PR-104A (Synonyms: SN 27858) |
| Catalog No.GC62490 |
Le PR-104A (SN 27858) est le métabolite alcoolique du promédicament phosphate PR-104. Le PR-104A est un agent de réticulation de l'ADN/un agent endommageant l'ADN et une cytotoxine. Activité antitumorale. Le PR-104A est métabolisé sous hypoxie par le NADPH À 1 électron:cytochrome P450 oxydoréductase. Le PR-104A peut être utilisé pour la recherche sur la leucémie aiguë lymphoblastique de la lignée T récidivante/réfractaire (T-ALL).
Products are for research use only. Not for human use. We do not sell to patients.
Cas No.: 680199-06-8
Sample solution is provided at 25 µL, 10mM.
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PR-104A (SN 27858) is the alcohol metabolite of phosphate prodrug PR-104. PR-104A is a hypoxia-selective DNA cross-linking agent/DNA-damaging agent and cytotoxin. Antitumor Activity[1]. PR-104A is metabolized under hypoxia by the 1-electron NADPH:cytochrome P450 oxidoreductase. PR-104A can be used for the research of relapsed/refractory T-lineage acute lymphoblastic leukemia (T-ALL)[2].
PR-104A (1-100 uM) shows antiproliferative potency in a panel of 10 human carcinoma cell lines following 4 hours exposures under aerobic and hypoxic conditions with the lowest IC50 (0.51 μM) in H460 non-small cell lung cancer cells and highest (7.3 μM) in PC3 prostate cells[1].
The phosphate ester "pre-prodrug" PR-104 is well tolerated in mice and converted rapidly to the corresponding prodrug PR-104A. H460 xenografts shows significant sensitivity to PR-104 (total dose 3.2 mmol/kg)[1].
[1]. Adam V Patterson, et al. Mechanism of action and preclinical antitumor activity of the novel hypoxia-activated DNA cross-linking agent PR-104. Clin Cancer Res. 2007 Jul 1;13(13):3922-32.
[2]. Donya Moradi Manesh, et al. AKR1C3 is a biomarker of sensitivity to PR-104 in preclinical models of T-cell acute lymphoblastic leukemia. Blood. 2015 Sep 3;126(10):1193-202.
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