
CAS 713112-69-7
:N-[3-[(benzoylcarbamothioylamino)carbamoyl]-4-(3,4-dimethoxyphenyl)-5-methylthiophen-2-yl]benzamide
Description:
N-[3-[(benzoylcarbamothioylamino)carbamoyl]-4-(3,4-dimethoxyphenyl)-5-methylthiophen-2-yl]benzamide, with CAS number 713112-69-7, is a synthetic organic compound characterized by its complex molecular structure, which includes multiple functional groups such as amides, thiophenes, and aromatic rings. This compound typically exhibits properties associated with both hydrophilicity and lipophilicity due to the presence of polar and non-polar regions within its structure. It may display biological activity, potentially serving as a pharmacophore in medicinal chemistry, particularly in the development of therapeutic agents. The presence of the thiophene ring and various substituents suggests that it could interact with biological targets, making it of interest in drug discovery. Additionally, its stability, solubility, and reactivity would depend on the specific conditions of use, including pH and solvent environment. As with many complex organic compounds, detailed characterization through techniques such as NMR, IR spectroscopy, and mass spectrometry would be essential for understanding its properties and potential applications.
Formula:C29H26N4O5S2
Synonyms:- N-[3-[(benzoylcarbamothioylamino)carbamoyl]-4-(3,4-dimethoxyphenyl)-5-methylthiophen-2-yl]benzamide
- 3-Thiophenecarboxylic acid, 2-(benzoylamino)-4-(3,4-dimethoxyphenyl)-5-methyl-, 2-[(benzoylamino)thioxomethyl]hydrazide
- SIC-19
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SIC-19
CAS:<p>SIC-19, a SIK2 inhibitor, functions by promoting the degradation of SIK2 protein via the ubiquitination pathway. It inhibits the growth of cancer cells and sensitizes cells, ovarian cancer organoids, and xenograft models to PARP inhibitors (such as Olaparib).</p>Formula:C29H26N4O5S2Color and Shape:SolidMolecular weight:574.67
