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Details

Stereochemistry RACEMIC
Molecular Formula C21H23NO4
Molecular Weight 353.4116
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FLAVODILOL

SMILES

CCCNCC(O)COC1=CC2=C(C=C1)C(=O)C=C(O2)C3=CC=CC=C3

InChI

InChIKey=KRBRHCLLOOCWQF-UHFFFAOYSA-N
InChI=1S/C21H23NO4/c1-2-10-22-13-16(23)14-25-17-8-9-18-19(24)12-20(26-21(18)11-17)15-6-4-3-5-7-15/h3-9,11-12,16,22-23H,2,10,13-14H2,1H3

HIDE SMILES / InChI

Molecular Formula C21H23NO4
Molecular Weight 353.4116
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Targets

Targets

Primary TargetPharmacologyConditionPotency
4.0 nM [Ki]
PubMed

PubMed

TitleDatePubMed
Flavones. 2. Synthesis and structure-activity relationship of flavodilol and its analogues, a novel class of antihypertensive agents with catecholamine depleting properties.
1989 Jan
Substance Class Chemical
Created
by admin
on Sat Dec 16 17:53:11 GMT 2023
Edited
by admin
on Sat Dec 16 17:53:11 GMT 2023
Record UNII
M8FR1KL85J
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FLAVODILOL
INN  
INN  
Official Name English
(±)-7-(2-HYDROXY-3-(PROPYLAMINO)PROPOXY)FLAVONE
Systematic Name English
flavodilol [INN]
Common Name English
4H-1-BENZOPYRAN-4-ONE, 7-(2-HYDROXY-3-(PROPYLAMINO)PROPOXY)-2-PHENYL-, (±)-
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C270
Created by admin on Sat Dec 16 17:53:12 GMT 2023 , Edited by admin on Sat Dec 16 17:53:12 GMT 2023
Code System Code Type Description
EVMPD
SUB07634MIG
Created by admin on Sat Dec 16 17:53:12 GMT 2023 , Edited by admin on Sat Dec 16 17:53:12 GMT 2023
PRIMARY
FDA UNII
M8FR1KL85J
Created by admin on Sat Dec 16 17:53:12 GMT 2023 , Edited by admin on Sat Dec 16 17:53:12 GMT 2023
PRIMARY
NCI_THESAURUS
C72783
Created by admin on Sat Dec 16 17:53:12 GMT 2023 , Edited by admin on Sat Dec 16 17:53:12 GMT 2023
PRIMARY
SMS_ID
100000080971
Created by admin on Sat Dec 16 17:53:12 GMT 2023 , Edited by admin on Sat Dec 16 17:53:12 GMT 2023
PRIMARY
EPA CompTox
DTXSID90868530
Created by admin on Sat Dec 16 17:53:12 GMT 2023 , Edited by admin on Sat Dec 16 17:53:12 GMT 2023
PRIMARY
CAS
79619-31-1
Created by admin on Sat Dec 16 17:53:12 GMT 2023 , Edited by admin on Sat Dec 16 17:53:12 GMT 2023
PRIMARY
ChEMBL
CHEMBL57185
Created by admin on Sat Dec 16 17:53:12 GMT 2023 , Edited by admin on Sat Dec 16 17:53:12 GMT 2023
PRIMARY
MESH
C058114
Created by admin on Sat Dec 16 17:53:12 GMT 2023 , Edited by admin on Sat Dec 16 17:53:12 GMT 2023
PRIMARY
INN
5279
Created by admin on Sat Dec 16 17:53:12 GMT 2023 , Edited by admin on Sat Dec 16 17:53:12 GMT 2023
PRIMARY
PUBCHEM
54410
Created by admin on Sat Dec 16 17:53:12 GMT 2023 , Edited by admin on Sat Dec 16 17:53:12 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
SALT/SOLVATE -> PARENT
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY