Template-constrained somatostatin analogues:: A biphenyl linker induces a type-V′ turn

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[42] Designed molecules that fold to mimic protein secondary structures [J]. CURRENT OPINION IN CHEMICAL BIOLOGY, 1999, 3 (06) : 714 - 723

[43] Template-constrained cyclic peptide analogues of somatostatin: Subtype-selective binding to somatostatin receptors and antiangiogenic activity [J]. BIOORGANIC & MEDICINAL CHEMISTRY, 2000, 8 (09) : 2229 - 2241

[44] HIGHLY-ACTIVE CYCLIC AND BICYCLIC SOMATOSTATIN ANALOGS OF REDUCED RING SIZE [J]. NATURE, 1979, 280 (5722) : 512 - 514

[45] Wang ZC, 1999, CHEM-EUR J, V5, P3273, DOI 10.1002/(SICI)1521-3765(19991105)5:11<3273::AID-CHEM3273>3.0.CO

[46] 2-3

[47] Wuthrich K., 1986, NMR PROTEINS NUCL AC, DOI DOI 10.1051/EPN/19861701011

[41] Identification of a potent heterocyclic ligand to somatostatin receptor subtype 5 by the synthesis and screening of β-turn mimetic libraries [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1999, 121 (09) : 1817 - 1825

[42] Designed molecules that fold to mimic protein secondary structures [J]. CURRENT OPINION IN CHEMICAL BIOLOGY, 1999, 3 (06) : 714 - 723

[43] Template-constrained cyclic peptide analogues of somatostatin: Subtype-selective binding to somatostatin receptors and antiangiogenic activity [J]. BIOORGANIC & MEDICINAL CHEMISTRY, 2000, 8 (09) : 2229 - 2241

[44] HIGHLY-ACTIVE CYCLIC AND BICYCLIC SOMATOSTATIN ANALOGS OF REDUCED RING SIZE [J]. NATURE, 1979, 280 (5722) : 512 - 514

[45] Wang ZC, 1999, CHEM-EUR J, V5, P3273, DOI 10.1002/(SICI)1521-3765(19991105)5:11<3273::AID-CHEM3273>3.0.CO

[46] 2-3

[47] Wuthrich K., 1986, NMR PROTEINS NUCL AC, DOI DOI 10.1051/EPN/19861701011