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SYS · ONLINEPASS · 63.0%
Open Assay
Independent Testing / Est. 2026
BATCH04·26·B
PASS63.0%
N27
PeptidesLongevity, MetabolicCoenzyme Q10 (injectable)

Coenzyme Q10 (injectable)

/ Coenzyme Q10 (ubiquinone); injectable research-grade preparation; mitochondrial electron transport cofactor
TIER 2 · TranslationalN = 0 · TESTING PENDINGMW 863.34 g·mol⁻¹

ALIAS · CoQ10 (injectable) · Ubiquinone · Coenzyme Q10

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Research use onlyAny dose figures below describe what specific cited studies used, reported factually. Nothing on this page is guidance for human use.READ FIRST →

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§ A · Identity
Primary sequence— sequence not captured —
MW · 863.34CLASS · Coenzyme Q10 (ubiquinone); injectable research-grade preparation; mitochondrial electron transport cofactorCATEGORY · Longevity, Metabolic

Tier 2. Small-to-moderate randomised trials of oral CoQ10 in heart failure (Q-SYMBIO), cardiac surgery preconditioning, and statin-associated myalgia. Injectable research-grade preparations sit outside FDA-approved channels in the US; oral ubiquinone and ubiquinol formulations are sold as dietary supplements and have generated most of the human evidence base.

§ B · Mechanism of action

Coenzyme Q10 (ubiquinone, 2,3-dimethoxy-5-methyl-6-decaprenyl-1,4-benzoquinone) is a lipid-soluble redox-active quinone that shuttles electrons from complexes I and II to complex III in the inner mitochondrial membrane electron transport chain. The reduced ubiquinol form additionally functions as an endogenous lipid-phase antioxidant, regenerating alpha-tocopherol from the tocopheroxyl radical and protecting membrane phospholipids from peroxidation.

Endogenous biosynthesis declines with age and is suppressed by HMG-CoA reductase inhibition, providing the mechanistic rationale for the statin-associated myalgia literature. Plasma CoQ10 rises with oral supplementation but tissue partitioning to mitochondria-rich organs (myocardium, skeletal muscle, brain) is limited and formulation-dependent; the ubiquinol form and lipid-emulsified preparations show higher relative bioavailability than crystalline ubiquinone in pharmacokinetic comparisons.

§ C · Human clinical evidence

Tier 2. The Q-SYMBIO trial (Mortensen and colleagues, JACC Heart Failure 2014) randomised 420 participants with chronic heart failure (NYHA III-IV) to CoQ10 100 mg three times daily or placebo for two years and reported reductions in the composite endpoint of major adverse cardiovascular events. Cardiac-surgery preconditioning trials (Rosenfeldt and colleagues 2007) reported myocardial recovery improvements. Multiple smaller trials in statin-associated myalgia have produced mixed results.

§ D · Primary literature
PubMed25282031Mortensen SA et al.The effect of coenzyme Q10 on morbidity and mortality in chronic heart failure: results from Q-SYMBIO: a randomized double-blind trial · JACC. Heart Failure · human-phase-3-rctCoQ10 100 mg three times daily for two years reduced the composite of unplanned hospitalisation for heart failure or cardiovascular death versus placebo in NYHA III-IV chronic heart failure.Limitations: Single trial; modest sample size for a hard-endpoint study; not independently replicated at scale.2014
§ F · Safety signal

Generally well-tolerated across decades of supplement use. Reported adverse events at oral doses up to 600 mg/day include mild gastrointestinal upset, headache, and rash. CoQ10 may reduce warfarin anticoagulation through structural similarity to vitamin K2; monitoring INR is recommended in concurrent use. Injectable research-grade preparations carry the additional concerns inherent to any non-approved parenteral product (sterility, endotoxin, identity, purity).

§ H · Regulatory status

Regulatory status

FDA status:
Not FDA-approved
§ I · Notable gaps and controversies

The injectable framing is largely a research-vendor presentation; the published clinical literature is predominantly oral. Tissue penetration of CoQ10 to mitochondria-rich organs is a longstanding pharmacokinetic concern and has driven development of mitochondrially-targeted analogs (MitoQ, idebenone) that are pharmacologically distinct from native ubiquinone. Q-SYMBIO has not been independently replicated at the same scale; subsequent meta-analyses (including a 2017 Cochrane review) have called for larger confirmatory trials.