Tulathromycin A A macrolide antibiotic

Tulathromycin A (CAS 217500-96-4)

Tulathromycin A | CAS 217500-96-4 is rated 5.0 out of 5 by 1.
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Synonym: (2R,3S,4R,5R,8R,10R,11R,12S,13S,14R)-13-[[2,6-Dideoxy-3-C-methyl-3-O-methyl-4-C-[(propylamino)methyl]-?-L-ribo-hexopyranosyl]oxy]-2-ethyl-3,4,10-trihydroxy-3,5,8,10,12,14-hexamethyl-11-[[3,4,6-trideoxy-3-(dimethylamino)-?-D-xylo-hexopyranosyl]oxy]-1-oxa-6-azacyclopentadecan-15-one; CP 472295; Draxxin; Tulathromycin
Application: A macrolide antibiotic
CAS Number: 217500-96-4
Purity: ≥97%
Molecular Weight: 806.08
Molecular Formula: C41H79N3O12
* Refer to Certificate of Analysis for lot specific data (including water content).
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Tulathromycin A is a triamilide antibiotic. Exists as an equilibrium mixture of two isomeric forms, Tulathromycin A (90%) and B (10%).

Physical State :
Solid
Solubility :
Soluble in DMSO, and methanol.
Storage :
Store at -20° C
Melting Point :
180-183 °C
Optical Activity :
α20D -34.72º, c = 0.53 in methanol
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
PubChem CID :
56841565
SMILES :
CCCNC[C@@]1([C@@H](O[C@H](C[C@@]1(C)OC)O[C@H]2[C@@H]([C@H]([C@](C[C@H](CN[C@@H]([C@H]([C@]([C@H](OC(=O)[C@@H]2C)CC)(C)O)O)C)C)(C)O)O[C@H]3[C@@H]([C@H](C[C@H](O3)C)N(C)C)O)C)C)O

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Certificate of Analysis

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Tulathromycin A  Product Citations

See how others have used Tulathromycin A. Click on the entry to view the PubMed entry .

Citations 1 to 2 of 2 total

PMID: # 28674821  Jansen, LJM. et al. 2017. Anal Bioanal Chem. 409: 4927-4941.

PMID: # 27259820  2016. Vet. Microbiol. 189: 1-7.

Citations 1 to 2 of 2 total

What is the solubility of this product?

Asked by: hawkeye11
This chemical, Tulathromycin A (CAS 217500-96-4), is slightly soluble in DMSO and Methanol.
Answered by: Chemical Support 1
Date published: 2017-03-16
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Rated 5 out of 5 by from Duquette et al Duquette et al. (PubMed ID 26000598) found that Tulathromycin showed immunomodulatory effects in leukocytes and anti-inflammatory effects in pigs in experimental models of A pleuropneumoniae infection by preventing the production of leukotriene B4. -SCBT Publication Review
Date published: 2015-03-11
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