Portoghese PS - Search Results

1

Selective naltrexone-derived opioid receptor antagonists.

Takemori AE, Portoghese PS. Takemori AE, et al. Among authors: portoghese ps. Annu Rev Pharmacol Toxicol. 1992;32:239-69. doi: 10.1146/annurev.pa.32.040192.001323. Annu Rev Pharmacol Toxicol. 1992. PMID: 1318671 Review.

2

Electrophilic N-benzylnaltrindoles as delta opioid receptor-selective antagonists.

Korlipara VL, Takemori AE, Portoghese PS. Korlipara VL, et al. Among authors: portoghese ps. J Med Chem. 1995 Apr 14;38(8):1337-43. doi: 10.1021/jm00008a012. J Med Chem. 1995. PMID: 7731019

3

kappa Opioid receptor selective affinity labels: electrophilic benzeneacetamides as kappa-selective opioid antagonists.

Chang AC, Takemori AE, Ojala WH, Gleason WB, Portoghese PS. Chang AC, et al. Among authors: portoghese ps. J Med Chem. 1994 Dec 23;37(26):4490-8. doi: 10.1021/jm00052a008. J Med Chem. 1994. PMID: 7799399

4

7'-Substituted amino acid conjugates of naltrindole. Hydrophilic groups as determinants of selective antagonism of delta 1 opioid receptor-mediated antinociception in mice.

Portoghese PS, Farouz-Grant F, Sultana M, Takemori AE. Portoghese PS, et al. J Med Chem. 1995 Feb 3;38(3):402-7. doi: 10.1021/jm00003a002. J Med Chem. 1995. PMID: 7853332

5

N-benzylnaltrindoles as long-acting delta-opioid receptor antagonists.

Korlipara VL, Takemori AE, Portoghese PS. Korlipara VL, et al. Among authors: portoghese ps. J Med Chem. 1994 Jun 10;37(12):1882-5. doi: 10.1021/jm00038a018. J Med Chem. 1994. PMID: 8021928

6

Synthesis and delta-opioid receptor antagonist activity of a naltrindole analogue with a regioisomeric indole moiety.

Portoghese PS, Ohkawa S, Moe ST, Takemori AE. Portoghese PS, et al. J Med Chem. 1994 Jun 10;37(12):1886-8. doi: 10.1021/jm00038a019. J Med Chem. 1994. PMID: 8021929

7

Lack of involvement of delta-1 opioid receptors in the development of physical dependence on morphine in mice.

Miyamoto Y, Bowen WD, Portoghese PS, Takemori AE. Miyamoto Y, et al. Among authors: portoghese ps. J Pharmacol Exp Ther. 1994 Jul;270(1):37-9. J Pharmacol Exp Ther. 1994. PMID: 8035333

8

Synthesis of naltrexone-derived delta-opioid antagonists. Role of conformation of the delta address moiety.

Portoghese PS, Sultana M, Moe ST, Takemori AE. Portoghese PS, et al. J Med Chem. 1994 Mar 4;37(5):579-85. doi: 10.1021/jm00031a006. J Med Chem. 1994. PMID: 8126697

9

Interaction of [D-Pen2,D-Pen5]enkephalin and [D-Ala2,Glu4]deltorphin with delta-opioid receptor subtypes in vivo.

Vanderah T, Takemori AE, Sultana M, Portoghese PS, Mosberg HI, Hruby VJ, Haaseth RC, Matsunaga TO, Porreca F. Vanderah T, et al. Among authors: portoghese ps. Eur J Pharmacol. 1994 Feb 3;252(2):133-7. doi: 10.1016/0014-2999(94)90588-6. Eur J Pharmacol. 1994. PMID: 8157053 Free article.

10

Structure-activity relationship of N17'-substituted norbinaltorphimine congeners. Role of the N17' basic group in the interaction with a putative address subsite on the kappa opioid receptor.

Portoghese PS, Lin CE, Farouz-Grant F, Takemori AE. Portoghese PS, et al. J Med Chem. 1994 May 13;37(10):1495-500. doi: 10.1021/jm00036a015. J Med Chem. 1994. PMID: 8182708

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