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S-(4-Hydroxybenzyl)glutathione

Cat. No. M11085
S-(4-Hydroxybenzyl)glutathione  Structure
Size Price Availability Quantity
10mg USD 400  USD400 In stock
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Quality Control & Documentation
Biological Activity

S-(4-Hydroxybenzyl)glutathione is a glutathione derivative. S-(4-Hydroxybenzyl)glutathione inhibits in vitro binding of erythoxylate to cerebral glutamate receptors,IC50 The value is 2 μM.

Chemical Information
Molecular Weight 413.45
Formula C17H23N3O7S
CAS Number 129636-38-0
Form Solid
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
Conversion of different model animals based on BSA (PMID: 27057123)
Species Mouse Rat Rabbit Guinea pig Hamster Dog
Weight (kg) 0.02 0.15 1.8 0.4 0.08 10
Body Surface Area (m2) 0.007 0.025 0.15 0.05 0.02 0.5
Km factor 3 6 12 8 5 20
Animal A (mg/kg) = Animal B (mg/kg) multiplied by  Animal B Km
Animal A Km

For example, to modify the dose of Compound A used for a mouse (20 mg/kg) to a dose based on the BSA for a rat, multiply 20 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for Compound A of 10 mg/kg.

References

[1] Jiamin Wang, et al. Talanta. A BODIPY-based turn-on fluorescent probe for the selective detection of hydrogen sulfide in solution and in cells

[2] Qing-Lan Guo, et al. J Asian Nat Prod Res. 4-Hydroxybenzyl-substituted glutathione derivatives from Gastrodia elata

[3] M La Marca, et al. Food Chem Toxicol. Structural influence of isothiocyanates on expression of cytochrome P450, phase II enzymes, and activation of Nrf2 in primary rat hepatocytes

[4] E Boyland, et al. Biochem J. Glutathione S-aralkyltransferase

[5] K Tajima, et al. Biochem Pharmacol. Formation of a glutathione conjugate from butylated hydroxytoluene by rat liver microsomes

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