2271-34-3 Usage
Description
(11E)-hexadec-11-enoic acid, also known as 11-hexadecenoic acid, is a naturally occurring unsaturated fatty acid found in the chemical composition of olives (Olea europaea Linn.). It is characterized by the presence of a double bond at the 11th carbon atom, which gives it unique chemical and biological properties.
Uses
Used in Pharmaceutical Industry:
(11E)-hexadec-11-enoic acid is used as an antidiabetic agent for its potential to modulate glucose metabolism and improve insulin sensitivity. This fatty acid has been identified for its ability to reduce blood glucose levels and improve glycemic control in diabetic patients.
Used in Food Industry:
(11E)-hexadec-11-enoic acid is used as a natural component in various food products, particularly in olive oil, due to its presence in olives. It contributes to the unique taste, aroma, and health benefits associated with olive oil consumption.
Used in Cosmetic Industry:
(11E)-hexadec-11-enoic acid can be used as an ingredient in cosmetic products, such as creams and lotions, due to its potential moisturizing and skin conditioning properties. Its presence in olive oil-based cosmetic formulations may provide additional health benefits to the skin.
Check Digit Verification of cas no
The CAS Registry Mumber 2271-34-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,7 and 1 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2271-34:
(6*2)+(5*2)+(4*7)+(3*1)+(2*3)+(1*4)=63
63 % 10 = 3
So 2271-34-3 is a valid CAS Registry Number.
2271-34-3Relevant articles and documents
Noren,Odham
, p. 573,574 (1973)
Synthesis and Characterization of Novel Acyl-Glycine Inhibitors of GlyT2
Mostyn, Shannon N.,Carland, Jane E.,Shimmon, Susan,Ryan, Renae M.,Rawling, Tristan,Vandenberg, Robert J.
, p. 1949 - 1959 (2017/09/26)
It has been demonstrated previously that the endogenous compound N-arachidonyl-glycine inhibits the glycine transporter GlyT2, stimulates glycinergic neurotransmission, and provides analgesia in animal models of neuropathic and inflammatory pain. However, it is a relatively weak inhibitor with an IC50 of 9 μM and is subject to oxidation via cyclooxygenase, limiting its therapeutic value. In this paper we describe the synthesis and testing of a novel series of monounsaturated C18 and C16 acyl-glycine molecules as inhibitors of the glycine transporter GlyT2. We demonstrate that they are up to 28 fold more potent that N-arachidonyl-glycine with no activity at the closely related GlyT1 transporter at concentrations up to 30 μM. This novel class of compounds show considerable promise as a first generation of GlyT2 transport inhibitors.
Electrochemical synthesis of (Z)-11-hexadecen-1-yl acetate - The pheromone of purple stem-borer (Sesamia inferens)
Singh,Misra
, p. 565 - 567 (2007/10/02)
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