Dr. Fadilah Fadilah

HOD
Departement of Medical Chemistry, Faculty of Medicine, Universitas Indonesia, Jakarta, Indonesia

Highest Degree
Ph.D. in Chemistry, Pharmacy from Universitas Indonesia, Indonesia

My URL
https://livedna.org/62.35164

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Area of Interest:

Biomedical Sciences
Drug Discovery
Pharmacology
Molecular Genetics
Computational Chemistry

Selected Publications

  1. Zuhri, U.M., E.H. Purwaningsih, F. Fadilah and N.D. Yuliana, 2022. Network pharmacology integrated molecular dynamics reveals the bioactive compounds and potential targets of Tinospora crispa Linn. as insulin sensitizer. PLoS ONE, Vol. 17. 10.1371/journal.pone.0251837.
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  2. Fatriansyah, J.F., A.G. Boanerges, S.R. Kurnianto, A.F. Pradana, Fadilah and S.N. Surip, 2022. Molecular dynamics simulation of ligands from Anredera cordifolia (Binahong) to the main protease (Mpro) of SARS-CoV-2. J. Trop. Med., Vol. 2022. 10.1155/2022/1178228.
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  3. Ahadini, P.A., A.I. Reihan, M.B.W. Utama, S. Khaerunnisa and F. Fadilah, 2022. In-silico study: Potential inhibitor of cyclin-dependent kinase 6 (CDK6) from natural plant compounds for melanoma treatment. Jurnal Ilmiah Mahasiswa Kedokteran Universitas Airlangga, 13: 93-99.
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  4. Fadilah, F., R. Andrajati, A. Arsianti, R.I. Paramita, L. Erlina and A. Yanuar, 2020. Synthesis and in vitro activity of eugenyl benzoate derivatives as BCL-2 inhibitor in colorectal cancer with QSAR and molecular docking approach. BioRxiv, 10.1101/2020.08.17.253591.
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  5. Fadilah, F., V.A. Widodo, R.P. Priawan, E.O. Joyo and H. Abdurrohman et al., 2019. Synthesis nanoparticle extract of clove (Syzygium aromaticum L.) and characterization by differential scanning colorimetry profiling and its activities as inhibitor of hela cell lines. Res. J. Pharm. Technol., 10.5958/0974-360x.2019.00566.3.
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  6. Fadilah, F., L. Wiyono, B.C. Edina, R.A. Rahmawati, L. Erlina, A. Tedjo and R.I. Paramita, 2019. In silico study and In vitro test of extract kaempferia pandurata roxb. as anti ER (+) reast cancer cell line MCF-7. Rese. J. Pharm. Technol., 10.5958/0974-360X.2019.00400.1.
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  7. Marcelia, M., A. Arsianti, J.O.T. Chan, S.J. Wijoyo and F. Fadilah et al., 2018. In vitro cytotoxicity of the synthesized gallic acid derivatives (N-alkyl gallamide) against breast MCF-7 cancer cells. Orient. J. Chem., 34: 2268-2272.
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  8. Kusmardi, K., T. Aryo, W.P. Eka, F. Fadilah, P.B. Pontjo and F. Wilzar, 2018. In silico, in vitro and in vivo tests of Ficus deltoidea jack leaves extract as inhibitor for beta-catenin expression in colon carcinogenesis model. Pharmacogn. J., 10: 808-813.
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  9. Kusmardi, K., A. Tedjo, F. Fadilah, A. Arsianti and R.I. Paramita, 2018. Identification by docking simulation and in vivo effect of essential oil from Cinnamommum burmannii as anti-obesity with leptin receptor in the olfactory system of mice balb C. Pharmacogn. J., 10: 875-879.
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  10. Fadilah, F., A. Arsianti, A. Yanuar, R. Andrajati, R.I. Paramita and E.H. Purwaningsih, 2018. Structure activity relationship analysis of antioxidant activity of simple benzene carboxylic acids group based on multiple linear regression. Oriental J. Chem., 34: 2656-2660.
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  11. Chan, J.O.T., A. Arsianti, M. Marcelia, S.J. Wijoyo and F. Fadilah et al., 2018. Synthesis and anticancer effect of 3,4,5-N-alkyl-benzamides on colon carcinoma HCT- 116 cells. Orient. J. Chem., 34: 1362-1367.
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  12. Arsianti, A., H. Astuti, Fadilah, D.M. Simadibrata and Z.M. Adyasa et al., 2018. Synthesis and in vitro antimalarial activity of alkyl esters gallate as a growth inhibitors of Plasmodium falciparum. Orient. J. Chem., 34: 655-662.
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  13. Fadilah, F., A. Yanuar, A. Arsianti, R. Andrajati and E.H. Purwaningsih, 2017. In silico study of aryl eugenol derivatives as anti-colorectal cancer by inducing of apoptosis. Asian J. Pharm. Clin. Res., 10: 345-349.
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  14. Fadilah, F., A. Yanuar, A. Arsianti and R. Andrajati, 2017. Phenylpropanoids, eugenol scaffold, and its derivatives as anticancer. Asian J. Pharm. Clin. Res., 10: 41-46.
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  15. Fadilah, A. Yanuar, A. Arsianti, R. Andrajati and R.I. Paramita, 2017. In silico study, synthesis, and cytotoxic activity of esterification of eugenol and gallic acid against HT-29 cell line. Orient. J. Chem., 33: 3009-3014.
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  16. Arsianti, A., H. Astuty, Fadilah, A. Bahtiar, H. Tanimoto and K. Kakiuchi, 2017. Design and screening of gallic acid derivatives as inhibitors of malarial dihydrofolate reductase (DHFR) by in silico docking. Asian J. Pharm. Clin. Res., 10: 330-334.
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  17. Arsianti, A., F. Fadilah, L. Erlina and R.I. Paramita, 2017. Molecular docking of antimycin A3 analogs and its aromatic segments as inhibitors of apoptosis protein marker BCL-XL and MCL-1. Asian J. Pharm. Clin. Res., 10: 317-322.
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  18. Arsianti, A., F. Fadilah, K. Kusmardi, G.Y. Sugiarta, H. Tanimoto and K. Kakiuchi, 2017. In silico study and cytotoxicity of the synthesized open-chain analogues of antimycin A3 against HEP-2 laryngeal cancer cells. Curr. Cancer Ther. Rev., 13: 129-136.
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  19. Arsianti, A., Fadilah, Fatmawaty, L.K. Wibisono and Kusmardi et al., 2016. Phytochemical composition and anticancer activity of seaweeds Ulva lactuca and Eucheuma cottonii against breast MCF-7 and colon HCT-116 cells. Asian J. Pharm. Clin. Res., 9: 115-119.
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  20. Vilar, S., G. Cozza and S. Moro, 2008. Medicinal chemistry and the molecular operating environment (MOE): Application of QSAR and molecular docking to drug discovery. Curr. Top. Med. Chem., 8: 1555-1572.
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Member since December, 2020