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Cat. No. Product Name Target Signaling Pathways
T70420 PHA 543613 hydrochloride

PHA-543613 hydrochloride acts as a potent and selective agonist for the α7 subtype of neural nicotinic acetylcholine receptors, with a high level of brain penetration and good oral bioavailability. It is under development as a possible treatment for cognitive deficits in schizophrenia.
T71930 aPKC-I

aPKC-I is an inhibitor of atypical protein kinase C (aPKC ) which inhibits both PKCζ and PKCι with high specificity and prevents VEGF-induced endothelial permeability in cell culture and in vivo, thereby blocking ischemia-reperfusion (IR)-induced permeability.
T16671 PS315

PKC Chromatin/Epigenetic; Cytoskeletal Signaling
PS315 inhibits the full-length and catalytic domain constructs of PKCζ (IC50=10 μM) and PKCη (IC50=30 μM). PS315 has anti-cancer activity. PS315 is a derivative of PS48 and is an allosteric PKC inhibitor by binding to the PIF-pocket of aPKC and inducing d
T61604 PKC-IN-4

PKC-IN-4 (compound 7l) is a highly potent and orally active inhibitor of atypical protein kinase C (aPKC), exhibiting an IC 50 value of 0.52 μM. In vitro studies have demonstrated that PKC-IN-4 effectively suppresses NF-κB activity induced by TNF-α. Moreover, this compound effectively impedes the permeability of the retinal vasculature, induced by both VEGF and TNFα. [1]

化合物

PHA 543613 hydrochloride
Cat.No: T70420
Synonym:
Target:
aPKC-I
Cat.No: T71930
Synonym:
Target:
PS315
Cat.No: T16671
Synonym:
Target: PKC
PKC-IN-4
Cat.No: T61604
Synonym:
Target:
TargetMol Loading
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