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Ezatiostat

CAS number:168682-53-9    molecular formula:C27H35N3O6S

overview

compound introduction

Information Ezatiostat Ezatiostat (TER199, TLK199, Telintra), a tripeptide analog of glutathione, is a peptidomimetic inhibitor of Glutathione S-transferase P1-1 (GSTP1-1) . Ezatiostat activates c-Jun NH2 terminal kinase (JNK1) and ERK1/ERK2 and induces apoptosis . Targets GSTP1-1 ; JNK1 ; ERK1/ERK2 In vitro Selection of a resistant clone of an HL60 tumor cell line through chronic exposure to Ezatiostat (TLK199) results in cells with elevated activities of c-Jun NH2 terminal kinase (JNK1) and ERK1/ERK2, and allows the cells to proliferate under stress conditions that induced high levels of apoptosis in the wild type cells. In vivo Ezatiostat (TLK199) stimulates both lymphocyte production and bone marrow progenitor (colony-forming unitgranulocyte macrophage) proliferation, but only in GST π +/+ and not in GST π -/- animals. Cell Research(from reference) Cell lines:Human myeloid leukemic cells (HL60) Concentrations:2.5 μM - 50 μM Incubation Time:8 h, 24 h

Specs

Chinese alias依扎替米沙坦
English aliasQ27095680 | NCGC00263221-01 | NCGC00263221-05 | TER 199 | Ezatiostat | Ezatiostat [INN] | Ezatiostat(TER199; TLK199) | SCHEMBL420400 | Glycine, L-gamma-glutamyl-S-(phenylmethyl)-L-cysteinyl-2-phenyl-, diethyl ester, (2R)- | J-690234 | TLK199 | TLK-199 | e
CAS number168682-53-9molecular formulaC27H35N3O6S
molecular weight529.65 g/molExact mass10mM in DMSO
PSA162.000 Ųlogp0.745

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