new aristolane sesquiterpenoid named rulepidol was isolated from the fruiting body of Russula lepida Fr. Its structure was elucidated as (1a alpha ,5 alpha ,7 alpha ,7a alpha, 7b alpha)-1, 1a,4,5,6,7,7a, 7b-octahydro-...new aristolane sesquiterpenoid named rulepidol was isolated from the fruiting body of Russula lepida Fr. Its structure was elucidated as (1a alpha ,5 alpha ,7 alpha ,7a alpha, 7b alpha)-1, 1a,4,5,6,7,7a, 7b-octahydro-5-hydroxy-1,1,7,7a-tetramethyl-5H-cyclopropa [alpha] naphthalen-2-one mainly by 1D and 2D-NMR techniques.展开更多
The carbon-13 nuclear magnetic resonance spectra of seventeen protoilludane ses- quiterpenoid aromatic esters from the artificially cultured mycelium of Armillaria mellea (Vahl.ex Fr.) Quel.have been analysed and assi...The carbon-13 nuclear magnetic resonance spectra of seventeen protoilludane ses- quiterpenoid aromatic esters from the artificially cultured mycelium of Armillaria mellea (Vahl.ex Fr.) Quel.have been analysed and assigned.All the ^(11)CNMR signals of the model compounds melleolide 5 and compounds 8,10,11,13,14,15,and 16 can be assigned on the basis of the multiplicity of the sig- nals in the off-resonance decoupled spectra or INEPT spectra.^(11)C-~1H COSY and long-range ^(13)C-~1H COSY.The assignments of the ^(13)CNMR spectra of other protoilludane sesquiterpenoid aromatic esters were completed by comparison with the model compounds as well as the electronic effects of substi- tuted group on the molecules.The present results indicate that ^(11)CNMR spectroscopy provides an ef- fective method for characterizing the protoilludane sesquiterpenoid aromatic esters.展开更多
A new eremophilane sesquiterpenoid, along with two known ones, was isolated from the ethyl acetate soluble fraction of the aerial part of Coleus xanthanthus C. Y. Wu et Y. C. Huang. Their structures were elucidate...A new eremophilane sesquiterpenoid, along with two known ones, was isolated from the ethyl acetate soluble fraction of the aerial part of Coleus xanthanthus C. Y. Wu et Y. C. Huang. Their structures were elucidated as 4,5,11_trimethyl_8,9_seco_1(10),7(11)_eremophiladien_8,12_olid_9_oic acid (1), 2,9_dioxoeuryopsin (2) and 9_oxoeuryopsin (3) by spectral methods. The 1H_NMR and 13 C NMR data of compounds 1, 2 and 3 were unambiguously assigned on the basis of two_dimensional NMR spectroscopy.展开更多
Two new sesquiterpenoid trialcohol isomers named 1 beta, 4 alpha 11 alpha -trihydroxyeudesmane (1) and Yunnanensehedychetriol (2), were isolated from the fresh rhizomes of Hedychium Yunnanense gagnep. Their structures...Two new sesquiterpenoid trialcohol isomers named 1 beta, 4 alpha 11 alpha -trihydroxyeudesmane (1) and Yunnanensehedychetriol (2), were isolated from the fresh rhizomes of Hedychium Yunnanense gagnep. Their structures were elucidated by spectroscopic methods.展开更多
Two novel fomannosane-type sesquiterpenoids,agrocybins H(1)and I(2),together with a known compound illudosin(3),were isolated from the culture broth of the mushroom Agrocybe salicacola.Their structures were elucidated...Two novel fomannosane-type sesquiterpenoids,agrocybins H(1)and I(2),together with a known compound illudosin(3),were isolated from the culture broth of the mushroom Agrocybe salicacola.Their structures were elucidated by extensive spectroscopic analysis.The relative stereochemistry of 1 was determined by the use of single crystal X-ray crystallographic diffraction.展开更多
A new sesquiterpenoid was obstained from the leaves of Magnolia delavayi. Its structure was determined as 8β-acetoxy-10α-ethyloxy-guaia-4α, 11-diol on the basis of spectral evidence.
