Pyrrolidinone

14,000,000 Leading Edge Experts on the ideXlab platform

Scan Science and Technology

Contact Leading Edge Experts & Companies

Scan Science and Technology

Contact Leading Edge Experts & Companies

The Experts below are selected from a list of 8871 Experts worldwide ranked by ideXlab platform

Isabel Vidal-tato - One of the best experts on this subject based on the ideXlab platform.

José M. Navaza - One of the best experts on this subject based on the ideXlab platform.

Alicia García-abuín - One of the best experts on this subject based on the ideXlab platform.

Guan-hu Bao - One of the best experts on this subject based on the ideXlab platform.

  • Flavoalkaloids with a Pyrrolidinone Ring from Chinese Ancient Cultivated Tea Xi-Gui.
    Journal of agricultural and food chemistry, 2018
    Co-Authors: Jian Cheng, Pu Wang, Xiaochun Wan, Ming-hua Qiu, Guan-hu Bao
    Abstract:

    Chinese Xi-Gui tea is one ancient cultivated variety of Camellia sinensis var. assamica. At present, it is used for producing expensive and elite tea in China. Five new flavoalkaloids, (−)-6-(5′′′S)-N-ethyl-2-Pyrrolidinone-epicatechin-3-O-gallate (ester-type catechins Pyrrolidinone E, etc-Pyrrolidinone E, 1), (−)-6-(5′′′R)-N-ethyl-2-Pyrrolidinone-epicatechin-3-O-gallate (etc-Pyrrolidinone F, 2) (−)-8-(5′′′S)-N-ethyl-2-Pyrrolidinone-epicatechin-3-O-gallate (etc-Pyrrolidinone G, 3a), (−)-8-(5′′′S)-N-ethyl-2-Pyrrolidinone-catechin-3-O-gallate (etc-Pyrrolidinone I, 4a), (−)-8-(5′′′R)-N-ethyl-2-Pyrrolidinone-catechin-3-O-gallate (etc-Pyrrolidinone J, 4b), and one new naturally occurring natural product (−)-8-(5′′′R)-N-ethyl-2-Pyrrolidinone-epicatechin-3-O-gallate (etc-Pyrrolidinone H, 3b) together with the known flavoalkaloids etc-Pyrrolidinones A–D (5, 6, 7a, and 7b) were detected and isolated from Xi-Gui green tea. Their structures were identified by comprehensive NMR spectroscopic analyses. Absolute configu...

  • Flavoalkaloids with a Pyrrolidinone Ring from Chinese Ancient Cultivated Tea Xi-Gui
    2018
    Co-Authors: Jian Cheng, Pu Wang, Xiaochun Wan, Ming-hua Qiu, Guan-hu Bao
    Abstract:

    Chinese Xi-Gui tea is one ancient cultivated variety of Camellia sinensis var. assamica. At present, it is used for producing expensive and elite tea in China. Five new flavoalkaloids, (−)-6-(5′′′S)-N-ethyl-2-Pyrrolidinone-epicatechin-3-O-gallate (ester-type catechins Pyrrolidinone E, etc-Pyrrolidinone E, 1), (−)-6-(5′′′R)-N-ethyl-2-Pyrrolidinone-epicatechin-3-O-gallate (etc-Pyrrolidinone F, 2) (−)-8-(5′′′S)-N-ethyl-2-Pyrrolidinone-epicatechin-3-O-gallate (etc-Pyrrolidinone G, 3a), (−)-8-(5′′′S)-N-ethyl-2-Pyrrolidinone-catechin-3-O-gallate (etc-Pyrrolidinone I, 4a), (−)-8-(5′′′R)-N-ethyl-2-Pyrrolidinone-catechin-3-O-gallate (etc-Pyrrolidinone J, 4b), and one new naturally occurring natural product (−)-8-(5′′′R)-N-ethyl-2-Pyrrolidinone-epicatechin-3-O-gallate (etc-Pyrrolidinone H, 3b) together with the known flavoalkaloids etc-Pyrrolidinones A–D (5, 6, 7a, and 7b) were detected and isolated from Xi-Gui green tea. Their structures were identified by comprehensive NMR spectroscopic analyses. Absolute configurations of 1–3 were established by comparison of the CD analyses with epicatechin-3-O-gallate (ECG). Compounds 1–4 were evaluated for their protection against high glucose induced cell senescence on human umbilical vein endothelia cells (HUVECs) and showed significant protection effects (p < 0.01) at both 1.0 and 10 μM. A discussion on the possible evolution of tea plants divergent from related food plants on the basis of phytochemical view is also provided

