-
1
-
-
0003177483
-
-
4, (R,R)-(-)1,2-bis[(O-methoxyphenyl)(phenyl) phosphino]ethane(1,5-cyclooctadiene)-rhodium(I) tetrafluoroborate; RP-HPLC, reverse-phase high performance liquid chromatography; TFA, trifluoroacetic acid; TLC, thin-layer chromatography.
-
(1985)
J. Biol. Chem.
, vol.260
, pp. 14-42
-
-
-
2
-
-
0016701344
-
Identification of two related pentapeptides from the brain with potent opiate agonist activity
-
Hughes, J.; Smith, T. W.; Kosterlitz, H. W.; Forthergill, L. A.; Morga, B. A.; Morris, H. R. Identification of two related pentapeptides from the brain with potent opiate agonist activity. Nature 1975, 258, 577-579.
-
(1975)
Nature
, vol.258
, pp. 577-579
-
-
Hughes, J.1
Smith, T.W.2
Kosterlitz, H.W.3
Forthergill, L.A.4
Morga, B.A.5
Morris, H.R.6
-
3
-
-
0017189685
-
Morphinomimetics activity of synthetic fragments of β-lipotropin and analogues
-
(a) Ling, N.; Guillemin, R. Morphinomimetics activity of synthetic fragments of β-lipotropin and analogues. Proc. Natl. Acad. Sci. U.S.A. 1976, 7, 3308-3310.
-
(1976)
Proc. Natl. Acad. Sci. U.S.A.
, vol.7
, pp. 3308-3310
-
-
Ling, N.1
Guillemin, R.2
-
4
-
-
0012720356
-
Opioid activity of a peptide β-lipotropin-(61-91), derived form β-lipotropin
-
(b) Cox, B. M.; Goldstein, A.; Li, C. H. Opioid activity of a peptide β-lipotropin-(61-91), derived form β-lipotropin. Proc. Natl. Acad. Sci. U.S.A. 1976, 73, 1821-1823.
-
(1976)
Proc. Natl. Acad. Sci. U.S.A.
, vol.73
, pp. 1821-1823
-
-
Cox, B.M.1
Goldstein, A.2
Li, C.H.3
-
5
-
-
0019638380
-
Porcine pituitary dynorphin: Complete amino acid sequence of the biologically active heptadecapeptide
-
Goldstein, A.; Fischli, W.; Lowney, L. I.; Hunkapilier, M.; Hood, L. Porcine pituitary dynorphin: Complete amino acid sequence of the biologically active heptadecapeptide. Proc. Natl. Acad. Sci. U.S.A. 1981, 78, 7219-7223.
-
(1981)
Proc. Natl. Acad. Sci. U.S.A.
, vol.78
, pp. 7219-7223
-
-
Goldstein, A.1
Fischli, W.2
Lowney, L.I.3
Hunkapilier, M.4
Hood, L.5
-
7
-
-
0030933655
-
A potent and selective endogenous agonist for the μ-opiate receptor
-
(a) Zadina, J. E.; Hackler, L.; Ge, L.-J.; Kastin, A. J. A potent and selective endogenous agonist for the μ-opiate receptor. Nature 1997, 386, 499-502.
-
(1997)
Nature
, vol.386
, pp. 499-502
-
-
Zadina, J.E.1
Hackler, L.2
Ge, L.-J.3
Kastin, A.J.4
-
8
-
-
0031426851
-
Isolation of relatively large amounts of endomorphin-1 and endomorphin-2 form human brain cortex
-
(b) Hackler, L.; Zadina, J. E.; Ge, L.-J.; Kastin, A. J. Isolation of relatively large amounts of endomorphin-1 and endomorphin-2 form human brain cortex. Peptides 1997, 18, 1635-1639.
-
(1997)
Peptides
, vol.18
, pp. 1635-1639
-
-
Hackler, L.1
Zadina, J.E.2
Ge, L.-J.3
Kastin, A.J.4
-
9
-
-
0030272919
-
The dermorphin peptide family
-
Melchiorri, P.; Negri, L. The dermorphin peptide family. Gen. Pharmacol. 1996, 27, 1099-1107.
-
(1996)
Gen. Pharmacol.
, vol.27
, pp. 1099-1107
-
-
Melchiorri, P.1
Negri, L.2
-
10
-
-
0032928689
-
What peptides these deltorphins be
-
Lazarus, L. H.; Bryant, S. D.; Cooper, P. S.; Salvadori, S. What peptides these deltorphins be. Prog. Neurobiol. 1999, 57, 377-420.
-
(1999)
Prog. Neurobiol.
, vol.57
, pp. 377-420
-
-
Lazarus, L.H.1
Bryant, S.D.2
Cooper, P.S.3
Salvadori, S.4
-
11
-
-
0024405504
-
Bivalent ligands and the message-address concept in the design of selective opioid receptor antagonists
-
Portoghese, P. S. Bivalent ligands and the message-address concept in the design of selective opioid receptor antagonists. Trends Pharmacol. Sci. 1989, 10, 230-235.
-
(1989)
Trends Pharmacol. Sci.
, vol.10
, pp. 230-235
-
-
Portoghese, P.S.1
-
12
-
-
0030880687
-
Evolution of the Dmt-Tic pharmacophore: N-terminal methylated derivatives with extraordinary δ opioid antagonist activity
-
(a) Salvadori, S.; Balboni, G.; Guerrini, R.; Tomatis, R.; Bianchi, C.; Bryant, S. D.; Copper, P. S.; Lazarus, L. H. Evolution of the Dmt-Tic pharmacophore: N-terminal methylated derivatives with extraordinary δ opioid antagonist activity. J. Med. Chem. 1997, 40, 3100-3108.
-
(1997)
J. Med. Chem.
, vol.40
, pp. 3100-3108
-
-
Salvadori, S.1
Balboni, G.2
Guerrini, R.3
Tomatis, R.4
Bianchi, C.5
Bryant, S.D.6
Copper, P.S.7
Lazarus, L.H.8
-
13
-
-
0033539134
-
2[Ψ] produces a potent analgesic effect, no physical dependence, and less tolerance that morphine in rats
-
2[Ψ] produces a potent analgesic effect, no physical dependence, and less tolerance that morphine in rats. J. Med. Chem. 1999, 42, 3520-3526.
-
(1999)
J. Med. Chem.
, vol.42
, pp. 3520-3526
-
-
Schiller, P.W.1
Fundytus, M.E.2
Merovitz, L.3
Weltrowska, G.4
Nguyen, T.M.-D.5
Lemieux, C.6
Chung, N.N.7
Coderre, T.J.8
-
14
-
-
0033518261
-
Further studies on the Dmt-Tic pharmacophore: Hydrophobic substituents at the C-terminus endow δ antagonists to manifest μ agonism or μ antagonism
-
(c) Salvadori, S.; Guerrini, R.; Balboni, G.; Bianchi, C.; Bryant, S. D.; Copper, P. S.; Lazarus, L. H. Further studies on the Dmt-Tic pharmacophore: Hydrophobic substituents at the C-terminus endow δ antagonists to manifest μ agonism or μ antagonism. J. Med. Chem. 1999, 42, 5010-5019.
-
(1999)
J. Med. Chem.
, vol.42
, pp. 5010-5019
-
-
Salvadori, S.1
Guerrini, R.2
Balboni, G.3
Bianchi, C.4
Bryant, S.D.5
Copper, P.S.6
Lazarus, L.H.7
-
15
-
-
0035913055
-
Novel C-terminus modifications of the Dmt-Tic motif: A new class of dipeptide analogues showing altered pharmacological profiles toward the opioid receptors
-
(d) Page, D.; Naismith, A.; Schmidt, R.; Coupal, M.; Labarre, M.; Gosselin, M.; Bellemare, D.; Payza, K.; Brown, W. Novel C-terminus modifications of the Dmt-Tic motif: A new class of dipeptide analogues showing altered pharmacological profiles toward the opioid receptors. J. Med. Chem. 2001, 44, 2387-2390.
