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1
Conformation-activity relationship in hexapeptides related to substance P.
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2
Design and synthesis of dimeric analogs of neurokinin A and B: effect of dimerization of COOH-terminal heptapeptides on receptor selection.
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3
Synthesis and some biological properties of the hexapeptide analog of substance P with a C-terminal thioamide group.
Pol J Pharmacol Pharm. 1990 Sep-Oct;42(5):483-90.
4
Synthesis and biological activity of NK-1 selective, N-backbone cyclic analogs of the C-terminal hexapeptide of substance P.
J Med Chem. 1996 Aug 2;39(16):3174-8. doi: 10.1021/jm960154i.
5
[Synthesis of cyclic and non-cyclic tachykinin partial sequences. 2. Synthesis of the homocyclic substance P(6-11) hexapeptide].
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6
Side chain methyl substitution in the delta-opioid receptor antagonist TIPP has an important effect on the activity profile.
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7
[Cyclic analogs of substance P. III. Cyclo (6(sup)gamma----oligomethylenediamine----11) substance P(6-11)-hexapeptides].
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8
Beta-methyl substitution of cyclohexylalanine in Dmt-Tic-Cha-Phe peptides results in highly potent delta opioid antagonists.
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9
N-acylated pentapeptides antagonists of substance P on guinea-pig ileum.
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10
In vitro activity and selectivity of glucosidic SP(6-11) analogues.
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