Articles

Found 16 Documents
Search

DUA DIMER RESVERATROL DARI KULIT BATANG SHOREA PARVIFOLIA (DIPTEROCARPACEAE) Rosyidah, Kholifatu; Juliawati, Lia Dewi; Syah, Yana Maolana; Hakim, Euis Holishotan; Achmad, Sjamsul Arifin; Makmur, Lukman
Jurnal Natur Indonesia Vol 12, No 2 (2010)
Publisher : Lembaga Penelitian dan Pengabdian kepada Masyarakat Universitas Riau

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (52.681 KB) | DOI: 10.31258/jnat.12.2.163-166

Abstract

Two resveratrol dimers, (-)-ampelopsin F dan (-)-laevifonol were isolated from aceton extract of the stem bark ofShorea parvifolia. The structures of these compounds were determined based on their spectroscopic data includingspectroscopy ultra violet (UV), infra red (IR), nuclear magnetic resonance (1H-NMR, 13C-NMR) and also were comparedto the reported data.
TURUNAN SENYAWA FLAVONOID DARI DAUN MACARANGA INVOLUCRATA (ROXB.) BAILL DARI BUTON TENGAH, SULAWESI TENGGARA Ilimu, Edi; Syah, Yana Maolana
Jurnal Kimia Valensi Jurnal Kimia VALENSI Volume 5, No. 1, May 2019
Publisher : Lembaga Penelitian dan Pengabdian Kepada Masyarakat Syarif Hidayatullah State Islamic Uni

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (1030.18 KB) | DOI: 10.15408/jkv.v5i1.7909

Abstract

Macaranga merupakan salah satu genus terbesar dari famili Euphorbiaceae yang terdiri dari 300 spesies dengan nama lokal mahang-mahangan. Tumbuhan Macaranga tersebar luas di wilayah Afrika dan Madagaskar di bagian barat hingga ke wilayah tropis Asia, Australia utara dan kepulauan Pasifik. Di Indonesia tumbuhan Macaranga tersebar di beberapa daerah yaitu daerah Papua, Maluku, Sulawesi, Kalimantan, Sumatera, Bangka, dan Jawa. Kajian fitokimia beberapa spesies Macaranga menunjukan adanya kelompok senyawa fenolik yaitu turunan flavonoid dan stilben, serta turunan terpenoid. Senyawa turunan fenolik tersebut memiliki keunikan dari struktur molekulnya, yaitu adanya subtituen tambahan dari metabolit terpenoid yaitu prenil (C5), geranil (C10), farnesil (C15), dan geranilgeranil (C20). Pada penelitian ini telah dilakukan isolasi metabolit sekunder dari daun M. involucrata (Roxb.) Baill dengan metode maserasi menggunakan pelarut aseton, kemudian dilanjutkan pemisahan dan pemurnian dengan menggunakan kromatografi cair vakum dan kromatografi radial untuk mendapatkan senyawa murni. Penentuan struktur dilakukan berdasarkan analisis data spektrum NMR 1D (1H-NMR dan13C-NMR), NMR 2D (NOESY, TOCSY, HSQC, dan HMBC), dan spektrum massa (MS). Berdasarkan metodologi tersebut, dua senyawa turunan flavon yaitu 5,7,4?-trihidroksi-3?(3-metilbut-2-enil)-3-metoksiflavon (1) dan makarangin (2), telah berhasil diisolasi dari tumbuhan ini. Berdasarkan hasil penelitian tersebut menunjukan daun M. involucrata (Roxb.) Baill yang berasal dari Kabupaten Buton Tengah, Sulawesi Tenggara menghasilkan senyawa fenolik turunan flavonoid. Kata kunci: Euphorbiaceae, Macaranga involucrata (Roxb.) Baill, flavon. Macaranga is one of the largest genera of the family Euphorbiaceae comprising 300 species with local name ?mahang-mahangan?. Macaranga is widespread in the region of Africa and the west of Madagascar to the tropical regions of Asia, northern Australia, and the Pacific islands. In Indonesia Macaranga spread in several areas:  Papua, Maluku, Sulawesi, Kalimantan, Sumatra, Bangka, and Java. Phytochemical studies showed the presence of several phenolic compounds such as flavonoids and stilbene derivatives. The phenolic compounds have a unique molecular structure with the addition of some substituents such as prenyl (C5), geranyl (C10), farnesyl (C15), and geranylgeranyl (C20). This research has been conducted on the isolation of secondary metabolites from the leaves of M. involucrata (Roxb.) Baill by maceration method using acetone, followed by separation and purification by using liquid vacuum chromatography and radial chromatography to obtain pure compounds. Determination of the structure is based on data analysis of 1D NMR spectrum (1H-NMR and 13C-NMR), 2D NMR (1H-1HCOSY, NOESY, TOCSY, HSQC, and HMBC), and mass spectra (MS). Based on this methodology, two flavone derivatives 5,7,4'-trihydroxy-3'(3-methylbut-2-enyl)-3-methoxy flavone (1) and macarangin (2), have been isolated from this plant. Based on these results showed that leaf of M. involucrata (Roxb.) Baill from Central Buton, Southeast Sulawesi produces phenolic compounds from flavonoid derivatives. Keywords: Euphorbiaceae, Macaranga involucrata (Roxb.) Baill, flavone.
Antibacterial Activity of Germacrone Sesquiterpene from Curcuma Xanthorrhiza Rhizomes Diastuti, Hartiwi; Syah, Yana Maolana; Juliawaty, Lia Dewi; Singgih, Marlia
ALCHEMY Jurnal Penelitian Kimia Vol 12, No 2 (2016): Alchemy Jurnal Penelitian Kimia
Publisher : UNIVERSITAS SEBELAS MARET (UNS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.20961/alchemy.12.2.1726.103-111

