Studies on Pellitorine Production and Antioxidant Activity of Explant Specific Calli of Anacyclus pyrethrum was written by Singh, Deepak Kumar;Babbar, Shashi Bhushan;Mir, Bilal Ahmad. And the article was included in Journal of Biologically Active Products from Nature in 2020.Recommanded Product: 18836-52-7 The following contents are mentioned in the article:
Anacyclus pyrethrum is a perennial and procumbent herb of immense medicinal value, largely due to the presence of an array of therapeutically active alkaloids such as Pellitorine. In this study, cotyledon, hypocotyl and root explants of A. pyrethrum were tested for their callogenic response and subsequent pellitorine accumulation on MS medium supplemented with 2, 4-D. At elevated concentrations of 2,4-D cotyledonary explants showed higher callogenic response than root and hypocotyl but at lower concentrations of 2,4-D, the results were observed the opposite. The calli of all the treatments were harvested after 30, 45, 60 and 75 days of inoculation. The calli of all the three explants were tested for pellitorine content after 30d, 45d, 60d, and 75d of the culture. Interestingly, calli of cotyledons harvested at 75d of inoculation accumulated maximum pellitorine content of 94.50μg/g dry weight indicating that the old callus is harvested for maximum economic benefit and large scale production of pellitorine. Antioxidant activity of calli raised from different explants and harvested after different time intervals were examined using DPPH (2,2-diphenyl-1-picrylhydrazyl) method. Thus, this study reports an efficient and reproducible protocol for successful callus induction from various explants of A. pyrethrum for large scale production of pellitorine and evaluation of antioxidant activities. This study involved multiple reactions and reactants, such as (2E,4E)-N-Isobutyldeca-2,4-dienamide (cas: 18836-52-7Recommanded Product: 18836-52-7).
(2E,4E)-N-Isobutyldeca-2,4-dienamide (cas: 18836-52-7) belongs to amides. The solubilities of amides and esters are roughly comparable. Typically amides are less soluble than comparable amines and carboxylic acids since these compounds can both donate and accept hydrogen bonds. Tertiary amides, with the important exception of N,N-dimethylformamide, exhibit low solubility in water. Amides are not in general accessible by the direct condensation of amines with carboxylic acids for two reasons: first, both components are readily deactivated by a transfer of a proton from the acid to the amine and second, the hydroxy unit on the carbonyl of the acid is a relatively poor leaving group. Nevertheless, the formation of five- and six-membered rings is often surprisingly simple provided that other factors can be brought into play to assist in the condensation.Recommanded Product: 18836-52-7
Referemce:
Amide – Wikipedia,
Amide – an overview | ScienceDirect Topics