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Guajadials C-F, four unusual meroterpenoids from Psidium guajava 被引量:6
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作者 Yuan GAO gen-tao li +3 位作者 Yan li Ping HAI Fei WANG Ji-Kai liU 《Natural Products and Bioprospecting》 CAS 2013年第1期14-19,共6页
Guajadials C-F(1-4),four sesquiterpenoid-based meroterpenoids with unprecedented skeletons were isolated from the leaves of Psidium guajava.Their structures and relative configurations were established by extensive sp... Guajadials C-F(1-4),four sesquiterpenoid-based meroterpenoids with unprecedented skeletons were isolated from the leaves of Psidium guajava.Their structures and relative configurations were established by extensive spectroscopic analysis.A possible biosynthetic pathway for 1-4 was also proposed. 展开更多
关键词 Psidium guajava meroterpenoid guajadial
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Nine New Farnesylphenols from the Basidiomycete Albatrellus Caeruleoporus 被引量:1
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作者 liang-Yan liu Zheng-Hui li +6 位作者 Gang-Qiang Wang Kun Wei Ze-Jun Dong Tao Feng gen-tao li Yan li Ji-Kai liu 《Natural Products and Bioprospecting》 CAS 2014年第2期119-128,共10页
Nine previously-unreported farnesylphenols,involving eight neogrifolin derivatives(1–8)and one grifolin analogue(9),together with three known compounds,were isolated from the fruiting bodies of the mushroom Albatrell... Nine previously-unreported farnesylphenols,involving eight neogrifolin derivatives(1–8)and one grifolin analogue(9),together with three known compounds,were isolated from the fruiting bodies of the mushroom Albatrellus caeruleoporus.Their structures were elucidated as(S)-17-hydroxy-18,20-ene-neogrifolin(1),(S)-18,19-dihydroxyneogrifolin(2),(S)-9-hydroxy-10,22-ene-neogrifolin(3),(9S,10R)-6,10-epoxy-9-hydroxyneo grifolin(4),(9S,10R)-6,9-epoxy-10-hydroxyneogrifolin(5),(-)-13,14-dihydroxyneogrifolin(6),albatrelin G(7),albatrelin H(8),and one grifolin analogue,(S)-10-hydroxygrifolin(9),grifolin(10),neogrifolin(11),and albatrellin(12)by extensive spectroscopic analyses and chemical methods.Compounds 7 and 8 showed weak cytotoxic activity to cell lines HL-60,SMMC-7721,A-549,and MCF-7,in vitro. 展开更多
关键词 Albatrellus caeruleoporus MUSHROOM POLYPORACEAE Farnesylphenols
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Identification and Cytotoxic Activities of Two New Trichothecenes and a New Cuparane-Type Sesquiterpenoid from the Cultures of the Mushroom Engleromyces goetzii
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作者 Yang Wang ling Zhang +4 位作者 gen-tao li Zheng-Hui li Ze-Jun Dong Yan li Ji-Kai liu 《Natural Products and Bioprospecting》 CAS 2015年第1期47-53,共7页
Engleromyces goetzii is a traditional medicinal mushroom that is widely used to treat infection,inflammation and cancer in Tibet,Sichuan and Yunnan provinces of China.Two new trichothecenes,engleromycones A and B(1 an... Engleromyces goetzii is a traditional medicinal mushroom that is widely used to treat infection,inflammation and cancer in Tibet,Sichuan and Yunnan provinces of China.Two new trichothecenes,engleromycones A and B(1 and 2),one new cuparane-type sesquiterpenoid named infuscol F(11),eight known trichothecene analogs,sambucinol(3),3-deoxysambucinol(4),trichothecolone(5),trichodermol(6),8-deoxytrichothecin(7),trichothecin(8),trichothecinol B(9)and trichothecinol A(10),and one known cyclopentanoid sesquiterpene cyclonerodiol(12)were isolated from the cultures of E.goetzii.The new compounds were elucidated through spectroscopic analyses.The anticancer effects of trichothecenes 1–10 were examined in the HL-60,SMMC-7721,A549,MCF-7,and SW-480 human cancer cell lines using an MTT assay.Trichothecinol A(10)significantly inhibited the growth of MCF-7 cells,with an IC50 value of 0.006 lM,which was comparable to the cytotoxic activity of the positive control,paclitaxel,indicating that trichothecinol A(10)represents a potential anticancer agent. 展开更多
关键词 Engleromyces goetzii TRICHOTHECENE Engleromycone Cuparane Infuscol MYCOTOXIN
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Synthesis and Anticancer Activity of 4b-Triazolepodophyllotoxin Glycosides
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作者 Cheng-Ting Zi gen-tao li +4 位作者 Yan li Jun Zhou Zhong-Tao Ding Zi-Hua Jiang Jiang-Miao Hu 《Natural Products and Bioprospecting》 CAS 2015年第2期83-90,共8页
A series of novel 4b-triazole-podophyllotoxin glycosides were synthesized by utilizing the Click reaction.Evaluation of cytotoxicity against a panel of five human cancer cell lines(HL-60,SMMC-7721,A-549,MCF-7,SW480)us... A series of novel 4b-triazole-podophyllotoxin glycosides were synthesized by utilizing the Click reaction.Evaluation of cytotoxicity against a panel of five human cancer cell lines(HL-60,SMMC-7721,A-549,MCF-7,SW480)using MTT assay shows that most of these compounds show weak cytotoxicity.It was observed that compound 16 shows the highest activity with IC50 values ranging from 2.85 to 7.28 lM,which is more potent than the control drugs etoposide and cisplatin against four of five cancer cell lines tested.Compound 16 is characterized with an a-D-galactosyl residue directly linked to the triazole ring and a 40-OH group on the E ring of the podophyllotoxin scaffold.HPLC investigation of representative compound indicates that incorporation of a sugar moiety seems to improve the chemical stability of the podophyllotoxin scaffold. 展开更多
关键词 Podophyllotoxin 4b-Triazole-podophyllotoxin GLYCOSIDES Click reaction ANTICANCER SYNTHESIS
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