Identification of novel bacterial urease inhibitors through molecular shape and structure based virtual screening approaches-Reference-Cited by-同舟云学术

Identification of novel bacterial urease inhibitors through molecular shape and structure based virtual screening approaches

Published:2020 Issue:27 Volume:10 Page:16061-16070
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Imran Muhammad¹²³⁴^ORCID,Waqar Saba⁵⁶⁷⁴,Ogata Koji⁸⁹¹⁰¹¹^ORCID,Ahmed Mahmood¹²³⁴^ORCID,Noreen Zobia⁵⁶⁷⁴,Javed Sundus⁵⁶⁷⁴,Bibi Nazia⁵⁶⁷⁴,Bokhari Habib⁵⁶⁷⁴,Amjad Asma⁵⁶⁷⁴,Muddassar Muhammad⁵⁶⁷⁴^ORCID

Affiliation:

1. School of Life Sciences

2. FC College University

3. Lahore

4. Pakistan

5. Department of Biosciences

6. COMSATS University Islamabad

7. Islamabad

8. Faculty of Pharmaceutical Sciences

9. Sanyo-Onoda City University

10. Yamaguchi

11. Japan

12. Renacon Pharma Limited

Abstract

The enzyme urease is an essential colonizing factor of the notorious carcinogenic pathogen Helicobacter pylori (H. pylori), conferring acid resistance to the bacterium.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2020/RA/D0RA02363A

Reference40 articles.

1. Synthesis, biological evaluation and molecular docking of N-phenyl thiosemicarbazones as urease inhibitors

2. 3-Arylpropionylhydroxamic acid derivatives as Helicobacter pylori urease inhibitors: Synthesis, molecular docking and biological evaluation

3. Helicobacter pylori Update: Gastric Cancer, Reliable Therapy, and Possible Benefits

4. Urease inhibitors as potential drugs for gastric and urinary tract infections: a patent review

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