Page last updated: 2024-09-05

eudesmane and sesquiterpenes

eudesmane has been researched along with sesquiterpenes in 66 studies

Compound Research Comparison

Studies (eudesmane)	Trials (eudesmane)	Recent Studies (post-2010) (eudesmane)	Studies (sesquiterpenes)	Trials (sesquiterpenes)	Recent Studies (post-2010) (sesquiterpenes)
93	0	53	17,489	536	7,668

Research

Studies (66)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	1 (1.52)	18.2507
2000's	25 (37.88)	29.6817
2010's	27 (40.91)	24.3611
2020's	13 (19.70)	2.80

Authors

Authors	Studies
Ahmed, AA; Balboul, BA; Mabry, TJ; Miao, B; Scott, AI; Williams, HH	1
Ito, Y; Masuoka, C; Nohara, T; Odake, Y; Ono, M	1
Nagasampagi, BA; Pujar, PP; Rojatkar, SR; Sawaikar, DD	1
Arias, JM; Dobado, JA; García-Granados, A; Melguizo, E; Molina, J; Parra, A; Simeó, Y; Viseras, B	1
Toyota, M	1
Fukushige, A; Hirai, A; Jiang, ZH; Kouno, I; Tanaka, T	1
Abdel-Razek, MH; Ahmed, AA; Hirata, T; Izumi, S; Nassar, MI; Ohta, S	1
Li, WD; Li, Y; Zhang, Z	1
Abdel-Ghani, HF; Ahmed, AA; El-Moghazy, SA; El-Shanawany, MA	1
Ahmed, AA; Ali, ET; Couladis, M; Gáti, T; Mabry, TJ; Mahmoud, AA; Tóth, G; Tzakou, O	1
García-Granados, A; Gutiérrez, MC; Parra, A; Rivas, F	1
Ahmed, AA; El-Maghraby, MA; Gani, A; Hassan, ME; Mohamed, Ael-H; Tzakou, O; Yannitsaros, A; Zeller, KP	1
Donadel, OJ; García, M; Giordano, OS; Sosa, ME; Tonn, CE	1
Gao, K; Jia, ZJ; Yang, ZD	1
Hamed, EM; Khanfar, MA; Sabri, SS; Zarga, MH; Zeller, KP	1
Guéritte, F; Sun, H; Xiao, Y; Zhang, Q; Zhao, Y; Zheng, Q	1
Adio, AM; König, WA; Muhle, H; Paul, C	1
Allemann, RK; Deligeorgopoulou, A; Forcat, S; Taylor, SE	1
Wu, B; Wu, LJ	1
Hajiwangoh, Z; Kaewbumrung, C; Phongpaichit, S; Rukachaisirikul, V	1
Ashurmetov, O; Consentino, LM; Kashiwada, Y; Kodzhimatov, OK; Lee, KH; Lin, AJ; Okasaka, M; Takaishi, Y	1
Baykan, S; Bedir, E; Karamenderes, C; Khan, IA; Pawar, R	1
Asakawa, Y; Bardón, A; Misico, R; Sierra, MG; Vera, N	1
Abou-Douh, AM	1
Baran, PS; Chen, K	1
Dai, SJ; Ren, Y; Shen, L	1
Allemann, RK; Faraldos, JA; Kariuki, B	1
Allemann, RK; Faraldos, JA	1
Allemann, RK; Antonczak, AK; Faraldos, JA; Fullerton, R; González, V; Tippmann, EM	1
Ando, M; Arao, K; Chen, Y; Hirano, S; Kataoka, T; Mitsui, T; Ogura, H; Shinozaki, M; Taketani, S; Tamura, R; Tang, W; Wang, L	1
Chen, Z; Feng, Z; Jiang, J; Li, Y; Yang, Y; Zhang, P	1
Choi, RJ; Chung, HS; Kang, SS; Kim, JS; Kim, YS; Lee, S; Lee, SY; Shin, HJ	1
Apostolides Arnold, N; Bruno, M; Caggia, S; Cardile, V; Formisano, C; Mari, A; Piacente, S; Rigano, D; Rosselli, S; Russo, A; Senatore, F	1
Fiorentino, A; Galasso, S; Gallicchio, M; Lorenz, P; Marciano, S; Monaco, P; Pacifico, S; Potenza, N; Stintzing, FC	1
Chen, Y; Dai, Y; Li, J; Liu, L; Qin, M; Qin, X; Wang, Q; Xie, G	1
Danova, K; Evstatieva, L; Meier, B; Riedl, R; Simmons, L; Todorova, M; Trendafilova, A; Wolfram, E	1
Al-Footy, KO; Al-Lihaibi, SS; Alarif, WM; Ayyad, SE; Badria, FA; Basaif, SA; Ghandourah, MA; Halid Ph, M; Zubair, MS	1
Bond, AD; Christensen, LP; Fretté, XC; Hyldgaard, MG; Jensen, KT; Purup, S; Qu, H	1
Ha, W; Jiang, HL; Shi, YP	1
Bai, W; Chen, JJ; Gao, K; Gobu, FR; Sun, M; Wu, CH; Zeng, J	1
Kong, LY; Li, RJ; Luo, J; Wang, P; Yaermaimaiti, S	1
Chen, SN; Gan, LS; Li, J; Liu, QF; Sheng, L; Yang, SP; Yu, Y; Yue, JM	1
Ding, LF; Li, Y; Peng, LY; Su, J; Tu, WC; Wu, XD; Yang, H; Zhao, QS	1
Feng, ZM; Jiang, JS; Xu, K; Yang, YN; Zhang, PC	1
Fukaya, H; Maeda, S; Matsuo, Y; Mimaki, Y; Ohba, C	1
