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Details

Stereochemistry ACHIRAL
Molecular Formula C14H18N4O4S2
Molecular Weight 370.447
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of THIOPHANATE

SMILES

CCOC(=O)NC(=S)NC1=C(NC(=S)NC(=O)OCC)C=CC=C1

InChI

InChIKey=YFNCATAIYKQPOO-UHFFFAOYSA-N
InChI=1S/C14H18N4O4S2/c1-3-21-13(19)17-11(23)15-9-7-5-6-8-10(9)16-12(24)18-14(20)22-4-2/h5-8H,3-4H2,1-2H3,(H2,15,17,19,23)(H2,16,18,20,24)

HIDE SMILES / InChI
Molecular Formula C14H18N4O4S2
Molecular Weight 370.447
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Unknown
139594
PubMed

PubMed

TitleDatePubMed
[Effects of Atractylodes macrocephala seeds coated with SCF on field diseases].
2002 Apr
On-line automated sample preparation for liquid chromatography using parallel supported liquid membrane extraction and microporous membrane liquid-liquid extraction.
2002 Oct 25
Effect of thiophanate-methyl on the reproduction and survival of the freshwater rotifer Brachionus calyciflorus Pallas.
2003 Oct
Histological and histomorphometric alterations in thyroid and adrenals of CD rat pups exposed in utero to methyl thiophanate.
2003 Sep-Oct
Re-identification and characterization of pathogens causing ugurassa (Flacourtia inermis) fruit anthracnose.
2004 Jan
A simple and rapid spectrophotometric method for determination of thiophanate-methyl in commercial formulations and its residues in foodstuffs.
2004 Jul-Aug
Effects of thiophanate-methyl and glyphosate on asexual and sexual reproduction in the rotifer Brachionus calyciflorus Pallas.
2004 Oct
[Determination of thiophanate-methyl residue in peppers by solid phase extraction-HPLC].
2005 May
Controlling fungal contamination in Chlamydomonas reinhardtii cultures.
2005 Oct
Neprilysin participates in skeletal muscle regeneration and is accumulated in abnormal muscle fibres of inclusion body myositis.
2006 Feb
The newt Triturus carnifex as a model for monitoring the ecotoxic impact of the fungicide thiophanate methyl: adverse effects on the adrenal gland.
2006 May
PPARalpha mediates the effects of the pesticide methyl thiophanate on liver of the lizard Podarcis sicula.
2007 Apr
Determination of thiophanate methyl and carbendazim residues in vegetable samples using microwave-assisted extraction.
2007 May 4
Morphological and functional changes in the thyroid gland of methyl thiophanate-injected lizards, Podarcis sicula.
2008 Aug
Rapid development of fungicide resistance by Sclerotinia homoeocarpa on turfgrass.
2008 Dec
Molecular characterization of benzimidazole-resistant isolates of Cladosporium fulvum.
2008 Jan
Assessment of methyl thiophanate-Cu (II) induced DNA damage in human lymphocytes.
2009 Aug
Determination of multi-class pesticides in wines by solid-phase extraction and liquid chromatography-tandem mass spectrometry.
2009 Jul 31
Flower-inhabiting Frankliniella Thrips (Thysanoptera: Thripidae), pesticides, and Fusarium hardlock in cotton.
2009 Jun
In vitro study on the interaction between thiophanate methyl and human serum albumin.
2009 Mar 3
Genotoxic fungicide methyl thiophanate as an oxidative stressor inducing 8-oxo-7,8-dihydro-2' -deoxyguanosine adducts in DNA and mutagenesis.
2010 Jan
Methyl thiophanate as a DNA minor groove binder produces MT-Cu(II)-DNA ternary complex preferably with AT rich region for initiation of DNA damage.
2010 Jul 1
Fungicide methyl thiophanate binding at sub-domain IIA of human serum albumin triggers conformational change and protein damage.
2010 Jul 1
High levels of miticides and agrochemicals in North American apiaries: implications for honey bee health.
2010 Mar 19
Dissipation study of thiophanate methyl residue in/on grapes (Vitis vinifera L.) in India.
2010 May
Identifying pesticide use patterns among flower growers to assess occupational exposure to mixtures.
2010 May
Acute human lethal toxicity of agricultural pesticides: a prospective cohort study.
2010 Oct 26
Patents

