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1. Full Text Strategic Redox Relay Enables A Scalable Synthesis of Ouabagenin, A Bioactive Cardenolide
by Hans Renata and Qianghui Zhou and Phil S. Baran
Science, ISSN 0036-8075, 1/2013, Volume 339, Issue 6115, pp. 59 - 63
Here, we report on a scalable route to the polyhydroxylated steroid ouabagenin with an unusual take on the age-old practice of steroid semisynthesis. The... 
Hydroxyls | Molecules | Hydrogen bonds | Ketones | Alkenes | REPORTS | Reagents | Tetrahedrons | Cardenolides | Oxidation | Steroids | OXIDATION | ALCOHOLS | OXYGEN | CROSS-COUPLING REACTIONS | STEROID GLYCOSIDES | BUFADIENOLIDES | OUABAIN | NATURAL-PRODUCTS | MULTIDISCIPLINARY SCIENCES | OLEFINS | Cardenolides - chemical synthesis | Ouabain - therapeutic use | Oxidation-Reduction | Humans | Ouabain - analogs & derivatives | Ouabain - chemistry | Ouabain - chemical synthesis | Cardenolides - therapeutic use | Cardenolides - chemistry | Heart Failure - drug therapy | Oxidation-reduction reaction | Chemical properties | Research | Chemical synthesis | Production processes | Methods | Enzymes | Chemical reactions | Molecular chemistry | Index Medicus | Synthesis | Photochemical | Olefins | Placing | Chemists | Showcases | Transformations | Carbon
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2. Full Text Cardiac Glycosides from the Seeds of Thevetia peruviana
by Tian, Dan-Mei and Cheng, Huo-Yun and Jiang, Miao-Miao and Shen, Wei-Zai and Tang, Jin-Shan and Yao, Xin-Sheng
Journal of Natural Products, ISSN 0163-3864, 01/2016, Volume 79, Issue 1, pp. 38 - 50
Investigation of the seeds of Thevetia peruviana resulted in the isolation of 15 new (2-16) and 18 known (1 and 17-33) cardiac glycosides. Eight... 
CARDENOLIDE GLYCOSIDES | CELLS | APOPTOSIS | CHEMISTRY, MEDICINAL | LEAVES | NERIIFOLIA | CANCER | 5-ALPHA-CARDENOLIDES | PLANT SCIENCES | CERBERA-ODOLLAM | PHARMACOLOGY & PHARMACY | ASCLEPIAS-CURASSAVICA | ANTIARIS-TOXICARIA | Cardiac Glycosides - pharmacology | Thevetia - chemistry | Humans | Drugs, Chinese Herbal - pharmacology | Antineoplastic Agents, Phytogenic - chemistry | Structure-Activity Relationship | Cardenolides - chemistry | Cardenolides - isolation & purification | Drugs, Chinese Herbal - chemistry | Cardiac Glycosides - chemistry | Inhibitory Concentration 50 | Nuclear Magnetic Resonance, Biomolecular | Molecular Structure | Seeds - chemistry | Antineoplastic Agents, Phytogenic - pharmacology | Cardiac Glycosides - isolation & purification | Drugs, Chinese Herbal - isolation & purification | Cardenolides - pharmacology | Antineoplastic Agents, Phytogenic - isolation & purification | Drug Screening Assays, Antitumor | Index Medicus
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3. Full Text First-in-human study of pbi-05204, an oleander-derived inhibitor of akt, fgf-2, nf-κΒ and p70s6k, in patients with advanced solid tumors
by Hong, D S and Henary, H and Falchook, G S and Naing, A and Fu, S and Moulder, S and Wheler, J J and Tsimberidou, A and Durand, J B and Khan, R and Yang, P and Johansen, M and Newman, R A and Kurzrock, R
Investigational New Drugs, ISSN 0167-6997, 12/2014, Volume 32, Issue 6, pp. 1204 - 1212
Background PBI-05204, a Nerium oleander extract (NOE) containing the cardiac glycoside oleandrin, inhibits the α-3 subunit of Na-K ATPase, as well as FGF-2... 
