Tildipirosin
CAS No. 328898-40-4
Tildipirosin( —— )
Catalog No. M20577 CAS No. 328898-40-4
Tildipirosin is a 16-membered macrolide used as an antibiotic in veterinary medicine. Like other macrolides it inhibits protein synthesis in bacteria and blocks the production of biofilms.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 88 | In Stock |
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| 5MG | 178 | In Stock |
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| 10MG | 295 | In Stock |
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| 25MG | 502 | In Stock |
|
| 50MG | 709 | In Stock |
|
| 100MG | 1008 | In Stock |
|
| 500MG | 2007 | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameTildipirosin
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NoteResearch use only, not for human use.
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Brief DescriptionTildipirosin is a 16-membered macrolide used as an antibiotic in veterinary medicine. Like other macrolides it inhibits protein synthesis in bacteria and blocks the production of biofilms.
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DescriptionTildipirosin is a 16-membered macrolide used as an antibiotic in veterinary medicine. Like other macrolides it inhibits protein synthesis in bacteria and blocks the production of biofilms.
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In VitroTildipirosin exhibits the inhibitory effect on C. coli species, and 23 of 31 (74%) isolates have MICs of 8 or 16 μg/mL while 8 of 31 (26%) have MIC >256 μg/mL. MICs against C. jejuni are 8-64 μg/mL. Tildipirosin against S. enterica and E. coli are 2-8 μg/mL. Tildipirosin inhibits the treponeme isolates form from CODD lesions from 19 sheep, with MIC90 of 0.0469 mg/L. The P. multocida B130 clones show the MIC of 0.25 mg/L for tildipirosin. The 10 P. multocida isolates that carry only erm(42) exhibit MIC of 16-32 mg/L for tildipirosin. The single M. haemolytica that harbours only erm(42) shows MIC of 32 mg/L for tildipirosin.
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In VivoThe mean percentage of lung consolidation for tildipirosin (4 mg/kg, s.c.)-treated calves is significantly lower than those for tulathromycin-treated and control calves. Metaphylactic administration of tildipirosin to calves 5 days prior to H somni challenge prevents subsequent culture of the pathogen from bronchial secretions and is more effective in minimizing clinical disease and lung lesions than is metaphylactic administration of tulathromycin.
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Synonyms——
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PathwayGPCR/G Protein
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TargetAntibacterial
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RecptorBacterial
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Research Area——
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Indication——
Chemical Information
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CAS Number328898-40-4
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Formula Weight734.02
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Molecular FormulaC41H71N3O8
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Purity>98% (HPLC)
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SolubilityDMSO:100 mg/mL (136.24 mM)
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SMILESCC[C@H]1OC(=O)C[C@@H](O)[C@H](C)[C@@H](O[C@@H]2O[C@H](C)[C@@H](O)[C@@H]([C@H]2O)N(C)C)[C@@H](CCN2CCCCC2)C[C@@H](C)C(=O)\C=C\C(\C)=C\[C@@H]1CN1CCCCC1
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Chemical Name(5S6S7R9R11E13E15R16R)-6-(((2R3R4S5S6R)-4-(dimethylamino)-35-dihydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)-16-ethyl-4-hydroxy-5913-trimethyl-7-(2-(piperidin-1-yl)ethyl)-15-(piperidin-1-ylmethyl)oxacyclohexadeca-1113-diene-210-dione
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Andersen N M Poehlsgaard J Warrass R et al. Inhibition of Protein Synthesis on the Ribosome by Tildipirosin Compared with Other Veterinary Macrolides[J]. Antimicrobial Agents and Chemotherapy 2012 56(11):6033-6036.
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