-
(2001)
J. Med. Chem.
, vol.44
, pp. 2387-2390
-
-
Page, D.1
Naismith, A.2
Schmidt, R.3
Coupal, M.4
Labarre, M.5
Gosselin, M.6
Bellemare, D.7
Payza, K.8
Brown, W.9
-
16
-
-
0037204052
-
Evaluation of the Dmt-Tic pharmacophore: Conversion of a potent δ opioid antagonist into a potent δ opioid agonist and ligands with mixed properties
-
(e) Balboni, G.; Guerrini, R.; Salvadori, S.; Bianchi, C.; Rizzi, D.; Bryant, S. D.; Lazarus, L. H. Evaluation of the Dmt-Tic pharmacophore: Conversion of a potent δ opioid antagonist into a potent δ opioid agonist and ligands with mixed properties. J. Med. Chem. 2002, 45, 713-720.
-
(2002)
J. Med. Chem.
, vol.45
, pp. 713-720
-
-
Balboni, G.1
Guerrini, R.2
Salvadori, S.3
Bianchi, C.4
Rizzi, D.5
Bryant, S.D.6
Lazarus, L.H.7
-
17
-
-
0345714625
-
Synthesis and opioid activity of N,N-dimethyl-Dmt-Tic-NH-CH(R)-R′ analogues: Acquisition of potent δ antagonism
-
(f) Balboni, G.; Salvadori, S.; Guerrini, R.; Negri, L.; Giannini, E.; Bryant, S. D.; Jinsmaa, J.; Lazarus, L. H. Synthesis and opioid activity of N,N-dimethyl-Dmt-Tic-NH-CH(R)-R′ analogues: Acquisition of potent δ antagonism. Bioorg. Med. Chem. 2003, 11, 5435-5441.
-
(2003)
Bioorg. Med. Chem.
, vol.11
, pp. 5435-5441
-
-
Balboni, G.1
Salvadori, S.2
Guerrini, R.3
Negri, L.4
Giannini, E.5
Bryant, S.D.6
Jinsmaa, J.7
Lazarus, L.H.8
-
18
-
-
0031857993
-
Design of δ-opioid peptide antagonists for emerging drug application
-
(a) Lazarus, L. H.; Bryant, S. D.; Cooper, P. S.; Guerrini, R.; Balboni, G.; Salvadori, S. Design of δ-opioid peptide antagonists for emerging drug application. Drug Discovery Today 1998, 3, 284-294.
-
(1998)
Drug Discovery Today
, vol.3
, pp. 284-294
-
-
Lazarus, L.H.1
Bryant, S.D.2
Cooper, P.S.3
Guerrini, R.4
Balboni, G.5
Salvadori, S.6
-
19
-
-
0037781997
-
Dmt and opioid peptides: A potent alliance
-
(b) Bryant, S. D.; Jinsmaa, Y.; Salvadori, S.; Okada, Y.; Lazarus, L. H. Dmt and opioid peptides: A potent alliance. Biopolymers (Pept. Sci.) 2003, 71, 86-102.
-
(2003)
Biopolymers (Pept. Sci.)
, vol.71
, pp. 86-102
-
-
Bryant, S.D.1
Jinsmaa, Y.2
Salvadori, S.3
Okada, Y.4
Lazarus, L.H.5
-
20
-
-
0026602250
-
Preparation and opioid activity of analogues of the analgesic dipeptide 2, 6-dimethyl-l-tyrosyl-N-(3-phenylpropyl)-d-alaninamide
-
(a) Chandrakumar, N. S.; Yonan, P. K.; Stapelfeld, A.; Savage, M.; Rorbacher, E.; Contreras, P. C.; Hammond, D. Preparation and opioid activity of analogues of the analgesic dipeptide 2, 6-dimethyl-l-tyrosyl-N-(3-phenylpropyl)- d-alaninamide. J. Med. Chem. 1992, 35, 223-233.
