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Products

Catalog NoChemical NameCAS NumberPurityChemical Structure
193123LY-33819162166616-75-5>98%
LY-3381916 is a potent, selective and brain penetrated inhibitor of IDO1 activity, bi
19364LR-90 245075-84-7>98%
LR-90 is an advanced glycation end product (AGE) inhibitor, inhibits inflammatory res
19357LCL5211226851-11-1>98%
LCL521 is an acid ceramidase (ACDase) inhibitor. LCL521 also inhibits the lysosomal a
1922710Larotaxel156294-36-9>98%
Larotaxel is a semi-synthetic derivative of the taxane 10-deacetylbaccatin III with p
192271Leniolisib1354690-24-6>98%
Leniolisib, also known CDZ173, is a potent phosphatidylinositol 3-kinase inhibitor (P
192261Leuprolide Acetate74381-53-6>98%
Leuprolide acetate is the acetate salt of a synthetic nonapeptide analogue of gonadot
192195LOXO-2922222755-14-6>98%
LOXO-292 (ARRY-192) is an oral and selective investigational drug in clinical develop
19122Lexibulin917111-49-0>98%
Lexibulin, also known as CYT997, is a n orally bioavailable small-molecule with tubul
1811302LP-2111052147-86-0>98%
LP-211 is a a selective agonist of the serotonin 5-HT7 receptor.
1811213LXH254 free base1800398-38-2>98%
LXH254 is an orally available inhibitor of all members of the serine/threonine protei
181172LY28283601231220-79-3>98%
LY2828360 is a novel potent, selective, and efficacious CB2 agonist.
1810262LP-533401 HCl1040526-12-2>98%
LP-533401 HCl is an inhibitor of tryptophan hydroxylase-1 (Tph-1), the initial enzyme
188101LP-9227611454808-95-7>98%
LP-922761 is a potent and selective AAK1 inhibitor with an in vitro IC50 value of 4.8
187165LM22B-10342777-54-2>98%
LM22B-10 is a TrkB and TrkC agonist. LM22B-10 exhibits neurotrophic activity (EC50 =
186278LY-32008821898283-02-7>98%
LY-3200882 is an orally active TGFbeta inhibitor. LY3200882 targets transforming grow
186275LX27611610954-97-6>98%
LX2761 is a locally acting SGLT1 inhibitor that is highly potent in vitro and delays
186156L685458292632-98-5>98%
L685458 is a potent and selective γ -secretase inhibitor.
186151Lometrexol disodium 120408-07-3>98%
Lometrexol is a folate analog antimetabolite with antineoplastic activity.
185312LB-1001632032-53-1>98%
LB-100 is a protein phosphatase 2A(PP2A)inhibitor.
185252LY28818351292290-38-0>98%
LY2881835 is a potent and selective GPR40 agonist potentially for treatment of type 2
185212LOXO-1952097002-61-2>98%
LOXO-195 is a potent and selective TRK inhibitor capable of addressing potential mech
184177Lanifibranor927961-18-0>98%
Lanifibranor, also known as IVA-337, is a peroxisome proliferator-activated receptors
184131LX-2343 333745-53-2>98%
LX-2343 is a neuroprotective agent for the treatment of Alzheimer's disease.
512194Lazertinib1903008-80-998% Min.
Description:Lazertinib is a an orally available third-generation, selective inhibi
18493LYN-16042088939-99-3>98%
LYN-1604 is a novel activator of ULK1, inducing cell death involved in ATF3, RAD21, a
18443LB42708226929-39-1>98%
LB42708 is a potent, orally active and selective nonpeptidic farnesyltransferase inhi
184314LLY-2832040291-27-6>98%
LLY-283 is a potent and selective SAM-competitive chemical probe for PRMT5.
1711249L-778123183499-57-2>98%
L-778,123 is an inhibitor of FPTase and GGPTase-I.
17101618LW6934593-90-5>98%
LW6 decreased HIF-1alpha protein expression without affecting HIF-1beta expression.
1710164LF3664969-54-4>98%
LF3 is a specific inhibitor of the classical Wnt signaling pathway by disrupting the