quinazolines has been researched along with 10-formyl-5,8-dideazafolate in 3 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 1 (33.33) | 18.2507 |
2000's | 2 (66.67) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Cook, RJ | 1 |
Krupenko, SA; Vlasov, AP; Wagner, C | 1 |
Caperelli, CA; Dahms, TE; Giroux, EL; Sainz, G; Smith, JL | 1 |
3 other study(ies) available for quinazolines and 10-formyl-5,8-dideazafolate
Article | Year |
---|---|
Use of 10-formyl-5,8-dideazafolate as substrate for rat 10-formyltetrahydrofolate dehydrogenase.
Topics: Acyltransferases; Animals; Folic Acid; Hydrolysis; Hydroxymethyl and Formyl Transferases; Leucovorin; Molecular Structure; NADP; Oxidoreductases Acting on CH-NH Group Donors; Phosphoribosylglycinamide Formyltransferase; Quinazolines; Rats; Spectrophotometry; Stereoisomerism | 1997 |
On the role of conserved histidine 106 in 10-formyltetrahydrofolate dehydrogenase catalysis: connection between hydrolase and dehydrogenase mechanisms.
Topics: Amino Acid Sequence; Animals; Binding Sites; Catalysis; Conserved Sequence; Folic Acid; Histidine; Hydrogen Bonding; Hydrolases; Models, Chemical; Models, Molecular; Molecular Sequence Data; Mutagenesis, Site-Directed; Oxidoreductases Acting on CH-NH Group Donors; Protein Folding; Protein Structure, Tertiary; Quinazolines; Sequence Homology, Amino Acid | 2001 |
The apo and ternary complex structures of a chemotherapeutic target: human glycinamide ribonucleotide transformylase.
Topics: Apoproteins; Binding Sites; Catalysis; Crystallography, X-Ray; Drug Design; Enzyme Inhibitors; Escherichia coli Proteins; Folic Acid; Humans; Hydrogen-Ion Concentration; Hydroxymethyl and Formyl Transferases; Models, Molecular; Phosphoribosylglycinamide Formyltransferase; Protein Binding; Protein Structure, Tertiary; Quinazolines; Substrate Specificity | 2005 |