-
1
-
-
0027070864
-
Peptide stability in drug development: A comparison of peptide reactivity in different biological media
-
M. F. Powell, H. Grey, F. Gaeta, A. Sette, and S. Colon. Peptide stability in drug development: a comparison of peptide reactivity in different biological media. J. Pharm. Sci. 81:731-735 (1992).
-
(1992)
J. Pharm. Sci.
, vol.81
, pp. 731-735
-
-
Powell, M.F.1
Grey, H.2
Gaeta, F.3
Sette, A.4
Colon, S.5
-
2
-
-
0019966290
-
Dynorphin-(1-13): Effects in non-tolerant and morphine -dependent rhesus monkeys
-
M. D. Aceto, W. L. Dewey, J. K. Chang, and N. M. Lee. Dynorphin-(1-13): effects in non-tolerant and morphine -dependent rhesus monkeys. Eur. J. Pharmacol. 83:139-142 (1982).
-
(1982)
Eur. J. Pharmacol.
, vol.83
, pp. 139-142
-
-
Aceto, M.D.1
Dewey, W.L.2
Chang, J.K.3
Lee, N.M.4
-
3
-
-
0023818946
-
Dynorphin A(1-13) attenuates withdrawal in morphine-dependent rats: Effect of route of administration
-
P. G. Green and N. M. Lee. Dynorphin A(1-13) attenuates withdrawal in morphine-dependent rats: Effect of route of administration. Eur. J. Pharmacol. 145:267-272 (1988).
-
(1988)
Eur. J. Pharmacol.
, vol.145
, pp. 267-272
-
-
Green, P.G.1
Lee, N.M.2
-
4
-
-
0026730434
-
Suppression by dynorphin A(1-13) of the expression of opiate withdrawal and tolerance in mice
-
A. E. Takemori, H. H. Loh, and N. M. Lee. Suppression by dynorphin A(1-13) of the expression of opiate withdrawal and tolerance in mice. Eur. J. Pharmacol. 221:223-226 (1992).
-
(1992)
Eur. J. Pharmacol.
, vol.221
, pp. 223-226
-
-
Takemori, A.E.1
Loh, H.H.2
Lee, N.M.3
-
5
-
-
0019962504
-
Suppression of withdrawal symptoms by dynorphin in heroin addicts
-
H. Wen and W. Ho. Suppression of withdrawal symptoms by dynorphin in heroin addicts. Eur. J. Pharmacol. 82:183-186 (1982).
-
(1982)
Eur. J. Pharmacol.
, vol.82
, pp. 183-186
-
-
Wen, H.1
Ho, W.2
-
6
-
-
0028903447
-
Dynorphin A modulates acute and chronic opioid effects
-
L. P. Hooke and N. M. Lee. Dynorphin A modulates acute and chronic opioid effects. J. Pharmacol. Exp. Ther. 273:292-297 (1995).
-
(1995)
J. Pharmacol. Exp. Ther.
, vol.273
, pp. 292-297
-
-
Hooke, L.P.1
Lee, N.M.2
-
7
-
-
0019779623
-
Possible regulatory role of dynorphin on morphine- and endorphin-dependent analgesia
-
F. C. Tulunay, M. F. Jen, J. K. Chang, H. H. Loh, and N. M. Lee. Possible regulatory role of dynorphin on morphine- and endorphin-dependent analgesia. J. Pharmacol. Exp. Ther. 219:296-298 (1981).
-
(1981)
J. Pharmacol. Exp. Ther.
, vol.219
, pp. 296-298
-
-
Tulunay, F.C.1
Jen, M.F.2
Chang, J.K.3
Loh, H.H.4
Lee, N.M.5
-
8
-
-
0028990456
-
1] Dynorphin A-(2-17) has naloxone-insensitive antinociceptive effect in the writhing assay
-
1] Dynorphin A-(2-17) has naloxone-insensitive antinociceptive effect in the writhing assay. J. Pharmacol. Exp. Ther. 273:802-807 (1995).
-
(1995)
J. Pharmacol. Exp. Ther.
, vol.273
, pp. 802-807
-
-
Hooke, L.P.1
He, L.2
Lee, N.M.3
-
9
-
-
0021340220
-
Comparison of the effectiveness of different opioid peptides in suppressing heroin withdrawal
-
H. L. Wen, W. K. K. Ho, and P. Y. Wen. Comparison of the effectiveness of different opioid peptides in suppressing heroin withdrawal. Eur. J. Pharmacol. 100:155-162 (1984).
