Reaction Details Report a problem with these data
Target
Dihydrofolate reductase
Ligand
BDBM50067856
Substrate
n/a
Meas. Tech.
ChEMBL_55108 (CHEMBL665435)
IC50
75.0±n/a nM
Citation
 Gangjee, A; Zhu, Y; Queener, SF 6-Substituted 2,4-diaminopyrido[3,2-d]pyrimidine analogues of piritrexim as inhibitors of dihydrofolate reductase from rat liver, Pneumocystis carinii, and Toxoplasma gondii and as antitumor agents. J Med Chem 41:4533-41 (1998) [PubMed]  Article 
Target
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:
MVRPLNCIVAVSQNMGIGKNGDLPWPLLRNEFKYFQRMTTTSSVEGKQNLVIMGRKTWFSIPEKNRPLKDRINIVLSRELKEPPQGAHFLAKSLDDALKLIEQPELASKVDMVWVVGGSSVYQEAMNQPGHLRLFVTRIMQEFESDTFFPEIDLEKYKLLPEYPGVLSEIQEEKGIKYKFEVYEKKD
  
Inhibitor
Name:
BDBM50067856
Synonyms:
6-(4-Methoxy-phenylsulfanyl)-pyrido[3,2-d]pyrimidine-2,4-diamine | CHEMBL137844
Type:
Small organic molecule
Emp. Form.:
C14H13N5OS
Mol. Mass.:
299.351
SMILES:
COc1ccc(Sc2ccc3nc(N)nc(N)c3n2)cc1
Structure:
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