Phase I | Medicine & Public Health | PBI-05204 | Nerium oleander | Oleandrin,NF-kB | Oncology | AKT | Pharmacology/Toxicology | Oleandrin NF-kB | Neoplasms - metabolism | Leukocytes, Mononuclear - metabolism | TOR Serine-Threonine Kinases - metabolism | Plant Extracts - pharmacology | Humans | Middle Aged | Cardenolides - therapeutic use | Male | Extracellular Signal-Regulated MAP Kinases - metabolism | Cardenolides - adverse effects | Adult | Female | Phytotherapy | Antineoplastic Agents, Phytogenic - therapeutic use | Proto-Oncogene Proteins c-akt - metabolism | Antineoplastic Agents, Phytogenic - pharmacokinetics | Cardenolides - blood | Antineoplastic Agents, Phytogenic - adverse effects | NF-kappa B - antagonists & inhibitors | Cardenolides - pharmacokinetics | Ribosomal Protein S6 Kinases, 70-kDa - metabolism | Ribosomal Protein S6 Kinases, 70-kDa - antagonists & inhibitors | Neoplasms - drug therapy | Sodium-Potassium-Exchanging ATPase - metabolism | Fibroblast Growth Factor 2 - antagonists & inhibitors | Maximum Tolerated Dose | Plant Extracts - pharmacokinetics | Nerium | Aged | Antineoplastic Agents, Phytogenic - pharmacology | Plant Extracts - therapeutic use | Cardenolides - pharmacology | Proto-Oncogene Proteins c-akt - antagonists & inhibitors | Plant Extracts - adverse effects | Index Medicus
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4. Full Text Community-wide convergent evolution in insect adaptation to toxic cardenolides by substitutions in the Na, K-ATPase
by Susanne Dobler and Safaa Dalla and Vera Wagschal and Anurag A. Agrawal
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 8/2012, Volume 109, Issue 32, pp. 13040 - 13045
The extent of convergent molecular evolution is largely unknown, yet is critical to understanding the genetics of adaptation. Target site insensitivity to... 
Enzymes | Adenosine triphosphatases | HeLa cells | Cardenolides | Amino acids | Herbivores | Phytophagous insects | Insect vectors | Insect genetics | Biological adaptation | Insect-plant interactions | Toxin resistance | Specialist herbivores | Target site insensitivity | Cardiac glycosides | GASTRIC H,K-ATPASE | ALPHA-SUBUNIT | toxin resistance | MILKWEED BUTTERFLIES | DIRECTED MUTAGENESIS | ONCOPELTUS-FASCIATUS | MULTIDISCIPLINARY SCIENCES | specialist herbivores | cardiac glycosides | HIGH-AFFINITY BINDING | CARDIAC-GLYCOSIDES | insect-plant interactions | target site insensitivity | OUABAIN-BINDING-SITE | AMINO-ACID-RESIDUES | RESISTANT SODIUM-CHANNELS | Amino Acid Sequence | Sodium-Potassium-Exchanging ATPase - genetics | Sodium-Potassium-Exchanging ATPase - chemistry | Species Specificity | Adaptation, Biological - genetics | Computational Biology | Models, Molecular | Molecular Sequence Data | DNA Primers - genetics | Cardenolides - chemistry | Phylogeny | Insecta - genetics | North America | Sequence Analysis, DNA | Mutation, Missense - genetics | Adaptation, Biological - physiology | Drug Resistance - genetics | Cardenolides - toxicity | Animals | Analysis of Variance | Base Sequence | Evolution, Molecular | Molecular evolution | Convergence (Biology) | Research | Insect-plant relationships | Butterflies & moths | Phylogenetics | Evolution | Toxicity | Animal behavior | Adenosine triphosphatase | Index Medicus | Biological Sciences | insect–plant interactions
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5. Full Text The Effects of Milkweed Induced Defense on Parasite Resistance in Monarch Butterflies, Danaus plexippus
by Tan, Wen-Hao and Tao, Leiling and Hoang, Kevin M and Hunter, Mark D and de Roode, Jacobus C
Journal of Chemical Ecology, ISSN 0098-0331, 11/2018, Volume 44, Issue 11, pp. 1040 - 1044
Many plants express induced defenses against herbivores through increasing the production of toxic secondary chemicals following damage. Phytochemical... 
