Search results for: 'purotoxin 1'
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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.
- BA3244 Thalidomide-NH-C2-PEG3-OHSummary: Thalidomide-NH-C2-PEG3-OH is an E3 ligaseligand-linker coupling (E3ligaseligand-linkerconjugate) comprising a Thalidomide-based ligand and 1 linker.
- BA3351 MurizatoclaxSummary: Murizatoclax (AMG397) is a potent, selective and orally active myeloid leukemia 1 inhibitor.
- BA3507 RIPK1-IN-4Summary: RIPK1-IN-4 is a potent inhibitor of type II kinase receptor-interacting protein 1 kinase.
- BA3508 OditrasertibSummary: Oditrasertib is a receptor-interacting protein kinase 1 inhibitor with values below 100 nM.
- BA4807 INCB059872Summary: INCB059872 is a potent, orally active, selective and irreversible inhibitor of lysine-specific demethylase 1.
- BA4891 UpadacitinibSummary: Upadacitinib (ABT-494) is a potent, orally active, selective Janus kinase 1 inhibitor.
- BA5284 AntalarminSummary: Antalarmin is a selective nonpeptide adrenocorticotropic hormone releasing factor receptor 1 antagonist.
- BA5332 TUG-499Summary: TUG-499 is a selective free fatty acid receptor 1 (or) (FreeFattyAcidReceptor) agonist.