Reaction Details |
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Target | Dihydrofolate reductase |
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Ligand | BDBM50011887 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_54103 |
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IC50 | 8500±n/a nM |
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Citation | Rosowsky, A; Forsch, RA; Bader, H; Freisheim, JH Synthesis and in vitro biological activity of new deaza analogues of folic acid, aminopterin, and methotrexate with an L-ornithine side chain. J Med Chem34:1447-54 (1991) [PubMed] |
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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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BDBM50011887 |
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n/a |
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Name | BDBM50011887 |
Synonyms: | 5-Amino-2-{4-[(2-amino-4-oxo-3,4-dihydro-pyrido[2,3-d]pyrimidin-6-ylmethyl)-amino]-benzoylamino}-pentanoic acid | CHEMBL35231 |
Type | Small organic molecule |
Emp. Form. | C20H23N7O4 |
Mol. Mass. | 425.4411 |
SMILES | NCCCC(NC(=O)c1ccc(NCc2cnc3nc(N)[nH]c(=O)c3c2)cc1)C(O)=O |
Structure |
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