Molekul: Jurnal Ilmiah Kimia
The MOLEKUL is dedicated to fostering advancements in all branches of chemistry and its diverse sub-disciplines. It aims to publish high-quality research encompassing a wide range of topics, including but not limited to Pharmaceutical Chemistry, Biological Activities of Synthetic Drugs, Environmental Chemistry, Biochemistry, Polymer Chemistry, Petroleum Chemistry, and Agricultural Chemistry. By providing a platform for rigorous scientific inquiry and dissemination of knowledge, the journal strives to contribute to the understanding, innovation, and practical applications of chemistry in various fields. We encourage submissions that explore new methodologies, elucidate fundamental principles, address pressing challenges, and demonstrate the potential for real-world impact. Our journal welcomes original research articles, reviews, and perspectives from researchers, scholars, and professionals across the global scientific community, promoting interdisciplinary collaboration and the advancement of chemical sciences. The scope of this journal encompasses a wide range of topics within the field of chemistry, with a particular focus on advancing knowledge and innovation in the following areas: 1. Theoretical Chemistry and Environmental Chemistry: This includes theoretical studies, computational modeling, and experimental investigations related to chemical reactivity, molecular structures, spectroscopy, and the environmental fate and impact of chemicals. 2. Materials Synthesis for Energy and Environmental Applications: The journal welcomes research on the synthesis, characterization, and application of materials for energy storage, catalysis, solar energy conversion, pollution mitigation, and sustainable environmental technologies. 3. Isolation, Purification, and Modification of Biomolecules: Manuscripts addressing the isolation, purification, and modification of biomolecules, such as proteins, nucleic acids, carbohydrates, and lipids, along with their applications in areas such as biotechnology, drug discovery, and diagnostics, are of particular interest. 4. Fabrication, Development, and Validation of Analytical Methods: The journal encourages submissions focusing on the development and optimization of analytical techniques, including chromatography, spectroscopy, electrochemistry, and mass spectrometry. Topics may include method validation, sample preparation, quality control, and applications in diverse fields.
Articles
218 Documents
<![CDATA[Kinetics Study on Thermal Degradation of Polystyrene and Sulfonated Polystyrene from Styrofoam Waste ]]>
<![CDATA[Pramono, Edi]]>;
<![CDATA[Dewi, Chintya]]>;
<![CDATA[Rahmawati, Fitria]]>
<![CDATA[ Molekul Vol 18 No 3 (2023) ]]>
Publisher : <![CDATA[Universitas Jenderal Soedirman ]]>
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DOI: 10.20884/1.jm.2023.18.3.7306
<![CDATA[This research studied kinetics of thermal degradation of polystyrene (PS), and sulfonated polustyrene (sPS) which were synthesized from styrofoam waste. The thermal study was conducted by thermogravimetric analysis (TGA) at various heating rate of 10, 15, 20 and 25 dpm. The kinetics parameters were determined by Coats Redfern (CR), Friedman (FM), Kissinger-Akahira-Sunose (KAS) and Ozawa-Flynn-Wall (OFW) models. TGA result found that PS has range thermal stability of 274 – 415 oC, but sPS has range thermal stability of 175 – 582 oC. Kinetic study to PS shows that the activation energy increases by the increasing of fraction conversion for all kinetics parameters with a regression value close to 1. While in sPS, the CR method shows an increase in activation energy value with an increasing fraction convertion. On the other hand, CR-FM-KAS and OFM methods obtained an increase in activation energy, then decreased at the fraction convertion above 0.6, and received negative activation energy. The kinetics model successfully explains the degradation of PS and sPS. In addition, the high thermal stability of sPS from styrofoam waste shows that this material has good potential as polymer electrolyte materials.]]>
<![CDATA[Immobilization of Urease from Psophocarpus tetragonolobus L. DC. using Natrium Alginate Supporting Matrix ]]>
<![CDATA[Zusfahair, Zusfahair]]>;
<![CDATA[Ningsih, Dian Riana]]>;
<![CDATA[Lestari, Puji]]>;
<![CDATA[Bilalodin, Bilalodin]]>;
<![CDATA[Aryanti, Eva]]>;
<![CDATA[Muslihah, Niken Istikhari]]>
<![CDATA[ Molekul Vol 19 No 1 (2024) ]]>
Publisher : <![CDATA[Universitas Jenderal Soedirman ]]>
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DOI: 10.20884/1.jm.2024.19.1.7335
<![CDATA[Urease is an enzyme that has the role to hydrolyzes urea into ammonia and carbon dioxide. Immobilization is one of the most efficient strategies to improve its activity recovery and properties of urease. This research started with the germination of winged beans for 8 days. The winged bean was extracted by grinding using a mortar and pestle and then added with phosphate buffer at pH 7. The solution was homogenized using a stirrer and then centrifuged in cold conditions so that an extract of urease was obtained. Urease extracts were immobilized using a chitosan-supporting matrix. Optimization of the immobilization process of urease extract includes the concentration of chitosan and sodium tripolyphosphate (TPP) and contact time. The obtained was free and immobilized urease activities then tested using the Nessler method and measured using a UV-Vis spectrophotometer with a wavelength of 500 nm. The obtained data were then statistically tested using ANOVA. Urease-chitosan beads were further tested in repeated use and analyzed with SEM-EDX (Scanning Electron Microscopy-Energy Dispersive X-ray). The results showed that the optimum conditions for making urease-chitosan beads were a concentration of 4% (w/v), 2.5% (w/v) TPP, and 60 minutes of contact time, resulting in an activity value of 15.076 U/mL, which can be used 5 times with 46% activity from the initial activity. The EDX analysis results after the addition of the enzyme showed atom composition changes leading to increasing carbon and nitrogen contents. The existence of phosphor showed that TPP was a chitosan cross-link compound. Keywords: Chitosan, immobilization, TPP, urease, winged bean]]>
<![CDATA[Immunostimulant Compounds Identification in Indonesian Underutilized Zingiberaceae Spices ]]>
<![CDATA[Rosalina, Dian]]>;
<![CDATA[Yuliana, Nancy Dewi]]>;
<![CDATA[Anggraeni, Ririn]]>;
<![CDATA[Prangdimurti, Endang]]>
<![CDATA[ Molekul Vol 18 No 3 (2023) ]]>
Publisher : <![CDATA[Universitas Jenderal Soedirman ]]>
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DOI: 10.20884/1.jm.2023.18.3.7589
<![CDATA[Spices are known for its health beneficial effect beside its function as flavouring and condiment. This study aimed to screen immunostimulant activities of 12 underutilized species of Zingiberaceae grown in Indonesia. The compound associated with immunostimulant activity in the most active sample was identified by linking the chromatogram profile of hexane, chloroform, ethyl acetate, methanol, and water fractions of the selected spices to its activity using orthogonal projection to the least square (OPLS) analysis, followed by LC-MS characterization. The result showed that Alpinia malaccensis and Zingiber ottensii had the highest lymphocyte cell proliferation index (SI) at concentrations of 400 ppm. A. malaccensis was chosen for the next step. The results of OPLS analysis showed that the retention time interval which strongly correlated with the immunostimulant activity was 27.0 – 28.5 minutes, which were abundant in methanol fraction. The mass spectra analysis of methanol fraction using UHPLC-HRMS showed that the respective retention time was attributed to flavokawain B. This compound was reported to increase rat splenocyte proliferation in vivo.]]>
<![CDATA[Physicochemical Properties and Biodegradability of Biofilm Based on Taro Starch and Duck Bone Gelatin ]]>
<![CDATA[Laksanawati, Trias Ayu]]>;
<![CDATA[Khirzin, Muhammad Habbib]]>;
<![CDATA[Amaniyah, Maghfirotul]]>;
<![CDATA[Meidayanti, Karina]]>;
<![CDATA[Deva, Bella Diah]]>
<![CDATA[ Molekul Vol 19 No 1 (2024) ]]>
Publisher : <![CDATA[Universitas Jenderal Soedirman ]]>
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DOI: 10.20884/1.jm.2024.19.1.7628
