(Q27125416)

Gene Ontology release 2020-05-02

Rhea release 113

3',5'-cyclic-AMP phosphodiesterase activity

1 reference

reference URL

http://geneontology.org/external2go/rhea2go

http://geneontology.org/external2go/rhea2go

1 February 2021

cAMP deaminase activity

1 reference

reference URL

cAMP biosynthetic process

1 February 2021

product

1 reference

cAMP catabolic process

reactant

1 reference

1 reference

cAMP receptor activity

reactant

1 reference

1 reference

cAMP metabolic process

participant

1 reference

1 reference

1 reference

cellular response to cAMP

reactant

1 reference

mass

328.044695±0 dalton

1 reference

MLS001333136 (English)

6 October 2016

chemical formula

C₁₀H₁₁N₅O₆P⁻

1 reference

based on heuristic

inferred from SMILES

canonical SMILES

C1C2C(C(C(O2)N3C=NC4=C3N=CN=C4N)O)OP(=O)(O1)[O-]

1 reference

MLS001333136 (English)

6 October 2016

isomeric SMILES

C1[C@@H]2[C@H]([C@H]([C@@H](O2)N3C=NC4=C3N=CN=C4N)O)OP(=O)(O1)[O-]

1 reference

https://reactome.org/PathwayBrowser/#/R-HSA-1430728&DTAB=MT

MLS001333136 (English)

6 October 2016

1 reference

Identifiers

InChI

InChI=1S/C10H12N5O6P/c11-8-5-9(13-2-12-8)15(3-14-5)10-6(16)7-4(20-10)1-19-22(17,18)21-7/h2-4,6-7,10,16H,1H2,(H,17,18)(H2,11,12,13)/p-1/t4-,6-,7-,10-/m1/s1

1 reference

MLS001333136 (English)

IVOMOUWHDPKRLL-KQYNXXCUSA-M

6 October 2016

InChIKey

2 references

MLS001333136 (English)

6 October 2016

ChEBI release 2020-09-01

2 references

3',5'-cyclic AMP(1-) (English)

IVOMOUWHDPKRLL-KQYNXXCUSA-M

6 October 2016

InChIKey

9 April 2021

https://commonchemistry.cas.org/detail?cas_rn=62906-31-4

1 reference

(4aR,6R,7R,7aS)-6-(6-Amino-9H-purin-9-yl)-7-hydroxytetrahydro-4H-furo[3,2-d][1,3,2]dioxaphosphinin-2-olate 2-oxide (English)

6 October 2016

1 reference

MLS001333136 (English)

6 October 2016

Reaxys registry number

3720459

1 reference

3',5'-cyclic AMP(1-) (English)

6 October 2016

ChEBI ID

58165

mapping relation type

1 reference