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diarylheptanoids (506) 506
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cyclic diarylheptanoids (44) 44
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1. Full Text Linear diarylheptanoids as potential anticancer therapeutics: synthesis, biological evaluation, and structure–activity relationship studies
by Motiur Rahman, A F. M and Lu, Yang and Lee, Hwa-Jong and Jo, Hyunji and Yin, Wencui and Alam, Mohammad Sayed and Cha, Hyochang and Kadi, Adnan A and Kwon, Youngjoo and Jahng, Yurngdong
Archives of Pharmacal Research, ISSN 0253-6269, 12/2018, Volume 41, Issue 12, pp. 1131 - 1148
In efforts to develop effective anticancer therapeutics with greater selectivity toward cancerous cell and reduced side-effects, such as emetic effects due to... 
Linear diarylheptanoids | Topoisomerase-IIα | Topoisomerase-I | Antiproliferative activity | Pharmacology/Toxicology | Pharmacy | GINGEROL-RELATED-COMPOUNDS | CHEMISTRY, MEDICINAL | ALPINIA-OFFICINARUM | INHIBITORY-ACTIVITY | CYTOTOXIC DIARYLHEPTANOIDS | CYCLIC DIARYLHEPTANOIDS | IN-VITRO | 1ST TOTAL-SYNTHESIS | NITRIC-OXIDE | PHARMACOLOGY & PHARMACY | Topoisomerase-II | FLUORESCEIN HYDRAZONES | RESPIRATORY SYNCYTIAL VIRUS | Diarylheptanoids - chemistry | Diarylheptanoids - pharmacology | Gram-Positive Bacteria - drug effects | Antineoplastic Agents - chemical synthesis | Humans | Structure-Activity Relationship | Antineoplastic Agents - chemistry | Anti-Bacterial Agents - chemical synthesis | Dose-Response Relationship, Drug | Microbial Sensitivity Tests | Gram-Negative Bacteria - drug effects | Diarylheptanoids - chemical synthesis | Anti-Bacterial Agents - chemistry | Gram-Negative Bacteria - growth & development | Cell Line, Tumor | Anti-Bacterial Agents - pharmacology | Antineoplastic Agents - pharmacology | Cell Proliferation - drug effects | Molecular Structure | Gram-Positive Bacteria - growth & development | Drug Screening Assays, Antitumor | Gastrointestinal agents | Microbiota (Symbiotic organisms) | Therapeutics | Drugstores | Plants | Antibacterial agents | Homeopathy | Materia medica and therapeutics
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2. Full Text Quali-quantitative analysis of the phenolic fraction of the flowers of Corylus avellana, source of the Italian PGI product "Nocciola di Giffoni": Isolation of antioxidant diarylheptanoids
by Masullo, M and Mari, A and Cerulli, A and Bottone, A and Kontek, B and Olas, B and Pizza, C and Piacente, S
PHYTOCHEMISTRY, ISSN 0031-9422, 10/2016, Volume 130, pp. 273 - 281
There is only limited information available on the chemical composition of the non-edible parts of Corylus avellana, source of the Italian PGI product... 
