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ChemicalBook--->CAS DataBase List--->99658-03-4

99658-03-4

99658-03-4 Structure

99658-03-4 Structure
IdentificationBack Directory
[Name]

ALPHA-HELICAL CRF (9-41)
[CAS]

99658-03-4
[Synonyms]

ALPHA-HELICAL CRF (9-41)
CORTICOTROPIN RELEASING FACTOR ANTAGONIST
ALPHA-HELICAL CORTICOTROPIN RELEASING FA CTOR
ALPHA-CORTICOTROPIN-RELEASING FACTOR 9-41, HELICAL
ALPHA-HELICAL CORTICOTROPIN RELEASING FACTOR (9-41)
alpha-Helical corticotropin releasing factor fragment
α-helical corticotropin releasing factor fragment (9-41)
ALPHA-HELICAL CORTICOTROPIN RELEASING FACTOR FRAGMENT (9-41)
methyl (2S)-2-[[(3R)-3-hydroxy-4-(phenylmethoxycarbonylamino)butanoyl]amino]-3-(2-iodophenyl)propanoate
ASP-LEU-THR-PHE-HIS-LEU-ARG-GLU-MET-LEU-GLU-MET-ALA-LYS-ALA-GLU-GLN-ALA-GLU-GLN-ALA-LEU-ASN-ARG-LEU-LEU-GLU-ALA-NH2
ASP-LEU-THR-PHE-HIS-LEU-LEU-ARG-GLU-MET-LEU-GLU-MET-ALA-LYS-ALA-GLU-GLN-GLU-ALA-GLU-GLN-ALA-ALA-LEU-ASN-ARG-LEU-LEU-LEU-GLU-GLU-ALA-NH2
H-ASP-LEU-THR-PHE-HIS-LEU-LEU-ARG-GLU-MET-LEU-GLU-MET-ALA-LYS-ALA-GLU-GLN-GLU-ALA-GLU-GLN-ALA-ALA-LEU-ASN-ARG-LEU-LEU-LEU-GLU-GLU-ALA-NH2
L-α-Aspartyl-L-leucyl-L-threonyl-L-phenylalanyl-L-histidyl-L-leucyl-L-leucyl-L-arginyl-L-α-glutamyl-L-methionyl-L-leucyl-L-α-glutamyl-L-methionyl-L-alanyl-L-lysyl-L-alanyl-L-α-glutamyl-L-glutaminyl-L-α-glutamyl-L-alanyl-L-α-glutamyl-L-glutaminyl-L-alanyl-L-alanyl-L-leucyl-L-asparaginyl-L-arginyl-L-leucyl-L-leucyl-L-leucyl-L-α-glutamyl-L-α-glutamyl-L-alanine
[Molecular Formula]

C22H25IN2O6
[MDL Number]

MFCD00081543
[MOL File]

99658-03-4.mol
[Molecular Weight]

540.348
Chemical PropertiesBack Directory
[storage temp. ]

−20°C
[form ]

powder
[color ]

white
Safety DataBack Directory
[WGK Germany ]

3
Hazard InformationBack Directory
[Biochem/physiol Actions]

The corticotropin releasing factor (CRF) antagonist α-helical CRF [9-41] exhibits 10-fold higher affinity for rat CRF2α receptors over human CRF2α receptors. It has been used to elucidate the role of CRF in various physiological systems. In colonic epithelium, it abolishes CRF-induced changes in ion secretion, and significantly inhibits CRF-stimulated conductance. It antagonizes the CRF-induced proinflammatory degranulation of perivascular mast cells that are activated in response to acute psychological stress and CRF secretion.
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