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.
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Menge
sc-221150
n.n.
C16H14ClN5O7PS ·(CH3CH2)3NH
25 µmol
(D) DT-2 A potent, cell permeable and highly selective polypeptide inhibitor of cGMP dependent protein kinase 1α.
H-8 • 2HCL A cAMP-dependent, cGMP-dependent, and Ca2+-phospholipid-dependent protein kinase inhibitor that potently blocks signaling pathways.
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Menge
sc-200526
84478-11-5
C12H15N3O2S ·2HCl
10 mg/50 mg
HA-1004 A potent inhibitor of cyclic AMP-dependent protein kinase and cyclic GMP-dependent protein kinase.
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Summenformel
Menge
sc-200537
91742-10-8
C12H15N5O2S ·2HCl
10 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.
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Menge
sc-200583
103745-39-7
C14H17N3O2S•2HCl
10 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.
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Menge
sc-3534
126643-37-6
C29H25N3O5
100 µg
PKG Inhibitor A specific cyclic GMP-dependent protein kinase inhibitor reported to block NMDA potentiation and GABA nitric oxide depression.
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sc-201161
82801-73-8
C38H74N18O10
1 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.
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Menge
sc-203989
172806-20-1
C18H14BrN5O6PS•Na
1 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.
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sc-202030
153660-04-9
C16H14ClN5O6PS2 ·Na
100 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.