Urease inhibitory potential of extracts and active phytochemicals of Hypochaeris radicata (Asteraceae)

• Published in: Natural product research Vol. 34; no. 4; pp. 553 - 557
• Main Authors: Abu-Izneid, Tareq, Rauf, Abdur, Saleem, Muhammad, Mansour, Nashwa, Abdelhady, Mohamed I. S., Ibrahim, Munjed M., Patel, Seema
• Format: Journal Article
• Language: English
• Published: England Taylor & Francis 16-02-2020; Taylor & Francis Ltd
• Subjects: Acetic acid; Asteraceae; Asteraceae - chemistry; Carbonic anhydrase; Carbonic anhydrases; Carbonic cnhydrase inhibition; Column chromatography; Enzyme Inhibitors - isolation & purification; Enzyme Inhibitors - pharmacology; Enzymes; Ethyl acetate; Hypochaeris radicata; Phytochemicals; Phytochemicals - analysis; Phytochemicals - isolation & purification; Phytochemicals - pharmacology; Plant Extracts - chemistry; Plant Extracts - pharmacology; Purification; Sesquiterpenes - analysis; Sesquiterpenes - chemistry; Sesquiterpenes - isolation & purification; Sesquiterpenes - pharmacology; Thiourea; Urease; Urease - antagonists & inhibitors; urease inhibition; phytochemicals; Hypochaeris radicata; urease inhibition; Carbonic cnhydrase inhibition
• ISSN: 1478-6419; 1478-6427
• DOI: 10.1080/14786419.2018.1489387

Urease inhibition potential of compound (1), guaiane-type sesquiterpene (2), confertin (3) and scopoletin (4) was carried out with high throughout mechanism-based assay. These compounds were isolated from Hypochaeris radicata L., an Asteraceae family member. The pure compounds were screened for their urease and carbonic anhydrase inhibitory activities. The ethyl acetate fractions were subjected to column chromatography, which resulted in the isolation and purification of four compounds (1-4). On evaluation, compounds (1-4) exhibited selective activity against urease enzyme with an IC
50
value of 180.11 ± 2.00, 27.18 ± 0.80, 24.12 ± 0.2 and 30.12 ± 1.10 µM respectively. The compounds (1-4) were found to be inactive against carbonic anhydrase enzyme. Thiourea was used as standard inhibitor (21 ± 0.14 µM) of urease enzyme.