T
T. Santisuk
Researcher at University of Illinois at Chicago
Publications - 14
Citations - 455
T. Santisuk is an academic researcher from University of Illinois at Chicago. The author has contributed to research in topics: Ring (chemistry) & Triterpene. The author has an hindex of 11, co-authored 14 publications receiving 428 citations. Previous affiliations of T. Santisuk include Virginia Tech College of Natural Resources and Environment & Mahidol University.
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Journal ArticleDOI
Plant anticancer agents, XLVIII. New cytotoxic flavonoids from Muntingia calabura roots.
Norito Kaneda,John M. Pezzuto,Djaja D. Soejarto,A. Douglas Kinghorn,Norman R. Farnsworth,T. Santisuk,Patoomratana Tuchinda,Jinda Udchachon,Vichai Reutrakul +8 more
TL;DR: Most of the isolates demonstrated cytotoxic activity when tested against cultured P-388 cells, with the flavans being more active than the flavones, and certain of these structurally related flavonoids exhibited somewhat selective activities when evaluated with a number of human cancer cell lines.
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Plant anticancer agents, L. cytotoxic triterpenes from Sandoricum koetjape stems.
Norito Kaneda,J. M. Pezzuto,A. D. Kinghorn,Norman R. Farnsworth,T. Santisuk,Patoomratana Tuchinda,Jinda Udchachon,Reutrakul +7 more
TL;DR: A new ring-A secotriterpene, koetjapic acid, and five known compounds, 3-oxo-olean-12-en-29-oic acid [2] (a novel natural product), katonic acid [3], (-)-alloaromadendrene, (-)-caryophyllene oxide, and (+)-spathulenol, have been isolated and characterized from a cytotoxic Et2O-soluble extract
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Three non-phenolic diarylheptanoids with anti-inflammatory activity from Curcuma xanthorrhiza.
P. Claeson,Ampai Panthong,Patoomratana Tuchinda,Vichai Reutrakul,D. Kanjanapothi,Walter C. Taylor,T. Santisuk +6 more
TL;DR: Three diarylheptanoids exerted significant anti-inflammatory activity in the assay of carrageenin-induced hind paw edema in rats and were identified by high-field 1H-NMR.
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Phenolic, iridoid and ionyl glycosides from Homalium ceylanicum
TL;DR: Salireposide, salirepin and two related novel phenolic glycosides named homaloside B [1-(2-methoxybenzoyloxy)methyl-5-hydroxyphenyl-β- d - glucopyranoside] and homalosides C [1-furoyloxymethyl-5 -hydroxymethylβ-d -glucopyranoide] were isolated from the n-butanol-soluble fraction of Homalium ceylanicum.
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Bioactive butenolides from Melodorum fruticosum
Patoomratana Tuchinda,Jinda Udchachon,Vichai Reutrakul,T. Santisuk,T. Santisuk,Walter C. Taylor,Norman R. Farnsworth,Norman R. Farnsworth,John M. Pezzuto,John M. Pezzuto,A. Douglas Kinghorn,A. Douglas Kinghorn +11 more
TL;DR: All butenolides showed cytotoxic activities in several tumour cell lines and the structures of the isolated compounds were elucidated by spectroscopic methods.