Phthalic anhydride (PA): a valuable substrate in organic transformations
K Nikoofar, M Sadathosainy - RSC advances, 2023 - pubs.rsc.org
This review has been centralized on applications of phthalic anhydride (PA) as a valuable
and significant heterocyclic substrate in two-and multicomponent organic reactions. The …
and significant heterocyclic substrate in two-and multicomponent organic reactions. The …
Design, synthesis, and biological evaluation of new challenging thalidomide analogs as potential anticancer immunomodulatory agents
Thalidomide and its analogs are immunomodulatory drugs that inhibit the production of
certain inflammatory mediators associated with cancer. In the present work, a new series of …
certain inflammatory mediators associated with cancer. In the present work, a new series of …
Phthalimides as anti-inflammatory agents
ABSTRACT Isoindoline-1, 3-dione, also referred as phthalimide, has gained recognition as
promising pharmacophore due to the documented biological activities of its derivatives …
promising pharmacophore due to the documented biological activities of its derivatives …
[HTML][HTML] Synthesis, in vitro and in vivo biological evaluation of novel lappaconitine derivatives as potential anti-inflammatory agents
L Pang, CY Liu, GH Gong, ZS Quan - Acta Pharmaceutica Sinica B, 2020 - Elsevier
Lappaconitine (LA), a natural compound with a novel C18-diterpenoid alkaloid skeleton,
displayed extensive biological profile. Recent research on LA is focused mainly on its anti …
displayed extensive biological profile. Recent research on LA is focused mainly on its anti …
Discovery of fusidic acid derivatives as novel STING inhibitors for treatment of sepsis
J Long, T Ying, L Zhang, T Yu, J Wu, Y Liu, X Li… - European Journal of …, 2022 - Elsevier
Sepsis is often caused by systemic inflammatory responses. Stimulator of interferon genes
(STING) could be a promising treatment target for sepsis. In this study, we report the design …
(STING) could be a promising treatment target for sepsis. In this study, we report the design …
Antitumor and immunomodulatory activities of thiosemicarbazones and 1, 3-Thiazoles in Jurkat and HT-29 cells
TAR Dos Santos, AC da Silva, EB Silva… - Biomedicine & …, 2016 - Elsevier
Cancer remains a high incidence and mortality disease, causing around 8.2 million of
deaths in the last year. Current chemotherapy needs to be expanded, making research for …
deaths in the last year. Current chemotherapy needs to be expanded, making research for …
Privileged structures in the design of potential drug candidates for neglected diseases
ACL Leite, JWP Espíndola… - Current Medicinal …, 2019 - ingentaconnect.com
Background: Privileged motifs are recurring in a wide range of biologically active
compounds that reach different pharmaceutical targets and pathways and could represent a …
compounds that reach different pharmaceutical targets and pathways and could represent a …
Phthalimido-thiazoles as building blocks and their effects on the growth and morphology of Trypanosoma cruzi
PAT de Moraes Gomes, AR Oliveira… - European journal of …, 2016 - Elsevier
Chagas disease is a parasitic infection caused by protozoan Trypanosoma cruzi that affects
approximately 6–7 million people worldwide. Benznidazole is the only drug approved for …
approximately 6–7 million people worldwide. Benznidazole is the only drug approved for …
Synthesis and biological evaluation of novel sinomenine derivatives as anti-inflammatory and analgesic agent
F Gao, Z Dai, T Zhang, Y Gu, D Cai, M Lu, Z Zhang… - RSC …, 2022 - pubs.rsc.org
Sinomenine (SIN) has long been known as an anti-inflammatory drug, while poor efficiency
and large-dose treatment had limited its further application. A series of novel SIN derivatives …
and large-dose treatment had limited its further application. A series of novel SIN derivatives …
[HTML][HTML] Improvement of in vivo anticancer and antiangiogenic potential of thalidomide derivatives
PM Da Costa, MP da Costa, AA Carvalho… - Chemico-Biological …, 2015 - Elsevier
The strategy of antiangiogenic drugs is based on inhibiting formation of new blood vessels
as alternative to limit cancer progression. In this work, we investigated the antitumor and …
as alternative to limit cancer progression. In this work, we investigated the antitumor and …