Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
---|---|---|---|---|
193123 | LY-3381916 | 2166616-75-5 | >98% | |
LY-3381916 is a potent, selective and brain penetrated inhibitor of IDO1 activity, bi | ||||
19364 | LR-90 | 245075-84-7 | >98% | |
LR-90 is an advanced glycation end product (AGE) inhibitor, inhibits inflammatory res | ||||
19357 | LCL521 | 1226851-11-1 | >98% | |
LCL521 is an acid ceramidase (ACDase) inhibitor. LCL521 also inhibits the lysosomal a | ||||
1922710 | Larotaxel | 156294-36-9 | >98% | |
Larotaxel is a semi-synthetic derivative of the taxane 10-deacetylbaccatin III with p | ||||
192271 | Leniolisib | 1354690-24-6 | >98% | |
Leniolisib, also known CDZ173, is a potent phosphatidylinositol 3-kinase inhibitor (P | ||||
192261 | Leuprolide Acetate | 74381-53-6 | >98% | |
Leuprolide acetate is the acetate salt of a synthetic nonapeptide analogue of gonadot | ||||
192195 | LOXO-292 | 2222755-14-6 | >98% | |
LOXO-292 (ARRY-192) is an oral and selective investigational drug in clinical develop | ||||
19122 | Lexibulin | 917111-49-0 | >98% | |
Lexibulin, also known as CYT997, is a n orally bioavailable small-molecule with tubul | ||||
1811302 | LP-211 | 1052147-86-0 | >98% | |
LP-211 is a a selective agonist of the serotonin 5-HT7 receptor. | ||||
1811213 | LXH254 free base | 1800398-38-2 | >98% | |
LXH254 is an orally available inhibitor of all members of the serine/threonine protei | ||||
181172 | LY2828360 | 1231220-79-3 | >98% | |
LY2828360 is a novel potent, selective, and efficacious CB2 agonist. | ||||
1810262 | LP-533401 HCl | 1040526-12-2 | >98% | |
LP-533401 HCl is an inhibitor of tryptophan hydroxylase-1 (Tph-1), the initial enzyme | ||||
188101 | LP-922761 | 1454808-95-7 | >98% | |
LP-922761 is a potent and selective AAK1 inhibitor with an in vitro IC50 value of 4.8 | ||||
187165 | LM22B-10 | 342777-54-2 | >98% | |
LM22B-10 is a TrkB and TrkC agonist. LM22B-10 exhibits neurotrophic activity (EC50 = | ||||
186278 | LY-3200882 | 1898283-02-7 | >98% | |
LY-3200882 is an orally active TGFbeta inhibitor. LY3200882 targets transforming grow | ||||
186275 | LX2761 | 1610954-97-6 | >98% | |
LX2761 is a locally acting SGLT1 inhibitor that is highly potent in vitro and delays | ||||
186156 | L685458 | 292632-98-5 | >98% | |
L685458 is a potent and selective γ -secretase inhibitor. | ||||
186151 | Lometrexol disodium | 120408-07-3 | >98% | |
Lometrexol is a folate analog antimetabolite with antineoplastic activity. | ||||
185312 | LB-100 | 1632032-53-1 | >98% | |
LB-100 is a protein phosphatase 2A(PP2A)inhibitor. | ||||
185252 | LY2881835 | 1292290-38-0 | >98% | |
LY2881835 is a potent and selective GPR40 agonist potentially for treatment of type 2 | ||||
185212 | LOXO-195 | 2097002-61-2 | >98% | |
LOXO-195 is a potent and selective TRK inhibitor capable of addressing potential mech | ||||
184177 | Lanifibranor | 927961-18-0 | >98% | |
Lanifibranor, also known as IVA-337, is a peroxisome proliferator-activated receptors | ||||
184131 | LX-2343 | 333745-53-2 | >98% | |
LX-2343 is a neuroprotective agent for the treatment of Alzheimer's disease. | ||||
512194 | Lazertinib | 1903008-80-9 | 98% Min. | |
Description:Lazertinib is a an orally available third-generation, selective inhibi | ||||
18493 | LYN-1604 | 2088939-99-3 | >98% | |
LYN-1604 is a novel activator of ULK1, inducing cell death involved in ATF3, RAD21, a | ||||
18443 | LB42708 | 226929-39-1 | >98% | |
LB42708 is a potent, orally active and selective nonpeptidic farnesyltransferase inhi | ||||
184314 | LLY-283 | 2040291-27-6 | >98% | |
LLY-283 is a potent and selective SAM-competitive chemical probe for PRMT5. | ||||
1711249 | L-778123 | 183499-57-2 | >98% | |
L-778,123 is an inhibitor of FPTase and GGPTase-I. | ||||
17101618 | LW6 | 934593-90-5 | >98% | |
LW6 decreased HIF-1alpha protein expression without affecting HIF-1beta expression. | ||||
1710164 | LF3 | 664969-54-4 | >98% | |
LF3 is a specific inhibitor of the classical Wnt signaling pathway by disrupting the |
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