Abstract

The aim of this research was to isolate and indentify the terpenoid compound from Curcuma xanthorrhiza rhizomes and its antibacterial activity. Isolation was carried out by using vacuum liquid chromatography and centrifugal chromatography. The structure was determined by NMR spectroscopy (1H-NMR, 13C-NMR 1D and 2D), then compare with data from literatures. Antibacterial test was carried out by using  microdillution methods and evaluated against eight bacteria. They are Bacillus subtilis, Staphylococcus aureus, Escherichia coli, Enterobacter aerogenes, Pseudomonas aeruginosa, Salmonella typhi, Shigella dysentriae and Vibrio cholerae. The result showed that the isolate was a white crystal which was indetified as germacron-type sesquiterpene. Germacron have highest activity againts P. aeruginosa, MIC 15.6 µg/mL and MBC 31.2 µg/mL.
Synthesis of quinine N-oxide and an NMR tutorial in its structure determination Aisyah, Aisyah; Tamaela, Nila Berghuis; Santoso, Joko; Syah, Yana Maolana; Mujahidin, Didin
Jurnal Penelitian Teh dan Kina Vol 17, No 1 (2014)
Publisher : Research Institute for Tea and Cinchona

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (637.555 KB) | DOI: 10.22302/pptk.jur.jptk.v17i1.45

Abstract

Cinchona alkaloids are one of abundant natural chiral pool for organocatalysts. The application of an N-oxide group containing molecule in asymmetric reaction is currently wide developed. The structure of quinine consist two amine groups that could be oxidized to the N-oxide groups at N-1’ of quinoline and at N-1 of quinuclidine moieties. The oxidation reaction took place selectively at quinuclidine moiety by controlling the concentration of oxidizing agents. In this study we showed that N-1-oxide quinine could be occurred chemo­selectively by using a low concentration of ozone thana palladium catalyzed oxidation. The structure of products N1-oxide quinine was elucidated by spectroscopy data including 1H-NMR, 13C-NMR, 2D-NMR, infra-red and mass spectrometry. The developed method is a chemoselectively and eco-friendly method for synthesis N1-oxide quinine.
METABOLITE PROFILE EVALUATION OF INDONESIAN ROASTED ROBUSTA COFFEES BY 1H NMR TECHNIQUE AND CHEMOMETRICS Happyana, Nizar; Hermawati, Elvira; Syah, Yana Maolana; Hakim, Euis Holisotan
Indonesian Journal of Chemistry ARTICLE IN PRESS
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (17.668 KB) | DOI: 10.22146/ijc.46492

