Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Nisachon Khunnawutmanotham"'
Autor:
Nisachon Khunnawutmanotham, Cherdchai Laongthipparos, Patchreenart Saparpakorn, Nitirat Chimnoi, Supanna Techasakul
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 14, Iss 1, Pp 2545-2552 (2018)
A series of 3-amino-6,7-dimethoxycoumarins conjugated with the N-benzylpyridinium moiety through an amide-bond linkage was synthesized and evaluated for their acetylcholinesterase inhibitory activity. A number of the benzylpyridinium derivatives exhi
Externí odkaz:
https://doaj.org/article/a4ac758bbe1b41bb89c9885da299fa0f
Autor:
Supanna Techasakul, Supa Hannongbua, Suda Louisirirotchanakul, Pornpan Pungpo, Patchareenart Saparpakorn, Nitirat Chimnoi, Nisachon Khunnawutmanotham
Publikováno v:
Molecules, Vol 12, Iss 2, Pp 218-230 (2007)
Based on the molecular modeling analysis against Y181CHIV-1 RT, dipyridodiazepinone derivatives containing an unsubstituted lactamnitrogen and 2-chloro-8-arylthiomethyl were synthesized via an efficientroute. Some of them were evaluated for their ant
Externí odkaz:
https://doaj.org/article/038fde6148c449759a751172fcf09fd2
Autor:
Sutatip Siripaisarnpipat, Narongsuk Chaichit, Supanna Techasakul, Nisachon Khunnawutmanotham, Supakit Achiwawanich
Publikováno v:
Acta Crystallographica Section E, Vol 67, Iss 1, Pp o112-o112 (2011)
In the title molecule, C17H10BrNO3, the mean planes of tricycle and bromophenyl fragments form a dihedral angle of 75.5 (1)°. In the crystal, π–π interactions [centroid–centroid distances = 3.556 (2) and 3.898 (8) Å] between the isoquinoline
Externí odkaz:
https://doaj.org/article/27de75ffafdf46f3b858541933509c4b
Autor:
Nisachon Khunnawutmanotham, Nitirat Chimnoi, Arunee Thitithanyanont, Patchreenart Saparpakorn, Kiattawee Choowongkomon, Pornpan Pungpo, Supa Hannongbua, Supanna Techasakul
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 5, Iss 1, p 36 (2009)
Ten dipyridodiazepinone derivatives were synthesized and evaluated for their anti HIV-1 reverse transcriptase activity against wild-type and mutant type enzymes, K103N and Y181C. Two of them were found to be promising inhibitors for HIV-1 RT.
Externí odkaz:
https://doaj.org/article/8011afa8e7814e68844df546e509b2bb
Autor:
Supanna Techasakul, Anuch Hasakunpaisarn, Nitirat Chimnoi, Phonchanok Nangkoed, Waraporn Wiwattanapaisarn, Nisachon Khunnawutmanotham
Publikováno v:
ChemistrySelect. 6:10221-10225
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ba2c6275ad8e788468ccbda37065d5e2
https://doi.org/10.1002/slct.202102590
https://doi.org/10.1002/slct.202102590
Autor:
Watthanachai Jumpathong, Chatchakorn Eurtivong, Nitirat Chimnoi, Nisachon Khunnawutmanotham, Supanna Techasakul
Publikováno v:
Journal of Chemical Research. 44:410-425
Acridine-based compounds possess anticancer activities by intercalating to DNA. Although they have chemotherapeutic potential, acridine-based compounds are not used to treat cancer. In this study, 2, N10-acridone derivatives are designed and synthesi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c456e655aec2494317b089823e86e213
https://doi.org/10.1177/1747519820902674
https://doi.org/10.1177/1747519820902674
Autor:
Charnsak Thongsornkleeb, Pavitra Laohapaisan, Nantamon Supantanapong, Lukana Ngiwsara, Nisachon Khunnawutmanotham, Warabhorn Rodphon, Jumreang Tummatorn, Kriengsak Lirdprapamongkol, Jisnuson Svasti, Onrapak Reamtong, Somsak Ruchirawat
Publikováno v:
ChemMedChem. 16(24)
Eighteen hybrid compounds between 8-bromo-2-fluoro-isocryptolepine (4) and 1,2,3-triazole were synthesized via azide rearrangement-annulation reaction. Compound 4 underwent regioselective N-propargylation and click reaction to form 8-bromo-2-fluoro-i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c7603100bed710e9390916393b79ec9
https://pubmed.ncbi.nlm.nih.gov/34610210
https://pubmed.ncbi.nlm.nih.gov/34610210
Autor:
Nopporn Thasana, Wachirasak Thaisaeng, Chatchakorn Eurtivong, Somsak Ruchirawat, Nisachon Khunnawutmanotham, Sakornrat Thorroad, Apiwan Jumraksa, Thanasan Nilsu, Wanlaya Thamnarak
Publikováno v:
Phytochemistry. 156:83-88
Phytochemical constituents in alkaloid extracts from three Thai club mosses Huperzia squarrosa, Huperzia phlegmaria and Phlegmariurus nummularifolius were investigated. Squarrosinoxide was an undescribed Lycopodium alkaloid from H. squarrosa possessi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02c4a9f426335f4a2a063ab9f5805865
https://doi.org/10.1016/j.phytochem.2018.09.001
https://doi.org/10.1016/j.phytochem.2018.09.001
Autor:
Nisachon Khunnawutmanotham, Watthanachai Jumpathong, Chatchakorn Eurtivong, Nitirat Chimnoi, Supanna Techasakul
Supplemental material, Supplementary_Information for Synthesis, cytotoxicity evaluation, and molecular modeling studies of 2,N10-substituted acridones as DNA-intercalating agents by Nisachon Khunnawutmanotham, Watthanachai Jumpathong, Chatchakorn Eur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1bcc438273f480c38c94f08425ab1739
Autor:
Patchreenart Saparpakorn, Cherdchai Laongthipparos, Nisachon Khunnawutmanotham, Supanna Techasakul, Nitirat Chimnoi
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 14, Iss 1, Pp 2545-2552 (2018)
Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry
A series of 3-amino-6,7-dimethoxycoumarins conjugated with the N-benzylpyridinium moiety through an amide-bond linkage was synthesized and evaluated for their acetylcholinesterase inhibitory activity. A number of the benzylpyridinium derivatives exhi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46e9076fc2c6f50c676f435a24ae0dbb
https://doi.org/10.3762/bjoc.14.231
https://doi.org/10.3762/bjoc.14.231