-
2
-
-
0034435822
-
Synthesis and evaluation of asperlicin analogues as non-peptidal cholecysto-kinin-antagonists
-
Lattmann E, Billington DC, Poyner DR. Synthesis and evaluation of asperlicin analogues as non-peptidal cholecysto-kinin-antagonists. Drug Des Discov. 2001;17:219-32.
-
(2001)
Drug Des Discov
, vol.17
, pp. 219-232
-
-
Lattmann, E.1
Billington, D.C.2
Poyner, D.R.3
-
3
-
-
9344219949
-
3-[2-(N-Phenylace-tamide)]-l,5- benzodiazepines: Orally active, binding selective CCK-A agonists
-
Wilson TM, Henke BR, Momtahen TM. 3-[2-(N-Phenylace-tamide)]-l,5- benzodiazepines: Orally active, binding selective CCK-A agonists. J Med Chem. 1996;39:3030-8.
-
(1996)
J Med Chem
, vol.39
, pp. 3030-3038
-
-
Wilson, T.M.1
Henke, B.R.2
Momtahen, T.M.3
-
4
-
-
0028314649
-
B/gastrin receptor antagonists containing a cationic solubi- lizing group
-
B/gastrin receptor antagonists containing a cationic solubi- lizing group. J Med Chem. 1994;37:719-31.
-
(1994)
J Med Chem
, vol.37
, pp. 719-731
-
-
Showell, G.A.1
Bourrain, S.2
Neduvelil, J.G.3
-
5
-
-
0037740724
-
Benzodiazepines as potent and selective bradykinin Bl antagonists
-
Wood MR, Homnick CF, Murphy KL. Benzodiazepines as potent and selective bradykinin Bl antagonists. J Med Chem. 2003;46:1803-17.
-
(2003)
J Med Chem
, vol.46
, pp. 1803-1817
-
-
Wood, M.R.1
Homnick, C.F.2
Murphy, K.L.3
-
6
-
-
0036711388
-
The gerbil elevated plus-maze II: Anxiolytic-like effects of selective neurokinin NK1 receptor antagonists
-
Varty GBP, Ursula C, Galen J. The gerbil elevated plus-maze II: anxiolytic-like effects of selective neurokinin NK1 receptor antagonists. Neuropsychopharmacology. 2002;27:371-84.
-
(2002)
Neuropsychopharmacology
, vol.27
, pp. 371-384
-
-
Varty, G.B.P.1
Ursula, C.2
Galen, J.3
-
7
-
-
0022343577
-
Opioid benzodizapine tifluadom and drug-induced hyperactivity in mice-lack of benzodiazepine-like effects
-
Sansone M, Castellano C, Pavone F. Opioid benzodizapine tifluadom and drug-induced hyperactivity in mice-lack of benzodiazepine-like effects. Pol J Pharmacol Pharm. 1985;37:585-91.
-
(1985)
Pol J Pharmacol Pharm
, vol.37
, pp. 585-591
-
-
Sansone, M.1
Castellano, C.2
Pavone, F.3
-
8
-
-
0021959870
-
The interaction of the two isomers of the opioid benzodiazepine tifluadom with binding sites and their analgesic and intestinal effects in rats
-
Petrillo P, Amato M, Tavani A. The interaction of the two isomers of the opioid benzodiazepine tifluadom with binding sites and their analgesic and intestinal effects in rats. Neuropeptides 1985;5:403-11.
-
(1985)
Neuropeptides
, vol.5
, pp. 403-411
-
-
Petrillo, P.1
Amato, M.2
Tavani, A.3
-
9
-
-
62249125768
-
-
Lattmann E, Offel M, Singh H. Aston University, PCT/GB2004/002252, 27/05/2004.
-
Lattmann E, Offel M, Singh H. Aston University, PCT/GB2004/002252, 27/05/2004.
-
-
-
-
10
-
-
0035822631
-
Time-dependent inhibition of protein tarnesyl-transferase by a benzodiazepine peptide mimetic
-
Roskoski R, Ritchie PA. Time-dependent inhibition of protein tarnesyl-transferase by a benzodiazepine peptide mimetic. Biochemistry. 2001;40:9329-35.
-
(2001)
Biochemistry
, vol.40
, pp. 9329-9335
-
-
Roskoski, R.1
Ritchie, P.A.2
-
11
-
-
62249191640
-
-
Sternbach LH, Reeder E, F. Hoffmann-La Roche AG, Swiss Patent 2.233.482, 11/12/1960
-
Sternbach LH, Reeder E. (F. Hoffmann-La Roche AG), Swiss Patent 2.233.482, 11/12/1960.
-
-
-
-
12
-
-
0142105290
-
Quinazolines and 1,4-ben-zodiazepines. 4,l,5-benzoxadiazocin-2-ones, a novel ring system
-
Stempel A, Douvan I, Reeder E. Quinazolines and 1,4-ben-zodiazepines. 4,l,5-benzoxadiazocin-2-ones, a novel ring system. J Org Chem. 1967;32:2417-22.