<![CDATA[Biofilm is an environmentally friendly plastic that is easily biodegradable. However, not all biodegradable plastics have the desired properties for packaging because they are made from renewable natural materials. The biofilm in this study was made from renewable natural raw materials that had never been used before, namely taro starch and duck bone gelatin. Mixing the two materials improve their physical properties and biodegradabilily This study was to to investigate the effect of adding duck bone gelatin 0%, 5%, 15%, 25% and 35% on physicochemical properties, namely color, oxygen permeability, and metal content (Pb and Cd) as well as biodegradability of biofilms. The method used in this research was solution casting. The results obtained from the color parameter with the highest lightness (L) value were produced in the addition of 15% of 85.26, for the highest value of color a was produced in the addition of 0%, namely 0.94, and the value of color b with the addition of 35% resulted in the highest color value of 1.67. The highest percentage of biodegradability was produced on day 14 with the addition of 35% duck bone gelatin in compost soil to produce a percentage of 100%, while for barren soil the yield was 54.54%-66.66%. The content of Cd and Pb in the biofilm is below the SNI limit. Biofilm is impermeable which can be used as food packaging. Keywords: Biodegradability, biofilm, gelatin, physicochemical, starch]]>
<![CDATA[Synthesis of Some New Amino Carbonyl Compounds by Mannich Reaction ]]>
<![CDATA[Dawood, Nagham]]>;
<![CDATA[Saeed, Banan]]>;
<![CDATA[Saeed, Zainab]]>
<![CDATA[ Molekul Vol 19 No 1 (2024) ]]>
Publisher : <![CDATA[Universitas Jenderal Soedirman ]]>
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DOI: 10.20884/1.jm.2024.19.1.7799
<![CDATA[Beta-aminocarbonyl compounds are important intermediates produced from Mannich condensation. In this research, benzaldehyde, para-hydroxy acetophenone or para-nitro acetophenone were reacted with a various of primary aromatic amines to give compounds (1-7) and (8-14), respectively. The chemical formulas of the synthesized compounds were confirmed by conducting some physical and spectroscopic measurements, such as, melting points, IR and H1-NMR spectrum. After testing the biological activity of some of the synthesized compounds (8,10,11,13) using Gram-positive (Streptococcus, and Staphylococcus aureus), Gram-negative (Klebsiella spp., and Escherichia coli) bacteria, as well as yeast strains, were chosen for this investigation (candidan albicans). Isolated bacteria were identified using standard methods of isolation and identification, including direct assays and culture on various media. Some theoretical tests have also been carried out such as SwissADME and cardioToxCSM prediction on all prepared compounds to predict their activity in terms of pharmacokinetic properties (ADME) and also predict their cardiotoxicity on some heart functions such as arrhythmia, cardiac failure, heart block, hERG toxicity, Hypertension (HT), and Myocardial Infarction (MI). Keywords: Secondary amines, aldehyde, Mannich condensation, antimicrobial activity.]]>
<![CDATA[Steroids Produced by Endophytic Fungus Lasiodiplodia Theobromae From Aglaia Argentea Blume and Their Cytotoxic Activity Against Hela Cervical Cancer Cell Lines ]]>
<![CDATA[Supratman, Unang]]>;
<![CDATA[Purbaya, Sari]]>;
<![CDATA[Harneti, Desi]]>;
<![CDATA[Wulandari, Asri Peni]]>;
<![CDATA[Mulyani, Yeni]]>;
<![CDATA[Azhari, Azmi]]>;
<![CDATA[Sari, Aprilia Permata]]>
<![CDATA[ Molekul Vol 18 No 3 (2023) ]]>
Publisher : <![CDATA[Universitas Jenderal Soedirman ]]>
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DOI: 10.20884/1.jm.2023.18.3.7824
<![CDATA[Three steroids, ergosterol (1), ergosterol peroxide (2) and stigmasterol (3) have been isolated from endophytic fungus, Lasiodiplodia theobromae derived from the root of Aglaia argentea Blume. The steroids were isolated by vacuum chromatography and column chromatography, the chemical structure was established following the analysis of 1D-NMR, 2D-NMR, IR, MS and by comparison with previously reported spectra data. Ergosterol peroxide (2) and stigmasterol (3) were reported for the first time isolated from Lasiodiplodia theobromae endophytic fungus. Cytotoxic activities of the compounds were tested with resazurin assay against HeLa cervical cancer cells, compound 2 displayed strongest cytotoxic activities against HeLa cervical cancer cells with IC50 values of 0.28 µM, while compounds 1 and 3 showed IC50 values of 0.34 µM and 27.32 µM, respectively]]>
<![CDATA[Synthesis, Activity Test and Molecular Docking of Novel Nitrophenylcalix[4]-2-methylresorcinarene Derivatives as Antimalarial Agent ]]>
<![CDATA[Nisa, Siti Astika]]>;
<![CDATA[Jumina, Jumina]]>;
<![CDATA[Mardjan, Muhammad Idham Darussalam]]>;
<![CDATA[Kurniawan, Yehezkiel Steven]]>
<![CDATA[ Molekul Vol 18 No 3 (2023) ]]>
Publisher : <![CDATA[Universitas Jenderal Soedirman ]]>
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DOI: 10.20884/1.jm.2023.18.3.7866
<![CDATA[This research involved the synthesis, antimalarial assay and molecular docking of novel nitrophenylcalix[4]-2-methylresorcinarene derivatives. Calix[4]-2-methylresorcinarene derivatives, i.e., 2N, 3N and 4N, were synthesized in a one-step reaction through the cyclo-condensation reaction between resorcinol and aldehydes, i.e., 2-nitrobenzaldehyde, 3-nitrobenzaldehyde and 4-nitrobenzaldehyde, respectively. The reaction was carried out through the reflux method with ethanol and hydrochloric acid 37% as the solvent and catalyst, respectively. The synthetic products were characterized using FTIR, 1H-NMR, 13C-NMR, and LC-MS spectrometers. Furthermore, the in vitro antimalarial assay was carried out against Plasmodium falciparum strain 3D7. The results showed that the 2N, 3N and 4N compounds were successfully synthesized in 86.4, 78.6 dan 95.7% yield, respectively. The antimalarial activity test of 2N, 3N and 4N gave IC50 values of 2.35, 1.68 and 1.79 µM, therefore, these compounds are classified as active antimalarial agents. Molecular docking performed against the PfLDH receptor showed that the 2N, 3N and 4N compounds had negative binding affinity values of -5.1, -6.1, and -6.0 kcal/mol and had specific interactions in the form of hydrogen bonds to the amino acid residues Arg109, Thr101 and Lys102 in the active site of the receptor. The molecular docking results agreed with the experimental antimalarial assay demonstrating the mechanism of action of nitrophenylcalix[4]-2-methylresorcinarenes as active antimalarial agents happened through the inhibition of the PfLDH receptor.]]>
<![CDATA[Potential Endophytic Fungi from the Leaves of Syzygium zeylanicum (L.) and Their Secondary Metabolite ]]>
<![CDATA[Elfita, Elfita]]>;
<![CDATA[Syarifah, Syarifah]]>;
<![CDATA[Widjajanty, Hary]]>;
<![CDATA[Setiawan, Arum]]>;
<![CDATA[Kurniawati, Alfia Rahma]]>
<![CDATA[ Molekul Vol 18 No 3 (2023) ]]>
Publisher : <![CDATA[Universitas Jenderal Soedirman ]]>
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DOI: 10.20884/1.jm.2023.18.3.7881
<![CDATA[Endophytic fungi coexist without harms in the host in some parts or all parts of its lifecycle. Endophytic fungi excrete specialized bioactive compounds beneficial for of its host; the compound itself can be different from what can be found on their host. Endophytic fungi are capable to excrete biologically significant secondary metabolites acting as antidiabetic, antioxidant, antimicrobial, and cytostatic agents. Endophytic fungi existence are common across different plants; including Syzygium zeylanicum that can be found in Indonesia. This study aims to isolate endophytic fungi found in leaves of Syzygium zeylanicum, L., to elucidate their characterized morphologically, and to examine its antimicrobial and antioxidant properties in addition to their chemical structures. Characterization of endophytic fungi was conducted by their macroscopic and microscopic features, followed by molecular characterization of highly bioactive metabolites. Antimicrobial activities were measured by disc diffusion method. Antioxidant properties were measured with DPPH. Secondary metabolites were chromatographically isolated and identified with spectroscopy techniques (NMR