S-4-Bromobenzylglutathione cyclopentyl diester

Base Information

Chemical Name:S-4-Bromobenzylglutathione cyclopentyl diester
CAS No.:166038-00-2
Molecular Formula:C₂₇H₃₈BrN₃O₆S
Molecular Weight:612.585
Hs Code.:
DSSTox Substance ID:DTXSID60937161
Nikkaji Number:J743.342E
Wikidata:Q82913371
ChEMBL ID:CHEMBL517039
Mol file:166038-00-2.mol

Synonyms:BrBzGSHCp2;S-4-bromobenzylglutathione cyclopentyl diester;S-p-bromobenzylglutathione dicyclopentyl ester

Suppliers and Price of S-4-Bromobenzylglutathione cyclopentyl diester

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

Total 6 raw suppliers

Chemical Property of S-4-Bromobenzylglutathione cyclopentyl diester

Chemical Property:

Vapor Pressure:5.64E-25mmHg at 25°C
Boiling Point:790.6°C at 760 mmHg
Flash Point:431.9°C
PSA：370.74000
Density:1.38g/cm³
LogP:2.71930
Storage Temp.:2-8°C
XLogP3:3.5
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:8
Rotatable Bond Count:16
Exact Mass:611.16647
Heavy Atom Count:38
Complexity:783

Purity/Quality:: 97% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CCC(C1)OC(=O)CNC(=O)C(CSCC2=CC=C(C=C2)Br)NC(=O)CCC(C(=O)OC3CCCC3)N
Isomeric SMILES:C1CCC(C1)OC(=O)CNC(=O)[C@H](CSCC2=CC=C(C=C2)Br)NC(=O)CC[C@@H](C(=O)OC3CCCC3)N
Uses S-p-Bromobenzylglutathione cyclopentyl diester has been used as an inhibitor of glyoxalase 1?(GLO-1) enzyme to treat HL-1 cardiomyocytes for stimulating aging-based glycative stress. It has also been used as an inhibitor of GLO-1 in hepatic stellate cells.

Technology Process of S-4-Bromobenzylglutathione cyclopentyl diester

There total 1 articles about S-4-Bromobenzylglutathione cyclopentyl diester 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: 71.0%