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Acta Biochim Pol ; 48(4): 1151-4, 2001.
Article in English | MEDLINE | ID: mdl-11995983

ABSTRACT

Linear and cyclic hymenistatin I (HS I) analogues with dipeptide segments Ile2-Pro3 Pro3-Pro4 and Val6-Pro7 replaced by their tetrazole analogues Ile2-psi[CN4]-Ala3', Pro3-psi[CN4]-Ala4 and Val6-psi[CN4]-Ala7 were synthesized by the solid phase peptide synthesis method and cyclized with the TBTU and/or HATU reagent. The peptides were examined for their immunosuppressive activity in the lymphocyte proliferation test (LPT).


Subject(s)
Immunosuppressive Agents/chemical synthesis , Immunosuppressive Agents/pharmacology , Peptides, Cyclic/chemistry , Peptides, Cyclic/pharmacology , Tetrazoles/chemistry , Amino Acid Sequence , Cell Division , Humans , Lymphocytes/cytology , Models, Chemical , Molecular Sequence Data , Peptide Biosynthesis , Peptides/chemistry
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