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1
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0021368643
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Conformational energy studies and in vitro and in vivo activity data on growth hormone-releasing peptides
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Momany, F. A.; Bowers, C. Y.; Reynolds, G. A.; Hong, A.; Newlander, K. Conformational energy studies and in vitro and in vivo activity data on growth hormone-releasing peptides. Endocrinology 1984, 114, 1531-1536.
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(1984)
Endocrinology
, vol.114
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Momany, F.A.1
Bowers, C.Y.2
Reynolds, G.A.3
Hong, A.4
Newlander, K.5
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2
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0021322884
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On the in vitro and in vivo activity of a new synthetic hexapeptide that acts on the pituitary to specifically release growth hormone
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Bowers, C. Y.; Momany, F. A.; Reynolds, G. A.; Hong, A. On the in vitro and in vivo activity of a new synthetic hexapeptide that acts on the pituitary to specifically release growth hormone. Endocrinology 1984, 114, 1537-1545.
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(1984)
Endocrinology
, vol.114
, pp. 1537-1545
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Bowers, C.Y.1
Momany, F.A.2
Reynolds, G.A.3
Hong, A.4
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3
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0027248530
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A nonpeptidyl growth hormone secretagogue
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Smith, R. G.; Cheng, K; Schoen, W. R.; Pong, S. S.; Hickey, H.; Jacks, T.; Butler, B.; Chan, W. W.-S.; Chaung, L.-Y. P.; Judith, F.; Taylor, J.; Wyvratt, M. J.; Fisher, M. H. A nonpeptidyl growth hormone secretagogue. Science 1993, 260, 1640-1643.
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(1993)
Science
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Smith, R.G.1
Cheng, K.2
Schoen, W.R.3
Pong, S.S.4
Hickey, H.5
Jacks, T.6
Butler, B.7
Chan, W.W.-S.8
Chaung, L.-Y.P.9
Judith, F.10
Taylor, J.11
Wyvratt, M.J.12
Fisher, M.H.13
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4
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0028294987
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A Novel 3-Substituted Benzazepinone Growth Hormone Secretagogue (L-692,429)
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Schoen, W. R.; Pisano, J. M.; Prendergast, K.; Wyvratt, M. J.; Fisher, M. H.; Cheng, K.; Chan, W. W.-S.; Butler, B.; Smith, R. G.; Ball, R. G. A Novel 3-Substituted Benzazepinone Growth Hormone Secretagogue (L-692,429). J. Med. Chem. 1994, 37, 897-906.
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Schoen, W.R.1
Pisano, J.M.2
Prendergast, K.3
Wyvratt, M.J.4
Fisher, M.H.5
Cheng, K.6
Chan, W.W.-S.7
Butler, B.8
Smith, R.G.9
Ball, R.G.10
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5
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0029129652
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Design and biological activity of L-163,-191 (MK-0677): A potent, orally active growth hormone secretagogue
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Patchett, A. A.; Nargund, R. P.; Tata, J. R.; Chen, M.-H.; Barakat, K. J.; Johnston, D. B. R.; Cheng, K.; Chan, W. W.-S.; Bulter, B.; Hickey, G.; Jacks, T.; Schleim, K.; Pong, S.-S.; Chaung, L.-Y. P.; Chen, H. Y.; Frazier, E.; Leung, K. H.; Chiu, S.-H. L.; Smith, R. G. Design and biological activity of L-163,-191 (MK-0677): A potent, orally active growth hormone secretagogue. Proc. Natl. Acad. Sci. U.S.A. 1995, 92, 7001-7005.
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Proc. Natl. Acad. Sci. U.S.A.
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Patchett, A.A.1
Nargund, R.P.2
Tata, J.R.3
Chen, M.-H.4
Barakat, K.J.5
Johnston, D.B.R.6
Cheng, K.7
Chan, W.W.-S.8
Bulter, B.9
Hickey, G.10
Jacks, T.11
Schleim, K.12
Pong, S.-S.13
Chaung, L.-Y.P.14
Chen, H.Y.15
Frazier, E.16
Leung, K.H.17
Chiu, S.-H.L.18
Smith, R.G.19
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6
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0030028275
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Identification of a new receptor for growth hormone secretagugues
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For characterization of the MK-0677 receptor, see: Pong, S.-S.; Chaung, L.-Y. P.; Dean, D. C.; Nargund, R. P.; Patchett, A. A.; Smith, R. G. Identification of a new receptor for growth hormone secretagugues. Mol. Endocrinol. 1996, 10, 57-61.
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Mol. Endocrinol.
