CHEBI:86012 - oxetanocin A

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ChEBI Name oxetanocin A
Definition A nucleoside analogue found in Bacillus megaterium in which an adenine moiety is attached to position 2 of a of an oxetane ring which is substituted at positions 3 and 4 by hydroxymethyl groups.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C10H13N5O3
Net Charge 0
Average Mass 251.24190
Monoisotopic Mass 251.10184
InChI InChI=1S/C10H13N5O3/c11-8-7-9(13-3-12-8)15(4-14-7)10-5(1-16)6(2-17)18-10/h3-6,10,16-17H,1-2H2,(H2,11,12,13)/t5-,6-,10-/m1/s1
SMILES Nc1ncnc2n(cnc12)[C@@H]1O[C@H](CO)[C@H]1CO
Metabolite of Species Details
Bacillus megaterium (NCBI:txid1404) of strain NK84-0218 See: PubMed
Roles Classification
Biological Role(s): anti-HIV agent
An antiviral agent that destroys or inhibits the replication of the human immunodeficiency virus.
bacterial metabolite
Any prokaryotic metabolite produced during a metabolic reaction in bacteria.
antibacterial agent
A substance (or active part thereof) that kills or slows the growth of bacteria.
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ChEBI Ontology
Outgoing oxetanocin A (CHEBI:86012) has functional parent adenine (CHEBI:16708)
oxetanocin A (CHEBI:86012) has role anti-HIV agent (CHEBI:64946)
oxetanocin A (CHEBI:86012) has role antibacterial agent (CHEBI:33282)
oxetanocin A (CHEBI:86012) has role bacterial metabolite (CHEBI:76969)
oxetanocin A (CHEBI:86012) is a diol (CHEBI:23824)
oxetanocin A (CHEBI:86012) is a nucleoside analogue (CHEBI:60783)
oxetanocin A (CHEBI:86012) is a oxetanes (CHEBI:38784)
oxetanocin A (CHEBI:86012) is a primary alcohol (CHEBI:15734)
Incoming oxetanocin A 4-(dihydrogen phosphate) (CHEBI:86011) has functional parent oxetanocin A (CHEBI:86012)
Synonyms Sources
(−)-oxetanocin ChEBI
(−)-oxetanocin A ChEBI
9-((2'R,3'R,4'S)-3',4'-bis(hydroxymethyl)-2'-oxetanyl)adenine ChEBI
9-[(2R,3R,4S)-3,4-bis(hydroxymethyl)-2-oxetanyl]adenine ChemIDplus
NK 84-0218 ChemIDplus
oxetanocin ChemIDplus
Manual Xref Database
EP0290817 Patent
View more database links
Registry Numbers Types Sources
103913-16-2 CAS Registry Number ChemIDplus
4297990 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
2787618 PubMed citation Europe PMC
3025147 PubMed citation Europe PMC
Last Modified
15 June 2015