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Teni Ernawati
Pusat Penelitian Kimia Lembaga Ilmu Pengetahuan Indonesia
Chemistry

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Sintesis N-Oktilsinamamid dan Aktivitasnya terhadap Sitotoksik Sel Kanker Leukemia P388 Teni Ernawati; Neneng Nurhalimah; Minarti Minarti
Jurnal Kimia Valensi Jurnal Kimia VALENSI Volume 3, No. 2, November 2017
Publisher : Syarif Hidayatullah State Islamic University

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (730.546 KB) | DOI: 10.15408/jkv.v0i0.5843

Abstract

Sintesis senyawa N-Oktilsinnamamid yang diturunkan dari senyawa metil trans-sinamat dengan menggunakan katalis basa telah dilakukan. Senyawa metil sinamat terlebih dahulu dikonversi menjadi asam sinamat melalui reaksi hidrolisis dengan basa menghasilkan asam sinamat. Selanjutnya asam sinamat diamidasi dengan menggunakan oktilamin dan 1,3 disikloheksilkarboodiimide (DCC) dan 4-dimetilaminopiridin (DMAP) sebagai katalis. Dari penelitian ini diperoleh rendemen hasil sintesis asam sinamat, sintesis N-Oktilsinnamami yang cukup baik. Hasil reaksi diidentifikasi dengan menggunakan 1H-NMR, 13C-NMR dan LC-MS. Uji sitotoksik senyawa N-Oktilsinamamid terhadap sel leukemia P388 diperoleh nilai IC50=6.71 µg/mL. Synthesis of N-Octylcinnamamide compound derived from methyl trans-cinnamate using abase catalyst has been done. First, The compound of methyl trans-cinnamate was converted into cinnamic acid by hydrolysis reaction with an alkaline condition. Furthermore cinnamic acid was amidated by using octylamine and 1,3 dicyclohexylcarbodiimide (DCC) and 4-dimethylaminopyridine (DMAP) as a catalyst. The results of this study were obtained synthesis of cinnamic and synthesis of N-Octylcinnamamide are good enough. Identification of this product was using by 1H-NMR, 13C-NMR and LC-MS.  Cytotoxic test of N-Octylcinnamamide against P388 leukemia cell was obtained IC50=6.71µg/mL.
Bioaktivitas Turunan Metil Sinamat Terhadap Pertumbuhan Bakteri Escherichia coli, Staphylococcus aureus, Bacillus subtilis, Pseudomonas aureugenosa dan Jamur Candida albicans Andri Budiana; Teni Ernawati
Jurnal Kimia Valensi Jurnal Kimia VALENSI Volume 1, No. 1, Mei 2015
Publisher : Syarif Hidayatullah State Islamic University

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (350.18 KB) | DOI: 10.15408/jkv.v0i0.3154

Abstract

Methyl cinnamic is a compound isolated from Alpinia malaccensis included in the family Zingiberaceae. A. malaccensis in Indonesia known as galangal forest. Some studies inform that ginger has anti-bacterial and pharmacologically galangal act as an antifungal. In this study the bioactivity of the compound methyl cinnamate and methyl cinnamic derivative which results cinnamic methyl esterification compound on the growth of Escherichia coli, Staphylococcus aureus, Bacillus subtilis, Pseudomonas aureugenosa and fungus Candida albicans. Methyl cinnamic derivative compounds tested are; cinnamic acid, cinnamic ethyl, butyl and 2-butyl cinnamic cinnamic. Anti-microbial test results showed that of the samples tested, cinnamic acid is able to inhibit microbial growth of S. aureus, B. subtilis, E. coli and P. aureugenosa and fungi C.albicans.DOI :http://dx.doi.org/10.15408/jkv.v0i0.3176 
Co-Authors Andri Budiana Minarti Minarti Neneng Nurhalimah