-
(1967)
J Org Chem
, vol.32
, pp. 2417-2422
-
-
Stempel, A.1
Douvan, I.2
Reeder, E.3
-
13
-
-
0001586662
-
Quinazolines and 1,4-benzodiaze-pines. The rearrangement of 6-chloro-2-chloromethyl-4-phenylquinazoline 3-oxide into 2-amino derivatives of 7- chloro-5-phenyl-3H-l,4-benzodiazepine 4-oxide
-
Sternbach LH, Reeder E. Quinazolines and 1,4-benzodiaze-pines. The rearrangement of 6-chloro-2-chloromethyl-4-phenylquinazoline 3-oxide into 2-amino derivatives of 7- chloro-5-phenyl-3H-l,4-benzodiazepine 4-oxide. J Org Chem. 1961;26:1111-8.
-
(1961)
J Org Chem
, vol.26
, pp. 1111-1118
-
-
Sternbach, L.H.1
Reeder, E.2
-
14
-
-
62249100205
-
Oxidation of quinazolines and 1,4-benzodiazepines
-
Avadagic A, Lesac A, Majer Z. Oxidation of quinazolines and 1,4-benzodiazepines. Helv Chim Acta. 1988;81:1567-77.
-
(1988)
Helv Chim Acta
, vol.81
, pp. 1567-1577
-
-
Avadagic, A.1
Lesac, A.2
Majer, Z.3
-
15
-
-
33845480788
-
Efficient synthesis of 3-hy-droxy-1,4-benzodiazepines oxazepam and lorazepam by new acetoxylation reaction of 3-position of 1 4-benzodiazepine ring
-
Cepanec I, Litvic M, Pogorelic I. Efficient synthesis of 3-hy-droxy-1,4-benzodiazepines oxazepam and lorazepam by new acetoxylation reaction of 3-position of 1 4-benzodiazepine ring. Org Proc Res Dev. 2006;10:1192-201.
-
(2006)
Org Proc Res Dev
, vol.10
, pp. 1192-1201
-
-
Cepanec, I.1
Litvic, M.2
Pogorelic, I.3
-
16
-
-
0013837872
-
Quinazolines and 1,4-benzodiazepines. Mechanism for ring enlargement of qui-nazoline 3-oxide with alkali to l,4-benzodiazepin-2-one dioxides
-
Stempel A, Reeder E, Sternbach LH. Quinazolines and 1,4-benzodiazepines. Mechanism for ring enlargement of qui-nazoline 3-oxide with alkali to l,4-benzodiazepin-2-one dioxides. J Org Chem. 1965:30:4267-73.
-
(1965)
J Org Chem
, vol.30
, pp. 4267-4273
-
-
Stempel, A.1
Reeder, E.2
Sternbach, L.H.3
-
17
-
-
0142105290
-
Quinazolines and 1,4-ben-zodiazepines. l,5-benzoxadiazocin-2-ones, a novel ring system
-
Stempel A, Douvan I, Reeder E. Quinazolines and 1,4-ben-zodiazepines. l,5-benzoxadiazocin-2-ones, a novel ring system. J. Org. Chem.1967;32: 2417-24.
-
(1967)
J. Org. Chem
, vol.32
, pp. 2417-2424
-
-
Stempel, A.1
Douvan, I.2
Reeder, E.3
-
18
-
-
0030036247
-
Biological Activity of YM022. Novel (3-amino substituted phenyl)urea derivatives of l,4-benzodiazepin-2-one as gastrin-cholecystokinin-B receptor agonists
-
Satoh M, Okamoto Y, Koshio H. Biological Activity of YM022. Novel (3-amino substituted phenyl)urea derivatives of l,4-benzodiazepin-2-one as gastrin-cholecystokinin-B receptor agonists. Chem Pharm Bull. 1996:44:1412-20.
-
(1996)
Chem Pharm Bull
, vol.44
, pp. 1412-1420
-
-
Satoh, M.1
Okamoto, Y.2
Koshio, H.3
-
19
-
-
62249203850
-
Synthesis of 3-substituted-amino/ arcyloxy-7-chloro-5-phenyl-l,3-dihydro-2H- l,l,4-benzodiazepin-2-ones as possible anxiolytics
-
Kulkarni YD, Abdi SHR, Sharma VL. Synthesis of 3-substituted-amino/ arcyloxy-7-chloro-5-phenyl-l,3-dihydro-2H- l,l,4-benzodiazepin-2-ones as possible anxiolytics. J Indian Chem Soc. 1986:425-31.
-
(1986)
J Indian Chem Soc
, pp. 425-431
-
-
Kulkarni, Y.D.1
Abdi, S.H.R.2
Sharma, V.L.3
-
20
-
-
62249189895
-
New synthesis of 3-(disubstituted- amino)-1,4-benzodiazepin-2-ones
-
Gatta F, Delgiudice MR, Settimj G. New synthesis of 3-(disubstituted- amino)-1,4-benzodiazepin-2-ones. Chem Comm. 1979;32:718-25.
