Updates on aldose reductase inhibitors for management of diabetic complications and non-diabetic diseases

A Singh Grewal, S Bhardwaj, D Pandita… - Mini reviews in …, 2016 - ingentaconnect.com
Diabetes mellitus occurrence has been associated to the modification of the physiological
levels of glucose and is often accompanied by several long-term complications, namely …

Recent studies of aldose reductase enzyme inhibition for diabetic complications

S Suzen, E Buyukbingol - Current medicinal chemistry, 2003 - ingentaconnect.com
Aldose reductase [ALR2; EC 1.1. 1.21], a key enzyme of polyol pathway, catalyzes NADPH-
dependent reduction of glucose to sorbitol (Sorbitol pathway), and an excessive …

Synthesis of 4-(thiazol-2-ylamino)-benzenesulfonamides with carbonic anhydrase I, II and IX inhibitory activity and cytotoxic effects against breast cancer cell lines

NMA Gawad, NH Amin, MT Elsaadi… - Bioorganic & medicinal …, 2016 - Elsevier
Abstract A series of 4-(thiazol-2-ylamino)-benzenesulfonamides was synthesized and
screened for their carbonic anhydrase (CA, EC 4.2. 1.1) inhibitory and cytotoxic activity on …

Synthesis, carbonic anhydrase inhibition and cytotoxic activity of novel chromone-based sulfonamide derivatives

FM Awadallah, TA El-Waei, MM Hanna… - European journal of …, 2015 - Elsevier
Four series of sulfonamides incorporating chromone moieties were synthesized and
assessed for their cytotoxic activity against MCF-7 and A-549 cell lines, considering the fact …

Synthesis and antimicrobial/antimalarial activities of novel naphthalimido trans-β-lactam derivatives

JA Rad, A Jarrahpour, C Latour, V Sinou… - Medicinal Chemistry …, 2017 - Springer
This paper describes for the first time the synthesis and microbiological assessment of some
new β-lactam derivatives containing a 1, 8-naphthalimide functional group. These …

Acyl sulfonamide anti-proliferatives: Benzene substituent structure− activity relationships for a novel class of antitumor agents

KL Lobb, PA Hipskind, JA Aikins… - Journal of medicinal …, 2004 - ACS Publications
Two closely related diaryl acylsulfonamides were recently reported as potent antitumor
agents against a broad spectrum of human tumor xenografts (colon, lung, breast, ovary, and …

Design, synthesis, and molecular docking of novel indole scaffold‐based VEGFR‐2 inhibitors as targeted anticancer agents

HM Roaiah, IAY Ghannam, IH Ali… - Archiv der …, 2018 - Wiley Online Library
A series of new indole derivatives 1–18 was synthesized and tested for their cytotoxic activity
on a panel of 60 tumor cell lines. Additionally, molecular docking was carried out to study …

Synthesis of some new thiazolopyrane and thiazolopyranopyrimidine derivatives bearing a sulfonamide moiety for evaluation as anticancer and radiosensitizing …

DA Abou El Ella, MM Ghorab, HI Heiba… - Medicinal Chemistry …, 2012 - Springer
A new series of thiazolopyrane 5a–d, 11–13 and thiazolopyranopyrimidine 6–10, 7b, 8b,
and 14 derivatives bearing a sulfonamide moiety were designed and synthesized. The …

[PDF][PDF] Synthesis of certain new thiazole derivatives bearing a sulfonamide moiety with expected anticancer and radiosensitizing activities

MM Ghorab, DAA El Ella, HI Heiba… - Journal of Materials …, 2011 - researchgate.net
New thiazolo [4, 5-d] pyrimidines 4a, b, thioxopropanoic acid ethyl ester 7 and 4-
oxothiazolidine benzenesulfonamides 9a-h were designed and synthesized. The molecular …

Synthesis and in vitro activity of novel 2-(benzylthio)-4-chloro-5-(1, 3, 4-oxadiazol-2-yl) benzenesulfonamide derivatives

K Brożewicz, J Sławiński - Monatshefte für Chemie-Chemical Monthly, 2012 - Springer
Two series of novel 4-chloro-2-(benzylthio)-5-(1, 3, 4-oxadiazol-2-yl) benzenesulfonamides
and their N-aroyl derivatives have been synthesized and evaluated for in vitro anticancer …