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Home API Fusidic Acid CS-T-52761

Diethanolamine Fusidate

Chemical Properties and Information

Product Code: CS-T-52761 API
Diethanolamine Fusidate
API Family
Fusidic Acid
Product Code
CS-T-52761

Diethanolamine Fusidate

Fusidic Acid API
Stock Status: In Stock
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CAT No.
CS-T-52761
CAS No.
16391-75-6
Molecular Formula
C₃₅H₅₉NO₈
Molecular Weight
621.84
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There is no hazardous surcharge associated with this product.
There is no packaging charge associated with this product.
For Research Purposes only. Not for Personal use.
All compounds supplied are strictly intended for laboratory, research, analytical, and scientific use only. They are not meant for human consumption, therapeutic use, or any form of clinical application.
CAS No.
16391-75-6
Product Code
CS-T-52761
M.F.
C₃₅H₅₉NO₈
M.W.
621.84
Smiles
O[C@]1([H])CC[C@@]2(C)[C@](CC[C@@]3(C)[C@@]2([H])[C@H](O)C[C@]4([H])[C@]3(C)C[C@@](OC(C)=O)([H])/C4=C(CC/C=C(C)\C)\C(O)=O)([H])[C@]1([H])C.OCCNCCO
Category
API
API Family
Fusidic Acid
Storage Condition
Store at refrigerator (2-8°C) for long term storage
IUPAC Name
(2Z)-2- [(3R,4S,5S,8S,9S,10S,11R,13R,14S,16S)-16-acetyloxy-3,11-dihydroxy-4,8,10,14-tetramethyl-2,3,4,5,6,7, 9,11,12,13,15,16-dodecahydro-1H-cyclopenta[a]phenanthren-17-ylidene]-6-methylhept-5-enoic acid;2-(2-hydroxyethylamino)ethanol
References
"Findon, G, et al,: Lab, Anim, Sci,, 41, 462 (1991); Parsons, R,L, et al,: Curr, Chemother, Proc, Int, Cong, Chemother,, 10, 384 (1978);"
Synonyms
Not available,
Application Notes
A bacteriostatic antibiotic with similar activity and better absorption after oral administration (in animals) than the sodium salt of Fusidic Acid . Inhibits protein synthesis in prokaryotes by inhibiting the ribosome-dependent activity of G factor and translocation of peptidyl-tRNA.
Purity by HPLC
Not less than 90 %
Hazard Compound
Refer MSDS for accurate information.
Overview
A bacteriostatic antibiotic with similar activity and better absorption after oral administration (in animals) than the sodium salt of Fusidic Acid . Inhibits protein synthesis in prokaryotes by inhibiting the ribosome-dependent activity of G factor and translocation of peptidyl-tRNA.
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