Reaction Details |
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Target | Dihydrofolate reductase |
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Ligand | BDBM18268 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_2260222 (CHEMBL5215233) |
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Ki | 0.040000±n/a nM |
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Citation | Bansal, R; Malhotra, A Therapeutic progression of quinazolines as targeted chemotherapeutic agents. Eur J Med Chem211:0 (2021) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Dihydrofolate reductase |
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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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BDBM18268 |
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n/a |
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Name | BDBM18268 |
Synonyms: | 5-methyl-6-{[(3,4,5-trimethoxyphenyl)amino]methyl}quinazoline-2,4-diamine | CHEMBL119 | TMQ | Trimetrexate | US11111252, Compound TMQ | US11530198, Example Trimetrexate |
Type | Small organic molecule |
Emp. Form. | C19H23N5O3 |
Mol. Mass. | 369.4176 |
SMILES | COc1cc(NCc2ccc3nc(N)nc(N)c3c2C)cc(OC)c1OC |
Structure |
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