecule inhibitor tar