Abstract

In this work, 1H NMR analysis along with chemometrics approach had been applied for investigating metabolite profiles of Indonesian roasted Robusta coffees obtained from Lampung and Aceh. In total, 24 compounds had been successfully detected in the 1H NMR spectra of the Robusta coffee extracts. Concentrations of some identified metabolites present in the coffees were determined by quantitative 1H NMR technique. Orthogonal projection to latent structure-discriminant analysis (OPLSDA) was used as a primary method for the chemometric approach. OPLSDA had classified clearly the Robusta coffee samples corresponding to their origin. Loading plot and S-plot of the OPLSDA revealed characteristic metabolites for each Robusta coffee. The results indicated that quinic acid, mannose, arabinoses, and acetic acid were an important discriminant compound for Lampung Robusta coffees. Meanwhile, lipids, lactic acid, and 5-caffeoylquinic acid were found as characteristic metabolites for Aceh Robusta coffee. This report provided knowledge about the chemical composition of Lampung and Aceh Robusta coffees and shed more light on the diversity of Indonesian Robusta coffees. Furthermore, it confirmed that 1H NMR analysis coupled with chemometrics was a powerful method for evaluating and classifying metabolite profiles of the roasted Robusta coffees.
IN VITRO ANTIBACTERIAL ACTIVITY OF CHALCONE DERIVATIVES FROM Kaempferia pandurata RHIZOMES AGAINST CLINICAL ISOLATE BACTERIA Marliyana, Soerya Dewi; Syah, Yana Maolana; Mujahidin, Didin -
ALCHEMY Jurnal Penelitian Kimia Vol 13, No 1 (2017): Alchemy Jurnal Penelitian Kimia
Publisher : UNIVERSITAS SEBELAS MARET (UNS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.20961/alchemy.13.1.4232.41-51

Abstract

In vitro antibacterial activity of chalcone derivatives from “temu kunci” (K. pandurta) rhizomes against clinical isolate bacteria has been done. Two chalcone derivatives, panduratin A (1) and 4-hydroxypanduratin A (2) were isolated from Kaempferia pandurata rhizomes. Isolation of the chemical components were done with extraction (maceration), vacuum liquid chromatography and radial chromatography methods. The structures were determined by NMR spectroscopy (1H-NMR, 13C-NMR, 1D and 2D), then compare with data from literatures. Antibacterial activity was carried out with reference to the CLSI microdilution method, against eight clinical isolate bacteria such as Bacillus subtilis, Staphylococcus aureus, Escherichia coli, Enterobacter aerogenes, Pseudomonas aeruginosa, Salmonella typhi, Shigella dysentriae and Vibrio cholerae. Compounds 1 and 2 showed significant antibacterial activity with highest activity against S. aureus and B. subtilis with MIC values of 2.4 to 18.8 µg/mL and MBC values of 4.8 to 37.5 µg/mL. These results showed these compounds as potential antibacterial agent for clinical isolate bacteria.
Senyawa Morusin dari Tumbuhan Murbei Hitam (Morus nigra) Ferlinahayati, Ferlinahayati; Hakim, Euis Holisotan; Syah, Yana Maolana; Juliawaty, Lia Dewi
Jurnal Penelitian Sains Vol 15, No 2 (2012)
Publisher : Faculty of Mathtmatics and Natural Sciences

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (584.537 KB)

Abstract

Tumbuhan murbei hitam merupakan salah satu spesies dari genus Morus. Tumbuhan dari genus ini telah dilaporkan kaya akan senyawa turunan fenol seperti flavonoid, 2-arilbenzofuran dan stilben. Dalam rangka pencarian senyawa turunan fenol dari tumbuhan murbei Indonesia maka telah berhasil diisolasi suatu senyawa flavon terprenilasi yaitu morusin dari ekstrak metanol kayu batang murbei hitam (M. nigra). Struktur senyawa tersebut telah ditetapkan berdasarkan data-data spektroskopi yang meliputi spektrum UV dan IR serta membandingkan KLTnya dengan senyawa morusin standar.
Artoindonesianin-E suatu senyawa baru turunan flavanon dari tumbuhan Artocarpus Champeden Hakim, Euis Holisotan; Aripin, Asep; Achmad, Sjamsul Arifin; Aimi, Norio; Kitajima, Mariko; Makmur, Lukman; Mujahidin, Didin; Syah, Yana Maolana; Takayama, Hiromitsu
Journal of Mathematical and Fundamental Sciences Vol 33, No 3 (2001)
Publisher : ITB Journal Publisher, LPPM ITB