Multiple Reaction Monitoring | GLYCOSIDES | FRUITS | STRUCTURAL ELUCIDATION | Diarylheptanoids | Antioxidant activity | BIOCHEMISTRY & MOLECULAR BIOLOGY | Hazelnut | ESI-MS | Flowers | TANDEM MASS-SPECTROMETRY | HAZELNUT BY-PRODUCTS | PLANT SCIENCES | FOOD SUPPLEMENTS | L. LEAVES | PROFILE | CYCLIZED DIARYLHEPTANOIDS | Corylus avellana | LC-ESI(QqQ)MS | Betulaceae | Plant Leaves - chemistry | Diarylheptanoids - chemistry | Antioxidants - chemistry | Diarylheptanoids - pharmacology | Humans | Hydrogen Peroxide - pharmacology | Flowers - chemistry | Diarylheptanoids - isolation & purification | Nuclear Magnetic Resonance, Biomolecular | Italy | Phenols - chemistry | Corylus - chemistry | Lipid Peroxidation | Antioxidants | Nuclear magnetic resonance spectroscopy | Drug discovery
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3. Full Text New Taste-Active 3‑(O‑β‑d‑Glucosyl)-2-oxoindole-3-acetic Acids and Diarylheptanoids in Cimiciato-Infected Hazelnuts
by Singldinger, Barbara and Dunkel, Andreas and Bahmann, Dominic and Bahmann, Claudia and Kadow, Daniel and Bisping, Bernward and Hofmann, Thomas
Journal of Agricultural and Food Chemistry, ISSN 0021-8561, 05/2018, Volume 66, Issue 18, pp. 4660 - 4673
Activity-guided fractionation in combination with sensory analytics, LC-TOF-MS, and 1D/2D-NMR spectroscopy enabled the identification of the bitter tasting... 
diarylheptanoids | asadanin | taste | Cimiciato | hazelnuts | Corylus avellana L | giffonin P | bitter | BITTER OFF-TASTE | HUMULUS-LUPULUS L | FOOD SCIENCE & TECHNOLOGY | LEAVES | BIORESPONSE | SENSORY CHARACTERIZATION | IDENTIFICATION | CORYLUS-AVELLANA L | CYCLIZED DIARYLHEPTANOIDS | DAUCUS-CAROTA L | AGRICULTURE, MULTIDISCIPLINARY | CHEMISTRY, APPLIED | DI GIFFONI | Diarylheptanoids - chemistry | Humans | Nuts - metabolism | Flavoring Agents - metabolism | Male | Chromatography, High Pressure Liquid | Young Adult | Tandem Mass Spectrometry | Diarylheptanoids - metabolism | Corylus - metabolism | Flavoring Agents - chemistry | Nuts - chemistry | Adult | Female | Taste | Corylus - chemistry
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4. TOTAL SYTNHESIS OF RHOIPTELOL B
by Tanaka, N and Takamura, H and Kadota, I
HETEROCYCLES, ISSN 0385-5414, 09/2018, Volume 97, Issue 2, pp. 1157 - 1164
A stereoselective total synthesis of rhoiptelol B, a diarylheptanoid isolated from the fruits of Rhoiptelea chiliantha, is described. The tetrahydropyran ring... 
ESTERS | CHEMISTRY, ORGANIC | DIARYLHEPTANOIDS
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5. Full Text Total Synthesis of Tedarene A
by Maurent, Kelly and Vanucci-Bacqué, Corinne and Saffon-Merceron, Nathalie and Baltas, Michel and Bedos-Belval, Florence
Journal of Natural Products, ISSN 0163-3864, 05/2017, Volume 80, Issue 5, pp. 1623 - 1630
Tedarene A is a macrocyclic diaryl ether heptanoid isolated from the marine sponge Tedania ignis showing an inhibitory effect against nitric oxide production.... 
CHEMISTRY, MEDICINAL | NATURALLY-OCCURRING DIARYLHEPTANOIDS | MACROCYCLES | PHARMACOLOGY & PHARMACY | AGENTS | ACEROSIDE-IV | PLANT SCIENCES | Propanols - chemistry | Diarylheptanoids - chemistry | Animals | Diarylheptanoids - chemical synthesis | Stereoisomerism | Diarylheptanoids - isolation & purification | Ethers - chemistry | Molecular Structure | Porifera - chemistry | Propanols - chemical synthesis | Chemical Sciences
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6. Full Text Oregonin from Alnus incana bark affects DNA methyltransferases expression and mitochondrial DNA copies in mouse embryonic fibroblasts
by Krasilnikova, Jelena and Lauberte, Liga and Stoyanova, Elena and Abadjieva, Desislava and Chervenkov, Mihail and Mori, Mattia and De Paolis, Elisa and Mladenova, Vanya and Telysheva, Galina and Botta, Bruno and Kistanova, Elena
Journal of Enzyme Inhibition and Medicinal Chemistry, ISSN 1475-6366, 01/2018, Volume 33, Issue 1, pp. 1055 - 1063
Oregonin is an open-chain diarylheptanoid isolated from Alnus incana bark that possesses remarkable antioxidant and anti-inflammatory properties, inhibits... 
DNA methyltransferases mRNAs | Alnus incana bark | Oregonin | mtDNA copy | CANCER-CELLS | PROMOTER HYPERMETHYLATION | METHYLATION | CHEMISTRY, MEDICINAL | CURCUMIN | BIOCHEMISTRY & MOLECULAR BIOLOGY | TRANSCRIPTION | NATURAL COMPOUNDS | GENE | COPY NUMBER | MAMMALIAN MITOCHONDRIA | DIARYLHEPTANOIDS | Cell Survival - drug effects | Diarylheptanoids - chemistry | DNA, Mitochondrial - metabolism | Diarylheptanoids - pharmacology | RNA, Messenger - genetics | Cells, Cultured | Structure-Activity Relationship | RNA, Messenger - metabolism | DNA (Cytosine-5-)-Methyltransferase 1 - biosynthesis | DNA (Cytosine-5-)-Methyltransferase 1 - metabolism | Plant Bark - chemistry | DNA (Cytosine-5-)-Methyltransferases - metabolism | Dose-Response Relationship, Drug | DNA (Cytosine-5-)-Methyltransferases - genetics | Animals | DNA (Cytosine-5-)-Methyltransferase 1 - genetics | Alnus - chemistry | Fibroblasts - drug effects | RNA, Messenger - antagonists & inhibitors | Diarylheptanoids - isolation & purification | Mice | Molecular Structure | DNA Methylation - drug effects | DNA (Cytosine-5-)-Methyltransferases - biosynthesis | Index Medicus
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7. Full Text Diarylheptanoids from the bark of black alder inhibit the growth of sensitive and multi-drug resistant non-small cell lung carcinoma cells
by Novaković, Miroslav and Pešić, Milica and Trifunović, Snežana and Vučković, Ivan and Todorović, Nina and Podolski-Renić, Ana and Dinić, Jelena and Stojković, Sonja and Tešević, Vele and Vajs, Vlatka and Milosavljević, Slobodan
Phytochemistry, ISSN 0031-9422, 01/2014, Volume 97, pp. 46 - 54
Ten hitherto unknown and ten known diarylheptanoids were isolated from the bark and exhibited significant cytotoxic activities against NCI-H460 and NCI-H460/R... 
Multi-drug resistance | HPLC-DAD | Black alder | Diarylheptanoids | NMR analysis | Anti-cancer activity | GLYCOSIDES | CURCUMIN | INNER BARK | BIOCHEMISTRY & MOLECULAR BIOLOGY | OREGONIN | PLANT SCIENCES | SEEDS | ABSOLUTE-CONFIGURATION | GENKWANIN | CONSTITUENTS | Cell Survival - drug effects | Diarylheptanoids - chemistry | Diarylheptanoids - pharmacology | Heptanes - pharmacology | Ilex - chemistry | Small Cell Lung Carcinoma | Antineoplastic Agents, Phytogenic - chemistry | Catechols - chemistry | Plant Bark - chemistry | Alnus - chemistry | Diarylheptanoids - isolation & purification | Catechols - pharmacology | Glycosides | Nuclear Magnetic Resonance, Biomolecular | Antineoplastic Agents, Phytogenic - pharmacology | Antineoplastic Agents, Phytogenic - isolation & purification | Drug Screening Assays, Antitumor | Drug resistance | Lung cancer, Non-small cell
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8. Full Text Anti-adipogenic activity of a new cyclic diarylheptanoid isolated from Alnus japonica on 3T3-L1 cells via modulation of PPARγ, C/EBPα and SREBP1c signaling
by Sung, Sang Hyun and Lee, Mina
Bioorganic & Medicinal Chemistry Letters, ISSN 0960-894X, 10/2015, Volume 25, Issue 20, pp. 4648 - 4651
Total methanolic extract of fruits exhibited significant anti-adipogenic activities in 3T3-L1 cells. A new cyclic diarylheptanoid ( ) along with ten known... 
