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Details

Stereochemistry ACHIRAL
Molecular Formula C7H5N3O2
Molecular Weight 163.1335
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 5-NITROINDAZOLE

SMILES

[O-][N+](=O)C1=CC=C2NN=CC2=C1

InChI

InChIKey=WSGURAYTCUVDQL-UHFFFAOYSA-N
InChI=1S/C7H5N3O2/c11-10(12)6-1-2-7-5(3-6)4-8-9-7/h1-4H,(H,8,9)

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Inhibition of the bioactivation of the neurotoxin MPTP by antioxidants, redox agents and monoamine oxidase inhibitors.
2011-08
Selective electrochemical discrimination between dopamine and phenethylamine-derived psychotropic drugs using electrodes modified with an acyclic receptor containing two terminal 3-alkoxy-5-nitroindazole rings.
2010-06
ESR and electrochemical study of 1,2-disubstituted 5-nitroindazolin-3-ones and 2-substituted 3-alkoxy-5-nitro-2H-indazoles: reactivity and free radical production capacity in the presence of biological systems.
2010-01
New potent 5-nitroindazole derivatives as inhibitors of Trypanosoma cruzi growth: synthesis, biological evaluation, and mechanism of action studies.
2009-12-15
Nitroindazole compounds inhibit the oxidative activation of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) neurotoxin to neurotoxic pyridinium cations by human monoamine oxidase (MAO).
2009-10
Molecular encapsulation of 5-nitroindazole derivatives in 2,6-dimethyl-beta-cyclodextrin: electrochemical and spectroscopic studies.
2009-07-01
Study of 5-nitroindazoles' anti-Trypanosoma cruzi mode of action: electrochemical behaviour and ESR spectroscopic studies.
2009-04
In vitro and in vivo antitrypanosomatid activity of 5-nitroindazoles.
2009-03
Comparative spectroscopic and electrochemical study of nitroindazoles: 3-alcoxy, 3-hydroxy and 3-oxo derivatives.
2008-08
Characterization, phase-solubility, and molecular modeling of inclusion complex of 5-nitroindazole derivative with cyclodextrins.
2008-05-01
ESR and electrochemical study of 5-nitroindazole derivatives with antiprotozoal activity.
2006-01
Synthesis and biological properties of new 5-nitroindazole derivatives.
2005-05-02
Conformational changes in nitric oxide synthases induced by chlorzoxazone and nitroindazoles: crystallographic and computational analyses of inhibitor potency.
2002-11-26
Patents
Name Type Language
NSC-5032
Preferred Name English
5-NITROINDAZOLE
Systematic Name English
INDAZOLE, 5-NITRO-
Systematic Name English
5-NITRO-1H-INDAZOLE
Systematic Name English
1H-INDAZOLE, 5-NITRO-
Systematic Name English
5-NITRO-1H-BENZOPYRAZOLE
Systematic Name English
NITROINDAZOLE, 5-
Systematic Name English
Code System Code Type Description
ECHA (EC/EINECS)
226-451-5
Created by admin on Mon Mar 31 19:16:09 GMT 2025 , Edited by admin on Mon Mar 31 19:16:09 GMT 2025
PRIMARY
NSC
5032
Created by admin on Mon Mar 31 19:16:09 GMT 2025 , Edited by admin on Mon Mar 31 19:16:09 GMT 2025
PRIMARY
PUBCHEM
21501
Created by admin on Mon Mar 31 19:16:09 GMT 2025 , Edited by admin on Mon Mar 31 19:16:09 GMT 2025
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DRUG BANK
DB04534
Created by admin on Mon Mar 31 19:16:09 GMT 2025 , Edited by admin on Mon Mar 31 19:16:09 GMT 2025
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EPA CompTox
DTXSID5049316
Created by admin on Mon Mar 31 19:16:09 GMT 2025 , Edited by admin on Mon Mar 31 19:16:09 GMT 2025
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FDA UNII
235Y7P37ZD
Created by admin on Mon Mar 31 19:16:09 GMT 2025 , Edited by admin on Mon Mar 31 19:16:09 GMT 2025
PRIMARY
CAS
5401-94-5
Created by admin on Mon Mar 31 19:16:09 GMT 2025 , Edited by admin on Mon Mar 31 19:16:09 GMT 2025
PRIMARY