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Products

Catalog NoChemical NameCAS NumberPurityChemical Structure
91001L18964232-83-398% 
L189 inhibits base excision repair (BER) and non-homologous end joining (NHEJ), which
82608Linagliptin668270-12-098% 
Linagliptin is a highly potent, selective DPP-4 inhibitor with IC50 of 1 nM.
81313Lurasidone hydrochloride367514-87-298% 
Lurasidone is an atypical antipsychotic developed by Dainippon Sumitomo Pharma, which
81001LRRK2-IN-11234480-84-297% 
LRRK2-IN-1 is a cell-permeable, ATP competitive, potent, and selective LRRK2 inhibito
71801LY28744551254473-64-798% 
1) Sponsor: Eli Lilly and Company.2) Phase:Phase 12) LY2874455 is potent, selective,
52806LDK3781032900-25-698% 
LDK378(Ceritinib) is potent inhibitor against ALK with IC50 of 0.2 nM, shows 40- and
52733LDN1931891062368-24-498% 
LDN193189(DM 3189) is a selective BMP signaling inhibitor, inhibits the transcription
52707LDN-2141171627503-67-698% 
LDN-214117 is a potent and selective ALK2 inhibitor with IC50 of 22 nM; > 100 fold
52588LDN-2128541432597-26-698% 
LDN-212854 is a potent and selectiveBMP receptorinhibitor with IC50 of 1.3 nM for ALK
52511LB-1001026680-07-898% 
LB-100 is a small-molecular protein phosphatase 2A(PP2A)inhibitor with IC50 of 0.85 M
52509LY-364947396129-53-698% 
LY364947 is a potent ATP-competitive inhibitor of TGFR-I with IC50 of 59 nM, exhibits
51504LH846639052-78-198% 
LH846 is a selective inhibitor of CK1 (IC50 values are 290 nM, 1.3 uM and 2.5 uM for
52309LY294002154447-36-698% 
LY294002 is the first synthetic molecule known to inhibitPI3K//withIC50of 0.5 M/0.57
52206LFM-A13244240-24-298% 
Selective Bruton's tyrosine kinase (BTK) inhibitor (IC50 = 2.5 M). Also inhibits poli
51703Luminespib ( NVP-AUY922 ; VER-52296 )747412-49-398%
NVP-AUY922 is an experimental drug candidate for the treatment of cancer. It was disc