Obesity | 3T3-L1 cells | Diarylheptanoids | Alnus japonica | Adipocyte differentiation | Betulaceae | Adipogenesis | CHEMISTRY, MEDICINAL | BARK | CHEMISTRY, ORGANIC | GENE | LIVER | HIRSUTA | BINDING | CONSTITUENTS | CCAAT-Enhancer-Binding Protein-alpha - metabolism | Diarylheptanoids - chemistry | Diarylheptanoids - pharmacology | Fruit - chemistry | Adipogenesis - drug effects | RNA, Messenger - genetics | Signal Transduction - genetics | Structure-Activity Relationship | 3T3-L1 Cells | Down-Regulation - drug effects | PPAR gamma - metabolism | Dose-Response Relationship, Drug | Animals | Alnus - chemistry | Signal Transduction - drug effects | Sterol Regulatory Element Binding Protein 1 - genetics | Diarylheptanoids - isolation & purification | CCAAT-Enhancer-Binding Protein-alpha - genetics | Mice | Molecular Structure | Adipogenesis - genetics | Sterol Regulatory Element Binding Protein 1 - metabolism | PPAR gamma - genetics
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9. Full Text Antioxidant activity of different species and varieties of turmeric (Curcuma spp): Isolation of active compounds
by Akter, Jesmin and Hossain, Md. Amzad and Takara, Kensaku and Islam, Md. Zahorul and Hou, De-Xing
Comparative Biochemistry and Physiology, Part C, ISSN 1532-0456, 01/2019, Volume 215, pp. 9 - 17
There are >80 species of turmeric ( .) and some species have multiple varieties, for example, ( . ) has 70 varieties. They could be different in their chemical... 
Turmeric | Phenolic | Ryudai gold | Active compound | Antioxidant | Flavonoid | CAPACITY | ASSAY | YIELD | BIOCHEMISTRY & MOLECULAR BIOLOGY | IDENTIFICATION | OXYGEN | ZOOLOGY | GROWTH | ENDOCRINOLOGY & METABOLISM | TOXICOLOGY | EXTRACTS | Free Radical Scavengers - pharmacology | Plant Extracts - chemistry | Curcumin - analogs & derivatives | Diarylheptanoids - chemistry | Antioxidants - chemistry | Species Specificity | Free Radical Scavengers - chemistry | Plant Extracts - pharmacology | Solvents - chemistry | Curcumin - chemistry | Diarylheptanoids - analysis | Spices - analysis | Osmolar Concentration | Rhizome - chemistry | Curcumin - analysis | Free Radical Scavengers - analysis | Molecular Structure | Methanol - chemistry | Antioxidants - analysis | Phytochemicals - chemistry | Diarylheptanoids - pharmacology | Oxidation-Reduction | Phytochemicals - analysis | Japan | Curcumin - pharmacology | Deoxyribose - chemistry | Curcumin - isolation & purification | Plant Breeding | Plant Extracts - isolation & purification | Antioxidants - pharmacology | Drug Discovery | Free Radical Scavengers - isolation & purification | Curcuma - growth & development | Phytochemicals - isolation & purification | Rhizome - growth & development | Antioxidants - isolation & purification | Diarylheptanoids - isolation & purification | Phytochemicals - pharmacology | Curcuma - chemistry | Antioxidants | Hydroxides | Chemical properties | Mass spectrometry | High performance liquid chromatography | Sugars | Isoflavones | Monosaccharides
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10. Full Text Diarylheptanoids from Curcuma kwangsiensis and their inhibitory activity on nitric oxide production in lipopolysaccharide-activated macrophages
by Li, Jun and Liao, Chun-Ru and Wei, Jun-Qi and Chen, Li-Xia and Zhao, Feng and Qiu, Feng
Bioorganic & Medicinal Chemistry Letters, ISSN 0960-894X, 09/2011, Volume 21, Issue 18, pp. 5363 - 5369
Eleven diarylheptanoids ( – ) were isolated from the rhizomes of , together with seven known compounds. All isolated compounds were evaluated for inhibitory... 