The fowers of Chrysanthemum indicum,i.e.Ye-ju-hua recorded in the Chinese Pharmacopoeia,has been widely used in China as an important heat-clearing and detoxifying herb for the treatment of infammation,headache,and ve...The fowers of Chrysanthemum indicum,i.e.Ye-ju-hua recorded in the Chinese Pharmacopoeia,has been widely used in China as an important heat-clearing and detoxifying herb for the treatment of infammation,headache,and vertigo.A phytochemical investigation of this herb has led to the isolation of two new eudesmane sesquiterpenoids,7-epi-eudesm4(15),11(13)-diene-1β,3β-diol(1)and 7-epi-1β-hydroxy-β-eudesmol(2).The molecular structures of these new sesquiterpenoids were established based on the comprehensive spectroscopic analyses,including NMR,MS,and IR,and comparing with the literatures.展开更多
Naturally occurring oplopanane sesquiterpenoids are rarely reported.A phytochemical investigation on the rhizomes of Homalomena occulta(Lours)has resulted in the discovery of six oplopanane sesquiterpenoids(1–6),incl...Naturally occurring oplopanane sesquiterpenoids are rarely reported.A phytochemical investigation on the rhizomes of Homalomena occulta(Lours)has resulted in the discovery of six oplopanane sesquiterpenoids(1–6),including four new(1–4)and one 3,5-seco-oplopanane(6),together with three previously reported sesquiterpenoids(7-9).In addition three new oplopananes(2a–4a)were also obtained by chemical transformation.All structures of these sesquiterpenoids were established based on the comprehensive spectroscopic analyses,including NMR,MS,and IR,and comparing with the literatures.展开更多
Soil-derived fungi represent an insufficiently tapped reservoir for discovering new and bioactive natural products(NPs),and despite an ever-increasing number of unknown NPs have been discovered over the past few decad...Soil-derived fungi represent an insufficiently tapped reservoir for discovering new and bioactive natural products(NPs),and despite an ever-increasing number of unknown NPs have been discovered over the past few decades,much of the hidden biosynthetic potential is still in an urgent need to be disclosed.In this research,a chemical inves-tigation was performed on a wetland soil-derived fungus Aspergillus calidoustus TJ403-EL05,leading to the isolation of a total of fourteen drimane sesquiterpenoids(1-14),incorporating three new ones,namely ustusols F-H(1-3).Their structures,comprising absolute configurations,were completely authenticated by widespread spectroscopic data,quantum chemical 13C NMR and ECD calculations,and X-ray crystallography experiments.Compound 14 exhibited moderate anti-inflammatory activity by inhibiting the LPS-induced NO release(IC_(50)=25.6μM).展开更多
Three new drimane sesquiterpenoids(1–3)together with the known 2a-hydroxyisodrimeninol(4),and a new isochromone derivative(5),were obtained from the solid cultures of fungal strain Pestalotiopsis sp.M-23,an endophyti...Three new drimane sesquiterpenoids(1–3)together with the known 2a-hydroxyisodrimeninol(4),and a new isochromone derivative(5),were obtained from the solid cultures of fungal strain Pestalotiopsis sp.M-23,an endophytic fungus isolated from the leaves of Leucosceptrum canum(Labiatae).Their structures were determined by comprehensive 1D and 2D NMR,and MS analyses.The metabolites were evaluated for their antibacterial activities,and compound 3 showed weak inhibitory activity against Bacillus subtilis.展开更多
A new protoilludane sesquiterpenoid aromatic ester,named armillarizin (1)has been isolated from the artificially cultured mycelium of Armillaria me- llea(Vahl.ex Fr)Quel.(Tricholomataceae).Its structure was deduced on...A new protoilludane sesquiterpenoid aromatic ester,named armillarizin (1)has been isolated from the artificially cultured mycelium of Armillaria me- llea(Vahl.ex Fr)Quel.(Tricholomataceae).Its structure was deduced on the ba- sis of spectral analyses.The relative configuration was established from the nuclear Overhauser effects and from the values of ~1H-~1H coupling constants.展开更多
