| Weight | 339.193 g/mol |
|---|---|
| Formula | C13H15BrN4O2 |
| Hydrogen Acceptors | 6 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 4 |
Brodimoprim (56518-41-3)
2,4-diamino-5-(4-bromo-3,5-dimethoxybenzyl)pyrimidine · Ro-10-5970 · Ro 10-5970
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- A 1H NMR study of the interactions and conformations of rationally designed brodimoprim analogues in complexes with Lactobacillus casei dihydrofolate reductase. (Journal of Medicinal Chemistry, 1984)
- Correlation of trimethoprim and brodimoprim physicochemical and lipid membrane interaction properties with their accumulation in human neutrophils. (Antimicrobial Agents and Chemotherapy, 1996)
- Relationships between structural and thermal properties of anhydrous and solvated crystalline forms of brodimoprim (Journal of Pharmaceutical Sciences, 2007)
- 1H/15N HSQC NMR Studies of Ligand Carboxylate Group Interactions with Arginine Residues in Complexes of Brodimoprim Analogues and Lactobacillus casei Dihydrofolate Reductase, (Biochemistry, 1999)
- Influence of subinhibitory concentrations of brodimoprim and trimethoprim on the adhesiveness, hydrophobicity, hemagglutination and motility of Escherichia coli (Chemotherapy, 1995)
- Solution structure of a brodimoprim analogue in its complex with Lactobacillus casei dihydrofolate reductase. (Biochemistry, 1995)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 2,4-diamino-5-(4-bromo-3,5-dimethoxybenzyl)pyrimidine
- Ro-10-5970
- Ro 10-5970
-
SMILESCOC1=CC(=CC(=C1Br)OC)CC2=CN=C(N=C2N)N
-
InChIKeyBFCRRLMMHNLSCP-UHFFFAOYSA-N
- Pubchem - Brodimoprim
- Wikipedia - brodimoprim
Brodimoprim is a structural derivative of trimethoprim. In brodimoprim, the 4-methoxy group of trimethoprim is replaced with a bromine atom. As trimethoprim, brodimoprim is a selective inhibitor of bacterial dihydrofolate reductase.
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