-
(1984)
Eur. J. Pharmacol.
, vol.100
, pp. 155-162
-
-
Wen, H.L.1
Ho, W.K.K.2
Wen, P.Y.3
-
11
-
-
0031745966
-
Effects of dynorphin A(1-13) on opiate withdrawal in humans
-
S. Specker, W. Wananukul, D. Hatsukami, K. Nolin, L. Hooke, M. J. Kreek, and P. R. Pentel. Effects of dynorphin A(1-13) on opiate withdrawal in humans. Psychopharmacology (Berl.) 137:326-332 (1998).
-
(1998)
Psychopharmacology (Berl.)
, vol.137
, pp. 326-332
-
-
Specker, S.1
Wananukul, W.2
Hatsukami, D.3
Nolin, K.4
Hooke, L.5
Kreek, M.J.6
Pentel, P.R.7
-
12
-
-
0029096691
-
Metabolism of dynorphin A(1-13) in human blood and plasma
-
S. Muller and G. Hochhaus. Metabolism of dynorphin A(1-13) in human blood and plasma. Pharm. Res. 12:1165-1170 (1995).
-
(1995)
Pharm. Res.
, vol.12
, pp. 1165-1170
-
-
Muller, S.1
Hochhaus, G.2
-
13
-
-
0031847602
-
Pharmacokinetics of intravenous dynorphin A(1-13) in opioid-naive and opioid-treated human volunteers
-
P. L. Gambus, T. W. Schnider, C. F. Minto, E. J. Youngs, V. Billard, W. G. Brose, G. Hochhaus, and S. L. Shafer. Pharmacokinetics of intravenous dynorphin A(1-13) in opioid-naive and opioid-treated human volunteers. Clin. Pharmacol. Ther. 64:27-38 (1998).
-
(1998)
Clin. Pharmacol. Ther.
, vol.64
, pp. 27-38
-
-
Gambus, P.L.1
Schnider, T.W.2
Minto, C.F.3
Youngs, E.J.4
Billard, V.5
Brose, W.G.6
Hochhaus, G.7
Shafer, S.L.8
-
14
-
-
0027464946
-
Effect of N-methyl substitution of the peptide bonds in luteinizing hormone-releasing hormone agonists
-
F. Haviv, T. D. Fitzpatrick, R. E. Swenson, C. J. Nichols, N. A. Mort, E. N. Bush, G. Diaz, G. Bammert, A. Nguyen, and N. S. Rhutasel. Effect of N-methyl substitution of the peptide bonds in luteinizing hormone-releasing hormone agonists. J. Med. Chem. 36:363-369 (1993).
-
(1993)
J. Med. Chem.
, vol.36
, pp. 363-369
-
-
Haviv, F.1
Fitzpatrick, T.D.2
Swenson, R.E.3
Nichols, C.J.4
Mort, N.A.5
Bush, E.N.6
Diaz, G.7
Bammert, G.8
Nguyen, A.9
Rhutasel, N.S.10
-
15
-
-
0021833338
-
Enkephalin pseudopeptides: Resistance to in vitro proteolytic degradation afforded by amide bond replacements extends to remote sites
-
D. E. Benovitzand and A. F. Spatola. Enkephalin pseudopeptides: resistance to in vitro proteolytic degradation afforded by amide bond replacements extends to remote sites. Peptides 6:257-261 (1985).
-
(1985)
Peptides
, vol.6
, pp. 257-261
-
-
Benovitzand, D.E.1
Spatola, A.F.2
-
17
-
-
0028808566
-
In vitro stability of some reduced peptide bond pseudopeptide analogues of dynorphin A
-
J. P. Meyer, T. J. Gillespie, S. Hom, V. J. Hruby, and T. P. Davis. In vitro stability of some reduced peptide bond pseudopeptide analogues of dynorphin A. Peptides 16:1215-1219 (1995).
