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BENZOTRIAZINONES AS VIRTUAL RING MIMICS OF ORTHO-METHOXYBENZAMIDES - NOVEL AND POTENT 5-HT3 RECEPTOR ANTAGONISTS
被引:27
作者
:
KING, FD
论文数:
0
引用数:
0
h-index:
0
机构:
SmithKline Beecham Pharmaceuticals, Coldharbour Road, Pinnacles Harlow, Essex
KING, FD
DABBS, S
论文数:
0
引用数:
0
h-index:
0
机构:
SmithKline Beecham Pharmaceuticals, Coldharbour Road, Pinnacles Harlow, Essex
DABBS, S
BERMUDEZ, J
论文数:
0
引用数:
0
h-index:
0
机构:
SmithKline Beecham Pharmaceuticals, Coldharbour Road, Pinnacles Harlow, Essex
BERMUDEZ, J
SANGER, GJ
论文数:
0
引用数:
0
h-index:
0
机构:
SmithKline Beecham Pharmaceuticals, Coldharbour Road, Pinnacles Harlow, Essex
SANGER, GJ
机构
:
[1]
SmithKline Beecham Pharmaceuticals, Coldharbour Road, Pinnacles Harlow, Essex
来源
:
JOURNAL OF MEDICINAL CHEMISTRY
|
1990年
/ 33卷
/ 11期
关键词
:
D O I
:
10.1021/jm00173a002
中图分类号
:
R914 [药物化学];
学科分类号
:
100701 ;
摘要
:
[No abstract available]
引用
收藏
页码:2942 / 2944
页数:3
相关论文
共 17 条
[1]
5-HYDROXYTRYPTAMINE (5-HT3) RECEPTOR ANTAGONISTS .1. INDAZOLE AND INDOLIZINE-3-CARBOXYLIC ACID-DERIVATIVES
BERMUDEZ, J
论文数:
0
引用数:
0
h-index:
0
机构:
BEECHAM PHARMACEUT,DIV RES,PINNACLES,HARLOW,ESSEX,ENGLAND
BEECHAM PHARMACEUT,DIV RES,PINNACLES,HARLOW,ESSEX,ENGLAND
BERMUDEZ, J
FAKE, CS
论文数:
0
引用数:
0
h-index:
0
机构:
BEECHAM PHARMACEUT,DIV RES,PINNACLES,HARLOW,ESSEX,ENGLAND
BEECHAM PHARMACEUT,DIV RES,PINNACLES,HARLOW,ESSEX,ENGLAND
FAKE, CS
JOINER, GF
论文数:
0
引用数:
0
h-index:
0
机构:
BEECHAM PHARMACEUT,DIV RES,PINNACLES,HARLOW,ESSEX,ENGLAND
BEECHAM PHARMACEUT,DIV RES,PINNACLES,HARLOW,ESSEX,ENGLAND
JOINER, GF
JOINER, KA
论文数:
0
引用数:
0
h-index:
0
机构:
BEECHAM PHARMACEUT,DIV RES,PINNACLES,HARLOW,ESSEX,ENGLAND
BEECHAM PHARMACEUT,DIV RES,PINNACLES,HARLOW,ESSEX,ENGLAND
JOINER, KA
KING, FD
论文数:
0
引用数:
0
h-index:
0
机构:
BEECHAM PHARMACEUT,DIV RES,PINNACLES,HARLOW,ESSEX,ENGLAND
BEECHAM PHARMACEUT,DIV RES,PINNACLES,HARLOW,ESSEX,ENGLAND
KING, FD
MINER, WD
论文数:
0
引用数:
0
h-index:
0
机构:
BEECHAM PHARMACEUT,DIV RES,PINNACLES,HARLOW,ESSEX,ENGLAND
BEECHAM PHARMACEUT,DIV RES,PINNACLES,HARLOW,ESSEX,ENGLAND
MINER, WD
SANGER, GJ
论文数:
0
引用数:
0
h-index:
0
机构:
BEECHAM PHARMACEUT,DIV RES,PINNACLES,HARLOW,ESSEX,ENGLAND
BEECHAM PHARMACEUT,DIV RES,PINNACLES,HARLOW,ESSEX,ENGLAND
SANGER, GJ
[J].
