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TargetDihydrofolate reductase
LigandBDBM50108174
Substrate/Competitorn/a
Meas. Tech.ChEMBL_52830 (CHEMBL665036)
IC50 2600±n/a nM
Citation Rosowsky, AForsch, RAQueener, SF Inhibition of Pneumocystis carinii, Toxoplasma gondii, and Mycobacterium avium dihydrofolate reductases by 2,4-diamino-5-[2-methoxy-5-(omega-carboxyalkyloxy)benzyl]pyrimidines: marked improvement in potency relative to trimethoprim and species selectivity relative to piritrexim. J Med Chem45:233-41 (2001) [PubMed]
More Info.:Get all data from this article,  Assay Method
 
Dihydrofolate reductase
Name:Dihydrofolate reductase
Synonyms:Dihydrofolate reductase (F31V) | dfrA17
Type:n/a
Mol. Mass.:17532.46
Organism:Escherichia coli
Description:n/a
Residue:157
Sequence:
MKISLISAVSESGVIGSGPDIPWSVKGEQLLFKALTYNQWLLVGRKTFDSMGVLPNRKYA
VVSKNGISSSNENVLVFPSIENALKELSKVTDHVYVSGGGQIYNSLIEKADIIHLSTVHV
EVEGDIKFPIMPENFNLVFEQFFMSNINYTYQIWKKG
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BDBM50108174
n/a
NameBDBM50108174
Synonyms:7-[3-(2,4-Diamino-pyrimidin-5-ylmethyl)-4-methoxy-phenoxy]-heptanoic acid | CHEMBL36310
TypeSmall organic molecule
Emp. Form.C19H26N4O4
Mol. Mass.374.4341
SMILESCOc1ccc(OCCCCCCC(O)=O)cc1Cc1cnc(N)nc1N
Structure
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