A novel dimeric eremophilane, ligulolide B, was isolated from the alcoholic extract of the whole plant of Ligularia virgaurea spp. oligocephala. The structure was elucidated by various spectroscopic methods including ...A novel dimeric eremophilane, ligulolide B, was isolated from the alcoholic extract of the whole plant of Ligularia virgaurea spp. oligocephala. The structure was elucidated by various spectroscopic methods including intensive 2D NMR techniques （^1H-^1H COSY, gHMQC, gHMBC and ^1H-^1H NOESY） and HR-ESI-MS.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
Six eremophilane sesquiterpenes were obtained from a marine fungus Penicillium sp. BL27-2. Their structures were elucidated as 3-acetyl-9, 7 （11）-dien-7a-hydroxy-8-oxoeremophilane （1）, 3-acetyl-13-deoxyphomenone ...Six eremophilane sesquiterpenes were obtained from a marine fungus Penicillium sp. BL27-2. Their structures were elucidated as 3-acetyl-9, 7 （11）-dien-7a-hydroxy-8-oxoeremophilane （1）, 3-acetyl-13-deoxyphomenone （2）, Sporogen-AO 1 （3）, 7-hydro- xypetasol （4）, 8a-hydroxy-13-deo -xyphomenone （5） and 6-dehydropetasol （6） based on detailed NMR analysis. 1 was a new compound and 2 was obtained as a new natural compound. These compounds were assayed for their cytotoxic activity on P388, A549, HL60, BEL7402 and K562 cell lines by the MTT method. The assay results suggested the epoxide rings in eremophilane molecules were essential for their activity, and acetylation could enhance their activity.展开更多
Two novel epimeric eremophilane sesquiterpenes, 7β-H-3α-angeloyl-9(10)-ene-11, 12-epoxy-8-oxoeremophilane (1) and 7β-H-3α-angeloyl-9(10)-ene-11, 12-epoxy-8-oxoeremophi- lane (2) were isolated from the methanol ext...Two novel epimeric eremophilane sesquiterpenes, 7β-H-3α-angeloyl-9(10)-ene-11, 12-epoxy-8-oxoeremophilane (1) and 7β-H-3α-angeloyl-9(10)-ene-11, 12-epoxy-8-oxoeremophi- lane (2) were isolated from the methanol extract of the flower of Cacalia tangutica (Franch.) Hand-Mazz. Their structures were characterized by 1D-, 2D-NMR (1H-1H COSY, HMQC, HMBC, 1H-1H NOESY) and HRESI-MS techniques.展开更多
A novel eremophilane dimer,named fischelactone（1）,was isolated from the roots of Ligularia fischeri.Complete structural elucidation of this compound was performed by HRESIMS,IR,1D NMR and 2D NMR（;H-;H COSY,HMBC,HMQ...A novel eremophilane dimer,named fischelactone（1）,was isolated from the roots of Ligularia fischeri.Complete structural elucidation of this compound was performed by HRESIMS,IR,1D NMR and 2D NMR（;H-;H COSY,HMBC,HMQC and NOESY） data.展开更多
Two new eremophilane sesquiterpenes 3β-angeloyloxy-8α-hydroxy-6β-methoxy eremophil-7 (11), 9 (10)-dien-8, 12-olide (1) and 3β-angeloyloxy-6β, 8α-dihydroxy-eremophi-7 (11), 9 (10)-dien-8, 12-olide (2) were isolat...Two new eremophilane sesquiterpenes 3β-angeloyloxy-8α-hydroxy-6β-methoxy eremophil-7 (11), 9 (10)-dien-8, 12-olide (1) and 3β-angeloyloxy-6β, 8α-dihydroxy-eremophi-7 (11), 9 (10)-dien-8, 12-olide (2) were isolated from Cacalia ainsliaeflora. Their structures were established by spectroscopic methods and 2D NMR experiments.展开更多
A new eremophilane-type sesquiterpene, 1α,8β,10β-trihydroxy-6β-（2-methylacryloy1）0xyeremophil-7（11）-en-8a,12-oide,was isolated from the roots of Ligularia virgaurea. Its structure was established on the basis ...A new eremophilane-type sesquiterpene, 1α,8β,10β-trihydroxy-6β-（2-methylacryloy1）0xyeremophil-7（11）-en-8a,12-oide,was isolated from the roots of Ligularia virgaurea. Its structure was established on the basis of various spectroscopic analyses, including the 1D, 2D NMR techniques and HR-ESI-MS.？ 2009 Zhan Xin Zhang. Published by Elsevier B.V. on behalf of Chinese Chemical Society. All rights reserved.展开更多
