DAFTAR PUSTAKA Anand, P., Kunnumakara, B., Thomas, S.G., 2008, Biological activities of curcumin and its analogues (Congeners) made by man and mother, Nature, 76:1590–1611. Anastas, P. T., Warner, J. C., 1998, Green Chemistry: Theory & Practice, Oxford Univ. Press, New York Aggarwal, B., Mishra, P.K., 2010, Curcumin and its Analogues: Potential Anticancer Agent, Medicinal Research Reviews, 30(5): 818-60 Aggarwal, B., Reddy, G.V., Reddanna, P., 2009, Eicosanoids in inflammation and cancer: the role of COX-2. Expert Rev Clin Immunol, 5(2):145-65 Akram, M., Uddin, S., Ahmed, K., Usmaghani, K., 2010, Curcuma Longa and Curcumin: A Review Articl, J. Plant Biol, 55(2): 65-70. Anand, P., Kunnumakara, B., Newman, R.A., Aggarwal, B.B., 2009, Bioavailibility of Curcumin : Problem and Promises, Molecular Pharmaceutics, 4(6): 807-18. Banditpuritat, J., Phutdhawong, W.S., and Phutdhawong, W., 2009, Microwaveinduced Acetylation of 2-methyl-5-hydroxy-1,4-naphthoquinone (Plumbagin), Maejo Int.J.Sci. Technol., 3(3), 366-70. Bhuiyan, M. M. H., Hossain, M. I., Mahmud, M. M., 2011, Microwave-assisted Efficient Synthesis of Chalcones as Probes for Antimicrobial Activities, Chemistry Journal ,1(1) : 21-8 Bembenek, S.D., Tounge, B. a, and Reynolds, C.H. 2009, Ligand efficiency and fragment-based drug discovery. Drug Discov, 14: 278–283. Bove, D., 2014, Computational Chemistry D. Bove, ed., New York: Nova Science Publishers,Inc. Chen, Y.-C. 2015. Beware of docking! Trends in Pharmacological Sciences, 36(2), 78–95. doi:10.1016/j.tips.2014.12.001 Christopher, C.C., Sundarananthavalli., Kulandaisami, A., 2011, Synthesis Characterisation,Analgesic,Antiinflammatory, Anti-ulcer, Wound healing and Antimicrobial effects of Curcuminoids. IJCRGG.2011;3(4):2040-2046.
144
Da’i, M., 2012, Perkembangan Riset Kurkumin: Sintesis dan Uji Aktivitasnya, Seminar Nasiponal Kunyit (Curcuma longa) Tinjauan Filosofis dan Ilmiah, Bagian Kimia Farmasi UGM, 12 Januari 2012. Eberhard, B., 2002, Structure Elucidation by NMR in Organic Chemistry Third Revi., Chichester: John Wiley & Sons Ltd. Departemen Kesehatan Republik Indonesia, 1995, Farmakope Indonesia. Edisi IV. Jakarta: Direktorat Jendral Pengawasan Obat dan Makanan, Hal 1002-35. Eufimia, C., 2014, ‘Penentuan Kondisi Optimum Sistem KCKT untuk Analisis Senyawa 1,5-bis(3’-etoksi-4’-hidroksifenil)-1,4-pentadien-3-on’ (EHP), Skripsi, Fakultas Farmasi Universitas Pancasila Jakarta. Geldenhuys, W.J., 2006, Optimizing the use of open source software applications in drug discovery. DDT, 11 (3/4), 127-32. Hart, H., Craine, L. E., Hart, D., 11th Ed, 2003, Organic Chemistry, Brooks Cole, Houghton Mifflin Co, pp.294-96. Hayes, B. L. 2004, Recent Advances in Microwave- Assisted Synthesis. Adrichimica ACTA, 37(2), 66–76. Huang, N., Shoichet, B.K., Irwin, J.J., 2006, Benchmarking sets for molecular docking. J. Med. Chem., 49, 6789-80 Istyastono, E. P., Riswanto, F.D., Yuliani, S.H., 2015, Computer-Aided Drug Repurposing: Acyclooxygenase-2 Inhibitor Celecoxib as A Ligand for Estrogen Alpha, Indones. J. Chem., 15(3), 274–280. Itokawa, H., Shi, S., Akiyama, T., 2008, Recent advances in the investigation of curcuminoids. , 13, pp.1–13. Jacobs, 2006, Microwave Assited Organic Synthesis (MAOS).
diakses pada 12 April 2013 Jawetz, Melnick, Adelberg, 2008, Mikrobiologi kedokteran edisi 20. Alih Bahasa Nugroho E, Maulany RF. Jakarta: Penerbit Buku Kedokteran;. Hal 1537,627-8. Jenie, U.A., Kardono, L.B., Hanafi, M., 2006, Teknik Modern Spektroskopi NMR, LIPI, Jakarta Kappe, C. O., Dallinger, D., & Murphree, S. S. 2009, Practical Microwave Synthesis for Organic Chemists (pp. 45–47, 161–182). Weinheim: WileyVCH.
