S-(4-Hydroxybenzyl)glutathione

Research use only, not for human use.

L-γ-Glutamyl-S-[(4-hydroxyphenyl)methyl] was isolated as the major principle responsible for the inhibition of the in vitro binding of kainic acid to brain glutamate receptors by water extracts of the plant Gastrodia elata.

L-γ-Glutamyl-S-[(4-hydroxyphenyl)methyl] was isolated as the major principle responsible for the inhibition of the in vitro binding of kainic acid to brain glutamate receptors by water extracts of the plant Gastrodia elata.(In Vitro):L-γ-Glutamyl-S-[(4-hydroxyphenyl)methyl] inhibits specific [3H]kainic acid binding to brain glutamate receptors with IC50 of 2 μM. The affinity (IC50 value) of the compound is slightly lower compared to glutamate and glutathione.

S-(4-Hydroxybenzyl)glutathione inhibits the binding of specific [3H]kainic acid to brain glutamate receptors, with an IC50 of 2 μM.

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L-γ-Glutamyl-S-[(4-hydroxyphenyl)methyl] | S-(4-Hydroxybenzyl)glutathione

Neuroscience

GluR

GluR

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129636-38-0

413.45

C17H23N3O7S

>98% (HPLC)

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N[C@@H](CCC(N[C@@H](CSCc(cc1)ccc1O)C(NCC(O)=O)=O)=O)C(O)=O

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(-20℃)

With Ice Pack

≥ 2 years