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Details

Stereochemistry ACHIRAL
Molecular Formula C19H14O8
Molecular Weight 370.3097
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FLAVODIC ACID

SMILES

OC(=O)COC1=CC(OCC(O)=O)=C2C(=O)C=C(OC2=C1)C3=CC=CC=C3

InChI

InChIKey=IGCSSLDDCHLXGL-UHFFFAOYSA-N
InChI=1S/C19H14O8/c20-13-8-14(11-4-2-1-3-5-11)27-16-7-12(25-9-17(21)22)6-15(19(13)16)26-10-18(23)24/h1-8H,9-10H2,(H,21,22)(H,23,24)

HIDE SMILES / InChI

Molecular Formula C19H14O8
Molecular Weight 370.3097
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Flavodic acid is a synthetic hydrosoluble derivative of natural flavonoids. It has been shown to reduce capiliary fragility and permeability. Sodium flavodate was marketed by the Italian pharmaceutical company Farmaceutici under tradename Pericel.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
PubMed

PubMed

TitleDatePubMed
Determination of sodium flavodate in body fluids by high-performance liquid chromatography: application to clinical pharmacokinetic studies.
1982 Jun 11
Phlebotonics for venous insufficiency.
2005 Jul 20
Phlebotonics for venous insufficiency.
2016 Apr 6
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:22:29 UTC 2023
Edited
by admin
on Fri Dec 15 16:22:29 UTC 2023
Record UNII
2Z9V171UEM
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FLAVODIC ACID
INN   WHO-DD  
INN  
Official Name English
Flavodic acid [WHO-DD]
Common Name English
((4-OXO-2-PHENYL-4H-1-BENZOPYRAN-5,7-DIYL)DIOXY)DIACETIC ACID
Systematic Name English
flavodic acid [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C1745
Created by admin on Fri Dec 15 16:22:29 UTC 2023 , Edited by admin on Fri Dec 15 16:22:29 UTC 2023
Code System Code Type Description
DRUG CENTRAL
1173
Created by admin on Fri Dec 15 16:22:29 UTC 2023 , Edited by admin on Fri Dec 15 16:22:29 UTC 2023
PRIMARY
NCI_THESAURUS
C65690
Created by admin on Fri Dec 15 16:22:29 UTC 2023 , Edited by admin on Fri Dec 15 16:22:29 UTC 2023
PRIMARY
INN
2680
Created by admin on Fri Dec 15 16:22:29 UTC 2023 , Edited by admin on Fri Dec 15 16:22:29 UTC 2023
PRIMARY
MESH
C002094
Created by admin on Fri Dec 15 16:22:29 UTC 2023 , Edited by admin on Fri Dec 15 16:22:29 UTC 2023
PRIMARY
ChEMBL
CHEMBL2107394
Created by admin on Fri Dec 15 16:22:29 UTC 2023 , Edited by admin on Fri Dec 15 16:22:29 UTC 2023
PRIMARY
EPA CompTox
DTXSID90190909
Created by admin on Fri Dec 15 16:22:29 UTC 2023 , Edited by admin on Fri Dec 15 16:22:29 UTC 2023
PRIMARY
SMS_ID
100000080989
Created by admin on Fri Dec 15 16:22:29 UTC 2023 , Edited by admin on Fri Dec 15 16:22:29 UTC 2023
PRIMARY
RXCUI
25060
Created by admin on Fri Dec 15 16:22:29 UTC 2023 , Edited by admin on Fri Dec 15 16:22:29 UTC 2023
PRIMARY RxNorm
PUBCHEM
71944
Created by admin on Fri Dec 15 16:22:29 UTC 2023 , Edited by admin on Fri Dec 15 16:22:29 UTC 2023
PRIMARY
EVMPD
SUB07633MIG
Created by admin on Fri Dec 15 16:22:29 UTC 2023 , Edited by admin on Fri Dec 15 16:22:29 UTC 2023
PRIMARY
FDA UNII
2Z9V171UEM
Created by admin on Fri Dec 15 16:22:29 UTC 2023 , Edited by admin on Fri Dec 15 16:22:29 UTC 2023
PRIMARY
CAS
37470-13-6
Created by admin on Fri Dec 15 16:22:29 UTC 2023 , Edited by admin on Fri Dec 15 16:22:29 UTC 2023
PRIMARY
ECHA (EC/EINECS)
253-517-0
Created by admin on Fri Dec 15 16:22:29 UTC 2023 , Edited by admin on Fri Dec 15 16:22:29 UTC 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY