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Catalog NoChemical NameCAS NumberPurityChemical Structure
20646TNG9082760481-53-4≧98.0%
TNG908 is a clinical stage MTA-cooperative PRMT5 inhibitor that is selectively active
20645CP-506 ( Synonyms: SN-36506 )2227304-19-898% Min.
CP-506 (SN-36506) is an hypoxia-activated prodrug of a DNA-alkylating nitrogen mustar
20524Zidesamtinib ( NVL-520 )2739829-00-4≧98.0%
Zidesamtinib ( NVL-520 ) is a novel brain-penetrant ROS1-selective tyrosine kinase in
20610Zavondemstat1851412-93-5≧98.0%
Zavondemstat is a KDM4 inhibitor with potential as an antineoplastic agent.
236271TP12872044686-42-0≧97.0%
Alvocidib Prodrug TP-1287 is an orally bioavailable, highly soluble phosphate prodrug
16122736Lirametostat ( CPI-1205 )1621862-70-1≧98.0%
Lirametostat ( CPI-1205 ) is a potent, selective, and cofactor-competitive inhibitor
230402BI 1015550 ( Nerandomilast )1423719-30-5≧98.0%
BI 1015550 ( Nerandomilast )is an oral, preferential inhibitor of phosphodiesterase 4
20455Camlipixant ( BLU-5937 )1621164-74-6≧98.0%
Camlipixant is an investigational, twice-daily oral P2X3 receptor antagonist for the
192142Upacicalcet1333218-50-0≧98.0%
Upacicalcet (formerly SK-1403/AJT240) is a novel non-peptide calcimimetic agent that
20553Tinengotinib ( TT-00420)2230490-29-4≧98.0%
Tinengotinib ( TT-00420) is a novel multiple kinase inhibitor that strongly inhibited
20548Pimicotinib ( ABSK02 )2253123-16-7≧98.0%
Pimicotinib is a novel small molecule inhibitor of CSF-1R, which is orally available,
20656IK-9302563892-44-2≧98.0%
IK-930 is a novel, selective, small molecule inhibitor of TEAD that prevents palmitat