30403-47-5 Usage
Description
1,2-Dihexanoyl-sn-glycerol is a lipid molecule that plays a significant role in cellular signaling and function. It is derived from sn-glycerol, a simple polyol compound, and has two hexanoyl groups attached to its first and second carbon atoms. This molecule is known for its ability to act as a bioregulator of protein kinase C (PKC) in human platelets, which is crucial for various cellular processes.
Uses
Used in Pharmaceutical Industry:
1,2-Dihexanoyl-sn-glycerol is used as a bioregulator for protein kinase C (PKC) in human platelets. Its role in regulating PKC is essential for maintaining proper cellular function and signaling, which can have implications in the development of therapeutic strategies for various diseases and conditions.
Used in Research and Development:
1,2-Dihexanoyl-sn-glycerol is also utilized in research and development for studying the role of PKC in cellular processes. By understanding the interactions between this lipid molecule and PKC, researchers can gain insights into the underlying mechanisms of various diseases and potentially develop targeted treatments.
Used in Drug Delivery Systems:
Similar to gallotannin, 1,2-dihexanoyl-sn-glycerol can be incorporated into drug delivery systems to enhance its applications and efficacy. By using various organic and metallic nanoparticles as carriers, the delivery, bioavailability, and therapeutic outcomes of this molecule can be improved, potentially leading to more effective treatments for a range of conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 30403-47-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,4,0 and 3 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 30403-47:
(7*3)+(6*0)+(5*4)+(4*0)+(3*3)+(2*4)+(1*7)=65
65 % 10 = 5
So 30403-47-5 is a valid CAS Registry Number.
30403-47-5Relevant articles and documents
Positional specificity and stereoselectivity of a lipase preparation from oat seeds acting on 1,2,3-trihexanoylglycerol
Ota, Yasuhide,Minesaki, Toshio,Oshima, Aki
, p. 166 - 167 (1997)
Oat seed lipase was extracted with 0.01 M calcium chloride solution containing 0.5% Triton X-100 and precipitated with ammonium sulfate. The precipitate was dissolved in phosphate buffer at pH 6.0 and the supernatant was used as the lipase preparation. The lipase was very selective in the ester positions of 1,2-trihexanoylglycerol, hydrolyzing sn-3 most quickly, sn-1 moderately, and sn-2 hardly at all.
Synthetic approaches to heavily lipidated phosphoglyceroinositides
Schlueter, Urs,Lu, Jun,Fraser-Reid, Bert
, p. 255 - 257 (2007/10/03)
(Matrix presented) Naturally occurring phosphoinositide glycoconjugates are equipped with varied acyl residues that are important for their biological activity and biosynthesis. This paper reports that acylation at O2 of the myo-inositol moiety can be ach
COSMETIC COMPOSITION
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, (2008/06/13)
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