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Details

Stereochemistry ACHIRAL
Molecular Formula C12H13NO2S
Molecular Weight 235.302
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CARBOXIN

SMILES

CC1=C(SCCO1)C(=O)NC2=CC=CC=C2

InChI

InChIKey=GYSSRZJIHXQEHQ-UHFFFAOYSA-N
InChI=1S/C12H13NO2S/c1-9-11(16-8-7-15-9)12(14)13-10-5-3-2-4-6-10/h2-6H,7-8H2,1H3,(H,13,14)

HIDE SMILES / InChI

Molecular Formula C12H13NO2S
Molecular Weight 235.302
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Oxathiin carboxanilide, a potent inhibitor of human immunodeficiency virus reproduction.
1991 Aug 1
Differences in the microflora of scarified and unscarified seeds of Karwinskia humboldtiana (Rhamnaceae).
2001
The carboxin-binding site on Paracoccus denitrificans succinate:quinone reductase identified by mutations.
2001 Apr
Photochemical behaviour of the systemic fungicide carboxin.
2002
[Inhibitors of complex I and II of the mitochondrial respiratory chain].
2002 Apr
Integration of the gene for carboxin resistance does not impact the Ustilago maydis-maize interaction.
2002 Jan
Succinate:quinone oxidoreductase in the bacteria Paracoccus denitrificans and Bacillus subtilis.
2002 Jan 17
Segmental analysis of molecular surface electrostatic potentials: application to enzyme inhibition.
2003 Apr
Construction of a homologous selectable marker gene for Lentinula edodes transformation.
2003 Sep
Stimulation by surangin B of endogenous amino acid release from synaptosomes.
2003 Sep 15
Flutolanil and carboxin resistance in Coprinus cinereus conferred by a mutation in the cytochrome b560 subunit of succinate dehydrogenase complex (Complex II).
2004 Oct
Evaluation of solid-phase extraction and stir-bar sorptive extraction for the determination of fungicide residues at low-microg kg(-1) levels in grapes by liquid chromatography-mass spectrometry.
2004 Oct 1
Phototransformation of carboxin in water. Toxicity of the pesticide and its sulfoxide to aquatic organisms.
2004 Oct 6
Biological protection of the main cereals against fungal specific diseases.
2005
Antifungal synergistic effect of scopoletin, a hydroxycoumarin isolated from Melia azedarach L. fruits.
2005 Apr 20
Evaluation of Several Approaches to Manage Meloidogyne incognita and Cotton Seedling Disease Complexes in the High Plains of Texas.
2005 Mar
Effect of fungicide seed treatments on N2-fixation and nodulation in pea, Pisum sativum L.
2006 Dec
Targeting antioxidative signal transduction and stress response system: control of pathogenic Aspergillus with phenolics that inhibit mitochondrial function.
2006 Jul
Molecular breeding of white rot fungus Pleurotus ostreatus by homologous expression of its versatile peroxidase MnP2.
2006 Jun
Transformation of Mucor circinelloides with autoreplicative vectors containing homologous and heterologous ARS elements and the dominant Cbx(r) carboxine-resistance gene.
2006 Mar
3-nitropropionic acid is a suicide inhibitor of mitochondrial respiration that, upon oxidation by complex II, forms a covalent adduct with a catalytic base arginine in the active site of the enzyme.
2006 Mar 3
Controlling food-contaminating fungi by targeting their antioxidative stress-response system with natural phenolic compounds.
2006 May
The effect of Pythium oligandrum and chitosan used in control of potato against late blight and the occurrence of fungal diseases on tuber peel.
2007
Soil bioassay for studying behavioral responses of wireworms (Coleoptera: Elateridae) to insecticide-treated wheat seed.
2007 Dec
Fungicide seed treatment efficacy against Microdochium nivale and M. majus in vitro and in vivo.
2008 Aug
Characterization of mutations in the iron-sulphur subunit of succinate dehydrogenase correlating with Boscalid resistance in Alternaria alternata from California pistachio.
2008 Jun
The dominant Hc.Sdh (R) carboxin-resistance gene of the ectomycorrhizal fungus Hebeloma cylindrosporum as a selectable marker for transformation.