Curcuma kwangsiensis | Diarylheptanoid | Macrophages | Inhibition of nitric oxide production | SESQUITERPENES | LONGA | CHEMISTRY, MEDICINAL | CHEMISTRY, ORGANIC | ZINGIBER-OFFICINALE | COMOSA | RHIZOMES | CONSTITUENTS | Macrophages - chemistry | Nitric Oxide - biosynthesis | Diarylheptanoids - chemistry | Diarylheptanoids - pharmacology | Magnetic Resonance Spectroscopy | Nitric Oxide - antagonists & inhibitors | Stereoisomerism | Structure-Activity Relationship | Dose-Response Relationship, Drug | Macrophages - metabolism | Diarylheptanoids - isolation & purification | Lipopolysaccharides - pharmacology | Macrophages - drug effects | Molecular Structure | Curcuma - chemistry | Nitric oxide
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11. Full Text The Garuganin and Garugamblin Diarylether Heptanoids: Total Synthesis and Determination of Chiral Properties Using Dynamic NMR
by Zhu, Zhi-Qiang and Salih, M. Quamar and Fynn, Edward and Bain, Alex D and Beaudry, Christopher M
The Journal of Organic Chemistry, ISSN 0022-3263, 04/2013, Volume 78, Issue 7, pp. 2881 - 2896
The synthesis of the garuganin and garugamblin diarylether heptanoids using an intramolecular Ullmann coupling is reported. Alkene stereoisomers, vinylogous... 
ACERACEAE PLANTS | O-IODOXYBENZOIC ACID | ACER-NIKOENSE | NATURAL-PRODUCTS | ACEROGENIN-A | BIPHENYL ETHER | CHEMISTRY, ORGANIC | CYTOTOXIC DIARYLHEPTANOIDS | CHEMICAL-EXCHANGE | CYCLIC DIARYLHEPTANOIDS | ACEROSIDE-IV | Diarylheptanoids - chemistry | Molecular Structure | Magnetic Resonance Spectroscopy | Diarylheptanoids - chemical synthesis | Usage | Ether | Chirality | Analysis | Racemization | Nuclear magnetic resonance spectroscopy | Chemical properties | Structure
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12. Efficacy of a diarylheptanoid derivative against Leishmania amazonensis
by Alves, Luciana Vignólio and Temporal, Rosane Maria and Cysne-Finkelstein, Léa and Leon, Leonor Laura
Efficacy of a diarylheptanoid derivative against Leishmania amazonensis, 12/2003
The activity of several diarylheptanoid derivatives (curcuminoids) was previously evaluated against Leishmania amazonensis   promastigotes and among them the... 
diarylheptanoid - treatment trial - Leishmania amazonensis   - leishmaniasis
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13. Full Text Evidence for pi-Stacking as a Source of Stereocontrol in the Synthesis of the Core Pyranochromene Ring System common to Calyxin I, Calyxin J, and Epicalyxin J
by Cakir, SP and Stokes, S and Sygula, A and Mead, KT
JOURNAL OF ORGANIC CHEMISTRY, ISSN 0022-3263, 10/2009, Volume 74, Issue 19, pp. 7529 - 7532
A diastereoselective Synthesis of the tetrahydropyrano-chromene ring system common to several natural product isolates of Alpinia blepharocalyx is reported. We... 