One novel spirolactone,aquilarisinolide(1),three new sesquiterpenoids,(2R,4S,5R,7R)-2-hydroxyeremophila-9,11-dien-8-one(2),(1R,4S,5S,7R,11R)-13-hydroxyepidaphnauran-9-en-8-one(3),and(4R,5S,7R,8S,10S,13R)-8,13-dihydrox...One novel spirolactone,aquilarisinolide(1),three new sesquiterpenoids,(2R,4S,5R,7R)-2-hydroxyeremophila-9,11-dien-8-one(2),(1R,4S,5S,7R,11R)-13-hydroxyepidaphnauran-9-en-8-one(3),and(4R,5S,7R,8S,10S,13R)-8,13-dihydroxyrotunda-1,11-dien-3-one(4),together with 13 known compounds(5-17)were isolated from the resinous heartwood of Aquilaria sinensis(Thymelaeaceae).The structures of the new compounds were elucidated based on the analysis of NMR and MS data and theoretical calculations their ECD spectra.The isolated compounds were evaluated for their protective activities against PC12 cell injury induced by corticosterone(CORT)and 1-methyl-4-phenylpyridine ion(MPP+),as well as inhibitory activities against BACE1.Compound 4,5,6-dihydroxy-2-(2-phenylethyl)chromone(5),daphnauranol B(7),6-methoxy-2-[2-(3-methyoxyphenyl)ethyl]chromone(10),isoagarotetrol(14),and 1-hydroxy-1,5-diphenylpentan-3-one(16)showed significant protective effects on CORT-induced injury in PC12 cells at a concentration of 20μM(P<0.001).Isoagarotetrol(14)showed a significant protective effect on MPP+-induced injury in PC12 cells at a concentration of 20μM(P<0.001),while compound 4 showed a moderate activity(P<0.01).The BACE1-inhibitory activities of all tested compounds were very weak with less than 30%inhibition at a concentration of 20μM.展开更多
Three non-isoprenoid botryane sesquiterpenoids,named boledulins A-C(1-3),have been isolated from the cultures of basidiomycete Boletus edulis Bull.The structures were established by means of spectroscopic methods.Bole...Three non-isoprenoid botryane sesquiterpenoids,named boledulins A-C(1-3),have been isolated from the cultures of basidiomycete Boletus edulis Bull.The structures were established by means of spectroscopic methods.Boledulin A(1)exhibited moderate inhibitory activity against five human cancer cell lines.展开更多
Dendrowardol C(1)-a novel sesquiterpenoid,with an unprecedented 4/5/6/6 tetracyclic carbon backbone,together with two known cyclopacamphane-type sesquiterpenoids;dendronobilin I(2)and dendrobane A(3)were isolated from...Dendrowardol C(1)-a novel sesquiterpenoid,with an unprecedented 4/5/6/6 tetracyclic carbon backbone,together with two known cyclopacamphane-type sesquiterpenoids;dendronobilin I(2)and dendrobane A(3)were isolated from the stems of Dendrobium wardianum Warner.The structure of 1 was established on the basis of spectroscopic data and the absolute configuration was determined by single-crystal X-ray diffraction crystallography.The hypothetical biosynthetic pathway of 1 was postulated.Compound 1 showed no cytotoxic activity against human tumor cell lines HL-60,SMMC-7721,A-549,MCF-7,and SW480.展开更多
Three new caryophyllene sesquiterpenoids,cytosporinols A-C(1-3),have been isolated from solid cultures of Cytospora sp.The structures of 1-3 were elucidated primarily by NMR spectroscopy,and 3 was further confirmed by...Three new caryophyllene sesquiterpenoids,cytosporinols A-C(1-3),have been isolated from solid cultures of Cytospora sp.The structures of 1-3 were elucidated primarily by NMR spectroscopy,and 3 was further confirmed by X-ray crystallography.The absolute configurations of the C-11 secondary alcohol in 1 and the 6,8-diol moiety in 3 were deduced using the modified Mosher and Snatzke’s method,respectively.Compounds 2 and 3 showed moderate cytotoxicity against HeLa cells.展开更多