2009 Apr
Why hypothetical protein KPN00728 of Klebsiella pneumoniae should be classified as chain C of succinate dehydrogenase?
2009 Dec
Pep1, a secreted effector protein of Ustilago maydis, is required for successful invasion of plant cells.
2009 Feb
Identification of three mutant loci conferring carboxin-resistance and development of a novel transformation system in Aspergillus oryzae.
2009 Jan
Transformation of an oleaginous zygomycete Mortierella alpina 1S-4 with the carboxin resistance gene conferred by mutation of the iron-sulfur subunit of succinate dehydrogenase.
2009 Jun
Quantifiable downregulation of endogenous genes in Agaricus bisporus mediated by expression of RNA hairpins.
2009 Mar
Investigating dominant selection markers for Coprinopsis cinerea: a carboxin resistance system and re-evaluation of hygromycin and phleomycin resistance vectors.
2009 Oct
Structure of Escherichia coli succinate:quinone oxidoreductase with an occupied and empty quinone-binding site.
2009 Oct 23
Toxicity of fungicides to natural bacterial communities in wetland water and sediment measured using leucine incorporation and potential denitrification.
2010 Feb
Activation of the cell wall integrity pathway promotes escape from G2 in the fungus Ustilago maydis.
2010 Jul 1
Fenretinide induces mitochondrial ROS and inhibits the mitochondrial respiratory chain in neuroblastoma.
2010 Mar
Investigating Agrobacterium-mediated transformation of Verticillium albo-atrum on plant surfaces.
2010 Oct 27
New capabilities for Mycosphaerella graminicola research.
2010 Sep
2-Methyl-4,4-dioxo-N-phenyl-5,6-di-hydro-1,4-oxathiine-3-carboxamide (Oxycarboxin).
2010 Sep 30
Environmental impact on vascular development predicted by high-throughput screening.
2011 Nov
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:05:35 GMT 2023
Edited
by admin
on Fri Dec 15 15:05:35 GMT 2023
Record UNII
5A8K850HDE
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CARBOXIN
HSDB   ISO   MI  
Common Name English
DCMO
Common Name English
VITAVAX
Brand Name English
CARBOXIN [HSDB]
Common Name English
CARBOXIN [ISO]
Common Name English
CARBATHIIN
Systematic Name English
NSC-263492
Code English
5,6-DIHYDRO-2-METHYL-N-PHENYL-1,4-OXATHIIN-3-CARBOXAMIDE
Systematic Name English
2,3-DIHYDRO-5-CARBOXANILIDO-6-METHYL-1,4-OXATHIIN
Common Name English
CARBOXIN [MI]
Common Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 90201
Created by admin on Fri Dec 15 15:05:35 GMT 2023 , Edited by admin on Fri Dec 15 15:05:35 GMT 2023
Code System Code Type Description
FDA UNII
5A8K850HDE
Created by admin on Fri Dec 15 15:05:35 GMT 2023 , Edited by admin on Fri Dec 15 15:05:35 GMT 2023
PRIMARY
CHEBI
3405
Created by admin on Fri Dec 15 15:05:35 GMT 2023 , Edited by admin on Fri Dec 15 15:05:35 GMT 2023
PRIMARY
MERCK INDEX
m3098
Created by admin on Fri Dec 15 15:05:35 GMT 2023 , Edited by admin on Fri Dec 15 15:05:35 GMT 2023
PRIMARY Merck Index
PUBCHEM
21307
Created by admin on Fri Dec 15 15:05:35 GMT 2023 , Edited by admin on Fri Dec 15 15:05:35 GMT 2023
PRIMARY
ECHA (EC/EINECS)
226-031-1
Created by admin on Fri Dec 15 15:05:35 GMT 2023 , Edited by admin on Fri Dec 15 15:05:35 GMT 2023
PRIMARY
EPA CompTox
DTXSID0023951
Created by admin on Fri Dec 15 15:05:35 GMT 2023 , Edited by admin on Fri Dec 15 15:05:35 GMT 2023
PRIMARY
ALANWOOD
carboxin
Created by admin on Fri Dec 15 15:05:35 GMT 2023 , Edited by admin on Fri Dec 15 15:05:35 GMT 2023
PRIMARY
NSC
263492
Created by admin on Fri Dec 15 15:05:35 GMT 2023 , Edited by admin on Fri Dec 15 15:05:35 GMT 2023
PRIMARY
CAS
5234-68-4
Created by admin on Fri Dec 15 15:05:35 GMT 2023 , Edited by admin on Fri Dec 15 15:05:35 GMT 2023
PRIMARY
HSDB
1532
Created by admin on Fri Dec 15 15:05:35 GMT 2023 , Edited by admin on Fri Dec 15 15:05:35 GMT 2023
PRIMARY
DRUG BANK
DB04657
Created by admin on Fri Dec 15 15:05:35 GMT 2023 , Edited by admin on Fri Dec 15 15:05:35 GMT 2023
PRIMARY