CAS 16391-75-6
:29-Nordammara-17(20),24-dien-21-oic acid, 16-(acetyloxy)-3,11-dihydroxy-, (3α,4α,8α,9β,11α,13α,14β,16β,17Z)-, compd. with 2,2′-iminobis[ethanol] (1:1)
Description:
29-Nordammara-17(20),24-dien-21-oic acid, 16-(acetyloxy)-3,11-dihydroxy-, is a complex organic compound characterized by its unique steroidal structure, which includes multiple hydroxyl groups and an acetyloxy functional group. This compound features a specific stereochemistry, denoted by its detailed configuration, which influences its biological activity and interactions. The presence of the 2,2′-iminobis[ethanol] indicates that it forms a 1:1 complex with this amine, potentially affecting its solubility and reactivity. The compound is likely to exhibit various pharmacological properties, given its structural features, which may include anti-inflammatory or other therapeutic effects. Its CAS number, 16391-75-6, allows for precise identification in chemical databases. Overall, the characteristics of this substance suggest it may have applications in medicinal chemistry or pharmacology, although specific biological activities would require further investigation through empirical studies.
Formula:C31H48O6·C4H11NO2
InChI:InChI=1S/C31H48O6.C4H11NO2/c1-17(2)9-8-10-20(28(35)36)26-22-15-24(34)27-29(5)13-12-23(33)18(3)21(29)11-14-30(27,6)31(22,7)16-25(26)37-19(4)32;6-3-1-5-2-4-7/h9,18,21-25,27,33-34H,8,10-16H2,1-7H3,(H,35,36);5-7H,1-4H2/b26-20-;/t18-,21-,22-,23+,24+,25-,27-,29-,30-,31-;/m0./s1
InChI key:InChIKey=OQZZCXRLEFBPLZ-JCJNLNMISA-N
SMILES:C[C@@]12[C@]3(C)[C@](/C(=C(\CCC=C(C)C)/C(O)=O)/[C@@H](OC(C)=O)C3)(C[C@@H](O)[C@]1([C@]4(C)[C@@](CC2)([C@H](C)[C@H](O)CC4)[H])[H])[H].N(CCO)CCO
Synonyms:- (2Z)-2-[(3alpha,4alpha,5alpha,8alpha,9xi,11alpha,13alpha,14beta,16beta,17Z)-16-(acetyloxy)-3,11-dihydroxy-4,8,10,14-tetramethylgonan-17-ylidene]-6-methylhept-5-enoic acid - 2,2'-iminodiethanol (1:1)
- (3alpha,8alpha,9beta,13alpha,14beta,16beta,17(Z))-16-(Acetyloxy)-3,11-dihydroxy-29-nordammara-17(20),24-dien-21-oic acid, compd. with 2,2'-iminobis(ethanol) (1:1)
- (4alpha,8alpha,9beta,13alpha,14beta,17Z)-16beta-Acetoxy-3alpha,11alpha-dihydroxy-29-nordammara-17(20),24-dien-21-oic acid, compound with 2,2'-iminodiethanol (1:1)
- 29-Nor-8α,9β,13α,14β-dammara-17(20),24-dien-21-oic acid, 3α,11α,16β-trihydroxy-, 16-acetate, compd. with 2,2′-iminodiethanol (1:1), (Z)-
- 29-Nordammara-17(20),24-dien-21-oic acid, 16-(acetyloxy)-3,11-dihydroxy-, (3α,4α,8α,9β,11α,13α,14β,16β,17Z)-, compd. with 2,2′-iminobis[ethanol] (1:1)
- Diethanolamine fusidate
- Ethanol, 2,2′-iminobis-, (3α,4α,8α,9β,11α,13α,14β,16β,17Z)-16-(acetyloxy)-3,11-dihydroxy-29-nordammara-17(20),24-dien-21-oate (salt)
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Found 7 products.
Diethanolamine fusidate
CAS:Diethanolamine fusidateFormula:C31H47NaO6 / C31H48O6Purity:81.2% / 77.8%Color and Shape:WhiteMolecular weight:538.32703 / 516.34509Diethanolamine Fusidate
CAS:Formula:C31H48O6·C4H11NO2Color and Shape:White To Off-White SolidMolecular weight:516.72 105.14Diethanolamine Fusidate
CAS:<p>Stability Hygroscopic<br>Applications 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 factor and translocation of peptidyl-tRNA.<br>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);<br></p>Formula:C31H48O6·C4H11NO2Color and Shape:NeatMolecular weight:621.84Diethanolamine Fusidate
CAS:Diethanolamine Fusidate: orally better-absorbed bacteriostatic antibiotic; inhibits protein synthesis in prokaryotes.Formula:C35H59NO8Color and Shape:SolidMolecular weight:621.86Diethanolamine fusidate
CAS:<p>Diethanolamine fusidate is an aminoglycoside antibiotic that inhibits protein synthesis in bacteria by binding to the ribosomes. It binds to bacterial 16S ribosomal RNA and inhibits protein synthesis, leading to cell death by inhibiting the production of proteins vital for cell division. Diethanolamine fusidate has been shown to be effective against methicillin-resistant Staphylococcus aureus (MRSA) and Pseudomonas aeruginosa, although is not active against acid-fast bacteria such as Mycobacterium tuberculosis or Mycobacterium avium complex. This drug also has anti-inflammatory properties, which may be due to its inhibition of prostaglandin synthesis.</p>Formula:C35H59NO8Purity:95%MinMolecular weight:621.84 g/mol







