Synthesis and biological activity of NK-1 selective, N-backbone cyclic analogs of the C-terminal hexapeptide of substance P. | J Med Chem;39(16): 3174-8, 1996 Aug 02. | MEDLINE

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Synthesis and biological activity of NK-1 selective, N-backbone cyclic analogs of the C-terminal hexapeptide of substance P.

Byk, G; Halle, D; Zeltser, I; Bitan, G; Selinger, Z; Gilon, C.

Affiliation

Byk G; Department of Organic Chemistry, Hebrew University of Jerusalem, Israel.

J Med Chem ; 39(16): 3174-8, 1996 Aug 02.

Article in En | MEDLINE | ID: mdl-8759639

Subject(s)

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Collection: 01-internacional Database: MEDLINE Main subject: Peptide Fragments / Peptides, Cyclic / Substance P / Receptors, Neurokinin-1 Limits: Animals Language: En Journal: J Med Chem Journal subject: QUIMICA Year: 1996 Document type: Article Affiliation country: Israel Country of publication: Estados Unidos

Search on Google

Collection: 01-internacional Database: MEDLINE Main subject: Peptide Fragments / Peptides, Cyclic / Substance P / Receptors, Neurokinin-1 Limits: Animals Language: En Journal: J Med Chem Journal subject: QUIMICA Year: 1996 Document type: Article Affiliation country: Israel Country of publication: Estados Unidos