16833-56-0 Usage
Description
(+)-Coronaric Acid, a mono-unsaturated, epoxide derivative of the di-saturated fatty acid linoleic acid, is a bioactive compound derived from the seed oils of plants in the sunflower family, such as Helianthus annuus and Xeranthemum annuum. It exhibits unique chemical properties and potential applications in various industries.
Uses
Used in Pharmaceutical Industry:
(+)-Coronaric Acid is used as a bioactive compound for its potential therapeutic applications. Its unique chemical structure allows it to interact with biological systems, making it a promising candidate for the development of new drugs and treatments.
Used in Nutraceutical Industry:
(+)-Coronaric Acid is used as a nutraceutical ingredient for its potential health benefits. It may be incorporated into dietary supplements and functional foods to support overall health and well-being.
Used in Cosmetic Industry:
(+)-Coronaric Acid is used as an active ingredient in the cosmetic industry for its potential skin health benefits. It may be included in skincare products to promote skin health and address various skin concerns.
Used in Agricultural Industry:
(+)-Coronaric Acid is used as a natural pesticide or growth promoter in the agricultural industry. Its bioactive properties may help protect crops from pests and diseases, while also promoting healthy plant growth.
Used in Research and Development:
(+)-Coronaric Acid is used as a research compound for studying its chemical properties, biological activities, and potential applications in various fields. This may lead to the discovery of new uses and applications for this unique compound.
Check Digit Verification of cas no
The CAS Registry Mumber 16833-56-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,8,3 and 3 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 16833-56:
(7*1)+(6*6)+(5*8)+(4*3)+(3*3)+(2*5)+(1*6)=120
120 % 10 = 0
So 16833-56-0 is a valid CAS Registry Number.
16833-56-0Relevant articles and documents
Molecular characterization of NbEH1 and NbEH2, two epoxide hydrolases from Nicotiana benthamiana
Huang, Fong-Chin,Schwab, Wilfried
, p. 6 - 15 (2013/07/11)
Plant epoxide hydrolases (EH) form two major clades, named EH1 and EH2. To gain a better understanding of the biochemical roles of the two classes, NbEH1.1 and NbEH2.1 were isolated from Nicotiana benthamiana and StEH from potato and heterologously expressed in Escherichia coli. The purified recombinant proteins were assayed with a variety of substrates. NbEH1.1 only accepted some aromatic epoxides, and displayed the highest enzyme activity towards phenyl glycidyl ether. In contrast, NbEH2.1 displayed a broad substrate range and similar substrate specificity as StEH. The latter enzymes showed activity towards all fatty acid epoxides examined. The activity (Vmax) of NbEH1.1 towards phenyl glycidyl ether was 10 times higher than that of NbEH2.1. On the contrary, NbEH2.1 converted cis-9,10-epoxystearic acid with Vmax of 3.83 μmol min mg-1 but NbEH1.1 could not hydrolyze cis-9,10- epoxystearic acid. Expression analysis revealed that NbEH1.1 is induced by infection with tobacco mosaic virus (TMV) and wounding, whereas NbEH2.1 is present at a relatively constant level, not influenced by treatment with TMV and wounding. NbEH1.1 transcripts were present predominantly in roots, whereas NbEH2.1 mRNAs were detected primarily in leaves and stems. Overall, these two types of tobacco EH enzymes are distinguished not only by their gene expression, but also by different substrate specificities. EH1 seems not to participate in cutin biosynthesis and it may play a role in generating signals for activation of certain defence and stress responses in tobacco. However, members of the EH2 group hydrate fatty acid epoxides and may be involved in cutin monomer production in plants.