SEEDS | CHEMISTRY, ORGANIC | ACIDS | ALPINIA-BLEPHAROCALYX | DERIVATIVES | DIARYLHEPTANOIDS | Alpinia - chemistry | Diarylheptanoids - chemistry | Cyclization | Diarylheptanoids - chemical synthesis | Stereoisomerism | Diarylheptanoids - isolation & purification | Molecular Structure
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14. Full Text Development and validation of an LC–MS/MS method for the determination of DPHB in rat plasma and its application in pharmacokinetic studies
by Wen, Qi and Li, Hai‐Long and Chen, Feng and Gong, Jing‐Wen and Guan, Wei‐Wei and Fu, Nai‐Guang and Tan, Yin‐Feng
Biomedical Chromatography, ISSN 0269-3879, 12/2018, Volume 32, Issue 12, pp. e4373 - n/a
The aim of the present study was to develop a rapid, specific and sensitive LC–MS/MS method for the determination of DPHB... 
diarylheptanoids | pharmacokinetic | LC–MS/MS | DPHB | 7‐(4″‐hydroxy‐3″‐methoxyphenyl)‐1‐phenyl‐4‐hepten‐3‐one | 7-(4″-hydroxy-3″-methoxyphenyl)-1-phenyl-4-hepten-3-one | CHEMISTRY, ANALYTICAL | VIRUS | 7-(4 ''-hydroxy-3 ''-methoxyphenyl)-1-phenyl-4-hepten-3-one | ALPINIA-OFFICINARUM | LESSER GALANGAL | BIOCHEMISTRY & MOLECULAR BIOLOGY | BIOCHEMICAL RESEARCH METHODS | LC-MS/MS | PHARMACOLOGY & PHARMACY | INHIBITORS | RHIZOMES | Diarylheptanoids - chemistry | Reproducibility of Results | Drug Stability | Rats | Linear Models | Male | Rats, Sprague-Dawley | Animals | Diarylheptanoids - pharmacokinetics | Sensitivity and Specificity | Chromatography, Liquid - methods | Tandem Mass Spectrometry - methods | Diarylheptanoids - blood
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15. Full Text Enantioselective Ullmann Ether Couplings: Syntheses of (−)-Myricatomentogenin, (−)-Jugcathanin, (+)-Galeon, and (+)-Pterocarine
by Salih, M. Quamar and Beaudry, Christopher M
Organic Letters, ISSN 1523-7060, 09/2013, Volume 15, Issue 17, pp. 4540 - 4543
The first enantioselective Ullmann cross-coupling reactions to prepare diaryl ethers are reported. The reactions were used to prepare the diarylether heptanoid... 
C-N | GARUGANIN | NATURAL-PRODUCTS | AMIDATION | CHEMISTRY, ORGANIC | BOND FORMATION | ARYL IODIDES | COPPER | CYTOTOXIC DIARYLHEPTANOIDS | EFFICIENT | ACEROGENINS | Biological Products - chemical synthesis | Biological Products - chemistry | Diarylheptanoids - chemistry | Molecular Structure | Diarylheptanoids - chemical synthesis | Stereoisomerism
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16. Full Text Two new compounds from the green peel of Juglans mandshurica
by Li, Jing and Xu, Kang-Ping and Zou, Zhen-Xing and Zou, Hui and Long, Hong-Ping and Tan, Lei-Hong and Liu, Rui-Huan and Wang, Yi-Kun and Xu, Ping-Sheng and Tan, Gui-Shan
Journal of Asian Natural Products Research, ISSN 1028-6020, 11/2017, Volume 19, Issue 11, pp. 1087 - 1092
A new cyclic diarylheptanoid (1) and a new flavone glucoside (2), along with seven known compounds, were isolated from the green peel of Juglans mandshurica.... 
