Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Tanapong Boonruangprapa"'
Autor:
Cheerapha Panyasiri, Sumalee Supothina, Sukitaya Veeranondha, Rungtiwa Chanthaket, Tanapong Boonruangprapa, Vanicha Vichai
Publikováno v:
Insects, Vol 13, Iss 8, p 684 (2022)
In a laboratory assay, it was shown that B. bassiana BCC48145, BCC2660, and P. lilacinum TBRC10638 were the three strains that exhibited the highest insecticidal activity against chili thrips, causing 92.5% and 91.86% and 92.3% corrected mortality, r
Externí odkaz:
https://doaj.org/article/d2c0c6ba420742eeb388c408767032ac
Autor:
Pattama Pittayakhajonwut, Chakapong Intaraudom, Nantiya Bunbamrung, Aibrohim Dramae, Tanapong Boonruangprapa, Wikorn Punyain
Publikováno v:
Fitoterapia. 138
Fourteen new compounds including thirteen drimane – phthalide derivatives (fendlerals A – C, fendlerins A – D, fendlerols A – B, fendleric acids A – C, fendlerinine G) and one terphenyl derivative (fendleryl E) along with eight known compou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a2107fc64db9b49a239efe64923c286
https://pubmed.ncbi.nlm.nih.gov/31476402
https://pubmed.ncbi.nlm.nih.gov/31476402
Autor:
Pranee Rachtawee, Vanicha Vichai, Chanikul Chutrakul, Sanisa Lapanun, Chanwit Suriyachadkun, Patchanee Auncharoen, Taridaporn Bunyapaiboonsri, Sumalee Supothina, Suwanee Chunhametha, Tanapong Boonruangprapa
Publikováno v:
Tetrahedron. 72:775-778
Three polycyclic tetrahydroxanthones, chrestoxanthones A−C, together with known albofungin and chloroalbofungin were isolated from the actinomycete Streptomyces chrestomyceticus BCC 24770. Their structures were elucidated by extensive spectroscopic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6e1d52ad46bc6b0e3d474f6c9262eff9
https://doi.org/10.1016/j.tet.2015.12.045
https://doi.org/10.1016/j.tet.2015.12.045
Autor:
Karoon Sadorn, Nattawut Boonyuen, Tanapong Boonruangprapa, Pattama Pittayakhajonwut, Siriporn Saepua, Pranee Rachtawee
Publikováno v:
Phytochemistry. 151
Eleven previously undescribed compounds, including cytosporanthraxanthone, xanthoquinodins A7–A10, ketoxanthoquinodin A6, xanthoquinodins B6–B8, and spiroxanthoquinodins A and B, and one synthetically known compound, 2-methoxy pinselin, as well a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3091589b7ccddd5ccefba8cef7a89460
https://pubmed.ncbi.nlm.nih.gov/29677644
https://pubmed.ncbi.nlm.nih.gov/29677644
Autor:
Siriporn Saepua, Jittra Kornsakulkarn, Tanapong Boonruangprapa, Chawanee Thongpanchang, Sumalee Suphothina
Publikováno v:
Phytochemistry Letters. 6:491-494
Four new β -carbolines 1–4 and two new indoles 5–6 were isolated together with thirteen known compounds from actinomycete, Actinomadura BCC 24717. Structures of the new compounds, 1–6, were determined by NMR spectroscopic and MS spectrometric
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f2cd17c3b03a897fc6ed183e31420fc2
https://doi.org/10.1016/j.phytol.2013.06.007
https://doi.org/10.1016/j.phytol.2013.06.007
Autor:
Vanicha Vichai, Patchanee Auncharoen, Sanisa Lapanun, Chanikul Chutrakul, Chanwit Suriyachadkun, Taridaporn Bunyapaiboonsri, Pranee Rachtawee, Suwanee Chunhametha, Sumalee Supothina, Tanapong Boonruangprapa
Publikováno v:
ChemInform. 47
Three polycyclic tetrahydroxanthones, chrestoxanthones A−C, together with known albofungin and chloroalbofungin were isolated from the actinomycete Streptomyces chrestomyceticus BCC 24770. Their structures were elucidated by extensive spectroscopic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::18fc55d0cc982b8126dcd8ff0d712c4d
https://doi.org/10.1002/chin.201621228
https://doi.org/10.1002/chin.201621228
Publikováno v:
The Journal of Antibiotics. 65:571-574
Torrubiellins A (1) and B (2), two new dimeric anthraquinones were isolated from the leafhopper pathogenic fungus Torrubiella sp. BCC 28517. The structures of the new compounds were elucidated by analyses of the NMR spectroscopic and mass spectrometr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb98fcfa8da77ffc56f53b3c7ed16ca7
https://doi.org/10.1038/ja.2012.76
https://doi.org/10.1038/ja.2012.76
Autor:
Pranee Rachtawee, Nattawut Boonyuen, Tanapong Boonruangprapa, Samran Prabpai, Kulvadee Dolsophon, Chawanee Thongpanchang, Jittra Kornsakulkarn, Palangpon Kongsaeree
Publikováno v:
Tetrahedron. 67:7540-7547
Eleven new dihydronaphthalenones 1–11, together with five known compounds; 5-hydroxydihydrofusarubin C (12), javanicin, bostrycoidin, anhydrofusarubin, and 3-O-methylfusarubin, were isolated from the endophytic fungus Fusarium sp. BCC14842 . Struct
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1f5936842e9f1690d30d6aaaab3a9caa
https://doi.org/10.1016/j.tet.2011.07.078
https://doi.org/10.1016/j.tet.2011.07.078
Autor:
Nattawut Rungjindamai, Umpava Pinruan, Tanapong Boonruangprapa, Masahiko Isaka, Panida Chinthanom
Publikováno v:
Journal of Natural Products. 73:683-687
Seven new eremophilane-type sesquiterpenoids (1-5, 7, and 8) and the known mairetolide F (6) were isolated from the endophytic Xylaria sp. BCC 21097. A new furofurandione (9) was also isolated from the fungal extract. The structures of the new compou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::299905dd6cb3d945e417d9c12f93e646
https://doi.org/10.1021/np100030x
https://doi.org/10.1021/np100030x
Autor:
Pranee Rachtawee, Palangpon Kongsaeree, Samran Prabpai, Chakapong Intaraudom, Tanapong Boonruangprapa, Pattama Pittayakhajonwut, Sutichai Nitthithanasilp
Publikováno v:
Phytochemistry. 120
Ten compounds including nine phenalenone derivatives (five bipolarides and four bipolarols) and a sesterterpene acid (bipolarenic acid), were isolated from a marine isolated of the fungus Lophiostoma bipolare (BCC25910), along with the known compound
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8cf795b2d1b1d57e239e674b611c83c
https://pubmed.ncbi.nlm.nih.gov/26582262
https://pubmed.ncbi.nlm.nih.gov/26582262