Category: 456-12-2

Jose, Sindhu; Ragunathan, V.; Arunachalam, Thangakumar; Joseph, Milesh; Madipatti, Satish published an article in 2016, the title of the article was Extraction, isolation and analytical characterisation of aegeline enantiomers from Aegle marmelos.Related Products of 456-12-2 And the article contains the following content:

Aegeline or N-[2-hydroxy-2(4-methoxyphenyl)-ethyl]-3-phenyl-2-propenamide is a main alkaloid isolated from the leaves of Aegle marmelos (bael). The plant is extensively used in the Indian traditional system of medicine viz. Ayurveda . It soothes impaired kapha, vata, body pain, poison, diarrhea, dysentery, vomiting and intermittent fever. Its leaves are known as a cure for asthma, inflammation, cough and diabetes. The leaves are trifoliate and aromatic They have a shape, intermediate between ovate and lanceolate with reticulate pinnate venation. The present work was undertaken to provide an easy and reliable method for the extraction and isolation of Aegeline (N-[2-hydroxy-2-(4-methoxyphenyl)ethyl]-3-phenyl-2-propenamide) using high performance liquid chromatog. (HPLC). The study also included the separation of the two enantiomers of Aegeline using chiral HPLC, its crystallog. structure, activity of the two enantiomers on cervical cancer and a NMR (NMR) method for the enantiomeric purity determination of collected fractions. Linear calibration curves were obtained over the range of 0.7 – 5mM for enantiomer-2 (R2 = 0.998). This study was undertaken with the intention to develop a fast and reliable method for the enantiomeric purity determination of Aegeline and related compounds The experimental process involved the reaction of N-(2-Hydroxy-2-(4-methoxyphenyl)ethyl)cinnamamide(cas: 456-12-2).Related Products of 456-12-2

The Article related to aegle leaf aegeline enantiomer anticancer, Plant Biochemistry: Composition and Products and other aspects.Related Products of 456-12-2

Referemce:
Amide – Wikipedia,
Amide – an overview | ScienceDirect Topics

On November 2, 1981, Sharma, B. R.; Rattan, R. K.; Sharma, Perveen published an article.Recommanded Product: N-(2-Hydroxy-2-(4-methoxyphenyl)ethyl)cinnamamide The title of the article was Constituents of Aegle marmelos. Part III. Marmeline, an alkaloid, and other components of unripe fruits of Aegle marmelos. And the article contained the following:

A new alkaloid, marmeline, was isolated from unripe fruits of A. marmelos and identified as N-2-hydroxy-2-[4-(3′,3′-dimethylallyloxy)phenyl]ethyl cinnamide. Aegeline, imperatorin, alloimperatorin, and xanthotoxol were also present. The experimental process involved the reaction of N-(2-Hydroxy-2-(4-methoxyphenyl)ethyl)cinnamamide(cas: 456-12-2).Recommanded Product: N-(2-Hydroxy-2-(4-methoxyphenyl)ethyl)cinnamamide

The Article related to aegle alkaloid marmeline structure, Plant Biochemistry: Composition and Products and other aspects.Recommanded Product: N-(2-Hydroxy-2-(4-methoxyphenyl)ethyl)cinnamamide

Referemce:
Amide – Wikipedia,
Amide – an overview | ScienceDirect Topics

On February 24, 1983, Govindachari, Tuticorin R.; Premila, Manakkal S. published an article.Computed Properties of 456-12-2 The title of the article was Some alkaloids from Aegle marmelos. And the article contained the following:

Four new alkaloids, 4-ROC6H4ZNHCOCH:CHPh [I ; R = CH2CH:CMe2, Z = (CH2)2, CH(OH)CH2; R = H, Z = CH(OH)CH2; R = Me, Z = CH:CH], were isolated from dry leaves of A. marmelos. Also isolated were aegeline [I ; R = H, Z = CH(OH)CH2] and a purple alkaloid of unknown structure. The experimental process involved the reaction of N-(2-Hydroxy-2-(4-methoxyphenyl)ethyl)cinnamamide(cas: 456-12-2).Computed Properties of 456-12-2

The Article related to aegle alkaloid structure, Plant Biochemistry: Composition and Products and other aspects.Computed Properties of 456-12-2

Referemce:
Amide – Wikipedia,
Amide – an overview | ScienceDirect Topics

Borde, Vinod U.; Pangrikar, Prashant P.; Wadikar, Madhukar S.; Tekale, Sunil U. published an article in 2011, the title of the article was Extraction and thin layer chromatography of alkaloids from Bael (Aegle marmelos) leaves.Recommanded Product: 456-12-2 And the article contains the following content:

Bael tree, (Aegle marmelos, Family – Rutaceae), is a sacred tree widely grown in Indian forests, Ceylon, Burma, Thailand and Indo-China. All parts of the tree are used for medicinal purpose. Some of the medicinal properties are astringent, antidiarreal, antidystentric, demulcent, stomachic, fever curing, insulin-promoter, anti-inflammatory, cardio tonic and cures ophthalmic, urinary trouble, palpitation and many more. Most of these properties are believed to be due to presence of bioactive alkaloids in Bael. This study was carried out to develop an easy method of extraction and separation of alkaloids from dried Bael leaves. Alkaloids from the dried leaves of Bael were extracted in 95% ethanol and separated with chloroform in presence of synthetic antioxidants butylated hydoxytoluene (BHT) and butylated hydroxyaniosole (BHA) by thin layer chromatog. BHT and BHA seem to protect alkaloids from their degradation/conversion to other components. The experimental process involved the reaction of N-(2-Hydroxy-2-(4-methoxyphenyl)ethyl)cinnamamide(cas: 456-12-2).Recommanded Product: 456-12-2

The Article related to aegle leaf butylated hydoxytoluene hydroxyanisole alkaloid, Plant Biochemistry: Composition and Products and other aspects.Recommanded Product: 456-12-2

Referemce:
Amide – Wikipedia,
Amide – an overview | ScienceDirect Topics

On January 31, 2009, Faizi, Shaheen; Farooqi, Fatima; Zikr-Ur-Rehman, Sadia; Naz, Aneela; Noor, Fatima; Ansari, Farheen; Ahmad, Aqeel; Khan, Shakeel Ahmed published an article.Category: amides-buliding-blocks The title of the article was Shahidine, a novel and highly labile oxazoline from Aegle marmelos: the parent compound of aegeline and related amides. And the article contained the following:

A rare alkaloid, shahidine (1), having an unstable oxazoline core has been isolated as a major constituent from the fresh leaves of Aegle marmelos. It is moisture-sensitive, and found to be the parent compound of aegeline and other amides, however, it is stable in DMSO. Its structure was established by spectroscopic anal. Biogenetically, oxazolines may be considered as the precursor of hydroxy amides and oxazoles found in plants. Shahidine (1) showed activity against a few Gram-pos. bacteria. The experimental process involved the reaction of N-(2-Hydroxy-2-(4-methoxyphenyl)ethyl)cinnamamide(cas: 456-12-2).Category: amides-buliding-blocks

The Article related to mol structure shahidine aegle alkaloid antibacterial anticancer, Plant Biochemistry: Composition and Products and other aspects.Category: amides-buliding-blocks

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Amide – Wikipedia,
Amide – an overview | ScienceDirect Topics

Della Casa de Marcano, D.; Hasegawa, M.; Castaldi, A. published an article in 1972, the title of the article was Neutral compounds and alkaloids of Zanthoxylum ocumarense.Computed Properties of 456-12-2 And the article contains the following content:

Bark of Z. ocumarense was extracted with benzene and chromatographed on Al2O3. A mixture of n-alkanes (C21H44-C33H68) lupeol, 尾-amyrin and 2 amides (I, m. 149-51掳, and II, m. 175-6掳) were detected. The bark was again extracted with hot MeOH to yield 3 quaternary bases, N-methyl-伪-(-)-canadine, (+)-laurifoline, and cheleritrine, 2 alkaloids, C20H16NO5Cl (III), m. 245掳, and C15H11NO3 (IV), m. 216掳; and hesperidin. III was obtained in low yield, and IV proved unstable. The experimental process involved the reaction of N-(2-Hydroxy-2-(4-methoxyphenyl)ethyl)cinnamamide(cas: 456-12-2).Computed Properties of 456-12-2

The Article related to zanthoxylum composition, alkaloid zanthoxylum, alkane zanthoxylum, amide zanthoxylum, Plant Biochemistry: Composition and Products and other aspects.Computed Properties of 456-12-2

Referemce:
Amide – Wikipedia,
Amide – an overview | ScienceDirect Topics

Nigam, Vinita; Vanisha, Nambiar published an article in 2018, the title of the article was Evaluation of antioxidant profile of wild and cultivated varieties of Aegle marmelos (L) correa leaves used as anti-diabetic agent.Recommanded Product: 456-12-2 And the article contains the following content:

Aim: The objective of the present study was to evaluate the total antioxidant activity of the wild variety of AM leaves from forest of Gir Somnath, Gujarat, India and cultivated variety from Central Horticultural Experiment Station, Vejalpur, Panchmahals, Gujarat to assess the role of this plant in ethanomedicine in India. Methods: The methanolic extracts of the leaves were screened for total antioxidant capacity through Ferric Reducing Antioxidant Potential (FRAP) and 1, 1-diphenyl-2-picrylhydrazyl (DPPH) radical scavenging assay; Total Phenol content (TPC) through spectrophotometric technique based on Folin Ciocalteau assay and for qual. estimation of phenols, High performance Liquid Chromatog. (HPLC) was used. Results: TPC of wild and cultivated variety was 7.6% and 6.5% resp. FRAP values and IC50 value (DPPH) for wild and cultivated variety were found to be 14.65渭mol/l and 11.80渭mol/l; 437渭g/mL and 620渭g/mL resp. Wild variety was found to be superior to the cultivated one. Conclusion: This study proved that the leaves of AM leaves have high antioxidant component. AM could be used as a potential preventive intervention for free radical mediated diseases such as diabetes and as neutraceutical in medicinal formulation. Further intervention trials are needed to prove the therapeutic potential of these leaves. The experimental process involved the reaction of N-(2-Hydroxy-2-(4-methoxyphenyl)ethyl)cinnamamide(cas: 456-12-2).Recommanded Product: 456-12-2