Juglans mandshurica | flavone glycoside | cytotoxicity | diarylheptanoid | CELLS | CHEMISTRY, MEDICINAL | BARK | PLANT SCIENCES | NAPHTHOQUINONES | ROOTS | PHARMACOLOGY & PHARMACY | CHEMISTRY, APPLIED | DIARYLHEPTANOIDS | Plant Extracts - chemistry | Diarylheptanoids - chemistry | Glucosides - pharmacology | Diarylheptanoids - pharmacology | Humans | Drugs, Chinese Herbal - pharmacology | Antineoplastic Agents, Phytogenic - chemistry | Flavones - chemistry | Hep G2 Cells | Glucosides - isolation & purification | Juglans - chemistry | Drugs, Chinese Herbal - chemistry | Diarylheptanoids - isolation & purification | K562 Cells | Glucosides - chemistry | Molecular Structure | Flavones - isolation & purification | Antineoplastic Agents, Phytogenic - pharmacology | Drugs, Chinese Herbal - isolation & purification | Flavones - pharmacology | Antineoplastic Agents, Phytogenic - isolation & purification | Drug Screening Assays, Antitumor | Cytotoxicity | Toxicity | Cell lines | Cancer
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17. Full Text Four new diarylheptanoids from Rhizoma Zingiberis
by Cui, Wan-Hua and Wang, Yan-Zhi and Li, Ze-Zhi and Guo, Yan and Gao, Mei-Ling and Cheng, Yong-Xian and Feng, Wei-Sheng
Journal of Asian Natural Products Research, ISSN 1028-6020, 01/2019, Volume 21, Issue 1, pp. 1 - 8
Four new diarylheptanoids, (1S, 3R, 5R, 6R)-1, 5-epoxy-3, 6 dihydroxy-1-(4-hydroxy-3, 5-dimethoxyphenyl)-7-(4-hydroxy-3-methoxyphenyl) heptane (1), (1R, 3R,... 
diarylheptanoids | cytotoxicity | Zingiberaceae | Rhizoma Zingiberis | CHEMISTRY, MEDICINAL | ALPINIA-OFFICINARUM | NITRIC-OXIDE | PHARMACOLOGY & PHARMACY | CHEMISTRY, APPLIED | PLANT SCIENCES | Diarylheptanoids - chemistry | Ginger - chemistry | Diarylheptanoids - pharmacology | Rhizome - chemistry | Humans | Diarylheptanoids - isolation & purification | Hep G2 Cells | Cytotoxicity | Nuclear magnetic resonance--NMR | Toxicity | Heptanes | Cell lines
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18. Full Text Compounds of Alpinia katsumadai as potential efflux inhibitors in Mycobacterium smegmatis
by Gröblacher, Barbara and Kunert, Olaf and Bucar, Franz
Bioorganic & Medicinal Chemistry, ISSN 0968-0896, 04/2012, Volume 20, Issue 8, pp. 2701 - 2706
Efflux pumps are one of the well established mechanisms that contribute to antibiotic resistance in bacteria, such as mycobacteria. As a result, the... 
