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Absorption and brain penetration of a high affinity, highly selective 5-HT2C receptor antagonist, RS-102221
被引:7
作者
:
Bonhaus, DW
论文数:
0
引用数:
0
h-index:
0
机构:
Roche Biosci, Palo Alto, CA 94304 USA
Roche Biosci, Palo Alto, CA 94304 USA
Bonhaus, DW
[
1
]
Rocha, CL
论文数:
0
引用数:
0
h-index:
0
机构:
Roche Biosci, Palo Alto, CA 94304 USA
Roche Biosci, Palo Alto, CA 94304 USA
Rocha, CL
[
1
]
Dawson, MW
论文数:
0
引用数:
0
h-index:
0
机构:
Roche Biosci, Palo Alto, CA 94304 USA
Roche Biosci, Palo Alto, CA 94304 USA
Dawson, MW
[
1
]
Eglen, RM
论文数:
0
引用数:
0
h-index:
0
机构:
Roche Biosci, Palo Alto, CA 94304 USA
Roche Biosci, Palo Alto, CA 94304 USA
Eglen, RM
[
1
]
机构
:
[1]
Roche Biosci, Palo Alto, CA 94304 USA
来源
:
ADVANCES IN SEROTONIN RECEPTOR RESEARCH: MOLECULAR BIOLOGY, SIGNAL TRANSDUCTION, AND THERAPEUTICS
|
1998年
/ 861卷
关键词
:
D O I
:
10.1111/j.1749-6632.1998.tb10218.x
中图分类号
:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号
:
071010 ;
081704 ;
摘要
:
引用
收藏
页码:269 / 269
页数:1
相关论文
共 3 条
[1]
RS-102221: A novel high affinity and selective, 5-HT2C receptor antagonist
[J].
Bonhaus, DW
论文数:
0
引用数:
0
h-index:
0
机构:
Institute of Pharmacology, Roche Bioscience, Neurobiology Unit, Palo Alto, CA 94304
Bonhaus, DW
;
Weinhardt, KK
论文数:
0
引用数:
0
h-index:
0
机构:
Institute of Pharmacology, Roche Bioscience, Neurobiology Unit, Palo Alto, CA 94304
Weinhardt, KK
;
Taylor, M
论文数:
0
引用数:
0
h-index:
0
机构:
Institute of Pharmacology, Roche Bioscience, Neurobiology Unit, Palo Alto, CA 94304
Taylor, M
;
Desouza, A
论文数:
0
引用数:
0
h-index:
0
机构:
Institute of Pharmacology, Roche Bioscience, Neurobiology Unit, Palo Alto, CA 94304
Desouza, A
;
Mcneeley, PM
论文数:
0
引用数:
0
h-index:
0
机构:
Institute of Pharmacology, Roche Bioscience, Neurobiology Unit, Palo Alto, CA 94304
Mcneeley, PM
;
Szczepanski, K
论文数:
0
引用数:
0
h-index:
0
机构:
Institute of Pharmacology, Roche Bioscience, Neurobiology Unit, Palo Alto, CA 94304
Szczepanski, K
;
Fontana, DJ
论文数:
0
引用数:
0
h-index:
0
机构:
Institute of Pharmacology, Roche Bioscience, Neurobiology Unit, Palo Alto, CA 94304
Fontana, DJ
;
Trinh, J
论文数:
0
引用数:
0
h-index:
0
机构:
Institute of Pharmacology, Roche Bioscience, Neurobiology Unit, Palo Alto, CA 94304
Trinh, J
;
Rocha, CL
论文数:
0
引用数:
0
h-index:
0
机构:
Institute of Pharmacology, Roche Bioscience, Neurobiology Unit, Palo Alto, CA 94304
Rocha, CL
;
Dawson, MW
论文数:
0
引用数:
0
h-index:
0
机构:
Institute of Pharmacology, Roche Bioscience, Neurobiology Unit, Palo Alto, CA 94304
Dawson, MW
;
Flippin, LA
论文数:
0
引用数:
0
h-index:
0
机构:
Institute of Pharmacology, Roche Bioscience, Neurobiology Unit, Palo Alto, CA 94304
Flippin, LA
;
Eglen, RM
论文数:
0
引用数:
0
h-index:
0
机构:
Institute of Pharmacology, Roche Bioscience, Neurobiology Unit, Palo Alto, CA 94304
Eglen, RM
.
NEUROPHARMACOLOGY,
1997,
36
(4-5)
:621
-629
[2]
HOYER D, 1994, PHARMACOL REV, V46, P157
[3]
Some benzenesulfonamido-substituted valerophenones that are selective antagonists for the 5-HT2C receptor
[J].
