ligands acting on targets

Application：(S)-ZINC-3573 has been used to investigate the biology of the primate-exclusive MRGPRX2 G protein-coupled receptor (GPCR).

Application：(S)-ZINC-3573 has been used to investigate the biology of the primate-exclusive MRGPRX2 G protein-coupled receptor (GPCR).

Application：(S)-ZINC-3573 has been used to investigate the biology of the primate-exclusive MRGPRX2 G protein-coupled receptor (GPCR).

Application：(S)-ZINC-3573 has been used to investigate the biology of the primate-exclusive MRGPRX2 G protein-coupled receptor (GPCR).

(S)-α-methylhistamine.

(S)-α-methylhistamine.

(S,R)-WT IDH1 Inhibitor 2 (GSK321) is a potent, selective mutant IDH1 inhibitor with IC 50 values of 2.9, 3.8, 4.6 and 46 nM for R132G, R132C, R132H and WT IDH1 , respectively, and &gt:100-fold selectivity over IDH2. (S,R)-WT IDH1 Inhibitor 2

(S,R)-WT IDH1 Inhibitor 2 (GSK321) is a potent, selective mutant IDH1 inhibitor with IC 50 values of 2.9, 3.8, 4.6 and 46 nM for R132G, R132C, R132H and WT IDH1 , respectively, and &gt:100-fold selectivity over IDH2. (S,R)-WT IDH1 Inhibitor 2

Information(S,R,S)-AHPC (MDK7526, VH032-NH2, VHL ligand 1) is the VH032-based VHL ligand used in the recruitment of the von Hippel-Lindau (VHL) protein. (S,R,S)-AHPC is potential useful for the targeted degradation of the androgen receptor .

Information(S,R,S)-AHPC (MDK7526, VH032-NH2, VHL ligand 1) is the VH032-based VHL ligand used in the recruitment of the von Hippel-Lindau (VHL) protein. (S,R,S)-AHPC is potential useful for the targeted degradation of the androgen receptor .

Information(S,R,S)-AHPC (MDK7526, VH032-NH2, VHL ligand 1) is the VH032-based VHL ligand used in the recruitment of the von Hippel-Lindau (VHL) protein. (S,R,S)-AHPC is potential useful for the targeted degradation of the androgen receptor .

Information(S,R,S)-AHPC (MDK7526, VH032-NH2, VHL ligand 1) is the VH032-based VHL ligand used in the recruitment of the von Hippel-Lindau (VHL) protein. (S,R,S)-AHPC is potential useful for the targeted degradation of the androgen receptor .