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79(14):1543-1556
Smiles: CC1N=CSC=1C1C=CC(=CC=1)[C@H](C)NC(=O)[C@H]1C[C@H](O)CN1C(=O)[C@@H](NC(=O)CCCCCCNC(=O)COC1=CC=CC=C1[C@@H](CCC1C=C(OC)C(=CC=1)OC)OC(=O)[C@@H]1CCCCN1C(=O)[C@@H](CC)C1=CC(OC)=C(OC)C(=C1)OC)C(C)(C)C
whereas it decreases the activity of both microsomal HMG-CoA reductase and cholesterol 7 alpha-hydroxylase and does not affect acyl-CoA: cholesterol acyltransferase (ACAT)
InChi: InChI=1S/C21H19ClN4O2/c1-24(2)14-8-6-7-13(11-14)20-19-16(12-18(27)25(20)3)23-26(21(19)28)17-10-5-4-9-15(17)22/h4-12
Tildipirosin Size:Solid 2 mg 79(14):1543-1556Tildipirosin (TIP) is a novel 16 membered ring macrolide authorized for the treatment of bovine and swine respiratory disease. Tildipirosin is developed to treat bacterial pathogens, including Mannheimia haemolytica and Pasteurella multocida, that cause respiratory tract infections in cattle and swine. Tildipirosin inhibits protein synthesis in bacteria and blocks the production of biofilms. Tildipirosin is particularly effective against Gram negative
US$ 1317.49
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