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Contents

   



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1 Medical uses  




2 References  













Tylvalosin







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From Wikipedia, the free encyclopedia
  

Tylvalosin
Clinical data
Trade namesAiviosin
AHFS/Drugs.comVeterinary Use
License data
Routes of
administration		By mouth
Drug classMacrolide antibiotic
ATCvet code
Legal status
Legal status
Identifiers
CAS Number
  • as tartrate: 63428-13-7
    • PubChem CID
    DrugBank
  • as tartrate: DBSALT001708
    • ChemSpider
  • as tartrate: 30790860
    • UNII
  • as tartrate: AL5667FY0W
    • KEGG
  • as tartrate: D10034
    • ChEMBL
    CompTox Dashboard (EPA)
    ECHA InfoCard100.058.284 Edit this at Wikidata
    Chemical and physical data
    FormulaC53H87NO19
    Molar mass1042.267 g·mol−1
    3D model (JSmol)
  • as tartrate: Interactive image

    • CC[C@H]1OC(=O)C[C@@H](OC(C)=O)[C@H](C)[C@@H](O[C@@H]2O[C@H](C)[C@@H](O[C@H]3C[C@@](C)(O)[C@@H](OC(=O)CC(C)C)[C@H](C)O3)[C@@H]([C@H]2O)N(C)C)[C@@H](CC=O)C[C@@H](C)C(=O)\C=C\C(\C)=C\[C@@H]1CO[C@@H]1O[C@H](C)[C@@H](O)[C@@H](OC)[C@H]1OC


    • as tartrate: O[C@H]([C@@H](O)C(O)=O)C(O)=O.CC[C@H]1OC(=O)C[C@@H](OC(C)=O)[C@H](C)[C@@H](O[C@@H]2O[C@H](C)[C@@H](O[C@H]3C[C@@](C)(O)[C@@H](OC(=O)CC(C)C)[C@H](C)O3)[C@@H]([C@H]2O)N(C)C)[C@@H](CC=O)C[C@@H](C)C(=O)\C=C\C(\C)=C\[C@@H]1CO[C@@H]1O[C@H](C)[C@@H](O)[C@@H](OC)[C@H]1OC

    • InChI=1S/C53H87NO19/c1-16-38-36(26-65-52-49(64-15)48(63-14)44(60)31(7)67-52)22-28(4)17-18-37(57)29(5)23-35(19-20-55)46(30(6)39(69-34(10)56)24-41(59)70-38)73-51-45(61)43(54(12)13)47(32(8)68-51)72-42-25-53(11,62)50(33(9)66-42)71-40(58)21-27(2)3/h17-18,20,22,27,29-33,35-36,38-39,42-52,60-62H,16,19,21,23-26H2,1-15H3/b18-17+,28-22+/t29-,30+,31-,32-,33+,35+,36-,38-,39-,42+,43-,44-,45-,46-,47-,48-,49-,50+,51+,52-,53-/m1/s1

    • Key:KCJJINQANFZSAM-HZDSEHBESA-N


    • as tartrate: InChI=1S/C53H87NO19.C4H6O6/c1-16-38-36(26-65-52-49(64-15)48(63-14)44(60)31(7)67-52)22-28(4)17-18-37(57)29(5)23-35(19-20-55)46(30(6)39(69-34(10)56)24-41(59)70-38)73-51-45(61)43(54(12)13)47(32(8)68-51)72-42-25-53(11,62)50(33(9)66-42)71-40(58)21-27(2)3;5-1(3(7)8)2(6)4(9)10/h17-18,20,22,27,29-33,35-36,38-39,42-52,60-62H,16,19,21,23-26H2,1-15H3;1-2,5-6H,(H,7,8)(H,9,10)/b18-17+,28-22+;/t29-,30+,31-,32-,33+,35+,36-,38-,39-,42+,43-,44-,45-,46-,47-,48-,49-,50+,51+,52-,53-;1-,2-/m11/s1

    • Key:OLLSDNUHBJHKJS-XKORHJEPSA-N

    Tylvalosin, sold under the brand name Aiviosin, is a macrolide antibiotic used for the treatment of bacterial infections in swine.[3] It is used as tylvalosin tartrate.[3]

    Medical uses[edit]

    Tylvalosin is indicated for the control of porcine proliferative enteropathy associated with Lawsonia intracellularis infection in groups of swine intended for slaughter and female swine intended for breeding in buildings experiencing an outbreak of PPE.[3] Not for use in male swine intended for breeding; and for the control of swine respiratory disease associated with Bordetella bronchiseptica, Glaesserella (Haemophilus) parasuis, Pasteurella multocida, Streptococcus suis, and Mycoplasma hyopneumoniae in groups of swine intended for slaughter and female swine intended for breeding in buildings experiencing an outbreak of swine respiratory disease.[3] Not for use in male swine intended for breeding.[3]

    References[edit]

    1. ^ "Aiviosin- tylvalosin granule". DailyMed. 29 November 2021. Retrieved 13 December 2023.
  • ^ "Aiviosin- tylvalosin tartrate granule, for solution". DailyMed. 29 November 2021. Retrieved 13 December 2023.
  • ^ a b c d e f "Freedom of Information Summary Aiviosin NADA 141-336" (PDF). Retrieved 13 December 2023. Public Domain This article incorporates text from this source, which is in the public domain.

    • Public Domain This article incorporates public domain material from US Food and Drug Administration. United States Department of Health and Human Services.


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    ●This page was last edited on 17 December 2023, at 03:19 (UTC).
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