145
Kappe, C. O., & Dallinger, D., 2012, Microwaves in Organic and Medicinal Chemistry (pp. 1–14). Weinheim: Wiley-VCH Kufareva, I., Rueda, M., Katritch, V., 2011, Status of GPCR modeling and docking as reflected by community-wide GPCR Dock 2010 assessment. Structure. Li, C., Anastas, T., 2012, Green Processes: Green Synthesis, Weinheim: WileyVCH, Vol 7, pp 23-24, 35-54, 60 Lidstrom, P., Tierner, J., Wather, B., and Westman, J., 2001, Microwave Assisted Organic Synthesis- A Review, Tetrahedron, 57, 9225-83. Lindell, M., 2003, Modeling of a System for Microwave Assisted Organic Synthesis-A Review, diakses pada 12 April 2013 <www.s3.kth.se/~kallej/grad_students/lindell_thesis03.pdf> Lu, F.C., 1995, Toksikologi dasar asas, organ sasaran, dan penelitian resiko, Edisi 2, Diterjemahkan oleh Edi Nugroho. Jakarta , UI Press. Majeed, M. Badmaer, V., Shivakumar, U., Rajendran, R. 1995, Curcuminoids: Antioxydant ,Phytonutrients McMurry, 2012, Organic Chemistry, 9th Ed, Thomson Brooks/Cole, Australia, United States, pp 1043-54 Meiyanto, 2011, Harapan dan tantangan pengembangan agen kemoprevensi kanker tepat sasaran. Pidato Pengukuhan Jabatan Guru Besar pada Fakultas Farmasi Universitas Gadjah Mada, Yogyakarta, h: 9 Mysinger, M.M., Shoichet, B. K.., 2012, Directory of Useful Decoys, Enhanced (DUD-E): Better Ligands and Decoys for Better Benchmarking. Mohan, S.B., Behera T.P., Ravi Kumar B.V.V., 2010, Microwave Irradiation Versus Conventional Method: Synthesis of Benzimidazolyl Chalcone Derivatives, International Journal of ChemTech Research, 2(3): 1634-37 Muegge, I., Rarey, M., Lipkowitz, K.B., Boyd, D.B., 2001, Reviews In Computational Chemistry. New York.; 17 :1-6. Mumpuni, E., Agus. N, Mayagustina, A., Arie, B.S., 2009, The Molecular Docking of 1,5-diphenil-1,4-pentadien-3-on derivates as The Inhibitor of COX-2 enzyme in Henk Timmerman International Seminar & Awards (HTSIA) on Structure Based Drug Design, Yogyakarta.
146
Mumpuni, E., Budi, I., Mayagustina, A., Arie, B.S., 2009, Docking Molekul Derivat 1,5-difenil-1,4-pentadien-3-on sebagai inhibitor enzim LOX-5, Seminar dan Konggres Nasional ISFI, Bidakara, Jakarta. Mumpuni, E., Indriana, P., Evi, L., Enjang, R., 2010, Sintesis dan uji antioksidan senyawa 1,5-bis(3’-etoksi-4’-hidroksifenil)-1,4-pentadien-3-on, Jurnal Ilmu Kefarmasian Indonesia, 8: Mumpuni, E., Rahayu, L., Nurrochmad, A., 2015, Toksisitas dan Antiinflamasi Senyawa 1,5-bis(3’-etoksi-4’-hidroksifenil)-1,4-pentadien-3-on, Jurnal Ilmu Kefarmasian Indonesia, 13(1): 45-49. Naga S. K., Shakira, M., Prasanthi, P., et al., 2008, Virtual screening for novel COX-2 inhibitors using the ZINC database. Biomedical Informatics Publishing Group. Nurfina, A.N., 1994, Synthesis of Some Symmetrical Curcumin Derivates and Their Anti-inflammatory Activities as well as Structure Activity Relationship, Dissertation, UGM Nurfina, A.N., Reksohadiprojo, M.S., Timmerman, H., Jenie, U.A., Sugiyanto, D., van der Goot, H., 1997, Synthesis of Some Symmetrical Curcumin Derivates and Their Anti-inflammatory Activity, Eur J Med Chem, 32: 321-28 Nurrochmad, A., Supardjan, A.M., Sardjiman, 1998, Penghambatan Siklooksigenase oleh Siklovalon dan Tiga Senyawa Analognya, Majalah Farmasi Indonesia, IX (4): 180-185. Nurrochmad, A., 2004, Pandangan Baru Kurkumin dan Aktivitasnya sebagai Antikanker, Biofarmasi 2 (2): 75-80 Oko, S., 2012, Sintesis senyawa p-metoksibenzil asetat dan p-etoksibenziltiol asetat dari minyak adas dengan metode sonikasi gelombang mikro dan penggerusan, Thesis, UGM Pavia, D.L., Lampman, G.M., Kriz, G.S., & Vyvyan, J.R., 2001, Introduction to Spectroscopy, 4th Ed, Department of Chemistry, Western Washongton University Bellingham, Washington Pelczar, M. J., Chan, J. C., 1996, Dasar-dasar mikrobiologi. Terj. Ratna Sri Hadioetomo, Teja Imas, S. Sutami, Tjitrosomo dan Tri Lestari Agka. Jakarta: Penerbit UI Press.; Hal 116-117,523,949,954. Pranowo, H.D., 2009, Peran kimia komputasi dalam desain molekul obat., Pengukuhan Guru Besar UGM, Yogyakarta
