cAMP-Dependent Protein Kinase Inhibitor-α (5-22) amide (human, mouse, rabbit, rat) structure
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Common Name | cAMP-Dependent Protein Kinase Inhibitor-α (5-22) amide (human, mouse, rabbit, rat) | ||
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| CAS Number | 100853-58-5 | Molecular Weight | 1969.17000 | |
| Density | N/A | Boiling Point | N/A | |
| Molecular Formula | C84H137N29O26 | Melting Point | N/A | |
| MSDS | N/A | Flash Point | N/A | |
Use of cAMP-Dependent Protein Kinase Inhibitor-α (5-22) amide (human, mouse, rabbit, rat)PKI(5-22)amide is the active inhibitory fragment of the inhibitor of the cyclic AMP-dependent protein kinase (PKA). PKI(5-22)amide inhibits PKA activation, but fails to attenuate homologous desensitization of CRF1 receptors[1][2]. |
| Name | h-thr-thr-tyr-ala-asp-phe-ile-ala-ser-gly-arg-thr-gly-arg-arg-asn-ala-ile-nh2 |
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| Synonym | More Synonyms |
| Description | PKI(5-22)amide is the active inhibitory fragment of the inhibitor of the cyclic AMP-dependent protein kinase (PKA). PKI(5-22)amide inhibits PKA activation, but fails to attenuate homologous desensitization of CRF1 receptors[1][2]. |
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| Related Catalog | |
| In Vitro | PKI(5-22)amide (1 μM; 1 min) fails to block CRF1 receptor (100 nM; 30 min) desensitization in Y-79 cells permeabilized with Streptolysin O (HY-135416)[1]. |
| References |
| Molecular Formula | C84H137N29O26 |
|---|---|
| Molecular Weight | 1969.17000 |
| Exact Mass | 1968.03000 |
| PSA | 931.05000 |
| PKI (5-22),AMIDE |
| CAMP-DEPENDENT PROTEIN KINASE INHIBITOR (5-22) AMIDE |
| PKI-a (5-22) aMide (huMan,Mouse,rabbit,rat),Wiptide |
| cAMP-Dependent Protein Kinase Inhibitor (5-22),amide,Wiptide |
| WIPTIDE |
| PROTEIN KINASE A INHIBITOR (5-22) AMIDE |
| TTYADFIASGRTGRRNAI-NH2 |
| CAMP DEPENDENT PK INHIBITOR (5-22) AMIDE |
| PKA INHIBITOR (5-22) AMIDE |
| THR-THR-TYR-ALA-ASP-PHE-ILE-ALA-SER-GLY-ARG-THR-GLY-ARG-ARG-ASN-ALA-ILE-NH2 |
| THR-THR-TYR-ALA-ASP-PHE-ILE-ALA-SER-GLY-ARG-THR-GLY-ARG-ARG-ASN-ALA-ILE-HIS-ASP: TTYADFIASGRTGRRNAIHD |