JOURNAL OF MEDICINAL CHEMISTRY,
1990,
33
(07)
: 1924
-
1929
[2]
5-HYDROXYTRYPTAMINE (5-HT3) RECEPTOR ANTAGONISTS .2. 1-INDOLINECARBOXAMIDES
BERMUDEZ, J
论文数:
0
引用数:
0
h-index:
0
机构:
BEECHAM PHARMACEUT,DIV RES,PINNACLES,HARLOW,ESSEX,ENGLAND
BEECHAM PHARMACEUT,DIV RES,PINNACLES,HARLOW,ESSEX,ENGLAND
BERMUDEZ, J
DABBS, S
论文数:
0
引用数:
0
h-index:
0
机构:
BEECHAM PHARMACEUT,DIV RES,PINNACLES,HARLOW,ESSEX,ENGLAND
BEECHAM PHARMACEUT,DIV RES,PINNACLES,HARLOW,ESSEX,ENGLAND
DABBS, S
JOINER, KA
论文数:
0
引用数:
0
h-index:
0
机构:
BEECHAM PHARMACEUT,DIV RES,PINNACLES,HARLOW,ESSEX,ENGLAND
BEECHAM PHARMACEUT,DIV RES,PINNACLES,HARLOW,ESSEX,ENGLAND
JOINER, KA
KING, FD
论文数:
0
引用数:
0
h-index:
0
机构:
BEECHAM PHARMACEUT,DIV RES,PINNACLES,HARLOW,ESSEX,ENGLAND
BEECHAM PHARMACEUT,DIV RES,PINNACLES,HARLOW,ESSEX,ENGLAND
KING, FD
[J].
JOURNAL OF MEDICINAL CHEMISTRY,
1990,
33
(07)
: 1929
-
1932
[3]
PHARMACOLOGICAL PROPERTIES OF GR38032F, A NOVEL ANTAGONIST AT 5-HT3 RECEPTORS
BUTLER, A
论文数:
0
引用数:
0
h-index:
0
机构:
GLAXO GRP RES LTD,DEPT NEUROPHARMACOL,WARE SG12 0DJ,HERTS,ENGLAND
GLAXO GRP RES LTD,DEPT NEUROPHARMACOL,WARE SG12 0DJ,HERTS,ENGLAND
BUTLER, A
HILL, JM
论文数:
0
引用数:
0
h-index:
0
机构:
GLAXO GRP RES LTD,DEPT NEUROPHARMACOL,WARE SG12 0DJ,HERTS,ENGLAND
GLAXO GRP RES LTD,DEPT NEUROPHARMACOL,WARE SG12 0DJ,HERTS,ENGLAND
HILL, JM
IRELAND, SJ
论文数:
0
引用数:
0
h-index:
0
机构:
GLAXO GRP RES LTD,DEPT NEUROPHARMACOL,WARE SG12 0DJ,HERTS,ENGLAND
GLAXO GRP RES LTD,DEPT NEUROPHARMACOL,WARE SG12 0DJ,HERTS,ENGLAND
IRELAND, SJ
JORDAN, CC
论文数:
0
引用数:
0
h-index:
0
机构:
GLAXO GRP RES LTD,DEPT NEUROPHARMACOL,WARE SG12 0DJ,HERTS,ENGLAND
GLAXO GRP RES LTD,DEPT NEUROPHARMACOL,WARE SG12 0DJ,HERTS,ENGLAND
JORDAN, CC
TYERS, MB
论文数:
0
引用数:
0
h-index:
0
机构:
GLAXO GRP RES LTD,DEPT NEUROPHARMACOL,WARE SG12 0DJ,HERTS,ENGLAND
GLAXO GRP RES LTD,DEPT NEUROPHARMACOL,WARE SG12 0DJ,HERTS,ENGLAND
TYERS, MB
[J].
