| Description |
A labelled analogue of Tildipirosin. Tildipirosinb is a novel 16-membered-ring macrolide used in veterinary medicine. Tildipirosin is used to treat bacterial pathogens including Mannheimia haemolytica and Pasteurella multocida that cause respiratory tract infections in cattle and swine. |
| Synonyms |
20-Deoxo-23-deoxy-5-O-[3,6-dideoxy-3-(dimethylamino)-β-D-glucopyranosyl]-20,23-di-1-piperidinyltylonolide-d10 |
| IUPAC Name |
(4R,5S,6S,7R,9R,11E,13E,15R,16R)-7-[2-(2,2,3,3,4,4,5,5,6,6-decadeuteriopiperidin-1-yl)ethyl]-6-[(2S,3S,4R,5R,6S)-4-(dimethylamino)-3,5-dihydroxy-6-methyloxan-2-yl]oxy-16-ethyl-4-hydroxy-5,9,13-trimethyl-15-(piperidin-1-ylmethyl)-1-oxacyclohexadeca-11,13-diene-2,10-dione |
| Related CAS |
328898-40-4 (unlabelled)
|
| Canonical SMILES |
CCC1C(C=C(C=CC(=O)C(CC(C(C(C(CC(=O)O1)O)C)OC2C(C(C(C(O2)C)O)N(C)C)O)CCN3CCCCC3)C)C)CN4CCCCC4 |
| InChI |
InChI=1S/C41H71N3O8/c1-8-35-32(26-44-20-13-10-14-21-44)23-27(2)15-16-33(45)28(3)24-31(17-22-43-18-11-9-12-19-43)40(29(4)34(46)25-36(47)51-35)52-41-39(49)37(42(6)7)38(48)30(5)50-41/h15-16,23,28-32,34-35,37-41,46,48-49H,8-14,17-22,24-26H2,1-7H3/b16-15+,27-23+/t28-,29+,30+,31+,32-,34-,35-,37-,38+,39+,40-,41-/m1/s1/i9D2,11D2,12D2,18D2,19D2 |
| InChI Key |
HNDXPZPJZGTJLJ-OEIVNSJOSA-N |
| Boiling Point |
846.8±65.0 °C at 760 mmHg |
| Melting Point |
115-120°C |
| Purity |
>98% |
| Density |
1.2±0.1 g/cm3 |
| Solubility |
Soluble in Chloroform, Methanol |
| Appearance |
White to Pale Yellow Solid |
| Storage |
Store at -20°C |
![Tildipirosin-[d10]](https://resource.bocsci.com/structure/tildipirosin-%5Bd10%5D.gif)
