Results 181 to 190 of about 104,731 (310)

Dearomative Nucleophilic Addition of Lithium Enolates to Electron-Poor Indoles. [PDF]

Chemphyschem
Roseau M, Hédouin M, Fressigné C, Legros J, Chataigner I.   +4 more
europepmc   +1 more source

Emission pattern and anti-insect function of indole from tea plant (<i>Camellia sinensis</i>) attacked by tea geometrids

, 2023
Jianlong Li, Guotai Jian, Jiajia Qian, Jinghua Xue, Chengshun Liu, Yongxia Jia, Bo Zhou, Jinchi Tang, Jie Yang, Lanting Zeng   +9 more
openalex   +1 more source

Deciphering the catalytic and pharmacological mechanisms of Coptis chinensis herbzymes to renovate intestinal microenvironment for colitis alleviation

BMEMat, EarlyView.
The synthesized CCzymes possess both antioxidant enzyme activity and pharmacological properties inherent to Coptis chinensis. By their antioxidant enzyme activity, CCzymes can attenuate oxidative stress within the inflammatory region of ulcerative colitis (UC), while their pharmacological activity acts on macrophage polarization and the intestinal ...
Zhichao Deng, Can Li, Yujie Zhang, Yuanyuan Zhu, Chenxi Xu, Bowen Gao, Mingxin Zhang, Martina H. Stenzel, Kelong Fan, Mingzhen Zhang, Yanyan Jiang   +10 more
wiley   +1 more source

Chemistry, Applications, and Synthesis Methods of Indole Derivatives: A Comprehensive Review. [PDF]

Chem Rec
Silva Moratório de Moraes R, Mestre Botelho AB, Tavares de Almeida Pinto G, Couto Rodrigues S, Miranda Martins MT, Alves Soares DL, Cardoso Cruz C, de Almeida Pinto A, Rodrigues Fintelman Dias F, Dias Fernandes P, Cunha AC.   +10 more
europepmc   +1 more source

Molecular bases of insect odorant receptor function: specificity and evolution

Biological Reviews, EarlyView.
ABSTRACT Insect odorant receptors (ORs) are a class of chemoreceptors that insects use to detect volatile cues in their environment. In recent years, major advances in the field of structural biology have made it possible to obtain the first structures of insect ORs.
Zibo Li, Abhinob Baruah, Sridevi Bhamidipati, Nicolas Montagné, Emmanuelle Jacquin‐Joly, Camille Meslin   +5 more
wiley   +1 more source

<i>Cis</i>-difluoromethyl hetarylative dearomatization by a radical docking-migration cascade. [PDF]

Chem Sci
Wang J, Kang H, Yang S, Cao Z, Chen X, Zhu C.   +5 more
europepmc   +1 more source

Green Synthesis of Iron-Based Nanoparticles Using Pomegranate Leaf Extracts: Characterization, Biomolecules and Indole Removal [PDF]

Huifang Sun, Yanjun Liu, Yifan Zhou, Zuliang Chen, Jianfeng Li   +4 more
openalex   +1 more source

Quantitative Profiling of Platelet-Rich Plasma Indole Markers by Direct-Matrix Derivatization Combined with LC-MS/MS in Patients with Neuroendocrine Tumors [PDF]

, 2019
Martijn van Faassen, Grytsje Bouma, Lotte D. de Hosson, Marloes A.M. Peters, Gürsah Kats‐Ugurlu, Elisabeth G.E. de Vries, Annemiek Walenkamp, Ido P. Kema   +7 more
openalex   +1 more source

Nutritional Content, Phytochemical Composition, and Physicochemical Properties of Different Quinoa (Chenopodium quinoa Willd.) Seed Varieties

Cereal Chemistry, EarlyView.
ABSTRACT Background and Objectives Quinoa (Chenopodium quinoa Willd.) is a pseudocereal with documented benefits for human health. The macronutrient composition and phytochemical content of the grain are known to vary depending on the variety and the growing location.
Vassilios Raikos, Shirley De Lima Sampaio, Helen E. Hayes, Gary J. Duncan, Donna Henderson, Nicholas J. Vaughan, Wendy R. Russell, Madalina Neacsu   +7 more
wiley   +1 more source

NaHMDS/B(C₆F₅)₃-promoted diastereoselective Friedel-Crafts alkylation of indoles/pyrroles with <i>N-tert</i>-butanesulfinylimines: towards the asymmetric synthesis of bisindole alkaloid Calcicamide B. [PDF]

RSC Adv
Zhang G, Chen X, Liu Y, Peng R, Xu M, Yan S, Xiao J, Liu Z, Min Q, Liao G, Wang X, Qin S.   +11 more
europepmc   +1 more source