BRITISH JOURNAL OF PHARMACOLOGY,
1988,
94
(02)
: 397
-
412
[4]
FAKE C S, 1987, British Journal of Pharmacology, V91, p335P
[5]
MDL-72222 - A POTENT AND HIGHLY SELECTIVE ANTAGONIST AT NEURONAL 5-HYDROXYTRYPTAMINE RECEPTORS
FOZARD, JR
论文数:
0
引用数:
0
h-index:
0
FOZARD, JR
[J].
NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY,
1984,
326
(01)
: 36
-
44
[6]
SUBSTITUTED BENZAMIDES WITH CONFORMATIONALLY RESTRICTED SIDE-CHAINS .1. QUINOLIZIDINE DERIVATIVES AS SELECTIVE GASTRIC PROKINETIC AGENTS
HADLEY, MS
论文数:
0
引用数:
0
h-index:
0
HADLEY, MS
KING, FD
论文数:
0
引用数:
0
h-index:
0
KING, FD
MCRITCHIE, B
论文数:
0
引用数:
0
h-index:
0
MCRITCHIE, B
TURNER, DH
论文数:
0
引用数:
0
h-index:
0
TURNER, DH
WATTS, EA
论文数:
0
引用数:
0
h-index:
0
WATTS, EA
[J].
JOURNAL OF MEDICINAL CHEMISTRY,
1985,
28
(12)
: 1843
-
1847
[7]
CONFORMATION-ACTIVITY RELATIONSHIP STUDY OF 5-HT3 RECEPTOR ANTAGONISTS AND A DEFINITION OF A MODEL FOR THIS RECEPTOR-SITE
HIBERT, MF
论文数:
0
引用数:
0
h-index:
0
机构:
Merrell Dow Research Institute, 67084 Strasbourg Cedex, 16, rue d'Ankara
HIBERT, MF
HOFFMANN, R
论文数:
0
引用数:
0
h-index:
0
机构:
Merrell Dow Research Institute, 67084 Strasbourg Cedex, 16, rue d'Ankara
HOFFMANN, R
MILLER, RC
论文数:
0
引用数:
0
h-index:
0
机构:
Merrell Dow Research Institute, 67084 Strasbourg Cedex, 16, rue d'Ankara
MILLER, RC
CARR, AA
论文数:
0
引用数:
0
h-index:
0
机构:
Merrell Dow Research Institute, 67084 Strasbourg Cedex, 16, rue d'Ankara
CARR, AA
[J].
JOURNAL OF MEDICINAL CHEMISTRY,
1990,
33
(06)
: 1594
-
1600
[8]
HIBERT MF, 1988, ACTUAL CHIM THER, V16, P37
[9]
KING F D, 1989, Drugs of the Future, V14, P875
[10]
KING FD, 1989, Patent No. 315390
←
1
2
→
共 17 条
[1]
5-HYDROXYTRYPTAMINE (5-HT3) RECEPTOR ANTAGONISTS .1. INDAZOLE AND INDOLIZINE-3-CARBOXYLIC ACID-DERIVATIVES
BERMUDEZ, J
论文数:
0
引用数:
0
h-index:
0
机构:
BEECHAM PHARMACEUT,DIV RES,PINNACLES,HARLOW,ESSEX,ENGLAND
