Tylosin tartrate

For research use only. Not for therapeutic Use.

  • CAT Number: A001141
  • CAS Number: 74610-55-2
  • Molecular Formula: C46H77NO17.C4H6O6
  • Molecular Weight: 1066.19
  • Purity: ≥95%
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Tylosin Tartrate(Cat No.:A001141)is an antibiotic used primarily in veterinary medicine for the treatment of various bacterial infections in animals, including respiratory and gastrointestinal infections. This macrolide antibiotic works by inhibiting bacterial protein synthesis, making it effective against a range of gram-positive and some gram-negative bacteria. Tylosin Tartrate is often used in poultry, swine, and cattle to prevent and control infections like mycoplasmosis. It is also employed in aquaculture to manage bacterial diseases in fish. Its stable form ensures effective treatment when administered in feed or water.


Catalog Number A001141
CAS Number 74610-55-2
Synonyms

NA

Molecular Formula C46H77NO17.C4H6O6
Purity ≥95%
Target Bacterial
Storage 3 years -20C powder
IUPAC Name (2R,3R)-2,3-dihydroxybutanedioic acid;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
InChI InChI=1S/C46H77NO17.C4H6O6/c1-13-33-30(22-58-45-42(57-12)41(56-11)37(52)26(5)60-45)18-23(2)14-15-31(49)24(3)19-29(16-17-48)39(25(4)32(50)20-34(51)62-33)64-44-38(53)36(47(9)10)40(27(6)61-44)63-35-21-46(8,55)43(54)28(7)59-35;5-1(3(7)8)2(6)4(9)10/h14-15,17-18,24-30,32-33,35-45,50,52-55H,13,16,19-22H2,1-12H3;1-2,5-6H,(H,7,8)(H,9,10)/b15-14+,23-18+;/t24-,25+,26-,27-,28+,29+,30-,32-,33-,35+,36-,37-,38-,39-,40-,41-,42-,43+,44+,45-,46-;1-,2-/m11/s1
InChIKey ICVKYYINQHWDLM-KBEWXLTPSA-N
SMILES CC[C@@H]1[C@H](/C=C(/C=C/C(=O)[C@@H](C[C@@H]([C@@H]([C@H]([C@@H](CC(=O)O1)O)C)O[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)C)O[C@H]3C[C@@]([C@H]([C@@H](O3)C)O)(C)O)N(C)C)O)CC=O)C)\C)CO[C@H]4[C@@H]([C@@H]([C@@H]([C@H](O4)C)O)OC)OC.[C@@H]([C@H](C(=O)O)O)(C(=O)O)O
Reference

<p>
Lovmar, Martin, and Tanel Tenson. /The Mechanism of Action of Macrolides, Lincosamides and Streptogramin B Reveals the Nascent Peptide Exit Path in the Ribosome./<em>Journal of Molecular Microbiology</em> 330.5 (2003): 1005-014.</p>
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