-
(1995)
Peptides
, vol.16
, pp. 1215-1219
-
-
Meyer, J.P.1
Gillespie, T.J.2
Hom, S.3
Hruby, V.J.4
Davis, T.P.5
-
18
-
-
0021905444
-
Dynamics and conformational energetics of a peptide hormone: Vasopressin
-
A. T. Hagler, D. J. Osguthorpe, P. Dauber-Osguthorpe, and J. C. Hempel. Dynamics and conformational energetics of a peptide hormone: vasopressin. Science 227:1309-1315 (1985).
-
(1985)
Science
, vol.227
, pp. 1309-1315
-
-
Hagler, A.T.1
Osguthorpe, D.J.2
Dauber-Osguthorpe, P.3
Hempel, J.C.4
-
19
-
-
0033829152
-
Dynorphin A(2-17) attenuates the unconditioned but not the conditioned effects of opiate withdrawal in the rat
-
T. S. Shippenberg, M. Funada, and C. G. Schutz. Dynorphin A(2-17) attenuates the unconditioned but not the conditioned effects of opiate withdrawal in the rat. Psychopharmacology (Berl.) 151:351-358 (2000).
-
(2000)
Psychopharmacology (Berl.)
, vol.151
, pp. 351-358
-
-
Shippenberg, T.S.1
Funada, M.2
Schutz, C.G.3
-
20
-
-
0034253821
-
Dynorphin: Friend or foe?
-
R. C. Caudle and A. J. Mannes. Dynorphin: friend or foe? Pain 87:235-239 (2000).
-
(2000)
Pain
, vol.87
, pp. 235-239
-
-
Caudle, R.C.1
Mannes, A.J.2
-
21
-
-
0020463686
-
Dynorphin(1-10)amide: A potent and selective analog of dynorphin(1-13)
-
S. Woo, J. Garzon, P. Sanchez-Blazquez, F. C. Tulunay, J. K. Chang, and H. H. Loh. Dynorphin(1-10)amide: a potent and selective analog of dynorphin(1-13). Life Sci. 31:1817-1820 (1982).
-
(1982)
Life Sci.
, vol.31
, pp. 1817-1820
-
-
Woo, S.1
Garzon, J.2
Sanchez-Blazquez, P.3
Tulunay, F.C.4
Chang, J.K.5
Loh, H.H.6
-
22
-
-
0029076399
-
Effects of high intravenous doses of dynorphin A(1-13) on tail flick latency and central nervous system histology in rats
-
P. R. Pentel, W. Wananukul, L. P. Hooke, C. R. N. Jones, D. Hatsukami, W. R. Anderson, and N. M. Lee. Effects of high intravenous doses of dynorphin A(1-13) on tail flick latency and central nervous system histology in rats. Pharm. Biochem. Behav. 51:387-390 (1995).
-
(1995)
Pharm. Biochem. Behav.
, vol.51
, pp. 387-390
-
-
Pentel, P.R.1
Wananukul, W.2
Hooke, L.P.3
Jones, C.R.N.4
Hatsukami, D.5
Anderson, W.R.6
Lee, N.M.7
-
23
-
-
0002261078
-
A method for determining loss of pain sensation
-
F. E. Damourand and D. L. Smith. A method for determining loss of pain sensation. J. Pharmacol. Exp. Ther. 72:74-79 (1941).
-
(1941)
J. Pharmacol. Exp. Ther.
, vol.72
, pp. 74-79
-
-
Damourand, F.E.1
Smith, D.L.2
-
24
-
-
0035201698
-
Buprenorphine substitution ameliorates spontaneous withdrawal in fentanyl-dependent rat pups
-
A. B. Lohmann and F. L. Smith. Buprenorphine substitution ameliorates spontaneous withdrawal in fentanyl-dependent rat pups. Pediatr. Res. 49:50-55 (2001).
-
(2001)
Pediatr. Res.
, vol.49
, pp. 50-55
-
-
Lohmann, A.B.1
Smith, F.L.2
-
25
-
-
0000977039
-
Some narcotic antagonists in the benzomorphan series
-
L. S. Harris and A. K. Pierson. Some narcotic antagonists in the benzomorphan series. J. Pharmacol. Exp. Ther. 143:141-148 (1964).
