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PKG Activators and Inhibitors

  • 8-(4-Chlorophenylthio)guanosine 3',5'-cyclic Monophosphate sodium salt
    Katalog #CAS NummerSummenformelMenge
    sc-20202951239-26-0C16H14ClN5O7PS ·Na1 mg/5 mg
  • 8-(4-Chlorophenylthio)guanosine 3',5'-cyclic Monophosphate triethylammonium salt
    Selective activator of cGMP-dependent protein kinase Iα, Iβ and type II as well as of cGMP-gated ion channels.
    Katalog #CAS NummerSummenformelMenge
    sc-20243254364-02-2C16H14ClN5O7PS ·C6H15N1 mg/5 mg
  • 8-pCPT-cGMP, TEA
    Selective membrane-permeable activator of protein kinase G that has a higher activation potential than cGMP. Does not significantly affect cGMP-regulated phosphodiesterases. Inhibits the thrombin-induced phosphorylation of human platelets mediated by myosin light chain kinase (MLCK) and protein kinase C (PKC). Note: 25 µmol = 14.73 mg.
    Katalog #CAS NummerSummenformelMenge
    sc-221150n.n.C16H14ClN5O7PS ·(CH3CH2)3NH25 µmol
  • (D) DT-2
    A potent, cell permeable and highly selective polypeptide inhibitor of cGMP dependent protein kinase 1α.
    Katalog #CAS NummerSummenformelMenge
    sc-361974n.n.C122H223N53O23 ·(free ·peptide)500 µg
  • Guanosine 3′,5′-cyclic Monophosphate, b-Phenyl-1,N2-etheno-8-bromo-, Sodium Salt
    A potent cell-permeable activator of protein kinase G type 1a and 1b. Reported to be one of the best known activators of PKG isozyme 1b. Also acts as an excellent muscle relaxant.
    Katalog #CAS NummerSummenformelMenge
    sc-203434144510-04-3C18H14BrN5O7P ·Na10 µmol
  • Guanosine-3',5'-cyclic Monophosphothioate, Sp-Isomer sodium salt
    Metabolically resistant activator of cGMP-dependent protein kinases (PKGs). Low membrane permeability.
    Katalog #CAS NummerSummenformelMenge
    sc-20306586562-10-9 (non-salt)C10H11N5O6SP ·Na500 µg/1 mg
  • H-8 • 2HCL
    A cAMP-dependent, cGMP-dependent, and Ca2+-phospholipid-dependent protein kinase inhibitor that potently blocks signaling pathways.
    Katalog #CAS NummerSummenformelMenge
    sc-20052684478-11-5C12H15N3O2S ·2HCl10 mg/50 mg
  • HA-1004
    A potent inhibitor of cyclic AMP-dependent protein kinase and cyclic GMP-dependent protein kinase.
    Katalog #CAS NummerSummenformelMenge
    sc-20053791742-10-8C12H15N5O2S ·2HCl10 mg/50 mg
  • HA-1077 dihydrochloride
    Shown to be an antiproliferative agent via inhibition of Rho kinase signaling pathways. Also has been reported to be a vasodilator by inhibition of Ca2+ channels.
    Katalog #CAS NummerSummenformelMenge
    sc-200583103745-39-7C14H17N3O2S•2HCl10 mg/50 mg
  • KT5823
    A derivative of K-252a, a selective inhibitor of PKG, and has been shown to dose dependently inhibits spontaneous apoptosis of neutrophils.
    Katalog #CAS NummerSummenformelMenge
    sc-3534126643-37-6C29H25N3O5100 µg
  • PKG Inhibitor
    A specific cyclic GMP-dependent protein kinase inhibitor reported to block NMDA potentiation and GABA nitric oxide depression.
    Katalog #CAS NummerSummenformelMenge
    sc-20116182801-73-8C38H74N18O101 mg
  • Rp-8-Br-PET-cyclic GMPS, Sodium Salt
    A metabolically-stable, competitive inhibitor of protein kinase G types 1a and 1b (Ki = 30 nM). Blocks cGMP-gated retinal type ion channels (IC50 = 25 µM) and the activation of purified PKA type II (Ki = 10 µM). More lipophilic and cell-permeable than Rp-8-pCPT-cGMPS . Note: 1 µmol = 0.56 mg.
    Katalog #CAS NummerSummenformelMenge
    sc-203989172806-20-1C18H14BrN5O6PS•Na1 µmol
  • Rp-8-pCPT-cyclic GMPS Sodium
    Potent selective inhibitor of cGK (also known as PKG) 1α, 1β and type II. Resistant to mammalian cyclic nucleotide-dependent phosphodiesterases. No metabolic side effects.
    Katalog #CAS NummerSummenformelMenge
    sc-202030153660-04-9C16H14ClN5O6PS2 ·Na100 µg/1 mg
  • Sp-8-pCPT-cyclic GMPS Sodium
    Potent activator of both cGMP-dependent protein kinase 1α, 1β and type II and cAMP-dependent protein kinase II. Excellent cell membrane permeability and phosphodiesterase stability.
    Katalog #CAS NummerSummenformelMenge
    sc-202433160385-87-5C16H14N5ClO6S2P ·Na1 mg