-
1
-
-
16444363347
-
Structure-activity relationships of arodyn, a novel dynorphin A (1-11) analogue
-
(Lebl, M. & Houghten, R.A., eds). American Peptide Society, San Diego, CA
-
Bennett, M.A., Murray, T.F. & Aldrich, J.V. (2001) Structure-activity relationships of arodyn, a novel dynorphin A (1-11) analogue. In: Peptides: Wave of the Future (Lebl, M. & Houghten, R.A., eds), pp. 894-895, American Peptide Society, San Diego, CA.
-
(2001)
Peptides: Wave of the Future
, pp. 894-895
-
-
Bennett, M.A.1
Murray, T.F.2
Aldrich, J.V.3
-
2
-
-
0012047617
-
Narcotic analgesics
-
(Abraham, D., ed.). John Wiley & Sons, Inc., New York, NY
-
Aldrich, J.V. & Vigil-Cruz, S. (2003) Narcotic analgesics. In: Burger's Medicinal Chemistry and Drug Discovery, Vol. 6 (Abraham, D., ed.), pp. 329-481. John Wiley & Sons, Inc., New York, NY.
-
(2003)
Burger's Medicinal Chemistry and Drug Discovery
, vol.6
, pp. 329-481
-
-
Aldrich, J.V.1
Vigil-Cruz, S.2
-
3
-
-
0034019066
-
An open-label study of a functional opioid κ antagonist in the treatment of opioid dependence
-
Rothman, R.B., Gorelick, D.A., Heishman, S.J., Eichmiller, P.R., Hill, B.H., Norbeck, J. & Liberto, J. (2000) An open-label study of a functional opioid κ antagonist in the treatment of opioid dependence. J. Substance Abuse Treat. 18, 277-281.
-
(2000)
J. Substance Abuse Treat
, vol.18
, pp. 277-281
-
-
Rothman, R.B.1
Gorelick, D.A.2
Heishman, S.J.3
Eichmiller, P.R.4
Hill, B.H.5
Norbeck, J.6
Liberto, J.7
-
4
-
-
0037381053
-
Antidepressant-like effects of kappa-opioid receptor antagonists in the forced swim test in rats
-
Mague, S.D., Pliakas, A.M., Todtenkopf, M.S., Tomasiewicz, H.C., Zhang, Y., Stevens, W.C. Jr, Jones, R.M., Portoghese, P.S. & Carlezon, W.A. Jr (2003) Antidepressant-like effects of kappa-opioid receptor antagonists in the forced swim test in rats. J. Pharmacol. Exp. Ther. 305, 323-330.
-
(2003)
J. Pharmacol. Exp. Ther.
, vol.305
, pp. 323-330
-
-
Mague, S.D.1
Pliakas, A.M.2
Todtenkopf, M.S.3
Tomasiewicz, H.C.4
Zhang, Y.5
Stevens Jr., W.C.6
Jones, R.M.7
Portoghese, P.S.8
Carlezon Jr., W.A.9
-
5
-
-
0023139286
-
Binaltorphimine and norbinaltorphimine, potent and selective kappa-opioid receptor antagonists
-
Portoghese, P.S., Nagase, H. & Takemori, A.E. (1987) Binaltorphimine and norbinaltorphimine, potent and selective kappa-opioid receptor antagonists. Life Sci 40, 1287-1292.
-
(1987)
Life Sci.
, vol.40
, pp. 1287-1292
-
-
Portoghese, P.S.1
Nagase, H.2
Takemori, A.E.3
-
6
-
-
0032705857
-
Intracisternal nor-binaltorphimine distinguishes central and peripheral κ-opioid antinociception in rhesus monkeys
-
Ko, M.C.H., Johnson, M.D., Butelman, E.R., Willmont, K.J., Mosberg, H.I. & Woods, J.H. (1999) Intracisternal nor-binaltorphimine distinguishes central and peripheral κ-opioid antinociception in rhesus monkeys. J. Pharmacol. Exp. Ther. 191, 1113-1120.
-
(1999)
J. Pharmacol. Exp. Ther.
, vol.191
, pp. 1113-1120
-
-
Ko, M.C.H.1
Johnson, M.D.2
Butelman, E.R.3
Willmont, K.J.4
Mosberg, H.I.5
Woods, J.H.6
-
7
-
-
0343191562
-
Potent and selective indolomorphinan antagonists of the kappa-opioid receptor
-
Stevens, W.C. Jr, Jones, R.M., Subramanian, G., Metzger, T.G., Ferguson, D.M. & Portoghese, P.S. (2000) Potent and selective indolomorphinan antagonists of the kappa-opioid receptor. J. Med. Chem. 43, 2759-2769.
