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Reaction Details
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TargetDihydrofolate reductase
LigandBDBM18071
Substrate/CompetitorBDBM18044
Meas. Tech.Enzyme Inhibition Assay
pH7±n/a
Temperature303.15±n/a K
Ki 9±n/a nM
IC50 90±20 nM
CommentsMIC=0.06 ug/mL.
Citation MUKHIJA, SBANDERA, MPARISI, SRIGO, SLIEB, SLOCIURO, SGILLESSEN, DISLAM, K AR-709-An Investigational diaminopyrimidine: Inhibition, Binding and Mode of Action. Interscience Conference on Antimicrobial Agents in Chemotherapy0:1-1 (2006)  
More Info.:Get all data from this article,   Solution Info,  Assay Method
 
Dihydrofolate reductase
Name:Dihydrofolate reductase
Synonyms:Dihydrofolate Reductase (DHFR) Mutant (I100L) | Tetrahydrofolate dehydrogenase
Type:Enzyme
Mol. Mass.:19700.70
Organism:Streptococcus pneumoniae (ATCC49619)
Description:n/a
Residue:168
Sequence:
MTKKIVAIWAQDEEGVIGKENRLPWHLPAELQHFKETTLNHAILMGRVTFDGMGRRLLPK
RETLILTRNPEEKIDGVATFQDVQSVLDWYQAQEKNLYILGGKQIFQAFEPYLDEVIVTH
IHARVEGDTYFPEELDLSLFETVSSKFYAKDEKNPYDFTIQYRKRKEV
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BDBM18071
BDBM18044
NameBDBM18071
Synonyms:5-chloro-3-({4-[(2,4-diaminopyrimidin-5-yl)methyl]-6,7-dimethoxy-1-benzofuran-2-yl}methyl)-N,N-dimethyl-1H-indole-2-carboxamide | AR-709
TypeSmall organic molecule
Emp. Form.C27H27ClN6O4
Mol. Mass.534.994
SMILESCOc1cc(Cc2cnc(N)nc2N)c2cc(Cc3c([nH]c4ccc(Cl)cc34)C(=O)N(C)C)oc2c1OC
Structure
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