CHEBI:140314 - 5'-triphosphoadenylyl-(2'→5')-adenosine

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ChEBI Name 5'-triphosphoadenylyl-(2'→5')-adenosine
ChEBI ID CHEBI:140314
ChEBI ASCII Name 5'-triphosphoadenylyl-(2'->5')-adenosine
Definition A (2'→5')-dinucleotide composed of two adenosine residues with a triphosphate group at the 5' terminus.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C20H28N10O19P4
Net Charge 0
Average Mass 836.388
Monoisotopic Mass 836.04827
InChI InChI=1S/C20H28N10O19P4/c21-15-9-17(25-3-23-15)29(5-27-9)19-13(33)11(31)7(45-19)1-43-51(37,38)47-14-12(32)8(2-44-52(39,40)49-53(41,42)48-50(34,35)36)46-20(14)30-6-28-10-16(22)24-4-26-18(10)30/h3-8,11-14,19-20,31-33H,1-2H2,(H,37,38)(H,39,40)(H,41,42)(H2,21,23,25)(H2,22,24,26)(H2,34,35,36)/t7-,8-,11-,12-,13-,14-,19-,20-/m1/s1
InChIKey YHHSPPDBQDMAPZ-XPWFQUROSA-N
SMILES P(OP(OP(OC[C@H]1O[C@@H](N2C=3N=CN=C(N)C3N=C2)[C@@H]([C@@H]1O)OP(=O)(OC[C@H]4O[C@H]([C@@H]([C@@H]4O)O)N5C=6N=CN=C(N)C6N=C5)O)(=O)O)(=O)O)(=O)(O)O
Metabolite of Species Details
Escherichia coli (NCBI:txid562) See: PubMed
Roles Classification
Biological Role(s): antiviral agent
A substance that destroys or inhibits replication of viruses.
bacterial metabolite
Any prokaryotic metabolite produced during a metabolic reaction in bacteria.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 5'-triphosphoadenylyl-(2'→5')-adenosine (CHEBI:140314) has role antiviral agent (CHEBI:22587)
5'-triphosphoadenylyl-(2'→5')-adenosine (CHEBI:140314) has role bacterial metabolite (CHEBI:76969)
5'-triphosphoadenylyl-(2'→5')-adenosine (CHEBI:140314) is a (2'→5')-dinucleotide (CHEBI:75800)
5'-triphosphoadenylyl-(2'→5')-adenosine (CHEBI:140314) is conjugate acid of 5'-triphosphoadenylyl-(2'→5')-adenosine(5−) (CHEBI:140294)
Incoming 5'-triphosphoadenylyl-(2'→5')-adenosine(5−) (CHEBI:140294) is conjugate base of 5'-triphosphoadenylyl-(2'→5')-adenosine (CHEBI:140314)
Synonym Source
pppA2'p5'A ChEBI
Registry Number Type Source
4646833 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
2482032 PubMed citation Europe PMC
2960522 PubMed citation Europe PMC
6090695 PubMed citation Europe PMC
6276660 PubMed citation Europe PMC
6933509 PubMed citation Europe PMC
9880533 PubMed citation Europe PMC
Last Modified
02 March 2018