Search results for: 'hg6 64 1'
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A1185 BMS-754807Target: Insulin and Insulin-like ReceptorsSummary: IGF-1R/InsR inhibitor,potent and selective -
BA3998 GNE-371Summary: GNE-371 is a highly efficient and selective chemical probe targeting the second bromo-terminal structural domain of human transcription initiation factor subunit 1 and transcription initiation factor-like subunit 1. -
P1130 Recombinant Human IL-19Summary: Human Interleukin-19 (IL-19) is encoded by the IL19 gene, which is located on the chromosome 1. - BA2567 PDP-PfpSummary: PDP-Pfp is the active molecule used to target TM4SF1 extracellular loop 1 (ECL1).
- BA7038 SupercinnamaldehydeSummary: Supercinnamaldehyde is a potent activator of transient receptor potential anchor protein 1 (TRPA1).
- BA7067 EpaminuradSummary: Epaminurad (UR-1102) is an orally potent and selective (uric acid transporter 1) inhibitor.
- BA7081 HSD-016Summary: HSD-016 is a potent, selective, orally active type 1 11β-hydroxysteroid dehydrogenase inhibitor.
- BA7101 CMS-121Summary: CMS-121 is a quinolone derivative and an orally active inhibitor of acetyl coenzyme A carboxylase 1.
- BA3169 S2116Summary: S2116, an N-alkylated trans-cyclopropylamine (TCP) derivative, is a potent lysine-specific demethylase 1 inhibitor.
- BA3171 S2157Summary: S2157, an N-alkylated trans-cyclopropylamine (TCP) derivative, is a potent lysine-specific demethylase 1 inhibitor.