-
(2000)
J. Med. Chem.
, vol.43
, pp. 2759-2769
-
-
Stevens Jr., W.C.1
Jones, R.M.2
Subramanian, G.3
Metzger, T.G.4
Ferguson, D.M.5
Portoghese, P.S.6
-
8
-
-
0034640189
-
5′-guanidinonaltrindole, a highly selective and potent kappa-opioid receptor antagonist
-
Jones, R.M. & Portoghese, P.S. (2000) 5′-Guanidinonaltrindole, a highly selective and potent kappa-opioid receptor antagonist. Eur. J. Pharmacol. 396, 49-52.
-
(2000)
Eur. J. Pharmacol.
, vol.396
, pp. 49-52
-
-
Jones, R.M.1
Portoghese, P.S.2
-
10
-
-
0036390018
-
Kappa opioid antagonist effects of the novel kappa antagonist 5′-guanidinonaltrindole (GNTI) in an assay of schedule-controlled behavior in rhesus monkeys
-
Negus, S.S., Mello, N.K., Linsenmayer, D.C., Jones, R.M. & Portoghese, P.S. (2002) Kappa opioid antagonist effects of the novel kappa antagonist 5′-guanidinonaltrindole (GNTI) in an assay of schedule-controlled behavior in rhesus monkeys. Psychopharmacology 163, 412-419.
-
(2002)
Psychopharmacology
, vol.163
, pp. 412-419
-
-
Negus, S.S.1
Mello, N.K.2
Linsenmayer, D.C.3
Jones, R.M.4
Portoghese, P.S.5
-
11
-
-
0035899186
-
4R)-dimethyl- 4-(3-hydroxyphenyl)piperidine derivative to possess highly potent and selective opioid kappa receptor antagonist activity
-
4R)-dimethyl-4-(3-hydroxyphenyl)piperidine derivative to possess highly potent and selective opioid kappa receptor antagonist activity. J. Med. Chem. 44, 1687-2690.
-
(2001)
J. Med. Chem.
, vol.44
, pp. 1687-2690
-
-
Thomas, J.B.1
Atkinson, R.N.2
Rothman, R.B.3
Fix, S.E.4
Mascarella, S.W.5
Vinson, N.A.6
Xu, H.7
Dersch, C.M.8
Lu, Y.9
Cantrell, B.E.10
Zimmerman, D.M.11
Carroll, F.I.12
-
12
-
-
0037783998
-
4R)-4-(3-hydroxyphenyl)-3,4-dimethyl-1-piperidinyl] methyl-2-methylpropyl)-1,2,3,4-tetrahydio-3-isoquinolinecarboxamide as a novel potent and selective opioid kappa receptor antagonist
-
4R)-4-(3-hydroxyphenyl)-3,4-dimethyl-1-piperidinyl] methyl-2-methylpropyl)-1,2,3,4-tetrahydio-3-isoquinolinecarboxamide as a novel potent and selective opioid kappa receptor antagonist. J. Med. Chem. 46, 3127-3137.
-
(2003)
J. Med. Chem.
, vol.46
, pp. 3127-3137
-
-
Thomas, J.B.1
Atkinson, R.N.2
Vinson, N.A.3
Catanzaro, J.L.4
Perretta, C.L.5
Fix, S.E.6
Mascarella, S.W.7
Rothman, R.B.8
Xu, H.9
Dersch, C.M.10
Cantrell, B.E.11
Zimmerman, D.M.12
Carroll, F.I.13
-
13
-
-
0842325908
-
Importance of phenolic address groups in opioid kappa receptor selective antagonists
-
Thomas, J.B., Fix, S.E., Rothman, R.B., Mascarella, S.W., Dersch, C.M., Cantrell, B.E., Zimmerman, D.M. & Carroll, F.I. (2004) Importance of phenolic address groups in opioid kappa receptor selective antagonists. J. Med. Chem. 47, 1070-1073.
-
(2004)
J. Med. Chem.
, vol.47
, pp. 1070-1073
-
-
Thomas, J.B.1
Fix, S.E.2
Rothman, R.B.3
Mascarella, S.W.4
Dersch, C.M.5
Cantrell, B.E.6
Zimmerman, D.M.7
Carroll, F.I.8
-
14
-
-
0028143479
-
Human κ opiate receptor second extracellular loop elevates dynorphin's affinity for human μ/κ chimeras
-
Wang, J.B., Johnson, P.S., Wu, J.M., Wang, W.F. & Uhl, G.R. (1994) Human κ opiate receptor second extracellular loop elevates dynorphin's affinity for human μ/κ chimeras. J. Biol. Chem. 269, 25966-25969.
