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PKA

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PKA

结构式 货号 产品名称 CAS号
HA-100 dihydrochloride 结构式
 BCP48930 HA-100 dihydrochloride 210297-47-5
HA-100 dihydrochloride is a protein kinase inhibitor, inhibiting superoxide release from human neutrophils (PMN).
A-3 Hydrochloride 结构式
 BCP37347 赤霉酸盐酸盐 78957-85-4
A-3 hydrochloride is an inhibitor of PKA, PKC, and casein kinase I and II, and MLCK.
8-Bromo-cAMP sodium salt 结构式
 BCP20617 8-溴腺苷-3',5'-环单磷酸钠 76939-46-3
8-Bromo-cAMP is a cell perbeable cyclic AMP (cAMP) analog and a PKA activator.
PKA Inhibitor (5-24) 结构式
 BCP35218 PKA Inhibitor (5-24) 99534-03-9
PKA Inhibitor (5-24) is a potent, competitive, and synthetic peptide inhibitor of PKA (cAMP-dependent protein kinase), with a Ki of 2.3 nM. PKI(5-24) corresponds to residues 5-24 in the naturally occurring heat-stable protein kinase inhibitor.
AT7867 dihydrochloride 结构式
 BCP30936 AT7867 dihydrochloride 1431697-86-7
AT7867 dihydrochloride is a potent ATP-competitive inhibitor of Akt1/Akt2/Akt3 and p70S6K/PKA with IC50s of 32 nM/17 nM/47 nM and 85 nM/20 nM, respectively.
Rp-8-bromo-Cyclic AMPS sodium salt 结构式
 BCP29965 Rp-8-bromo-Cyclic AMPS sodium salt 925456-59-3
Rp-8-bromo-Cyclic AMPS (Rp-8-bromo-cAMPS) is a cell-permeable cAMP analog that combines an exocyclic sulfur substitution in the equatorial position of the cyclophosphate ring with a bromine substitution in the adenine base of cAMP.
TX-1918 结构式
 BCP16358 TX-1918 503473-32-3
TX-1918 is a cell-permeable tyrphostin derivative that inhibits eukaryotic elongation factor-2 kinase (eEF-2K; IC50 = 440 nM).
Fasudil 结构式
 BCP26821 法舒地尔 103745-39-7
Fasudil, a Rho-kinase inhibitor, has been shown to reduce portal venous pressure in cirrhotic rats.
Fasudil hydrochloride 结构式
 BCP26351 盐酸法舒地尔 105628-07-7
Fasudil Hydrochloride is a potent inhibitor of ROCK1, PKA, PKC, and MLCK with Kis of 0.33 μM, 1.0 μM, 9.3 μM and 55 μM, respectively.
Dibutyryl adenosine cyclophosphate calcium 结构式
 BCP23536 二丁酰环磷腺苷钙 938448-87-4
Bucladesine calcium salt(DC2797 calcium salt) is a membrane permeable selective activator of PKA.
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