Creatinol O-Phosphate

Creatinol O-Phosphate (COP) is a synthetic creatine analogue developed in the 1970s-80s for cardioprotection. Injected COP (1-3g IV) showed benefits for arrhythmias and protecting cardiac tissue during ischemia. However, research ceased decades ago and oral bioavailability is unknown. Sold in pre-workout supplements for supposed muscle performance benefits, but NO evidence supports oral use for exercise. The cardioprotective research was via injection only. Essentially an abandoned pharmaceutical with unclear oral effects.

Quick Answer

What it is

Creatinol O-Phosphate (COP) is a synthetic creatine analogue developed in the 1970s-80s for cardioprotection. Injected COP (1-3g IV) showed benefits for arrhythmias and protecting cardiac tissue during ischemia.

Key findings

  • Grade B: Ventricular Arrhythmia Reduction (IV Administration)
  • Grade C: Myocardial Ischemia Protection (IV Administration)
  • Grade D: Cardiac Hemodynamic Function (IV Administration)

Safety

No specific caution or interaction language was detected in the current summary/outcome notes.

ℹ️ Quick Facts: Creatinol O-Phosphate

Quick Facts: Creatinol O-Phosphate

  • Best Evidence:Grade B
  • Conditions Studied:3
  • Research Outcomes:3
  • Grade B Findings:1
  • Key Effect:Cardiovascular Disease
Outcomes by grade:
A0
B1
C1
D1
3 conditions · 3 outcomes

Detailed Outcomes

|
B
Ventricular Arrhythmia Reduction (IV Administration)
Multiple human clinical trials from the late 1970s, including double-blind studies, found that intravenous COP (1-3g) reduced ventricular premature beats and showed antiarrhythmic effectiveness in patients with ischemic heart disease. All evidence is limited to IV injection; no data exists for oral administration.
moderateImproves
C
Myocardial Ischemia Protection (IV Administration)
A double-blind clinical trial found IV COP improved outcomes in patients with inadequate coronary circulation. Animal studies in rats and mice showed COP protected against isoprenaline-induced cardiac enzyme elevation and CaCl2-induced ventricular fibrillation. An in vitro NMR study in perfused Xenopus heart confirmed effects on cardiac energy metabolism. All evidence is from IV or direct perfusion, not oral dosing.
moderateImproves
D
Cardiac Hemodynamic Function (IV Administration)
A single preclinical study in conscious and anaesthetized dogs examined the effects of IV COP on haemodynamics and cardiac metabolism, providing early evidence of cardiovascular activity. No human replication or oral bioavailability data exists.
smallImproves

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