WebH-89 dihydrochloride is an inhibitor of PKA and MSK, inhibits cyclic-AMP response element binding protein-mediated MAPK phosphatase-1 induction by lipopolysaccharide. … WebBiological target: H-89 dihydrochloride is a potent and selective inhibitor of protein kinase A (PKA) with an IC50 of 48 nM. In vitro activity: Mouse embryonic fibroblast (MEF), human bronchial epithelial (hBE), human bone osteosarcoma epithelial (U20S), hepatocellular carcinoma (HepG2), human pancreatic carcinoma (MIA PaCa-2), and mouse myoblast …
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WebH89 dihydrochloride, Kinase inhibitor (ab120341) Specific References (5) Description: Kinase inhibitor. NKH 477 (Colforsin daropate), an adenylyl cyclase activator (ab120240) Description: Water-soluble analogue of forskolin (ab120058), an adenylyl cyclase activator. 2-APB, Ca2+ release modulator (ab120124) WebH89 Dihydrochloride is a potent and selective inhibitor of cAMP-dependent protein kinase (PKA). It has also been shown to inhibit CaM kinase II, casein kinase I and MYLK, as …
WebH-89, Dihydrochloride - 2040089. 2040089. Reference overview. Pub Med ID. Characterization of activators and inhibitors of protein kinase C mu. Johannes, F J, et … Webwith the protein kinase A (PKA) antagonist, H89, and the protein kinase C (PKC) antagonist, calphostin C, and fever was induced using lipopolysaccharide (LPS) in order to detect the expression of TRPV1 and phosphorylated (p-)TRPV1, the intracellular Ca 2+ concentration [(Ca) i] of hypothalami and rat body temperature.
WebH-89 Dihydrochloride C20H22BrCl2N3O2S CID 5702541 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological ... WebAKT3+AKT2+cAMP Protein Kinase Catalytic subunit+ROCK2 (1) ... H89 dihydrochloride, Kinase inhibitor (ab120341) Specific References (6) Description: Kinase inhibitor. A-3 hydrochloride, PKA, PKG, Casein Kinase I and II inhibitor (ab143761) Description: Inhibits cAMP and cGMP dependent protein kinases. Also inhibits MLC kinase, casein kinase I ...
WebNov 15, 2024 · In this experiment, after injection of LPS, the expressions of TRPV1, p-TRPV1 and (Ca 2+) i in the PO/AH area increased and the temperature rose; and after a meantime injection of the PKA inhibitor H89 (1 or 1.5 µg/site) or the PKC inhibitor calphostin C (200 ng/site), the expressions of p-TRPV1 in the PO/AH area were …
WebOct 8, 2016 · H-89 is a potent and selective inhibitor of cyclic AMP-dependent protein kinase (protein kinase A) with IC50 of 48 nM and has weak inhibition on PKG, PKC, … batik kembangWebH 89 dihydrochloride is a protein kinase A inhibitor that also inhibits several other kinases (IC 50 values are 80, 120, 135, 270, 2600 and 2800 nM for S6K1, MSK1, PKA, ROCKII, … batik kemasan pngWebH-89 is a protein kinase inhibitor with greatest effect on protein kinase A (PKA). [2] H-89, derived from H-8 (N- [2- (methylamino)ethyl]-5-isoquinoline-sulfonamide), [3] was initially believed to act specifically as an inhibitor of PKA, [4] being 30 times more potent than H … te mračne noći film online s prijevodomWebH-89 Dihydrochloride C20H22BrCl2N3O2S CID 5702541 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, … batik kembang bayemWebIn the present study, using an in vivo experimental method, rat brain ventricles were injected with the protein kinase A (PKA) antagonist, H89, and the protein kinase C (PKC) antagonist, calphostin C, and fever was induced using lipopolysaccharide (LPS) in order to detect the expression of TRPV1 and phosphorylated (p‑)TRPV1, the intracellular ... batik kembang semanggiWebFeb 7, 2024 · Purpose: This study aimed to explore the role of the protein kinase A (PKA) pathway in proliferative vitreoretinopathy (PVR) and the effect of the PKA inhibitor H89 … temraza maskWebA cell-permeable, selective, reversible, ATP-competitive and potent inhibitor of protein kinase A (K i = 48 nM). View Price and Availability. Sigma-Aldrich. B1427. H-89 … batik kembang kenanga