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Diethanolamine Fusidate _Molecular_structure_CAS_16391-75-6)
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Diethanolamine Fusidate

Catalog No. D441880 Name Toronto Research Chemicals
CAS Number 16391-75-6 Website http://www.trc-canada.com
M. F. C35H59NO8 Telephone +1 (416) 665-9696
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Storage Chembase ID: 167106

SYNONYMS

IUPAC name
2-[(1S,2S,6S,7S,10S,11S,13R,14Z,15R,17R)-13-(acetyloxy)-5,17-dihydroxy-2,6,10,11-tetramethyltetracyclo[8.7.0.02,7.011,15]heptadecan-14-ylidene]-6-methylhept-5-enoic acid; 2-[(2-hydroxyethyl)amino]ethan-1-ol
IUPAC Traditional name
2-[(1S,2S,6S,7S,10S,11S,13R,14Z,15R,17R)-13-(acetyloxy)-5,17-dihydroxy-2,6,10,11-tetramethyltetracyclo[8.7.0.02,7.011,15]heptadecan-14-ylidene]-6-methylhept-5-enoic acid; diethanolamine
Synonyms
(3,4α,8α,9β,11α,13α,14β,16β,17Z)-16-(Acetyloxy)-3,11-dihydroxy-29-nordammara-17(20),24-dien-21-oic Acid compd. with 2,2'-Iminobis[ethanol]
2,2'-Iminobis(ethanol) (3,4α,8α,9β,11α,13α,14β,16β,17Z)-16-(acetyloxy)- 3,11-dihydroxy-29-nordammara-17(20),24-dien-21-oate

DATABASE IDS

CAS Number 16391-75-6

PROPERTIES

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DETAILS

Description (English)
A bacteriostatic antibiotic with similar activity and better absorption after oral administration (in animals) than the sodium salt of Fusidic Acid (F865500). Inhibits protein synthesis in prokaryotes by inhibiting the ribosome-dependent activity of G fac

REFERENCES

  • Findon, G. et al.: Lab. Anim. Sci., 41, 462 (1991)
  • Parsons, R.L. et al.: Curr. Chemother. Proc. Int. Cong. Chemother., 10, 384 (1991)