CHEBI:84604 - 2-(6-aminohexylamino)-cAMP

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ChEBI Name 2-(6-aminohexylamino)-cAMP
ChEBI ID CHEBI:84604
Definition A 3',5'-cyclic purine nucleotide that is 3',5'-cyclic AMP in which the hydrogen at position 2 on the purine fragment is replaced by a 6-aminohexylamino group
Stars This entity has been manually annotated by the ChEBI Team.
Submitter Margaret Duesbury
jyoti.khadake
Secondary ChEBI IDs CHEBI:64394
Supplier Information
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Formula C16H26N7O6P
Net Charge 0
Average Mass 443.39470
Monoisotopic Mass 443.16822
InChI InChI=1S/C16H26N7O6P/c17-5-3-1-2-4-6-19-16-21-13(18)10-14(22-16)23(8-20-10)15-11(24)12-9(28-15)7-27-30(25,26)29-12/h8-9,11-12,15,24H,1-7,17H2,(H,25,26)(H3,18,19,21,22)/t9-,11-,12-,15-/m1/s1
InChIKey RGMLRJHDNMCVGX-SDBHATRESA-N
SMILES NCCCCCCNc1nc(N)c2ncn([C@@H]3O[C@@H]4COP(O)(=O)O[C@H]4[C@H]3O)c2n1
Roles Classification
Chemical Role(s): Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 2-(6-aminohexylamino)-cAMP (CHEBI:84604) has functional parent 3',5'-cyclic AMP (CHEBI:17489)
2-(6-aminohexylamino)-cAMP (CHEBI:84604) is a 3',5'-cyclic purine nucleotide (CHEBI:19834)
2-(6-aminohexylamino)-cAMP (CHEBI:84604) is a adenyl ribonucleotide (CHEBI:61296)
2-(6-aminohexylamino)-cAMP (CHEBI:84604) is a primary amino compound (CHEBI:50994)
2-(6-aminohexylamino)-cAMP (CHEBI:84604) is a secondary amino compound (CHEBI:50995)
IUPAC Name
(4aR,6R,7R,7aS)-6-{6-amino-2-[(6-aminohexyl)amino]-9H-purin-9-yl}-2,7-dihydroxytetrahydro-2H,4H-2λ5-furo[3,2-d][1,3,2]dioxaphosphinin-2-one
Synonyms Sources
2-(6-aminohexylamino)-3',5'-cyclic AMP ChEBI
2-(6-aminohexylamino)adenosine 3',5'-(cyclic)phosphate JCBN
2-(6-aminohexylamino)adenosine 3',5'-(hydrogen phosphate) ChEBI
2-(6-aminohexylamino)adenosine 3',5'-cyclic monophosphate ChEBI
2-(6-aminohexylamino)adenosine cyclic 3',5'-phosphate ChEBI
2-(6-aminohexylamino)adenosine-3',5'-cyclic monophosphate ChEBI
2-AHA-cAMP ChEBI
Citations Waiting for Citations Types Sources
19119138 PubMed citation Europe PMC
24605759 PubMed citation SUBMITTER
Last Modified
15 January 2020