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Details

Stereochemistry ACHIRAL
Molecular Formula C14H10ClNO4
Molecular Weight 291.687
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LOBENZARIT

SMILES

OC(=O)C1=C(NC2=C(C=CC(Cl)=C2)C(O)=O)C=CC=C1

InChI

InChIKey=UGDPYGKWIHHBMB-UHFFFAOYSA-N
InChI=1S/C14H10ClNO4/c15-8-5-6-10(14(19)20)12(7-8)16-11-4-2-1-3-9(11)13(17)18/h1-7,16H,(H,17,18)(H,19,20)

HIDE SMILES / InChI

Molecular Formula C14H10ClNO4
Molecular Weight 291.687
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Description
Curator's Comment: description was created based on several sources, including: https://www.ncbi.nlm.nih.gov/pubmed/9161931 | http://www.rad-ar.or.jp/siori/english/kekka.cgi?n=750

Lobenzarit is an immunomodulator and antioxidative agent, which has been used successfully in Japan for the treatment of rheumatoid arthritis. Lobenzarit is a scavenger of oxygen-free radicals such as hydroxyl radicals, superoxide, peroxyl and singlet oxygen. Side effects of this medicine are: decreased/considerably increased urinary volume, bloody urine, frequent urination.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: P00390
Gene ID: 2936.0
Gene Symbol: GSR
Target Organism: Homo sapiens (Human)
Target ID: Glutathione S-transferases (rat)
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
CARFENIL

Approved Use

This medicine improves immune abnormality and reduces inflammation and swelling of joints and so on. It is usually used to treat chronic rheumatoid arthritis.

Launch Date

1986
PubMed

PubMed

TitleDatePubMed
Study of the critical points in lobenzarit disodium hydrophilic matrices for controlled drug delivery.
2006 May
Estimation of the percolation thresholds in lobenzarit disodium native dextran matrix tablets.
2007 Dec 28
Investigation of the influence of particle size on the excipient percolation thresholds of HPMC hydrophilic matrix tablets.
2007 Oct
Estimation of the percolation thresholds in ternary lobenzarit disodium-dextran-HPMC hydrophilic matrices tablets: effects of initial porosity.
2009 Nov 5
Patents

Sample Use Guides

2 tablets (80 mg of the active ingredient) at a time, 3 times a day, in combination with other antiphlogistic analgesic
Route of Administration: Oral
In Vitro Use Guide
The Iobenzarit at concentrations of 1, 30, 100 and 1000 uM Iobenzarit had no inhibitory effect on various rat liver microsomal P-450 activities: on the ethoxyresorufin O-dealkylation activity, on the pentoxyresorufin O-deaikylation activity or on the p-nitrophenol hydroxylation activity, when measured in liver microsomes isolated from rats induced with beta-naphthoflavone, phenobarbital and pyrazol.
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:15:36 GMT 2023
Edited
by admin
on Fri Dec 15 16:15:36 GMT 2023
Record UNII
915EE91P39
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LOBENZARIT
INN   MI   WHO-DD  
INN  
Official Name English
LOBENZARIT [MI]
Common Name English
Lobenzarit [WHO-DD]
Common Name English
4-CHLORO-2,2'-IMINODIBENZOATE
Systematic Name English
lobenzarit [INN]
Common Name English
BENZOIC ACID, 2-((2-CARBOXYPHENYL)AMINO)-4-CHLORO-
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C275
Created by admin on Fri Dec 15 16:15:36 GMT 2023 , Edited by admin on Fri Dec 15 16:15:36 GMT 2023
Code System Code Type Description
NCI_THESAURUS
C83889
Created by admin on Fri Dec 15 16:15:36 GMT 2023 , Edited by admin on Fri Dec 15 16:15:36 GMT 2023
PRIMARY
INN
5106
Created by admin on Fri Dec 15 16:15:36 GMT 2023 , Edited by admin on Fri Dec 15 16:15:36 GMT 2023
PRIMARY
MERCK INDEX
m6880
Created by admin on Fri Dec 15 16:15:36 GMT 2023 , Edited by admin on Fri Dec 15 16:15:36 GMT 2023
PRIMARY Merck Index
MESH
C015735
Created by admin on Fri Dec 15 16:15:36 GMT 2023 , Edited by admin on Fri Dec 15 16:15:36 GMT 2023
PRIMARY
FDA UNII
915EE91P39
Created by admin on Fri Dec 15 16:15:36 GMT 2023 , Edited by admin on Fri Dec 15 16:15:36 GMT 2023
PRIMARY
EVMPD
SUB08543MIG
Created by admin on Fri Dec 15 16:15:36 GMT 2023 , Edited by admin on Fri Dec 15 16:15:36 GMT 2023
PRIMARY
EPA CompTox
DTXSID20212709
Created by admin on Fri Dec 15 16:15:36 GMT 2023 , Edited by admin on Fri Dec 15 16:15:36 GMT 2023
PRIMARY
PUBCHEM
3946
Created by admin on Fri Dec 15 16:15:36 GMT 2023 , Edited by admin on Fri Dec 15 16:15:36 GMT 2023
PRIMARY
WIKIPEDIA
LOBENZARIT
Created by admin on Fri Dec 15 16:15:36 GMT 2023 , Edited by admin on Fri Dec 15 16:15:36 GMT 2023
PRIMARY
ChEMBL
CHEMBL1986706
Created by admin on Fri Dec 15 16:15:36 GMT 2023 , Edited by admin on Fri Dec 15 16:15:36 GMT 2023
PRIMARY
SMS_ID
100000082529
Created by admin on Fri Dec 15 16:15:36 GMT 2023 , Edited by admin on Fri Dec 15 16:15:36 GMT 2023
PRIMARY
DRUG CENTRAL
1591
Created by admin on Fri Dec 15 16:15:36 GMT 2023 , Edited by admin on Fri Dec 15 16:15:36 GMT 2023
PRIMARY
CAS
63329-53-3
Created by admin on Fri Dec 15 16:15:36 GMT 2023 , Edited by admin on Fri Dec 15 16:15:36 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY