- Product Details
Keywords
- Iguratimod
- 123663-49-0
- 99
Quick Details
- ProName: Iguratimod
- CasNo: 123663-49-0
- Molecular Formula: C17H14N2O6S
- Appearance: White to off-white powder
- Application: intermediate
- DeliveryTime: in stock
- PackAge: according to the need of packing
- Port: Shanghai
- ProductionCapacity: 10 Kilogram/Day
- Purity: 99
- Storage: 2-8°C
- Transportation: SEA/COURIER/AIR
- LimitNum: 100 Gram
Superiority
Iguratimod Basic information
Product Name: Iguratimod
Synonyms: IGURATIMOD;iguratimod( R&D);T 614;N-[7-methanesulfonamido-4-oxo-6-(phenoxy)chromen-3-yl]formamide;3-(Formylamino)-7-(methylsulfonylamino)-6-phenoxy-4H-1-benzopyran-4-one;N-[3-(Formylamino)-4-oxo-6-phenoxy-4H-1-benzopyran-7-yl]methanesulfonamide;IguratiMod (T 614);N-(7-(MethylsulfonaMido)-4-oxo-6-phenoxy-4H-chroMen-3-yl)forMaMide
CAS: 123663-49-0
MF: C17H14N2O6S
MW: 374.37
EINECS: 808-127-0
Product Categories: Pharmaceutical intermediate;Pharmaceuticals;API;123663-49-0
Mol File: 123663-49-0.mol
Details
Iguratimod Chemical Properties
Melting point 238.0 to 242.0 °C
Boiling point 580.6±60.0 °C(Predicted)
density 1.52±0.1 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
solubility DMSO (Slightly)
pka 5.58±0.20(Predicted)
form Solid
color White to Off-White
Safety Information
HS Code 2935.90.9500
MSDS Information
Iguratimod Usage And Synthesis
Description
In August 2011, China’s State FDA approved Simcere Pharmaceutical Group’s new drug application for iguratimod (T-614), a disease modifying anti-rheumatic drug (DMARD) for the treatment of rheumatoid arthritis (RA). Preclinical in vivo studies indicated that iguratimod was effective in an established adjuvant-induced arthritis model (ED40=3.6 mg/kg) in rats and also efficacious in a type II collagen-induced arthritis model in DBA/1J mice at 30 mg and 100 mg/kg.
Originator Toyama (Japan)
Uses Iguratimod acts as an anti-inflammatory agent, used primarily in the treatment of rheumatoid arthritis.
Definition ChEBI: Iguratimod is an organic molecular entity.
Brand name Iremod
Clinical Use Iguratimod, which was discovered by Toyama Pharmaceuticals and jointly co-developed with Eisai in Japan, was approved by the PMDA (Pharmaceuticals and Medical Devices Agency) of Japan on June 29, 2012 for the treatment of rheumatoid arthritis. This drug was also independently developed by Simcere Pharmaceutical Group and is marked as Iremod® in China. The drug exhibited inhibitory effects on granuloma inflammation, and was shown to be efficacious for the prevention of joint destruction in adjuvant arthritis.