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Volumn 2, Issue 7, 2011, Pages 650-654

Carbocyclic 5′-nor "reverse" fleximers. Design, synthesis, and preliminary biological activity

(6) Zimmermann, Sarah C a Sadler, Joshua M a Andrei, Graciela b Snoeck, Robert b Balzarini, Jan b Seley Radtke, Katherine L a

a UNIVERSITY OF MARYLAND BALTIMORE COUNTY (United States)

b REGA INSTITUTE FOR MEDICAL RESEARCH (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

1 [4' HYDROXY 2' CYCLOPENTEN 1' YL] 5 (FURAN 2 YLL)URACIL; 1 [4' HYDROXY 2' CYCLOPENTEN 1' YL] 5 (THIAZOL 5 YL)URACIL; 1 [4' HYDROXY 2' CYCLOPENTEN 1' YL] 5 (THIOPHENE 2 YL)URACIL; ANTIVIRUS AGENT; CARBOCYCLIC NUCLEOSIDE; DRUG METABOLIZING ENZYME; NUCLEOSIDE DERIVATIVE; PURINE; PYRIMIDINE; UNCLASSIFIED DRUG;

ANIMAL CELL; ANTIVIRAL ACTIVITY; ARTICLE; CHEMICAL MODIFICATION; CONCENTRATION RESPONSE; CONTROLLED STUDY; DRUG CYTOTOXICITY; DRUG DESIGN; DRUG SCREENING; DRUG STRUCTURE; DRUG SYNTHESIS; HUMAN; HUMAN CELL; NONHUMAN; PRIORITY JOURNAL;

EID: 79960154798 PISSN: 20402503 EISSN: 20402511 Source Type: Journal
DOI: 10.1039/c1md00094b Document Type: Article

Times cited : (20)

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