| Weight | 916.112 g/mol |
|---|---|
| Formula | C46H77NO17 |
| Hydrogen Acceptors | 18 |
| Hydrogen Donors | 5 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 13 |
Tylosin (1401-69-0)
Score:
#325 in Microbiology
,
#2706 in Biology
,
#3383 in Chemistry
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- Sorption and mobility of metronidazole, olaquindox, oxytetracycline and tylosin in soil (Chemosphere, 2000)
- Use of oxytetracycline and tylosin in intensive calf farming: evaluation of transfer to manure and soil (Chemosphere, 2003)
- A tylosin ketoreductase reveals how chirality is determined in polyketides (Chemistry & Biology, 2007)
- Determination of the distribution coefficient (logKd) of oxytetracycline, tylosin A, olaquindox and metronidazole in manure (Chemosphere, 2002)
- The effect of pH and ionic strength on the sorption of sulfachloropyridazine, tylosin, and oxytetracycline to soil. (Environmental Toxicology and Chemistry, 2006)
- Effects of the antibiotics oxytetracycline and tylosin on soil fauna. (Chemosphere, 2000)
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Predict GHS Hazards for Any Chemical in silico.
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SMILESCCC1C(C=C(C=CC(=O)C(CC(C(C(C(CC(=O)O1)O)C)OC2C(C(C(C(O2)C)OC3CC(C(C(O3)C)O)(C)O)N(C)C)O)CC=O)C)C)COC4C(C(C(C(O4)C)O)OC)OC
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InChIKeyWBPYTXDJUQJLPQ-UHFFFAOYSA-N
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