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Signaling Pathways
- Angiogenesis/Protein Tyrosine Kinase
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- Epigenetics
-
GPCR/G Protein
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Neuro Signaling Pathway
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Protease/Metabolic Enzyme
- COMT
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Research Areas
- Metabolic Disease
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Nature products
Antibodies
Peptides
Catalysts
Impurities
Intermediate
- Amino acid
- Ammonia Series
- Azaindazole
- Pyridazine Series
- Nucleoside Series
- Quinazoline
- Pyrazole Series
- Boric acid
- Pyrimidine Series
- Quinoline Series
- Pyrrole Series
- Thiophene Series
- Saccharide
- Azaindole
- Indole Series
- Piperidine Series
- Indazole Series
- Heterocyclic Series
- Benzene Series
- Pyridine Series
Raw Materials
PKA
Chemical Structure | Cat. No. | Product Name | CAS No. |
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BCP48930 | HA-100 dihydrochloride New | 210297-47-5 | |
HA-100 dihydrochloride is a protein kinase inhibitor, inhibiting superoxide release from human neutrophils (PMN).
|
BCP37347 | A-3 Hydrochloride New | 78957-85-4 | |
A-3 hydrochloride is an inhibitor of PKA, PKC, and casein kinase I and II, and MLCK.
|
BCP20617 | 8-Bromo-cAMP sodium salt New | 76939-46-3 | |
8-Bromo-cAMP is a cell perbeable cyclic AMP (cAMP) analog and a PKA activator.
|
BCP35218 | PKA Inhibitor (5-24) New | 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.
|
BCP30936 | AT7867 dihydrochloride New | 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.
|
BCP29965 | Rp-8-bromo-Cyclic AMPS sodium salt New | 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.
|
BCP16358 | TX-1918 New | 503473-32-3 | |
TX-1918 is a cell-permeable tyrphostin derivative that inhibits eukaryotic elongation factor-2 kinase (eEF-2K; IC50 = 440 nM).
|
BCP26821 | Fasudil | 103745-39-7 | |
Fasudil, a Rho-kinase inhibitor, has been shown to reduce portal venous pressure in cirrhotic rats.
|
BCP26351 | Fasudil hydrochloride | 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.
|
BCP23536 | Dibutyryl adenosine cyclophosphate calcium | 938448-87-4 | |
Bucladesine calcium salt(DC2797 calcium salt) is a membrane permeable selective activator of PKA.
|