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

Details

Stereochemistry ACHIRAL
Molecular Formula C24H30N2O3
Molecular Weight 394.5066
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CHROMAFENOZIDE

SMILES

CC1=CC(=CC(C)=C1)C(=O)N(NC(=O)C2=C(C)C3=C(OCCC3)C=C2)C(C)(C)C

InChI

InChIKey=HPNSNYBUADCFDR-UHFFFAOYSA-N
InChI=1S/C24H30N2O3/c1-15-12-16(2)14-18(13-15)23(28)26(24(4,5)6)25-22(27)20-9-10-21-19(17(20)3)8-7-11-29-21/h9-10,12-14H,7-8,11H2,1-6H3,(H,25,27)

HIDE SMILES / InChI

Molecular Formula C24H30N2O3
Molecular Weight 394.5066
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Potent and selective partial ecdysone agonist activity of chromafenozide in Sf9 cells.
2002 Apr 12
Binding mode of ecdysone agonists to the receptor: comparative modeling and docking studies.
2003 Feb
Synthesis and insecticidal activity of benzoheterocyclic analogues of N'-benzoyl-N-(tert-butyl)benzohydrazide: Part 3. Modification of N-tert-butylhydrazine moiety.
2003 Jan
Classical and three-dimensional QSAR for the inhibition of [3H]ponasterone A binding by diacylhydrazine-type ecdysone agonists to insect Sf-9 cells.
2005 Feb 15
Towards Coleoptera-specific high-throughput screening systems for compounds with ecdysone activity: development of EcR reporter assays using weevil (Anthonomus grandis)-derived cell lines and in silico analysis of ligand binding to A. grandis EcR ligand-binding pocket.
2009 Aug
N'-Benzoyl-N-tert-butyl-2-chloro-N'-{[3-(6-chloro-3-pyrid-ylmethyl)-2-nitrimino-imidazolidin-1-yl]sulfan-yl}benzo-hydrazide.
2009 Aug 12
Acute human lethal toxicity of agricultural pesticides: a prospective cohort study.
2010 Oct 26
[Determination of five diacylhydrazine insecticide residues in welsh onion using high performance liquid chromatography-tandem mass spectrometry].
2010 Sep
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 19:51:53 GMT 2023
Edited
by admin
on Fri Dec 15 19:51:53 GMT 2023
Record UNII
2ODM465D5M
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CHROMAFENOZIDE
ISO   MI  
Common Name English
ANS-118
Common Name English
CHROMAFENOZIDE [MI]
Common Name English
MATRIC
Common Name English
3,4-DIHYDRO-5-METHYL-2H-1-BENZOPYRAN-6-CARBOXYLIC ACID 2-(3,5-DIMETHYLBENZOYL)-2-(1,1-DIMETHYLETHYL)HYDRAZIDE
Common Name English
CHROMAFENOZIDE [ISO]
Common Name English
Code System Code Type Description
CAS
143807-66-3
Created by admin on Fri Dec 15 19:51:53 GMT 2023 , Edited by admin on Fri Dec 15 19:51:53 GMT 2023
PRIMARY
EPA CompTox
DTXSID4057976
Created by admin on Fri Dec 15 19:51:53 GMT 2023 , Edited by admin on Fri Dec 15 19:51:53 GMT 2023
PRIMARY
PUBCHEM
10157484
Created by admin on Fri Dec 15 19:51:53 GMT 2023 , Edited by admin on Fri Dec 15 19:51:53 GMT 2023
PRIMARY
ALANWOOD
chromafenozide
Created by admin on Fri Dec 15 19:51:53 GMT 2023 , Edited by admin on Fri Dec 15 19:51:53 GMT 2023
PRIMARY
CHEBI
38450
Created by admin on Fri Dec 15 19:51:53 GMT 2023 , Edited by admin on Fri Dec 15 19:51:53 GMT 2023
PRIMARY
MERCK INDEX
m3493
Created by admin on Fri Dec 15 19:51:53 GMT 2023 , Edited by admin on Fri Dec 15 19:51:53 GMT 2023
PRIMARY Merck Index
FDA UNII
2ODM465D5M
Created by admin on Fri Dec 15 19:51:53 GMT 2023 , Edited by admin on Fri Dec 15 19:51:53 GMT 2023
PRIMARY
MESH
C454111
Created by admin on Fri Dec 15 19:51:53 GMT 2023 , Edited by admin on Fri Dec 15 19:51:53 GMT 2023
PRIMARY