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Catalog NoChemical NameCAS NumberPurityChemical Structure
122203Dalcetrapib211513-37-098% 
Dalcetrapib is a rhCETP inhibitor with IC50 of 0.2 M that increases the plasma HDL ch
2062004((1R,2S)-2-(3-fluorophenyl)-2-(hydroxymethyl)cyclopropyl)methyl acetate1369768-29-5≧95.0%
2073106Lerociclib HCl (G1T38 HCl)2097938-59-3≧98.0%
Lerociclib HCl (G1T38)is a novel, selective,differentiated oral CDK4/6 inhibitor with
2071535Danicopan1903768-17-1≧98.0%
Danicopan, aslo known as ACH-4471 and ACH-0144471, is a highly potent, orally active
122518SB-742457 ( Intepirdine )607742-69-898% 
SB-742457(Intepirdine) is a highly selective 5-HT6 receptor antagonist with pKi of 9.
26188Firibastat ( QGC-001 )648927-86-0≧98.0%
Firibastat, (originally named QGC001) is the first drug candidate of a new class of c
20103001ASN0072055597-12-9≧98.0%
ASN007 , a novel oral ERK inhibitor , has shown anti-tumor activity in both solid tum
2105071AP1189 acetate959850-74-9≧98.0%
AP1189 is a melanocortin receptor agonist on MC1 and MC3 receptors.
2091501AB-6802105904-82-198% Min.
AB-680 is highly potent, reversible and selective CD73 inhibitor. AB680 to be a rever
185235Trilaciclib (G1T28)1374743-00-6>98%
TRILACICLIB (G1T28), A HIGHLY POTENT, TRANSIENT CDK 4/6 INHIBITOR WITHIC50s OF 1 nM A
52023DCC-2036(Rebastinib)1020172-07-998%
Rebastinib(DCC-2036;DCC2036) is an inhibitor of tyrosine kinases TIE2 and ABL1.Rebast
20103003ML3801627138-52-6≧98.0%
ML380 is a highly potent and the first CNS penetrant M5 positive allosteric modulator