35775-65-6

Propionylmaridomycin Chemical Structure
35775-65-6

Chemical Structure

Propionylmaridomycin

  • CAS No.: 35775-65-6
  • Formula:C46H75NO17
  • Molecular Weight:914.08

IUPAC Name: (1R,3R,7R,8R,9S,10R,12R,13S,16R,E)-9-(((2R,3S,4S,5R,6R)-4-(dimethylamino)-3-hydroxy-5-(((2S,4S,5S,6S)-4-hydroxy-4,6-dimethyl-5-((3-methylbutanoyl)oxy)tetrahydro-2H-pyran-2-yl)oxy)-6-methyltetrahydro-2H-pyran-2-yl)oxy)-8-methoxy-3,12-dimethyl-5-oxo-10-(2-o

InChIKey: YOEZGCFEDPFSHG-IHBICIFHSA-N

SMILES: C[C@H]1[C@@H]([C@@](O)(C[C@H](O[C@@H]2[C@@H](N(C)C)[C@@H]([C@@H](O[C@@H]3[C@@H]([C@@H](CC(O[C@@H](C[C@@H]4[C@@H](/C=C/[C@@H](OC(CC)=O)[C@@H](C[C@@H]3CC=O)C)O4)C)=O)OC(CC)=O)OC)O[C@@H]2C)O)O1)C)OC(CC(C)C)=O

Biological Activity: Propionylmaridomycin is a macrolide antibiotic with antibacterial activity. Propionylmaridomycin is rapidly absorbed from the gastrointestinal tract and rapidly distributed to tissues. Propionylmaridomycin radioactivity levels in the liver, kidneys, and lungs were significantly higher than in plasma, while distribution to the brain was less. Propionylmaridomycin is excreted primarily through the feces, and the high fecal recovery rate is due to unabsorbed compounds and biliary excretion of compounds and their metabolites. Propionylmaridomycin exhibits the highest antibacterial activity in the lungs. Propionylmaridomycin is completely converted to several metabolites in rats, of which 4''-depropionyl-9-propionylmaridomycin was identified as the major metabolite[1].

Cat. No. Product Name Purity Description Pricing
HY-137263
Propionylmaridomycin Propionylmaridomycin is a macrolide antibiotic with antibacterial activity. Propionylmaridomycin is rapidly absorbed from the gastrointestinal tract and rapidly distributed to tissues. Propionylmaridomycin radioactivity levels in the liver, kidneys, and lungs were significantly higher than in plasma, while distribution to the brain was less. Propionylmaridomycin is excreted primarily through the feces, and the high fecal recovery rate is due to unabsorbed compounds and biliary excretion of compounds and their metabolites. Propionylmaridomycin exhibits the highest antibacterial activity in the lungs. Propionylmaridomycin is completely converted to several metabolites in rats, of which 4''-depropionyl-9-propionylmaridomycin was identified as the major metabolite.
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