Chemical compound
Pharmaceutical compound
Mitoquinone mesylate Trade names MitoQ
10-(4,5-dimethoxy-2-methyl-3,6-dioxocyclohexa-1,4-dien-1-yl)decyl-triphenylphosphanium methanesulfonate
CAS Number PubChem CID ChemSpider UNII ChEMBL CompTox Dashboard (EPA ) Formula C 38 H 47 O 7 P S Molar mass 678.82 g·mol−1 3D model (JSmol )
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-]
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
Key:GVZFUVXPTPGOQT-UHFFFAOYSA-M
Mitoquinone mesylate (MitoQ ) is a synthetic analogue of coenzyme Q10 which has antioxidant effects. It was first developed in New Zealand in the late 1990s.[ 1] It has significantly improved bioavailability and improved mitochondrial penetration compared to coenzyme Q10,[ 2] [ 3] and has shown potential in a number of medical indications,[ 4] [ 5] [ 6] [ 7] being widely sold as a dietary supplement .[ 8] [ 9]
A 2014 review found insufficient evidence for the use of mitoquinone mesylate in Parkinson's disease and other movement disorders.[ 10]
See also
References
^ US abandoned 20060229278 , Taylor K, Smith R, "Mitoquinone derivatives used as mitochondrially targeted antioxidants.", published 12 October 2006, assigned to Antipodean Pharmaceuticals Inc
^ Battogtokh G, Choi YS, Kang DS, Park SJ, Shim MS, Huh KM, et al. (October 2018). "Mitochondria-targeting drug conjugates for cytotoxic, anti-oxidizing and sensing purposes: current strategies and future perspectives" . Acta Pharmaceutica Sinica B . 8 (6): 862– 880. doi :10.1016/j.apsb.2018.05.006 . PMC 6251809 . PMID 30505656 .
^ Gutierrez-Mariscal FM, Arenas-de Larriva AP, Limia-Perez L, Romero-Cabrera JL, Yubero-Serrano EM, López-Miranda J (October 2020). "Coenzyme Q10 Supplementation for the Reduction of Oxidative Stress: Clinical Implications in the Treatment of Chronic Diseases" . International Journal of Molecular Sciences . 21 (21): 7870. doi :10.3390/ijms21217870 . PMC 7660335 . PMID 33114148 .
^ Silva FS, Simoes RF, Couto R, Oliveira PJ (2016). "Targeting Mitochondria in Cardiovascular Diseases". Current Pharmaceutical Design . 22 (37): 5698– 5717. doi :10.2174/1381612822666160822150243 . PMID 27549376 .
^ Kezic A, Spasojevic I, Lezaic V, Bajcetic M (2016). "Mitochondria-Targeted Antioxidants: Future Perspectives in Kidney Ischemia Reperfusion Injury" . Oxidative Medicine and Cellular Longevity . 2016 : 2950503. doi :10.1155/2016/2950503 . PMC 4894993 . PMID 27313826 .
^ Oliver DM, Reddy PH (April 2019). "Small molecules as therapeutic drugs for Alzheimer's disease" . Molecular and Cellular Neurosciences . 96 : 47– 62. doi :10.1016/j.mcn.2019.03.001 . PMC 6510253 . PMID 30877034 .
^ Ismail H, Shakkour Z, Tabet M, Abdelhady S, Kobaisi A, Abedi R, et al. (October 2020). "Traumatic Brain Injury: Oxidative Stress and Novel Anti-Oxidants Such as Mitoquinone and Edaravone" . Antioxidants . 9 (10): 943. doi :10.3390/antiox9100943 . PMC 7601591 . PMID 33019512 .
^ Braakhuis AJ, Nagulan R, Somerville V (2018). "The Effect of MitoQ on Aging-Related Biomarkers: A Systematic Review and Meta-Analysis" . Oxidative Medicine and Cellular Longevity . 2018 : 8575263. doi :10.1155/2018/8575263 . PMC 6079400 . PMID 30116495 .
^
^ Liu J, Wang LN (January 2014). "Mitochondrial enhancement for neurodegenerative movement disorders: a systematic review of trials involving creatine, coenzyme Q10, idebenone and mitoquinone". CNS Drugs . 28 (1): 63– 8. doi :10.1007/s40263-013-0124-4 . PMID 24242074 . S2CID 207486107 .
Food antioxidants Fuel antioxidants Measurements
Information related to Mitoquinone mesylate