About 4 results found for searched term "AR antagonist 1 hydrochloride" (0.279 seconds)
Cat.No. | Name | Target |
---|---|---|
M43417 | AR antagonist 1 hydrochloride | Ligand for E3 Ligase |
AR antagonist 1 hydrochloride is a potent androgen receptor (AR) antagonist and binds to E3 ligase ligands with weak binding affinities to VHL protein in the synthesis of PROTAC ARD-266. | ||
M7590 | A3 hydrochloride | PKA |
A-3 hydrochloride | ||
A-3 Hydrochloride is A potent, cellular permeable, reversible, atP-competitive, non-selective antagonist targeting multiple kinases. A-3 Hydrochloride is an inhibitor of PKA (Ki=4.3 µM), casein kinase II (Ki=5.1 µM), and myosin light chain kinase (MLCK) (Ki=7.4 µM). A-3 hydrochloride also inhibited PKC and casein kinase I activity with Ki of 47 µM and 80 µM, respectively. | ||
M25555 | BIIE-0246 hydrochloride | Neuropeptide Receptor |
AR-H 053591 hydrochloride | ||
BIIE-0246 hydrochloride (AR-H 053591 hydrochloride) is a potent and selective NPY2R (neuropeptide Y receptor 2) antagonist with an IC50 value of 15 nM for rat [125I]PYY3-36. BIIE-0246 hydrochloride decreases the expression of p-AKT S473, P-p44/42 MAPK under the NPY-stimulated. BIIE-0246 hydrochloride reduces albuminuria in ADR nephropathy. | ||
M59054 | ENMD-1068 hydrochloride | PAR |
ENMD1068 HCl | ||
ENMD-1068 hydrochloride is a selective protease-activated receptor 2 (PAR2) antagonist. ENMD-1068 hydrochloride reduces hepatic stellate cell activation and collagen expression by inhibiting TGF-β1/Smad signaling. |
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