Dimethoxycurcumin-d6
Dimethoxycurcumin-d6 (DiMC-d6; CHC 004-d6; Di-O-methylcurcumin-d6) is the deuterated-labeled Dimethoxycurcumin (HY-100977). Dimethoxycurcumin (DiMC) is a curcuminoid compound found in Curcuma longa. Dimethoxycurcumin is also an orally active thioredoxin reductase inhibitor (IC50 = 5.4 μM) and androgen receptor antagonist. Dimethoxycurcumin inhibits thioredoxin reductase, leading to oxidized thioredoxin accumulation, ROS production, DNA damage, glutathione depletion, mitochondrial membrane potential decrease, ATP depletion, S phase arrest, and apoptosis. Dimethoxycurcumin inhibits NF-κB, NADPH oxidase subunits, ATP synthase subunits, CDK4, cyclin-D1, FASN, ACC, and the IRS2-PI3K-Akt pathway, while activating AMPK, ERK, and JNK. Dimethoxycurcumin can be used for research on cancer, arsenic-induced hepatotoxicity, and tuberculosis.
For research use only. We do not sell to patients.
- CAS No.: 3006902-95-7
- Formula: C23H18D6O6
- Molecular Weight:402.47
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
All AMPK Isoforms
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Biological Activity
Description
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thioredoxin reductase 5.4 μM (IC50) |
Androgen receptor |
NF-κB |
CDK4 |
cyclin-D1 |
FASN |
ACC |
IRS2 |
PI3K |
Akt |
AMPK |
ERK |
JNK |
Application
1. This compound can be used as a tracer
2. This compound can be used as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS.
Chemical Information
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CAS No. 3006902-95-7
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Unlabeled CAS 160096-59-3
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Molecular Weight 402.47
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Formula C23H18D6O6
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SMILES
COC1=C(C=CC(/C=C/C(CC(/C=C/C2=CC(OC)=C(C=C2)OC([2H])([2H])[2H])=O)=O)=C1)OC([2H])([2H])[2H]
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Synonyms
DiMC-d6; CHC 004-d6; Di-O-methylcurcumin-d6
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
Purity & Documentation
References
[4]. Patwardhan RS, et al. Dimethoxycurcumin, a metabolically stable analogue of curcumin, exhibits anti-inflammatory activities in murine and human lymphocytes. Biochemical pharmacology. 2011 Sep 15;82(6):642-57. [Content Brief]
[8]. Yoon MJ, et al. Stronger proteasomal inhibition and higher CHOP induction are responsible for more effective induction of paraptosis by dimethoxycurcumin than curcumin. Cell death & disease. 2014 Mar 13;5(3):e1112. [Content Brief]
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
Keywords
- Dimethoxycurcumin-d6
- 3006902-95-7
- DiMC-d6
- CHC 004-d6
- Di-O-methylcurcumin-d6
- Isotope-Labeled Compounds
- Androgen Receptor
- Reactive Oxygen Species (ROS)
- Apoptosis
- NF-κB
- CDK
- Fatty Acid Synthase (FASN)
- Acetyl-CoA Carboxylase
- PI3K
- Akt
- AMPK
- ERK
- JNK
- HCT116
- androgen receptor
- 786-O
- Curcuma longa
- Mycobacterium tuberculosis H37Ra
- A549
- RAW264.7
- thioredoxin reductase
- MCF7
- MDA-MB 435S
- Inhibitor
- inhibitor
- inhibit