Two new drimane sesquiterpenoids(1 and 2),as well as five known compounds(3-7),were isolated from the basidiomycete Trichaptum biforme.The structures of new compounds were elucidated by extensive spectroscopic methods...Two new drimane sesquiterpenoids(1 and 2),as well as five known compounds(3-7),were isolated from the basidiomycete Trichaptum biforme.The structures of new compounds were elucidated by extensive spectroscopic methods,and the known compounds were identified by comparing their spectroscopic data with those reported in the literature.The cytotoxicities results against five human cancer cell lines of compounds 1 and 2 were negligible.展开更多
Two new seco-sativene sesquiterpenoids,bipolenins D(1)and E(2),a new seco-longifolene sesquiterpenoid,bipolenin F(3),together with three known analogues(4–6),were obtained from cultures of endophytic fungus Bipolaris...Two new seco-sativene sesquiterpenoids,bipolenins D(1)and E(2),a new seco-longifolene sesquiterpenoid,bipolenin F(3),together with three known analogues(4–6),were obtained from cultures of endophytic fungus Bipolaris eleusines.Their structures were established by MS and NMR data.Compounds 1–6 showed no activity to five human cancer cell lines.展开更多
In the^(1)H NMR-guided fractionation of extracts from the edible mushroom Lactarius deliciosus,two new azulene-type sesquiterpenoids,7-isopropenyl-4-methyl-azulene-1-carboxylic acid(1)and 15-hydroxy-3,6-dihydrolactar...In the^(1)H NMR-guided fractionation of extracts from the edible mushroom Lactarius deliciosus,two new azulene-type sesquiterpenoids,7-isopropenyl-4-methyl-azulene-1-carboxylic acid(1)and 15-hydroxy-3,6-dihydrolactarazulene(2),together with seven known compounds were characterized.Their structures were determined on basis of spectroscopic evidence,as well as by comparing with literature data.Amongst the known metabolites,the^(13)C NMR assignment of 15-hydroxy-6,7-dihydrolactarazulene(3)is reported here for the first time.Moreover,7-acetyl-4-methylazulene-1-carbaldehyde(5)displayed a moderate antibacterial activity against Staphylococcus aureus.展开更多
One previously undescribed angeloylated noreudesmane sesquiterpenoid,dobinin O(1),along with four known eudesmane sesquiterpenoids(2-5)were isolated from the peeled roots of Dobinea delavayi.Their structures were eluc...One previously undescribed angeloylated noreudesmane sesquiterpenoid,dobinin O(1),along with four known eudesmane sesquiterpenoids(2-5)were isolated from the peeled roots of Dobinea delavayi.Their structures were elucidated by extensive spectroscopic data analyses.In addition,compound 1 exhibited moderate antimalarial activity against Plasmodium yoelii BY265RFP with the inhibition ratio of 17.8±13.3%at the dose of 30 mg/kg/day.展开更多
文摘new aristolane sesquiterpenoid named rulepidol was isolated from the fruiting body of Russula lepida Fr. Its structure was elucidated as (1a alpha ,5 alpha ,7 alpha ,7a alpha, 7b alpha)-1, 1a,4,5,6,7,7a, 7b-octahydro-5-hydroxy-1,1,7,7a-tetramethyl-5H-cyclopropa [alpha] naphthalen-2-one mainly by 1D and 2D-NMR techniques.
文摘The carbon-13 nuclear magnetic resonance spectra of seventeen protoilludane ses- quiterpenoid aromatic esters from the artificially cultured mycelium of Armillaria mellea (Vahl.ex Fr.) Quel.have been analysed and assigned.All the ^(11)CNMR signals of the model compounds melleolide 5 and compounds 8,10,11,13,14,15,and 16 can be assigned on the basis of the multiplicity of the sig- nals in the off-resonance decoupled spectra or INEPT spectra.^(11)C-~1H COSY and long-range ^(13)C-~1H COSY.The assignments of the ^(13)CNMR spectra of other protoilludane sesquiterpenoid aromatic esters were completed by comparison with the model compounds as well as the electronic effects of substi- tuted group on the molecules.The present results indicate that ^(11)CNMR spectroscopy provides an ef- fective method for characterizing the protoilludane sesquiterpenoid aromatic esters.
