Page last updated: 2024-10-15

6-methyltetrahydropterin

Cross-References

ID SourceID
PubMed CID135443397
CHEMBL ID344471
CHEBI ID166567
SCHEMBL ID584982
MeSH IDM0068344

Synonyms (29)

Synonym
CHEBI:166567
942-41-6
2-amino-6-methyl-5,6,7,8-tetrahydro-3h-pteridin-4-one
CHEMBL344471 ,
6-methyltetrahydropterin
bdbm50378559
c9ao82g1r1 ,
tyrosine hydroxylase pteridine cofactor
4(1h)-pteridinone, 2-amino-5,6,7,8-tetrahydro-6-methyl-
2-amino-6-methyl-5,6,7,8-tetrahydro-4(3h)-pteridinone
6-methyltetrahydropteridine
unii-c9ao82g1r1
6-mph4
6-methyl-5,6,7,8-tetrahydrobiopterin
mph4
SCHEMBL584982
dl-6-methyl-5,6,7,8-tetrahydropterin
6-methyltetrahydropterin, (+/-)-
6-methyl-5,6,7,8-tetrahydropterin
2-amino-4-hydroxy-6-methyl-5,6,7,8-tetrahydropteridine
4(3h)-pteridinone, 2-amino-5,6,7,8-tetrahydro-6-methyl-
2-amino-6-methyl-1,4,5,6,7,8-hexahydropteridin-4-one
2-amino-5,6,7,8-tetrahydro-6-methyl-4(1h)-pteridinone
DTXSID40912476
2-amino-6-methyl-5,6,7,8-tetrahydropteridin-4(1h)-one
Q27275350
2-amino-6-methyl-5,6,7,8-tetrahydropteridin-4(3h)-one
SB47599
CS-0436315
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
pterins
[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 (1)

Inhibition Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (4)

Assay IDTitleYearJournalArticle
AID228546Michaelis-Menten constant was determined for the compound1983Journal of medicinal chemistry, Apr, Volume: 26, Issue:4
Preparation of 2-amino-4(3H)-oxopyrimido[5,4-b] [1,4]thiazines (5-thiapterins) and their evaluation as cofactors for phenylalanine hydroxylase.
AID444560Inhibition of Bacillus anthracis DHPS expressed in Escherichia coli BL21 (DE3) after 30 mins2010Journal of medicinal chemistry, Jan-14, Volume: 53, Issue:1
Structural studies of pterin-based inhibitors of dihydropteroate synthase.
AID157599Tested for competitive binding inhibition against phenylalanine hydroxylase in rat liver; ND denotes no data1983Journal of medicinal chemistry, Apr, Volume: 26, Issue:4
Preparation of 2-amino-4(3H)-oxopyrimido[5,4-b] [1,4]thiazines (5-thiapterins) and their evaluation as cofactors for phenylalanine hydroxylase.
AID444559Inhibition of Bacillus anthracis DHPS expressed in Escherichia coli BL21 (DE3) at 500 uM after 30 mins2010Journal of medicinal chemistry, Jan-14, Volume: 53, Issue:1
Structural studies of pterin-based inhibitors of dihydropteroate synthase.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (51)

TimeframeStudies, This Drug (%)All Drugs %
pre-199024 (47.06)18.7374
1990's14 (27.45)18.2507
2000's9 (17.65)29.6817
2010's4 (7.84)24.3611
2020's0 (0.00)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 Studies2 (3.92%)4.05%
Observational0 (0.00%)0.25%
Other49 (96.08%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]