BEECHAM PHARMACEUT,DIV RES,PINNACLES,HARLOW,ESSEX,ENGLAND
BERMUDEZ, J
FAKE, CS
论文数:
0
引用数:
0
h-index:
0
机构:
BEECHAM PHARMACEUT,DIV RES,PINNACLES,HARLOW,ESSEX,ENGLAND
BEECHAM PHARMACEUT,DIV RES,PINNACLES,HARLOW,ESSEX,ENGLAND
FAKE, CS
JOINER, GF
论文数:
0
引用数:
0
h-index:
0
机构:
BEECHAM PHARMACEUT,DIV RES,PINNACLES,HARLOW,ESSEX,ENGLAND
BEECHAM PHARMACEUT,DIV RES,PINNACLES,HARLOW,ESSEX,ENGLAND
JOINER, GF
JOINER, KA
论文数:
0
引用数:
0
h-index:
0
机构:
BEECHAM PHARMACEUT,DIV RES,PINNACLES,HARLOW,ESSEX,ENGLAND
BEECHAM PHARMACEUT,DIV RES,PINNACLES,HARLOW,ESSEX,ENGLAND
JOINER, KA
KING, FD
论文数:
0
引用数:
0
h-index:
0
机构:
BEECHAM PHARMACEUT,DIV RES,PINNACLES,HARLOW,ESSEX,ENGLAND
BEECHAM PHARMACEUT,DIV RES,PINNACLES,HARLOW,ESSEX,ENGLAND
KING, FD
MINER, WD
论文数:
0
引用数:
0
h-index:
0
机构:
BEECHAM PHARMACEUT,DIV RES,PINNACLES,HARLOW,ESSEX,ENGLAND
BEECHAM PHARMACEUT,DIV RES,PINNACLES,HARLOW,ESSEX,ENGLAND
MINER, WD
SANGER, GJ
论文数:
0
引用数:
0
h-index:
0
机构:
BEECHAM PHARMACEUT,DIV RES,PINNACLES,HARLOW,ESSEX,ENGLAND
BEECHAM PHARMACEUT,DIV RES,PINNACLES,HARLOW,ESSEX,ENGLAND
SANGER, GJ
[J].
JOURNAL OF MEDICINAL CHEMISTRY,
1990,
33
(07)
: 1924
-
1929
[2]
5-HYDROXYTRYPTAMINE (5-HT3) RECEPTOR ANTAGONISTS .2. 1-INDOLINECARBOXAMIDES
BERMUDEZ, J
论文数:
0
引用数:
0
h-index:
0
机构:
BEECHAM PHARMACEUT,DIV RES,PINNACLES,HARLOW,ESSEX,ENGLAND
BEECHAM PHARMACEUT,DIV RES,PINNACLES,HARLOW,ESSEX,ENGLAND
BERMUDEZ, J
DABBS, S
论文数:
0
引用数:
0
h-index:
0
机构:
BEECHAM PHARMACEUT,DIV RES,PINNACLES,HARLOW,ESSEX,ENGLAND
BEECHAM PHARMACEUT,DIV RES,PINNACLES,HARLOW,ESSEX,ENGLAND
DABBS, S
JOINER, KA
论文数:
0
引用数:
0
h-index:
0
机构:
BEECHAM PHARMACEUT,DIV RES,PINNACLES,HARLOW,ESSEX,ENGLAND
BEECHAM PHARMACEUT,DIV RES,PINNACLES,HARLOW,ESSEX,ENGLAND
JOINER, KA
KING, FD
论文数:
0
引用数:
0
h-index:
0
机构:
BEECHAM PHARMACEUT,DIV RES,PINNACLES,HARLOW,ESSEX,ENGLAND
BEECHAM PHARMACEUT,DIV RES,PINNACLES,HARLOW,ESSEX,ENGLAND
KING, FD
[J].
JOURNAL OF MEDICINAL CHEMISTRY,
1990,
33
(07)
: 1929
-
1932
[3]
PHARMACOLOGICAL PROPERTIES OF GR38032F, A NOVEL ANTAGONIST AT 5-HT3 RECEPTORS
BUTLER, A
论文数:
0
引用数:
0
h-index:
0
机构:
GLAXO GRP RES LTD,DEPT NEUROPHARMACOL,WARE SG12 0DJ,HERTS,ENGLAND
GLAXO GRP RES LTD,DEPT NEUROPHARMACOL,WARE SG12 0DJ,HERTS,ENGLAND
BUTLER, A
HILL, JM
论文数:
0
引用数:
0
h-index:
0
机构:
GLAXO GRP RES LTD,DEPT NEUROPHARMACOL,WARE SG12 0DJ,HERTS,ENGLAND
GLAXO GRP RES LTD,DEPT NEUROPHARMACOL,WARE SG12 0DJ,HERTS,ENGLAND
HILL, JM
IRELAND, SJ
论文数:
0
引用数:
0
h-index:
0
机构:
GLAXO GRP RES LTD,DEPT NEUROPHARMACOL,WARE SG12 0DJ,HERTS,ENGLAND
GLAXO GRP RES LTD,DEPT NEUROPHARMACOL,WARE SG12 0DJ,HERTS,ENGLAND
IRELAND, SJ
JORDAN, CC
论文数:
0
引用数:
0
h-index:
0
机构:
GLAXO GRP RES LTD,DEPT NEUROPHARMACOL,WARE SG12 0DJ,HERTS,ENGLAND
GLAXO GRP RES LTD,DEPT NEUROPHARMACOL,WARE SG12 0DJ,HERTS,ENGLAND
JORDAN, CC
TYERS, MB
论文数:
0
引用数:
0
h-index:
0
机构:
GLAXO GRP RES LTD,DEPT NEUROPHARMACOL,WARE SG12 0DJ,HERTS,ENGLAND
GLAXO GRP RES LTD,DEPT NEUROPHARMACOL,WARE SG12 0DJ,HERTS,ENGLAND
TYERS, MB
[J].
BRITISH JOURNAL OF PHARMACOLOGY,
1988,
94
(02)
: 397
-
412
[4]
FAKE C S, 1987, British Journal of Pharmacology, V91, p335P
[5]
MDL-72222 - A POTENT AND HIGHLY SELECTIVE ANTAGONIST AT NEURONAL 5-HYDROXYTRYPTAMINE RECEPTORS
FOZARD, JR
论文数:
0
引用数:
0
h-index:
0
FOZARD, JR
[J].
NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY,
1984,
326
(01)
: 36
-
44
[6]
SUBSTITUTED BENZAMIDES WITH CONFORMATIONALLY RESTRICTED SIDE-CHAINS .1. QUINOLIZIDINE DERIVATIVES AS SELECTIVE GASTRIC PROKINETIC AGENTS
HADLEY, MS
论文数:
0
引用数:
0
h-index:
0
HADLEY, MS
KING, FD
论文数:
0
引用数:
0
h-index:
0
KING, FD
MCRITCHIE, B
论文数:
0
引用数:
0
h-index:
0
MCRITCHIE, B
TURNER, DH
论文数:
0
引用数:
0
h-index:
0
TURNER, DH
WATTS, EA
论文数:
0
引用数:
0
h-index:
0
WATTS, EA
[J].
JOURNAL OF MEDICINAL CHEMISTRY,
1985,
28
(12)
: 1843
-
1847
[7]
CONFORMATION-ACTIVITY RELATIONSHIP STUDY OF 5-HT3 RECEPTOR ANTAGONISTS AND A DEFINITION OF A MODEL FOR THIS RECEPTOR-SITE
HIBERT, MF
论文数:
0
引用数:
0
h-index:
0
机构:
Merrell Dow Research Institute, 67084 Strasbourg Cedex, 16, rue d'Ankara
HIBERT, MF
HOFFMANN, R
论文数:
0
引用数:
0
h-index:
0
机构:
Merrell Dow Research Institute, 67084 Strasbourg Cedex, 16, rue d'Ankara
HOFFMANN, R
MILLER, RC
论文数:
0
引用数:
0
h-index:
0
机构:
Merrell Dow Research Institute, 67084 Strasbourg Cedex, 16, rue d'Ankara
MILLER, RC
CARR, AA
论文数:
0
引用数:
0
h-index:
0
机构:
Merrell Dow Research Institute, 67084 Strasbourg Cedex, 16, rue d'Ankara
CARR, AA
[J].
JOURNAL OF MEDICINAL CHEMISTRY,
1990,
33
(06)
: 1594
-
1600
[8]
HIBERT MF, 1988, ACTUAL CHIM THER, V16, P37
[9]
KING F D, 1989, Drugs of the Future, V14, P875
[10]
KING FD, 1989, Patent No. 315390
←
1
2
→