Bambang Purwono
Bambang Purwono
Email yang diverifikasi di ugm.ac.id
Judul
Dikutip oleh
Dikutip oleh
Tahun
Tetrazolo [1, 5-a] quinolines and 1, 2, 3-Triazolo [1, 5-a] quinazolines by the Action of Cyanocarbanions on 2-azidoarylcarbonyl Compounds
TC Porter, RK Smalley, M Teguiche, B Purwono
Synthesis 1997 (07), 773-777, 1997
411997
Chalcone analogue as potent anti-malarial compounds against Plasmodium falciparum: Synthesis, biological evaluation, and docking simulation study
J Syahri, E Yuanita, BA Nurohmah, R Armunanto, B Purwono
Asian Pacific Journal of Tropical Biomedicine 7 (8), 675-679, 2017
322017
Terapan analisis hansch untuk aktivitas antioksidan senyawa turunan flavon/flavonol
I Tahir, K Wijaya, D Widianingsih
Makalah Seminar Khemometri 25, 2003
312003
Synthesis and biological activity of novel bis-indole inhibitors of bacterial transcription initiation complex formation
M Mielczarek, RV Devakaram, C Ma, X Yang, H Kandemir, B Purwono, ...
Organic & biomolecular chemistry 12 (18), 2882-2894, 2014
292014
Pengantar Praktikum Kimia Organik
C Anwar, P Bambang, DP Harno, DW Titik
Universitas Gajah Mada, Yogyakarta, 1994
281994
The nitration of some 4, 6-dimethoxyindoles
AW Jones, B Purwono, PK Bowyer, PSR Mitchell, N Kumar, SJ Nugent, ...
Tetrahedron 60 (47), 10779-10786, 2004
252004
Syntheses of azo-imine derivatives from vanillin as an acid base indicator
B Purwono, C Anwar, A Hanapi
Indonesian Journal of Chemistry 13 (1), 1-6, 2013
182013
Xanthone as Antimalarial: QSAR Analysis, Synthesis, Molecular Docking and In vitro Antimalarial Evaluation
J Syahri, E Yuanita, BA Nurohmah, MH Wathon, R Syafri, R Armunanto, ...
Orient. J. Chem 33 (1), 29-40, 2017
172017
Structure–antioxidant activities relationship analysis of isoeugenol, eugenol, vanilin and their derivatives
N Aini, B Purwono, I Tahir
Indonesian Journal of Chemistry 7 (1), 61-66, 2007
152007
Antibacterial and antifungal activity of three monosaccharide monomyristate derivatives
J Jumina, M Mutmainah, B Purwono, YS Kurniawan, YM Syah
Molecules 24 (20), 3692, 2019
112019
Synthesis, biological evaluation, QSAR analysis, and molecular docking of chalcone derivatives for antimalarial activity
J Syahri, K Rullah, R Armunanto, E Yuanita, BA Nurohmah, MFFM Aluwi, ...
parasite 4, 8, 2016
112016
Terapan Analisis Hansch Untuk Aktivitas Antioksidan Senyawa Turunan Flavon
I Tahir, K Wijaya, D Wdianingsih, B Purwono
Flavonol. Jogjakarta. Makalah Seminar Khemometri. Jurusan Kimia FMIPA UGM, 2003
102003
isoxazolo [4, 3-c] quinolines from o-azidobenzonitrile oxide by sequential carbanion attack and intramolecular aza-Wittig reaction
B Purwono, RK Smalley, TC Porter
Synlett, 231-232, 1992
101992
Design of New Potential Antimalaria Compound Based on   QSAR Analysis of Chalcone Derivatives 
RA Jufrizal Syahri, Bambang Purwono
International Journal of Pharmaceutical Sciences Review and Research  36 ((2 …, 2016
92016
B. and Wahyunngsih, TD: Micellar Catalytic Effect of Cetyltrimethylammonium Bromide on O-Allylation of Eugenal by Allyl Bromide. Inter
P Hernawan
J. Engineering & Technology IJET-IJENS 12 (1), 1-4, 2012
72012
Analisa hubungan struktur-aktivitas antioksidan dari isoeugenol, eugenol, vanilin dan turunannya
N Aini, B Purwono, I Tahir
Indonesian Journal of Chemistry 7 (1), 61-66, 2007
72007
QSAR study of flavone/flavonol analogues as the antiradical compounds based on Hansch analysis
I Tahir, K Wijaya, B Purwono, D Widianingsih
Indonesian Journal of Chemistry 3 (1), 48-54, 2010
62010
Chalcone Based Colorimetric Sensor for Anions: Experimental and TD-DFT Study
BP Adita Silvia Fitriana, Harno Dwi Pranowo
Indones. J. Chem., 16 (1), 80-86, 2016
52016
Aminoalkylated chalcone: Synthesis, biological evaluation, and docking simulation as potent antimalarial agents
J Syahri, H Nasution, BA Nurohmah, B Purwono, E Yuanita
J Appl Pharm Sci 10 (06), 001-005, 2020
42020
Molecular docking analysis on epidermal growth factor receptor Wild Type (EGFRwt) with quinazoline derivative compounds as tyrosine kinase inhibitors
H Rasyid, R Armunanto, B Purwono
Applied Science and Engineering Progress 10 (4), 293-299, 2017
42017
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