Molecules 2020, 25, 308
14 of 15
5.
6.
Wang, P.; Pradhan, K.; Zhong, X.; Mao, X. Isoniazid metabolism and hepatotoxicity. Acta Pharm. Sinica B
Bedia, K.K.; Elçin, O.; Seda, U.; Fatma, K.; Nathaly, S.; Sevim, R.; Dimoglo, A. Synthesis and characterization
of novel hydrazide–hydrazones and the study of their structure-antituberculosis activity. Eur. J. Med. Chem.
7.
8.
9.
Rollas, S.; Küçükgüzel, S.G. Biological activities of hydrazine derivatives. Molecules 2007, 12, 1910–1939.
Eldehna, W.M.; Fares, M.; Abdel-Aziz, M.M.; Abdel-Aziz, H.A. Design, synthesis and antitubercular activity
of certain nicotinic acid hydrazides. Molecules 2015, 20, 8800–8815. [CrossRef] [PubMed]
Kumari, D.; Bansal, H. Benzohydrazides: As potential bio-active agents. Pharma Innov. J. 2018, 7, 543–550.
10. Abbas, A.; Ali, B.; Kanwal, K.M.; Khan, K.M.; Iqbal, J.; Ur Rahman, S.; Zaib, S.; Perveen, S. Synthesis and
in vitro urease inhibitory activity of benzohydrazide derivatives, in silico and kinetic studies. Bioorg. Chem.
11. Timmins, G.S.; Deretic, V. Mechanisms of action of isoniazid. Mol. Microb. 2006, 62, 1220–1227. [CrossRef]
12. Wengenack, N.L.; Rusnak, F. Evidence for isoniazid-dependent free radical generation catalyzed by
Mycobacterium tuberculosis KatG and the isoniazid-resistant mutant KatG(S315T). Biochemistry 2001, 40,
13. Khan, S.R.; Morgan, A.G.M.; Michail, K.; Srivastava, N.; Whittal, R.M.; Aljuhani, N.; Siraki, A.G. Metabolism
of isoniazid by neutrophil myeloperoxidase leads to isoniazid-NAD+ adduct formation: A comparison of the
reactivity of isoniazid with its known human metabolites. Biochem. Pharmacol. 2016, 106, 46–55. [CrossRef]
14. Dong, J.; Ren, Y.; Sun, S.; Yang, J.; Nan, C.; Shi, H.; Xu, J.; Duan, J.; Shi, T.; Elding, L.I. Kinetics and mechanism
of oxidation of the anti-tubercular prodrug isoniazid and its analog by iridium (IV) as models for biological
redox systems. Dalton Trans. 2017, 46, 8377–8386. [CrossRef]
15. Pelizzetti, E.; Mentasti, E.; Baiocchi, C. Kinetics and mechanism of oxidation of quinols by
hexachloroiridate(IV) in aqueous acidic perchlorate media. J. Phys. Chem. 1976, 80, 2979–2982. [CrossRef]
16. Pelizzetti, E.; Mentasti, E.; Pramauro, E. Outer-sphere oxidation of ascorbic acid. Inorg. Chem. 1978, 17,
17. Stanbury, D.M. Reactions involving the hydrazinium free radical; oxidation of hydrazine by hexachloroiridate.
Inorg. Chem. 1984, 23, 2879–2882. [CrossRef]
18. Hubbard, C.D.; Gerhard, A.; van Eldik, R. Electrostriction and counter ion effects in an outer-sphere electron
transfer reaction. Kinetics of the reduction of hexachloroiridate(IV) by iodide ion. Dalton Trans. 2001
,
19. Bhattari, N.; Stanburry, D.M. Oxidation of glutathione by hexachloroiridate(IV), dicyanobis(bipyridine)
iron(III), and tetracyano (bipyridine)iron(III). Inorg. Chem. 2012, 51, 13303–13311. [CrossRef]
20. Kim, E.; Winkler, T.E.; Kitchen, C.; Kang, M.; Banis, G.; Bentley, W.E.; Kelly, D.L.; Ghodssi, R.; Payne, G.F.
Redox probing for chemical information of oxidative stress. Anal. Chem. 2017, 89, 1583–1592. [CrossRef]
21. Katouaha, H.A.; Al-Fahemia, J.H.; Elghalbana, M.G.; Saada, F.A.; Althagafia, I.A.; El-Metwaly, N.M.;
Khedra, A.M. Synthesis of new Cu(II)-benzohydrazide nanometer complexes, spectral, modeling, CT-DNA
binding with potential anti-inflammatory and anti-allergic theoretical feature. Mater. Sci. Eng. C: Mater. Biol.
22. Jim
é
nez-Pulido, S.B.; Linares-Ord ñez, F.M.; Mart
ó
ínez-Martos, J.M.; Moreno-Carretero, M.N.;
Quir
ó
s-Oloz bal, M.; Ram rez-Expósito, M.J. Metal complexes with the ligand derived from
á
í
6-acetyl-1,3,7-trimethyllumazine and benzohydrazide. Molecular structures of two new Co(II) and Rh(III)
complexes and analysis of in vitro antitumor activity. J. Inorg. Biochem. 2008, 102, 1677–1683. [CrossRef]
23. Yang, P.; Lim, L.H.; Chuanprasit, P.; Hirao, H.; Zhou, J. Nickel–catalyzed enantioselective reductive amination
of ketones with both arylamines and benzhydrazide. Angew. Chem. Int. Ed. 2016, 55, 12083–12087. [CrossRef]
24. Shewale, S.A.; Phadkule, A.N.; Gokavi, G.S. Kinetics and mechanism of oxidation of benzohydrazide by
bromate catalyzed by vanadium (IV) in aqueous acidic medium. Int. J. Chem. Kinet. 2008, 40, 151–159.