Alkaloids for cancer prevention and therapy: Current progress and future perspectives

A Mondal, A Gandhi, C Fimognari, AG Atanasov… - European journal of …, 2019 - Elsevier
Alkaloids are important chemical compounds that serve as a rich source for drug discovery.
Numerous alkaloids screened from medicinal plants and herbs showed antiproliferative and …

Rutaecarpine: a promising cardiovascular protective alkaloid from Evodia rutaecarpa (Wu Zhu Yu)

K Tian, J Li, S Xu - Pharmacological Research, 2019 - Elsevier
Rutaecarpine is a bioactive alkaloid isolated from Evodia rutaecarpa (Wu Zhu Yu, Family:
Rutaceae), a versatile medicinal herb which is clinically used to treat headache, abdominal …

Electrosynthesis of CF3‐Substituted Polycyclic Quinazolinones via Cascade Trifluoromethylation/Cyclization of Unactivated Alkene

L Liu, W Zhang, C Xu, J He, Z Xu… - Advanced Synthesis …, 2022 - Wiley Online Library
An atom and step economy cascade trifluoromethylation/cyclization of unactivated alkene
with Langlois reagent as a CF3 source is described. A variety of polycyclic quinazolinones …

[HTML][HTML] Phytotherapeutic applications of alkaloids in treating breast cancer

S Rampogu, T Balasubramaniyam, JH Lee - Biomedicine & …, 2022 - Elsevier
Breast cancer is one of the major causes of mortality in women worldwide. The current
treatments available are radiation therapy (RT), surgery, endocrine (hormone) therapy (ET) …

Structure–activity relationships and computational investigations into the development of potent and balanced dual-acting butyrylcholinesterase inhibitors and human …

D Dolles, M Hoffmann, S Gunesch… - Journal of medicinal …, 2018 - ACS Publications
The enzyme butyrylcholinesterase (BChE) and the human cannabinoid receptor 2 (h CB2R)
represent promising targets for pharmacotherapy in the later stages of Alzheimer's disease …

Catalyst-free cyclization of anthranils and cyclic amines: one-step synthesis of rutaecarpine

J Li, ZB Wang, Y Xu, XC Lu, SR Zhu… - Chemical Communications, 2019 - pubs.rsc.org
An efficient synthesis of a variety of quinazolinone derivatives via a direct cyclization
reaction between commercially available anthranils and cyclic amines is described. The …

Promising derivatives of rutaecarpine with diverse pharmacological activities

D Li, Z Huang, X Xu, Y Li - Frontiers in Chemistry, 2023 - frontiersin.org
Rutaecarpine (RUT) is a natural pentacyclic indolopyridoquinazolinone alkaloid first isolated
from one of the most famous traditional Chinese herbs, Evodia rutaecarpa, which is used for …

Electrosynthesis of polycyclic quinazolinones and rutaecarpine from isatoic anhydrides and cyclic amines

X Chen, X Zhang, S Lu, P Sun - RSC advances, 2020 - pubs.rsc.org
A direct decarboxylative cyclization between readily available isatoic anhydrides and cyclic
amines was established to construct polycyclic fused quinazolinones employing …

A novel superparamagnetic powerful guanidine-functionalized γ-Fe 2 O 3 based sulfonic acid recyclable and efficient heterogeneous catalyst for microwave-assisted …

FH Norouzi, N Foroughifar, A Khajeh-Amiri, H Pasdar - RSC advances, 2021 - pubs.rsc.org
The novel organic–inorganic nanohybrid superparamagnetic (γ-Fe2O3@ CPTMS–
guanidine@ SO3H) nanocatalyst modified with sulfonic acid represents an efficient and …

[HTML][HTML] Rutaecarpine analogues with potent anti-inflammation to alleviate acute ulcerative colitis via regulating TLR4/MAPK/NF-κB pathway

LQ Qin, ZY Gu, NY Chen, PD Liu, LS Lan, XW Li… - Results in …, 2024 - Elsevier
Natural products are a rich resource in drug discovery. In the report, series novel
rutaecarpine-derived compounds with potent anti-inflammatory activity and therapeutic …