64043-42-1 Usage
Uses
Used in Pharmaceutical Industry:
Cardiolipin is used as a biological marker for indicating pathological states. Its levels can be monitored to assess mitochondrial dysfunction and oxidative stress, which are often associated with various diseases, including neurodegenerative disorders, cardiovascular diseases, and cancer.
Used in Diagnostic Applications:
Cardiolipin is used as a diagnostic tool to detect and monitor mitochondrial dysfunction in various diseases. Its analysis can provide valuable insights into the underlying mechanisms of the disease and help in the development of targeted therapies.
Used in Drug Development:
Cardiolipin can be used in the development of drugs targeting mitochondrial function. Its unique interactions with proteins and enzymes make it a promising candidate for the design of novel therapeutic agents that can modulate mitochondrial activity and improve cellular metabolism.
Used in Nutritional Supplements:
Cardiolipin can be used as a nutritional supplement to support mitochondrial health and function. Its supplementation may help improve energy production, reduce oxidative stress, and support overall health and well-being.
Check Digit Verification of cas no
The CAS Registry Mumber 64043-42-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,0,4 and 3 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 64043-42:
(7*6)+(6*4)+(5*0)+(4*4)+(3*3)+(2*4)+(1*2)=101
101 % 10 = 1
So 64043-42-1 is a valid CAS Registry Number.
64043-42-1Relevant articles and documents
A Short, Flexible Route to Symmetrically and Unsymmetrically Substituted Diphoshatidyglycerols (Cardiolipins)
Keana, John F. W.,Shimizu, Masato,Jernstedt, Karen K.
, p. 2297 - 2299 (2007/10/02)
Phosphatidyglycerol methyl esters 2a,b undergo selective phosphorylation on the primary alcohol with phosphatidic acid 3a to give, after methylation of the crude product for purposes of purification and then didemethylation, symmetrically substituted DPG 5a and unsymmetrically substituted DPG 5b, respectively, in moderate overall yield.