Life Sciences | Biochemistry, general | Entomology | Induction | Biological Microscopy | Ecology | Agriculture | Herbivory | Asclepias | Ophryocystis elektroscirrha | Trophic interactions | PLANT | HERBIVORE | CARDENOLIDES | BIOCHEMISTRY & MOLECULAR BIOLOGY | DISEASE | ECOLOGY | TRAITS | Plant Leaves - chemistry | Plant Leaves - parasitology | Asclepias - parasitology | Asclepias - chemistry | Cardenolides - chemistry | Chromatography, High Pressure Liquid | Herbivory - drug effects | Animals | Plant Leaves - metabolism | Cardenolides - isolation & purification | Larva - drug effects | Butterflies - physiology | Larva - growth & development | Asclepias - metabolism | Butterflies - growth & development | Host-Parasite Interactions | Cardenolides - pharmacology | Disease susceptibility | Plants | Monarch butterfly | Butterflies | Parasite resistance | Plant protection | Interspecific | Parasites | Chemicals | Chemical damage | Disease resistance | Organic chemistry | Trophic relationships | Butterflies & moths | Caterpillars | Toxins | Herbivores | Fitness | Index Medicus
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6. Full Text Cytotoxic cardenolides and sesquiterpenoids from the fruits of Reevesia formosana
by Hsiao, Pei-Yu and Lee, Shiow-Ju and Chen, Ih-Sheng and Hsu, Hsing-Yu and Chang, Hsun-Shuo
Phytochemistry, ISSN 0031-9422, 10/2016, Volume 130, pp. 282 - 290
Bioassay-guided fractionation of the fruits of led to isolation of three cardenolides (reevesioside J, reevesioside K, and -reevesioside K), three... 
Cardenolides | Cytotoxicity | Reevesia formosana | Sterculiaceae | Sesquiterpenoids | OXIDATION | ROOT | ACIDS | BIOCHEMISTRY & MOLECULAR BIOLOGY | PLANT SCIENCES | SEEDS | CHEMICAL-CONSTITUENTS | GROWTH | LIGNANS | DERIVATIVES | NEOLIGNAN GLYCOSIDES | RHIZOMES | Sesquiterpenes - isolation & purification | Sesquiterpenes - chemistry | Fruit - chemistry | Humans | Sterculiaceae - chemistry | Antineoplastic Agents, Phytogenic - chemistry | Cardenolides - chemistry | Glycosides - pharmacology | Hep G2 Cells | MCF-7 Cells | Cardenolides - isolation & purification | Glycosides - isolation & purification | Female | Cell Proliferation - drug effects | Sesquiterpenes - pharmacology | Antineoplastic Agents, Phytogenic - pharmacology | Glycosides - chemistry | Sesterterpenes | Cardenolides - pharmacology | Antineoplastic Agents, Phytogenic - isolation & purification | Drug Screening Assays, Antitumor | Drugstores | Medical colleges | Research institutes | Fruit | Pharmacy | Sesquiterpenes | Index Medicus
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7. Full Text Cytotoxicity of cardenolides and cardenolide glycosides from Asclepias curassavica
by Li, Jun-Zhu and Qing, Chen and Chen, Chang-Xiang and Hao, Xiao-Jiang and Liu, Hai-Yang
Bioorganic & Medicinal Chemistry Letters, ISSN 0960-894X, 2009, Volume 19, Issue 7, pp. 1956 - 1959
A new cardenolide and a new doubly linked cardenolide glycoside together with eleven known compounds were isolated from the aerial part of and their cytotoxic... 
Cardenolide glycoside | Cytotoxicity | Cardenolide | Asclepias curassavica | Asclepiadaceae | CHEMISTRY, MEDICINAL | CHEMISTRY, ORGANIC | STEROIDAL GLYCOSIDES | FRUTICOSA | Cell Line | Cardenolides - toxicity | Cardenolides - isolation & purification | Glycosides - toxicity | Humans | Glycosides - isolation & purification | Asclepias - chemistry | Cardenolides - chemistry | Glycosides - chemistry | Index Medicus
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8. Full Text Calotropin: A Cardenolide from Calotropis gigantea that Inhibits Wnt Signaling by Increasing Casein Kinase 1α in Colon Cancer Cells
by Park, Hyun Young and Toume, Kazufumi and Arai, Midori A and Sadhu, Samir K and Ahmed, Firoj and Ishibashi, Masami
ChemBioChem, ISSN 1439-4227, 04/2014, Volume 15, Issue 6, pp. 872 - 878
Wnt signaling plays key roles in embryonic development and various human diseases. Activity‐guided testing to isolate Wnt signaling inhibitors from the... 
