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TargetDihydrofolate reductase
LigandBDBM50081906
Substrate/Competitorn/a
Meas. Tech.ChEMBL_53497 (CHEMBL665621)
Ki 19±n/a nM
Citation Chowdhury, SFVillamor, VBGuerrero, RHLeal, IBrun, RCroft, SLGoodman, JMMaes, LRuiz-Perez, LMPacanowska, DGGilbert, IH Design, synthesis, and evaluation of inhibitors of trypanosomal and leishmanial dihydrofolate reductase. J Med Chem42:4300-12 (1999) [PubMed]
More Info.:Get all data from this article,  Assay Method
 
Dihydrofolate reductase
Name:Dihydrofolate reductase
Synonyms:DHFR | DYR_HUMAN | Dihydrofolate reductase (DHFR) | Tetrahydrofolate dehydrogenase
Type:Enzyme
Mol. Mass.:21453.99
Organism:Homo sapiens (Human)
Description:Recombinant human DHFR.
Residue:187
Sequence:
MVGSLNCIVAVSQNMGIGKNGDLPWPPLRNEFRYFQRMTTTSSVEGKQNLVIMGKKTWFS
IPEKNRPLKGRINLVLSRELKEPPQGAHFLSRSLDDALKLTEQPELANKVDMVWIVGGSS
VYKEAMNHPGHLKLFVTRIMQDFESDTFFPEIDLEKYKLLPEYPGVLSDVQEEKGIKYKF
EVYEKND
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  Blast E-value cutoff:
BDBM50081906
n/a
NameBDBM50081906
Synonyms:6-Ethyl-5-(3-heptyloxy-benzyl)-pyrimidine-2,4-diamine | CHEMBL135935
TypeSmall organic molecule
Emp. Form.C20H30N4O
Mol. Mass.342.4784
SMILESCCCCCCCOc1cccc(Cc2c(N)nc(N)nc2CC)c1
Structure
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