文摘A new eremophilane sesquiterpenoid, along with two known ones, was isolated from the ethyl acetate soluble fraction of the aerial part of Coleus xanthanthus C. Y. Wu et Y. C. Huang. Their structures were elucidated as 4,5,11_trimethyl_8,9_seco_1(10),7(11)_eremophiladien_8,12_olid_9_oic acid (1), 2,9_dioxoeuryopsin (2) and 9_oxoeuryopsin (3) by spectral methods. The 1H_NMR and 13 C NMR data of compounds 1, 2 and 3 were unambiguously assigned on the basis of two_dimensional NMR spectroscopy.
文摘Two new sesquiterpenoid trialcohol isomers named 1 beta, 4 alpha 11 alpha -trihydroxyeudesmane (1) and Yunnanensehedychetriol (2), were isolated from the fresh rhizomes of Hedychium Yunnanense gagnep. Their structures were elucidated by spectroscopic methods.
文摘Two novel fomannosane-type sesquiterpenoids,agrocybins H(1)and I(2),together with a known compound illudosin(3),were isolated from the culture broth of the mushroom Agrocybe salicacola.Their structures were elucidated by extensive spectroscopic analysis.The relative stereochemistry of 1 was determined by the use of single crystal X-ray crystallographic diffraction.
文摘A new sesquiterpenoid was obstained from the leaves of Magnolia delavayi. Its structure was determined as 8β-acetoxy-10α-ethyloxy-guaia-4α, 11-diol on the basis of spectral evidence.
基金supported by National Natural Science Foundation of China(Nos.81673325,81711540311,and 21705156)the International Partnership Program of CAS(No.153631KYSB20160004)+1 种基金Gansu Province Key International S&T Cooperation Project(No.18YF1WA127)CAS Pioneer Hundred Talents Program.
文摘The fowers of Chrysanthemum indicum,i.e.Ye-ju-hua recorded in the Chinese Pharmacopoeia,has been widely used in China as an important heat-clearing and detoxifying herb for the treatment of infammation,headache,and vertigo.A phytochemical investigation of this herb has led to the isolation of two new eudesmane sesquiterpenoids,7-epi-eudesm4(15),11(13)-diene-1β,3β-diol(1)and 7-epi-1β-hydroxy-β-eudesmol(2).The molecular structures of these new sesquiterpenoids were established based on the comprehensive spectroscopic analyses,including NMR,MS,and IR,and comparing with the literatures.
基金The work was financially supported by the National Nature Science Foundation of China(Nos.21375136 and 21575150)the scientific research project of Central Asia Drug Discovery and Development Centre of Chinese Academy of Sciences(No.CAM201404)the CAS Pioneer Hundred Talents Program.
文摘Naturally occurring oplopanane sesquiterpenoids are rarely reported.A phytochemical investigation on the rhizomes of Homalomena occulta(Lours)has resulted in the discovery of six oplopanane sesquiterpenoids(1–6),including four new(1–4)and one 3,5-seco-oplopanane(6),together with three previously reported sesquiterpenoids(7-9).In addition three new oplopananes(2a–4a)were also obtained by chemical transformation.All structures of these sesquiterpenoids were established based on the comprehensive spectroscopic analyses,including NMR,MS,and IR,and comparing with the literatures.
基金The National Natural Science Foundation for Distinguished Young Scholars,81725021,Yonghui Zhangthe National Natural Science Foundation of China,Nos.81573316,31870326+4 种基金the Innovative Research Groups of the National Natural Science Foundation of China,No.81721005,Yonghui Zhangthe Fundamental Research Funds for the Central Universities,No.2020kfyXJJS083,Zhengxi Huthe National Key R&D Program of China,No.2021YFA0910500,Yonghui Zhangthe Research and Development Program of Hubei Province,No.2020BCA058,Jianping Wangthe Chinese Medicine Research Foundation of Health Commission of Hubei Province,No.ZY2021Z019,Jianping Wang.
