Downregulation of tumor necrosis factor and other proinflammatory biomarkers by polyphenols

SC Gupta, AK Tyagi, P Deshmukh-Taskar… - Archives of biochemistry …, 2014 - Elsevier
Human tumor necrosis factor (TNF), first isolated by our group as an anticancer agent, has
been now shown to be a primary mediator of inflammation. Till today 19 different members of …

Therapeutic significance of β-glucuronidase activity and its inhibitors: A review

P Awolade, N Cele, N Kerru, L Gummidi… - European journal of …, 2020 - Elsevier
The emergence of disease and dearth of effective pharmacological agents on most
therapeutic fronts, constitutes a major threat to global public health and man's existence …

Development of novel pyrazole, imidazo [1, 2-b] pyrazole, and pyrazolo [1, 5-a] pyrimidine derivatives as a new class of COX-2 inhibitors with immunomodulatory …

R Ayman, MS Abusaif, AM Radwan… - European Journal of …, 2023 - Elsevier
Searching for new compounds with anti-inflammatory properties is a significant target since
inflammation is a major cause of pain. A series of pyrazole, imidazopyrazolone, and …

[HTML][HTML] Evaluation of anti-inflammatory activity of selected medicinal plants used in Indian traditional medication system in vitro as well as in vivo

RU Shaikh, MM Pund, RN Gacche - Journal of traditional and …, 2016 - Elsevier
The present study was carried out to evaluate in vivo and in vitro anti-inflammatory potential
of selected medicinal plants used in Indian traditional medication. The sequentially extracted …

Chemical Characterization and Anti-Inflammatory Activity of Phytoconstituents from Swertia alata

S Bajaj, S Fuloria, V Subramaniyan, DU Meenakshi… - Plants, 2021 - mdpi.com
Swertia alata CB Clarke (Gentianaceae) is a well-reported plant in the traditional system of
medicine. The present study was intended to isolate the phytoconstituents from the ethanolic …

Curcumin analogues and derivatives with anti-proliferative and anti-inflammatory activity: Structural characteristics and molecular targets

E Chainoglou, D Hadjipavlou-Litina - Expert opinion on drug …, 2019 - Taylor & Francis
ABSTRACT Introduction: Curcumin (Diferuloylmethane) is a natural phenolic compound,
which belongs to the curcuminoid family, presenting pleiotropic activity and low …

Synthesis and cytotoxicity evaluation of novel asymmetrical mono-carbonyl analogs of curcumin (AMACs) against Vero, HeLa, and MCF7 Cell Lines

P Wiji Prasetyaningrum, A Bahtiar, H Hayun - Scientia pharmaceutica, 2018 - mdpi.com
A series of novel asymmetrical mono-carbonyl analogs of curcumin (AMACs) were
synthesized and evaluated for cytotoxic activity using BSLT and MTT assay against Vero …

Synthesis, in vitro, in silico and DFT studies of indole curcumin derivatives as potential anticancer agents

A Parthiban, R Sivasankar, B Rajdev, RN Asha… - Journal of Molecular …, 2022 - Elsevier
The curcumin derivatives were synthesized for the first time using simple starting materials
through a three-component reaction, yielding high purity compounds. The synthesized …

Development of antioxidant COX-2 inhibitors as radioprotective agents for radiation therapy—a hypothesis-driven review

M Laube, T Kniess, J Pietzsch - Antioxidants, 2016 - mdpi.com
Radiation therapy (RT) evolved to be a primary treatment modality for cancer patients.
Unfortunately, the cure or relief of symptoms is still accompanied by radiation-induced side …

Screening of curcumin‐derived isoxazole, pyrazoles, and pyrimidines for their anti‐inflammatory, antinociceptive, and cyclooxygenase‐2 inhibition

M Ahmed, MA Qadir, A Hameed… - Chemical Biology & …, 2018 - Wiley Online Library
Curcumin has shown pharmacological properties against different phenotypes of various
disease models. Different synthetic routes have been employed to develop its numerous …