9 results for "Protein Kinase A Inhibitors" in Products

Protein Kinase A Inhibitors

The cAMP-dependent protein kinase (PKA) holoenzyme is composed of two regulatory and two catalytic subunits, designated PKA R and PKA C, respectively. Upon PKA R subunit binding to the second messenger cAMP, active PKA C subunits are released, initiating a phosphorylation cascade that regulates such cellular functions as metabolism, ion transport, and gene transcription. Catalytic PKA subunit isoforms, Cα, Cβ and, in humans, Cγ, have been identified.

Protein kinase A inhibitor

Chemical Name: N-[2-[[3-(4-Bromophenyl)-2-propenyl]amino]ethyl]-5-isoquinolinesulfonamide dihydrochloride
Purity: ≥98%
Protein kinase A inhibitor
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Selective protein kinase A inhibitor

Chemical Name: (9R,10S,12S)-2,3,9,10,11,12-Hexahydro-10-hydroxy-9-methyl-1-oxo-9,12-epoxy-1H-diindolo[1,2,3-fg:3',2',1'-kl]pyrrolo[3,4-i][1,6]benzodiazocine-10-carboxylic acid, hexyl ester
Purity: ≥97%
Selective protein kinase A inhibitor
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Cell-permeable protein kinase A inhibitor

Alternate Names: Protein kinase inhibitor-(14-22)-amide,myristoylated
Purity: ≥95%
Cell-permeable protein kinase A inhibitor
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Inhibitor of cyclic nucleotide dependent- and Rho-kinases

Alternate Names: HA 1077
Purity: ≥98%
Inhibitor of cyclic nucleotide dependent- and Rho-kinases
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Potent protein kinase A inhibitor

Alternate Names: Protein kinase inhibitor-(6-22)-amide,PKI-(6-22)-amide
Purity: ≥95%
Potent protein kinase A inhibitor
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Staurosporine synthesized to Ancillary Material Grade

Chemical Name: [9S-(9α,10β,11β,13α)]-2,3,10,11,12,13-Hexahydro-10-methoxy-9-methyl-11-(methylamino)-9,13-epoxy-1H,9H-diindolo[1,2,3-gh:3',2',1'-lm]pyrrolo[3,4-j][1,7]benzodiazonin-1-one
Purity: ≥98%
Staurosporine synthesized to Ancillary Material Grade
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Potent pan-Akt and PKA inhibitor

Chemical Name: 4-(4-Chlorophenyl)-4-[4-(1H-pyrazol-4-yl)phenyl]piperidine hydrochloride
Purity: ≥98%
Potent pan-Akt and PKA inhibitor
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High affinity PKA inhibitor

Purity: ≥95%
High affinity PKA inhibitor
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cAMP antagonist

Chemical Name: (R)-Adenosine, cyclic 3',5'-(hydrogenphosphorothioate) triethylammonium
Purity: ≥98%
cAMP antagonist
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