, vol.10
, pp. 57-61
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Pong, S.-S.1
Chaung, L.-Y.P.2
Dean, D.C.3
Nargund, R.P.4
Patchett, A.A.5
Smith, R.G.6
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7
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0024396484
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Binding of a growth hormone releasing hexapeptide to specific hypothalamic and pituitary binding sites
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Walker, R. F.; Shu, A. Y.; Codd, E. E. Binding of a growth hormone releasing hexapeptide to specific hypothalamic and pituitary binding sites. Neuropharmacology 1989, 28, 1139-1144.
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Neuropharmacology
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, pp. 1139-1144
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Walker, R.F.1
Shu, A.Y.2
Codd, E.E.3
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8
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0025901021
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Demonstration and characterization of the specific binding of growth hormone-releasing peptide to rat anterior pituitary and hypothalamic membranes
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Bowers, C. Y.; Veeraragavan, K.; Sethumadhavan, K. Demonstration and characterization of the specific binding of growth hormone-releasing peptide to rat anterior pituitary and hypothalamic membranes. Biochem. Biophys. Res. Commun. 1991, 178, 31-37.
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(1991)
Biochem. Biophys. Res. Commun.
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Bowers, C.Y.1
Veeraragavan, K.2
Sethumadhavan, K.3
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9
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0002762422
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Selection and synthesis of receptor-specific radioligands
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Hulme, E. C , Ed.; Oxford University Press: Oxford
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McFarthing, K. G. Selection and synthesis of receptor-specific radioligands. In Receptor-Ligand Interactions: A Practical Approach; Hulme, E. C , Ed.; Oxford University Press: Oxford, 1992; pp 1-18.
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(1992)
Receptor-Ligand Interactions: A Practical Approach
, pp. 1-18
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McFarthing, K.G.1
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10
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15844402859
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note
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35S]sulfonyl chloride and its use to prepare corresponding sulfonamides.
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12
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15844372108
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note
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Of critical importance to the success of subsequent coupling, excess oxalyl chloride was effectively removed by washing the dichloromethane solution with 0.5% sodium bicarbonate solution. This was accompanied by small amounts of methane[35]sulfonyl chloride hydrolysis (10-15%). The solution was then dried over sodium sulfate and concentrated by atmospheric distillation.
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13
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0021260262
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A new reagent for the selective, high-yield N-dealkylation of tetriary amines: Improved syntheses of naltrexone and nalbuphine
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Olofson, R. A.; Martz, J. T.; Senet, J.-P.; Piteau, M.; Malfroot, T. A new reagent for the selective, high-yield N-dealkylation of tetriary amines: improved syntheses of naltrexone and nalbuphine. J. Org. Chem. 1984, 49, 2081-2082.
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J. Org. Chem.
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, pp. 2081-2082
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Olofson, R.A.1
Martz, J.T.2
Senet, J.-P.3
Piteau, M.4
Malfroot, T.5
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14
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0003161990
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The return of sulfenes
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35S]sulfonamide via minute amounts of a highly reactive sulfene intermediate apparently requires high concentrations of 7 (with an attentuated indoline nitrogen nucleophile) in order to compete effectively with trace amounts of water. For a review of sulfenes, see: King, J. K. The return of sulfenes. Acc. Chem. Res. 1975, 8, 10-17.
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Acc. Chem. Res.
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, pp. 10-17
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King, J.K.1
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15
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15844418111
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note
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32S corresponding to a specific activity of 1110 Ci/mmol.
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16
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15844411128
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note
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35S]-3a demonstrated remarkable stability (<0.5% loss of radiochemical purity/month) when stored at -20 °C as a solution in 15% methanol-water solution containing a trace of hydrochloric acid.
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17
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0344565333
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In vitro labelling of proteins
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Slater, R. J., Ed.; Oxford University Press: Oxford
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Enhanced hydrophilicity (water solubility) is usually inversely related to the observed "stickiness" of the radioligand which often severely restricts its usefulness in various receptor preparations, see: Bailey, G. S. In vitro labelling of proteins. In Radioisotopes in Biology: A Practical Approach; Slater, R. J., Ed.; Oxford University Press: Oxford, 1990; pp 191-206.
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Radioisotopes in Biology: A Practical Approach
, pp. 191-206
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Bailey, G.S.1
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18
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0015816824
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"Aromatic" substiturent constants for structure-activity correlations
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Hansch, C.; Leo, A.; Unger, S. H.; Kim, K. H.; Nikaitam, D.; Lien, E. J. "Aromatic" substiturent constants for structure-activity correlations. J. Med. Chem. 1973, 16, 1207-1216.
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J. Med. Chem.
, vol.16
, pp. 1207-1216
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Hansch, C.1
Leo, A.2
Unger, S.H.3
Kim, K.H.4
Nikaitam, D.5
Lien, E.J.6
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