Edaglitazone

Base Information

Chemical Name:Edaglitazone
CAS No.:213411-83-7
Molecular Formula:C₂₄H₂₀N₂O₄S₂
Molecular Weight:464.566
Hs Code.:
UNII:8GKF7V499B,59LQZ96XUU,QP6GWW0LZD
DSSTox Substance ID:DTXSID00870240
Nikkaji Number:J1.244.260B
Wikidata:Q27077152
NCI Thesaurus Code:C75189
Pharos Ligand ID:A1ZKUB2335ZZ
Metabolomics Workbench ID:149816
ChEMBL ID:CHEMBL3990804
Mol file:213411-83-7.mol

Synonyms:5-((4-(2-(5-methyl-2-phenyloxazol-4-yl)ethoxy)benzo(b)thiophen-7-yl)methyl)thiazolidine-2,4-dione;BM 13.1258;BM-13.1258;BM-131258;BM13.1258;edaglitazone

Suppliers and Price of Edaglitazone

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

TRC
Edaglitazone
50mg
$ 530.00

Tocris
Edaglitazone ≥98%(HPLC)
50
$ 668.00

Tocris
Edaglitazone ≥98%(HPLC)
10
$ 159.00

Cayman Chemical
Edaglitazone
10mg
$ 148.00

Cayman Chemical
Edaglitazone
5mg
$ 87.00

Cayman Chemical
Edaglitazone
25mg
$ 348.00

American Custom Chemicals Corporation
5-((4-(2-(5-METHYL-2-PHENYLOXAZOL-4-YL)ETHOXY)BENZO[B]THIOPHEN-7-YL)METHYL)THIAZOLIDINE-2,4-DIONE 95.00%
5MG
$ 504.52

AK Scientific
Edaglitazone
5mg
$ 217.00

Total 4 raw suppliers

Chemical Property of Edaglitazone

Chemical Property:

Melting Point:208 °C
PSA：138.46000
Density:1.375g/cm³
LogP:5.65620
XLogP3:5.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:7
Exact Mass:464.08644947
Heavy Atom Count:32
Complexity:689

Purity/Quality:

97% ^*data from raw suppliers

Edaglitazone ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=C(N=C(O1)C2=CC=CC=C2)CCOC3=C4C=CSC4=C(C=C3)CC5C(=O)NC(=O)S5
Description Edaglitazone is an agonist of peroxisome proliferator-activated receptor γ (PPARγ). It activates PPARγ in a reporter assay using CV-1 cells expressing murine PPARγ2 when used at concentrations ranging from 0.1 to 1 μM. Edaglitazone (1, 5, and 25 μM) increases [3H]2-deoxyglucose transport in the presence and absence of insulin and increases glycogen synthesis in the presence of insulin in soleus muscle strips isolated from obese rats.
Uses Treatment of Type 2 diabetes. Edaglitazone possesses anti-diabetic properties and is a thiazolidinedione peroxisome proliferator-activated receptor gamma (PPARγ) agonist. Also, it is a cytochrome P 450 2C19 (CYP2C19) substrate.

Technology Process of Edaglitazone

There total 3 articles about Edaglitazone which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 95.9%

: 5-{[4-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]benzo[b]thien-7-yl]methylene}-2,4-thiazolidinedione

: 892128-35-7,892128-36-8,213411-83-7
5-{4-[2-(5-methyl-2-phenyloxazol-4-yl)-ethoxy]-benzo[b]thiophen-7-ylmethyl}-thiazolidine-2,4-dione

Guidance literature:: With Dowtherm A; diethyl 2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate; at 20 ℃; for 2h; Product distribution / selectivity;