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Detail of > 20064-19-1

  • CAS Number:
  • 20064-19-1
  • Name:
  • 1-Propanaminium, 3-carboxy-N,N,N-trimethyl-2-(1-oxopropoxy)-, inner salt, (R)-

  • Formula:
  • C10H19NO4
  • Molecular Structure:
  • Molecular Weight:
  • 217.2622
  • Density:
  • g/cm3
  • Boiling Point:
  • °Cat760mmHg
  • Flash Point:
  • °C
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CAS No. 

20064-19-1 1-Propanaminium, 3-carboxy-N,N,N-trimethyl-2-(1-oxopropoxy)-, inner salt, (R)-

Name:Propionyl L-Carnitine HCL
China (Mainland)   56
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  • Address:1518 Minsheng Rd,Pudong area,Shanghai
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    Reference

    The propionyl-L-carnitine hypothesis: an alternative approach to treating heart failure
    The propionyl-L-carnitine hypothesis: an alternative approach to treating heart failure. Ferrari, Roberto; De Giuli, Federica (Chair of Cardiology, University of Brescia, Brescia 25123, Italy). Journal of Cardiac Failure, 3(3), 217-224 (English) 1997 Churchill Livingstone. CODEN: JCFAF9. ISSN: 1071-9164. DOCUMENT TYPE: Journal CA Section: 1 (Pharmacology) Propionyl-L-carnitine (PLC) is a naturally occurring compd. that has been considered for the treatment of congestive heart failure (CHF). The rationale for its use in this pathol. is related to its effects on cardiac and skeletal muscle. Chronic treatment with PLC improves the contraction of isolated and aerobic perfused rabbit hearts. The compd. improves energy metab. and myocardial contractility in different exptl. models of heart failure, such as pressure-overloaded rats, infarct model of heart failure, and rabbit with streptozotocin-induced diabetes. In general, the effect of PLC is apparent in situations of high energy demand such as those induced by increased workload. It therefore seems likely that PLC is able to correct some metabolic steps of the process that leads to heart failure. In addn., PLC may be helpful in heart failure because of its specific action on peripheral skeletal muscle.In this article, certain chemicals are used. One of their cas registry numbers is 20064-19-1 Administration of PLC in patients with CHF improves skeletal muscle metab. by increasing pyruvate flux into the Krebs cycle and by decreasing lactate prodn. These effects occur in the absence of major hemodynamic and neuroendocrinol. changes and may underlie the ability of PLC to increase exercise performance in patients with heart failure. In a randomized study of 50 patients with mild CHF, PLC increased the maximal exercise time, reduced lactate prodn., and improved left ventricular ejection fraction. There have been two large-scale trials on the effects of PLC on both cardiac and peripheral muscle function in CHF. One is ongoing; the other one, which just ended, failed to show an improvement in exercise capacity in the population studied. A benefit was evident only in a subgroup of patients with preserved ejection fraction and impaired baseline exercise duration. .

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