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Description: Oltipraz (RP 35972; NSC 347901), a potential anticancer agent, is a potent Nrf2 activator and an inducer of Phase II detoxification enzymes such as glutathione-S-transferase (GST). Oltipraz is a synthetic, substituted 1, 2-dithiole-3-thione originally used in humans as an antischistosomal agent. Oltipraz has been classified as a monofunctional inducer since it advantageously elevates Phase II detoxification enzymes, while only slightly altering the expression of the Phase I “activating” enzymes.
References: Proc Natl Acad Sci U S A. 2001 Mar 13; 98(6):3410-5; Mol Cancer Ther. 2009 Oct; 8(10):2791-802.
Chemical Name: 4-methyl-5-(pyrazin-2-yl)-3H-1, 2-dithiole-3-thione
InChi Key: CKNAQFVBEHDJQV-UHFFFAOYSA-N
InChi Code: InChI=1S/C8H6N2S3/c1-5-7(12-13-8(5)11)6-4-9-2-3-10-6/h2-4H, 1H3
SMILES Code: S=C1SSC(C2=NC=CN=C2)=C1C
CD-1400; CD1400; CD 1400
Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.
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