Search results for: 'hg6 64 1'
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BA2262 LP-935509Summary: LP-935509 is an orally potent, selective, ATP-competitive, and blood-brain barrier-crossing inhibitor of junctional protein-2-related kinase 1. - BA2791 DC661Summary: DC661 is a potent inhibitor of palmitoyl protein thioesterase 1, inhibits autophagy, and acts as an anti-lysosomal agent.
- BA6784 BAY-8002Summary: BAY-8002 is a potent, selective, orally available inhibitor of monocarboxylic acid transporter protein subtype 1.
- BA3112 M47Summary: M47 is a small molecule that selectively destabilizes cryptorchidin 1 (CRY1) and increases the degradation of CRY1 in the nucleus.
- BA3504 PK68Summary: PK68 is a potent and specific type II inhibitor of receptor-interacting kinase 1 (RIPK1) with oral activity.
- BA4978 GivosiranSummary: Givosiran (ALN-AS1) is a small interfering RNA that targets hepatic aminocellulose synthase 1 messenger RNA.
- BA5221 OMDM-6Summary: OMDM-6 is a mixed agonist of the receptor (=75 nM) and cannabinoid type 1 receptor (=3.2 μM).
- BA5446 GemilukastSummary: Gemilukast is an orally active, potent dual inhibitor of cysteinyl leukotriene 1 and 2 receptors (and).
- BA5467 ASP-4058Summary: ASP-4058 is a selective, orally active, second generation agonist of sphingosine phosphate receptors 1 and 5.
- BA7821 PHD-1-IN-1Summary: PHD-1-IN-1 is an orally active, potent structural domain 1 inhibitor of the hypoxia-inducible factor prolyl hydroxylase.