Efflux pumps | Fatty acids | MDR resistance | Mycobacteria | Diarylheptanoids | TRANSPORT | CHEMISTRY, MEDICINAL | PUMPS | BIOCHEMISTRY & MOLECULAR BIOLOGY | RESISTANCE | CHEMISTRY, ORGANIC | ETHIDIUM-BROMIDE EFFLUX | Alpinia - chemistry | Mycobacterium smegmatis - growth & development | Plant Extracts - chemistry | Diarylheptanoids - chemistry | Antitubercular Agents - chemistry | Diarylheptanoids - pharmacology | Plant Extracts - pharmacology | Antitubercular Agents - pharmacology | Plant Extracts - isolation & purification | Antitubercular Agents - isolation & purification | Antibiotics, Antitubercular - pharmacology | Microbial Sensitivity Tests | Antibiotics, Antitubercular - chemistry | Diarylheptanoids - isolation & purification | Mycobacterium smegmatis - drug effects | Antibiotics, Antitubercular - isolation & purification | Molecular Structure | Seeds - chemistry | Drug resistance in microorganisms | Antimicrobial agents | Flavonoids | Antibiotics | Rifampin | Antibiotic resistance | Minimum inhibitory concentration
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19. Full Text Anti-neuroinflammatory diarylheptanoids from the rhizomes of Dioscorea nipponica
by Woo, Kyeong Wan and Moon, Eunjung and Kwon, Oh Wook and Lee, Kang Ro and Lee, Sung Ok and Kim, Sun Yeou and Choi, Sang Zin and Son, Mi Won
Bioorganic & Medicinal Chemistry Letters, ISSN 0960-894X, 07/2013, Volume 23, Issue 13, pp. 3806 - 3809
In a continuing search for bioactive constituents from Dioscoreaceae medicinal plants, two new cyclic diarylheptanoids, diosniponol A ( ) and B ( ), together... 
Dioscorea nipponica | Diarylheptanoids | Nitric oxide | Anti-neuroinflammation | Dioscoreaceae | CHEMISTRY, MEDICINAL | MACROPHAGES | INHIBITORY-ACTIVITY | LEAVES | CHEMISTRY, ORGANIC | MAKINO | AMOMUM-TSAO-KO | STEMS | NITRIC-OXIDE PRODUCTION | ZINGIBER-OFFICINALE | BV2 MICROGLIA | CONSTITUENTS | Cell Line | Nitric Oxide - biosynthesis | Diarylheptanoids - chemistry | Diarylheptanoids - pharmacology | Nitric Oxide - antagonists & inhibitors | Anti-Inflammatory Agents, Non-Steroidal - chemistry | Anti-Inflammatory Agents, Non-Steroidal - isolation & purification | Anti-Inflammatory Agents, Non-Steroidal - pharmacology | Animals | Rhizome - chemistry | Diarylheptanoids - isolation & purification | Mice | Molecular Structure | Dioscorea - chemistry | Index Medicus | Mass spectroscopy
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20. Full Text A comprehensive investigation of anti-inflammatory diarylheptanoids from the leaves of Alnus formosana
by Lai, Yi-Chun and Chen, Chien-Kuang and Lin, Wan-Wan and Lee, Shoei-Sheng
Phytochemistry, ISSN 0031-9422, 2012, Volume 73, Issue 1, pp. 84 - 94
This study led to the characterization of 27 diarylheptanoids, including 13 hitherto unknown compounds. Compound and alnuside A ( ) were found to possess... 
Alnus formosana | HPLC-SPE-NMR | Anti-inflammatory | Diarylheptanoids | Betulaceae | GLYCOSIDES | SERRULATOIDES | JAPONICA | TRITERPENOIDS | FEMALE FLOWERS | BARK | BIOCHEMISTRY & MOLECULAR BIOLOGY | PLANT SCIENCES | ANTITUMOR AGENTS | CHEMICAL-CONSTITUENTS | CURCUMIN ANALOGS | CYTOTOXIC AGENTS | Plant Leaves - chemistry | Nitric Oxide - biosynthesis | Diarylheptanoids - chemistry | Diarylheptanoids - pharmacology | Anti-Inflammatory Agents - pharmacology | Chromatography, High Pressure Liquid | Animals | Anti-Inflammatory Agents - chemistry | Alnus - chemistry | Diarylheptanoids - isolation & purification | Lipopolysaccharides - pharmacology | Taiwan | Inhibitory Concentration 50 | Nuclear Magnetic Resonance, Biomolecular | Anti-Inflammatory Agents - isolation & purification | Mice | Molecular Structure | Anti-inflammatory drugs | Investigations
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