Structure and properties of carbocyclic 5′-Nor oligodeoxynucleotides
Synthesis of carbocyclic nucleosides as potential antiviral agents
Synthesis of carbocyclic nucleosides bearing a cyclopropane ring
Synthesis of carbocyclic 5′-Nor uridine and cytidine derivatives
Carbocyclic L-Nucleoside Analogs as Potential Antiviral Agents
Synthesis of telomere-mimic carbocyclic 5′-nor oligodeoxynucleotides
Synthesis of carbocyclic nucleosides and their SAH hydrolase inhibitory activities
Synthesis and chirality analysis of carbocyclic 5′-Nor nucleosides
Synthetic study on carbocyclic analogs of cyclic ADP-ribose, a novel second messenger: An efficient synthesis of cyclic IDP-carbocyclic-ribose
Synthesis of conformationally locked carbocyclic nucleoside phosphonates to probe the active site of HIV-1 RT
Synthesis of conformationally locked carbocyclic 1,3-diazepinone nucleosides as inhibitors of cytidine deaminase
Conformationally-2',4'-Locked Aza-ENA and Carbocyclic ribo-Thymidine
Synthesis of 5″-substituted cyclic ADP-carbocyclic-ribose as biological tools
Conformationally-2′,4′-Locked Aza-ENA and Carbocyclic ribo-Thymidine
“Reverse Fleximers”: Introduction of a series of 5-substituted carbocyclic uridine analogues
Inhibition of vertebrate telomerases by the triphosphate derivatives of carbocyclic oxetanocin analogs
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1 describing any cyclic molecular structure containing only carbon atoms in the ring or rings; describing any compound having such a stucture. See also homocyclic (def. 1). Compare heterocyclic (def. 1).
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