-
(1979)
Chem Comm
, vol.32
, pp. 718-725
-
-
Gatta, F.1
Delgiudice, M.R.2
Settimj, G.3
-
21
-
-
0024529827
-
Benzodiazepine gastrin and brain cholecystokinin receptor ligands
-
Bock MG, DiPardo RM, Evans BE. Benzodiazepine gastrin and brain cholecystokinin receptor ligands. J Med Chem. 1989;32:13-26.
-
(1989)
J Med Chem
, vol.32
, pp. 13-26
-
-
Bock, M.G.1
DiPardo, R.M.2
Evans, B.E.3
-
22
-
-
62249197094
-
Sintesi di 2-E 3-amino 1,4-benzodizepine.
-
Gatta F, Delgiudice MR, Pandolfi C. Sintesi di 2-E 3-amino 1,4-benzodizepine. Farmaco. 1982;27:343-51.
-
(1982)
Farmaco
, vol.27
, pp. 343-351
-
-
Gatta, F.1
Delgiudice, M.R.2
Pandolfi, C.3
-
23
-
-
33646153757
-
Synthesis of substituted 3-anilino-5-phenyl-1,3-dihydro-2H- 1,4-benzodiazepinones and their evaluation as cholecystokinin ligands
-
Offel M, Lattmann P, Singh H. Synthesis of substituted 3-anilino-5-phenyl-1,3-dihydro-2H- 1,4-benzodiazepinones and their evaluation as cholecystokinin ligands. Arch Pharm. 2006;339:163-78.
-
(2006)
Arch Pharm
, vol.339
, pp. 163-178
-
-
Offel, M.1
Lattmann, P.2
Singh, H.3
-
24
-
-
0036933446
-
Combinatorial solid phase synthesis of multiply-substituted 1,4-benzodiaze-pines and affinity studies on the CCK2 receptor
-
Lattmann E, Billington DC, Poyner DR. Combinatorial solid phase synthesis of multiply-substituted 1,4-benzodiaze-pines and affinity studies on the CCK2 receptor. Drug Des Discov. 2002;18:9-21.
-
(2002)
Drug Des Discov
, vol.18
, pp. 9-21
-
-
Lattmann, E.1
Billington, D.C.2
Poyner, D.R.3
-
25
-
-
33644782623
-
Synthesis and evaluation of N-(3-oxo-2,3-dihydro-lH-pyrazol-4-yl)-lH-indole-carboxamide as cholecystokinin antagonists
-
Lattmann E, Singh H, Boonprakob Y. Synthesis and evaluation of N-(3-oxo-2,3-dihydro-lH-pyrazol-4-yl)-lH-indole-carboxamide as cholecystokinin antagonists. J Pharm Pharm. 2006;58:1-17.
-
(2006)
J Pharm Pharm
, vol.58
, pp. 1-17
-
-
Lattmann, E.1
Singh, H.2
Boonprakob, Y.3
-
26
-
-
20344380203
-
Synthesis and evaluation of N-(5-methyl-3-oxol,2-diphenyl-2,3-dihydro- lH-pyrazol-4yl)-N-phenylureas as cholecystokinin antagonists
-
Lattmann E, Sattayasai J, Boonprakob Y. Synthesis and evaluation of N-(5-methyl-3-oxol,2-diphenyl-2,3-dihydro- lH-pyrazol-4yl)-N-phenylureas as cholecystokinin antagonists. Arzneimittelforschung. 2005;55:251-64.
-
(2005)
Arzneimittelforschung
, vol.55
, pp. 251-264
-
-
Lattmann, E.1
Sattayasai, J.2
Boonprakob, Y.3
-
27
-
-
0037648758
-
The cholecystokinin antagonist proglumide enhances the analgesic effect of dihydrocodeine
-
McCleane GJ. The cholecystokinin antagonist proglumide enhances the analgesic effect of dihydrocodeine. Clin J Pain. 2003;19:200-4.
-
(2003)
Clin J Pain
, vol.19
, pp. 200-204
-
-
McCleane, G.J.1
-
28
-
-
0037468288
-
A randomised, double blind, placebo controlled crossover study of the cholecystokinin 2 antagonist L-365,260 as an adjunct to strong opioids in chronic human neuropathic pain
-
McCleane GJ. A randomised, double blind, placebo controlled crossover study of the cholecystokinin 2 antagonist L-365,260 as an adjunct to strong opioids in chronic human neuropathic pain. Neurosci Lett. 2003;338:151-63.
-
(2003)
Neurosci Lett
, vol.338
, pp. 151-163
-
-
McCleane, G.J.1
-
29
-
-
33644778139
-
Management of neuropathic pain using a CCK antagonist devazepide as an adjunct to strong opiates [abstract]
-
San Francisco, p
-
Simpson K. Management of neuropathic pain using a CCK antagonist devazepide as an adjunct to strong opiates [abstract]. In: International conference on the mechanism and treatment of neuropathic pain; 2001; San Francisco, p. 397, no. 118.
-
(2001)
International conference on the mechanism and treatment of neuropathic pain
, Issue.118
, pp. 397
-
-
Simpson, K.1
|