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Volumn 23, Issue 5, 2015, Pages 1157-1168
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Design, synthesis, and biological evaluation of novel 2-methylpiperazine derivatives as potent CCR5 antagonists
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Author keywords
2 Methylpiperazine derivatives; Anti HIV 1 agent; CCR5 antagonist
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Indexed keywords
1 ACETYL N (3 CHLORO 4 METHYLPHENYL) N [3 [2 METHYL 4 (4 METHYLBENZYL)PIPERAZIN 1 YL]PROPYL]PIPERIDINE 4 CARBOXAMIDE;
1 ACETYL N (3 CHLORO 4 METHYLPHENYL) N [3 [4 (2 FLUOROBENZYL) 2 METHYLPIPERAZIN 1 YL]PROPYL]PIPERIDINE 4 CARBOXAMIDE;
1 ACETYL N (3 CHLORO 4 METHYLPHENYL) N [3 [4 (4 CYANOBENZYL) 2 METHYLPIPERAZIN 1 YL]PROPYL]PIPERIDINE 4 CARBOXAMIDE;
1 ACETYL N (3 CHLORO 4 METHYLPHENYL) N [3 [4 (4 FLUOROBENZOYL) 2 METHYLPIPERAZIN 1 YL]PROPYL]PIPERIDINE 4 CARBOXAMIDE;
1 ACETYL N (3 CHLORO 4 METHYLPHENYL) N [3 [4 (4 FLUOROBENZYL) 1,4 DIAZEPAN 1 YL]PROPYL]PIPERIDINE 4 CARBOXAMIDE;
1 ACETYL N (3 CHLORO 4 METHYLPHENYL) N [3 [4 (4 FLUOROBENZYL) 2 METHYLPIPERAZIN 1 YL]PROPYL] 1 (METHYLSULFONYL)PIPERIDINE 4 CARBOXAMIDE;
1 ACETYL N (3 CHLORO 4 METHYLPHENYL) N [3 [4 (4 FLUOROBENZYL) 2 METHYLPIPERAZIN 1 YL]PROPYL]PIPERIDINE 3 CARBOXAMIDE;
1 ACETYL N (3 CHLORO 4 METHYLPHENYL) N [3 [4 (4 FLUOROBENZYL) 2 METHYLPIPERAZIN 1 YL]PROPYL]PIPERIDINE 4 CARBOXAMIDE;
1 ACETYL N (3 CHLORO 4 METHYLPHENYL) N [3 [4 (4 FLUOROPHENYLSULFONYL) 2 METHYLPIPERAZIN 1 YL]PROPYL]PIPERIDINE 4 CARBOXAMIDE;
1 ACETYL N (3 CHLORO 4 METHYLPHENYL) N [3 [5 (4 FLUOROBENZYL) 2 ,5 DIAZABICYCLO[2.2.1]HEPTAN 2 YL]PROPYL]PIPERIDINE 4 CARBOXAMIDE;
1 ACETYL N (3 CHLOROPHENYL) N [3 [4 (4 FLUOROBENZYL) 2 METHYLPIPERAZIN 1 YL]PROPYL]PIPERIDINE 4 CARBOXAMIDE;
1 ACETYL N [3 (4 BENZYL 2 METHYLPIPERAZIN 1 YL)PROPYL] N (3 CHLORO 4 METHYLPHENYL)PIPERIDINE 4 CARBOXAMIDE;
1 ACETYL N [3 [4 (4 FLUOROBENZYL) 2 METHYLPIPERAZIN 1 YL]PROPYL] N PHENYLPIPERIDINE 4 CARBOXAMIDE;
1 BENZOYL N (3 CHLORO 4 METHYLPHENYL) N [3 [4 (4 FLUOROBENZYL) 2 METHYLPIPERAZIN 1 YL]PROPYL]PIPERIDINE 4 CARBOXAMIDE;
2 METHYLPIPERAZINE DERIVATIVE;
ANTIVIRUS AGENT;
CALCIUM;
CHEMOKINE RECEPTOR CCR5 ANTAGONIST;
MARAVIROC;
N (3 CHLORO 4 METHYLPHENYL) 4 FLUORO N [3 [4 (4 FLUOROBENZYL) 2 METHYLPIPERAZIN 1 YL]PROPYL]BENZAMIDE;
N (3 CHLORO 4 METHYLPHENYL) N [3 [4 (4 FLUOROBENZYL) 2 METHYLPIPERAZIN 1 YL]PROPYL]ACETAMIDE;
UNCLASSIFIED DRUG;
2-METHYLPIPERAZINE;
ANTI HUMAN IMMUNODEFICIENCY VIRUS AGENT;
CCR5 PROTEIN, HUMAN;
CHEMOKINE RECEPTOR CCR5;
PIPERAZINE DERIVATIVE;
ANTIVIRAL ACTIVITY;
ARTICLE;
BIOLOGICAL ACTIVITY;
CALCIUM MOBILIZATION ASSAY;
CONTROLLED STUDY;
DRUG DESIGN;
DRUG DETERMINATION;
DRUG EFFECT;
DRUG POTENCY;
DRUG SCREENING;
DRUG STRUCTURE;
DRUG SYNTHESIS;
GROWTH INHIBITION;
HUMAN IMMUNODEFICIENCY VIRUS 1;
NONHUMAN;
VIRUS IDENTIFICATION;
VIRUS INFECTIVITY;
ANIMAL;
CHEMISTRY;
CHO CELL LINE;
CRICETULUS;
DRUG EFFECTS;
HAMSTER;
HUMAN;
PATHOGENICITY;
SYNTHESIS;
HUMAN IMMUNODEFICIENCY VIRUS 1;
ANIMALS;
ANTI-HIV AGENTS;
CHO CELLS;
CRICETINAE;
CRICETULUS;
DRUG DESIGN;
HIV-1;
HUMANS;
PIPERAZINES;
RECEPTORS, CCR5;
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EID: 84923083716
PISSN: 09680896
EISSN: 14643391
Source Type: Journal
DOI: 10.1016/j.bmc.2014.12.052 Document Type: Article |
Times cited : (13)
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References (8)
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