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Details

Stereochemistry RACEMIC
Molecular Formula C21H23NO4.C4H4O4
Molecular Weight 469.4838
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of FLAVODILOL MALEATE

SMILES

OC(=O)\C=C/C(O)=O.CCCNCC(O)COC1=CC2=C(C=C1)C(=O)C=C(O2)C3=CC=CC=C3

InChI

InChIKey=AEAIVULHCUHDDP-BTJKTKAUSA-N
InChI=1S/C21H23NO4.C4H4O4/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;5-3(6)1-2-4(7)8/h3-9,11-12,16,22-23H,2,10,13-14H2,1H3;1-2H,(H,5,6)(H,7,8)/b;2-1-

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 ( + / - )

Molecular Formula C4H4O4
Molecular Weight 116.0722
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 1
Optical Activity NONE

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
Flavodilol: a new antihypertensive agent.
1989 Jul
Flavodilol: a new antihypertensive agent that preferentially depletes peripheral biogenic amines.
1989 Jul
Disposition of flavodilol in laboratory animals.
1989 Jul-Aug
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:19:26 GMT 2023
Edited
by admin
on Fri Dec 15 16:19:26 GMT 2023
Record UNII
Y0DFC0D3Q8
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FLAVODILOL MALEATE
USAN  
USAN  
Official Name English
(±)-7-(2-HYDROXY-3-(PROPYLAMINO)PROPOXY)FLAVONE MALEATE (1:1) (SALT)
Common Name English
4H-1-BENZOPYRAN-4-ONE, 7-(2-HYDROXY-3-(PROPYLAMINO)PROPOXY)-2-PHENYL-, (±)-, (Z)-2-BUTENEDIOATE (1:1) (SALT)
Common Name English
PR-877-53OL
Code English
PR-877-530L
Code English
FLAVODILOL MALEATE [USAN]
Common Name English
Code System Code Type Description
FDA UNII
Y0DFC0D3Q8
Created by admin on Fri Dec 15 16:19:26 GMT 2023 , Edited by admin on Fri Dec 15 16:19:26 GMT 2023
PRIMARY
ChEMBL
CHEMBL57185
Created by admin on Fri Dec 15 16:19:26 GMT 2023 , Edited by admin on Fri Dec 15 16:19:26 GMT 2023
PRIMARY
NCI_THESAURUS
C169985
Created by admin on Fri Dec 15 16:19:26 GMT 2023 , Edited by admin on Fri Dec 15 16:19:26 GMT 2023
PRIMARY
PUBCHEM
6435382
Created by admin on Fri Dec 15 16:19:26 GMT 2023 , Edited by admin on Fri Dec 15 16:19:26 GMT 2023
PRIMARY
CAS
79619-32-2
Created by admin on Fri Dec 15 16:19:26 GMT 2023 , Edited by admin on Fri Dec 15 16:19:26 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
PARENT -> SALT/SOLVATE
Related Record Type Details
ACTIVE MOIETY