Powder: -20°C for 3 years | In solvent: -80°C for 1 year
Amifostine thiol (WR-1065), the active metabolite of cytoprotector Amifostine, serves as a cytoprotective agent possessing radioprotective properties. It activates p53 via a JNK-dependent signaling pathway[1][2][3].
Pack Size | Availability | Price/USD | Quantity |
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2 mg | 5 days | $ 58.00 |
Description | Amifostine thiol (WR-1065), the active metabolite of cytoprotector Amifostine, serves as a cytoprotective agent possessing radioprotective properties. It activates p53 via a JNK-dependent signaling pathway[1][2][3]. |
In vitro | Amifostine thiol mitigates both immediate and delayed adverse effects of radiation exposure across a range of linear energy transfer (LET) levels, including DNA damage and G1-phase arrest[1]. It provides protection to RKO36 cells against chromosomal damage and death caused by ionizing radiation, also safeguarding these cells from delayed genomic instability when administered at a concentration of 4 mM for 30 minutes[1]. While cytotoxic to RKO36 cells at millimolar concentrations, particularly with continuous exposure[1], at 40 μM, it effectively prevents delayed genomic instability, albeit without guarding against immediate chromosomal damage or cell death[1]. Additionally, amifostine thiol activates JNK, which leads to p53 phosphorylation at threonine 81[2], and alters phosphorylation of topoisomerase IIα, influencing its activity and affecting cell cycle progression in CHO AA8 cells[3]. |
Molecular Weight | 134.24 |
Formula | C5H14N2S |
CAS No. | 31098-42-7 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
H2O: 250 mg/mL (1862.34 mM)
DMSO: < 1 mg/mL (insoluble or slightly Soluble)
You can also refer to dose conversion for different animals. More
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Amifostine thiol 31098-42-7 inhibitor inhibit