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TargetDihydrofolate reductase
LigandBDBM50135142
Substrate/Competitorn/a
Meas. Tech.ChEMBL_1888457 (CHEMBL4390134)
IC50 500±n/a nM
Citation Shah, KQueener, SCody, VPace, JGangjee, A Development of substituted pyrido[3,2-d]pyrimidines as potent and selective dihydrofolate reductase inhibitors for pneumocystis pneumonia infection. Bioorg Med Chem Lett29:1874-1880 (2019) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Dihydrofolate reductase
Name:Dihydrofolate reductase
Synonyms:DYR_RAT | Dhfr | Dihydrofolate reductase (DHFR) | Dihydrofolate reductase; P. carinii vs rat | Tetrahydrofolate dehydrogenase
Type:Enzyme
Mol. Mass.:21638.84
Organism:Rattus norvegicus (rat)
Description:n/a
Residue:187
Sequence:
MVRPLNCIVAVSQNMGIGKNGDLPWPLLRNEFKYFQRMTTTSSVEGKQNLVIMGRKTWFS
IPEKNRPLKDRINIVLSRELKEPPQGAHFLAKSLDDALKLIEQPELASKVDMVWVVGGSS
VYQEAMNQPGHLRLFVTRIMQEFESDTFFPEIDLEKYKLLPEYPGVLSEIQEEKGIKYKF
EVYEKKD
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BDBM50135142
n/a
NameBDBM50135142
Synonyms:6-[(2,5-Dimethoxy-phenylamino)-methyl]-pyrido[2,3-d]pyrimidine-2,4-diamine | CHEMBL424135
TypeSmall organic molecule
Emp. Form.C16H18N6O2
Mol. Mass.326.3531
SMILESCOc1ccc(OC)c(NCc2cnc3nc(N)nc(N)c3c2)c1
Structure
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