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Catalog NoChemical NameCAS NumberPurityChemical Structure
112191Aprocitentan1103522-45-798% Min.
Aprocitentan is an orally active, dual endothelin (ET) receptor antagonist developed
6121401Vadadustat ( AKB-6548 )1000025-07-998% 
Vadadustat (AKB-6548), a novel, titratable, oral hypoxia-inducible factor prolyl hydr
1662118MK-8931 ( Verubecestat )1286770-55-598% by HPLC/HNMR 
Verubecestat(MK-8931) is a small-molecule inhibitor of beta-secretase cleaving enzyme
6112701JPH203 ( KYT-0353 )1037592-40-7≧98.0%
JPH203(also known as KYT-0353) is a potent and selective LAT1 selective ( L-type amin
615201CLEFMA1246964-32-898% Min.
CLEFMA has anti-proliferative activity in H441 cells. CLEFMA may induce autophagic ce
174192RG7800 ( RO6885247 )1449598-06-4≧98.0%
RG7800(RO6885247) is a small molecule modifier of survival motor neuron 2 splicing.
111013MGCD-265-analog875337-44-3≧98.0%
MGCD-265-analog is a tyrosine kinase inhibitor that selectively targets MET and Axl.M
121805L-778123 hydrochloride253863-00-298%
L-778123 hydrochloride is an inhibitor of FPTase and GGPTase-I with IC50 of 2 nM and
51703Luminespib ( NVP-AUY922 ; VER-52296 )747412-49-398%
NVP-AUY922 is an experimental drug candidate for the treatment of cancer. It was disc
122805Balipodect ( TAK-063 )1238697-26-198% 
Balipodect (TAK 063 ) is a novel PDE10A inhibitor. It has shown high inhibitory activ
51608SSR128129E848318-25-298% 
SSR128129E is an orally-active and allostericFGFR1inhibitor withIC50of 1.9 M, while n
71161SBI02069651884220-36-398% 
SBI0206965 is a potent and selective autophagy Kinase ULK1 Inhibitor. Many tumors bec