Two eremophilane-type sesquiterpenoids from the rhizomes of Ligularia veitchiana（Hemsl.） Greenm were isolated and determined as 10α,11-endoperoxide-1（2）-en-7α-hydroeremophilane（1） and 1（10）-en-2-oxo-7α-isop...Two eremophilane-type sesquiterpenoids from the rhizomes of Ligularia veitchiana（Hemsl.） Greenm were isolated and determined as 10α,11-endoperoxide-1（2）-en-7α-hydroeremophilane（1） and 1（10）-en-2-oxo-7α-isopropanol-eremophilane（2）.Compound 1 was a new compound and compound 2 was a new natural product.The structures of the two compounds were established by means of spectral methods including 1^H NMR,13^C NMR,2D NMR and MS.展开更多
Four new eremophilane type sesquiterpenes were isolated from the roots of Cacalia roborowskii (Maxim) Ling. Their structures were established as 8-oxo-eremophila-6, 9-dien-12-oic acid (1), 3 beta-acetoxyl-8-oxo-eremop...Four new eremophilane type sesquiterpenes were isolated from the roots of Cacalia roborowskii (Maxim) Ling. Their structures were established as 8-oxo-eremophila-6, 9-dien-12-oic acid (1), 3 beta-acetoxyl-8-oxo-eremophila-6, 9-dien-12-oic acid (2), 3 beta-angeloyoxyl-8-oxo-eremophilad, 9-dien-12-oic acid (3) and 3 beta-(2-methylbutyryloxyl)-8-oxo-eremophilia-6,9-dien-12-oic acid (4) by means of 1D and 2D NMR spectroscopy.展开更多
From Senecio tsoongianus, two pairs of enantiomeric isomers, tsoongianolides A (1) and B (2), tsoongianolides C (3) and D (4) were isolated. Their structures were elucidated by 1D and 2D-NMR techniques and X-ray diffr...From Senecio tsoongianus, two pairs of enantiomeric isomers, tsoongianolides A (1) and B (2), tsoongianolides C (3) and D (4) were isolated. Their structures were elucidated by 1D and 2D-NMR techniques and X-ray diffractions. The cytotoxicity to KB cell of 1 and 2 is also reported.展开更多
Two new eremophilane sesquiterpenes, 15β-formic ether-6-oxo-furanoeremophilane （1） and 6α, 15β-epoxy eremophila-7（11）-en-8α, 12-olide （2） were isolation from the roots of Ligularia macrophylla. Their structu...Two new eremophilane sesquiterpenes, 15β-formic ether-6-oxo-furanoeremophilane （1） and 6α, 15β-epoxy eremophila-7（11）-en-8α, 12-olide （2） were isolation from the roots of Ligularia macrophylla. Their structures were deduced from spectroscopic methods and 2D NMR experiments.展开更多
Two new eremophilane sesquiterpenes, 3β-angeloyloxy-8-oxo-eremophil-6(7)-en-12-oic acid 1 and 3β-angeloyloxy-10β-hydroxy-8-oxo-eremophil-6 (7)-en-12-oic acid 2, and a novel nor-eremophilane derivative, 3β-angeloyl...Two new eremophilane sesquiterpenes, 3β-angeloyloxy-8-oxo-eremophil-6(7)-en-12-oic acid 1 and 3β-angeloyloxy-10β-hydroxy-8-oxo-eremophil-6 (7)-en-12-oic acid 2, and a novel nor-eremophilane derivative, 3β-angeloyloxy-10β-hydroxy-8-oxo-eremophil-6(7)-en 3 were isolated from the roots of Cacalia ainsliaeflora. Their structures were elucidated by spectroscopic methods, including 2D NMR.展开更多
基金supported by the Foundation for the"Bairen Jihua"of Chinese Academy of Sciences(CAS)in 2000the National Natural Science Foundation of China(NNSFC 20021001,20372029,20475057).
文摘A novel dimeric eremophilane, ligulolide B, was isolated from the alcoholic extract of the whole plant of Ligularia virgaurea spp. oligocephala. The structure was elucidated by various spectroscopic methods including intensive 2D NMR techniques （^1H-^1H COSY, gHMQC, gHMBC and ^1H-^1H NOESY） and HR-ESI-MS.
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Six eremophilane sesquiterpenes were obtained from a marine fungus Penicillium sp. BL27-2. Their structures were elucidated as 3-acetyl-9, 7 （11）-dien-7a-hydroxy-8-oxoeremophilane （1）, 3-acetyl-13-deoxyphomenone （2）, Sporogen-AO 1 （3）, 7-hydro- xypetasol （4）, 8a-hydroxy-13-deo -xyphomenone （5） and 6-dehydropetasol （6） based on detailed NMR analysis. 1 was a new compound and 2 was obtained as a new natural compound. These compounds were assayed for their cytotoxic activity on P388, A549, HL60, BEL7402 and K562 cell lines by the MTT method. The assay results suggested the epoxide rings in eremophilane molecules were essential for their activity, and acetylation could enhance their activity.
