Determine the necessary mass, volume, or concentration for preparing a solution.
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| SKU | Size | Availability |
Price | Qty |
|---|---|---|---|---|
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I129330-250mg
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250mg |
3
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$48.90
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I129330-1g
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1g |
4
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$96.90
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I129330-5g
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5g |
2
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$164.90
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I129330-25g
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25g |
2
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$494.90
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I129330-100g
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100g |
2
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$1,479.90
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Potent antioxidant and neuroprotective agent
| Synonyms | BRN 2001459 | IDEBENONE [MART.] | FR114 | Idebenone, >=98% (HPLC) | 2-(10-Hydroxydecyl)-5,6-dimethoxy-3-methyl-1,4-benzoquinone | 6-(10-Hydroxydecyl)-2,3-dimethoxy-5-methyl-1,4-benzoquinone | HB6PN45W4J | Pharmakon1600-01505755 | SR-01000759378 | Idebenon |
|---|---|
| Specifications & Purity | ≥98% |
| Biochemical and Physiological Mechanisms | Idebenone, a neuroprotective agent, has been shown to act as a free radical scavenger and protect mitochondrial membranes against lipid peroxidation. This compound has also been found to prevent platelet aggregation and recover cholinergic and monoaminerg |
| Shipped In | Normal |
| Mechanism of action | Antioxidant and mitochondrial electron carrier |
| Note | Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details. |
| Product Description |
Idebenone is a synthetic analog of coenzyme Q10 (CoQ10) and a brain stimulant. application: Idebenone has been used:to treat mutant myocilin (mMYOC) cells for drug treatment assay,to validate C2C12 secondary cell screening assay to treat obese mice, to test whether idebenone and CoQ10 bind directly to peroxisome proliferator-activated receptor (PPAR)LBDs, His-tagged PPARα, δ and γ LBDs |
Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Lipids and lipid-like molecules |
| Class | Prenol lipids |
| Subclass | Quinone and hydroquinone lipids |
| Intermediate Tree Nodes | Prenylquinones |
| Direct Parent | Ubiquinones |
| Alternative Parents | Fatty alcohols P-benzoquinones Vinylogous esters Primary alcohols Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aliphatic homomonocyclic compounds |
| Substituents | Ubiquinone skeleton - Fatty alcohol - P-benzoquinone - Quinone - Fatty acyl - Vinylogous ester - Cyclic ketone - Ketone - Alcohol - Hydrocarbon derivative - Primary alcohol - Organic oxide - Organooxygen compound - Organic oxygen compound - Carbonyl group - Aliphatic homomonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as ubiquinones. These are coenzyme Q derivatives containing a 5, 6-dimethoxy-3-methyl(1,4-benzoquinone) moiety to which an isoprenyl group is attached at ring position 2(or 6). |
| External Descriptors | primary alcohol - benzoquinones |
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| ALogP | 4.3 |
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| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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| Pubchem Sid | 488179783 |
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| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488179783 |
| IUPAC Name | 2-(10-hydroxydecyl)-5,6-dimethoxy-3-methylcyclohexa-2,5-diene-1,4-dione |
| INCHI | InChI=1S/C19H30O5/c1-14-15(12-10-8-6-4-5-7-9-11-13-20)17(22)19(24-3)18(23-2)16(14)21/h20H,4-13H2,1-3H3 |
| InChIKey | JGPMMRGNQUBGND-UHFFFAOYSA-N |
| Smiles | CC1=C(C(=O)C(=C(C1=O)OC)OC)CCCCCCCCCCO |
| Isomeric SMILES | CC1=C(C(=O)C(=C(C1=O)OC)OC)CCCCCCCCCCO |
| RTECS | GU5290000 |
| Molecular Weight | 338.44 |
| Reaxy-Rn | 2001459 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2001459&ln= |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
| Certificate of Analysis | Jan 09, 2025 | I129330 | |
| Certificate of Analysis | Jan 09, 2025 | I129330 | |
| Certificate of Analysis | Aug 02, 2024 | I129330 | |
| Certificate of Analysis | Aug 02, 2024 | I129330 | |
| Certificate of Analysis | Aug 02, 2024 | I129330 | |
| Certificate of Analysis | Aug 02, 2024 | I129330 | |
| Certificate of Analysis | Jun 27, 2024 | I129330 | |
| Certificate of Analysis | Sep 21, 2023 | I129330 | |
| Certificate of Analysis | Sep 21, 2023 | I129330 | |
| Certificate of Analysis | Sep 21, 2023 | I129330 | |
| Certificate of Analysis | Sep 21, 2023 | I129330 | |
| Certificate of Analysis | Sep 14, 2023 | I129330 | |
| Certificate of Analysis | Mar 10, 2023 | I129330 | |
| Certificate of Analysis | Oct 14, 2022 | I129330 |
| Solubility | Soluble in DMSO (>25 mg/ml), ethanol (>25 mg/ml), methanol, and chloroform. Insoluble in water. |
|---|---|
| Melt Point(°C) | 53℃ |
| Molecular Weight | 338.400 g/mol |
| XLogP3 | 4.300 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 12 |
| Exact Mass | 338.209 Da |
| Monoisotopic Mass | 338.209 Da |
| Topological Polar Surface Area | 72.800 Ų |
| Heavy Atom Count | 24 |
| Formal Charge | 0 |
| Complexity | 502.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
Starting at $45.90
| 1. Zhiwen Li, Zhilin Zhou, Jianghua Wang, Tingxian Tao, Yingqiang Fu. (2023) Aggregation-induced emission enhancement N, S-CQDs for selective detection of CIP in the environment. NANOTECHNOLOGY, 34 (39): (395503). |
| 2. Xiao Tu, Jiaxin Hu, Jinghao Peng, Qihan Chen, Yangle Zhao, Zemao Gu. (2025) Discovery of thymoquinone analogues with high anthelmintic activity against monogenean infections in goldfish (Carassius auratus). VETERINARY PARASITOLOGY, 334 (110401). |
| 3. Haiyan Zhu, Yijing Yang, Yenan Duan, Xin Zheng, Zixiong Lin, Jie Zhou. (2024) Nrf2/FSP1/CoQ10 axis-mediated ferroptosis is involved in sodium aescinate-induced nephrotoxicity. ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 759 (110100). |