Volume 27, Issue 23
Natural Products
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ChemInform Abstract: Design and Comprehensive Conformational Studies of Tyr1-cyclo(D-Pen2- Gly3-Phe4-L-3-Mpt5) and Tyr1-cyclo(D-Pen2-Gly3-Phe4-D-3-Mpt5): Novel Conformationally Constrained Opioid Peptides.

G. V. NIKIFOROVICH

G. V. NIKIFOROVICH

Cent. Mol. Des., Washington Univ., St. Louis, MO 63130, USA

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K. E. KOEVER

K. E. KOEVER

Cent. Mol. Des., Washington Univ., St. Louis, MO 63130, USA

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S. A. KOLODZIEJ

S. A. KOLODZIEJ

Cent. Mol. Des., Washington Univ., St. Louis, MO 63130, USA

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B. NOCK

B. NOCK

Cent. Mol. Des., Washington Univ., St. Louis, MO 63130, USA

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C. GEORGE

C. GEORGE

Cent. Mol. Des., Washington Univ., St. Louis, MO 63130, USA

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J. R. DESCHAMPS

J. R. DESCHAMPS

Cent. Mol. Des., Washington Univ., St. Louis, MO 63130, USA

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J. L. FLIPPEN-ANDERSON

J. L. FLIPPEN-ANDERSON

Cent. Mol. Des., Washington Univ., St. Louis, MO 63130, USA

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G. R. MARSHALL

G. R. MARSHALL

Cent. Mol. Des., Washington Univ., St. Louis, MO 63130, USA

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First published: June 4, 1996

Abstract

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ChemInform Abstract

Employing energy calculations the two title compounds are designed and their structures studied by homo- and heteronuclear NMR spectroscopy and X-ray analysis. The compounds are tested for their binding to . delta.-, μ-, and ϰ-opioid receptors. The solution conformations are compared to their suggested δ-receptor-bound conformers.

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