Patents

JP2000356603A
1
JP2001084954A
1
JP2001183293A
1
JP2003014894A
1
JP2005030908A
1
JP2005537627A
1
JP2006525250A
40
JP2007527852A
15
JP2008509189A
188
JP2010096559A
1
JP2011509959A
61
JP2011509971A
151
JP2582885B2
6
JP4651384B2
1
JP4657199B2
31
JP4711974B2
3
JP4728220B2
15
JPH00558820A
1
JPH00564580A
1
JPH01209343A
1
JPH0197842A
1
JPH02147843A
1
JPH02176447A
1
JPH02226049A
1
JPH03255337A
1
JPH03255359A
1
JPH0326942A
1
JPH04131747A
1
JPH04131748A
1
JPH04292844A
1
JPH05148109A
2
JPH05155706A
2
JPH05218164A
1
JPH0558820A
1
JPH0564580A
1
JPH0644554A
1
JPH0694607A
1
JPH0694612A
1
JPH0694618A
1
JPH07277909A
2
JPH07316004A
1
JPH08101121A
1
JPH08145880A
1
JPH0961357A
1
JPH0996607A
1
JPH10109909A
1
JPH10160667A
1
JPH10267845A
1
JPH1030984A
1
JPS05942308A
1
JPS05973506A
1
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:47:22 GMT 2023
Edited
by admin
on Fri Dec 15 15:47:22 GMT 2023
Record UNII
5Q0Y96D5I8
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
THIOPHANATE
HSDB   ISO   MART.   MI  
Common Name English
THIOPHANATE [MI]
Common Name English
DIETHYL 4,4'-(O-PHENYLENE)BIS(3-THIOALLOPHANATE)
Common Name English
THIOPHANATE [MART.]
Common Name English
DIETHYL N,N'-(1,2-PHENYLENEBIS(IMINOCARBONOTHIOYL))BIS(CARBAMATE)
Systematic Name English
NSC-170810
Code English
THIOPHANATE [ISO]
Common Name English
THIOPHANATE [HSDB]
Common Name English
Classification Tree Code System Code
WHO-VATC QP52AC04
Created by admin on Fri Dec 15 15:47:22 GMT 2023 , Edited by admin on Fri Dec 15 15:47:22 GMT 2023
EPA PESTICIDE CODE 103401
Created by admin on Fri Dec 15 15:47:22 GMT 2023 , Edited by admin on Fri Dec 15 15:47:22 GMT 2023
NCI_THESAURUS C737
Created by admin on Fri Dec 15 15:47:22 GMT 2023 , Edited by admin on Fri Dec 15 15:47:22 GMT 2023
Code System Code Type Description
MERCK INDEX
m10775
Created by admin on Fri Dec 15 15:47:22 GMT 2023 , Edited by admin on Fri Dec 15 15:47:22 GMT 2023
PRIMARY Merck Index
NCI_THESAURUS
C76880
Created by admin on Fri Dec 15 15:47:22 GMT 2023 , Edited by admin on Fri Dec 15 15:47:22 GMT 2023
PRIMARY
MESH
D013875
Created by admin on Fri Dec 15 15:47:22 GMT 2023 , Edited by admin on Fri Dec 15 15:47:22 GMT 2023
PRIMARY
NSC
170810
Created by admin on Fri Dec 15 15:47:22 GMT 2023 , Edited by admin on Fri Dec 15 15:47:22 GMT 2023
PRIMARY
FDA UNII
5Q0Y96D5I8
Created by admin on Fri Dec 15 15:47:22 GMT 2023 , Edited by admin on Fri Dec 15 15:47:22 GMT 2023
PRIMARY
EPA CompTox
DTXSID3034531
Created by admin on Fri Dec 15 15:47:22 GMT 2023 , Edited by admin on Fri Dec 15 15:47:22 GMT 2023
PRIMARY
ChEMBL
CHEMBL2103777
Created by admin on Fri Dec 15 15:47:22 GMT 2023 , Edited by admin on Fri Dec 15 15:47:22 GMT 2023
PRIMARY
CHEBI
82060
Created by admin on Fri Dec 15 15:47:22 GMT 2023 , Edited by admin on Fri Dec 15 15:47:22 GMT 2023
PRIMARY
ECHA (EC/EINECS)
245-741-2
Created by admin on Fri Dec 15 15:47:22 GMT 2023 , Edited by admin on Fri Dec 15 15:47:22 GMT 2023
PRIMARY
CAS
23564-06-9
Created by admin on Fri Dec 15 15:47:22 GMT 2023 , Edited by admin on Fri Dec 15 15:47:22 GMT 2023
PRIMARY
ALANWOOD
thiophanate
Created by admin on Fri Dec 15 15:47:22 GMT 2023 , Edited by admin on Fri Dec 15 15:47:22 GMT 2023
PRIMARY
SMS_ID
300000029425
Created by admin on Fri Dec 15 15:47:22 GMT 2023 , Edited by admin on Fri Dec 15 15:47:22 GMT 2023
PRIMARY
PUBCHEM
3032792
Created by admin on Fri Dec 15 15:47:22 GMT 2023 , Edited by admin on Fri Dec 15 15:47:22 GMT 2023
PRIMARY
HSDB
6938
Created by admin on Fri Dec 15 15:47:22 GMT 2023 , Edited by admin on Fri Dec 15 15:47:22 GMT 2023
PRIMARY
NIH
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