The Article related to antioxidant aegle correa leaves antidiabetic sugar ethanomedicine neutraceutical gujarat, Pharmaceuticals: Formulation and Compounding and other aspects.Recommanded Product: 456-12-2

Referemce:
Amide – Wikipedia,
Amide – an overview | ScienceDirect Topics

On April 30, 1979, Patra, A.; Mukhopadhyay, A. K.; Ghosh, A. published an article.Recommanded Product: N-(2-Hydroxy-2-(4-methoxyphenyl)ethyl)cinnamamide The title of the article was Constituents of Aegle marmelos: carbon-13 NMR spectra of aurapten and marmin. And the article contained the following:

Chem. reinvestigation of A. marmelos yielded aurapten, marmin, umbelliferone, and lupeol from the bark and lupeol, sitosterol, and aegeline from the leaves. 13C NMR shifts of aurapten and marmin are discussed. The experimental process involved the reaction of N-(2-Hydroxy-2-(4-methoxyphenyl)ethyl)cinnamamide(cas: 456-12-2).Recommanded Product: N-(2-Hydroxy-2-(4-methoxyphenyl)ethyl)cinnamamide

The Article related to aegle aurapten marmin nmr, aegelin aegle, umbelliferone aegle, lupeol aegle, sitosterol aegle, Plant Biochemistry: Composition and Products and other aspects.Recommanded Product: N-(2-Hydroxy-2-(4-methoxyphenyl)ethyl)cinnamamide

Referemce:
Amide – Wikipedia,
Amide – an overview | ScienceDirect Topics

On August 31, 2010, Ali, Muhammad Shaiq; Shahnaz; Tabassum, Sobia; Ogunwande, Isiaka Ajani; Pervez, Muhammad Kashif; Ibrahim, Oladosu Adebayo published an article.Safety of N-(2-Hydroxy-2-(4-methoxyphenyl)ethyl)cinnamamide The title of the article was Naturally occurring antifungal aromatic esters and amides. And the article contained the following:

During the search of antifungal natural products from terrestrial plants, a new long chained aromatic ester named grandiflorate (1) along with spatazoate (2) from Portulaca grandiflora and N-[2-methoxy-2-(4-methoxyphenyl) ethyl]-trans-cinnamide (3) and aegeline (4) from Solanum erianthum of Nigeria were isolated and tested against six fungal species. The known constituents 2-4 have not been reported so far from mentioned investigated plants. Structures of the isolated compounds were elucidated with the aid of spectroscopic techniques including two dimensional NMR experiments Among the compounds 1-4, the esters (1-2) found more potent than amides (3-4) against Candida albicans and Aspergillus flavus. The new compound grandiflorate (1) gave response against all tested fungal species while aegeline (4) was found to give lowest inhibition during this study. The experimental process involved the reaction of N-(2-Hydroxy-2-(4-methoxyphenyl)ethyl)cinnamamide(cas: 456-12-2).Safety of N-(2-Hydroxy-2-(4-methoxyphenyl)ethyl)cinnamamide

The Article related to grandiflorate structure spatazoate fungicide portulaca, methoxymethoxyphenylethylcinnamide aegeline solanum fungicide, Plant Biochemistry: Composition and Products and other aspects.Safety of N-(2-Hydroxy-2-(4-methoxyphenyl)ethyl)cinnamamide

Referemce:
Amide – Wikipedia,
Amide – an overview | ScienceDirect Topics

Ellis, J.; Gellert, E.; Summons, R. E. published an article in 1972, the title of the article was Alkaloids of Mitrella kentii (Annonaceae).Formula: C18H19NO3 And the article contains the following content:

Bark extracts of Mitrella kentii yielded 4 alkaloids: liriodenine, anonine, asimilobine, and egeline. The experimental process involved the reaction of N-(2-Hydroxy-2-(4-methoxyphenyl)ethyl)cinnamamide(cas: 456-12-2).Formula: C18H19NO3

The Article related to mitrella bark alkaloid, liriodenine mitrella bark, anonaine mitrella bark, asimilobine mitrella bark, egeline mitrella bark, Plant Biochemistry: Composition and Products and other aspects.Formula: C18H19NO3

Referemce:
Amide – Wikipedia,
Amide – an overview | ScienceDirect Topics