| Weight | 260.297 g/mol |
|---|---|
| Formula | C13H16N4O2 |
| Hydrogen Acceptors | 6 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 4 |
DIAVERIDINE (5355-16-8)
diaveridine monohydrochloride · EGIS-5645 · 2,4-diamino-5-(3,4-dimethoxybenzyl)pyrimidine
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- The diffusion of selected sulfonamides, trimethoprim, and diaveridine into prostatic fluid of dogs. (Investigative urology, 1971)
- The genotoxicity of diaveridine and trimethoprim. (Environmental Toxicology and Pharmacology, 1997)
- Treatment of experimental avian coccidiosis with a soluble combination of sulphaquinoxaline and diaveridine (Veterinary Record, 1965)
- An improved synthesis of diaveridine, trimethoprim, and closely related 2,4-diaminopyrimidines. (Journal of Medicinal Chemistry, 1971)
- Characterization of in vitro metabolites of trimethoprim and diaveridine in pig liver microsomes by liquid chromatography combined with hybrid ion trap/time-of-flight mass spectrometry. (Biomedical Chromatography, 2012)
- Determination of residual diaveridine and sulfaquinoxaline in Hen's egg, chicken plasma and tissues by high-performance liquid chromatography. (Chemical & Pharmaceutical Bulletin, 1981)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - diaveridine monohydrochloride
- EGIS-5645
- 2,4-diamino-5-(3,4-dimethoxybenzyl)pyrimidine
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SMILESCOC1=C(C=C(C=C1)CC2=CN=C(N=C2N)N)OC
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DIAVERIDINE
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