-
(1994)
J. Biol. Chem.
, vol.269
, pp. 25966-25969
-
-
Wang, J.B.1
Johnson, P.S.2
Wu, J.M.3
Wang, W.F.4
Uhl, G.R.5
-
15
-
-
0028104682
-
Differential binding domains of peptide and non-peptide ligands in the cloned rat κ opioid receptor
-
Xue, J.-C., Chen, C., Zhu, J., Kunapuli, S., DeRiel, J.K., Yu, L. & Liu-Chen, L.-Y. (1994) Differential binding domains of peptide and non-peptide ligands in the cloned rat κ opioid receptor. J. Biol. Chem. 169, 30195-30199.
-
(1994)
J. Biol. Chem.
, vol.169
, pp. 30195-30199
-
-
Xue, J.-C.1
Chen, C.2
Zhu, J.3
Kunapuli, S.4
DeRiel, J.K.5
Yu, L.6
Liu-Chen, L.-Y.7
-
16
-
-
0029017044
-
A chimeric study of the molecular basis of affinity and selectivity of the κ and the δ opioid receptors: Potential role of extracellular domains
-
Meng, F., Hoversten, M.T., Thompson, R.C., Taylor, L., Watson, S.J. & Akil, H. (1995) A chimeric study of the molecular basis of affinity and selectivity of the κ and the δ opioid receptors: potential role of extracellular domains. J. Biol. Chem. 170, 12730-12736.
-
(1995)
J. Biol. Chem.
, vol.170
, pp. 12730-12736
-
-
Meng, F.1
Hoversten, M.T.2
Thompson, R.C.3
Taylor, L.4
Watson, S.J.5
Akil, H.6
-
17
-
-
0030769046
-
Molecular simulation of dynorphin A-(1-10) binding to extracellular loop 2 of the κ-opioid receptor. A model for activation
-
Paterlini, G., Portoghese, P.S. & Perguson, D.M. (1997) Molecular simulation of dynorphin A-(1-10) binding to extracellular loop 2 of the κ-opioid receptor. A model for activation. J. Med. Chem. 40, 3254-3262.
-
(1997)
J. Med. Chem.
, vol.40
, pp. 3254-3262
-
-
Paterlini, G.1
Portoghese, P.S.2
Perguson, D.M.3
-
18
-
-
0034611604
-
Isosteric replacement of acidic with neutral residues in extracellular loop-2 of the κ-opioid receptor does not affect dynorphin A(1-13) affinity and function
-
Ferguson, D.M., Kramer, S., Metzger, T.G., Law, P.Y. & Portoghese, P.S. (2000) Isosteric replacement of acidic with neutral residues in extracellular loop-2 of the κ-opioid receptor does not affect dynorphin A(1-13) affinity and function. J. Med. Chem. 43, 1251-1252.
-
(2000)
J. Med. Chem.
, vol.43
, pp. 1251-1252
-
-
Ferguson, D.M.1
Kramer, S.2
Metzger, T.G.3
Law, P.Y.4
Portoghese, P.S.5
-
19
-
-
0033549868
-
A novel acetylated analogue of dynorphin A-(1-11) amide as a κ-opioid receptor antagonist
-
Wan, Q., Murray, T.F. & Aldrich, J.V. (1999) A novel acetylated analogue of dynorphin A-(1-11) amide as a κ-opioid receptor antagonist. J. Med. Chem. 42, 3011-3013.
-
(1999)
J. Med. Chem.
, vol.42
, pp. 3011-3013
-
-
Wan, Q.1
Murray, T.F.2
Aldrich, J.V.3
-
20
-
-
0345158331
-
Specific receptor for the opioid peptide dynorphin: Structure-activity relationships
-
Chavkin, C. & Goldstein, A. (1981) Specific receptor for the opioid peptide dynorphin: structure-activity relationships. Proc. Natl. Acad. Sci. USA 78, 6543-6547.
-
(1981)
Proc. Natl. Acad. Sci. USA
, vol.78
, pp. 6543-6547
-
-
Chavkin, C.1
Goldstein, A.2
-
21
-
-
0017620408
-
ACTH: A short introductory review
-
Schwyzer, R. (1977) ACTH: A short introductory review. Ann. NY Acad. Sci. 197, 3-16.
-
(1977)
Ann. NY Acad. Sci.
, vol.197
, pp. 3-16
-
-
Schwyzer, R.1
-
22
-
-
0034644221
-
2: A dynorphin analogue with high selectivity for the κ opioid receptor
-
2: A dynorphin analogue with high selectivity for the κ opioid receptor. J. Med. Chem. 43, 2698-2702.
