CAS 16391-75-6
:29-Nordammara-17(20),24-dieno-21-ácido oico, 16-(acetiloxi)-3,11-dihidroxi-, (3α,4α,8α,9β,11α,13α,14β,16β,17Z)-, comp. con 2,2′-iminobis[etanol] (1:1)
Descripción:
29-Nordammara-17(20),24-dien-21-ácido oico, 16-(acetyloxy)-3,11-dihidroxi-, es un compuesto orgánico complejo caracterizado por su estructura esteroidal única, que incluye múltiples grupos hidroxilo y un grupo funcional acetyloxy. Este compuesto presenta una estereoequilibrio específico, denotado por su configuración detallada, que influye en su actividad biológica e interacciones. La presencia de 2,2′-iminobis[etanol] indica que forma un complejo 1:1 con esta amina, lo que podría afectar su solubilidad y reactividad. Es probable que el compuesto exhiba diversas propiedades farmacológicas, dadas sus características estructurales, que pueden incluir efectos antiinflamatorios u otros efectos terapéuticos. Su número CAS, 16391-75-6, permite una identificación precisa en bases de datos químicas. En general, las características de esta sustancia sugieren que puede tener aplicaciones en química medicinal o farmacología, aunque las actividades biológicas específicas requerirían una investigación adicional a través de estudios empíricos.
Fórmula: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
Clave InChI: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
Sinónimos:- (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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Encontrado 7 productos.
Diethanolamine fusidate
CAS:Diethanolamine fusidateFórmula:C31H47NaO6 / C31H48O6Pureza:81.2% / 77.8%Forma y color:WhitePeso molecular:538.32703 / 516.34509Diethanolamine Fusidate
CAS:Fórmula:C31H48O6·C4H11NO2Forma y color:White To Off-White SolidPeso molecular: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>Fórmula:C31H48O6·C4H11NO2Forma y color:NeatPeso molecular:621.84Diethanolamine Fusidate
CAS:Diethanolamine Fusidate: orally better-absorbed bacteriostatic antibiotic; inhibits protein synthesis in prokaryotes.Fórmula:C35H59NO8Forma y color:SolidPeso molecular: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>Fórmula:C35H59NO8Pureza:95%MinPeso molecular:621.84 g/mol







