CHEBI:131825 - 8,5'-cyclo-2'-deoxyadenosine

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ChEBI Name 8,5'-cyclo-2'-deoxyadenosine ChEBI ID CHEBI:131825 Definition An organic heterotetracyclic compound obtained by intramolecular formation of a C-C bond between positions 8 and 5' of 2'-deoxyadenosine. Stars This entity has been manually annotated by the ChEBI Team. Supplier Information Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search Formula C10H11N5O3 Net Charge 0 Average Mass 249.226 Monoisotopic Mass 249.08619 InChI InChI=1S/C10H11N5O3/c11-8-5-9(13-2-12-8)15-4-1-3(16)7(18-4)6(17)10(15)14-5/h2-4,6-7,16-17H,1H2,(H2,11,12,13)/t3-,4+,6-,7-/m0/s1 InChIKey MBVGIEDXZGVICG-FXZMZVCPSA-N SMILES [C@H]12N3C=4N=CN=C(C4N=C3[C@H]([C@]([C@H](C1)O)(O2)[H])O)N Metabolite of Species Details Mycoplasma genitalium (NCBI:txid2097) See: PubMed Roles Classification Chemical Role(s): Bronsted base A molecular entity capable of accepting a hydron from a donor (Bronsted acid). (via organic amino compound ) Biological Role(s): Mycoplasma genitalium metabolite Any bacterial metabolite produced during a metabolic reaction in Mycoplasma genitalium. View more via ChEBI Ontology ChEBI Ontology Outgoing 8,5'-cyclo-2'-deoxyadenosine (CHEBI:131825) has functional parent 2'-deoxyadenosine (CHEBI:17256) 8,5'-cyclo-2'-deoxyadenosine (CHEBI:131825) has role Mycoplasma genitalium metabolite (CHEBI:131604) 8,5'-cyclo-2'-deoxyadenosine (CHEBI:131825) is a N-glycosyl compound (CHEBI:21731) 8,5'-cyclo-2'-deoxyadenosine (CHEBI:131825) is a aromatic amine (CHEBI:33860) 8,5'-cyclo-2'-deoxyadenosine (CHEBI:131825) is a bridged compound (CHEBI:35990) 8,5'-cyclo-2'-deoxyadenosine (CHEBI:131825) is a diol (CHEBI:23824) 8,5'-cyclo-2'-deoxyadenosine (CHEBI:131825) is a organic heterotetracyclic compound (CHEBI:38163) IUPAC Name (6R,7S,8S,10R)-4-amino-7,8,9,10-tetrahydro-6H-7,10-epoxyazepino[1,2-e]purine-6,8-diol Synonyms Sources 2'-Deoxy-8,5'-cycloadenosine ChemIDplus 8,5'-Cda ChemIDplus cyclo-dA ChEBI cyclodA ChEBI Registry Numbers Types Sources 117182-88-4 CAS Registry Number ChemIDplus 8118367 Reaxys Registry Number Reaxys Citations Types Sources 22817898 PubMed citation Europe PMC 23961697 PubMed citation Europe PMC 24471831 PubMed citation Europe PMC 25034731 PubMed citation Europe PMC 25605892 PubMed citation Europe PMC 26344223 PubMed citation Europe PMC Last Modified 21 April 2016