Page last updated: 2024-10-15

6-hydroxymethyl-7,8-dihydropterin

Description

2-amino-6-(hydroxymethyl)-7,8-dihydropteridin-4-one : A dihydropterin that is 7,8-dihydropteridin-4-one substituted at positions 2 and 6 by amino and hydroxymethyl groups respectively. [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]

2-amino-6-(hydroxymethyl)-7,8-dihydropteridin-4-ol : A dihydropterin that is 7,8-dihydropteridin-4-ol substituted at positions 2 and 6 by amino and hydroxymethyl groups respectively. [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 CID135398568
CHEMBL ID1233322
CHEBI ID17083
CHEBI ID44841
SCHEMBL ID230712
MeSH IDM0475106

Synonyms (31)

Synonym
CHEMBL1233322
CHEBI:17083 ,
2-amino-6-(hydroxymethyl)-7,8-dihydropteridin-4-ol
2-amino-6-hydroxymethyl-7,8-dihydro-3h-pteridin-4-one
2-amino-4-hydroxy-6-hydroxy-methyl-dihydropteridine
2-amino-7,8-dihydro-4-hydroxy-6-(hydroxymethyl)pteridine
2-amino-4-hydroxy-6-(hydroxymethyl)dihydropteridine
3672-03-5
4(1h)-pteridinone, 2-amino-7,8-dihydro-6-(hydroxymethyl)-
2-amino-4-hydroxy-6-(hydroxymethyl)-7,8-dihydropteridine
6-pteridinemethanol, 2-amino-7,8-dihydro-4-hydroxy-
7,8-dihydro-6-(hydroxymethyl)pterin
2-amino-4-hydroxy-6-hydroxymethyl-7,8-dihydropteridine
2-amino-6-(hydroxymethyl)-7,8-dihydropteridin-4-one
C01300
2-amino-6-(hydroxymethyl)-7,8-dihydropteridin-4(3h)-one
6-(hydroxymethyl)-7,8-dihydropterin
6-hydroxymethyl-7,8-dihydropterin
DB02119
2QX0
2-amino-6-(hydroxymethyl)-7,8-dihydro-3h-pteridin-4-one
CHEBI:44841
SCHEMBL230712
DTXSID00274264
2-amino-7,8-dihydro-6-(hydroxymethyl)-4(3h)-pteridinone
Q27093187
2-amino-6-(hydroxymethyl)-1,4,7,8-tetrahydropteridin-4-one
b46l5lr2xm ,
unii-b46l5lr2xm
4(3h)-pteridinone, 2-amino-7,8-dihydro-6-(hydroxymethyl)-
PD008538
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (1)

RoleDescription
Saccharomyces cerevisiae metaboliteAny fungal metabolite produced during a metabolic reaction in Baker's yeast (Saccharomyces cerevisiae).
[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 (1)

ClassDescription
dihydropterin
dihydropterin
[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]

Pathways (6)

PathwayProteinsCompounds
Folate Biosynthesis1126
GTP Degradation and Molybdenum Cofactor Biosynthesis1020
Tetrahydrofolate Biosynthesis829
superpathway of tetrahydrofolate biosynthesis1029
tetrahydrofolate biosynthesis II1232
6-hydroxymethyl-dihydropterin diphosphate biosynthesis I417

Bioassays (2)

Assay IDTitleYearJournalArticle
AID1682980Binding affinity to Escherichia coli BL21 (DE3) HPPK in presence of ATP and MgCl2 by fluorimetry2021Bioorganic & medicinal chemistry, 01-01, Volume: 29Bisubstrate inhibitors of 6-hydroxymethyl-7,8-dihydropterin pyrophosphokinase: Transition state analogs for high affinity binding.
AID1146850Inhibition of Escherichia coli dihydroneopterin aldolase assessed as [14C]glycolaldehyde formation using [14C]neopterin substrate by scintillation counting1977Journal of medicinal chemistry, Sep, Volume: 20, Issue:9
Inhibitors of folate biosynthesis. 1. Inhibition of dihydroneopterin aldolase by pteridine derivatives.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (17)

TimeframeStudies, This Drug (%)All Drugs %
pre-19901 (5.88)18.7374
1990's0 (0.00)18.2507
2000's6 (35.29)29.6817
2010's9 (52.94)24.3611
2020's1 (5.88)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 (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other17 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]