Results 281 to 290 of about 103,462 (335)

BPM31510 Increases the CoQ Pool in Chemically Induced CoQ-Deficient Cells, CoQ-Deficient Patient Fibroblasts, and in Metabolically Active Murine Tissues. [PDF]

FASEB J
Aristizabal-Henao JJ, Wessel SR, Stopka SA, Karmacharya S, Van Cura D, Pesini A, Nickerson KR, Grover K, Zavidij O, Ravi A, Mota AL, Rosen KM, Nastke MD, Cox MK, Narain NR, Modur V, Quinzii CM, Gesta S, Kiebish MA.   +18 more
europepmc   +1 more source

Advances in cardiovascular supplementation: mechanisms, efficacy, and clinical perspectives. [PDF]

Front Mol Biosci
Wu X, Fang T.
europepmc   +1 more source

Effects Of Exogenous Coenzyme Q 10 And Zinc Supplementation On Performance and Muscular Injury In Young Amateur Boxers

, 2019
Çiğdem Karakükçü, Yahya Polat, Yasemin Altuner Torun, Adile Ortaköylüoğlu, Yavuz Katırcılar   +4 more
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Cellular factories for coenzyme Q(10) production

Cellular factories for coenzyme Q(10) production
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Coenzyme Q ₄ is a functional substitute for coenzyme Q ₁₀ and can be targeted to the mitochondria

2023
ABSTRACT Coenzyme Q 10 (CoQ 10 ) is an important cofactor and antioxidant for numerous cellular processes, and its deficiency has been linked to human disorders including mitochondrial disease, heart failure, Parkinson’s disease, and hypertension.
Laura H. Steenberge, Andrew Y. Sung, Jing Fan, David J. Pagliarini   +3 more
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Coenzyme Q. XXIV. On the significance of coenzyme Q 10 in human tissues

Archives of Biochemistry and Biophysics, 1961
Abstract Several organs and tissues of three humans have been examined for coenzyme Q content. The liver, heart, spleen, kidney, pancreas, and adrenals contain relatively high concentrations of coenzyme Q 10, indicating that studies of the functional relationship of coenzyme Q to diseases involving any of these organs might be important.
P H, GALE, F R, KONIUSZY, A C, PAGE, K, FOLKERS, H, SIEGEL   +4 more
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Synthesis of Coenzyme Q₁₀

European Journal of Organic Chemistry, 2012
AbstractA practical synthesis of coenzyme Q10 has been developed. The route features an improved Friedel–Crafts allylation of tetramethoxytoluene with a para‐chlorobenzenesulfonyl‐substituted C5 allylic chloride at 40 °C. Replacement of the methyl ether protecting groups of the para‐hydroquinone by methoxymethyl groups at Q1 stage proceeded efficiently,
Eun‐Taek Oh, Hee Jin Kim, Jung Taek Oh, Liang Su, Inkyun Yun, Kyunggu Nam, Jae‐Hong Min, Joon Woo Kim, Sangho Koo   +8 more
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