Gong, Y; Li, HF; Li, YX; Pang, XY; Yan, Y; Zhu, Y	1
Ding, LF; Gong, X; Li, Y; Peng, LY; Tu, WC; Wu, XD; Xu, ZZ; Yang, H; Zhao, QS; Zhong, WW	1
Chen, R; Dai, J; Liu, J; Tan, Z; Xie, K; Zhang, M; Zhao, J	1
Akssira, M; Berteina-Raboin, S; Zaki, M	1
Bedir, E; Demir, S; Karaalp, C	1
Dhaouadi, H; El Mokni, R; Ercolano, G; Formisano, C; Hammami, S; Ianaro, A; Rigano, D; Sirignano, C; Snene, A; Taglialatela-Scafati, O	1
Cuong, NX; Dang, NH; Huong, NT; Kiem, PV; Minh, CV; Nam, NH; Ngoc, NT; Thanh, NV; The, HV; Thung, DC; Tuan, VS	1
Dao, TT; Hien, TT; Shi, YP; Yang, JL; Zhao, YM	1
Cheng, YX; Ren, Z; Wang, SX; Yan, YM; Zhang, L	1
Katsutani, K; Matsunami, K; Mizuta, T; Otsuka, H; Sugimoto, S; Yamano, Y	1
Cuong, NX; Hanh, TTH; Quang, TH; Vinh, LB	1
Cao, DH; Ji, KL; Lu, JM; Sun, P; Wu, M; Xiao, CF; Xu, YK; Yue, JR	1
Chen, JJ; He, XF; Huang, XY; Li, TZ; Ma, YB; Wang, Y; Zhang, XM	1
Chen, SL; Chiou, SF; Dai, CF; Fu, CW; Lin, CC; Lin, YC; Sheu, JH; Wang, HC	1
Dong, J; Geng, J; Li, T; Qin, Q; Yao, X; Yu, Y; Zhou, M	1
Ao, ZY; Chen, JY; Chen, LP; Fan, YW; Jiang, DX; Lian, X; Pan, YC; Wu, JW; Zhang, WJ	1
Naini, AA; Riyadi, SA; Supratman, U	1
Bi, D; Chen, Y; Huang, J; Li, H; Li, Q; Ni, D; Wang, H; Wang, M; Wang, W; Xiao, W; Yang, R	1
Chang, WQ; Fu, XJ; Han, JJ; Li, Y; Liang, Z; Lou, HX; Lv, DX; Xu, ZJ; Yuan, SZ; Zhang, JZ; Zhou, JC; Zhu, MZ	1
Fang, X; Gao, J; Guan, S; Liu, X; Zhang, Q; Zhang, X; Zhang, Y	1
Ding, LF; Hu, GX; Li, ZJ; Liu, YY; Shen, MX; Su, J; Wang, QH; Wu, XD; Zhu, GF	1

Reviews

3 review(s) available for eudesmane and sesquiterpenes

Article	Year
[Phytochemical study of liverworts Conocephalum conicum and Chiloscyphus polyanthos]. Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan, 2000, Volume: 120, Issue:12 Topics: Lichens; Molecular Conformation; Naphthalenes; Sesquiterpenes; Sesquiterpenes, Eudesmane; Stereoisomerism	2000
[Advances in studies on chemical constituents of Senecio]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica, 2003, Volume: 28, Issue:2 Topics: Animals; Anti-Bacterial Agents; Antineoplastic Agents, Phytogenic; Chromatography, High Pressure Liquid; Humans; Molecular Structure; Plants, Medicinal; Pyrrolizidine Alkaloids; Senecio; Sesquiterpenes; Sesquiterpenes, Eudesmane	2003
Sesquiterpenoids from Meliaceae Family and Their Biological Activities. Molecules (Basel, Switzerland), 2023, Jun-20, Volume: 28, Issue:12 Topics: Flowers; Medicine, Traditional; Meliaceae; Molecular Structure; Sesquiterpenes; Sesquiterpenes, Eudesmane	2023

Other Studies

63 other study(ies) available for eudesmane and sesquiterpenes

Article	Year
Eudesmane derivatives from Iva frutescens. Phytochemistry, 1998, Volume: 47, Issue:3 Topics: Naphthalenes; Nuclear Magnetic Resonance, Biomolecular; Plants; Sesquiterpenes; Sesquiterpenes, Eudesmane	1998
Eudesmane derivatives from Tessaria integrifolia. Phytochemistry, 2000, Volume: 53, Issue:4 Topics: Asteraceae; Enzyme Activation; Hyaluronoglucosaminidase; Magnetic Resonance Spectroscopy; Naphthalenes; Plant Extracts; Sesquiterpenes; Sesquiterpenes, Eudesmane	2000
Eudesmanoids from Sphaeranthus indicus. Fitoterapia, 2000, Volume: 71, Issue:3 Topics: Asteraceae; Humans; Naphthalenes; Plant Extracts; Plants, Medicinal; Sesquiterpenes; Sesquiterpenes, Eudesmane	2000
