{"id":2252,"date":"2018-10-18T15:23:50","date_gmt":"2018-10-18T08:23:50","guid":{"rendered":"https:\/\/www.its.ac.id\/kimia\/?page_id=2252"},"modified":"2025-04-09T11:58:09","modified_gmt":"2025-04-09T04:58:09","slug":"natural-material-chemistry-laboratory-and-synthesis","status":"publish","type":"page","link":"https:\/\/www.its.ac.id\/kimia\/en\/facilities\/laboratory\/natural-material-chemistry-laboratory-and-synthesis\/","title":{"rendered":"Natural Material Chemistry Laboratory and Synthesis"},"content":{"rendered":"

[vc_row][vc_column][vc_tta_accordion][vc_tta_section title=”About” tab_id=”1518428298141-3646fd64-f224″][vc_column_text]Natural Produtcs and Chemical Synthesis<\/strong><\/em><\/p>\n

Bioactive chemicals, fragrance & flavors, and Energetic Materials<\/em>[\/vc_column_text][\/vc_tta_section][vc_tta_section title=”Research Topics” tab_id=”1518428645712-0de4c0cf-78e0″][vc_column_text]BIOACTIVE CHEMICALS<\/span><\/p>\n

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  1. Natural ingredients that are active and have the potential as anti-cancer, anti-diabetic and anti-malarial agents of the genus Clusiaceae<\/span><\/li>\n
  2. Correlation data on the structure and bioactivity of natural material compounds<\/span><\/li>\n
  3. Synthesis of derivatives and analogues of active and potential natural ingredients<\/span><\/li>\n
  4. Nitroaromatic compounds are found as natural materials which among others are found in mangrove plants. The study succeeded in synthesizing 2 itoaromatic compounds, 1 was studied for its activity in inhibiting the growth of Candida albicans, Fusarium graminearum, Aspergillus niger<\/span><\/li>\n
  5. The study succeeded in synthesizing trisindolina natural compounds and 25 derivatives. As lead compound, trisindolina shows activity as antibiotics and anti-cancer. The bioactivity test shows that:<\/span><\/li>\n
  6. a) 5 trisindolina derivatives were tested and showed antibiotic activity against E. coli (gram negative) and S. aureus (gram positive), b) 13 trisindolina derivatives were tested and cytotoxic against cervical and colon cancer cells, c) 4 were tested and inhibited the growth of Mycobacterium tuberculosis H37Rv and isolates of pulmonary tuberculosis patients Px 1 and Px 2<\/span><\/li>\n
  7. Computational study of Quantitative Structure-Activity Relationship (QSAR) and molecular docking to obtain the optimal structure of trisindolina derivatives as anti-cancer<\/span><\/li>\n
  8. Synthesis, in vitro testing and in vivo compounds from computational studies<\/span><\/li>\n<\/ol>\n

    FRAGRANCE (PEWANGI) AND FLAVOR (PERISA)<\/span><\/p>\n

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    1. Synthesis of homonuclear, heteronuclear polymer complexes and metalorganic framework with various structures, and the results of cytotoxicity tests on cancer cells<\/span><\/li>\n
    2. Essential oil exploration 18 species of family Myrtaceae<\/span><\/li>\n
    3. Utilization of clove leaf waste for the manufacture of clove leaf oil. The separation and purification of eugenol from clove leaf oil, and its transformation into fragrans \/ flavor: vanillin, vanillil alcohol, Isobutavan\u00ae and its 3 analogues, 2 Isobutavan\u00ae derivatives, and their sensor data<\/span><\/li>\n
    4. Separation of safrol from commercial mace oil, and its transformation into fragrans \/ flavor: isosafrol, heliotropin\u00ae, piperonil alcohol, 7 piperonyl esters, and sensor data<\/span><\/li>\n
    5. Synthesis of new Isobutavan\u00ae derivatives along with their sensor data<\/span><\/li>\n
    6. The transformation of heliotropin\u00ae into analogous commercial fragrans compounds of Methyl diantilis\u00ae as well as sensory data<\/span><\/li>\n
    7. The transformation of heliotropin\u00ae into analog compounds fragrans oxymes and ether oxymes ester groups along with their sensor data<\/span><\/li>\n
    8. Optimization of fragrans synthesis and flavor using new catalysts<\/span><\/li>\n<\/ol>\n

      ENERGETIC MATERIALS<\/span><\/p>\n

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      1. Manufacture of pilot plant diazodinitrofenol scale in cooperation with PT. Pindad<\/span><\/li>\n
      2. The design and production of energetic materials through cooperation partners (PT. Pindad, PT Dahana, LAPAN, etc.)<\/span><\/li>\n<\/ol>\n

        [\/vc_column_text][\/vc_tta_section][vc_tta_section title=”Head of Laboratory” tab_id=”1518420491061-9d0a4081-88f4″][vc_column_text]Prof. Mardi Santoso, Ph.D<\/a>[\/vc_column_text][\/vc_tta_section][vc_tta_section title=”Laboratory Member” tab_id=”1518420491162-b7b8bf2d-b77e”][vc_column_text]<\/p>\n