Synthesis of 2‐Aryl‐12 H ‐benzothiazolo[2,3‐ b ]quinazolin‐12‐ones and Their Activity Against Monoamine Oxidases-Reference-Cited by-同舟云学术

Synthesis of 2‐Aryl‐12 H ‐benzothiazolo[2,3‐ b ]quinazolin‐12‐ones and Their Activity Against Monoamine Oxidases

Published:2019-10-09 Issue:37 Volume:4 Page:11071-11076
ISSN:2365-6549
Container-title:ChemistrySelect
language:en
Short-container-title:ChemistrySelect

Author:

Jafari Behzad¹,Jalil Saquib²,Zaib Sumera²,Iqbal Jamshed²,Safarov Sayfidin¹³,Khalikova Muattar¹³,Isobaev Muzafar¹³,Munshi Ali¹⁴,Rahman Qamar¹⁴,Ospanov Meirambek¹⁵,Yelibayeva Nazym¹⁵,Kelzhanova Nazken¹⁵,Abilov Zharylkasyn A.⁵,Turmukhanova Mirgul Z.⁵,Kalugin Sergey N.⁵,Ehlers Peter¹,Langer Peter¹⁶^ORCID

Affiliation:

1. Institut für ChemieUniversität Rostock Albert-Einstein-Str. 3a 18059 Rostock Germany

2. Centre for Advanced Drug ResearchCOMSATS University Islamabad Abbottabad Campus Abbottabad- 22060 Pakistan.

3. Institute of ChemistryTajikistan Academy of Sciences, ul. Aini 299 Dushanbe 734063 Tajikistan.

4. Amity UniversityLucknow Campus, Viraj Khand-5, Gomti Nagar Lucknow– 226010 India

5. Al-Farabi Kazakh National University Al-Farabi ave. 71 050040 Almaty Kazakhstan.

6. Leibniz Institut für Katalyse an der Universität Rostock e.V. (LIKAT) Albert-Einstein-Str. 29a 18059 Rostock Germany.

Funder

Higher Education Commision, Pakistan

Publisher

Wiley

Subject

General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/slct.201902245

Reference33 articles.

2. MAO inhibitory activity of bromo-2-phenylbenzofurans: synthesis, in vitro study, and docking calculations

3. Design, synthesis and biological evaluation of lazabemide derivatives as inhibitors of monoamine oxidase

4. The therapeutic potential of monoamine oxidase inhibitors

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3. Synthesis and Antitumor Activity of 3-Hydrazone Quinazolinone Derivatives;Chinese Journal of Organic Chemistry;2023

4. Synthesis of 2‐Alkynyl‐ and2‐Amino‐12 H ‐benzothiazolo[2,3‐ b ]quinazolin‐12‐ones and Their Inhibitory Potential against Monoamine Oxidase A and B;ChemistrySelect;2019-12-17