ID and 2D). Four endophytic fungi isolates were obtained: Penicillium citrinum (SZ1), Colletotrichum lindemuthianum (SZ2), Aspergillus nidulan (SZ3), Scopulariopsis asperula (SZ4). Penicillium citrinum (SZ1) showed antimicrobial activities against four different bacteria (71.3% against E. coli; 74.1% against S. aureus; 76.2% against S. typhi; and dan76.9% against B. subtilis). Antioxidant activity ini all ekstrak of endophytic fungi showed very activity (IC50 SZ3 extract = 3.85 µg/mL). Potential endophytic fungi SZ1 was molecularly identified as Penicillium citrinum. Extracts from SZ1 fungi contains bioactive 4-hydroxy-2-(4-hydroxyphenyl)-ɣ-butyrolactone-3-yl) methyl acetate. The newly obtained substance could be developed into antimicrobial and antioxidant agents in further studies.]]>
<![CDATA[The Sesquiterpenoids from Aglaia cucullata Peel Fruit and Their Cytotoxic Activities Against B16-F10 and HeLa Cancer Cell Lines ]]>
<![CDATA[Supratman, Unang]]>;
<![CDATA[Anjari, Intan Hawina]]>;
<![CDATA[Harneti, Desi]]>;
<![CDATA[Naini, Al Arofatus]]>;
<![CDATA[Farabi, Kindi]]>;
<![CDATA[Anwar, Risyandi]]>
<![CDATA[ Molekul Vol 18 No 3 (2023) ]]>
Publisher : <![CDATA[Universitas Jenderal Soedirman ]]>
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DOI: 10.20884/1.jm.2023.18.3.7900
<![CDATA[Sesquiterpenoids are terpenoid derivative compounds that have a diverse chemical structure and pharmacological effects. Sesquiterpenoids can be found in many plants of Aglaia which is the large source of natural compounds in the Meliaceae family. This research was aimed to elucidate the structure of sesquiterpenoids from the peel fruit of Aglaia cucullata and their cytotoxic activities against two human cancer cell lines. The n-hexane extract was separated and further purified by various chromatographic methods to yiled three sesquiterpenoids. The structure of these sesquiterpenoids were identified by spectroscopy analysis including MS, IR, 1H-NMR, 13C-NMR and DEPT as well as compared with spectral data which reported previously. The sesquiterpenoid compounds 1-3 were identified as spathulenol (1), alismol (2), and 10-oxo-isodauc-3-en-15-al (3). The cytotoxic activity of three sesquiterpenoid compounds were tested against HeLa cervical cancer cell and B16-F10 skin cancer cell using the PrestoBlue method. Compound 2 exhibited the highest activity against both HeLa and B16-F10 cancer cell lines with IC50 48.11 μg/mL and 57.05 μg/mL, respectively.]]>
<![CDATA[Antimicrobial Activity of Natural Solid Soap with a Combination of Liquid Cheese Waste, Turmeric (Curcuma longa), and Dragon Fruit (Hylocereus polyrhizus) Peel ]]>
<![CDATA[Estikomah, Solikah Ana]]>;
<![CDATA[Suranto, Suranto]]>;
<![CDATA[Susilowati, Ari]]>;
<![CDATA[Masykuri, Mohammad]]>
<![CDATA[ Molekul Vol 18 No 3 (2023) ]]>
Publisher : <![CDATA[Universitas Jenderal Soedirman ]]>
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DOI: 10.20884/1.jm.2023.18.3.8039
<![CDATA[Yoghurt whey is a product from fermented cheese liquid waste. Yoghurt cheese liquid waste has been known to contain lactoferrin. Lactoferrin functions as an antimicrobial. yoghurt made from whey has not been widely utilized as a solid soap ingredient. This research focuses on producing solid natural soap made of yoghurt whey with added natural dye turmeric and dragon fruit peel, soap quality testing, and analysis of the soap's antibacterial activity toward Staphylococcus aureus. The solid soap was processed through the saponification reaction between palm oil, coconut oil, zaitun oil, and canola oil with sodium hydroxide. Variations of yogurt whey used in this study yoghurt 25%,75%,100% whey) was added natural dye (turmeric and dragon fruit peel). The quality test was done by determining free alkali, water content, pH, and foam height. Antibacterial activity test using the well diffusion method. The result shows that the quality test yoghurt soap meets with INS (Indonesia National Standard) 2016, for all the criteria. Performs inhibition against bacteria Staphylococcus aureus. Yoghurt whey is potently used as an antibacterial agent in the manufacture of natural solid soap.]]>