-
(1964)
J. Pharmacol. Exp. Ther.
, vol.143
, pp. 141-148
-
-
Harris, L.S.1
Pierson, A.K.2
-
26
-
-
0011118368
-
Novel activity of human angiotensin I converting enzyme: Release of the NH2- and COOH-terminal tripeptides from the luteinizing hormone-releasing hormone
-
R. A. Skidgel and E. G. Erdos. Novel activity of human angiotensin I converting enzyme: release of the NH2- and COOH-terminal tripeptides from the luteinizing hormone-releasing hormone. Proc. Natl. Acad. Sci. USA 82:1025-1029 (1985).
-
(1985)
Proc. Natl. Acad. Sci. USA
, vol.82
, pp. 1025-1029
-
-
Skidgel, R.A.1
Erdos, E.G.2
-
27
-
-
0021175531
-
Hydrolysis of substance p and neurotensin by converting enzyme and neutral endopeptidase
-
R. A. Skidgel, S. Engelbrecht, A. R. Johnson, and E. G. Erdos. Hydrolysis of substance p and neurotensin by converting enzyme and neutral endopeptidase. Peptides 5:769-776 (1984).
-
(1984)
Peptides
, vol.5
, pp. 769-776
-
-
Skidgel, R.A.1
Engelbrecht, S.2
Johnson, A.R.3
Erdos, E.G.4
-
29
-
-
0019332139
-
Binding of peptide substrates and inhibitors of angiotensin-converting enzyme. Importance of the COOH-terminal dipeptide sequence
-
H. S. Cheung, F. L. Wang, M. A. Ondetti, E. F. Sabo, and D. W. Cushman. Binding of peptide substrates and inhibitors of angiotensin-converting enzyme. Importance of the COOH-terminal dipeptide sequence. J. Biol. Chem. 255:401-407 (1980).
-
(1980)
J. Biol. Chem.
, vol.255
, pp. 401-407
-
-
Cheung, H.S.1
Wang, F.L.2
Ondetti, M.A.3
Sabo, E.F.4
Cushman, D.W.5
-
30
-
-
0022377047
-
High enkephalyl peptide degradation, due to angiotensin-converting enzyme-like activity in human CSF
-
I. Lantzand and L. Terenius. High enkephalyl peptide degradation, due to angiotensin-converting enzyme-like activity in human CSF. FEBS Lett. 193:31-34 (1985).
-
(1985)
FEBS Lett.
, vol.193
, pp. 31-34
-
-
Lantzand, I.1
Terenius, L.2
-
31
-
-
0027364033
-
Syntheses, opioid binding affinities, and potencies of dynorphin A analogues substituted in positions, 1, 6, 7, 8 and 10
-
A. M. Kawasaki, R. J. Knapp, A. Walton, W. S. Wire, T. Zalewska, H. I. Yamamura, F. Porreca, T. F. Burks, and V. J. Hruby. Syntheses, opioid binding affinities, and potencies of dynorphin A analogues substituted in positions, 1, 6, 7, 8 and 10. Int. J. Pept. Protein Res. 42:411-419 (1993).
-
(1993)
Int. J. Pept. Protein Res.
, vol.42
, 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
-
32
-
-
0027366630
-
Suppression by dynorphin a and [des-Tyr1]-dynorphin a peptides of the expression of opiate withdrawal and tolerance in morphine-dependent mice
-
A. E. Takemori, H. H. Loh, and N. M. Lee. Suppression by dynorphin A and [des-Tyr1]-dynorphin A peptides of the expression of opiate withdrawal and tolerance in morphine-dependent mice. J. Pharmacol. Exp. Ther. 266:121-124 (1993).
-
(1993)
J. Pharmacol. Exp. Ther.
, vol.266
, pp. 121-124
-
-
Takemori, A.E.1
Loh, H.H.2
Lee, N.M.3
-
33
-
-
0025213406
-
Analgesia produced by E-2078, a systemically active dynorphin analog, in mice
-
T. Nakazawa, Y. Furuya, T. Kaneko, K. Yamatsu, H. Yoshino, and S. Tachibana. Analgesia produced by E-2078, a systemically active dynorphin analog, in mice. J. Pharmacol. Exp. Ther. 252:1247-1254 (1990).
-
(1990)
J. Pharmacol. Exp. Ther.
, vol.252
, pp. 1247-1254
-
-
Nakazawa, T.1
Furuya, Y.2
Kaneko, T.3
Yamatsu, K.4
Yoshino, H.5
Tachibana, S.6
|