Regioselective enzymatic acylations of polyhydroxylated eudesmanes: semisynthesis, theoretical calculations, and biotransformation of cyclic sulfites. The Journal of organic chemistry, 2000, Dec-01, Volume: 65, Issue:24 Topics: Acylation; Biotransformation; Dealkylation; Lipase; Magnetic Resonance Spectroscopy; Molecular Conformation; Naphthalenes; Rhizopus; Sesquiterpenes; Sesquiterpenes, Eudesmane; Sulfites	2000
New eudesmane sesquiterpenes from the root of Lindera strychnifolia. Journal of natural products, 2001, Volume: 64, Issue:3 Topics: China; Drugs, Chinese Herbal; Lauraceae; Naphthalenes; Plant Extracts; Plant Roots; Plants, Medicinal; Sesquiterpenes; Sesquiterpenes, Eudesmane	2001
An eudesmanolide and a carotane from Ferula sinaica. Phytochemistry, 2001, Volume: 57, Issue:4 Topics: Biological Factors; Egypt; Ferula; Medicine, Traditional; Naphthalenes; Phytotherapy; Plant Leaves; Plants, Medicinal; Plants, Toxic; Sesquiterpenes; Sesquiterpenes, Eudesmane	2001
Novel approach for the stereocontrolled construction of eudesmane skeleton: a concise synthesis of (+/-)-balanitol. Organic letters, 2001, Aug-09, Volume: 3, Issue:16 Topics: Catalysis; Cyclization; Hydrogenation; Indicators and Reagents; Japan; Molecular Conformation; Naphthalenes; Plants, Medicinal; Sesquiterpenes; Sesquiterpenes, Eudesmane; Stereoisomerism	2001
A new eudesmane derivative from Onopordon ambiguum. Fitoterapia, 2002, Volume: 73, Issue:1 Topics: Asteraceae; Humans; Magnetic Resonance Spectroscopy; Phytotherapy; Plant Extracts; Sesquiterpenes; Sesquiterpenes, Eudesmane	2002
Two highly oxygenated eudesmanes and 10 lignans from Achillea holosericea. Phytochemistry, 2002, Volume: 59, Issue:8 Topics: Asteraceae; Lignans; Magnetic Resonance Spectroscopy; Molecular Conformation; Sesquiterpenes; Sesquiterpenes, Eudesmane	2002
Chemical-microbiological synthesis of cryptomeridiol derivatives by Gliocladium roseum: semisynthesis of 11-hydroxyeudesmanolides. Journal of natural products, 2002, Volume: 65, Issue:7 Topics: Ascomycota; Biotransformation; Gliocladium; Molecular Conformation; Molecular Structure; Nuclear Magnetic Resonance, Biomolecular; Oxidation-Reduction; Sesquiterpenes; Sesquiterpenes, Eudesmane; Spain; Spectrophotometry, Infrared	2002
Three pyrone glucosidic derivatives from Conyza albida. Planta medica, 2002, Volume: 68, Issue:7 Topics: Asteraceae; Glucosides; Magnetic Resonance Spectroscopy; Molecular Conformation; Pyrones; Sesquiterpenes; Sesquiterpenes, Eudesmane	2002
Allelochemical effects of eudesmane and eremophilane sesquiterpenes on Tribolium castaneum larvae. Journal of chemical ecology, 2003, Volume: 29, Issue:1 Topics: Administration, Topical; Animals; Biological Assay; Chemoreceptor Cells; Larva; Movement; Naphthalenes; Polycyclic Sesquiterpenes; Sesquiterpenes; Sesquiterpenes, Eudesmane; Tribolium	2003
Eudesmane derivatives and other constituents from Saussurea parviflora. Phytochemistry, 2003, Volume: 62, Issue:8 Topics: Antineoplastic Agents, Phytogenic; Carcinoma, Hepatocellular; Cell Survival; Chemical Fractionation; Drug Screening Assays, Antitumor; Female; Humans; Liver Neoplasms; Nuclear Magnetic Resonance, Biomolecular; Ovarian Neoplasms; Plants, Medicinal; Saussurea; Sesquiterpenes; Sesquiterpenes, Eudesmane; Tumor Cells, Cultured	2003
A new eudesmane type sesquiterpene from Inula viscosa. Natural product research, 2003, Volume: 17, Issue:2 Topics: Humans; Inula; Magnetic Resonance Spectroscopy; Phytotherapy; Plant Extracts; Sesquiterpenes; Sesquiterpenes, Eudesmane	2003