Joelle Pérard-viret - One of the best experts on this subject based on the ideXlab platform.

  • In silico studies, synthesis and binding evaluation of substituted 2-Pyrrolidinones as peptidomimetics of RGD tripeptide sequence
    Tetrahedron, 2015
    Co-Authors: Valérie Toum, Julie Bolley, Yoann Lalatonne, Carole Barbey, Laurence Motte, Marc Lecouvey, Jacques Royer, Nathalie Dupont, Joelle Pérard-viret
    Abstract:

    In silico optimisation, synthesis and binding evaluation of αvβ3 integrin's affinity for precursors of a new RGD peptidomimetics family are presented. The 2-Pyrrolidinone building block was obtained by condensation of L-lysine with dimethoxydihydrofuran followed by reduction. The ring was functionalised functionalized with a carboxylic acid and a guanidinium appendage. On the Pyrrolidinone heterocycle, the effects on affinity of position, length and relative .geometry of the two acid or basic functionalized side chains introduced on the Pyrrolidinone ring have been previously evaluated by docking studies. Peptidomimetics have finally been evaluated by competition binding assays for αvβ3 integrin's affinity using radio-ligands.

  • In silico studies, synthesis and binding evaluation of substituted 2-Pyrrolidinones as peptidomimetics of RGD tripeptide sequence
    European journal of medicinal chemistry, 2015
    Co-Authors: Valérie Toum, Julie Bolley, Yoann Lalatonne, Carole Barbey, Laurence Motte, Marc Lecouvey, Jacques Royer, Nathalie Dupont, Joelle Pérard-viret
    Abstract:

    In silico optimisation, synthesis and binding evaluation of αvβ3 integrin's affinity for precursors of a new RGD peptidomimetics family are presented. The 2-Pyrrolidinone building block was obtained by condensation of l-lysine with dimethoxydihydrofuran followed by reduction. The ring was functionalized with a carboxylic acid and a guanidinium appendage. On the Pyrrolidinone heterocycle, the effects on affinity of position, length and relative geometry of the two acid or basic functionalized side chains introduced on the Pyrrolidinone ring have been previously evaluated by docking studies. Peptidomimetics have finally been evaluated by competition binding assays for αvβ3 integrin's affinity using radio-ligands.

  • An expeditiousAn expeditious total synthesis of (±)-jamtine using condensation between imine and acid anhydride total synthesis of (±)-jamtine using condensation between imines and acid anhydride
    Tetrahedron Letters, 2010
    Co-Authors: Joelle Pérard-viret, Florence Souquet, Marie-line Manisse, Jacques Royer
    Abstract:

    In silico optimisation, synthesis and binding evaluation of avb3 integrin's affinity for precursors of a new RGD peptidomimetics family are presented. The 2-Pyrrolidinone building block was obtained by condensation of L-lysine with dimethoxydihydrofuran followed by reduction. The ring was functionalized with a carboxylic acid and a guanidinium appendage. On the Pyrrolidinone heterocycle, the effects on affinity of position, length and relative geometry of the two acid or basic functionalized side chains introduced on the Pyrrolidinone ring have been previously evaluated by docking studies. Peptidomimetics have finally been evaluated by competition binding assays for avb3 integrin's affinity using radioligands