Citation: S. Chaki et A. Nakazato, Recent advances in feeding suppressing agents: potential therapeutic strategy for the treatment of obesity, EXPERT OP T, 11(11), 2001, pp. 1677-1692
Authors:
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Citation: T. Kumagai et al., Synthesis and structure-affinity relationships of 4-(5-aryl-1,2,3,6-tetrahydropyridino)pyrimidine derivatives as corticotropin-releasing factor(1) receptor antagonists, BIO MED CH, 9(5), 2001, pp. 1349-1355
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Citation: T. Kumagai et al., Chemical modification of aryl-1,2,3,6-tetrahydropyridinopyrimidine derivative to discover corticotropin-releasing factor(1) receptor antagonists: Aryl-1,2,3,6-tetrahydropyridino-purine, -3H-1,2,3-triazolo[4,5-d]pyrimidine, -purin-8-one, and -7H-pyrrolo[2,3-d]pyrimidine derivatives, BIO MED CH, 9(5), 2001, pp. 1357-1363
Authors:
Takamori, K
Kawashima, N
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Citation: K. Takamori et al., Involvement of the hypothalamus-pituitary-adrenal axis in antidepressant activity of corticotropin-releasing factor subtype 1 receptor antagonists inthe rat learned helplessness test, PHARM BIO B, 69(3-4), 2001, pp. 445-449
Authors:
Takamori, K
Kawashima, N
Chaki, S
Nakazato, A
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Citation: K. Takamori et al., Involvement of corticotropin-releasing factor subtype 1 receptor in the acquisition phase of learned helplessness in rats, LIFE SCI, 69(11), 2001, pp. 1241-1248
Authors:
Kawashima, N
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Citation: N. Kawashima et al., Neuropharmacological profiles of a novel atypical antipsychotic, NRA0562, in rats (vol 423, pg 27, 2001), EUR J PHARM, 428(3), 2001, pp. 389-390
Authors:
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Citation: I. Miyata et al., Localization and characterization of a short isoform of the corticotropin-releasing factor receptor type 2 alpha (CRF2 alpha-tr) in the rat brain, BIOC BIOP R, 280(2), 2001, pp. 553-557
Authors:
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Citation: A. Nakazato et al., Design, synthesis and structure-affinity relationships of 4-methylidenepiperidine and 4-aryl-1,2,3,6-tetrahydropyridine derivatives as corticotropin-releasing factor(1) receptor antagonists, BIO MED CH, 8(5), 2000, pp. 1183-1193
Authors:
Nakazato, A
Kumagai, T
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Suzuki, Y
Chaki, S
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Okuyama, S
Citation: A. Nakazato et al., Synthesis, SARs, and pharmacological characterization of 2-amino-3 or 6-fluorobicyclo[3.1.0]hexane-2,6-dicarboxylic acid derivatives as potent, selective, and orally active group II metabotropic glutamate receptor agonists, J MED CHEM, 43(25), 2000, pp. 4893-4909
Authors:
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Citation: T. Funakoshi et al., In vivo receptor labeling of peripheral benzodiazepine receptor by ex vivobinding of [H-3]PK11195, RES COM M P, 105(1-2), 1999, pp. 35-41
Authors:
Nakazato, A
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Citation: A. Nakazato et al., Chemical modification of apomorphine to discover sigma ligands: 6H-dibenzo[b,d]pyran and carbazole analogues, BIO MED CH, 7(9), 1999, pp. 2027-2035
Authors:
Chaki, S
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Citation: S. Chaki et al., A novel layout optimization technique for miniaturization and accurate design of MMICs, IEICE TR EL, E82C(11), 1999, pp. 1960-1967
Authors:
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Vera, ES
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Citation: Y. Inoue et al., A global multimedia research collaberation between the University of Chileand NTT Laboratories, NTT REVIEW, 11(2), 1999, pp. 34-37
Authors:
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Citation: N. Kawashima et al., Effects of NRA0045, NRA0160, and NRA0215 on regional Fos-like immunoreactivity in the rat brain, GEN PHARM, 32(6), 1999, pp. 637-646
Authors:
Kawashima, N
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Citation: N. Kawashima et al., Effects of selective dopamine D-4 receptor blockers, NRA0160 and L-745,870, on A9 and A10 dopamine neurons in rats, LIFE SCI, 65(24), 1999, pp. 2561-2571
Authors:
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Kawashima, N
Chaki, S
Yoshikawa, R
Funakoshi, T
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Ikeda, Y
Kumagai, T
Nakazato, A
Nagamine, M
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Citation: S. Okuyama et al., A selective dopamine D-4 receptor antagonist, NRA0160: A preclinical neuropharmacological profile, LIFE SCI, 65(20), 1999, pp. 2109-2125
Authors:
Okuyama, S
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Suzuki, Y
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Nakazato, A
Nagamine, M
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Citation: S. Okuyama et al., Neuropharmacological profile of peripheral benzodiazepine receptor agonists, DAA1097 and DAA1106, LIFE SCI, 64(16), 1999, pp. 1455-1464
Authors:
Okuyama, S
Chaki, S
Kawashima, N
Suzuki, Y
Ogawa, SI
Nakazato, A
Kumagai, T
Okubo, T
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Citation: S. Okuyama et al., Receptor binding, behavioral, and electrophysiological profiles of nonpeptide corticotropin-releasing factor subtype 1 receptor antagonists CRA1000 and CRA1001, J PHARM EXP, 289(2), 1999, pp. 926-935
Authors:
Nakazato, A
Ohta, K
Sekiguchi, Y
Okuyama, S
Chaki, S
Kawashima, Y
Hatayama, K
Citation: A. Nakazato et al., Design, synthesis, structure-activity relationships, and biological characterization of novel arylalkoxyphenylalkylamine sigma ligands as potential antipsychotic drugs, J MED CHEM, 42(6), 1999, pp. 1076-1087
Authors:
Nakazato, A
Kumagai, T
Ohta, K
Chaki, S
Okuyama, S
Tomisawa, K
Citation: A. Nakazato et al., Synthesis and SAR of 1-alkyl-2-phenylethylamine derivatives designed from N,N-dipropyl-4-methoxy-3-(2-phenylethoxy)phenylethylamine to discover sigma(1) ligands, J MED CHEM, 42(19), 1999, pp. 3965-3970
Authors:
Chaki, S
Funakoshi, T
Yoshikawa, R
Okuyama, S
Okubo, T
Nakazato, A
Nagamine, M
Tomisawa, K
Citation: S. Chaki et al., Binding characteristics of [H-3]DAA1106, a novel and selective ligand for peripheral benzodiazepine receptors, EUR J PHARM, 371(2-3), 1999, pp. 197-204
Authors:
Chaki, S
Okuyama, S
Nakazato, A
Kumagai, T
Okubo, T
Ikeda, Y
Oshida, Y
Hamajima, Y
Tomisawa, K
Citation: S. Chaki et al., In vitro pharmacological profile of nonpeptide CRF1 receptor antagonists, CRA1000 and CRA1001, EUR J PHARM, 371(2-3), 1999, pp. 205-211