Page last updated: 2024-10-15

2-amino-4-hydroxy-6-formylpteridine

Description

2-amino-4-hydroxy-6-formylpteridine: pteridine precursor in biosynthesis of dihydropteroate; structure [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

6-formylpterin : Pterin carrying a formyl group at position 6. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Cross-References

ID SourceID
PubMed CID135409352
CHEMBL ID3314206
CHEBI ID70981
SCHEMBL ID398501
SCHEMBL ID23270838
MeSH IDM0047803

Synonyms (40)

Synonym
OPREA1_253099
712-30-1
pterin-6-aldehyde
6-formylpterin
2-amino-4-hydroxy-6-formylpteridine
AKOS000276932
2-amino-4-oxo-1h-pteridine-6-carbaldehyde
FT-0661826
6-pteridinecarboxaldehyde, 2-amino-3,4-dihydro-4-oxo-
2-amino-4-oxo-3,4-dihydropteridine-6-carbaldehyde
2-amino-4-hydroxy-pteridine-6-carbaldehyde
EPITOPE ID:178098
2-amino-4-hydroxy-6-pteridylcarboxaldehyde
2-amino-6-formylpteridin-4-one
2-amino-1,4-dihydro-4-oxo-6-pteridinecarboxaldehyde
2-amino-4-hydroxypteridine-6-carboxaldehyde
2-amino-3,4-dihydro-4-oxo-6-pteridinecarboxaldehyde
2-amino-4-hydroxy-6-pteridinecarboxaldehyde
CHEBI:70981 ,
6-formyl pterin
LLJAQDVNMGLRBD-UHFFFAOYSA-N
CHEMBL3314206 ,
DTXSID20221396
2-amino-4-hydroxy-6-formylpteridin
SCHEMBL398501
Q27139229
bdbm50497925
BCP31588
folic acid impurity 5
6-formylpterin;pterin-6-aldehyde; 2-amino-4-hydroxy-6-formylpteridine
SCHEMBL23270838
CS-0064810
AT22350
6-fp
2-amino-4-oxo-4,8-dihydropteridine-6-carbaldehyde
AS-79159
2-amino-4-oxo-3h-pteridine-6-carbaldehyde
PD018821
AKOS040754964
HY-113978
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (2)

RoleDescription
EC 1.17.3.2 (xanthine oxidase) inhibitorAn EC 1.17.3.* (oxidoreductase acting on CH or CH2 with oxygen as acceptor) inhibitor that interferes with the action of xanthine oxidase (EC 1.17.3.2).
reactive oxygen species generatorAny entity used to generate reactive oxygen species.
[role information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Drug Classes (2)

ClassDescription
pterins
aldehydeA compound RC(=O)H, in which a carbonyl group is bonded to one hydrogen atom and to one R group.
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Protein Targets (2)

Inhibition Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Xanthine dehydrogenase Rhodobacter capsulatusKi0.10360.10360.10360.1036AID1185464
Xanthine dehydrogenase/oxidaseBos taurus (cattle)Ki0.00180.00010.83862.6000AID1185460
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Biological Processes (1)

Processvia Protein(s)Taxonomy
xanthine catabolic processXanthine dehydrogenase/oxidaseBos taurus (cattle)
[Information is prepared from geneontology information from the June-17-2024 release]

Molecular Functions (9)

Processvia Protein(s)Taxonomy
xanthine dehydrogenase activityXanthine dehydrogenase/oxidaseBos taurus (cattle)
xanthine oxidase activityXanthine dehydrogenase/oxidaseBos taurus (cattle)
iron ion bindingXanthine dehydrogenase/oxidaseBos taurus (cattle)
molybdenum ion bindingXanthine dehydrogenase/oxidaseBos taurus (cattle)
protein homodimerization activityXanthine dehydrogenase/oxidaseBos taurus (cattle)
molybdopterin cofactor bindingXanthine dehydrogenase/oxidaseBos taurus (cattle)
flavin adenine dinucleotide bindingXanthine dehydrogenase/oxidaseBos taurus (cattle)
2 iron, 2 sulfur cluster bindingXanthine dehydrogenase/oxidaseBos taurus (cattle)
FAD bindingXanthine dehydrogenase/oxidaseBos taurus (cattle)
[Information is prepared from geneontology information from the June-17-2024 release]

Ceullar Components (3)

Processvia Protein(s)Taxonomy
extracellular spaceXanthine dehydrogenase/oxidaseBos taurus (cattle)
peroxisomeXanthine dehydrogenase/oxidaseBos taurus (cattle)
xanthine dehydrogenase complexXanthine dehydrogenase/oxidaseBos taurus (cattle)
[Information is prepared from geneontology information from the June-17-2024 release]

Bioassays (2)

Assay IDTitleYearJournalArticle
AID1185464Inhibition of Rhodobacter capsulatus xanthine dehydrogenase2014Journal of natural products, Jul-25, Volume: 77, Issue:7
X-ray crystal structure of a xanthine oxidase complex with the flavonoid inhibitor quercetin.
AID1185460Inhibition of bovine milk xanthine oxidoreductase by spectrophotometry2014Journal of natural products, Jul-25, Volume: 77, Issue:7
X-ray crystal structure of a xanthine oxidase complex with the flavonoid inhibitor quercetin.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (48)

TimeframeStudies, This Drug (%)All Drugs %
pre-199014 (29.17)18.7374
1990's2 (4.17)18.2507
2000's24 (50.00)29.6817
2010's7 (14.58)24.3611
2020's1 (2.08)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials1 (2.08%)5.53%
Reviews2 (4.17%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other45 (93.75%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]