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
SMILES
CC1=CC(=CC(C)=C1)C(=O)N(NC(=O)C2=CC=C3OCCCC3=C2C)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)
| 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
| Title | Date | PubMed |
|---|---|---|
| Acute human lethal toxicity of agricultural pesticides: a prospective cohort study. | 2010-10-26 |
|
| [Determination of five diacylhydrazine insecticide residues in welsh onion using high performance liquid chromatography-tandem mass spectrometry]. | 2010-09 |
|
| N'-Benzoyl-N-tert-butyl-2-chloro-N'-{[3-(6-chloro-3-pyrid-ylmethyl)-2-nitrimino-imidazolidin-1-yl]sulfan-yl}benzo-hydrazide. | 2009-08-12 |
|
| 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. | 2009-08 |
|
| QSAR and mode of action studies of insecticidal ecdysone agonists. | 2007-03-17 |
|
| Classical and three-dimensional QSAR for the inhibition of [3H]ponasterone A binding by diacylhydrazine-type ecdysone agonists to insect Sf-9 cells. | 2005-02-15 |
|
| Nonsteroidal ecdysone agonists. | 2005 |
|
| Binding mode of ecdysone agonists to the receptor: comparative modeling and docking studies. | 2003-02 |
|
| Synthesis and insecticidal activity of benzoheterocyclic analogues of N'-benzoyl-N-(tert-butyl)benzohydrazide: Part 3. Modification of N-tert-butylhydrazine moiety. | 2003-01 |
|
| Synthesis and insecticidal activity of benzoheterocyclic analogues of N'-benzoyl-N-(tert-butyl)benzohydrazide: Part 2. Introduction of substituents on the benzene rings of the benzoheterocycle moiety. | 2003-01 |
|
| Potent and selective partial ecdysone agonist activity of chromafenozide in Sf9 cells. | 2002-04-12 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:59:24 GMT 2025
by
admin
on
Mon Mar 31 19:59:24 GMT 2025
|
| Record UNII |
2ODM465D5M
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Preferred Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
143807-66-3
Created by
admin on Mon Mar 31 19:59:24 GMT 2025 , Edited by admin on Mon Mar 31 19:59:24 GMT 2025
|
PRIMARY | |||
|
DTXSID4057976
Created by
admin on Mon Mar 31 19:59:24 GMT 2025 , Edited by admin on Mon Mar 31 19:59:24 GMT 2025
|
PRIMARY | |||
|
10157484
Created by
admin on Mon Mar 31 19:59:24 GMT 2025 , Edited by admin on Mon Mar 31 19:59:24 GMT 2025
|
PRIMARY | |||
|
chromafenozide
Created by
admin on Mon Mar 31 19:59:24 GMT 2025 , Edited by admin on Mon Mar 31 19:59:24 GMT 2025
|
PRIMARY | |||
|
38450
Created by
admin on Mon Mar 31 19:59:24 GMT 2025 , Edited by admin on Mon Mar 31 19:59:24 GMT 2025
|
PRIMARY | |||
|
m3493
Created by
admin on Mon Mar 31 19:59:24 GMT 2025 , Edited by admin on Mon Mar 31 19:59:24 GMT 2025
|
PRIMARY | Merck Index | ||
|
2ODM465D5M
Created by
admin on Mon Mar 31 19:59:24 GMT 2025 , Edited by admin on Mon Mar 31 19:59:24 GMT 2025
|
PRIMARY | |||
|
C454111
Created by
admin on Mon Mar 31 19:59:24 GMT 2025 , Edited by admin on Mon Mar 31 19:59:24 GMT 2025
|
PRIMARY |