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CAS 2410075-64-6

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3-Piperidinebutanamide, β-[[(2S)-2-[(2-benzofuranylcarbonyl)amino]-3-cyclohexyl-1-oxopropyl]amino]-α,2-dioxo-N-(phenylmethyl)-, (βS,3S)-

Description:
3-Piperidinebutanamide, β-[[(2S)-2-[(2-benzofuranylcarbonyl)amino]-3-cyclohexyl-1-oxopropyl]amino]-α,2-dioxo-N-(phenylmethyl)-, (βS,3S)- is a complex organic compound characterized by its multi-functional structure, which includes a piperidine ring, a benzofuran moiety, and various amide and carbonyl groups. This compound exhibits properties typical of amides, such as potential solubility in polar solvents and the ability to engage in hydrogen bonding due to the presence of nitrogen and oxygen atoms. The stereochemistry indicated by the (βS,3S) configuration suggests specific spatial arrangements that may influence its biological activity and interactions with other molecules. The presence of a cyclohexyl group and a phenylmethyl substituent may contribute to its hydrophobic characteristics, potentially affecting its pharmacokinetics and bioavailability. Overall, this compound's intricate structure suggests it may have applications in medicinal chemistry, particularly in the development of pharmaceuticals targeting specific biological pathways. However, detailed studies would be necessary to fully elucidate its properties and potential uses.
Formula:C34H40N4O6
Synonyms:
  • 3-Piperidinebutanamide, β-[[(2S)-2-[(2-benzofuranylcarbonyl)amino]-3-cyclohexyl-1-oxopropyl]amino]-α,2-dioxo-N-(phenylmethyl)-, (βS,3S)-
  • CTSL/CAPN1-IN-2
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  • CTSL/CAPN1-IN-2

    CAS:
    <p>CTSL/CAPN1-IN-2 (Compound 14b) serves as an orally active inhibitor targeting both CTSL and CAPN1, manifesting IC50 values of 6.88 nM for CTSL and 347.6 nM for CAPN1 respectively. This compound not only displays anti-inflammatory attributes but also features favorable pharmacokinetic properties. Moreover, CTSL/CAPN1-IN-2 shows extensive antiviral effects against coronaviruses by inhibiting viral entry [1].</p>
    Formula:C34H40N4O6
    Color and Shape:Solid
    Molecular weight:600.7