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (416.394 KB)

Abstract

Sari. Suatu senyawabaru turunan flavanon, yakni 5,7-dihidroksi-2',4',6'-trimetoksiflavanon yang diberi nama artoindonesianin-E(1 ), telah ditemukan untuk pertama kalinya bersama-samad engan artokarpin (2) dan heteroflavanon-A (3) pada ekstrak benzena kulit batang tumbuhan Artocarpus champeden Spreng (Moraceae), suatu tumbuhan yang endemik untuk Indonesia, serta dikenal dengan narna Cempedak. Struktur molekul senyawa tersebut telah ditetapkan berdasarkan data fisika dan spekroskopi (MS, 1H dan 13C NMR).Artoindonesianin-E a New Flavanone Derivative from Artocarpus ChampedenAbstract. A new flavanone derivative, 5,7-dihydroxy-2',4',6'-trimethoxyflavanone named artoindonesianin-E (1) had been isolated for the first time, together with artocarpin (2) and heteroflavanone-A (3) from benzene extract of the tree bark of Artocarpus champeden Spreng. (Moraceae), a species endemic to Indonesia and locally known as Cempedak. The structure of this compound was elucidated based on physical and spectroscopic data (MS, 1H and 13C NMR).
Synthesis and Characterization of Oligomer 4-Vinylpyridine as A Corrosion Inhibitor for Mild Steel in CO2 Saturated Brine Solution Ilim, Ilim; Jefferson, Alan; Simanjuntak, Wasinton; Jeannin, Marc; Syah, Yana Maolana; Bundjali, Bunbun; Buchari, Buchari
Indonesian Journal of Chemistry Vol 16, No 2 (2016)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (392.016 KB) | DOI: 10.22146/ijc.21164

Abstract

In this work, the oligomer of 4-vinylpyridine designated as O(4-VP) was synthesized by hydrogen peroxide initiated chain growth polymerization and characterized in terms of molecular weight and structure by matrix assisted laser desorption ionization time of flight mass spectroscopy (MALDI-TOF MS). The oligomer was tested as corrosion inhibitor of mild steel in brine solution saturated with carbon dioxide, with the main purpose to investigate the effect of inhibitor concentrations and temperatures on the inhibition activity defined in terms of corrosion rate and percent of protection. The inhibition tests were carried out using the methods of weight loss (WL) and linear polarization (LP). Characterization using MALDI-TOF MS revealed that the oligomer has the mass (m/z) in the range 200-2400, which corresponds to chain length of 2-22 repeating units. The results of corrosion rate measurements show that the corrosion rate with the use of oligomer is significantly lower than that without inhibitor, demonstrating that the oligomer functioned as effective corrosion inhibitor, while the 4-vinyl pyridine monomer was found to promote the corrosion. It was also found that the protection by the oligomer increased with increasing temperature and it was predicted the oligomer was chemically adsorbed by the surface of the metal.
FLAVANONES FROM THE WOOD OF Morus nigra WITH CYTOTOXIC ACTIVITY Ferlinahayati, Ferlinahayati; Syah, Yana Maolana; Juliawaty, Lia Dewi; Hakim, Euis Holisotan
Indonesian Journal of Chemistry Vol 13, No 3 (2013)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (192.38 KB) | DOI: 10.22146/ijc.21277

Abstract

Two flavanone derivatives, norartocarpanone (1) and euchrenone a7 (2) had been isolated for the first time from the methanol extract of the wood of Morus nigra. The structures of these compounds were determined base on spectral evidence, including UV, IR, and NMR. The first compound also confirmed by comparison with the reported data. Cytotoxic properties of these compounds were evaluated against murine leukemia P-388 cells. Euchrenone a7 (2) was found more cytotoxic than norartocarpanone (1) with their IC50 7.8 and 12.7 mg/mL respectively.