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About This Item
Empirical Formula (Hill Notation):
C27H35N3O6S
CAS Number:
Molecular Weight:
529.65
UNSPSC Code:
12352200
NACRES:
NA.77
Assay:
≥98% (HPLC)
Form:
powder
Quality Segment
assay
≥98% (HPLC)
form
powder
color
white to beige
solubility
DMSO: 5 mg/mL, clear (warmed)
storage temp.
2-8°C
SMILES string
S(C[C@H](NC(=O)CC[C@H](N)C(=O)OCC)C(=O)N[C@H](c2ccccc2)C(=O)OCC)Cc1ccccc1
InChI
1S/C27H35N3O6S/c1-3-35-26(33)21(28)15-16-23(31)29-22(18-37-17-19-11-7-5-8-12-19)25(32)30-24(27(34)36-4-2)20-13-9-6-10-14-20/h5-14,21-22,24H,3-4,15-18,28H2,1-2H3,(H,29,31)(H,30,32)/t21-,22-,24+/m0/s1
InChI key
GWEJFLVSOGNLSS-WPFOTENUSA-N
Application
Ezatiostat has been used as glutathione S-transferase P1 (GSTP1) inhibitor:
- to study its effects on peroxiredoxin 6 (PRDX6) inhibition in neonatal rat testicular gonocytes
- for the incubation of bronchial epithelial cells in proteolysis assay
- to study its effects on the cystine-glutamate antiporter xCT (SLC7A11) expression in tumor cells
Biochem/physiol Actions
Ezatiostat is an inhibitor of glutathione S-transferase P1-1 (GSTP1-1) with hematopoiesis-stimulating activity.
Ezatiostat is an inhibitor of glutathione S-transferase P1-1 (GSTP1-1) with hematopoiesis-stimulating activity. After intracellular de-esterification, the active form of ezatiostat binds to and inhibits GST P1-1, leading to activation of Jun kinase (JNK), a key regulator of cellular growth and differentiation of blood precursor cells, thereby restoring JNK and MAPK pathway activities and promoting MAPK-mediated cellular proliferation and differentiation. Ezatiostat promotes the proliferation and maturation of hematopoietic precursor cells, granulocytes, monocytes, erythrocytes and platelets. Ezatiostat has recently been given orphan drug designation for it for the treatment of myelodysplastic syndrome.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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