A Practical Method of N ‐Methylpyrrole Disulfonamides Synthesis: Computational Studies, Carbonic Anhydrase Inhibition and Electrochemical DNA Binding Investigations-Reference-Cited by-同舟云学术

A Practical Method of N ‐Methylpyrrole Disulfonamides Synthesis: Computational Studies, Carbonic Anhydrase Inhibition and Electrochemical DNA Binding Investigations

Published:2021-08-02 Issue:29 Volume:6 Page:7376-7383
ISSN:2365-6549
Container-title:ChemistrySelect
language:en
Short-container-title:ChemistrySelect

Author:

Abas Mujahid¹,Nazir Yasir¹²,Ashraf Zaman¹,Iqbal Zafar¹,Raza Hussain³,Hassan Mubashir⁴,Jabeen Erum¹,Bais Abdul¹

Affiliation:

1. Department of Chemistry Allama Iqbal Open University Islamabad 44000 Pakistan

2. Faculty of Sciences Department of Chemistry University of Sialkot 51300 Pakistan

3. Department of Biological Sciences College of Natural Sciences Kongju National University Gongju 314-701 Korea

4. Institute of Molecular Biology and Biotechnology The University of Lahore Lahore Pakistan

Publisher

Wiley

Subject

General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/slct.202101854

Reference24 articles.

1. Synthesis of 3-[5-(biphenyl-4-yl)pyrrol-2-yl]-1-phenylprop-2-yn-1-ones by palladium-free cross-coupling between pyrroles and haloalkynes on aluminum oxide

2. Multiple Binding Modes of Inhibitors to Carbonic Anhydrases: How to Design Specific Drugs Targeting 15 Different Isoforms?

3. Carbonic anhydrase inhibitors

4. Combining the tail and the ring approaches for obtaining potent and isoform-selective carbonic anhydrase inhibitors: Solution and X-ray crystallographic studies

5. Imaging the hypoxia surrogate marker CA IX requires expression and catalytic activity for binding fluorescent sulfonamide inhibitors

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