-
(1992)
J. Med. Chem.
, vol.35
, pp. 223-233
-
-
Chandrakumar, N.S.1
Yonan, P.K.2
Stapelfeld, A.3
Savage, M.4
Rorbacher, E.5
Contreras, P.C.6
Hammond, D.7
-
21
-
-
0026578014
-
5]enkephalin
-
5]enkephalin. J. Med. Chem. 1992, 35, 684-687.
-
(1992)
J. Med. Chem.
, vol.35
, pp. 684-687
-
-
Hansen, J.D.W.1
Stapelfeld, A.2
Savage, M.A.3
Reichman, M.4
Hammond, D.L.5
Haaseth, R.C.6
Mosberg, H.I.7
-
22
-
-
0032713301
-
Biological properties of opioid peptides replacing Tyr at position 1 by 2,6-dimethyl-Tyr
-
(c) Sasaki, Y.; Suto, T.; Ambo, A.; Ouchi, H.; Yamamoto Y. Biological properties of opioid peptides replacing Tyr at position 1 by 2,6-dimethyl-Tyr. Chem. Pharm. Bull. 1999, 47, 1506-1509.
-
(1999)
Chem. Pharm. Bull.
, vol.47
, pp. 1506-1509
-
-
Sasaki, Y.1
Suto, T.2
Ambo, A.3
Ouchi, H.4
Yamamoto, Y.5
-
23
-
-
0034000876
-
Novel ligands lacking a positive charge for the δ-and μ-opioid receptors
-
(d) Schiller, P. W.; Berezowska, I.; Nguyen, T. M.-D.; Schimidt, R.; Lemieux, C.; Chung, N. N.; Falcone-Hindley, M. L.; Yao, W.; Liu, J.; Iwama, S.; Smith, A. B.; Hirschmann, R. Novel ligands lacking a positive charge for the δ-and μ-opioid receptors. J. Med. Chem. 2000, 43, 551-559.
-
(2000)
J. Med. Chem.
, vol.43
, pp. 551-559
-
-
Schiller, P.W.1
Berezowska, I.2
Nguyen, T.M.-D.3
Schimidt, R.4
Lemieux, C.5
Chung, N.N.6
Falcone-Hindley, M.L.7
Yao, W.8
Liu, J.9
Iwama, S.10
Smith, A.B.11
Hirschmann, R.12
-
24
-
-
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. 2001, 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
Lemiex, C.5
Chung, N.N.6
Schiller, P.W.7
-
25
-
-
0035847697
-
Enkephalin analogues with 2′,6′-dimethylphenylalanine replacing phenylalanine in position 4
-
(f) Sasaki, Y.; Hirabuki, M.; Ambo, A.; Ouchi, H.; Yamamoto, Y. Enkephalin analogues with 2′,6′-dimethylphenylalanine replacing phenylalanine in position 4. Bioorg. Med. Chem. Lett. 2001, 11, 327-329.
-
(2001)
Bioorg. Med. Chem. Lett.
, vol.11
, pp. 327-329
-
-
Sasaki, Y.1
Hirabuki, M.2
Ambo, A.3
Ouchi, H.4
Yamamoto, Y.5
-
26
-
-
0037468538
-
2,6-Dimethyltyrosine analogues of a stereodiversified ligand library: Highly potent, selective, nonpeptidic μ opioid receptor agonists
-
(g) Harrison, B. A.; Pasternak, G. W.; Verdine, G. L. 2,6-Dimethyltyrosine analogues of a stereodiversified ligand library: Highly potent, selective, nonpeptidic μ opioid receptor agonists. J. Med. Chem. 2003, 46, 677-680.
-
(2003)
J. Med. Chem.
, vol.46
, pp. 677-680
-
-
Harrison, B.A.1
Pasternak, G.W.2
Verdine, G.L.3
-
27
-
-
1542511365
-
A chimeric opioid peptide with mixed μ agonist/δ antagonist properties
-
(h) Weltrowska, G.; Lemieux, C.; Chung, N. N.; Schiller, P. W. A chimeric opioid peptide with mixed μ agonist/δ antagonist properties. J. Pept. Res. 2004, 63, 63-68.
