CAS 16391-75-6
:29-Nordammara-17(20),24-dieno-21-acido oico, 16-(acetilossi)-3,11-diidrossi-, (3α,4α,8α,9β,11α,13α,14β,16β,17Z)-, comp. con 2,2′-iminobis[etanolo] (1:1)
Descrizione:
29-Nordammara-17(20),24-dien-21-acido oico, 16-(acetyloxy)-3,11-diidrossi-, è un composto organico complesso caratterizzato dalla sua unica struttura steroidea, che include più gruppi idrossilici e un gruppo funzionale acetyloxy. Questo composto presenta una stereochimica specifica, denotata dalla sua configurazione dettagliata, che influenza la sua attività biologica e le interazioni. La presenza di 2,2′-iminobis[etanolo] indica che forma un complesso 1:1 con questa ammina, potenzialmente influenzando la sua solubilità e reattività. Il composto è probabile che mostri varie proprietà farmacologiche, date le sue caratteristiche strutturali, che possono includere effetti anti-infiammatori o altri effetti terapeutici. Il suo numero CAS, 16391-75-6, consente un'identificazione precisa nei database chimici. In generale, le caratteristiche di questa sostanza suggeriscono che potrebbe avere applicazioni in chimica medicinale o farmacologia, sebbene specifiche attività biologiche richiederebbero ulteriori indagini attraverso studi empirici.
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
Sinonimi:- (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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7 prodotti.
Diethanolamine fusidate
CAS:Diethanolamine fusidateFormula:C31H47NaO6 / C31H48O6Purezza:81.2% / 77.8%Colore e forma:WhitePeso molecolare:538.32703 / 516.34509Diethanolamine Fusidate
CAS:Formula:C31H48O6·C4H11NO2Colore e forma:White To Off-White SolidPeso molecolare: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·C4H11NO2Colore e forma:NeatPeso molecolare:621.84Diethanolamine Fusidate
CAS:Diethanolamine Fusidate: orally better-absorbed bacteriostatic antibiotic; inhibits protein synthesis in prokaryotes.Formula:C35H59NO8Colore e forma:SolidPeso molecolare: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:C35H59NO8Purezza:95%MinPeso molecolare:621.84 g/mol







