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1.
Prostaglandin E2 receptors are differentially expressed in subpopulations of granulosa cells from primate periovulatory follicles.
Biol Reprod
; 85(5): 916-23, 2011 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-21753194
2.
14-O-Heterocyclic-substituted naltrexone derivatives as non-peptide mu opioid receptor selective antagonists: design, synthesis, and biological studies.
Bioorg Med Chem Lett
; 19(6): 1825-9, 2009 Mar 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-19217280
3.
The LIF receptor antagonist PEGLA is effectively delivered to the uterine endometrium and blocks LIF activity in cynomolgus monkeys.
Contraception
; 87(6): 813-23, 2013 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-23121824
4.
Design, synthesis, and biological evaluation of 14-heteroaromatic-substituted naltrexone derivatives: pharmacological profile switch from mu opioid receptor selectivity to mu/kappa opioid receptor dual selectivity.
J Med Chem
; 56(22): 9156-69, 2013 Nov 27.
Artículo
en Inglés
| MEDLINE | ID: mdl-24144240
5.
Design, synthesis, and biological evaluation of 6alpha- and 6beta-N-heterocyclic substituted naltrexamine derivatives as mu opioid receptor selective antagonists.
J Med Chem
; 52(5): 1416-27, 2009 Mar 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-19199782
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