DIPEA‐Assisted Efficient One‐Pot Three‐Component Synthesis of Novel β‐Carboline Tethered Pyran Derivatives

N Banyal, CC Malakar, R Kumar, V Singh - ChemistrySelect, 2024 - Wiley Online Library
A potential DIPEA‐assisted approach has been unfolded for the synthesis of novel β‐
carboline tethered‐4H‐pyran derivatives via one‐pot condensation of 1‐formyl‐9H‐β …

An A-ring substituted evodiamine derivative with potent anticancer activity against human non-small cell lung cancer cells by targeting heat shock protein 70

HY Min, Y Lim, H Kwon, HJ Boo, SY Hyun… - Biochemical …, 2023 - Elsevier
The heat shock protein (HSP) system is essential for the conformational stability and function
of several proteins. Therefore, the development of efficacious HSP-targeting anticancer …

Design and synthesis of 1, 3-benzothiazinone derivatives as potential anti-inflammatory agents

J Li, X Fan, J Deng, Y Liang, S Ma, Y Lu… - Bioorganic & Medicinal …, 2020 - Elsevier
Abstract A series of 1, 3-benzothiazinone derivatives were designed and synthesized for
pharmacological assessments. Among the synthesized 19 compounds, some compounds …

An Expeditious Approach for the Synthesis of β‐Carboline− Pyrazole‐Based Molecular Hybrids

D Singh, P Sharma, R Kumar… - Asian Journal of …, 2018 - Wiley Online Library
A simple and highly efficient one‐pot, metal‐free approach has been developed for the
synthesis of β‐carboline− pyrazole/− pyrazoline‐based molecular hybrids. The synthesis of …

Ortho‐Functionalization of Benzimidates and Benzamidines

G Borah, B Dam, BK Patel - ChemistrySelect, 2022 - Wiley Online Library
In recent years, benzimidates and benzamidines have received tremendous importance as
starting materials owing to their electronic properties and high reactivity. Their application as …

Gerüstdiversitätsbasierte Synthese und ihre Anwendung bei der Sonden‐und Wirkstoffsuche

M Garcia‐Castro, S Zimmermann… - Angewandte …, 2016 - Wiley Online Library
Die Gerüstdiversität ist ein entscheidendes Merkmal von Verbindungskollektionen, das
einen großen Einfluss auf deren Erfolg beim biologischen Screening hat. Die Synthese …

Advances in antitumor research of CA-4 analogs carrying quinoline scaffold

C Wang, J Chang, S Yang, L Shi, Y Zhang… - Frontiers in …, 2022 - frontiersin.org
Combretastatin A-4 (CA-4) is a potent inhibitor of tubulin polymerization and a colchicine
binding site inhibitor (CBSI). The structure-activity relationship study of CA-4 showed that the …

Recent Advance on the Synthesis of 3, 3'-Bisindolylmethane Derivatives under Transition-Metal-Free Catalytic Conditions

Z Zhenguo, L Xiaoxiao, Z Xinlong, Y Yalin… - Chinese Journal of …, 2021 - sioc-journal.cn
Bisindolylmethanes (3, 3'-BIMs) compounds are important indole alkyloads and their units
are widely found in various natural products, functional materials and synthetic …

Rutaecarpine-inspired scaffold-hopping strategy and Ullmann cross-coupling based synthetic approach: Identification of pyridopyrimidinone-indole based novel …

M Yadav, N Roy, K Mandal, M Nagpure… - Bioorganic & Medicinal …, 2024 - Elsevier
Natural products as starting templates have shown historically major contribution to
development of drugs. Inspired by the structure–function of an anticancer natural alkaloid …

Bioactivation of herbal constituents: Mechanisms and toxicological relevance

B Wen, P Gorycki - Drug Metabolism Reviews, 2019 - Taylor & Francis
The increase in the application of herbal medicines and dietary products over the last
decades has been accompanied with a substantial increase in case reports of herb-induced …