ChemicalBook--->CAS DataBase List--->26289-39-4

26289-39-4

26289-39-4 Structure

26289-39-4 Structure
IdentificationBack Directory
[Name]

S-(2,4-Dinitrophenyl)-Glutathione
[CAS]

26289-39-4
[Synonyms]

Dinitrophenylglutathione
2,4-Dinitrophenyl-S-glutathione
γGlu-S-(2,4-Dinitrophenyl)-L-Cys-Gly-OH
L-γGlu-S-(2,4-Dinitrophenyl)-L-Cys-Gly-OH
N-[L-γ-Glutamyl-S-(2,4-dinitrophenyl)-L-cysteinyl]glycine
[Molecular Formula]

C16H19N5O10S
[MOL File]

26289-39-4.mol
[Molecular Weight]

473.41
Chemical PropertiesBack Directory
[Appearance]

Light Yellow Solid
[Melting point ]

210-212° dec.
[Boiling point ]

895.1±65.0 °C(Predicted)
[density ]

1.61±0.1 g/cm3(Predicted)
[storage temp. ]

-20°C Freezer
[solubility ]

Water: Slightly Soluble
[form ]

A solid
[pka]

2.21±0.10(Predicted)
Hazard InformationBack Directory
[Chemical Properties]

Light Yellow Solid
[Uses]

A substrate for Glutathione-S-Transferase, with a kinetically determined dissociation constant of 7uM
[Definition]

ChEBI: A Glu-Cys-Gly tripeptide glutathione conjugate containing a 2,4-dinitrophenyl substituent on the S of Cys.
[Description]

S-(2,4-Dinitrophenyl)-glutathione is a substrate for glutathione-S-transferase with a kinetic dissociation constant of 7 μM. In vitro, it is transported by multidrug resistance protein 1 (MDR1) and MDR3, which are transporters that confer resistance to some chemotherapeutics.
[References]

[1] V L SCHRAMM. Kinetic studies and active site-binding properties of glutathione S-transferase using spin-labeled glutathione, a product analogue.[J]. The Journal of Biological Chemistry, 1984, 259 2: 714-722.
[2] H ZENG. Transport of amphipathic anions by human multidrug resistance protein 3.[J]. Cancer research, 2000, 60 17: 4779-4784.
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