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EC 2.4.2.4 (thymidine phosphorylase) inhibitor

An EC 2.4.2.* (pentosyltransferase) inhibitor that interferes with the action of thymidine phosphorylase (EC 2.4.2.4).

ChEBI ID: 90878

Members (2)

MemberDefinitionClass
5-chloro-6-(1-(2-iminopyrrolidinyl) methyl)uracil hydrochlorideA hydrochloride obtained by combining tipiracil with one equivalent of hydrochloric acid. Used in combination with trifluridine, a nucleoside metabolic inhibitor, for treatment of advanced/relapsed unresectable colorectal cancer.tipiracil hydrochloride
ma-1A member of the class of pyrimidones that is uracil substituted by chloro and (2-iminopyrrolidin-1-yl)methyl groups at positions 5 and 6 respectively. Used (as the hydrochloride salt) in combination with trifluridine, a nucleoside metabolic inhibitor, for treatment of advanced/relapsed unresectable colorectal cancer.tipiracil

Research

Studies (127)

TimeframeStudies, Drugs with This Role(%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's8 (6.30)29.6817
2010's29 (22.83)24.3611
2020's90 (70.87)2.80

Study Types

Publication TypeStudies, Drugs with this Role (%)All Drugs (%)
Trials31 (24.22%)5.53%
Reviews7 (5.47%)6.00%
Case Studies7 (5.47%)4.05%
Observational8 (6.25%)0.25%
Other75 (58.59%)84.16%

Protein Targets (3)

Potency Measurements

ProteinTaxonomyMeasurementAverage (mM)Bioassay(s)Drugs
Spike glycoproteinSevere acute respiratory syndrome-related coronavirusPotency39.810711

Inhibition Measurements

ProteinTaxonomyMeasurementAverage (mM)Bioassay(s)Drugs
Thymidine phosphorylaseEscherichia coli K-12IC500.022755
Thymidine phosphorylaseHomo sapiens (human)IC500.03111212
Thymidine phosphorylaseEscherichia coli K-12Ki0.035011
Thymidine phosphorylaseHomo sapiens (human)Ki0.011599