U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C20H22N2O
Molecular Weight 306.4015
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FENAZAQUIN

SMILES

CC(C)(C)C1=CC=C(CCOC2=NC=NC3=C2C=CC=C3)C=C1

InChI

InChIKey=DMYHGDXADUDKCQ-UHFFFAOYSA-N
InChI=1S/C20H22N2O/c1-20(2,3)16-10-8-15(9-11-16)12-13-23-19-17-6-4-5-7-18(17)21-14-22-19/h4-11,14H,12-13H2,1-3H3

HIDE SMILES / InChI

Molecular Formula C20H22N2O
Molecular Weight 306.4015
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Effect of household processing on fenazaquin residues in okra fruits.
2010-02
Evaluation of the efficacy of Oberon (Spiromesifen), to contain infestations of mites and whiteflies on Capsicum annuum L.
2010
Evaluation of the efficacy and selectivity of Oberon (Spiromesifen) for the control of Tetranychus urticae on strawberry.
2010
Multi-residue analysis of 30 currently used pesticides in fine airborne particulate matter (PM 2.5) by microwave-assisted extraction and liquid chromatography-tandem mass spectrometry.
2009-12-18
Pesticide extraction from table grapes and plums using ionic liquid based dispersive liquid-liquid microextraction.
2009-12
Ionic liquid based dispersive liquid-liquid microextraction for the extraction of pesticides from bananas.
2009-10-23
Antimutagenic and antigenotoxic effects of vegetable matrices on the activity of pesticides.
2009-07
Exposure to pesticides residues from consumption of Italian blood oranges.
2009-07
Resistance mechanisms to mitochondrial electron transport inhibitors in a field-collected strain of Tetranychus urticae Koch (Acari: Tetranychidae).
2009-02
Side-effects of fenazaquin on a cellular model of Paramecium.
2009
Application of hollow fibre liquid phase microextraction for the multiresidue determination of pesticides in alcoholic beverages by ultra-high pressure liquid chromatography coupled to tandem mass spectrometry.
2008-10-24
Efficacy of five selected acaricides against Tetranychus urticae (Acari: Tetranychidae) and their side effects on relevant natural enemies occurring in citrus orchards.
2008-08
Modification and re-validation of the ethyl acetate-based multi-residue method for pesticides in produce.
2007-11
Mechanism of toxicity of pesticides acting at complex I: relevance to environmental etiologies of Parkinson's disease.
2007-03
Multiple resistance and biochemical mechanisms of pyridaben resistance in Tetranychus urticae (Acari: Tetranychidae).
2006-06
Investigation in tea on fate of fenazaquin residue and its transfer in brew.
2006-04
Metabolism of fenazaquin, an acaricide in tea plant.
2005-09
Fenpyroximate resistance in Tetranychus urticae (Acari: Tetranychidae): cross-resistance and biochemical resistance mechanisms.
2004-10
Application of liquid chromatography with electrospray tandem mass spectrometry to the determination of a new generation of pesticides in processed fruits and vegetables.
2004-05-21
Investigation in tea on fate of fenazaquin residue and its transfer in brew.
2004-03
Photodecomposition of an acaricide, fenazaquin, in aqueous alcoholic solution.
2003-07-02
Synthesis and fungicidal activity of a series of novel aryloxylepidines.
2001-09
Incidence and inheritance of resistance to METI-acaricides in European strains of the two-spotted spider mite (Tetranychus urticae) (Acari: Tetranychidae).
2001-05
NADH: ubiquinone oxidoreductase inhibitors block induction of ornithine decarboxylase activity in MCF-7 human breast cancer cells.
1998-11
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 19:16:07 GMT 2025
Edited
by admin
on Mon Mar 31 19:16:07 GMT 2025
Record UNII
DK5Q534WEE
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FENAZAQUIN
ISO   MI  
Common Name English
MAGISTER
Preferred Name English
DE-436
Code English
FENAZAQUIN [ISO]
Common Name English
4-(2-(4-(1,1-DIMETHYLETHYL)PHENYL)ETHOXY)QUINAZOLINE
Systematic Name English
4-(2-(4-(TERT-BUTYL)PHENYL)ETHOXY)QUINAZOLINE
Systematic Name English
4-TERT-BUTYLPHENETHYL QUINAZOLIN-4-YL ETHER
Systematic Name English
EL-436
Code English
FENAZAQUIN [MI]
Common Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 44501
Created by admin on Mon Mar 31 19:16:07 GMT 2025 , Edited by admin on Mon Mar 31 19:16:07 GMT 2025
Code System Code Type Description
CHEBI
38593
Created by admin on Mon Mar 31 19:16:07 GMT 2025 , Edited by admin on Mon Mar 31 19:16:07 GMT 2025
PRIMARY
EPA CompTox
DTXSID4040476
Created by admin on Mon Mar 31 19:16:07 GMT 2025 , Edited by admin on Mon Mar 31 19:16:07 GMT 2025
PRIMARY
FDA UNII
DK5Q534WEE
Created by admin on Mon Mar 31 19:16:07 GMT 2025 , Edited by admin on Mon Mar 31 19:16:07 GMT 2025
PRIMARY
PUBCHEM
86356
Created by admin on Mon Mar 31 19:16:07 GMT 2025 , Edited by admin on Mon Mar 31 19:16:07 GMT 2025
PRIMARY
HSDB
7948
Created by admin on Mon Mar 31 19:16:07 GMT 2025 , Edited by admin on Mon Mar 31 19:16:07 GMT 2025
PRIMARY
ALANWOOD
fenazaquin
Created by admin on Mon Mar 31 19:16:07 GMT 2025 , Edited by admin on Mon Mar 31 19:16:07 GMT 2025
PRIMARY
CAS
120928-09-8
Created by admin on Mon Mar 31 19:16:07 GMT 2025 , Edited by admin on Mon Mar 31 19:16:07 GMT 2025
PRIMARY
MESH
C087876
Created by admin on Mon Mar 31 19:16:07 GMT 2025 , Edited by admin on Mon Mar 31 19:16:07 GMT 2025
PRIMARY
MERCK INDEX
m5263
Created by admin on Mon Mar 31 19:16:07 GMT 2025 , Edited by admin on Mon Mar 31 19:16:07 GMT 2025
PRIMARY Merck Index