methiocarb

Synonyms: "mercaptodimethur", "metmercapturon", "methiocarbe", "grandslam", "lizetan", "mesurol", "certan", "draza", "mesurol phenol"

Source: methiocarb is an n-methyl carbamate pesticide. It is used as a bird repellent, insecticide, acaricide and molluscicide.

Identifiers:

IUPAC Name: (3,5-dimethyl-4-methylsulfanylphenyl) N-methylcarbamate
CAS Number: 2032-65-7
PubChem ID: 16248
InChiKey: YFBPRJGDJKVWAH-UHFFFAOYSA-N
Canonical SMILES: CC1=CC(=CC(=C1SC)C)OC(=O)NC

Structural Properties:

Molecular Formula: C11H15NO2S
Molecular Weight: 225,307

Pharmacophore Features:

Number of bond donors: 1
Number of bond acceptors: 1
Number of atoms different from hydrogen: 15

Downloads

2D structure (.sdf)
3D structure (.sdf)
3D structure (.mol2)
3D structure (.pdb)
3D structure (.pdbqt)

Search Similar molecules

Similarity from: % to %

Toxicological Information

ACToR (Aggregated Computational Toxicology Resource)

HSDB (Hazardous Substances Data Bank)

CTD (Comparative Toxicogenomics Database)

Evidence Supporting This Chemical as an Endocrine Disruptor
TEDX List of Potential Endocrine Disruptors


Casale GP, Vennerstrom JL, Bavari S, Wang T. 1993. Inhibition of interleukin 2 driven proliferation of mouse CTLL2 cells, by selected carbamate and organophosphate insecticides and congeners of carbaryl. Immunopharmacology & Immunotoxicology 15(2 & 3):199-215.
Kojima H, Katsura E, Takeuchi S, Niiyama K, Kobayashi K. 2004. Screening for estrogen and androgen receptor activities in 200 pesticides by in vitro reporter gene assays using Chinese hamster ovary cells. Environ Health Perspect 112(5):524-531.

External Links

Keywords


2D-structure

3D-structure

Jmol viewer