147
Pranowo, H.D., Kadir, A.R.H., 2011, Pengantar Kimia Komputasi, Lubuk Agung , Bandung Prasojo, S.L., Hartanto, F. A.D., Yuniarti, N., Ikawati, Z., Istyastono, E.P., 2010, Dockingof1-Phenylsulfonamide-3-trifluoromethyl-5-parabromophenylpyrazole to cyclooxygenase-2 using PLANTS, Indonesian Journal of Chemistry, 10, 348-51 Pratiwi, S. T., 2008, Mikrobiologi Farmasi. Jakarta: Erlangga; Hal 188-91. Rao, M.N.A., 1997, Antioxidant properties of curcumin. Departement of Pharmaceutical Chemistry College of Pharmaceutical Science. Manipal, India, 39-42 Ravindran, J., Prasad, S. & Aggarwal, B.B., 2009, Curcumin and Cancer Cells : How Many Ways Can Curry Kill Tumor Cells Selectively , 11(3). Ronald, B., Levi, M.,Wilson, N., 2008, Nonsteroidal Anti-Inflamatory Drugs in Foye’s Principles of Medicinal Chemistry, 6thed, Wolters Kluwer, Lippincott Williams&Wilkins, Philadelphia- Tokyo Robinson, Ehlers, T., Hubbard, R.B., .,2003, Design, Synthesis and Biological Evaluation of Angiogenesis Inhibitors: Aromatic Enone and Dienone Analogues of Curcumin, Bioorg. Med. Chem, 13: 115-17 Rotella, D., 2015, Green Chemistry Strategies for Drug Discovery Series, Editors : (P. Emily & M. Julie, Eds.) (pp. 1–11), Cambridge: The Royal Society of Chemistry. Stankovic, I., 2004, Chemical and Technical Assessment 61st, JECFA., 1(8): 1–8. Santosa, Juari, S., 2008, Kimia Hijau Sebagai Pilar Utama Pembangunan Lestari. Yogyakarta: FMIPA, Universitas Gajah Mada. Sardjiman, 2000, ‘Synthesis of Some new series of Curcumin anlogues, antioxidative, anti-inflammatory,antibacterial activities and QualitativeStructure Activity Relationships’, Dissertation, Gadjah Mada University, Yogyakarta Sastroamidjojo, H., 2007, Spektroskopi, Cetakan ketiga, Liberty, Yogyakarta Shi, S. Z. and Jiann, Y. H., 2003, Microwave-assisted wet chemical synthesis : advantages, significance, and steps to industrialization, Journal of Minerals & Materials Characterization & Engineering, 2(2): 101-10
148
Silverstein, R.M., Bassler, G.G., and Morrill, T.C., 2002, Spectrometric Identification of Organic Compounds, 6th Ed, alih bahasa Hartono, A.J, Erlangga, Jakarta., Silverstein, R.M., Bassler, G.G., and Morrill, T.C., 2005, 7 Ed, Spectrometric Identification of Organic Compounds, John Wiley &Sons, New York Supardjan, A.M., 1999, ‘Synthesis and anti-inflammatory activity of some 4substitued curcumin derivates’, Dissertation, Gadjah Mada University, Yogyakarta Supardjan, A.M., Permatasari I., 2006, Sintesis senyawa bahan alam 1,5 bis(4’hidroksi-3’metoksifenil)-1,4-pentadien-3-on. Majalah Obat Tradisional. Vol II April-Juni 2006; (36). Hal. 15-20. Supardjan, A.M., Muhammad Da’I., 2005, Hubungan Struktur dan Aktivitas Sitotoksik Turunan Kurkumin Terhadap Sel Myeloma, Majalah Farmasi Indonesia ; 100-04 Utomo, P., 2010, Green Chemistry dengan Kimia Katalis, Prosiding Seminar Nasional Penelitian, Pendidikan dan Penerapan MIPA, Fakultas MIPA, Universitas Negeri Yogyakarta, 15 Mei 2010 Windholz, M.. The Merck Index. 13th ed. Rahway: Merck 7 Co., Inc; 2001. p 69,3881 Wade, L.G., 2006, Organic Chemistry, 6 ed, Pearson Prentice Hall, USA, pp 1056-75 Warren, Stuart, 2008, Organic Synthesis: The Disconection Approach, John Wiley & Sons, Chicester Yuniarti, N., Ikawati, Z., Istyastono, E. P., 2011, The importance of ARG513 as a hydrogen bond anchor to discover COX-2 inhibitors in a virtual screening campaign, Bioinformation, 6, 164-6. Yuniarti, N., Istyastono, E.P., 2012, In vitro and In Silico Studies on Curcumin and Its Analogues as Dual Inhibitiors for cyclooxygenase-1 (COX-1) and cyclooxygenase-2 (COX-2) , ITB J.Sci, Vol 44 A, No.1, 51-56 __________, WiDR tanggal 19 Desember 2013
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