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| Product | Description | |
|---|---|---|
| Oltipraz | ?98% (HPLC), powder. Group: Fluorescence/luminescence spectroscopy. |  |
| Oltipraz | Oltipraz, a promising cancer chemopreventive agent, is a bifunctional inducer, modulating both phase I and II drug-metabolizing enzymes to enhance carcinogen detoxification. Uses: Anticarcinogenic agents. Synonyms: CD1400; CD 1400; CD-1400. Grades: >98%. CAS No. 64224-21-1. Molecular formula: C8H6N2S3. Mole weight: 226.33. |  |
| Oltipraz | Oltipraz has an inhibitory effect on HIF-1α activation in a time-dependent manner, completely abrogating HIF-1α induction at ≥10 μM concentrations, the IC 50 of Oltipraz for HIF-1α inhibition is 10 μM. Oltipraz is a potent Nrf2 activator. Uses: Scientific research. Group: Signaling pathways. Alternative Names: RP 35972; NSC 347901. CAS No. 64224-21-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg; 200 mg; 500 mg. Product ID: HY-12519. |  |
| Oltipraz | Oltipraz is a synthetic, substituted 1,2-dithiole-3-thione previously used in humans as an antischistosomal agent. Animal studies have demonstrated that oltipraz is a potent inducer of Phase II detoxification enzymes, most notably glutathione-S-transferase (GST). Oltipraz is now known to be used for tumor prevention purposes. Group: Biochemicals. Alternative Names: 4-Methyl-5-pyrazinyl-3H-1,2-dithiole-3-thione; NSC 347901; RP 35972. Grades: Highly Purified. CAS No. 64224-21-1. Pack Sizes: 25mg. US Biological Life Sciences. |  Worldwide |
| Oltipraz metabolite M2 | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
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