Marcellino Rudyanto, Drs., Apt., MSi., PhD

Year

Education

1990

Bachelor of Science (Drs), Pharmaceutical Science, Faculty of Pharmacy, Universitas Airlangga, Indonesia

1991

Apothecary (Apt), Faculty of Pharmacy, Universitas Airlangga, Indonesia

1996

Master of Science (MSi), Organic Chemistry, Institute Technology Bandung, Indonesia

2002

Doctor of Philosophy (PhD), Pharmaceutical Chemistry, Tohoku University, Japan

 

Courses

Organic Chemistry I, Organic Chemistry II, Synthetic Chemistry, Introduction to Drug Synthesis, Drug Synthesis, Spectroscopic Identification of Organic Compounds, Pharmaceutical Polymer.

 

Research Interests

  • Synthesis of biologically active compounds
  • Development of synthetic methodology
  • Drug development

 

Selected Publications

  1. Dini Kesuma, Siswandono, Bambang Tri Purwanto, Marcellino Rudyanto. 2018. SynthesisofN-(phenylcarbamothioyl)-benzamide derivatives and their cytotoxic activity against MCF-7 cells J. Chin. Pharm. Sci. 27(10), 665-671. http://www.jcps.ac.cn/fileup/HTML/1003-1057(2018)10-696-07.shtml
  2. Dini Kesuma, Siswandono, Bambang Tri Purwanto, Marcellino Rudyanto. 2018. Docking, Synthesis and Cytotoxic Test on Human Breast Cancer Cell Line T47D of N-(Phenylcarbamothiioyl)-Benzamide..World J. Pharm. Res., 7(7), 70-78. https://wjpr.net/dashboard/archive_show/2018/VOLUME%207,%20APRIL%20ISSUE%207
  3. Alvan F. Shalas, Siswandono, Marcellino Rudyanto. 2018. Synthesis and Pain Inhibition Activity of the Analogs of 1-Allyl-3-Benzoylthiourea for New Analgesic Lead Compound Discovery. J. Young Pharm., 10(1), 12-15. http://www.jyoungpharm.org/article/1082
  4. Alvan F. Shalas, Siswandono, Marcellino Rudyanto. 2016. Synthesis and Structure-Activity Relationship of 1-Allyl-3-(2-Chlorobenzoyl)-thiourea as Analgesic. Int. J. Pharm. Pharm. Sci. 8(6), 297-298. https://innovareacademics.in/journals/index.php/ijpps/article/view/11184
  5. Marcellino Rudyanto, Tri Widiandani, Achmad Syahrani. 2015. Benzoxazine and Aminomethyl Derivatives of Eugenol: Cytotoxicity on MCF-7 Cell Line. Int. J. Pharm. Pharm. Sci. 7(5), 229-232. https://innovareacademics.in/journals/index.php/ijpps/article/view/4109
  6. Marcellino Rudyanto, Juni Ekowati, Tri Widiandani, Toshio Honda. 2014. Synthesis and Brine Shrimp Lethality Test of Some Benzoxazine and Aminomethyl Derivatives of Eugenol. Int. J. Pharm. Pharm. Sci. 6(2), 96-98. https://innovareacademics.in/journal/ijpps/Vol6Issue2/8467.pdf
  7. Marcellino Rudyanto, Koichi Kobayashi, Toshio Honda. 2009. Synthetic Studies on Isocoumarins and Isocarbostyril Derivatives Having an Alkyl Substituent at the 3-Position: Total Syntesis of Scoparines A and B. Heterocycles 79, 753-764. https://www.heterocycles.jp/newlibrary/libraries/journal/79/1/page:3
  8. Marcellino Rudyanto, Yuichiro Tomizawa. Hiroshi Morita, Toshio Honda. 2008. First Total Synthesis of Cassiarin A. Organic Letters 10, 1921-1922. https://pubs.acs.org/doi/10.1021/ol8004112
  9. Shiori Oshimi, Yuichiro Tomizawa, Yusuke Hirasawa, Toshio Honda, Wiwied Ekasari, Aty Widyawaruyanti, Marcellino Rudyanto, Gunawan Indrayanto, Noor Cholies Zaini, Hiroshi Morita. 2008. Chrobisiamone A, a New Bischromone from Cassia siamea and a Biomimetic Transformation of 5-Acetonyl-7-hydroxy-2-methylchromone into Cassiarin A. Bioorg. Med. Chem. Lett. 18, 3761-3763. https://www.sciencedirect.com/science/article/pii/S0960894X08005398?via%3Dihub
  10. Marcellino Rudyanto, Natsuko Kagawa, Masahiro Toyota, Masataka Ihara, 2002. A Concise Synthesis of A Potential Key Intermediate for 12-Epi-Mycalamide A. Heterocycles 58, 655-658. https://www.heterocycles.jp/newlibrary/libraries/journal/58/1/hetero44@pharm.hokudai.ac.jp/page:3
  11. Masahiro Toyota, Marcellino Rudyanto, Masatakan Ihara. 2002. Some Aspects of Palladium-Catalyzed Cycloalkenylation: Developments of Environmentally Benign Catalytic Conditions and Demonstration of Tandem Cycloalkenylation. J. Org. Chem. 67, 3374-3386. https://pubs.acs.org/toc/joceah/67/10
  12. Masahiro Toyota, Marcellino Rudyanto, Masatakan Ihara. 2000. Application of palladium-catalyzed cycloalkenylation reaction to terpenoid synthesis – novel approach to tricyclo[5.3.1.02,6]-undecane derivative and its transformation into tricyclo[5.3.1]undecane ring system.. Tetrahedron Lett. 41, 8929-8932. https://www.sciencedirect.com/journal/tetrahedron-letters/vol/41/issue/46

 

Contact

Marcellino Rudyanto, Drs., Apt., MSi., PhD

E-mail instansi marcellino-r@ff.unair.ac.id


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