文摘Soil-derived fungi represent an insufficiently tapped reservoir for discovering new and bioactive natural products(NPs),and despite an ever-increasing number of unknown NPs have been discovered over the past few decades,much of the hidden biosynthetic potential is still in an urgent need to be disclosed.In this research,a chemical inves-tigation was performed on a wetland soil-derived fungus Aspergillus calidoustus TJ403-EL05,leading to the isolation of a total of fourteen drimane sesquiterpenoids(1-14),incorporating three new ones,namely ustusols F-H(1-3).Their structures,comprising absolute configurations,were completely authenticated by widespread spectroscopic data,quantum chemical 13C NMR and ECD calculations,and X-ray crystallography experiments.Compound 14 exhibited moderate anti-inflammatory activity by inhibiting the LPS-induced NO release(IC_(50)=25.6μM).
基金This work was supported financially by the National Natural Science Foundation of China(Nos.31525005,U1202263,31570362)the Youth Innovation Promotion association of Chinese Academy of Sciences(awarded to Shi-Hong Luo)+1 种基金the“Western Light”Program of Chinese Academy of Sciences(awarded to Shi-Hong Luo)the“Hundred Talents Program”of the Chinese Academy of Sciences(awarded to Sheng-Hong Li).
文摘Three new drimane sesquiterpenoids(1–3)together with the known 2a-hydroxyisodrimeninol(4),and a new isochromone derivative(5),were obtained from the solid cultures of fungal strain Pestalotiopsis sp.M-23,an endophytic fungus isolated from the leaves of Leucosceptrum canum(Labiatae).Their structures were determined by comprehensive 1D and 2D NMR,and MS analyses.The metabolites were evaluated for their antibacterial activities,and compound 3 showed weak inhibitory activity against Bacillus subtilis.
文摘A new protoilludane sesquiterpenoid aromatic ester,named armillarizin (1)has been isolated from the artificially cultured mycelium of Armillaria me- llea(Vahl.ex Fr)Quel.(Tricholomataceae).Its structure was deduced on the ba- sis of spectral analyses.The relative configuration was established from the nuclear Overhauser effects and from the values of ~1H-~1H coupling constants.
文摘One novel spirolactone,aquilarisinolide(1),three new sesquiterpenoids,(2R,4S,5R,7R)-2-hydroxyeremophila-9,11-dien-8-one(2),(1R,4S,5S,7R,11R)-13-hydroxyepidaphnauran-9-en-8-one(3),and(4R,5S,7R,8S,10S,13R)-8,13-dihydroxyrotunda-1,11-dien-3-one(4),together with 13 known compounds(5-17)were isolated from the resinous heartwood of Aquilaria sinensis(Thymelaeaceae).The structures of the new compounds were elucidated based on the analysis of NMR and MS data and theoretical calculations their ECD spectra.The isolated compounds were evaluated for their protective activities against PC12 cell injury induced by corticosterone(CORT)and 1-methyl-4-phenylpyridine ion(MPP+),as well as inhibitory activities against BACE1.Compound 4,5,6-dihydroxy-2-(2-phenylethyl)chromone(5),daphnauranol B(7),6-methoxy-2-[2-(3-methyoxyphenyl)ethyl]chromone(10),isoagarotetrol(14),and 1-hydroxy-1,5-diphenylpentan-3-one(16)showed significant protective effects on CORT-induced injury in PC12 cells at a concentration of 20μM(P<0.001).Isoagarotetrol(14)showed a significant protective effect on MPP+-induced injury in PC12 cells at a concentration of 20μM(P<0.001),while compound 4 showed a moderate activity(P<0.01).The BACE1-inhibitory activities of all tested compounds were very weak with less than 30%inhibition at a concentration of 20μM.
基金This work was supported in part by the National Natural Sci This project was supported by the National Basic Research Program of China(973 Program,2009CB522300)the National Natural Sciences Foundation of China(30830113)MOST(2009ZX09501-029).
文摘Three non-isoprenoid botryane sesquiterpenoids,named boledulins A-C(1-3),have been isolated from the cultures of basidiomycete Boletus edulis Bull.The structures were established by means of spectroscopic methods.Boledulin A(1)exhibited moderate inhibitory activity against five human cancer cell lines.
基金This work was financially supported by the National Natural and Science Foundations of China(No.30800090)"Xi-Bu-Zhi-Guang"project(No.2009312D11017)from Chinese Academy of Sciencesthe Fund of the State Key Laboratory of Phytochemistry and Plant Resources in West China(P2010-ZZ012).
