Tylosin

Chemical Information
Tylosin is a macrolide antibiotic that is tylonolide having mono- and diglycosyl moieties attached to two of its hydroxy groups. It is found naturally as a fermentation product of Streptomyces fradiae. It has a role as a xenobiotic, an allergen, a bacterial metabolite and an environmental contaminant. It is an aldehyde, a leucomycin, a macrolide antibiotic, an enone, a disaccharide derivative and a monosaccharide derivative. It is functionally related to a tylactone. It is a conjugate base of a tylosin(1+).
| CAS Number | 1401-69-0 |
| PubChem CID | 5280440 |
| IUPAC Name | 2-[(4R,5S,6S,7R,9R,11E,13E,15R,16R)-6-[(2R,3R,4R,5S,6R)-5-[(2S,4R,5S,6S)-4,5-dihydroxy-4,6-dimethyloxan-2-yl]oxy-4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy-16-ethyl-4-hydroxy-15-[[(2R,3R,4R,5R,6R)-5-hydroxy-3,4-dimethoxy-6-methyloxan-2-yl]oxymethyl]-5,9,13-trimethyl-2,10-dioxo-1-oxacyclohexadeca-11,13-dien-7-yl]acetaldehyde |
| Molecular Formula | C46H77NO17 |
| Molecular Weight | 916.1 |
| XLogP | 1 |
| Topological Polar Surface Area | 239 |
| Hydrogen Bond Donor Count | 5 |
| Hydrogen Bond Acceptor Count | 18 |
| Rotatable Bond Count | 13 |
| Heavy Atom Count | 64 |
| Formal Charge | 0 |
| Complexity | 1560 |
| Property | Value |
|---|---|
| Molecular Weight | 916.1 |
| XLogP3 | 1 |
| Hydrogen Bond Donor Count | 5 |
| Hydrogen Bond Acceptor Count | 18 |
| Rotatable Bond Count | 13 |
| Exact Mass | 915.51914999 |
| Monoisotopic Mass | 915.51914999 |
| Topological Polar Surface Area | 239 Ų |
| Heavy Atom Count | 64 |
| Formal Charge | 0 |
| Complexity | 1560 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 21 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 2 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently-Bonded Unit Count | 1 |
| Compound Is Canonicalized | Yes |
Alternative Products
| Catalog | Name |
|---|---|
| MBS3601676-01 | Tylosin |
| IAA02648-01 | Tylosin A |
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