Reaction Details |
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Target | Dihydrofolate reductase |
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Ligand | BDBM50387407 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_828283 (CHEMBL2050302) |
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IC50 | >16000±n/a nM |
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Citation | Gangjee, A; Zhao, Y; Ihnat, MA; Thorpe, JE; Bailey-Downs, LC; Kisliuk, RL Novel tricyclic indeno[2,1-d]pyrimidines with dual antiangiogenic and cytotoxic activities as potent antitumor agents. Bioorg Med Chem20:4217-25 (2012) [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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BDBM50387407 |
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n/a |
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Name | BDBM50387407 |
Synonyms: | CHEMBL2047253 |
Type | Small organic molecule |
Emp. Form. | C17H12ClFN4 |
Mol. Mass. | 326.755 |
SMILES | Nc1nc2cc3ccccc3c2c(Nc2ccc(Cl)cc2F)[nH]1 |
Structure |
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