基金supported by Foundation of“Bairen Jihua”of CAS in 2000NNSFC(No.20372029 and 20475057).
文摘Two novel epimeric eremophilane sesquiterpenes, 7β-H-3α-angeloyl-9(10)-ene-11, 12-epoxy-8-oxoeremophilane (1) and 7β-H-3α-angeloyl-9(10)-ene-11, 12-epoxy-8-oxoeremophi- lane (2) were isolated from the methanol extract of the flower of Cacalia tangutica (Franch.) Hand-Mazz. Their structures were characterized by 1D-, 2D-NMR (1H-1H COSY, HMQC, HMBC, 1H-1H NOESY) and HRESI-MS techniques.
基金financially supported by State Key Laboratory of Applied Organic Chemistry,Lanzhou University, China and Natural Science Foundation of Shandong Province,China(No.Y2008D23).
文摘A novel eremophilane dimer,named fischelactone（1）,was isolated from the roots of Ligularia fischeri.Complete structural elucidation of this compound was performed by HRESIMS,IR,1D NMR and 2D NMR（;H-;H COSY,HMBC,HMQC and NOESY） data.
基金This work was supported by the National Natural Sciencc Foundation of China No.29972017the Foundation of the Ministry of Education of China for Doctoral Program No.98073003
文摘Two new eremophilane sesquiterpenes 3β-angeloyloxy-8α-hydroxy-6β-methoxy eremophil-7 (11), 9 (10)-dien-8, 12-olide (1) and 3β-angeloyloxy-6β, 8α-dihydroxy-eremophi-7 (11), 9 (10)-dien-8, 12-olide (2) were isolated from Cacalia ainsliaeflora. Their structures were established by spectroscopic methods and 2D NMR experiments.
文摘A new eremophilane-type sesquiterpene, 1α,8β,10β-trihydroxy-6β-（2-methylacryloy1）0xyeremophil-7（11）-en-8a,12-oide,was isolated from the roots of Ligularia virgaurea. Its structure was established on the basis of various spectroscopic analyses, including the 1D, 2D NMR techniques and HR-ESI-MS.？ 2009 Zhan Xin Zhang. Published by Elsevier B.V. on behalf of Chinese Chemical Society. All rights reserved.
文摘Two eremophilane-type sesquiterpenoids from the rhizomes of Ligularia veitchiana（Hemsl.） Greenm were isolated and determined as 10α,11-endoperoxide-1（2）-en-7α-hydroeremophilane（1） and 1（10）-en-2-oxo-7α-isopropanol-eremophilane（2）.Compound 1 was a new compound and compound 2 was a new natural product.The structures of the two compounds were established by means of spectral methods including 1^H NMR,13^C NMR,2D NMR and MS.
文摘Four new eremophilane type sesquiterpenes were isolated from the roots of Cacalia roborowskii (Maxim) Ling. Their structures were established as 8-oxo-eremophila-6, 9-dien-12-oic acid (1), 3 beta-acetoxyl-8-oxo-eremophila-6, 9-dien-12-oic acid (2), 3 beta-angeloyoxyl-8-oxo-eremophilad, 9-dien-12-oic acid (3) and 3 beta-(2-methylbutyryloxyl)-8-oxo-eremophilia-6,9-dien-12-oic acid (4) by means of 1D and 2D NMR spectroscopy.
基金This work is financially supported in part by the Life Sciences Special Fund of Chinese Academy of Sciences Supported by the Ministry of Finance (STZ-00-24) the Yunnan Province Foundation of Applied Basic Research (2000C0072M) the Chine-France PRA (g
文摘From Senecio tsoongianus, two pairs of enantiomeric isomers, tsoongianolides A (1) and B (2), tsoongianolides C (3) and D (4) were isolated. Their structures were elucidated by 1D and 2D-NMR techniques and X-ray diffractions. The cytotoxicity to KB cell of 1 and 2 is also reported.
基金This work was supported by the National Natural Science Foundation of China(No.29972017).
文摘Two new eremophilane sesquiterpenes, 15β-formic ether-6-oxo-furanoeremophilane （1） and 6α, 15β-epoxy eremophila-7（11）-en-8α, 12-olide （2） were isolation from the roots of Ligularia macrophylla. Their structures were deduced from spectroscopic methods and 2D NMR experiments.
文摘Two new eremophilane sesquiterpenes, 3β-angeloyloxy-8-oxo-eremophil-6(7)-en-12-oic acid 1 and 3β-angeloyloxy-10β-hydroxy-8-oxo-eremophil-6 (7)-en-12-oic acid 2, and a novel nor-eremophilane derivative, 3β-angeloyloxy-10β-hydroxy-8-oxo-eremophil-6(7)-en 3 were isolated from the roots of Cacalia ainsliaeflora. Their structures were elucidated by spectroscopic methods, including 2D NMR.