natural products | Calotropis gigantea | Wnt signaling | cardenolides | casein kinase 1alpha | signal transduction | GLYCOSIDES | ACTIVATION | CHEMISTRY, MEDICINAL | MECHANISM | PROCERA | BIOCHEMISTRY & MOLECULAR BIOLOGY | BETA-CATENIN | PATHWAY | GROWTH | DISEASE | MUTATIONS | CARCINOMA | Humans | Casein Kinase Ialpha - antagonists & inhibitors | Casein Kinase Ialpha - genetics | Cardenolides - chemistry | RNA, Messenger - metabolism | Wnt Proteins - metabolism | beta Catenin - metabolism | Colonic Neoplasms - metabolism | Calotropis - metabolism | Signal Transduction - drug effects | Cardenolides - isolation & purification | beta Catenin - antagonists & inhibitors | Colonic Neoplasms - pathology | Cell Line, Tumor | Phosphorylation - drug effects | Wnt Proteins - antagonists & inhibitors | Calotropis - chemistry | Casein Kinase Ialpha - metabolism | Cardenolides - pharmacology | Index Medicus
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9. Full Text Two new cyototoxic cardenolides from the whole plants of Adonis multiflora Nishikawa & Koki Ito
by Jung, Jae-Woo and Baek, Nam-In and Hwang-Bo, Jeon and Lee, Seung-Su and Park, Ji-Hae and Seo, Kyeong-Hwa and Kwon, Jung-Hwa and Oh, Eun-Ji and Lee, Dae-Young and Chung, In-Sik and Bang, Myun-Ho
Molecules, ISSN 1420-3049, 11/2015, Volume 20, Issue 11, pp. 20823 - 20831
A phytochemical investigation of the whole plants of Adonis multiflora Nishikawa & Koki Ito. resulted in the isolation and identification of two new... 
Adonioside B | Cardenolide | Adonioside A | Adonis multiflora | Cytotoxic activity | SEEDS | adonioside A | CHEMISTRY, ORGANIC | adonioside B | cardenolide | cytotoxic activity | CYTOTOXIC CARDENOLIDE | CARDIAC-GLYCOSIDES | Cell Survival - drug effects | Plant Extracts - chemistry | Plant Extracts - pharmacology | Humans | Adonis - chemistry | Antineoplastic Agents, Phytogenic - chemistry | Plant Extracts - isolation & purification | Cardenolides - chemistry | Hep G2 Cells | Cardenolides - isolation & purification | Cell Line, Tumor | Inhibitory Concentration 50 | Nuclear Magnetic Resonance, Biomolecular | Antineoplastic Agents, Phytogenic - pharmacology | Cardenolides - pharmacology
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10. Full Text Cytotoxic cardenolides from the latex of Calotropis procera
by Mohamed, Nadia H and Liu, Miaomiao and Liu, Xueting and Abdel-Mageed, Wael M and Alwahibi, Lamya H and Dai, Huanqin and Ismail, Mady Ahmed and Badr, Gamal and Quinn, Ronald J and Zhang, Lixin and Shoreit, Ahmed A.M
Bioorganic & Medicinal Chemistry Letters, ISSN 0960-894X, 10/2015, Volume 25, Issue 20, pp. 4615 - 4620
Three new cardenolides ( , and ), along with eight known ones, were isolated from the latex of . The structural determination was accomplished by the 1D- and... 
