Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
---|---|---|---|---|
010802 | LX7101 | 1192189-69-7 | 98% | |
LX7101 is a potent inhibitor of LIMK1/2, ROCK2 and PKA, with IC50 of 24/1.6, 10, and | ||||
010435 | Loratadine | 79794-75-5 | 98% | |
Loratadine is a selective inverse peripheral histamine H1-receptor agonist with an IC | ||||
122909 | LY2584702 free base | 1082949-67-4 | 98% | |
LY2584702 is an orally available inhibitor of p70S6K signaling; inhibits p70S6K and p | ||||
122907 | LY2584702 tosylate | 1082949-68-5 | 98% | |
LY-2584702 tosylate salt is an orally available inhibitor of p70S6K signaling; inhibi | ||||
122835 | L-779450 | 303727-31-3 | 98% | |
L-779450 is a potent, selective and ATP-competitive Raf kinase inhibitor (IC50 = 10 n | ||||
122830 | LDN193189 Hydrochloride | 1062368-62-0 | 98% | |
LDN193189 Hydrochloride is a selective BMP signaling inhibitor, inhibits the transcri | ||||
122820 | LCL161 | 1005342-46-0 | 98% | |
LCL161 is an orally bioavailable SMAC mimetic and inhibitor of Inhibitor of Apoptosis | ||||
122803 | Lexibulin | 917111-44-5 | 98% | |
Lexibulin is an orally bioavailable small-molecule with tubulin-inhibiting, vascular- | ||||
122509 | LY2228820 | 862507-23-1 | 98% | |
LY2228820 is a novel and potent p38MAPK inhibitor (the IC50 for p38MAPK and p38MAPK w | ||||
122218 | LY2608204 | 1234703-40-2 | 98% | |
LY2608204 is a activator of glucokinase (GK) with EC50 of 42 nM. | ||||
121805 | L-778123 hydrochloride | 253863-00-2 | 98% | |
L-778123 hydrochloride is an inhibitor of FPTase and GGPTase-I with IC50 of 2 nM and | ||||
121506 | Laquinimod | 248281-84-7 | 98% | |
Laquinimod is an experimental immunomodulator developed by Active Biotech and Teva. | ||||
121435 | LY2811376 | 1194044-20-6 | 98% | |
LY2811376 is a BACE1 inhibitor with marked Ab-lowering effects in animal models. | ||||
121427 | LY2886721 | 1262036-50-9 | 98% | |
LY2886721 is an BACE inhibitor used for the treatment of Alzheimer's Disease. | ||||
121416 | Linifanib | 796967-16-3 | 98% | |
Linifanib is a novel, potent ATP-competitive VEGFR/PDGFR inhibitor for KDR, CSF-1R, F | ||||
5121102 | LY2090314 | 603288-22-8 | 98% by HPLC | |
LY2090314 (LY) is a glycogen synthase kinase 3 inhibitor with preclinical efficacy in | ||||
120422 | LMK 235 | 1418033-25-6 | 98% | |
LMK 235 is a selective histone deacetylase (HDAC) 4 and HDAC5 inhibitor, which demons | ||||
110606 | LDN-57444 | 668467-91-2 | 98% | |
LDN-57444 is a Uch-L1 inhibitor with Ki= 0.4 M. Ubiquitin carboxy-terminal hydrolase | ||||
110603 | Leuprolide | 53714-56-0 | 98% | |
Leuprolide is an agonist at pituitary GnRH receptors. | ||||
101914 | LY2409881 trihydrochloride | 946518-60-1 | 98% | |
LY2409881 trihydrochloride is a novel selective inhibitor of IKK2 with IC50 of 30 nM; | ||||
91810 | LHW090-A7 | 1308256-94-1 | 98% | |
Coming soon! | ||||
91001 | L189 | 64232-83-3 | 98% | |
L189 inhibits base excision repair (BER) and non-homologous end joining (NHEJ), which | ||||
82608 | Linagliptin | 668270-12-0 | 98% | |
Linagliptin is a highly potent, selective DPP-4 inhibitor with IC50 of 1 nM. | ||||
81313 | Lurasidone hydrochloride | 367514-87-2 | 98% | |
Lurasidone is an atypical antipsychotic developed by Dainippon Sumitomo Pharma, which | ||||
81001 | LRRK2-IN-1 | 1234480-84-2 | 97% | |
LRRK2-IN-1 is a cell-permeable, ATP competitive, potent, and selective LRRK2 inhibito | ||||
71801 | LY2874455 | 1254473-64-7 | 98% | |
1) Sponsor: Eli Lilly and Company.2) Phase:Phase 12) LY2874455 is potent, selective, | ||||
52806 | LDK378 | 1032900-25-6 | 98% | |
LDK378(Ceritinib) is potent inhibitor against ALK with IC50 of 0.2 nM, shows 40- and | ||||
52733 | LDN193189 | 1062368-24-4 | 98% | |
LDN193189(DM 3189) is a selective BMP signaling inhibitor, inhibits the transcription | ||||
52721 | Lorcaserin Hydrochloride | 846589-98-8 | 98% | |
Lorcaserin HCl(APD-356 Hcl) is a selective full agonist of human 5-HT2C receptor with | ||||
52707 | LDN-214117 | 1627503-67-6 | 98% | |
LDN-214117 is a potent and selective ALK2 inhibitor with IC50 of 22 nM; > 100 fold |
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