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ChemicalBook--->CAS DataBase List--->64224-21-1

64224-21-1

64224-21-1 Structure

64224-21-1 Structure
IdentificationBack Directory
[Name]

OLTIPRAZ
[CAS]

64224-21-1
[Synonyms]

OLTIPRAZ
RP-35972
CCRIS 4048
NSC 347901
BRN 0978110
OLTIPRAZ USP/EP/BP
Oltipraz (RP 35972
Oltipraz (NSC-347901)
4-methyl-5-pyrazin-2-yldithiole-3-thione
4-methyl-5-pyrazin-2-yl-dithiole-3-thione
4-methyl-5-pyrazinyl-3h-2-dithiole-3-thione
4-methyl-5-pyrazinyl-3h-1,2-dithiole-3-thione
4-methyl-5-pyrazin-2-yl-1,2-dithiole-3-thione
4-Methyl-5-(2-pyrazinyl)-1,2-dithiole-3-thione
5-(2-pyrazinyl)-4-methyl-1,2-dithiole-3-thione
4-Methyl-5-(2-pyrazinyl)-3H-1,2-dithiole-3-thione
4-Methyl-5-(pyrazin-2-yl)-3H-1,2-dithiole-3-thione
3H-1,2-Dithiole-3-thione,4-methyl-5-(2-pyrazinyl)-
[EINECS(EC#)]

264-736-6
[Molecular Formula]

C8H6N2S3
[MDL Number]

MFCD00868499
[MOL File]

64224-21-1.mol
[Molecular Weight]

226.34
Chemical PropertiesBack Directory
[Melting point ]

165-166
[Boiling point ]

408.1±55.0 °C(Predicted)
[density ]

1.51±0.1 g/cm3(Predicted)
[RTECS ]

JP1293000
[storage temp. ]

2-8°C
[solubility ]

DMSO: >20mg/mL
[form ]

Solid
[pka]

0.18±0.10(Predicted)
[color ]

red
[Sensitive ]

Light Sensitive
[Stability:]

Stable for 2 years from date of purchase as supplied. Solutions in DMSO may be stored at -20° for up to 1 month.
[InChIKey]

CKNAQFVBEHDJQV-UHFFFAOYSA-N
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

26-36/37/39-36/37
[WGK Germany ]

3
Hazard InformationBack Directory
[Description]

Oltipraz (64224-21-1) upregulates the transcription factor NRF2 and prevents insulin resistance and obesity induced by high fat diet in C57BL/6J mice.1 Attenuates the progression of fibrosis in a rat model of nonalcoholic steatohepatitis.2 Oltipaz attenuates chronic hypoxia-induced cardiopulmonary alterations in mice.3 Promotes liver regeneration after partial hepatectomy.4 Off target effects: Activates constitutive androstane receptor (CAR).5
[Chemical Properties]

Dark Red Solid
[Uses]

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 detoxi fication enzymes, most notably glutathione-S-transferase (GST). Oltipraz is now known to be used for tumor prevention purposes.
[Uses]

schistosomicide, antineoplastic
[Definition]

ChEBI: A 1,2-dithiole that is 3H-1,2-dithiole-3-thione substituted at positions 4 and 5 by methyl and pyrazin-2-yl groups respectively.
[General Description]

Oltipraz, a dithiol derivative, is a member of dithiolethiones class of organosulfur compounds. It has anti-tumor, antioxidative, anti- inflammatory and radioprotective properties. It provides protection from numerous carcinogens. Oltipraz functions as a schistosomicide.
[Biochem/physiol Actions]

Oltipraz is an activator of Nrf2. Nrf2 (NF-E2-related factor 2) is a transcription factor that binds to antioxidant response elements (AREs) and activates these genes. Oltipraz activates Nrf2 and subsequently elevates expression of the detoxification genes encoding anti-oxidant and multidrug resistance-associated proteins to mediate its chemopreventive efficacy.
[Enzyme inhibitor]

This schistosomicide (FW = 226.35 g/mol; CAS 64224-21-1), also known as 5- (2-pyrazinyl) -4-methyl-1,2-dithiole-3-thione, is used to treat disease caused by parasitic flatworms and is also a potent cancer chemopreventive agent. Oltipraz was found to protect against chemically induced carcinogens within the lung, stomach, colon, and urinary bladder. The anti-HIV activity of the pharmaceutical is believed to be due to its ability to irreversibly inhibit HIV reverse transcriptase. Target (s) : CYP1A2 (1-3); CYP3A4; HIV I reverse transcriptase; RNA-directed DNA polymerase. 1. Sofowora, Choo, Mayo, Shyr & Wilkinson Cancer Chemother. Pharmaco
[storage]

Store at -20°C
[References]

1) Yu?et al. (2011),?Oltipraz upregulates the nuclear factor (erythroid-derived 2)-like 2 (NRF2) antioxidant system and prevents insulin resistance and obesity induced by a high-fat diet in C57BL/6J mice; Diabetologia,?54?922 2) Shimozono?et al. (2013),?Nrf2 activators attenuate the progression of nonalcoholic steatohepatitis-related fibrosis in a dietary rat model; Mol. Pharmacol,?84?62 3) Eba?et al. (2013),?The nuclear factor erythroid 2-related factor 2 activator oltipraz attenuates chronic hypoxia-induced cardiopulmonary alterations in mice; Am. J. Respir. Cell. Mol. Biol.,?49?324 4) Cho?et al. (2009), Oltipraz promotion of liver regeneration after partial hepatectomy: the role of PI3-kinase dependent C/EBPbeta and cyclin E regulation; Arch. Pharm. Res.,?32?625 5) Merrell?et al. (2008),?The Nrf2 activator oltipraz also activates the constitutive androstane receptor; Drug Metab. Dispos.,?36?1716
Spectrum DetailBack Directory
[Spectrum Detail]

OLTIPRAZ(64224-21-1)1HNMR
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