Eudesmane derivatives from Laggera pterodonta. Fitoterapia, 2003, Volume: 74, Issue:5 Topics: Antineoplastic Agents; Asteraceae; Cell Division; Humans; Phytotherapy; Plant Extracts; Sesquiterpenes; Sesquiterpenes, Eudesmane; Tumor Cells, Cultured	2003
Volatile constituents in the liverwort Tritomaria polita. Phytochemistry, 2003, Volume: 64, Issue:2 Topics: Gas Chromatography-Mass Spectrometry; Hepatophyta; Nuclear Magnetic Resonance, Biomolecular; Oils, Volatile; Sesquiterpenes; Sesquiterpenes, Eudesmane; Volatilization	2003
Stabilisation of eudesmane cation by tryptophan 334 during aristolochene synthase catalysis. Chemical communications (Cambridge, England), 2003, Sep-07, Issue:17 Topics: Catalysis; Cations; Isomerases; Penicillium; Polyisoprenyl Phosphates; Sesquiterpenes; Sesquiterpenes, Eudesmane; Tryptophan	2003
Eudesmane sesquiterpenes from the aquatic fungus Beltrania rhombica. Chemical & pharmaceutical bulletin, 2005, Volume: 53, Issue:2 Topics: Anti-Bacterial Agents; Antifungal Agents; Bacteria; Fermentation; Fungi; Magnetic Resonance Spectroscopy; Microbial Sensitivity Tests; Sesquiterpenes; Sesquiterpenes, Eudesmane	2005
Terpenoids from Juniperus polycarpus var. seravschanica. Phytochemistry, 2006, Volume: 67, Issue:24 Topics: Abietanes; Animals; Antimalarials; Diterpenes; Fruit; Juniperus; Magnetic Resonance Spectroscopy; Molecular Structure; Plant Extracts; Plasmodium falciparum; Sesquiterpenes; Sesquiterpenes, Eudesmane; Terpenes	2006
Elemanolide sesquiterpenes and eudesmane sesquiterpene glycosides from Centaurea hierapolitana. Phytochemistry, 2007, Volume: 68, Issue:5 Topics: Centaurea; Flavones; Glycosides; Hydrolysis; Mass Spectrometry; Models, Molecular; Molecular Conformation; Plant Components, Aerial; Plant Structures; Sesquiterpenes; Sesquiterpenes, Eudesmane; Spectrophotometry, Infrared	2007
Eudesmanes from Pluchea sagittalis. Their antifeedant activity on Spodoptera frugiperda. Phytochemistry, 2008, Volume: 69, Issue:8 Topics: Animals; Asteraceae; Crystallography, X-Ray; Feeding Behavior; Larva; Molecular Structure; Plant Components, Aerial; Plant Preparations; Sesquiterpenes; Sesquiterpenes, Eudesmane; Spodoptera	2008
New eudesmane derivatives and other sesquiterpenes from the epigeal parts of Dittrichia graveolens. Chemical & pharmaceutical bulletin, 2008, Volume: 56, Issue:11 Topics: Analgesics, Non-Narcotic; Animals; Anti-Bacterial Agents; Anti-Inflammatory Agents, Non-Steroidal; Antifungal Agents; Bacteria; Body Temperature; Edema; Fever; Fungi; Inula; Magnetic Resonance Spectroscopy; Male; Microbial Sensitivity Tests; Plant Extracts; Rats; Sesquiterpenes; Sesquiterpenes, Eudesmane	2008
Total synthesis of eudesmane terpenes by site-selective C-H oxidations. Nature, 2009, Jun-11, Volume: 459, Issue:7248 Topics: Biological Products; Biomimetics; Carbon; Hydrogen; Molecular Structure; Oxidation-Reduction; Sesquiterpenes; Sesquiterpenes, Eudesmane	2009
Two new eudesmane-type sesquiterpenoids from Olanum lyratum. Natural product research, 2009, Volume: 23, Issue:13 Topics: Animals; Antineoplastic Agents; Cell Line, Tumor; Cell Survival; Drugs, Chinese Herbal; HT29 Cells; Humans; Magnetic Resonance Spectroscopy; Mice; Molecular Structure; Sesquiterpenes; Sesquiterpenes, Eudesmane; Solanaceae	2009
