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Details

Stereochemistry ACHIRAL
Molecular Formula C8H6N2O2
Molecular Weight 162.1454
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 5-NITROINDOLE

SMILES

[O-][N+](=O)C1=CC=C2NC=CC2=C1

InChI

InChIKey=OZFPSOBLQZPIAV-UHFFFAOYSA-N
InChI=1S/C8H6N2O2/c11-10(12)7-1-2-8-6(5-7)3-4-9-8/h1-5,9H

HIDE SMILES / InChI

Molecular Formula C8H6N2O2
Molecular Weight 162.1454
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
An efficient conversion of 5-nitroisatin into 5-nitroindole derivative.
2001 Mar 26
[Enhancing the stability of oligonucleotide duplexes. The effect of adding 1-(2'-deoxy-beta-d-ribofuranosyl)-5-nitroindole].
2002 Jan-Feb
Method for detection of single-base mismatches using bimolecular beacons.
2002 Mar 20
Facile polymerization of dNTPs bearing unnatural base analogues by DNA polymerase alpha and Klenow fragment (DNA polymerase I).
2003 Sep 9
Generic expansion of the substrate spectrum of a DNA polymerase by directed evolution.
2004 Jun
Novel anellated pyrazoloquinolin-3-ones: synthesis and in vitro BZR activity.
2005 May 16
Large fragment Bst DNA polymerase for whole genome amplification of DNA from formalin-fixed paraffin-embedded tissues.
2006 Dec 12
1H NMR spectral studies on the polymerization mechanism of indole and its derivatives.
2006 Mar 1
Solution structure and dynamics of DNA duplexes containing the universal base analogues 5-nitroindole and 5-nitroindole 3-carboxamide.
2007
Synthesis of a universal 5-nitroindole ribonucleotide and incorporation into RNA by a viral RNA-dependent RNA polymerase.
2007 Aug 13
Analysis of multiple single nucleotide polymorphisms closely positioned in the ovine PRNP gene using linear fluorescent probes and melting curve analysis.
2007 Aug 3
[Spectral analysis of the effect of different polymerization potential on electrosynthesized poly (5-nitroindole) films].
2007 Jun
Thiazole orange and Cy3: improvement of fluorescent DNA probes with use of short range electron transfer.
2008 Jun 6
[Oligodeoxynucleotides containing substituted 4-nitroindoles: synthesis and study of their DNA duplexes].
2008 Mar-Apr
Primer fabrication using polymerase mediated oligonucleotide synthesis.
2009 Jul 31
Potential benefits of sequential inhibitor-mutagen treatments of RNA virus infections.
2009 Nov
Evolving a polymerase for hydrophobic base analogues.
2009 Oct 21
Replication of a universal nucleobase provides unique insight into the role of entropy during DNA polymerization and pyrophosphorolysis.
2010 Apr 13
Template-directed ligation of tethered mononucleotides by t4 DNA ligase for kinase ribozyme selection.
2010 Aug 24
A multi-step process of viral adaptation to a mutagenic nucleoside analogue by modulation of transition types leads to extinction-escape.
2010 Aug 26
Cationic nucleoside lipids derived from universal bases: A rational approach for siRNA transfection.
2010 Jun 16
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 18:35:48 GMT 2023
Edited
by admin
on Fri Dec 15 18:35:48 GMT 2023
Record UNII
O2BHX6EDBN
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
5-NITROINDOLE
Systematic Name English
5-NITRO-1H-INDOLE
Systematic Name English
NITROINDOLE, 5-
Systematic Name English
NSC-520594
Code English
INDOLE, 5-NITRO-
Systematic Name English
1H-INDOLE, 5-NITRO-
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID80210403
Created by admin on Fri Dec 15 18:35:48 GMT 2023 , Edited by admin on Fri Dec 15 18:35:48 GMT 2023
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FDA UNII
O2BHX6EDBN
Created by admin on Fri Dec 15 18:35:48 GMT 2023 , Edited by admin on Fri Dec 15 18:35:48 GMT 2023
PRIMARY
CAS
6146-52-7
Created by admin on Fri Dec 15 18:35:48 GMT 2023 , Edited by admin on Fri Dec 15 18:35:48 GMT 2023
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PUBCHEM
22523
Created by admin on Fri Dec 15 18:35:48 GMT 2023 , Edited by admin on Fri Dec 15 18:35:48 GMT 2023
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NSC
520594
Created by admin on Fri Dec 15 18:35:48 GMT 2023 , Edited by admin on Fri Dec 15 18:35:48 GMT 2023
PRIMARY
ECHA (EC/EINECS)
228-153-0
Created by admin on Fri Dec 15 18:35:48 GMT 2023 , Edited by admin on Fri Dec 15 18:35:48 GMT 2023
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