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Mivotilate

Names

[ CAS No. ]:
130112-42-4

[ Name ]:
Mivotilate

[Synonym ]:
propan-2-yl 2-(1,3-dithietan-2-ylidene)-3-[(4-methyl-1,3-thiazol-2-yl)amino]-3-oxopropanoate
Mivotilate

Biological Activity

[Description]:

Mivotilate is a nontoxic, potent activator of the aryl hydrocarbon receptor (AhR), and acts as a hepatoprotective agent.

[Related Catalog]:

Signaling Pathways >> Immunology/Inflammation >> Aryl Hydrocarbon Receptor
Research Areas >> Others

[Target]

Aryl hydrocarbon receptor[1]


[In Vitro]

Mivotilate is a nontoxic, potent activator of the aryl hydrocarbon receptor. Mivotilate (YH439) has a novel activation mode that tolerates mutation of histidine 285 to tyrosine[1]. Mivotilate induces cytochromes P4501A1/2 (CYP1A1/2) through the aryl hydrocarbon (Ah) receptor[3].

[In Vivo]

Mivotilate (YH439, 150 mg/kg, p.o.) reduces CYP2E1-mediated NDMA demethylase activity in rats, but shows no obvious effect on NADPH-dependent P450 oxidoreductase activity. Mivotilate (75-300 mg/kg) rapidly decreases immunoreactive CYP2E1 protein. Mivotilate (150 mg/kg, p.o.) inhibits the transcription of CYP2E1 in rats[2].

[Animal admin]

Male outbred Sprague-Dawley rats (weighing 100-150 g) are kept on a 12-h light-dark cycle with NIH 31 autoclavable rat die and water ad libitum. After a single oral administration of Mivotilate (75, 150, and 300 mg/kg body wt, diluted in corn oil), the animals are sacrificed at different times as indicated. Livers from control (corn oil-treated), starved (2 days) and Mivotilate-treated animals (n = 5 per group) are immediately excised, freeze-clamped, and processed further. Another group of rats (n = 3) is treated with phenobarbital (100 mg/kg/day) by intraperitoneal injection for 2 days and sacrificed 24 h after the last dose[2].

[References]

[1]. Whelan F, et al. Amino acid substitutions in the aryl hydrocarbon receptor ligand binding domain reveal YH439 as an atypical AhR activator. Mol Pharmacol. 2010 Jun;77(6):1037-46.

[2]. Jeong KS, et al. Transcriptional inhibition of cytochrome P4502E1 by a synthetic compound, YH439. Arch Biochem Biophys. 1996 Feb 1;326(1):137-44.

[3]. Lee IJ, et al. Transcriptional induction of the cytochrome P4501A1 gene by a thiazolium compound, YH439. Mol Pharmacol. 1996 Jun;49(6):980-8.


[Related Small Molecules]

Pifithrin-α hydrobromide | StemRegenin 1 (SR1) | FICZ | L-Kynurenine | ITE | Diosmin | PDM 2 | Indole-3-carbinol | 1,4-Chrysenequinone | CAY 10465 | Benvitimod (Tapinarof)

Chemical & Physical Properties

[ Density]:
1.467g/cm3

[ Molecular Formula ]:
C12H14N2O3S3

[ Molecular Weight ]:
330.44600

[ Exact Mass ]:
330.01700

[ PSA ]:
147.13000

[ LogP ]:
3.06370

[ Index of Refraction ]:
1.68

[ Storage condition ]:
2-8℃

MSDS

Safety Information

[ RIDADR ]:
NONH for all modes of transport

Articles

Identification of residues in the N-terminal PAS domains important for dimerization of Arnt and AhR.

Nucleic Acids Res. 39 , 3695-709, (2011)

The basic helix-loop-helix (bHLH).PAS dimeric transcription factors have crucial roles in development, stress response, oxygen homeostasis and neurogenesis. Their target gene specificity depends in pa...


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Related Compounds

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