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Casokefamide

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Casokefamide
Clinical data
Other namesL-tyrosyl-D-alanyl-L-phenylalanyl-D-alanyl-L-tyrosinamide
ATC code
  • None
Identifiers
  • (2S)-2-[(2R)-2-[(2S)-2-[(2R)-2-[(2S)-2-amino-3-(4-hydroxyphenyl)propanamido]propanamido]-3-phenylpropanamido]propanamido]-3-(4-hydroxyphenyl)propanamide
CAS Number
PubChemCID
ChemSpider
UNII
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC33H40N6O7
Molar mass632.718g·mol−1
3D model (JSmol)
  • O=C(N[C@@H](C(=O)N[C@H](C(=O)N[C@@H](C(=O)N[C@H](C(=O)N)Cc1ccc(O)cc1)C)Cc2ccccc2)C)[C@@H](N)Cc3ccc(O)cc3
  • InChI=1S/C33H40N6O7/c1-19(36-32(45)26(34)16-22-8-12-24(40)13-9-22)31(44)39-28(18-21-6-4-3-5-7-21)33(46)37-20(2)30(43)38-27(29(35)42)17-23-10-14-25(41)15-11-23/h3-15,19-20,26-28,40-41H,16-18,34H2,1-2H3,(H2,35,42)(H,36,45)(H,37,46)(H,38,43)(H,39,44)/t19-,20-,26+,27+,28+/m1/s1
  • Key:XDRHVZLDLNGKLM-FLVVDCEDSA-N

Casokefamide(INN), also known asβ-casomorphin 4027(β-CM-4027) and[D-Ala2,4,Tyr5]-β-casomorphin-5-amide,is aperipherally-specific,syntheticopioid pentapeptidewith theamino acid sequenceTyr-D-Ala-Phe-D-Ala-Tyr-NH2.[1]Derived from theβ-casomorphinsequence, it was designed with the intention of improving resistance todigestive enzymesso that it could be used as anantidiarrhealmedicine.[1][2]Unlike other casomorphins, which are generallyselectiveμ-opioid receptoragonists,casokefamide binds to both the μ- andδ-opioid receptors.[1]In aclinical study,casokefamide was found to be effective via the oral route for the treatment of chronicdiarrhea,and did not produce anyside effects.[2]However, further clinical development was not pursued and it was never marketed.

See also

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References

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  1. ^abcBrantl V, Picone D, Amodeo P, Temussi PA (March 1993). "Solution structure of casokefamide".Biochemical and Biophysical Research Communications.191(3): 853–9.doi:10.1006/bbrc.1993.1295.PMID8466524.
  2. ^abSchulte-Frohlinde E, Reindl W, Bierling D, et al. (March 2000). "Effects of oral casokefamide on plasma levels, tolerance, and intestinal transit in man".Peptides.21(3): 439–42.doi:10.1016/S0196-9781(00)00166-2.PMID10793229.S2CID44670226.