Cardenolides | Cytotoxicity | Antimicrobial activity | Calotropis procera | Asclepiadaceae | GLYCOSIDES | CHEMISTRY, MEDICINAL | ANTHELMINTIC ACTIVITY | STEREOCHEMISTRY | RATS | CHEMISTRY, ORGANIC | MODEL | CARDIOTONIC STEROIDS | ASCLEPIAS-FRUTICOSA | PERGULARIA-TOMENTOSA | ANTICANCER THERAPY | CONSTITUENTS | Humans | Bacteria - drug effects | Antifungal Agents - chemistry | Structure-Activity Relationship | Dose-Response Relationship, Drug | Microbial Sensitivity Tests | Cardenolides - isolation & purification | Anti-Bacterial Agents - chemistry | Molecular Structure | Calotropis - chemistry | Antifungal Agents - pharmacology | Fungi - drug effects | Latex - chemistry | Antineoplastic Agents, Phytogenic - chemistry | Anti-Bacterial Agents - isolation & purification | Cardenolides - chemistry | Antifungal Agents - isolation & purification | Cell Line, Tumor | Anti-Bacterial Agents - pharmacology | Cell Proliferation - drug effects | HeLa Cells | Antineoplastic Agents, Phytogenic - pharmacology | Cardenolides - pharmacology | Antineoplastic Agents, Phytogenic - isolation & purification | Drug Screening Assays, Antitumor | Index Medicus
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11. Full Text Biotechnological approaches for biomass and cardenolide production in Digitalis purpurea L
by Pérez-Alonso, Naivy and Chong-Pérez, Borys and Capote, Alina and Pérez, Anabel and Gerth, André and Angenon, Geert and Jiménez, Elio
Methods in Molecular Biology, ISSN 1064-3745, 04/2016, Volume 1391, pp. 81 - 102
Digitalis purpurea L. is one of the main economically viable sources of cardenolides (cardiac glycosides) for the pharmaceutical industry. Nevertheless,... 
Cardenolides | Secondary metabolites | Foxglove | Genetic transformation | Temporary immersion system | Digitalis - genetics | Transformation, Genetic | Cardenolides - analysis | Digitalis - microbiology | Cell Culture Techniques - instrumentation | Cardenolides - metabolism | Agrobacterium tumefaciens - genetics | Biosynthetic Pathways | Biomass | Cell Culture Techniques - methods | Equipment Design | Biotechnology - methods | Digitalis - chemistry | Cardenolides - isolation & purification | Digitalis - metabolism | Biotechnology - instrumentation | Index Medicus
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12. Full Text A convergent total synthesis of 19-hydroxysarmentogenin
by Mukai, Ken and Urabe, Daisuke and Kasuya, Satoshi and Aoki, Naoto and Inoue, Masayuki
Angewandte Chemie - International Edition, ISSN 1433-7851, 05/2013, Volume 52, Issue 20, pp. 5300 - 5304
  19 in 19: A convergent total synthesis of 19-hydroxysarmentogenin has been achieved, starting from three simple fragments. The desired product was... 
radical reactions | aldol reaction | steroids | total synthesis | convergent strategy | ENANTIOSELECTIVE SYNTHESIS | CARDENOLIDES | OUABAGENIN | (+)-DIGITOXIGENIN | CHEMISTRY, MULTIDISCIPLINARY | ANIONIC POLYCYCLIZATION | OUABAIN | RING | RADICAL CYCLIZATION | CONSTRUCTION | Cardenolides - chemical synthesis | Biological Products - chemical synthesis | Biological Products - chemistry | Bufanolides - chemical synthesis | Stereoisomerism | Models, Molecular | Crystallography, X-Ray | Bufanolides - chemistry | Celastraceae - chemistry | Molecular Structure | Cardenolides - chemistry | Synthesis | Universities and colleges | Organic compounds | Index Medicus | Fragments | Formations
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13. Full Text Characterization of the anticancer properties of monoglycosidic cardenolides isolated from Nerium oleander and Streptocaulon tomentosum
by Rashan, Luay J and Franke, Katrin and Khine, Myint Myint and Kelter, Gerhard and Fiebig, Heinz H and Neumann, Joachim and Wessjohann, Ludger A
Journal of Ethnopharmacology, ISSN 0378-8741, 04/2011, Volume 134, Issue 3, pp. 781 - 788
Monoglycosidic cardenolides possessing the 3 ,14 -dihydroxy-5 -card-20(22)-enolide structure with or without an acetoxy group at C-16 are the most active... 