Weinhardt, KK
论文数:
0
引用数:
0
h-index:
0
机构:
Roche Bioscience, Neurobiology Unit, Palo Alto, CA 94304-1397
Weinhardt, KK
;
Bonhaus, DW
论文数:
0
引用数:
0
h-index:
0
机构:
Roche Bioscience, Neurobiology Unit, Palo Alto, CA 94304-1397
Bonhaus, DW
;
DeSouza, A
论文数:
0
引用数:
0
h-index:
0
机构:
Roche Bioscience, Neurobiology Unit, Palo Alto, CA 94304-1397
DeSouza, A
.
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS,
1996,
6
(22)
:2687
-2692
←
1
→
共 3 条
[1]
RS-102221: A novel high affinity and selective, 5-HT2C receptor antagonist
[J].
Bonhaus, DW
论文数:
0
引用数:
0
h-index:
0
机构:
Institute of Pharmacology, Roche Bioscience, Neurobiology Unit, Palo Alto, CA 94304
Bonhaus, DW
;
Weinhardt, KK
论文数:
0
引用数:
0
h-index:
0
机构:
Institute of Pharmacology, Roche Bioscience, Neurobiology Unit, Palo Alto, CA 94304
Weinhardt, KK
;
Taylor, M
论文数:
0
引用数:
0
h-index:
0
机构:
Institute of Pharmacology, Roche Bioscience, Neurobiology Unit, Palo Alto, CA 94304
Taylor, M
;
Desouza, A
论文数:
0
引用数:
0
h-index:
0
机构:
Institute of Pharmacology, Roche Bioscience, Neurobiology Unit, Palo Alto, CA 94304
Desouza, A
;
Mcneeley, PM
论文数:
0
引用数:
0
h-index:
0
机构:
Institute of Pharmacology, Roche Bioscience, Neurobiology Unit, Palo Alto, CA 94304
Mcneeley, PM
;
Szczepanski, K
论文数:
0
引用数:
0
h-index:
0
机构:
Institute of Pharmacology, Roche Bioscience, Neurobiology Unit, Palo Alto, CA 94304
Szczepanski, K
;
Fontana, DJ
论文数:
0
引用数:
0
h-index:
0
机构:
Institute of Pharmacology, Roche Bioscience, Neurobiology Unit, Palo Alto, CA 94304
Fontana, DJ
;
Trinh, J
论文数:
0
引用数:
0
h-index:
0
机构:
Institute of Pharmacology, Roche Bioscience, Neurobiology Unit, Palo Alto, CA 94304
Trinh, J
;
Rocha, CL
论文数:
0
引用数:
0
h-index:
0
机构:
Institute of Pharmacology, Roche Bioscience, Neurobiology Unit, Palo Alto, CA 94304
Rocha, CL
;
Dawson, MW
论文数:
0
引用数:
0
h-index:
0
机构:
Institute of Pharmacology, Roche Bioscience, Neurobiology Unit, Palo Alto, CA 94304
Dawson, MW
;
Flippin, LA
论文数:
0
引用数:
0
h-index:
0
机构:
Institute of Pharmacology, Roche Bioscience, Neurobiology Unit, Palo Alto, CA 94304
Flippin, LA
;
Eglen, RM
论文数:
0
引用数:
0
h-index:
0
机构:
Institute of Pharmacology, Roche Bioscience, Neurobiology Unit, Palo Alto, CA 94304
Eglen, RM
.
NEUROPHARMACOLOGY,
1997,
36
(4-5)
:621
-629
[2]
HOYER D, 1994, PHARMACOL REV, V46, P157
[3]
Some benzenesulfonamido-substituted valerophenones that are selective antagonists for the 5-HT2C receptor
[J].
Weinhardt, KK
论文数:
0
引用数:
0
h-index:
0
机构:
Roche Bioscience, Neurobiology Unit, Palo Alto, CA 94304-1397
Weinhardt, KK
;
Bonhaus, DW
论文数:
0
引用数:
0
h-index:
0
机构:
Roche Bioscience, Neurobiology Unit, Palo Alto, CA 94304-1397
Bonhaus, DW
;
DeSouza, A
论文数:
0
引用数:
0
h-index:
0
机构:
Roche Bioscience, Neurobiology Unit, Palo Alto, CA 94304-1397
DeSouza, A
.
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS,
1996,
6
(22)
:2687
-2692
←
1
→