IBRIGAMPAR

Investigational

Details

Stereochemistry	ACHIRAL
Molecular Formula	C21H12Cl4N2O3S
Molecular Weight	514.209
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

ClC1=CC=C(C(Cl)=C1)S(=O)(=O)NC2=CC(Cl)=C(OC3=CN=C4C=CC=CC4=C3)C(Cl)=C2

InChI

InChIKey=NMRWDFUZLLQSBN-UHFFFAOYSA-N

InChI=1S/C21H12Cl4N2O3S/c22-13-5-6-20(16(23)8-13)31(28,29)27-14-9-17(24)21(18(25)10-14)30-15-7-12-3-1-2-4-19(12)26-11-15/h1-11,27H

HIDE SMILES / InChI

Molecular Formula	C21H12Cl4N2O3S
Molecular Weight	514.209
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Description
Sources: https://web.archive.org/web/20171004070815/http://www.intekrin.com:80/programs-int131.html
Curator's Comment: description was created based on several sources, including https://www.ncbi.nlm.nih.gov/pubmed/19337960

INT-131, a novel, non-thiazolidinedione (TZD), selective peroxisome proliferator-activated receptor (PPAR) gamma modulator and partial agonist, which was investigated in phase II of clinical trial for the treatment of type 2 diabetes mellitus (non-insulin dependent diabetes) and Multiple Sclerosis, Relapsing Remitting. The concept of selective modulation involves targeting and activating specific genes to minimize side effects while maintaining therapeutic benefits. In vitro, INT-131 attenuated adipogenic properties, indicating moderate PPAR gamma activation/cofactor recruitment compared with the full agonistic properties of TZD compounds.

Originator

Approval Year

Targets

Primary Target	Pharmacology	Condition	Potency
Peroxisome proliferator-activated receptor gamma 118 Target ID: CHEMBL235 Sources: https://www.ncbi.nlm.nih.gov/pubmed/23294830	Partial Agonist 297

Conditions

Condition	Modality	Targets	Highest Phase	Product
Type 2 diabetes mellitus 262 Sources: https://www.ncbi.nlm.nih.gov/pubmed/19337960	Primary		Phase II 1147	Unknown Approved Use Unknown
Multiple sclerosis, relapsing remitting 2 Sources: https://clinicaltrials.gov/ct2/show/NCT02638038	Primary		Phase II 1147	Unknown Approved Use Unknown

Overview

CYP3A4	CYP2C9	CYP2D6	hERG
inhibitor 2252	inhibitor 2438	inhibitor 2507

OverviewOther

Other Inhibitor	Other Substrate	Other Inducer
P-gp 1741

Drug as perpetrator

Target	Modality	Activity
CYP2D6 2546	inhibitor 4027 Sources: https://pubchem.ncbi.nlm.nih.gov/bioassay/1645840#sid=363680393	inconclusive [IC50 21.3174 uM]
P-gp 1932	inhibitor 4027 Sources: https://pubchem.ncbi.nlm.nih.gov/bioassay/1346987#sid=363680393	inconclusive [IC50 29.0929 uM]
CYP3A4 2633	inhibitor 4027 Sources: https://pubmed.ncbi.nlm.nih.gov/23294830/	yes [IC50 25 uM]
CYP2C9 2497	inhibitor 4027 Sources: https://pubchem.ncbi.nlm.nih.gov/bioassay/1645842#sid=363680393	yes [IC50 3.0112 uM]

Sourcing

Vendor/Aggregator	ID	URL
Axon MedChem	2019	https://www.axonmedchem.com/product/2019
ChemShuttle	139037	https://www.chemshuttle.com/catalogsearch/result/?q=139037
eMolecules	46024421	https://orderbb.emolecules.com/search/#?query=46024421
HongKong Chemhere	315224-26-1
MolPort	MolPort-042-665-800	https://www.molport.com/shop/molecule-link/MolPort-042-665-800
MuseChem	I002041	https://www.musechem.com/product/I002041.html
Nanjing Pope Bio-tech	NSTH-C016864
Norris Pharm	NSTH-C016864
Ryan Scientific	101-94008	https://ryansci.com/products?q=101-94008&list_q=&search_type=exact

PubMed

Title	Date	PubMed

Patents

Sample Use Guides

In Vivo Use Guide

1.0 mg, Once daily

Route of Administration: Oral

In Vitro Use Guide

Unknown

Substance Class	Chemical Created by `admin` on `Mon Mar 31 22:12:03 GMT 2025` Edited by `admin` on `Mon Mar 31 22:12:03 GMT 2025`
Record UNII	E7ILQ6U50J
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

AMG-131

Preferred Name

English

IBRIGAMPAR

Official Name

English

T0903131

Code

English

CHS-131

Code

English

INT-131

Code

English

2,4-DICHLORO-N-(3,5-DICHLORO-4-((QUINOLIN-3- YL)OXY)PHENYL)BENZENE-1-SULFONAMIDE

Systematic Name

English

ibrigampar [INN]

Common Name

English

T131

Code

English

T-0903131

Code

English

BENZENESULFONAMIDE, 2,4-DICHLORO-N-(3,5-DICHLORO-4-(3-QUINOLINYLOXY)PHENYL)-

Systematic Name

English

Code System Code Type Description

DRUG BANK

DB05490