-
(2004)
J. Pept. Res.
, vol.63
, pp. 63-68
-
-
Weltrowska, G.1
Lemieux, C.2
Chung, N.N.3
Schiller, P.W.4
-
28
-
-
0037401355
-
1]endomorphin-2 analogues: Enhanced activity and cis orientation of the Dmt-Pro amide bond
-
1]endomorphin-2 analogues: Enhanced activity and cis orientation of the Dmt-Pro amide bond. Bioorg. Med. Chem. 2003, 11, 1983-1984.
-
(2003)
Bioorg. Med. Chem.
, vol.11
, pp. 1983-1984
-
-
Okada, Y.1
Fujita, Y.2
Motoyama, T.3
Tsuda, Y.4
Yokoi, T.5
Li, T.6
Sasaki, Y.7
Ambo, A.8
Jinsmaa, Y.9
Bryant, S.D.10
Lazarus, L.H.11
-
29
-
-
3042599035
-
Development of potent bifunctional endomorphin-2 analogues with mixed μ/δ-opioid agonist and δ-opioid antagonist properties
-
(b) Fujita, Y.; Tsuda, Y.; Li, T.; Motoyama, T.; Takahashi, M.; Shimizu, Y.; Yokoi, T.; Sasaki, Y.; Ambo, A.; Kita, A.; Jinsmaa, Y.; Bryant, S. D.; Lazarus, L. H.; Okada, Y. Development of potent bifunctional endomorphin-2 analogues with mixed μ/δ-opioid agonist and δ-opioid antagonist properties. J. Med. Chem. 2004, 47, 3591-3599.
-
(2004)
J. Med. Chem.
, vol.47
, pp. 3591-3599
-
-
Fujita, Y.1
Tsuda, Y.2
Li, T.3
Motoyama, T.4
Takahashi, M.5
Shimizu, Y.6
Yokoi, T.7
Sasaki, Y.8
Ambo, A.9
Kita, A.10
Jinsmaa, Y.11
Bryant, S.D.12
Lazarus, L.H.13
Okada, Y.14
-
30
-
-
0038155285
-
Unique high-affinity synthetic μ-opioid receptor agonists with central-and systemic-mediated analgesia
-
Okada, Y.; Tsuda, Y.; Fujita, Y.; Yokoi, T.; Sasaki, Y.; Ambo, A.; Konishi, R.; Nagata, M.; Salvadori, S.; Jinsmaa, Y.; Bryant, S. D.; Lazarus, L. H. Unique high-affinity synthetic μ-opioid receptor agonists with central-and systemic-mediated analgesia. J. Med. Chem. 2003, 46, 3201-3209.
-
(2003)
J. Med. Chem.
, vol.46
, pp. 3201-3209
-
-
Okada, Y.1
Tsuda, Y.2
Fujita, Y.3
Yokoi, T.4
Sasaki, Y.5
Ambo, A.6
Konishi, R.7
Nagata, M.8
Salvadori, S.9
Jinsmaa, Y.10
Bryant, S.D.11
Lazarus, L.H.12
-
31
-
-
2342572941
-
n]-2(1H)-pyrazinone with central-mediated analgesia
-
n]-2(1H)-pyrazinone with central-mediated analgesia. J. Med. Chem. 2004, 47, 2599-2610.
-
(2004)
J. Med. Chem.
, vol.47
, pp. 2599-2610
-
-
Jinsmaa, Y.1
Miyazaki, A.2
Fujita, Y.3
Li, T.4
Fujisawa, Y.5
Shiotani, K.6
Tsuda, Y.7
Yokoi, T.8
Ambo, A.9
Sasaki, Y.10
Bryant, S.D.11
Lazarus, L.H.12
Okada, Y.13
-
32
-
-
0017355395
-
Comparison of the analgesic properties of lipotropin C-fragment and stabilized enkephalins in the rat
-
Bradbury, A. F.; Smyth, D. G.; Snell, C. R.; Deakin, J. E. W.; Wendlandt, S. Comparison of the analgesic properties of lipotropin C-fragment and stabilized enkephalins in the rat. Biochem. Biophy. Res. Commun. 1977, 74, 748-754.
-
(1977)
Biochem. Biophy. Res. Commun.
, vol.74
, pp. 748-754
-
-
Bradbury, A.F.1
Smyth, D.G.2
Snell, C.R.3
Deakin, J.E.W.4
Wendlandt, S.5
-
33
-
-
0017334225
-
Evidence for topographical analogy between methionine-enkephalin and morphine derivatives
-
Schiller, P. W.; Yam, C. H.; Lis, M. Evidence for topographical analogy between methionine-enkephalin and morphine derivatives. Biochemistry 1977, 16, 1831-1838.
-
(1977)
Biochemistry
, vol.16
, pp. 1831-1838
-
-
Schiller, P.W.1
Yam, C.H.2
Lis, M.3
-
35
-
-
0026647625
-
5] enkephalin with δ opioid receptor selectivity
-
5] enkephalin with δ opioid receptor selectivity. J. Med. Chem. 1992, 35, 2384-2391.
-
(1992)
J. Med. Chem.
, vol.35
, pp. 2384-2391
-
-
Toth, G.1
Russell, K.C.2
Landis, G.3
Kramer, T.H.4
Fang, L.5
Knapp, R.6
Davis, P.7
Burks, T.F.8
Yamamura, H.I.9
Hruby, V.10
-
36
-
-
0019130301
-
Tyrosine-modified analogues of methionine-enkephalin and their effects on the mouse vas deferens
-
Coy, D. H.; Kastin, A. J. Tyrosine-modified analogues of methionine-enkephalin and their effects on the mouse vas deferens. Peptides 1980, 1, 175-177.
-
(1980)
Peptides
, vol.1
, pp. 175-177
-
-
Coy, D.H.1
Kastin, A.J.2
-
37
-
-
0020513524
-
Structure-activity studies of dermorphin. Synthesis and some pharmacological data of dermorphin and its 1-substituted analogues
-
Darlak, K.; Grzonka, Z.; Janicki, P.; Czlonkowski, A.; Gumulka, W. Structure-activity studies of dermorphin. Synthesis and some pharmacological data of dermorphin and its 1-substituted analogues. J. Med. Chem. 1983, 26, 1445-1457.
-
(1983)
J. Med. Chem.
, vol.26
, pp. 1445-1457
-
-
Darlak, K.1
Grzonka, Z.2
Janicki, P.3
Czlonkowski, A.4
Gumulka, W.5
-
38
-
-
0033748070
-
Synthesis and in vitro opioid activity profiles of DALDA analogues
-
Schiller, P. W.; Nguyen, T. M.-D.; Berezowska, I.; Dupuis, S.; Weltrowska, G.; Chang, N. N.; Lemieux, C. Synthesis and in vitro opioid activity profiles of DALDA analogues. Eur. J. Med. Chem. 2000, 35, 895-901.
-
(2000)
Eur. J. Med. Chem.
, vol.35
, pp. 895-901
-
-
Schiller, P.W.1
Nguyen, T.M.-D.2
Berezowska, I.3
Dupuis, S.4
Weltrowska, G.5
Chang, N.N.6
Lemieux, C.7
-
39
-
-
0037356635
-
Endomorphin 2 analogues containing Dmp residue as an aromatic amino acid surrogate with high μ-opioid receptor affinity and selectivity
-
Sasaki, Y.; Sasaki, A.; Niizuma, H.; Goto, H.; Ambo, A. Endomorphin 2 analogues containing Dmp residue as an aromatic amino acid surrogate with high μ-opioid receptor affinity and selectivity. Bioorg. Med. Chem. 2003, 11, 675-678.
-
(2003)
Bioorg. Med. Chem.
, vol.11
, pp. 675-678
-
-
Sasaki, Y.1
Sasaki, A.2
Niizuma, H.3
Goto, H.4
Ambo, A.5
-
40
-
-
0037424706
-
Dermorphin tetrapeptide analogues with 2′,6′- dimethylphenylalanine (Dmp) substituted for aromatic amino acids have high μ opioid receptor binding and biological activities
-
Ambo, A.; Niizuma, H.; Sasaki, A.; Kohara, H.; Sasaki, Y. Dermorphin tetrapeptide analogues with 2′,6′-dimethylphenylalanine (Dmp) substituted for aromatic amino acids have high μ opioid receptor binding and biological activities. Bioorg. Med. Chem. Lett. 2003, 13, 1269-1272.
-
(2003)
Bioorg. Med. Chem. Lett.
, vol.13
, pp. 1269-1272
-
-
Ambo, A.1
Niizuma, H.2
Sasaki, A.3
Kohara, H.4
Sasaki, Y.5
-
41
-
-
0026740967
-
A convenient asymmetric synthesis of the unnatural amino acid 2,6-dimethyl-L-tyrosine
-
Dygos, J. H.; Yonan, E. E.; Scaros, M. G.; Goodmonson, O. J.; Getman, D. P.; Periana, R. A.; Beck, G. R. A convenient asymmetric synthesis of the unnatural amino acid 2,6-dimethyl-L-tyrosine. Synthesis 1992, 741-743.
-
(1992)
Synthesis
, pp. 741-743
-
-
Dygos, J.H.1
Yonan, E.E.2
Scaros, M.G.3
Goodmonson, O.J.4
Getman, D.P.5
Periana, R.A.6
Beck, G.R.7
-
42
-
-
0035939193
-
Large-scale asymmetric synthesis of novel sterically constrained 2′,6′-dimethyl- and α-2′,6′-trimethyltyrosine and -phenylalanine derivatives via alkylation of chiral equivalents of nucleophilic glycine and alanine
-
(a) Soloshonok, V. A.; Tang, X.; Hruby, V. J. Large-scale asymmetric synthesis of novel sterically constrained 2′,6′-dimethyl- and α-2′,6′-trimethyltyrosine and -phenylalanine derivatives via alkylation of chiral equivalents of nucleophilic glycine and alanine. Tetrahedron 2001, 57, 6375-6328.
-
(2001)
Tetrahedron
, vol.57
, pp. 6375-6328
-
-
Soloshonok, V.A.1
Tang, X.2
Hruby, V.J.3
-
43
-
-
0034725677
-
Convenient, asymmetric synthesis of enantiomerically pure 2′,6′-dimethyltyrosine (DMT) via alkylation of chiral equivalents of nucleophilic glycine
-
(b) Tang, X.; Soloshonok, V. A.; Hruby, V. J. Convenient, asymmetric synthesis of enantiomerically pure 2′,6′-dimethyltyrosine (DMT) via alkylation of chiral equivalents of nucleophilic glycine. Tetrahedron: Asymmetry 2000, 11, 2917-2925.
-
(2000)
Tetrahedron: Asymmetry
, vol.11
, pp. 2917-2925
-
-
Tang, X.1
Soloshonok, V.A.2
Hruby, V.J.3
-
44
-
-
37049052033
-
Pyrylium salts obtained by diacylation of olefins. Part II. The two pyrylium salts formed in diacetylation of 2-methylbut-2-ene
-
Balaban, A. T.; Nenitzescu, C. D. Pyrylium salts obtained by diacylation of olefins. Part II. The two pyrylium salts formed in diacetylation of 2-methylbut-2-ene. J. Chem. Soc. 1961, 3553-3561.
-
(1961)
J. Chem. Soc.
, pp. 3553-3561
-
-
Balaban, A.T.1
Nenitzescu, C.D.2
-
45
-
-
0032873933
-
Hapten design in the development of competitive enzyme-linked immunosorbent assays for genotoxic metabolites of alachlor
-
Tessier, D. M.; Clark, J. M. Hapten design in the development of competitive enzyme-linked immunosorbent assays for genotoxic metabolites of alachlor. J. Agric. Food Chem. 1999, 47, 3925-3933.
-
(1999)
J. Agric. Food Chem.
, vol.47
, pp. 3925-3933
-
-
Tessier, D.M.1
Clark, J.M.2
-
46
-
-
12344251104
-
Autoxidation of 1,3,5-triisopropylbenzene, a new synthesis of phloroglucinol
-
Seidel, F.; Schulze, M.; Baltz, H. Autoxidation of 1,3,5- triisopropylbenzene, a new synthesis of phloroglucinol. J. Prakt. Chem. 1956, 3, 278-298.
-
(1956)
J. Prakt. Chem.
, vol.3
, pp. 278-298
-
-
Seidel, F.1
Schulze, M.2
Baltz, H.3
-
47
-
-
0000702671
-
Palladium-catalyzed vinylation of organic halides
-
Heck, R. F. Palladium-catalyzed vinylation of organic halides. Org. React. 1982, 25, 345-390.
-
(1982)
Org. React.
, vol.25
, pp. 345-390
-
-
Heck, R.F.1
-
48
-
-
0011947794
-
Computational chemistry and opioidmimetics: Receptor ligand interaction of three classes of biologically potent peptides
-
Martinez, J., Fehrentz, J.-A., Eds.; EDK: Paris
-
Bryant, S. D.; Salvadori, S.; Okada, Y.; Takahshi, M.; Sasaki, Y.; Lazarus, L. H. Computational chemistry and opioidmimetics: Receptor ligand interaction of three classes of biologically potent peptides. In Peptides 2000, Martinez, J., Fehrentz, J.-A., Eds.; EDK: Paris, 2000; pp 407-408.
-
(2000)
Peptides 2000
, pp. 407-408
-
-
Bryant, S.D.1
Salvadori, S.2
Okada, Y.3
Takahshi, M.4
Sasaki, Y.5
Lazarus, L.H.6
-
49
-
-
0023028494
-
Design and synthesis of conformationally constrained somatostatin analogues with high potency and specificity for μ opioid receptors
-
Pelton, J. T.; Kazmierski, W.; Gulya, K.; Yamamura, H. I.; Hruby, V. J. Design and synthesis of conformationally constrained somatostatin analogues with high potency and specificity for μ opioid receptors. J. Med. Chem. 1986, 29, 2370-2375.
-
(1986)
J. Med. Chem.
, vol.29
, pp. 2370-2375
-
-
Pelton, J.T.1
Kazmierski, W.2
Gulya, K.3
Yamamura, H.I.4
Hruby, V.J.5
-
50
-
-
0025734366
-
Function of negative charge in the "address domain" of deltorphins
-
(a) Lazarus, L. H.; Salvadori, S.; Santagaga, V.; Tomatis, R.; Wilson, W. E. Function of negative charge in the "address domain" of deltorphins. J. Med. Chem. 1991, 34, 1350-1355.
-
(1991)
J. Med. Chem.
, vol.34
, pp. 1350-1355
-
-
Lazarus, L.H.1
Salvadori, S.2
Santagaga, V.3
Tomatis, R.4
Wilson, W.E.5
-
51
-
-
0027511496
-
Interaction of deltorphin with opioid receptors: Molecular determinants for affinity and selectivity
-
(b) Lazarus, L. H.; Salvadori, S.; Attila, M.; Grieco, P.; Bundy, D. M.; Wilson, W. E.; Tomatis, R. Interaction of deltorphin with opioid receptors: Molecular determinants for affinity and selectivity. Peptides 1993, 14, 21-28.
-
(1993)
Peptides
, vol.14
, pp. 21-28
-
-
Lazarus, L.H.1
Salvadori, S.2
Attila, M.3
Grieco, P.4
Bundy, D.M.5
Wilson, W.E.6
Tomatis, R.7
|