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Details

Stereochemistry ACHIRAL
Molecular Formula C10H11N3OS
Molecular Weight 221.279
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of METHABENZTHIAZURON

SMILES

CNC(=O)N(C)C1=NC2=C(S1)C=CC=C2

InChI

InChIKey=RRVIAQKBTUQODI-UHFFFAOYSA-N
InChI=1S/C10H11N3OS/c1-11-9(14)13(2)10-12-7-5-3-4-6-8(7)15-10/h3-6H,1-2H3,(H,11,14)

HIDE SMILES / InChI

Molecular Formula C10H11N3OS
Molecular Weight 221.279
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Fate of two herbicides in zero-tension lysimeters and in field soil.
2010-09-14
Rate of loss of simazine, terbuthylazine, isoproturon, and methabenzthiazuron during soil solarization.
2009-07-22
Multiresidue analysis of pesticides with hydrolyzable functionality in cooked vegetables by liquid chromatography tandem mass spectrometry.
2009-07
Simultaneous determination of ethidimuron, methabenzthiazuron, and their two major degradation products in soil.
2006-10-04
[Effect of adenovirus-mediated mutant exogenous P27kip1 gene expression on the chemosensitivities of cholangiocarcinoma cell line].
2006-10-01
Inhibitory effect of caffeic acid phenethyl ester on the growth of SW480 colorectal tumor cells involves beta-catenin associated signaling pathway down-regulation.
2006-08-21
Toxicity assessment of 40 herbicides to the green alga Raphidocelis subcapitata.
2006-03
[Effects of cyclooxygenase-2 antisense vector on proliferation and sensitivity to cisplatin of H1299 cells].
2005-10-20
Phototransformation of methabenthiazuron in the presence of nitrate and nitrite ions.
2005-09
Effect of caffeic acid phenethyl ester on proliferation and apoptosis of colorectal cancer cells in vitro.
2005-07-14
Celecoxib inhibits proliferation and induces apoptosis via cyclooxygenase-2 pathway in human pancreatic carcinoma cells.
2005
Effects of cyclooxygenase-2 antisense vector on proliferation of human cholangiocarcinoma cells.
2004-06
Microwave-assisted solvent extraction of the herbicide methabenzthiazuron from soils and some soil natural organic and inorganic constituents. Influence of environmental factors on its extractability.
2003-12
Sequential bio- and phototransformation of the herbicide methabenzthiazuron in water.
2003-09
Celecoxib inhibits proliferation and induces apoptosis via prostaglandin E2 pathway in human cholangiocarcinoma cell lines.
2003-06
Bile from a patient with anomalous pancreaticobiliary ductal union promotes the proliferation of human cholangiocarcinoma cells via COX-2 pathway.
2003-05
[The regulatory effect of human bone morphogenetic protein 7 gene transfer on the proliferation and differentiation of rabbit bone marrow mesenchymal stem cells].
2003-02
Proliferative activity of bile from congenital choledochal cyst patients.
2003-01
Overexpression of bcl-2 protects hepatoma cell line HCC-9204 from ethanol-induced apoptosis.
2002-01
Adsorption of methabenzthiazuron on six allophanic and nonallophanic soils: effect of organic matter amendment.
2001-01
The w/w+ SMART is a useful tool for the evaluation of pesticides.
1994-07
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:53:05 GMT 2025
Edited
by admin
on Mon Mar 31 18:53:05 GMT 2025
Record UNII
82NPF43P0X
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
METHABENZTHIAZURON
ISO   MI  
Common Name English
TRIBUNIL
Preferred Name English
BAYER 5633
Code English
TRIBUNIL (BAYER)
Brand Name English
BAYER 74283
Code English
MBU
Common Name English
N-2-BENZOTHIAZOLYL-N,N'-DIMETHYLUREA
Systematic Name English
1-(2-BENZOTHIAZOLYL)-1,3-DIMETHYLUREA
Systematic Name English
METABENZTHIAZURON
Common Name English
1-(1,3-BENZOTHIAZOL-2-YL)-1,3-DIMETHYLUREA
Systematic Name English
METHABENZTHIAZURON [MI]
Common Name English
METHABENZTHIAZURON [ISO]
Common Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 281300
Created by admin on Mon Mar 31 18:53:05 GMT 2025 , Edited by admin on Mon Mar 31 18:53:05 GMT 2025
Code System Code Type Description
MERCK INDEX
m7281
Created by admin on Mon Mar 31 18:53:05 GMT 2025 , Edited by admin on Mon Mar 31 18:53:05 GMT 2025
PRIMARY Merck Index
PUBCHEM
29216
Created by admin on Mon Mar 31 18:53:05 GMT 2025 , Edited by admin on Mon Mar 31 18:53:05 GMT 2025
PRIMARY
EPA CompTox
DTXSID0037570
Created by admin on Mon Mar 31 18:53:05 GMT 2025 , Edited by admin on Mon Mar 31 18:53:05 GMT 2025
PRIMARY
ALANWOOD
methabenzthiazuron
Created by admin on Mon Mar 31 18:53:05 GMT 2025 , Edited by admin on Mon Mar 31 18:53:05 GMT 2025
PRIMARY
FDA UNII
82NPF43P0X
Created by admin on Mon Mar 31 18:53:05 GMT 2025 , Edited by admin on Mon Mar 31 18:53:05 GMT 2025
PRIMARY
ECHA (EC/EINECS)
242-505-0
Created by admin on Mon Mar 31 18:53:05 GMT 2025 , Edited by admin on Mon Mar 31 18:53:05 GMT 2025
PRIMARY
CAS
18691-97-9
Created by admin on Mon Mar 31 18:53:05 GMT 2025 , Edited by admin on Mon Mar 31 18:53:05 GMT 2025
PRIMARY