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Mitoquinone (MitoQ10) mesylate - 10mM in DMSO, high purity , CAS No.845959-50-4

    Grade & Purity:
  • 10mM in DMSO
In stock
Item Number
M426202
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M426202-1ml
1ml
Available within 8-12 weeks(?)
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$1,000.90

ROS Inhibitors

Basic Description

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 

Taxonomic Classification

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

Product Properties

ALogP 6.675
hba_count 4
Rotatable Bond 16

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

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=

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Chemical and Physical Properties

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

Solution Calculators

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