Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C6H5N3O |
| Molecular Weight | 135.1234 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
ON1N=NC2=C1C=CC=C2
InChI
InChIKey=ASOKPJOREAFHNY-UHFFFAOYSA-N
InChI=1S/C6H5N3O/c10-9-6-4-2-1-3-5(6)7-8-9/h1-4,10H
| Molecular Formula | C6H5N3O |
| Molecular Weight | 135.1234 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Solid phase synthesis of hydrophobic difficult sequence peptides on BDDMA-PS support. | 2001 Dec |
|
| Differential regulation of laccase gene expression in Pleurotus sajor-caju. | 2001 Jul |
|
| Pycnoporus cinnabarinus laccases: an interesting tool for food or non-food applications. | 2003 |
|
| Removal of estrogenic activities of 17beta-estradiol and ethinylestradiol by ligninolytic enzymes from white rot fungi. | 2003 Apr |
|
| Purification, molecular characterization and reactivity with aromatic compounds of a laccase from basidiomycete Trametes sp. strain AH28-2. | 2003 Feb |
|
| On the mechanism of the laccase-mediator system in the oxidation of lignin. | 2003 Nov 7 |
|
| Modification of malachite green by Fomes sclerodermeus and reduction of toxicity to Phanerochaete chrysosporium. | 2004 Feb 16 |
|
| Spectrophotometric, EPR and kinetic characterisation of the >N-O* radical from 1-hydroxybenzotriazole, a key reactive species in mediated enzymatic oxidations. | 2004 Oct 21 |
|
| O-selectivity and utility of phosphorylation mediated by phosphite triester intermediates in the N-unprotected phosphoramidite method. | 2004 Sep 8 |
|
| Fully automated synthesis of (phospho)peptide arrays in microtiter plate wells provides efficient access to protein tyrosine kinase characterization. | 2005 Jan 12 |
|
| Role of 1-hydroxybenzotriazole in oxidation by laccase from Trametes versicolor. Kinetic analysis of the laccase-1-hydroxybenzotriazole couple. | 2006 Dec |
|
| Applicability of Coriolopsis rigida for biodegradation of polycyclic aromatic hydrocarbons. | 2006 Jul |
|
| [Synthesis and immunomodulating activity of new glycopeptides of glycyrrhizic acid containing residues of L-glutamic acid]. | 2006 Nov-Dec |
|
| Heterologous expression of lcc1 gene from Trametes trogii in Pichia pastoris and characterization of the recombinant enzyme. | 2006 Oct 12 |
|
| Transformation of polycyclic aromatic hydrocarbons by laccase is strongly enhanced by phenolic compounds present in soil. | 2007 Apr 15 |
|
| Laccase-catalyzed conversion of natural and synthetic hormones from a municipal wastewater. | 2007 Aug |
|
| O6-(benzotriazol-1-yl)inosine derivatives: easily synthesized, reactive nucleosides. | 2007 Jan 31 |
|
| Design and synthesis of a 3,4-dehydroproline amide discovery library. | 2007 Jul-Aug |
|
| Redox-mediated decolorization of Direct Red 23 and Direct Blue 80 catalyzed by bioaffinity-based immobilized tomato (Lycopersicon esculentum) peroxidase. | 2008 Oct |
|
| Stereochemical preference in the reactions of N-protected L-amino acid 1-hydroxybenzotriazole esters with racemic amino acid derivatives. | 2009 |
|
| Effect of metal ions on reactive dye decolorization by laccase from Ganoderma lucidum. | 2009 Aug 30 |
|
| Steroids linked with amide bond-extended cholesterol. | 2009 Jan |
|
| Human neutrophil elastase responsive delivery from poly(ethylene glycol) hydrogels. | 2009 Jun 8 |
|
| Using both xylanase and laccase enzymes for pulp bleaching. | 2009 Mar |
|
| Decolorization of textile effluent by bitter gourd peroxidase immobilized on concanavalin A layered calcium alginate-starch beads. | 2009 May 30 |
|
| COMU: a safer and more effective replacement for benzotriazole-based uronium coupling reagents. | 2009 Sep 21 |
|
| Oxyma: an efficient additive for peptide synthesis to replace the benzotriazole-based HOBt and HOAt with a lower risk of explosion. | 2009 Sep 21 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 02:08:29 GMT 2023
by
admin
on
Sat Dec 16 02:08:29 GMT 2023
|
| Record UNII |
A2T929DMG4
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
75771
Created by
admin on Sat Dec 16 02:08:29 GMT 2023 , Edited by admin on Sat Dec 16 02:08:29 GMT 2023
|
PRIMARY | |||
|
219-989-7
Created by
admin on Sat Dec 16 02:08:29 GMT 2023 , Edited by admin on Sat Dec 16 02:08:29 GMT 2023
|
PRIMARY | |||
|
1-Hydroxybenzotriazole
Created by
admin on Sat Dec 16 02:08:29 GMT 2023 , Edited by admin on Sat Dec 16 02:08:29 GMT 2023
|
PRIMARY | |||
|
m6121
Created by
admin on Sat Dec 16 02:08:29 GMT 2023 , Edited by admin on Sat Dec 16 02:08:29 GMT 2023
|
PRIMARY | Merck Index | ||
|
C011852
Created by
admin on Sat Dec 16 02:08:29 GMT 2023 , Edited by admin on Sat Dec 16 02:08:29 GMT 2023
|
PRIMARY | |||
|
2592-95-2
Created by
admin on Sat Dec 16 02:08:29 GMT 2023 , Edited by admin on Sat Dec 16 02:08:29 GMT 2023
|
PRIMARY | |||
|
DTXSID3044627
Created by
admin on Sat Dec 16 02:08:29 GMT 2023 , Edited by admin on Sat Dec 16 02:08:29 GMT 2023
|
PRIMARY | |||
|
A2T929DMG4
Created by
admin on Sat Dec 16 02:08:29 GMT 2023 , Edited by admin on Sat Dec 16 02:08:29 GMT 2023
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
SALT/SOLVATE -> PARENT |
|
||
|
SOLVATE->ANHYDROUS |
|