Streptocaulon tomentosum | Breastin | Cardenolides | Nerium oleander | Anticancer activity | ANTIPROLIFERATIVE ACTIVITY | CHEMISTRY, MEDICINAL | ASSAY | LEAVES | CANCER-CELL-LINES | TRITERPENES | CARDIAC-GLYCOSIDES | PLANT SCIENCES | IN-VITRO | INTEGRATIVE & COMPLEMENTARY MEDICINE | BIOACTIVE CARDENOLIDES | GROWTH | ROOTS | PHARMACOLOGY & PHARMACY | Immunohistochemistry | Magnetic Resonance Spectroscopy | Apocynaceae - chemistry | Humans | Cell Division - drug effects | Cardenolides - isolation & purification | Cell Line, Tumor | Inhibitory Concentration 50 | Nerium - chemistry | Antineoplastic Agents, Phytogenic - pharmacology | Cell Cycle - drug effects | Cardenolides - pharmacology | Drug Screening Assays, Antitumor | Care and treatment | Universities and colleges | Chemical properties | Analysis | Cancer | Leaves | Roots | Cell cycle | Plasma membranes | Antitumor activity | Cytotoxicity | Tumor cell lines | Index Medicus
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14. Full Text Elaeodendron orientale as a source of cytotoxic cardenolides
by Osorio, Alex A and López, Manuel R and Jiménez, Ignacio A and Moujir, Laila M and Rodríguez, Matías L and Bazzocchi, Isabel L
Phytochemistry, ISSN 0031-9422, 09/2014, Volume 105, pp. 60 - 67
A series of natural cardenolide glycosides exhibited cytotoxicity against human cancer cell lines and selectivity on normal Vero cells higher than digoxin.... 
Antiproliferative | Cardenolides | Elaeodendron orientale | Celastraceae | Human cancer cell lines | SERIES | GLAUCUM | BIOCHEMISTRY & MOLECULAR BIOLOGY | DEATH | CARDIOTONIC STEROIDS | IDENTIFICATION | MADAGASCAR RAIN-FOREST | CARDIAC-GLYCOSIDES | PLANT SCIENCES | THERAPY | ANODENDRON-AFFINE | NA+/K+-ATPASE | Plant Leaves - chemistry | Humans | Cercopithecus aethiops | Antineoplastic Agents, Phytogenic - chemistry | Cardenolides - chemistry | Digoxin - pharmacology | Animals | Cardenolides - isolation & purification | X-Ray Diffraction | HL-60 Cells | Nuclear Magnetic Resonance, Biomolecular | Celastraceae - chemistry | Molecular Structure | HeLa Cells | Antineoplastic Agents, Phytogenic - pharmacology | Vero Cells | Cardenolides - pharmacology | Antineoplastic Agents, Phytogenic - isolation & purification | Index Medicus
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15. Full Text Toxicity of the spiny thick‐foot Pachypodium
by Agrawal, Anurag A and Ali, Aliya and Daisy Johnson, M and Hastings, Amy P and Burge, Dylan and Weber, Marjorie G
American Journal of Botany, ISSN 0002-9122, 04/2018, Volume 105, Issue 4, pp. 677 - 686
PREMISE OF THE STUDY: Pachypodium (Apocynaceae) is a genus of iconic stem-succulent and poisonous plants endemic to Madagascar and southern Africa. We tested... 
sodium‐potassium pump | cardiac glycoside | chemical ecology | Madagascar | plant–insect interactions | Apocynaceae | ase | Danaus plexippus | southern Africa | cardenolide | monarch butterfly | ATP | stem‐succulent milkweeds | ATPase | stem-succulent milkweeds | K | Na | sodium-potassium pump | ARMS-RACE | Na+/K+-ATPase | CARDENOLIDES | PATTERNS | PLANT DEFENSES | PLANT SCIENCES | EVOLUTION | plant-insect interactions | MILKWEEDS ASCLEPIAS | BUTTERFLIES LEPIDOPTERA | DEFENSE-ESCALATION | Plant Leaves - chemistry | Sodium-Potassium-Exchanging ATPase - antagonists & inhibitors | Plant Extracts - toxicity | Apocynaceae - chemistry | Chromatography, High Pressure Liquid | Phylogeny | Plant Leaves - toxicity | Cardenolides - toxicity | Animals | Cardenolides - isolation & purification | Larva - drug effects | Cardiac Glycosides - toxicity | Butterflies - drug effects | Biological Assay | Apocynaceae - toxicity | Asclepias - toxicity | Toxicity | Bioassays | Liquid chromatography | Na+/K+-exchanging ATPase | High-performance liquid chromatography | Butterflies | Mode of action | Cardiac glycosides | Endemic plants | Poisons | Leaves | Glycosides | Caterpillars | Toxins | Flowers & plants | Inhibition | Glucosides | Index Medicus
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