U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C10H6O4
Molecular Weight 190.1522
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CHROMOCARB

SMILES

OC(=O)C1=CC(=O)C2=CC=CC=C2O1

InChI

InChIKey=RVMGXWBCQGAWBR-UHFFFAOYSA-N
InChI=1S/C10H6O4/c11-7-5-9(10(12)13)14-8-4-2-1-3-6(7)8/h1-5H,(H,12,13)

HIDE SMILES / InChI

Molecular Formula C10H6O4
Molecular Weight 190.1522
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Chromocarb is benzo-γ-pyrone derivative with vasoprotection activity used to eliminate lipoperoxidation post-vitrectomy. Peroral treatment of rats with chromocarb significantly reduced the degradation of the vascular wall by intravenous collagenase, as demonstrated by a lesser permeability increase of the blood-brain barrier, a shorter recovery time, lower hydroxyproline levels in the cerebrospinal fluid and a lesser decrease of the collagen content of the brain capillary basal lamina.

Originator

Sources: Berichte der Deutschen Chemischen Gesellschaft [Abteilung] B: Abhandlungen (1933), 66B, 1168-77.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
PubMed

PubMed

TitleDatePubMed
Leukotrienes, antileukotrienes and asthma.
2008 Jun
Chromone-2- and -3-carboxylic acids inhibit differently monoamine oxidases A and B.
2010 May 1
Patents

Sample Use Guides

rats: 50 mg/kg daily in drinking water for 30 days
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:32:53 UTC 2023
Edited
by admin
on Fri Dec 15 16:32:53 UTC 2023
Record UNII
FY38S0790W
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CHROMOCARB
INN   MI   WHO-DD  
INN  
Official Name English
chromocarb [INN]
Common Name English
Chromocarb [WHO-DD]
Common Name English
CHROMOCARB [MI]
Common Name English
NSC-758218
Code English
Classification Tree Code System Code
NCI_THESAURUS C29698
Created by admin on Fri Dec 15 16:32:53 UTC 2023 , Edited by admin on Fri Dec 15 16:32:53 UTC 2023
Code System Code Type Description
NCI_THESAURUS
C78116
Created by admin on Fri Dec 15 16:32:53 UTC 2023 , Edited by admin on Fri Dec 15 16:32:53 UTC 2023
PRIMARY
EVMPD
SUB06221MIG
Created by admin on Fri Dec 15 16:32:53 UTC 2023 , Edited by admin on Fri Dec 15 16:32:53 UTC 2023
PRIMARY
INN
2786
Created by admin on Fri Dec 15 16:32:53 UTC 2023 , Edited by admin on Fri Dec 15 16:32:53 UTC 2023
PRIMARY
DRUG CENTRAL
628
Created by admin on Fri Dec 15 16:32:53 UTC 2023 , Edited by admin on Fri Dec 15 16:32:53 UTC 2023
PRIMARY
PUBCHEM
2741
Created by admin on Fri Dec 15 16:32:53 UTC 2023 , Edited by admin on Fri Dec 15 16:32:53 UTC 2023
PRIMARY
SMS_ID
100000081878
Created by admin on Fri Dec 15 16:32:53 UTC 2023 , Edited by admin on Fri Dec 15 16:32:53 UTC 2023
PRIMARY
NSC
758218
Created by admin on Fri Dec 15 16:32:53 UTC 2023 , Edited by admin on Fri Dec 15 16:32:53 UTC 2023
PRIMARY
MERCK INDEX
m3511
Created by admin on Fri Dec 15 16:32:53 UTC 2023 , Edited by admin on Fri Dec 15 16:32:53 UTC 2023
PRIMARY Merck Index
CAS
4940-39-0
Created by admin on Fri Dec 15 16:32:53 UTC 2023 , Edited by admin on Fri Dec 15 16:32:53 UTC 2023
PRIMARY
FDA UNII
FY38S0790W
Created by admin on Fri Dec 15 16:32:53 UTC 2023 , Edited by admin on Fri Dec 15 16:32:53 UTC 2023
PRIMARY
EPA CompTox
DTXSID6045878
Created by admin on Fri Dec 15 16:32:53 UTC 2023 , Edited by admin on Fri Dec 15 16:32:53 UTC 2023
PRIMARY
ChEMBL
CHEMBL83628
Created by admin on Fri Dec 15 16:32:53 UTC 2023 , Edited by admin on Fri Dec 15 16:32:53 UTC 2023
PRIMARY
ECHA (EC/EINECS)
225-583-0
Created by admin on Fri Dec 15 16:32:53 UTC 2023 , Edited by admin on Fri Dec 15 16:32:53 UTC 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY