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Volumn 23, Issue 16, 2013, Pages 4696-4700
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Synthesis and the 5-HT6 receptor antagonistic effect of 3-arylsulfonylamino-5,6-dihydro-6-substituted pyrazolo[3,4]pyridinones for neuropathic pain treatment
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Author keywords
5 HT6 receptor antagonist; Arylsufonylamino 5,6 dihydro pyrazolo 3,4 c pyridine 7 one; Neuropathic pain; Synthesis
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Indexed keywords
3 PHENYLSULFONYL 8 (1 PIPERAZINYL)QUINOLINE;
4 AMINO N [2,6 BIS(METHYLAMINO) 4 PYRIDINYL]BENZENESULFONAMIDE;
4 AMINO N [2,6 BIS(METHYLAMINO) 4 PYRIMIDINYL]BENZENESULFONAMIDE;
AVN 211;
BVT 74316;
SAM 532;
SB 258585;
SB 737050A;
SEROTONIN 6 ANTAGONIST;
SEROTONIN 6 RECEPTOR;
UNCLASSIFIED DRUG;
ENZYME INHIBITOR;
PYRAZOLE DERIVATIVE;
PYRIDONE DERIVATIVE;
SEROTONIN RECEPTOR;
PROTEIN BINDING;
ALKYLATION;
ANIMAL EXPERIMENT;
ANIMAL MODEL;
ARTICLE;
DRUG DESIGN;
HUMAN;
HUMAN CELL;
IN VITRO STUDY;
NEUROPATHIC PAIN;
NONHUMAN;
POLYMERIZATION;
RAT;
STRUCTURE ACTIVITY RELATION;
SUBSTITUTION REACTION;
5-HT(6) RECEPTOR ANTAGONIST;
ANIMAL;
ARYLSUFONYLAMINO-5,6-DIHYDRO-PYRAZOLO[3,4-C]PYRIDINE-7-ONE;
CHEMICAL STRUCTURE;
CHEMISTRY;
DISEASE MODEL;
DRUG EFFECT;
DRUG STABILITY;
IC 50;
METABOLISM;
NEURALGIA;
PROTEIN BINDING;
SYNTHESIS;
DRUG EFFECTS;
IC50;
ANIMALIA;
RATTUS;
5-HT(6) RECEPTOR ANTAGONIST;
ARYLSUFONYLAMINO-5,6-DIHYDRO-PYRAZOLO[3,4-C]PYRIDINE-7-ONE;
NEUROPATHIC PAIN;
SYNTHESIS;
ANIMALS;
DISEASE MODELS, ANIMAL;
DRUG STABILITY;
ENZYME INHIBITORS;
INHIBITORY CONCENTRATION 50;
MOLECULAR STRUCTURE;
NEURALGIA;
PROTEIN BINDING;
PYRAZOLES;
PYRIDONES;
RATS;
RECEPTORS, SEROTONIN;
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EID: 84880601634
PISSN: 0960894X
EISSN: 14643405
Source Type: Journal
DOI: 10.1016/j.bmcl.2013.05.100 Document Type: Article |
Times cited : (13)
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References (22)
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