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BREMONT B
MALAGIE I
JACQUOT C
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SERRAZ I
ANDRIEUX J
BREMONT B
MATHEALLAINMAT M
PONCET A
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LANGLOIS M
Citation: S. Sicsic et al., 3-DIMENSIONAL QUANTITATIVE STRUCTURE-ACTIVITY RELATIONSHIP OF MELATONIN RECEPTOR LIGANDS - A COMPARATIVE MOLECULAR-FIELD ANALYSIS STUDY, Journal of medicinal chemistry, 40(5), 1997, pp. 739-748
Authors:
YANG DL
SOULIER JL
SICSIC S
MATHEALLAINMAT M
BREMONT B
CROCI T
CARDAMONE R
AUREGGI G
LANGLOIS M
Citation: Dl. Yang et al., NEW ESTERS OF 4-AMINO-5-CHLORO-2-METHOXYBENZOIC ACID AS POTENT AGONISTS AND ANTAGONISTS FOR 5-HT4 RECEPTORS, Journal of medicinal chemistry, 40(4), 1997, pp. 608-621
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BREMONT B
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LANGLOIS M
Citation: Jl. Soulier et al., ARYLCARBAMATE DERIVATIVES OF 1-PIPERIDINEETHANOL AS POTENT LIGANDS FOR 5-HT4 RECEPTORS, Journal of medicinal chemistry, 40(11), 1997, pp. 1755-1761
Authors:
TRILLAT AC
MALAGIE I
LANGLOIS M
MATHEALLAINMAT M
BREMONT B
DESAINTFUSCIEN E
JACQUOT C
GARDIER AM
Citation: Ac. Trillat et al., ENHANCEMENT OF SSRIS EFFECTS BY 5-HT1A AUTORECEPTOR BLOCKADE IN RATS - IN-VIVO MICRODIALYSIS AND BEHAVIORAL-STUDIES, British Journal of Pharmacology, 122, 1997, pp. 298-298
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BREMONT B
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Citation: D. Yang et al., SEROTONINERGIC PROPERTIES OF NEW CONFORMATIONALLY RESTRICTED BENZAMIDES, European journal of medicinal chemistry, 31(3), 1996, pp. 231-239
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MATHEALLAINMAT M
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DANGYCAYE AL
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BREMONT B
BENATALAH Z
LANGLOIS M
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DELAGRANGE P
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SHEN SR
BREMONT B
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MATHEALLAINMAT M
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Citation: Sr. Shen et al., STRUCTURE-ACTIVITY-RELATIONSHIPS FOR SUBSTRATES AND INHIBITORS OF PINEAL 5-HYDROXYTRYPTAMINE-N-ACETYLTRANSFERASE - PRELIMINARY STUDIES, European journal of pharmacology, 307(2), 1996, pp. 133-140
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Citation: M. Langlois et al., DESIGN AND SYNTHESIS OF NEW NAPHTHALENIC DERIVATIVES AS LIGANDS FOR 2-[I-125]IODOMELATONIN BINDING-SITES, Journal of medicinal chemistry, 38(12), 1995, pp. 2050-2060
Authors:
LANGLOIS M
SOULIER JL
MATHEALLAINMAT M
GALLAIS C
BREMONT B
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Citation: M. Langlois et al., N-CHLOROMETHYL QUINUCLIDINIUM DERIVATIVES - A NEW CLASS OF IRREVERSIBLE LIGANDS FOR 5-HT3 RECEPTORS, Bioorganic & medicinal chemistry letters, 4(7), 1994, pp. 945-948
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ZHANG L
YANG D
BREMONT B
SHEN S
MANARA L
CROCI T
Citation: M. Langlois et al., DESIGN OF A POTENT 5-HT4 RECEPTOR AGONIST WITH NANOMOLAR AFFINITY, Bioorganic & medicinal chemistry letters, 4(12), 1994, pp. 1433-1436
Authors:
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SOULIER JL
RAMPILLON V
GALLAIS C
BREMONT B
SHEN S
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GIUDICE A
SUREAU F
Citation: M. Langlois et al., SYNTHESIS OF QUINAZOLINE-2,4-DIONE AND NAPHTHALIMIDE DERIVATIVES AS NEW 5-HT3 RECEPTOR ANTAGONISTS, European journal of medicinal chemistry, 29(12), 1994, pp. 925-940
Citation: M. Langlois et al., SYNTHESIS OF NEW DERIVATIVES OF 8-OH-DPAT - INFLUENCE OF SUBSTITUTIONON THE AROMATIC RING ON THE PHARMACOLOGICAL PROFILE, Bioorganic & medicinal chemistry letters, 3(10), 1993, pp. 2035-2038
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SOULIER JL
YANG D
BREMONT B
FLORAC C
RAMPILLON V
GIUDICE A
Citation: M. Langlois et al., STRUCTURAL-ANALYSIS OF 5-HT(3) RECEPTOR ANTAGONISTS - SYNTHESIS AND PHARMACOLOGICAL ACTIVITY OF VARIOUS AROMATIC ESTERS OR AMIDES DERIVED FROM TROPANE AND 1,2,6-TRISUBSTITUTED PIPERIDINE, European journal of medicinal chemistry, 28(11), 1993, pp. 869-880