Tetrahydroisoquinoline based 5-nitro-2-furoic acid derivatives: a promising new approach for anti-tubercular agents?
New Journal of Chemistry Pub Date: 2023-07-25 DOI: 10.1039/D3NJ01907A
Abstract
We designed, synthesized, and tested twenty-six novel tetrahydroisoquinoline carbohydrazide compounds for their anti-mycobacterial activity. Utilizing mass spectrometry, 1H NMR, 13C NMR, and elemental analysis, all the synthesized derivative structures were confirmed. The final analogs were tested for their ability to inhibit Mycobacterium tuberculosis (Mtb). The Mtb inhibitory activity outcomes varied from 0.78 to 25 μg mL?1. Among all the investigated analogues, compounds NFT-12, NFT-19, and NFT-20 exhibited substantial activity with a MIC of 0.78 μg mL?1 against Mtb H37Rv. Furthermore, the NFT-11 compound showed excellent activity with a MIC of 1.56 μg mL?1. The majority of the compounds showed very good activity compared to the standard drug rifampicin (MIC 3.12 μg mL?1). The most active compounds, NFT-12, NFT-19, and NFT-20, demonstrated selectivity over the normal human embryonic kidney cell line (HEK293T) with a selectivity index of >40. To determine whether the designed compounds exhibit synergistic effects or not, drug–inhibitor combination studies were carried out for the most active compounds using the standard drugs isoniazid, rifampicin, ciprofloxacin, and streptomycin. The improvement in pharmacological activities (x/y coefficients) demonstrates the effectiveness of the compounds NFT-12, NFT-19, and NFT-20 with isoniazid. The expected binding site of the test ligand at the active site of the chosen target proteins was determined using molecular docking studies. The most active compounds NFT-12, NFT-19, and NFT-20 were used in the docking experiments to determine the binding pattern at the active site with the Mycobacterium tuberculosis InhA (PDB ID: 4OHU, 1.60 ?).
Recommended Literature
- [1] An aptamer-based keypad lock system? Yaqing Liu,Jiangtao Ren,Jing Li,Jiyang Liu,Erkang WangChem. Commun., 2012,48, 802-804 10.1039/C1CC15979H
- [2] Aggregation of biologically important peptides and proteins: inhibition or acceleration depending on protein and metal ion concentrations Benjamin Gabriel Poulson,Kacper Szczepski,Joanna Izabela Lachowicz,Lukasz Jaremko,Abdul-Hamid Emwas,Mariusz JaremkoRSC Adv., 2020,10, 215-227 10.1039/C9RA09350H
- [3] An amorphous Cu–In–S nanoparticle-based precursor ink with improved atom economy for CuInSe2 solar cells with 10.85% efficiency? Green Chem., 2017,19, 1268-1277 10.1039/C6GC03280J
- [4] Alternative donor substrates for inverting and retaining glycosyltransferases? Luke L. Lairson,Warren W. WakarchukChem. Commun., 2007, 365-367 10.1039/B614636H
- [5] Alt-proteins: A promising future 10.1002/fsat.3701_10.x
- [6] Acetyl protected thiol methacrylic polymers as effective ligands to keep quantum dots in luminescent standby mode? Marta Liras,Isabel Quijada-Garrido,Marta Palacios-Cuesta,Sonia Mu?oz-Durieux,Olga GarcíaPolym. Chem., 2014,5, 433-442 10.1039/C3PY00987D
- [7] An apparatus for testing water by measurement of its electrical conductivity Analyst, 1912,37, 538-543 10.1039/AN9123700538
- [8] An integrated cathode and solid electrolyte via in situ polymerization with significantly reduced interface resistance? Jialiang Yuan,Ran Dong,Yuan Li,Yang Liu,Zhuo Zheng,Yuxia Liu,Yan Sun,Benhe Zhong,Zhenguo Wu,Xiaodong GuoChem. Commun., 2021,57, 13004-13007 10.1039/D1CC04485K
- [9] Alternative synthesis of the anti-baldness compound RU58841? RSC Adv., 2014,4, 14143-14148 10.1039/C4RA00332B
- [10] An artificial enzyme cascade amplification strategy for highly sensitive and specific detection of breast cancer-derived exosomes? Huiying Xu,Lu Zheng,Yu Zhou,Bang-Ce YeAnalyst, 2021,146, 5542-5549 10.1039/D1AN01071A
Journal Name:New Journal of Chemistry
research_products
-
CAS no.: 89640-58-4