N1509
S-(4-Nitrobenzyl)glutathione
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About This Item
Empirical Formula (Hill Notation):
C17H22N4O8S
CAS Number:
Molecular Weight:
442.44
UNSPSC Code:
12352200
PubChem Substance ID:
MDL number:
storage temp.
2-8°C
SMILES string
NC(CCC(=O)NC(CSCc1ccc(cc1)N(=O)=O)C(=O)NCC(O)=O)C(O)=O
InChI
1S/C17H22N4O8S/c18-12(17(26)27)5-6-14(22)20-13(16(25)19-7-15(23)24)9-30-8-10-1-3-11(4-2-10)21(28)29/h1-4,12-13H,5-9,18H2,(H,19,25)(H,20,22)(H,23,24)(H,26,27)
InChI key
OAWORKDPTSAMBZ-UHFFFAOYSA-N
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Regulatory Information
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M T Vincenzini et al.
Biochimica et biophysica acta, 1073(3), 571-579 (1991-04-09)
The epithelium of the small intestine act by the formation of GSH-S-conjugation, as a first line of defence against various ingested toxic chemicals. GSH and GSH-dependent enzymes are present in the gastrointestinal wall. We and others have characterized the GSH-specific
L Bousset et al.
Biochemistry, 40(45), 13564-13573 (2001-11-07)
The [URE3] phenotype in yeast Saccharomyces cerevisiae is due to an altered prion form of Ure2p, a protein involved in nitrogen catabolism. To understand possible conformational changes at the origin of prion propagation, we previously solved the crystal structure of
J D deBethizy et al.
Biochemical and biophysical research communications, 114(2), 500-504 (1983-07-29)
[14C]-4-Nitrotoluene was metabolized by rat liver postmitochondrial supernatant containing NADPH, reduced glutathione and a sulfate activating system to 4-nitrobenzyl alcohol, 4-nitrobenzyl sulfate, and S-(4-nitrobenzyl) glutathione. Formation of both sulfur-containing metabolites was dependent on the presence of a sulfate activating system.