
CAS 6019-39-2
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7 produits concernés.
5-benzoylaminoindole
CAS :Formule :C15H12N2ODegré de pureté :98%Couleur et forme :SolidMasse moléculaire :236.2686OAC-2
CAS :Formule :C15H12N2ODegré de pureté :>97.0%(HPLC)(qNMR)Couleur et forme :White to Brown powder to crystalMasse moléculaire :236.27OAC2
CAS :<p>OAC2, an Oct4 activator, boosts iPSC creation from embryonic fibroblasts, similar to OAC1.</p>Formule :C15H12N2ODegré de pureté :99.58% - ≥95%Couleur et forme :SolidMasse moléculaire :236.27N-(1H-Indol-5-yl)benzamide
CAS :Produit contrôlé<p>Applications N-(1H-Indol-5-yl)benzamide is a octamer-binding transcription factor 4 activating compound that activated Oct4 and Nanog promoters, which are essential regulators of embryonic stem cell (ESC) pluripotency and key to the reprogramming process.<br>References Li, W.D., et al.: Proceed. Nation. Acad. Sci. U.S.A., et al.: 109, 20853 (2012);<br></p>Formule :C15H12N2OCouleur et forme :NeatMasse moléculaire :236.27N-(1H-Indol-5-yl)benzamide
CAS :<p>N-(1H-Indol-5-yl)benzamide is a tetraaryl compound that acts as a catalyst. It has been shown to be active against Gram-positive bacteria, such as Streptococcus pneumoniae and Staphylococcus aureus, at 10 μM. This compound has high activity against these bacteria and is more stable at higher temperatures. N-(1H-Indol-5-yl)benzamide has also been shown to have good stability in the presence of clarithromycin, which is an antibiotic used to treat bacterial infections. This drug can form a complex with clavulanic acid (a β-lactamase inhibitor) and thus can inhibit bacterial growth by binding to the ribosomal RNA of the bacteria. The molecular weight of N-(1H-indol-5-yl)benzamide is 169 g/mol and its functional groups are hydroxyl, carbonyl, and car</p>Formule :C15H12N2ODegré de pureté :Min. 95%Masse moléculaire :236.27 g/mol






