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| SKU | Size | Availability |
Price | Qty |
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M426202-1ml
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1ml |
Available within 8-12 weeks(?)
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$1,000.90
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ROS Inhibitors
| Synonyms | Mitoquinone mesylate | 845959-50-4 | Mitoquinone methanesulfonate | MitoQ | Mitoquinone (mesylate) | UNII-6E01CG547T | 6E01CG547T | Phosphonium, (10-(4,5-dimethoxy-2-methyl-3,6-dioxo-1,4-cyclohexadien-1-yl)decyl)triphenyl-, methanesulfonate (1:1) | 10-(4,5-dimethoxy-2-me |
|---|---|
| Specifications & Purity | 10mM in DMSO |
| Biochemical and Physiological Mechanisms | Mitoquinone mesylate (MitoQ, MitoQ10, Mitoubiquinone) is a TPP-based, mitochondria-targeted antioxidant that blocks H2O2-induced intracellular ROS responses and protects against oxidative damage. This product is a waxy solid. |
| Storage Temp | Store at -80°C |
| Shipped In |
Ice chest + Ice pads This product requires cold chain shipping. Ground and other economy services are not available. |
| Product Description |
Information Mitoquinone (MitoQ10) mesylate Mitoquinone mesylate (MitoQ, MitoQ10, Mitoubiquinone) is a TPP-based, mitochondria -targeted antioxidant that blocks H 2 O 2 -induced intracellular ROS responses and protects against oxidative damage. This product is a waxy solid. Targets mitochondria ; ROS In vitro Mitoquinone blocks H2O2-induced intracellular ROS responses inmurine pancreatic acinar cells. Mitoquinone does not reduce mitochondrial depolarisation induced by either cholecystokinin (CCK) or bile acid TLCS. Mitoquinone increases basal and CCK-induced cell death in a plate-reader assay. In vivo In a TLCS-induced AP model Mitoquinone treatment is not protective. In AP induced by caerulein hyperstimulation (CER-AP), Mitoquinone exerts mixed effects. Thus, partial amelioration of histopathology scores is observed but without reduction of the biochemical markers pancreatic trypsin or serumamylase. Lungmyeloperoxidase and interleukin-6 are concurrently increased by Mitoquinone in CER-AP. Mitoquinone causes biphasic effects on ROS production in isolated polymorphonuclear leukocytes, inhibiting an acute increase but elevating later levels. Cell Research(from reference) Cell lines:Pancreatic Acinar Cells Concentrations:1 μM, 10 μM Incubation Time:200 s, 400 s, 600 s, 800 s, 1000 s |
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 | P-benzoquinones Phenylphosphines and derivatives Vinylogous esters Sulfonyls Organosulfonic acids Alkanesulfonic acids Organophosphorus compounds Organic oxides Hydrocarbon derivatives Organic cations |
| Molecular Framework | Not available |
| Substituents | Triphenylphosphine - Ubiquinone skeleton - P-benzoquinone - Quinone - Phenylphosphine - Monocyclic benzene moiety - Benzenoid - Vinylogous ester - Alkanesulfonic acid - Sulfonyl - Organosulfonic acid - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Ketone - Cyclic ketone - Organic oxygen compound - Carbonyl group - Hydrocarbon derivative - Organosulfur compound - Organophosphorus compound - Organooxygen compound - Organic oxide - Organic cation - Aromatic 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 | Not available |
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| ALogP | 6.675 |
|---|---|
| hba_count | 4 |
| Rotatable Bond | 16 |
| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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| IUPAC Name | 10-(4,5-dimethoxy-2-methyl-3,6-dioxocyclohexa-1,4-dien-1-yl)decyl-triphenylphosphanium;methanesulfonate |
|---|---|
| INCHI | InChI=1S/C37H44O4P.CH4O3S/c1-29-33(35(39)37(41-3)36(40-2)34(29)38)27-19-8-6-4-5-7-9-20-28-42(30-21-13-10-14-22-30,31-23-15-11-16-24-31)32-25-17-12-18-26-32;1-5(2,3)4/h10-18,21-26H,4-9,19-20,27-28H2,1-3H3;1H3,(H,2,3,4)/q+1;/p-1 |
| InChIKey | GVZFUVXPTPGOQT-UHFFFAOYSA-M |
| Smiles | CC1=C(C(=O)C(=C(C1=O)OC)OC)CCCCCCCCCC[P+](C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4.CS(=O)(=O)[O-] |
| Isomeric SMILES | CC1=C(C(=O)C(=C(C1=O)OC)OC)CCCCCCCCCC[P+](C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4.CS(=O)(=O)[O-] |
| Molecular Weight | 678.81 |
| Reaxy-Rn | 12274395 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=12274395&ln= |
| Molecular Weight | 678.800 g/mol |
|---|---|
| XLogP3 | |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 7 |
| Rotatable Bond Count | 16 |
| Exact Mass | 678.278 Da |
| Monoisotopic Mass | 678.278 Da |
| Topological Polar Surface Area | 118.000 Ų |
| Heavy Atom Count | 47 |
| Formal Charge | 0 |
| Complexity | 965.000 |
| 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 | 2 |