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Tetrazole regioisomers in the development of nitro group-containing antitubercular agents

https://doi.org/10.1039/c4md00301b
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/(sici)1097-458x(199703)35:3<209::aid-omr40>3.0.co;2-6openalex-snapshot
Discrimination of Structural Isomers ofN-Methylated andN-tert-Butylated Tetrazoles by13C and15N NMR. Long-Range15N,1H Coupling Constants
inferredcites →https://doi.org/10.1002/cmdc.201200339openalex-snapshot
Recent Advances in the Research of Heterocyclic Compounds as Antitubercular Agents
inferredcites →https://doi.org/10.1002/ejoc.201200469openalex-snapshot
Synthesis and Functionalization of 5‐Substituted Tetrazoles
inferredcites →https://doi.org/10.1002/emmm.201303575openalex-snapshot
Towards a new combination therapy for tuberculosis with next generation benzothiazinones
inferredcites →https://doi.org/10.1002/hc.20293openalex-snapshot
Synthesis of novel 5‐aryl‐1 H ‐tetrazoles
inferredcites →https://doi.org/10.1002/med.21262openalex-snapshot
Antituberculosis Drug Research: A Critical Overview
inferredcites →https://doi.org/10.1016/j.bmc.2012.06.007openalex-snapshot
Synthesis and biological evaluation of new N-acyl-homoserine-lactone analogues, based on triazole and tetrazole scaffolds, acting as LuxR-dependent quorum sensing modulators
inferredcites →https://doi.org/10.1016/j.ejmech.2004.10.004openalex-snapshot
Synthesis and antimycobacterial activity of 2-substituted halogenobenzimidazoles
inferredcites →https://doi.org/10.1016/j.ejmech.2007.02.023openalex-snapshot
Carbamoyl tetrazoles as inhibitors of endocannabinoid inactivation: A critical revisitation
inferredcites →https://doi.org/10.1016/j.ejmech.2014.05.069openalex-snapshot
1-Substituted-5-[(3,5-dinitrobenzyl)sulfanyl]-1H-tetrazoles and their isosteric analogs: A new class of selective antitubercular agents active against drug-susceptible and multidrug-resistant mycobacteria
inferredcites →https://doi.org/10.1016/j.tet.2013.07.103openalex-snapshot
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inferredcites →https://doi.org/10.1016/s0223-5234(02)01342-9openalex-snapshot
Synthesis and preliminary evaluation of benzimidazole derivatives as antimicrobial agents
inferredcites →https://doi.org/10.1016/s0960-894x(02)00697-2openalex-snapshot
Heterocyclic benzazole derivatives with antimycobacterial In vitro activity
inferredcites →https://doi.org/10.1021/ja211042ropenalex-snapshot
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inferredcites →https://doi.org/10.1021/jm800136bopenalex-snapshot
Optimization of the Central Heterocycle of α-Ketoheterocycle Inhibitors of Fatty Acid Amide Hydrolase
inferredcites →https://doi.org/10.1021/jm960404vopenalex-snapshot
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inferredcites →https://doi.org/10.1023/a:1026125230589openalex-snapshot
2-Substituted and 2,5-Disubstituted Tetrazoles
inferredcites →https://doi.org/10.1038/nrd4001openalex-snapshot
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inferredcites →https://doi.org/10.1056/nejmoa1112433openalex-snapshot
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inferredcites →https://doi.org/10.1093/infdis/jis034openalex-snapshot
New Drugs for the Treatment of Tuberculosis: Needs, Challenges, Promise, and Prospects for the Future
inferredcites →https://doi.org/10.1111/j.1747-0285.2009.00909.xopenalex-snapshot
Heme Oxygenase Inhibition by 2‐Oxy‐substituted 1‐Azolyl‐4‐phenylbutanes: Effect of Variation of the Azole Moiety. X‐Ray Crystal Structure of Human Heme Oxygenase‐1 in Complex with 4‐Phenyl‐1‐(1H‐1,2,4‐triazol‐1‐yl)‐2‐butanone†
inferredcites →https://doi.org/10.1126/science.1171583openalex-snapshot
Benzothiazinones Kill Mycobacterium tuberculosis by Blocking Arabinan Synthesis
inferredcites →https://doi.org/10.1128/aac.00665-06openalex-snapshot
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inferredcites →https://doi.org/10.1128/aac.49.6.2294-2301.2005openalex-snapshot
Preclinical Testing of the Nitroimidazopyran PA-824 for Activity against Mycobacterium tuberculosis in a Series of In Vitro and In Vivo Models
inferredcites →https://doi.org/10.1134/s1070428006040014openalex-snapshot
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inferredcites →https://doi.org/10.1134/s1070428006110017openalex-snapshot
Protolytic equilibria in tetrazoles
inferredcites →https://doi.org/10.1134/s1070428009010217openalex-snapshot
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inferredcites →https://doi.org/10.1248/yakushi1947.112.9_622openalex-snapshot
Orally Active Cephalosporins. I. Synthesis and Structure-Activity Relationships of 7β-[2-(R)-Amino-2-phenylacetamido]-3-(1H-1, 2, 3-triazol-4-yl) alkylthiomethyl-3-cephem-4-carboxylic Acid and Related Compounds
inferredcites →https://doi.org/10.1371/journal.pmed.0030466openalex-snapshot
OPC-67683, a Nitro-Dihydro-Imidazooxazole Derivative with Promising Action against Tuberculosis In Vitro and In Mice
inferredcites →https://doi.org/10.1371/journal.ppat.1000645openalex-snapshot
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inferredcites →https://doi.org/10.2174/157340612800493593openalex-snapshot
