Name Index L

LHW090-A7 (Catalog# : 91810, Cas# : 1308256-94-1)Coming soon!
L189 (Catalog# : 91001, Cas# : 64232-83-3)L189 inhibits base excision repair (BER) and non-homologous end joining (NHEJ), which
Linagliptin (Catalog# : 82608, Cas# : 668270-12-0)Linagliptin is a highly potent, selective DPP-4 inhibitor with IC50 of 1 nM.
Lurasidone hydrochloride (Catalog# : 81313, Cas# : 367514-87-2)Lurasidone is an atypical antipsychotic developed by Dainippon Sumitomo Pharma, which
LRRK2-IN-1 (Catalog# : 81001, Cas# : 1234480-84-2)LRRK2-IN-1 is a cell-permeable, ATP competitive, potent, and selective LRRK2 inhibito
LY2874455 (Catalog# : 71801, Cas# : 1254473-64-7)1) Sponsor: Eli Lilly and Company.2) Phase:Phase 12) LY2874455 is potent, selective,
LDK378 (Catalog# : 52806, Cas# : 1032900-25-6)LDK378(Ceritinib) is potent inhibitor against ALK with IC50 of 0.2 nM, shows 40- and
LDN193189 (Catalog# : 52733, Cas# : 1062368-24-4)LDN193189(DM 3189) is a selective BMP signaling inhibitor, inhibits the transcription
LDN-214117 (Catalog# : 52707, Cas# : 1627503-67-6)LDN-214117 is a potent and selective ALK2 inhibitor with IC50 of 22 nM; > 100 fold
LDN-212854 (Catalog# : 52588, Cas# : 1432597-26-6)LDN-212854 is a potent and selectiveBMP receptorinhibitor with IC50 of 1.3 nM for ALK
LB-100 (Catalog# : 52511, Cas# : 1026680-07-8)LB-100 is a small-molecular protein phosphatase 2A(PP2A)inhibitor with IC50 of 0.85 M
LY-364947 (Catalog# : 52509, Cas# : 396129-53-6)LY364947 is a potent ATP-competitive inhibitor of TGFR-I with IC50 of 59 nM, exhibits
LH846 (Catalog# : 51504, Cas# : 639052-78-1)LH846 is a selective inhibitor of CK1 (IC50 values are 290 nM, 1.3 uM and 2.5 uM for
LY294002 (Catalog# : 52309, Cas# : 154447-36-6)LY294002 is the first synthetic molecule known to inhibitPI3K//withIC50of 0.5 M/0.57
LFM-A13 (Catalog# : 52206, Cas# : 244240-24-2)Selective Bruton's tyrosine kinase (BTK) inhibitor (IC50 = 2.5 M). Also inhibits poli
Luminespib ( NVP-AUY922 ; VER-52296 ) (Catalog# : 51703, Cas# : 747412-49-3)NVP-AUY922 is an experimental drug candidate for the treatment of cancer. It was disc

MGD-28 (Catalog# : 25073, Cas# : 2991818-13-2)MGD-28 is a potent molecular glue degrader that demonstrates significant in vitro eff
TG101209 analog 1 (Catalog# : 25072)TG101209 analog 1 (Compound 8h) is an inhibitor of BUB1B with an IC50 of 10.36 μ M.
AT-007 (Catalog# : 25071, Cas# : 2170729-29-8)AT-007 is an orally active central nervous system (CNS) penetrant Aldose Reductase in
TAK-653 (Catalog# : 25070, Cas# : 1358751-06-0)TAK-653 is a novel AMPA receptor potentiator, strictly potentiating a glutamate-induc
Emavusertib (Catalog# : 25069, Cas# : 1801344-14-8)Emavusertib, also known as CA-4948 is a potent IRAK4/FLT3 inhibitor with anti-tumor a
Roginolisib (Catalog# : 25068, Cas# : 1305267-37-1)Roginolisib, also known as MSC2360844 and IOA-244, is a potent, orally active and sel
NT219 (Catalog# : 25067, Cas# : 1198078-60-2)NT219 is a novel inhibitor of the insulin/igf signaling cascade (iis), mediating a lo
SPB linker (Catalog# : 25066, Cas# : 858128-57-1)SPB is a agent-linker conjugate for ADC with potent anti-inflammatory activity by usi
JTE-151 (Catalog# : 20594, Cas# : 1404380-58-0)JTE-151 is a novel RORγ inverse agonist.
Ecopipam ( SCH 39166 ) (Catalog# : 25065, Cas# : 112108-01-7)Ecopipam ( SCH 39166 ) is a Selective Dopamine Receptor D1/D5 Antagonist used in the

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