{"type":"standard","title":"Carbocyclic nucleoside","displaytitle":"Carbocyclic nucleoside","namespace":{"id":0,"text":""},"wikibase_item":"Q25323875","titles":{"canonical":"Carbocyclic_nucleoside","normalized":"Carbocyclic nucleoside","display":"Carbocyclic nucleoside"},"pageid":49809924,"thumbnail":{"source":"https://upload.wikimedia.org/wikipedia/commons/thumb/a/a9/Generic_ribonucleoside_with_gycosidic_bond_and_carbocyclic_ribonucleoside_analogue.svg/330px-Generic_ribonucleoside_with_gycosidic_bond_and_carbocyclic_ribonucleoside_analogue.svg.png","width":320,"height":113},"originalimage":{"source":"https://upload.wikimedia.org/wikipedia/commons/thumb/a/a9/Generic_ribonucleoside_with_gycosidic_bond_and_carbocyclic_ribonucleoside_analogue.svg/11593px-Generic_ribonucleoside_with_gycosidic_bond_and_carbocyclic_ribonucleoside_analogue.svg.png","width":12881,"height":4551},"lang":"en","dir":"ltr","revision":"1225033364","tid":"031df6d0-17c7-11ef-9bdd-0ce88c7c1bfd","timestamp":"2024-05-21T23:08:19Z","description":"Class of chemical compounds","description_source":"local","content_urls":{"desktop":{"page":"https://en.wikipedia.org/wiki/Carbocyclic_nucleoside","revisions":"https://en.wikipedia.org/wiki/Carbocyclic_nucleoside?action=history","edit":"https://en.wikipedia.org/wiki/Carbocyclic_nucleoside?action=edit","talk":"https://en.wikipedia.org/wiki/Talk:Carbocyclic_nucleoside"},"mobile":{"page":"https://en.m.wikipedia.org/wiki/Carbocyclic_nucleoside","revisions":"https://en.m.wikipedia.org/wiki/Special:History/Carbocyclic_nucleoside","edit":"https://en.m.wikipedia.org/wiki/Carbocyclic_nucleoside?action=edit","talk":"https://en.m.wikipedia.org/wiki/Talk:Carbocyclic_nucleoside"}},"extract":"Carbocyclic nucleosides are nucleoside analogues in which a methylene group has replaced the oxygen atom of the furanose ring.\nThese analogues have the nucleobase attached at a simple alkyl carbon rather than being part of a hemiaminal ether linkage. As a result, they have increased chemical stability. They also have increased metabolic stability because they are unaffected by phosphorylases and hydrolases that cleave the glycosidic bond between the nucleobase and furanose ring of nucleosides. They retain many of the biological properties of the original nucleosides with respect to recognition by various enzymes and receptors.","extract_html":"
Carbocyclic nucleosides are nucleoside analogues in which a methylene group has replaced the oxygen atom of the furanose ring.\nThese analogues have the nucleobase attached at a simple alkyl carbon rather than being part of a hemiaminal ether linkage. As a result, they have increased chemical stability. They also have increased metabolic stability because they are unaffected by phosphorylases and hydrolases that cleave the glycosidic bond between the nucleobase and furanose ring of nucleosides. They retain many of the biological properties of the original nucleosides with respect to recognition by various enzymes and receptors.
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{"fact":"There are approximately 100 breeds of cat.","length":42}
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