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Volumn 18, Issue 12, 2010, Pages 4374-4384
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Design, synthesis, and biological evaluation of novel coxsackievirus B3 inhibitors
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Author keywords
6 Chloropurine; Bicyclo 2.2.1 heptane; Coxsackievirus B3; Fluorination; Mitsunobu reaction
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Indexed keywords
5 (6 CHLORO 9H PURIN 9 YL)BICYCLO[2.2.1]HEPTAN 2 OL;
5 (6 CHLORO 9H PURIN 9 YL)BICYCLO[2.2.1]HEPTAN 2 ONE;
5 (6 CHLORO 9H PURIN 9 YL)BICYCLO[2.2.1]HEPTANE 2,3 DIOL;
6 (6 CHLORO 9H PURIN 9 YL)BICYCLO[2.2.1]HEPTAN 2 OL;
6 (6 CHLORO 9H PURIN 9 YL)BICYCLO[2.2.1]HEPTAN 2 ONE;
6 CHLORO 9 (1,2,3,4 TETRAHYDROANTHRACEN 2 YL) 9H PURINE;
6 CHLORO 9 (1,7,7 TRIMETHYLBICYCLO[2.2.1]HEPT 2 YL] 9H PURINE;
6 CHLORO 9 (3 OXATRICYCLO[3.2.1.0]OCT 6 YL) 9H PURINE;
6 CHLORO 9 (3,3 DIMETHYLBICYCLO[2.2.1]HEPT 2 YL) 9H PURINE;
6 CHLORO 9 (4 OXATRICYCLO[4.2.1.0]NON 2 YL) 9H PURINE;
6 CHLORO 9 (4 OXATRICYCLO[4.2.1.0]NON 9 YL] 9H PURINE;
6 CHLORO 9 (5 FLUOROBICYCLO[2.2.1]HEPT 2 YL) 9H PURINE;
6 CHLORO 9 (5 PHENYLBICYCLO[2.2.1]HEPT 2 YL) 9H PURINE;
6 CHLORO 9 (5,5 DIFLUOROBICYCLO[2.2.1]HEPT 2 YL) 9H PURINE;
6 CHLORO 9 (6 FLUOROBICYCLO[2.2.1]HEPT 2 YL) 9H PURINE;
6 CHLORO 9 (6 PHENYLBICYCLO[2.2.1]HEPT 2 YL) 9H PURINE;
6 CHLORO 9 (6,6 DIFLUOROBICYCLO[2.2.1]HEPT 2 YL] 9H PURINE;
6 CHLORO 9 (TRICYCLO[2.2.1.0]HEPT 3 YL) 9H PURINE;
6 CHLORO 9 (TRICYCLO[5.2.1.0]DEC 8 YL] 9H PURINE;
6 CHLORO 9 (TRICYCLO[6.2.1.0]UNDECA 2,4,6 TRIEN 9 YL] 9H PURINE;
9 (BICYCLO[2.2.1]HEPT 2 YL) 6 CHLORO 9H PURINE;
9 (BICYCLO[2.2.1]HEPT 2 YLMETHYL) 6 CHLORO 9H PURINE;
9 (BICYCLO[2.2.1]HEPT 5 EN 2 YL) 6 CHLORO 9H PURINE;
9 (BICYCLO[2.2.1]HEPT 5 EN 2 YLMETHYL) 6 CHLORO 9H PURINE;
9,9' BICYCLO[2.2.1]HEPT 5 ENE 2,3 DIYLBIS (6 CHLORO 9H PURINE);
9,9' BICYCLO[2.2.1]HEPTANE 2,3 DIYLBIS(6 CHLORO 9H PURINE);
9,9' BICYCLO[2.2.1]HEPTANE 2,5 DIYLBIS (6 CHLORO 9H PURINE);
9,9' BICYCLO[2.2.1]HEPTANE 2,6 DIYLBIS(6 CHLORO 9H PURINE);
ANTIVIRUS AGENT;
PURINE DERIVATIVE;
UNCLASSIFIED DRUG;
6-CHLOROPURINE;
BICYCLO COMPOUND;
BICYCLO(2.2.1)HEPTENE;
ARTICLE;
CONTROLLED STUDY;
COXSACKIE VIRUS B3;
CYTOTOXICITY;
DRUG DESIGN;
DRUG SCREENING;
DRUG SYNTHESIS;
VIRUS INHIBITION;
ANIMAL;
CHEMISTRY;
CHLOROCEBUS AETHIOPS;
DRUG EFFECTS;
ENTEROVIRUS;
HUMAN;
STRUCTURE ACTIVITY RELATION;
SYNTHESIS;
VERO CELL LINE;
ANIMALS;
ANTIVIRAL AGENTS;
BICYCLO COMPOUNDS;
CERCOPITHECUS AETHIOPS;
DRUG DESIGN;
ENTEROVIRUS B, HUMAN;
HUMANS;
PURINES;
STRUCTURE-ACTIVITY RELATIONSHIP;
VERO CELLS;
COXSACKIEVIRUS;
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EID: 77953130838
PISSN: 09680896
EISSN: None
Source Type: Journal
DOI: 10.1016/j.bmc.2010.04.081 Document Type: Article |
Times cited : (39)
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References (24)
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