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Volumn 42, Issue 7, 2003, Pages 776-778

Design and synthesis of γ-dipeptide derivatives with submicromolar affinities for human somatostatin receptors

Author keywords

Hormones; Peptides; Peptidomimetics; Somatostatin

Indexed keywords

AMINO ACIDS; CHEMICAL BONDS; HORMONES; SYNTHESIS (CHEMICAL);

EID: 0037450183     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200390205     Document Type: Article
Times cited : (66)

References (23)
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    • note
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    • The choice of a 2-naphthylacetyl group at the N-terminus was inspired by previous observations: The naphthyl group may be considered to mimic the benzyl side chain of a Phe residue, which precedes the Trp in the peptide chain of somatostatin: S. J. Hocart, R. Jain, W. A. Murphy, J. E. Taylor, B. Morgan, D. H. Coy, J. Med. Chem. 1998, 41, 1146-1154; A. J. Souers, A. A. Virgilio, A. Rosenquist, W. Fenuik, J. A. Ellman, J. Am. Chem. Soc. 1999, 121, 1817-1825.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.