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inferredcites →https://doi.org/10.4161/cib.2.3.7926openalex-snapshot
The mechanism of action of PA-824

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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inferred← citeshttps://doi.org/10.1002/ddr.21606openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ddr.21638openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/med.21454openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/slct.201600286openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/slct.202000641openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/slct.202002238openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10934-022-01369-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11172-016-1394-zopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s13738-018-1325-zopenalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.bioorg.2024.107646openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.bioorg.2026.109894openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.biopha.2024.116399openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.bmc.2015.10.029openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.bmc.2017.08.010openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.bmcl.2018.07.005openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.bmcl.2023.129391openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.cbi.2022.110078openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.cbi.2023.110735openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.ejmech.2016.11.041openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.ejmech.2017.02.058openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.ejmech.2018.12.001openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.ejmech.2019.111882openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.ejmech.2020.112886openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.ejmech.2023.115301openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.ica.2019.01.039openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.ica.2025.122857openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tet.2015.07.034openalex-snapshot
An efficient access to (1H-tetrazol-5-yl)furoxan ammonium salts via a two-step dehydration/[3+2]-cycloaddition strategy
inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.11.049openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.jmedchem.3c00925openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.jmedchem.5b00608openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.jmedchem.9b00912openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acsmedchemlett.8b00177openalex-snapshot
Identification of N-Benzyl 3,5-Dinitrobenzamides Derived from PBTZ169 as Antitubercular Agents
inferred← citeshttps://doi.org/10.1039/c5nj00211gopenalex-snapshot
Application of a functionalized mesoporous silica catalyst to the synthesis of tetrazoles
inferred← citeshttps://doi.org/10.1039/d4md00060aopenalex-snapshot
Carltonine-derived compounds for targeted butyrylcholinesterase inhibition
inferred← citeshttps://doi.org/10.1039/d5cc05872dopenalex-snapshot
Electro-oxidative [3+2] cycloaddition for the synthesis of 5-selenyltetrazoles
inferred← citeshttps://doi.org/10.1063/5.0127508openalex-snapshot
Microwave assisted synthesis of tetrazole derivative
inferred← citeshttps://doi.org/10.1070/rcr4864openalex-snapshot
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inferred← citeshttps://doi.org/10.1080/00304948.2024.2368904openalex-snapshot
Manganese (II) Chloride Tetrahydrate as an Efficient Catalyst for the Preparation of 5-Aryl-1 H -tetrazoles via [3 + 2] Cycloaddition of Sodium Azide and Nitriles
inferred← citeshttps://doi.org/10.1080/00304948.2025.2550319openalex-snapshot
An Efficient and Expeditious Synthesis of Tetrazoles with Meglumine as a Reusable Catalyst
inferred← citeshttps://doi.org/10.1080/00397911.2017.1401639openalex-snapshot
Synthesis and antibacterial evaluation of new sulfanyltetrazole derivatives bearing piperidine dithiocarbamate moiety
inferred← citeshttps://doi.org/10.1080/00397911.2018.1519077openalex-snapshot
Fe3O4-Graphene oxide nanocomposite: Synthesis of 5-sulfanyl tetrazole derivatives of alkyls, indoles, and pyrroles
inferred← citeshttps://doi.org/10.1080/00397911.2019.1679185openalex-snapshot
ZSM-5 catalyzed one pot three-component synthesis of 5-substituted-1H-tetrazoles from aldehyde
inferred← citeshttps://doi.org/10.1080/21505594.2016.1256536openalex-snapshot
Early diagnosis and effective treatment regimens are the keys to tackle antimicrobial resistance in tuberculosis (TB): A report from Euroscicon's international TB Summit 2016
inferred← citeshttps://doi.org/10.1134/s1070428025602602openalex-snapshot
Pharmacological Potential and Medicinal Applications of Substituted Tetrazole Analogs (A Review)
inferred← citeshttps://doi.org/10.2174/9789815165258123120005openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/ijms24119124openalex-snapshot
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