Target
Dihydrofolate reductase
Ligand
BDBM50029769
Substrate
n/a
Meas. Tech.
ChEMBL_53494 (CHEMBL665618)
IC50
3300±n/a nM
Citation
 Rosowsky, AMota, CEWright, JEFreisheim, JHHeusner, JJMcCormack, JJQueener, SF 2,4-Diaminothieno[2,3-d]pyrimidine analogues of trimetrexate and piritrexim as potential inhibitors of Pneumocystis carinii and Toxoplasma gondii dihydrofolate reductase. J Med Chem 36:3103-12 (1993) [PubMed]
Target
Name:
Dihydrofolate reductase
Synonyms:
Bacterial dihydrofolate reductase | DYR_ECOLI | Dihydrofolate Reductase (DHFR) | Tetrahydrofolate dehydrogenase | folA | tmrA
Type:
Enzyme
Mol. Mass.:
17991.61
Organism:
Escherichia coli
Description:
E. coli DHFR was expressed in BL21, and purified to homogeneity.
Residue:
159
Sequence:
MISLIAALAVDRVIGMENAMPWNLPADLAWFKRNTLNKPVIMGRHTWESIGRPLPGRKNIILSSQPGTDDRVTWVKSVDEAIAACGDVPEIMVIGGGRVYEQFLPKAQKLYLTHIDAEVEGDTHFPDYEPDDWESVFSEFHDADAQNSHSYCFEILERR
  
Inhibitor
Name:
BDBM50029769
Synonyms:
6-[2-(2,5-Dimethoxy-phenyl)-ethyl]-5-methyl-thieno[2,3-d]pyrimidine-2,4-diamine | CHEMBL322585
Type:
Small organic molecule
Emp. Form.:
C17H20N4O2S
Mol. Mass.:
344.431
SMILES:
COc1ccc(OC)c(CCc2sc3nc(N)nc(N)c3c2C)c1
Structure:
Search PDB for entries with ligand similarity: