An overview on the synthetic urease inhibitors with structure-activity relationship and molecular docking

W Yang, Q Feng, Z Peng, G Wang - European Journal of Medicinal …, 2022 - Elsevier
Urease is a kind of enzyme which could be found in various bacteria, fungi, plants, and
algae, which can quickly catalyze the hydrolysis of urea into ammonia and carbon dioxide …

A review on 'sulfonamides': their chemistry and pharmacological potentials for designing therapeutic drugs in medical science

W Zafar, SH Sumrra, AU Hassan… - Journal of Coordination …, 2023 - Taylor & Francis
The discovery of new chemical entities having enhanced bioactivities and improved
functionalities to overcome the prevailing antibiotic resistance and emerging diseases has …

Tetrabutylammonium bromide (TBAB): a neutral and efficient catalyst for the synthesis of biscoumarin and 3, 4-dihydropyrano [c] chromene derivatives in water and …

JM Khurana, S Kumar - Tetrahedron Letters, 2009 - Elsevier
A simple, efficient and ecofriendly procedure has been developed using
tetrabutylammonium bromide as catalyst for the synthesis of biscoumarin and dihydropyrano …

Synthesis of biscoumarin and 3, 4-dihydropyrano [c] chromene derivatives catalysed by sodium dodecyl sulfate (SDS) in neat water

H Mehrabi, H Abusaidi - Journal of the Iranian Chemical Society, 2010 - Springer
Iranian Chemical Society Synthesis of Biscoumarin and 3,4-Dihydropyrano[c]chromene
Derivatives Catalysed by Sodium Dodecyl Sulfa Page 1 J. Iran. Chem. Soc., Vol. 7, No. 4 …

Design, synthesis and mechanistic study of new benzenesulfonamide derivatives as anticancer and antimicrobial agents via carbonic anhydrase IX inhibition

MTM Nemr, AM AboulMagd, HM Hassan, AA Hamed… - RSC …, 2021 - pubs.rsc.org
Changes in gene expression cause uncontrolled cell proliferation and consequently tumor
hypoxia. The tumor cells shift their metabolism to anaerobic glycolysis with a significant …

Identification of antibacterial and antifungal pharmacophore sites for potent bacteria and fungi inhibition: indolenyl sulfonamide derivatives

ZH Chohan, MH Youssoufi, A Jarrahpour… - European Journal of …, 2010 - Elsevier
Synthesis of seven new indolenyl sulfonamides, have been prepared by the condensation
reaction of indole-3-carboxaldehyde with different sulfonamides such as, sulphanilamide …

4‐Hydroxycoumarin: A versatile substrate for transition‐metal‐free multicomponent synthesis of bioactive heterocycles

B Borah, K Dhar Dwivedi… - Asian Journal of Organic …, 2021 - Wiley Online Library
One‐pot multi‐component reactions especially under transition‐metal‐free catalysis served
as an efficient, and environmentally friendly method for the construction of value‐added …

[HTML][HTML] Synthetic approaches and biological activities of 4-hydroxycoumarin derivatives

JC Jung, OS Park - Molecules, 2009 - mdpi.com
Molecules | Free Full-Text | Synthetic Approaches and Biological Activities of 4-Hydroxycoumarin
Derivatives Next Article in Journal New Cucurbitane Triterpenoids and Steroidal Glycoside …

An efficient one-pot three-component synthesis of tetrahydrobenzo [b] pyran and 3, 4-dihydropyrano [c] chromene derivatives using starch solution as catalyst

N Hazeri, MT Maghsoodlou, F Mir, M Kangani… - Chinese Journal of …, 2014 - Elsevier
Abstract Tetrahydrobenzo [b] pyran and 3, 4-dihydropyrano [c] chromene derivatives were
synthesized via a one-pot three-component condensation of aromatic aldehydes with …

Synthesis of some novel coumarin isoxazol sulfonamide hybrid compounds, 3D-QSAR studies, and antibacterial evaluation

SN Esfahani, MS Damavandi, P Sadeghi, Z Nazifi… - Scientific reports, 2021 - nature.com
With the progressive and ever-increasing antibacterial resistance pathway, the need for
novel antibiotic design becomes critical. Sulfonamides are one of the more effective …