Intermediacy of eudesmane cation during catalysis by aristolochene synthase. The Journal of organic chemistry, 2010, Feb-19, Volume: 75, Issue:4 Topics: Binding Sites; Catalysis; Cations; Crown Compounds; Crystallography, X-Ray; Cyclization; Isomerases; Models, Molecular; Penicillium; Sesquiterpenes; Sesquiterpenes, Eudesmane; Sesquiterpenes, Germacrane; Stereoisomerism	2010
Inhibition of (+)-aristolochene synthase with iminium salts resembling eudesmane cation. Organic letters, 2011, Mar-04, Volume: 13, Issue:5 Topics: Aspergillus; Catalysis; Cyclization; Imines; Isomerases; Models, Molecular; Molecular Structure; Nicotiana; Penicillium; Salts; Sesquiterpenes; Sesquiterpenes, Eudesmane; Sesquiterpenes, Germacrane; Stereoisomerism	2011
Probing eudesmane cation-π interactions in catalysis by aristolochene synthase with non-canonical amino acids. Journal of the American Chemical Society, 2011, Sep-07, Volume: 133, Issue:35 Topics: Amino Acids; Cations; Isomerases; Models, Molecular; Mutation; Penicillium; Sesquiterpenes; Sesquiterpenes, Eudesmane; Sesquiterpenes, Germacrane	2011
Eudesmane-type sesquiterpene lactones inhibit multiple steps in the NF-κB signaling pathway induced by inflammatory cytokines. Bioorganic & medicinal chemistry letters, 2012, Jan-01, Volume: 22, Issue:1 Topics: Algorithms; Cell Line, Tumor; Chemistry, Pharmaceutical; Cytokines; Dimerization; Drug Design; Humans; Inflammation; Inhibitory Concentration 50; Intercellular Adhesion Molecule-1; Interleukin-1alpha; Ketones; Lactones; Models, Chemical; NF-kappa B; Sesquiterpenes; Sesquiterpenes, Eudesmane; Signal Transduction; Time Factors; Tumor Necrosis Factor-alpha	2012
Hepatoprotective glycosides from Leonurus japonicus Houtt. Carbohydrate research, 2012, Feb-01, Volume: 348 Topics: Carbohydrate Sequence; Cell Line; Cytoprotection; Glucosides; Glycosides; Guaiacol; Hepatocytes; Humans; Leonurus; Magnetic Resonance Spectroscopy; Mass Spectrometry; Molecular Structure; Plant Extracts; Sesquiterpenes; Sesquiterpenes, Eudesmane; Trisaccharides	2012
Sesquiterpenes and other constituents from Dendranthema zawadskii var. latilobum. Chemical & pharmaceutical bulletin, 2012, Volume: 60, Issue:3 Topics: Animals; Cells, Cultured; Chrysanthemum; Flavonoids; Inhibitory Concentration 50; Lipopolysaccharides; Macrophages; Mice; Nitric Oxide; Plant Extracts; Sesquiterpenes; Sesquiterpenes, Eudesmane; Sesquiterpenes, Germacrane; Spectrum Analysis	2012
Phytochemical profile and apoptotic activity of Onopordum cynarocephalum. Planta medica, 2012, Volume: 78, Issue:15 Topics: Antineoplastic Agents, Phytogenic; Apoptosis; Caspase 3; Cell Line, Tumor; Cell Proliferation; DNA Fragmentation; Dose-Response Relationship, Drug; Furans; HSP70 Heat-Shock Proteins; Humans; Inhibitory Concentration 50; Lignans; Molecular Structure; Monocyclic Sesquiterpenes; Onopordum; Plant Components, Aerial; Plant Extracts; Plants, Medicinal; PTEN Phosphohydrolase; Sesquiterpenes; Sesquiterpenes, Eudesmane	2012
Apolar Laurus nobilis leaf extracts induce cytotoxicity and apoptosis towards three nervous system cell lines. Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 2013, Volume: 62 Topics: Animals; Antioxidants; Apoptosis; Cell Line; Cell Line, Tumor; Gas Chromatography-Mass Spectrometry; Glioma; Humans; Lactones; Laurus; Neuroblastoma; Neuroprotective Agents; Plant Extracts; Plant Leaves; Rats; Sesquiterpenes; Sesquiterpenes, Eudesmane; Terpenes	2013
Four new eudesmane-type sesquiterpenes from the basal leaves of Salvia plebeia R. Br. Fitoterapia, 2014, Volume: 94 Topics: Animals; Cell Line; Crystallography, X-Ray; Drugs, Chinese Herbal; Lactones; Magnetic Resonance Spectroscopy; Medicine, Chinese Traditional; Mice; Molecular Structure; Nitric Oxide; Plant Leaves; Salvia; Sesquiterpenes; Sesquiterpenes, Eudesmane	2014
Highly oxygenated sesquiterpenes in Artemisia alba Turra. Phytochemistry, 2015, Volume: 110 Topics: Alcohols; Artemisia; Molecular Structure; Nuclear Magnetic Resonance, Biomolecular; Oxygen; Sesquiterpenes; Sesquiterpenes, Eudesmane; Sesquiterpenes, Guaiane	2015
The role of new eudesmane-type sesquiterpenoid and known eudesmane derivatives from the red alga Laurencia obtusa as potential antifungal-antitumour agents. Natural product research, 2016, Volume: 30, Issue:10 Topics: Antifungal Agents; Antineoplastic Agents; Fungi; Humans; Laurencia; MCF-7 Cells; Microbial Sensitivity Tests; Molecular Structure; Sesquiterpenes; Sesquiterpenes, Eudesmane	2016
Guaianolides and a seco-Eudesmane from the Resinous Exudates of Cushion Bush (Leucophyta brownii) and Evaluation of Their Cytostatic and Anti-inflammatory Activity. Journal of natural products, 2015, Aug-28, Volume: 78, Issue:8 Topics: Animals; Anti-Inflammatory Agents; Asteraceae; Crystallography, X-Ray; Cytostatic Agents; Drug Screening Assays, Antitumor; HT29 Cells; Humans; Lactones; Mice; Molecular Structure; Resins, Plant; Sesquiterpenes; Sesquiterpenes, Eudesmane; Sesquiterpenes, Guaiane	2015
New eudesmane-type sesquiterpenoids from the root bark of Pseudolarix kaempferi. Journal of Asian natural products research, 2015, Volume: 17, Issue:12 Topics: Drugs, Chinese Herbal; Molecular Structure; Nuclear Magnetic Resonance, Biomolecular; Pinaceae; Plant Bark; Sesquiterpenes; Sesquiterpenes, Eudesmane	2015
Sesquiterpenoids from the roots of Vladimiria muliensis. Journal of Asian natural products research, 2015, Volume: 17, Issue:12 Topics: Asteraceae; Drugs, Chinese Herbal; Humans; Molecular Structure; Plant Roots; Sesquiterpenes; Sesquiterpenes, Eudesmane; Sesquiterpenes, Guaiane	2015
Sesquiterpenoids from the seeds of Sarcandra glabra and the potential anti-inflammatory effects. Fitoterapia, 2016, Volume: 111 Topics: Animals; Anti-Inflammatory Agents; Drugs, Chinese Herbal; Furans; Macrophages; Magnoliopsida; Mice; Molecular Structure; Nitric Oxide; RAW 264.7 Cells; Seeds; Sesquiterpenes; Sesquiterpenes, Eudesmane	2016
Eucarobustols A-I, Conjugates of Sesquiterpenoids and Acylphloroglucinols from Eucalyptus robusta. Journal of natural products, 2016, 05-27, Volume: 79, Issue:5 Topics: Drugs, Chinese Herbal; Eucalyptus; Inhibitory Concentration 50; Molecular Structure; Nuclear Magnetic Resonance, Biomolecular; Plant Leaves; Protein Tyrosine Phosphatase, Non-Receptor Type 1; Sesquiterpenes; Sesquiterpenes, Eudesmane; Sesquiterpenes, Guaiane	2016
Bioactive sesquiterpenoids from the flowers of Inula japonica. Phytochemistry, 2016, Volume: 129 Topics: Animals; Crystallography, X-Ray; Flowers; HL-60 Cells; Humans; Inhibitory Concentration 50; Inula; Lipopolysaccharides; Macrophages; Mice; Molecular Conformation; Molecular Structure; Nitric Oxide; Sesquiterpenes; Sesquiterpenes, Eudesmane; Sesquiterpenes, Guaiane	2016
Eight new eudesmane- and eremophilane-type sesquiterpenoids from Atractylodes lancea. Fitoterapia, 2016, Volume: 114 Topics: Acetaminophen; Atractylodes; Hep G2 Cells; Humans; Molecular Structure; Polycyclic Sesquiterpenes; Rhizome; Sesquiterpenes; Sesquiterpenes, Eudesmane	2016
Vetiverianines A, B, and C: Sesquiterpenoids from Vetiveria zizanioides Roots. Journal of natural products, 2016, 09-23, Volume: 79, Issue:9 Topics: Antineoplastic Agents, Phytogenic; Chrysopogon; Crystallography, X-Ray; Drug Screening Assays, Antitumor; HL-60 Cells; Humans; Japan; Molecular Structure; Plant Roots; Sesquiterpenes; Sesquiterpenes, Eudesmane	2016
Sesquiterpenes from the whole plants of Parasenecio roborowskii. Fitoterapia, 2017, Volume: 116 Topics: Animals; Antineoplastic Agents, Phytogenic; Asteraceae; Cell Line, Tumor; Humans; Melanoma, Experimental; Mice; Molecular Structure; Sesquiterpenes; Sesquiterpenes, Eudesmane	2017
Sesquiterpenoids from the twigs and leaves of Fokienia hodginsii. Journal of Asian natural products research, 2017, Volume: 19, Issue:7 Topics: Antineoplastic Agents, Phytogenic; Drug Screening Assays, Antitumor; Drugs, Chinese Herbal; HL-60 Cells; Humans; Molecular Structure; Plant Leaves; Plant Stems; Sesquiterpenes; Sesquiterpenes, Eudesmane	2017
Sesquiterpenoids from the cultured mycelia of Ganoderma capense. Fitoterapia, 2017, Volume: 118 Topics: Cell Line, Tumor; Ganoderma; Humans; Molecular Structure; Mycelium; Polycyclic Sesquiterpenes; Sesquiterpenes; Sesquiterpenes, Eudesmane	2017
Modification of Natural Eudesmane Scaffolds via Mizoroki-Heck Reactions. Molecules (Basel, Switzerland), 2017, Apr-20, Volume: 22, Issue:4 Topics: Biological Products; Magnetic Resonance Spectroscopy; Molecular Structure; Plant Extracts; Sesquiterpenes; Sesquiterpenes, Eudesmane	2017
Specialized metabolites from the aerial parts of Centaurea polyclada DC. Phytochemistry, 2017, Volume: 143 Topics: Centaurea; Lactones; Molecular Structure; Nuclear Magnetic Resonance, Biomolecular; Plant Components, Aerial; Plants, Medicinal; Sesquiterpenes; Sesquiterpenes, Eudesmane; Turkey	2017
Antiproliferative metabolites from the Northern African endemic plant Daucus virgatus (Apiaceae). Phytochemistry, 2017, Volume: 143 Topics: Antineoplastic Agents, Phytogenic; Apiaceae; Cell Proliferation; Drug Screening Assays, Antitumor; Humans; Isocoumarins; Molecular Structure; Nuclear Magnetic Resonance, Biomolecular; Phytoalexins; Plant Components, Aerial; Sesquiterpenes; Sesquiterpenes, Eudesmane	2017
Eudesmane and aromadendrane sesquiterpenoids from the Vietnamese soft coral Sinularia erecta. Natural product research, 2018, Volume: 32, Issue:15 Topics: Animals; Anthozoa; Antineoplastic Agents; Cell Line, Tumor; Drug Screening Assays, Antitumor; HeLa Cells; Humans; Inhibitory Concentration 50; Magnetic Resonance Spectroscopy; Molecular Structure; Sesquiterpenes; Sesquiterpenes, Eudesmane; Sesquiterpenes, Guaiane	2018
Further sesquiterpenoids from the rhizomes of Homalomena occulta and their anti-inflammatory activity. Bioorganic & medicinal chemistry letters, 2019, 05-15, Volume: 29, Issue:10 Topics: Animals; Anti-Inflammatory Agents; Araceae; Cyclooxygenase 2; Drug Evaluation, Preclinical; Gene Expression Regulation; Medicine, Chinese Traditional; Mice; Molecular Structure; Plant Extracts; RAW 264.7 Cells; Rhizome; RNA, Messenger; Sesquiterpenes; Sesquiterpenes, Eudesmane; Sesquiterpenes, Guaiane; Structure-Activity Relationship	2019
Three new sesquiterpenoids with cytotoxic activity from Natural product research, 2021, Volume: 35, Issue:6 Topics: Artemisia; Carbon-13 Magnetic Resonance Spectroscopy; Cell Death; Cell Line, Tumor; Humans; Plant Leaves; Proton Magnetic Resonance Spectroscopy; Sesquiterpenes; Sesquiterpenes, Eudesmane	2021
Eudesmane-type sesquiterpene glycosides: sonneratiosides A-E and eudesmol β-D-glucopyranoside from the leaves of Sonneratia alba. Journal of natural medicines, 2020, Volume: 74, Issue:1 Topics: Arbutin; Glycosides; Lythraceae; Molecular Structure; Monophenol Monooxygenase; Naphthalenes; Plant Leaves; Sesquiterpenes; Sesquiterpenes, Eudesmane	2020
Two new eudesmane sesquiterpene glucosides from the aerial parts of Natural product research, 2023, Volume: 37, Issue:9 Topics: Artemisia; Glucosides; Humans; Molecular Structure; Neoplasms; Plant Components, Aerial; Sesquiterpenes; Sesquiterpenes, Eudesmane	2023
Croargoids A-G, Eudesmane Sesquiterpenes from the Bark of Molecules (Basel, Switzerland), 2022, Sep-27, Volume: 27, Issue:19 Topics: Carbon; Croton; Lactones; Molecular Structure; Plant Bark; Sesquiterpenes; Sesquiterpenes, Eudesmane	2022
Artemleucolides A-L, eudesmane-type sesquiterpenoids from Artemisia leucophylla and their antihepatoma cytotoxicity. Fitoterapia, 2023, Volume: 165 Topics: Artemisia; Humans; Molecular Structure; Sesquiterpenes; Sesquiterpenes, Eudesmane	2023
New Verticillene Diterpenoids, Eudesmane Sesquiterpenoids, and Hydroperoxysteroids from the Further Chemical Investigation of a Taiwanese Soft Coral Molecules (Basel, Switzerland), 2023, Feb-04, Volume: 28, Issue:4 Topics: Animals; Anthozoa; Diterpenes; Magnetic Resonance Spectroscopy; Molecular Structure; Sesquiterpenes; Sesquiterpenes, Eudesmane	2023
Structurally diverse new eudesmane sesquiterpenoids with anti-inflammatory activity from the fruits of Alpinia oxyphylla. Bioorganic chemistry, 2023, Volume: 134 Topics: Alpinia; Anti-Inflammatory Agents; Cyclooxygenase 2; Fruit; Interleukin-6; Lipopolysaccharides; Molecular Structure; Sesquiterpenes; Sesquiterpenes, Eudesmane; Tumor Necrosis Factor-alpha	2023
Four new eudesmane-type and one new eremophilane-type sesquiterpenes from the whole plant of Carpesium abrotanoides L. Fitoterapia, 2023, Volume: 169 Topics: Asteraceae; COVID-19; Magnetic Resonance Spectroscopy; Molecular Structure; Polycyclic Sesquiterpenes; SARS-CoV-2; Sesquiterpenes; Sesquiterpenes, Eudesmane	2023
Two New Eudesmane-Type Sesquiterpene from Clonostachys sp. Y6-1and Their Cytotoxic Activity. Chemistry & biodiversity, 2023, Volume: 20, Issue:9 Topics: Antineoplastic Agents; Magnetic Resonance Spectroscopy; Molecular Structure; Sesquiterpenes; Sesquiterpenes, Eudesmane	2023
Ent-eudesmane sesquiterpenoids from the Chinese liverwort Chiloscyphus polyanthus. Phytochemistry, 2023, Volume: 214 Topics: Antifungal Agents; Antineoplastic Agents; China; Hep G2 Cells; Hepatophyta; Humans; Molecular Structure; Sesquiterpenes; Sesquiterpenes, Eudesmane	2023
Eudesmane sesquiterpenoid glycosides from the leaves of Pittosporum lenticellatum with anti-neuroinflammatory activity. Phytochemistry, 2023, Volume: 215 Topics: Glycosides; Magnetic Resonance Spectroscopy; Molecular Docking Simulation; Molecular Structure; Nitric Oxide; Sesquiterpenes; Sesquiterpenes, Eudesmane	2023
Eudesmane-type sesquiterpenoids from the aerial parts of Artemisia lavandulaefolia and their anti-pancreatic cancer activities. Phytochemistry, 2023, Volume: 216 Topics: Artemisia; Molecular Structure; Pancreatic Neoplasms; Plant Components, Aerial; Sesquiterpenes; Sesquiterpenes, Eudesmane	2023