:: Last Update ::
  14-08-2021

LUELAK  LOMLIM

Tel No ::  074-288929
E-mail Address ::  luelak.l@psu.ac.th
Homepage ::  -



 
Education ::
  - ѪʵúѳԵ, Ѫʵ, ŧóԷ, 2539
  - ѪʵҺѳԵ, Ѫ, ŧóԷ, 2542
  - Doktor der Naturwissenschaften, Medicinal Chemistry, Friedrich-Alexander University, Erlangen-Nuernberg, 2549

Main Fields of Scientific Interests ::
  - Design and synthesis of Anti-Alzheimer's Drug
- Development of Polymer conjugate as drug delivery system


Fields of specialist ::
  - Medicinal Chemistry, Organic Chemistry


Research ::

  Publication ::
  1. Suwanhom, P., Saetang, J., Khongkow, P., Nualnoi, T., Tipmanee, V., Lomlim, L. Synthesis, Biological Evaluation, and In Silico Studies of New Acetylcholinesterase Inhibitors Based on Quinoxaline Scaffold.  Molecules, 26:  4895, 2021.
  2. Suwanhom, P., Nualnoi, T., Khongkow, P., Lee, V.S., Lomlim, L. Synthesis and Evaluation of Chromone-2-Carboxamido-Alkylamines as Potent Acetylcholinesterase Inhibitors.  Med. Chem. Res., 29(3):  564-574, 2020.
  3. Kara, J., Suwanhom, P., Wattanapiromsakul, C., Nualnoi, T., Puripattanavong, J., Khongkow, P., Lee, V.S., Gaurav, A., and Lomlim, L. Synthesis of 2-(2-Oxo-2H-chromen-4-yl)acetamides as Potent Acetylcholinesterase Inhibitors and Molecular Insights into Binding Interactions .  Arch Pharm Chem Life Sci, 7:  e1800310, 2019.
  4. Petrat W., Wattanapiromsakul C., Nualnoi T., Sabri N.H., Lee V.S., Lomlim L. Cholinesterase inhibitory activity, kinetic and a molecular docking studies of N-(1-substituted-1H-1,2,3-triazole-4-yl)-aralkylamide derivatives.  Walailak Journal of Science and Technology, 14:  687-701, 2017.
  5. Suksuwan,A., Lomlim,L., Dickert, F.L., Suedee R.  Tracking the chemical surface properties of racemic thalidomide and its enantiomers using a biomimetic functional surface on a quartz crystal microbalance.  J. Appl.Polym. Sci., 42309:  (1-14), 2015.
  6. Suksuwan A., Lomlim L., Rungrotmongkol T., Nakpheng T., Dickert F., Suedee R.  The composite nanomaterials containing (R)-thalidomide-molecularly imprinted polymers as a recognition system for enantioselective-controlled release and targeted drug delivery.  J. Appl.Polym. Sci., 41930:  (p 1-21), 2015.
  7. Plyduang T, Lomlim L, Yuenyongsawad S, Wiwattanapatapee R Carboxymethylcellulose-tetrahydrocurcumin conjugates for colon-specific delivery of a novel anti-cancer agent, 4-amino tetrahydrocurcumin.  Eur. J. Pharm. Biopharm., 88:  351-360, 2014.
  8. Puripattanavong, J., Songkram, C., Lomlim, L., Amnuaikit, T. Development of concentrated emulsion containing nicotiana tabacum extract for use as pesticide.  Journal of Applied Pharmaceutical Science, 3(11):  16-21, 2013.
  9. Kara, J., Wattanapiromsakul, C. and Lomlim, L.  Isoindoline-1,3-dione derivatives of 1-benzylpiperazine as acetylcholinesterase inhibitors. .  SDU Res. J. Sci .& Tech., 6(1):  141-158, 2013.
  10. Lomlim, L., Einsiedel, J., Heinemann, F.W., Meyer, K., Gmeiner, P.  Proline derived spirobarbiturates as highly effective beta-turn mimetics incorporating polar and functionalizable constraint elements.  J. Org. Chem., 73:  3608-3611, 2008.
  11. Wiwattanawongsa, K., Tantishaiyakul, V., Lomlim, L., Rojanasakul, Y., Pinsuwan, S., Keawnopparat, S. Experimental and computational studies of epithelial transport of mefenamic acid ester prodrugs.  Pharm. Res., 22:  721-727, 2005.
  12. Lomlim, L., Jirayupong, N., Plubrukarn, A. Heat-accelerated degradation of solid-state andrographolide.  Chem. Pharm. Bull., 51:  24-26, 2003.
  13. Wiwattanapatapee R., Lomlim L., Saramunee K. Dendrimer conjugates for colonic delivery of 5-aminosalicylic acid.  J. Controlled Release, 88:  1-9, 2003.
  14. Lomlim, L., Patarapanich, C., and Teerawanichapong, A.  Synthesis of amide derivatives of valproic acid.  Thai J. Pharm. Sci., 23 (Suppl.):  48, 1999.