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Details

Stereochemistry ACHIRAL
Molecular Formula C16H11F3N2O2
Molecular Weight 320.2659
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of AMINOFLAVONE

SMILES

CC1=C(F)C(N)=C2C(=O)C=C(OC2=C1F)C3=CC=C(N)C(F)=C3

InChI

InChIKey=RTUZVPPGTJRELI-UHFFFAOYSA-N
InChI=1S/C16H11F3N2O2/c1-6-13(18)15(21)12-10(22)5-11(23-16(12)14(6)19)7-2-3-9(20)8(17)4-7/h2-5H,20-21H2,1H3

HIDE SMILES / InChI

Molecular Formula C16H11F3N2O2
Molecular Weight 320.2659
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Substituted flavones as aryl hydrocarbon (Ah) receptor agonists and antagonists.
1996 Apr 26
Aminoflavone induces oxidative DNA damage and reactive oxidative species-mediated apoptosis in breast cancer cells.
2008 Apr 1
Patents

Patents

Substance Class Chemical
Created
by admin
on Sat Dec 16 06:40:14 GMT 2023
Edited
by admin
on Sat Dec 16 06:40:14 GMT 2023
Record UNII
2EXS38428U
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
AMINOFLAVONE
Common Name English
4H-1-BENZOPYRAN-4-ONE, 5-AMINO-2-(4-AMINO-3-FLUOROPHENYL)-6,8-DIFLUORO-7-METHYL-
Systematic Name English
5-AMINO-2-(4-AMINO-3-FLUOROPHENYL)-6,8-DIFLUORO-7-METHYL-4H-1-BENZOPYRAN-4-ONE
Systematic Name English
NSC-686288
Code English
Code System Code Type Description
EPA CompTox
DTXSID50167854
Created by admin on Sat Dec 16 06:40:14 GMT 2023 , Edited by admin on Sat Dec 16 06:40:14 GMT 2023
PRIMARY
CAS
165179-35-1
Created by admin on Sat Dec 16 06:40:14 GMT 2023 , Edited by admin on Sat Dec 16 06:40:14 GMT 2023
PRIMARY
PUBCHEM
389710
Created by admin on Sat Dec 16 06:40:14 GMT 2023 , Edited by admin on Sat Dec 16 06:40:14 GMT 2023
PRIMARY
FDA UNII
2EXS38428U
Created by admin on Sat Dec 16 06:40:14 GMT 2023 , Edited by admin on Sat Dec 16 06:40:14 GMT 2023
PRIMARY
NSC
686288
Created by admin on Sat Dec 16 06:40:14 GMT 2023 , Edited by admin on Sat Dec 16 06:40:14 GMT 2023
PRIMARY
Related Record Type Details
TARGET -> ACTIVATOR
Related Record Type Details
ACTIVE MOIETY