文摘Dendrowardol C(1)-a novel sesquiterpenoid,with an unprecedented 4/5/6/6 tetracyclic carbon backbone,together with two known cyclopacamphane-type sesquiterpenoids;dendronobilin I(2)and dendrobane A(3)were isolated from the stems of Dendrobium wardianum Warner.The structure of 1 was established on the basis of spectroscopic data and the absolute configuration was determined by single-crystal X-ray diffraction crystallography.The hypothetical biosynthetic pathway of 1 was postulated.Compound 1 showed no cytotoxic activity against human tumor cell lines HL-60,SMMC-7721,A-549,MCF-7,and SW480.
基金support from the National Natural Science Foundation of China(30925039)the Beijing Natural Science Foundation(5111003)+1 种基金the Ministry of Science and Technology of China(2009CB522300,2010ZX09401-403)the Chinese Academy of Sciences(KSCX2-EW-G-6).
文摘Three new caryophyllene sesquiterpenoids,cytosporinols A-C(1-3),have been isolated from solid cultures of Cytospora sp.The structures of 1-3 were elucidated primarily by NMR spectroscopy,and 3 was further confirmed by X-ray crystallography.The absolute configurations of the C-11 secondary alcohol in 1 and the 6,8-diol moiety in 3 were deduced using the modified Mosher and Snatzke’s method,respectively.Compounds 2 and 3 showed moderate cytotoxicity against HeLa cells.
基金This project was supported by the National Basic Research Program of China(973 Program,2009CB522300)the National Natural Sciences Foundation of China(U1132607)Youth Innovation Promotion Association of Chinese Academy of Sciences.
文摘Two new drimane sesquiterpenoids(1 and 2),as well as five known compounds(3-7),were isolated from the basidiomycete Trichaptum biforme.The structures of new compounds were elucidated by extensive spectroscopic methods,and the known compounds were identified by comparing their spectroscopic data with those reported in the literature.The cytotoxicities results against five human cancer cell lines of compounds 1 and 2 were negligible.
基金National Natural Science Foundation of China(31560010,31260342)China Agricultural Research System(CARS-10)Natural Science Fund of Yunnan province(2013ZA007)。
文摘Two new seco-sativene sesquiterpenoids,bipolenins D(1)and E(2),a new seco-longifolene sesquiterpenoid,bipolenin F(3),together with three known analogues(4–6),were obtained from cultures of endophytic fungus Bipolaris eleusines.Their structures were established by MS and NMR data.Compounds 1–6 showed no activity to five human cancer cell lines.
基金the Natural Science Foundation for a Chinese Government Scholarship Fund for Study Abroad(31470414,20140101126JC).
文摘In the^(1)H NMR-guided fractionation of extracts from the edible mushroom Lactarius deliciosus,two new azulene-type sesquiterpenoids,7-isopropenyl-4-methyl-azulene-1-carboxylic acid(1)and 15-hydroxy-3,6-dihydrolactarazulene(2),together with seven known compounds were characterized.Their structures were determined on basis of spectroscopic evidence,as well as by comparing with literature data.Amongst the known metabolites,the^(13)C NMR assignment of 15-hydroxy-6,7-dihydrolactarazulene(3)is reported here for the first time.Moreover,7-acetyl-4-methylazulene-1-carbaldehyde(5)displayed a moderate antibacterial activity against Staphylococcus aureus.
基金supported by the National Natural Science Foundation of China(Nos.81960637 and 81460532)the Innovation Team Project of Dali University for the Development and Utilization of Characteristic Medicinal Plants in Western Yunnan&Bai Nationality Medicines(No.ZKLX2019106).
文摘One previously undescribed angeloylated noreudesmane sesquiterpenoid,dobinin O(1),along with four known eudesmane sesquiterpenoids(2-5)were isolated from the peeled roots of Dobinea delavayi.Their structures were elucidated by extensive spectroscopic data analyses.In addition,compound 1 exhibited moderate antimalarial activity against Plasmodium yoelii BY265RFP with the inhibition ratio of 17.8±13.3%at the dose of 30 mg/kg/day.
