![L-gamma-glutamyl-N-[S-(1H-indol-3-ylmethyl)-L-cysteinyl]glycine](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fcas-image%2Fthumb-webp%2F200033-l-gamma-glutamyl-n-s-1h-indol-3-ylmethyl-l-cysteinyl-glycine.webp&w=3840&q=75)
CAS 101038-93-1: L-gamma-glutamyl-N-[S-(1H-indol-3-ylmethyl)-L-cysteinyl]glycine
Formula:C19H24N4O6S
InChI:InChI=1/C19H24N4O6S/c20-13(19(28)29)5-6-16(24)23(8-17(25)26)18(27)14(21)10-30-9-11-7-22-15-4-2-1-3-12(11)15/h1-4,7,13-14,22H,5-6,8-10,20-21H2,(H,25,26)(H,28,29)/t13-,14-/m0/s1
SMILES:c1ccc2c(c1)c(c[nH]2)CSC[C@@H](C(=O)N(CC(=O)O)C(=O)CC[C@@H](C(=O)O)N)N
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3-Glutathionyl-S-methylindole
CAS:3-Glutathionyl-S-methylindole is a reactive compound that is metabolized by cytochromes P450 2A13 and CYP2A13. It has been shown to be a potent nasal irritant in animals and humans. 3-Glutathionyl-S-methylindole is also an epoxidation product of indole, which is found in the tissues of mammals and birds. The reaction system for this compound has been characterized, with kinetic parameters established. The profile of 3-glutathionyl-S-methylindole has been determined to be similar to those of glutathione and cyp2a13. The enzyme activity profiles have been studied in rats, leading to the conclusion that 3-glutathionyl-s methylindole is metabolized by cytochrome P450 2A13 and CYP2A13.Formula:C19H24N4O6SPurity:Min. 95%Molecular weight:436.48 g/mol