-
(2000)
J. Med. Chem.
, vol.43
, pp. 2698-2702
-
-
Schlechtingen, G.1
Zhang, L.2
Maycock, A.3
DeHaven, R.N.4
Daubert, J.D.5
Cassel, J.6
Chung, N.N.7
Schiller, P.W.8
Goodman, M.9
-
23
-
-
0035855594
-
2 analogues lacking an N-terminal amino group: Potent and selective κ opioid antagonists
-
2 analogues lacking an N-terminal amino group: Potent and selective κ opioid antagonists. J. Med. Chem. 44, 3048-3053.
-
(2001)
J. Med. Chem.
, vol.44
, pp. 3048-3053
-
-
Lu, Y.1
Nguyen, T.M.-D.2
Weltrowska, G.3
Berezowska, I.4
Lemieux, C.5
Chung, N.N.6
Schiller, P.W.7
-
24
-
-
0027372945
-
Acetalins: Opioid receptor antagonists determined through the use of synthetic peptide combinatorial libraries
-
Dooley, C.T., Chung, N.N., Schiller, P.W. & Houghten, R.A. (1993) Acetalins: opioid receptor antagonists determined through the use of synthetic peptide combinatorial libraries. Proc. Natl. Acad. Sci. USA 90, 10811-10815.
-
(1993)
Proc. Natl. Acad. Sci. USA
, vol.90
, pp. 10811-10815
-
-
Dooley, C.T.1
Chung, N.N.2
Schiller, P.W.3
Houghten, R.A.4
-
26
-
-
0012051289
-
The use of the message-address concept in the design of potential antagonists based on dynorphin A
-
(Kaumaya, T.P. & Hodges, R.S., eds). Mayflower Scientific Ltd., West Midlands, UK
-
Kulkarni, S.N., Choi, H., Murray, T.F., DeLander, G.E. & Aldrich, J.V. (1996) The use of the message-address concept in the design of potential antagonists based on dynorphin A. In: Peptides: Chemistry, Structure and Biology (Kaumaya, T.P. & Hodges, R.S., eds), pp. 655-656, Mayflower Scientific Ltd., West Midlands, UK.
-
(1996)
Peptides: Chemistry, Structure and Biology
, pp. 655-656
-
-
Kulkarni, S.N.1
Choi, H.2
Murray, T.F.3
DeLander, G.E.4
Aldrich, J.V.5
-
27
-
-
0012077131
-
-
Pacifichem 2000, Honolulu, HI
-
Aldrich, J.V., Wan, Q. & Murray, T.F. (2000) Identification of Novel Kappa Opioid Receptor Selective Peptides from a Combinatorial Library. Pacifichem 2000, Honolulu, HI.
-
(2000)
Identification of Novel Kappa Opioid Receptor Selective Peptides from a Combinatorial Library
-
-
Aldrich, J.V.1
Wan, Q.2
Murray, T.F.3
-
28
-
-
0037137590
-
Identification of arodyn, a novel acetylated dynorphin A-(1-11) analogue, as a kappa opioid receptor antagonist
-
Bennett, M.A., Murray, T.F. & Aldrich, J.V. (2002) Identification of arodyn, a novel acetylated dynorphin A-(1-11) analogue, as a kappa opioid receptor antagonist. J. Med. Chem. 45, 5617-5619.
-
(2002)
J. Med. Chem.
, vol.45
, pp. 5617-5619
-
-
Bennett, M.A.1
Murray, T.F.2
Aldrich, J.V.3
-
29
-
-
2942735425
-
An inexpensive, manually operated, solid-phase, parallel synthesizer
-
Vig, B.S. & Aldrich, J.V. (2003) An inexpensive, manually operated, solid-phase, parallel synthesizer. Aldrichimica Acta 37, 2.
-
(2003)
Aldrichimica Acta
, vol.37
, pp. 2
-
-
Vig, B.S.1
Aldrich, J.V.2
-
30
-
-
33845312505
-
Advantageous application of azabenzotriazole (triazolopyridine)-based coupling reagents to solid-phase peptide synthesis
-
Carpino, L.A., El-Faham, A., Minor, C.A. & Albericio, F. (1994) Advantageous application of azabenzotriazole (triazolopyridine)-based coupling reagents to solid-phase peptide synthesis. J. Chem. Soc., Chem. Comm, 101-103.
-
(1994)
J. Chem. Soc., Chem. Comm.
, pp. 101-103
-
-
Carpino, L.A.1
El-Faham, A.2
Minor, C.A.3
Albericio, F.4
-
31
-
-
0014772602
-
Color test for detection of free terminal amino groups in the solid-phase synthesis of peptides
-
Kaiser, E., Colescott, R.L., Bossinger, C.D. & Cook, P.L. (1970) Color test for detection of free terminal amino groups in the solid-phase synthesis of peptides. Anal. Biochem 34, 595-598.
-
(1970)
Anal. Biochem.
, vol.34
, pp. 595-598
-
-
Kaiser, E.1
Colescott, R.L.2
Bossinger, C.D.3
Cook, P.L.4
-
32
-
-
0029330768
-
Detection of secondary amines on solid phase
-
Vojkovsky, T. (1995) Detection of secondary amines on solid phase. Pept. Res. 8, 236-237.
-
(1995)
Pept. Res.
, vol.8
, pp. 236-237
-
-
Vojkovsky, T.1
-
34
-
-
0031003877
-
Synthesis and opioid activity of conformationally constrained dynorphin A analogues. 2. Conformational constraint in the "address" sequence
-
Arttamangkul, S., Ishmael, J.E., Murray, T.F., Grandy, D.K., DeLander, G.E., Kieffer, B.L. & Aldrich, I.V. (1997) Synthesis and opioid activity of conformationally constrained dynorphin A analogues. 2. Conformational constraint in the "address" sequence. J. Med. Chem. 40, 1211-1218.
-
(1997)
J. Med. Chem.
, vol.40
, pp. 1211-1218
-
-
Arttamangkul, S.1
Ishmael, J.E.2
Murray, T.F.3
Grandy, D.K.4
DeLander, G.E.5
Kieffer, B.L.6
Aldrich, I.V.7
-
37
-
-
0026494942
-
Effect of modification of the basic residues of dynorphin A-(1-13] amide on κ opioid receptor selectivity and opioid activity
-
Snyder, K.R., Story, S.C., Heidt, M.E., Murray, T.F., DeLander, G.E. & Aldrich, J.V. (1992) Effect of modification of the basic residues of dynorphin A-(1-13] amide on κ opioid receptor selectivity and opioid activity. J. Med. Chem. 35, 4330-4333.
-
(1992)
J. Med. Chem.
, vol.35
, pp. 4330-4333
-
-
Snyder, K.R.1
Story, S.C.2
Heidt, M.E.3
Murray, T.F.4
DeLander, G.E.5
Aldrich, J.V.6
-
38
-
-
0021259551
-
Dynorphin-(1-13) I. Structure-function relationships of Ala-containing analogs
-
Turcotte, A., Lalonde, J.-M., St-Pierre, S. & Lemaire, S. (1984) Dynorphin-(1-13) I. Structure-function relationships of Ala-containing analogs. Int. J. Pept. Protein Res. 13, 361-367.
-
(1984)
Int. J. Pept. Protein Res.
, vol.13
, pp. 361-367
-
-
Turcotte, A.1
Lalonde, J.-M.2
St-Pierre, S.3
Lemaire, S.4
-
39
-
-
0027364033
-
Syntheses, opioid binding affinities, and potencies of dynorphin A analogues substituted in positions 1, 6, 7, 8 and 10
-
Kawasaki, A.M., Knapp, R.J., Walton, A., Wire, W.S., Zalewska, T., Yamamura, H.I., Porreca, F., Burks, T.F. & Hruby, V.J. (1993) Syntheses, opioid binding affinities, and potencies of dynorphin A analogues substituted in positions 1, 6, 7, 8 and 10. Int. J. Pept. Protein Res. 41, 411-419.
-
(1993)
Int. J. Pept. Protein Res.
, vol.41
, pp. 411-419
-
-
Kawasaki, A.M.1
Knapp, R.J.2
Walton, A.3
Wire, W.S.4
Zalewska, T.5
Yamamura, H.I.6
Porreca, F.7
Burks, T.F.8
Hruby, V.J.9
-
40
-
-
0033600840
-
Ligands for κ-opioid and ORL1 receptors identified from a conformationally constrained peptide combinatorial library
-
Becker, J.A.J., Wallace, A., Garzon, A., Ingallinella, P., Bianchi, E., Cortese, R., Simonin, F., Kieffer, B.L. & Pessi, A. (1999) Ligands for κ-opioid and ORL1 receptors identified from a conformationally constrained peptide combinatorial library. J. Biol Chem. 274, 27513-27522.
-
(1999)
J. Biol Chem.
, vol.274
, pp. 27513-27522
-
-
Becker, J.A.J.1
Wallace, A.2
Garzon, A.3
Ingallinella, P.4
Bianchi, E.5
Cortese, R.6
Simonin, F.7
Kieffer, B.L.8
Pessi, A.9
|