Compound ID | 1967
Class: Diaminopyrimidine
Spectrum of activity: | Gram-positive |
Details of activity: | Inhibits dihydrofolic acid reductase and thus, the synthesis of purine |
Description: | Synthetic compound. Trimethoprim derivative |
Year first mentioned: | 1984 |
Development status: | Inactive |
Chemical structure(s): | |
Canonical SMILES: | COC1=CC(=CC(=C1Br)OC)CC2=C(N)N=C(N)N=C2 |
Isomeric SMILES: | COC1=CC(=CC(=C1Br)OC)CC2=CN=C(N=C2N)N |
InChI: | InChI=1S/C13H15BrN4O2/c1-19-9-4-7(5-10(20-2)11(9)14)3-8-6-17-13(16)18-12(8)15/h4-6H,3H2,1-2H3,(H4,15,16,17,18) |
InChI Key: | BFCRRLMMHNLSCP-UHFFFAOYSA-N |
Structure link: | https://pubchem.ncbi.nlm.nih.gov/compound/68760 |
External links: | |
Guide to Pharmacology: | brodimoprim |
Main Source: | https://www.karger.com/Article/Abstract/238239 |
Citations: |
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