13699-47-3 Usage
Classification
Phospholipid compound
Lipid class
Belongs to the class of lipids
Research and pharmaceutical applications
Widely used due to its ability to interact with cell membranes and modulate cellular signaling pathways
Therapeutic potential
Studied for potential therapeutic effects in the treatment of lung injury, cancer, and neurodegenerative diseases
Drug delivery
Used in the development of liposomal formulations
Biomimetic membrane model
Utilized for studying lipid-protein interactions and membrane biophysics
Check Digit Verification of cas no
The CAS Registry Mumber 13699-47-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,6,9 and 9 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 13699-47:
(7*1)+(6*3)+(5*6)+(4*9)+(3*9)+(2*4)+(1*7)=133
133 % 10 = 3
So 13699-47-3 is a valid CAS Registry Number.
InChI:InChI=1/C28H56NO8P/c1-6-8-10-12-14-16-18-20-27(30)34-24-26(25-36-38(32,33)35-23-22-29(3,4)5)37-28(31)21-19-17-15-13-11-9-7-2/h26H,6-25H2,1-5H3
13699-47-3Relevant articles and documents
Selective Acylation of Nucleosides, Nucleotides, and Glycerol-3-phosphocholine in Water
Fernández-García, Christian,Powner, Matthew W.
supporting information, p. 78 - 83 (2016/12/26)
A convenient selective synthesis of 2′,3′-di-O-acetyl-nucleotide-5′-phosphates, 2′,3′-di-O-acetyl-nucleotide-5′-triphosphates and 2′,3′,5′-tri-O-acetyl-nucleosides in water has been developed. Furthermore, a long-chain selective glycerol-3-phosphocholine diacylation is elucidated. These reactions are environmentally benign, rapid, high yielding, and the products are readily purified. Importantly, this reaction may indicate a prebiotically plausible reaction pathway for the selective acylation of key metabolites to facilitate their incorporation into protometabolism.
