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1. Full Text Efficacy and safety of the dipeptidyl peptidase‐4 inhibitor sitagliptin compared with α‐glucosidase inhibitor in Japanese patients with type 2 diabetes inadequately controlled on sulfonylurea alone (SUCCESS‐2): a multicenter, randomized, open‐label, non‐inferiority trial
by Kobayashi, K and Yokoh, H and Sato, Y and Takemoto, M and Uchida, D and Kanatsuka, A and Kuribayashi, N and Terano, T and Hashimoto, N and Sakurai, K and Hanaoka, H and Ishikawa, K and Onishi, S and Yokote, K and Success Study Grp and SUCCESS Study Group
Diabetes, Obesity and Metabolism, ISSN 1462-8902, 08/2014, Volume 16, Issue 8, pp. 761 - 765
We assessed the efficacy and safety of sitagliptin compared with α‐glucosidase inhibitor ( αGI ) in 120 of Japanese patients with type 2 diabetes mellitus (... 
type 2 diabetes | DPP‐IV | inhibitor | sulphonylureas | α‐glucosidase inhibitor | randomized trial | Type 2 diabetes | Randomized trial | α-glucosidase inhibitor | Sulphonylureas | DPP-IV inhibitor | VOGLIBOSE | MONOTHERAPY | HYPERGLYCEMIA | DOUBLE-BLIND TRIAL | alpha-glucosidase inhibitor | ENDOCRINOLOGY & METABOLISM | MELLITUS | Glycated Hemoglobin A - analysis | Triazoles - adverse effects | Glycoside Hydrolase Inhibitors - adverse effects | Dipeptidyl-Peptidase IV Inhibitors - adverse effects | Dipeptidyl-Peptidase IV Inhibitors - therapeutic use | Humans | Middle Aged | Glycoside Hydrolase Inhibitors - therapeutic use | Male | Pyrazines - therapeutic use | Hypoglycemia - prevention & control | 1-Deoxynojirimycin - therapeutic use | Drug Therapy, Combination - adverse effects | Inositol - therapeutic use | Inositol - adverse effects | 1-Deoxynojirimycin - analogs & derivatives | Female | 1-Deoxynojirimycin - adverse effects | Sitagliptin Phosphate | Hypoglycemia - chemically induced | Triazoles - therapeutic use | Hypoglycemic Agents - therapeutic use | Hyperglycemia - prevention & control | Japan | Sulfonylurea Compounds - therapeutic use | Inositol - analogs & derivatives | Diabetes Mellitus, Type 2 - blood | Gastrointestinal Agents - therapeutic use | Pyrazines - adverse effects | Aged | Gastrointestinal Agents - adverse effects | Diabetes Mellitus, Type 2 - drug therapy | alpha-Glucosidases - metabolism | alpha-Glucosidases - chemistry | Index Medicus
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2. Full Text A fluorescence resonance energy transfer (FRET) based "Turn-On" nanofluorescence sensor using a nitrogen-doped carbon dot-hexagonal cobalt oxyhydroxide nanosheet architecture and application to α-glucosidase inhibitor screening
by Li, Guoliang and Kong, Weiheng and Zhao, Mei and Lu, Shuaimin and Gong, Peiwei and Chen, Guang and Xia, Lian and Wang, Hua and You, Jinmao and Wu, Yongning
Biosensors and Bioelectronics, ISSN 0956-5663, 05/2016, Volume 79, pp. 728 - 735
The medicines targeted at α-glucosidase played an important role in anti-diabetes and anti-HIV therapy. Unfortunately, the method based on fluorescent assay... 
Enzyme inhibition | Fluorescence resonance energy transfer | Nitrogen-doped carbon dots | α-Glucosidase | ELECTROCHEMISTRY | CHEMISTRY, ANALYTICAL | NANOSCIENCE & NANOTECHNOLOGY | ASCORBIC-ACID | GREEN | QUANTUM DOTS | BIOPHYSICS | LUMINESCENCE | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | alpha-Glucosidase | Acarbose - pharmacology | Drug Evaluation, Preclinical - methods | Nanostructures - ultrastructure | Ascorbic Acid - analysis | Oxides - chemistry | Glycoside Hydrolase Inhibitors - pharmacology | Carbon - chemistry | Ascorbic Acid - metabolism | Nitrogen - chemistry | Nanostructures - chemistry | Fluorescence Resonance Energy Transfer - methods | Cobalt - chemistry | alpha-Glucosidases - metabolism | Index Medicus | Screening | Platforms | Fretting | Inhibitors | Fluorescence | Nanostructure | Sensors | Carbon
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3. Full Text Diphlorethohydroxycarmalol isolated from Ishige okamurae, a brown algae, a potent α-glucosidase and α-amylase inhibitor, alleviates postprandial hyperglycemia in diabetic mice
by Heo, Soo-Jin and Hwang, Ji-Young and Choi, Jung-In and Han, Ji-Sook and Kim, Hak-Ju and Jeon, You-Jin
European Journal of Pharmacology, ISSN 0014-2999, 2009, Volume 615, Issue 1, pp. 252 - 256
This study was designed to investigate whether diphlorethohydroxycarmalol (DPHC) may inhibit α-glucosidase and α-amylase activities, and alleviate postprandial... 
α-glucosidase | Postprandial hyperglycemia | Diphlorethohydroxycarmalol | α-amylase | Diabetes | Hypoglycemic Agents - therapeutic use | alpha-Amylases - antagonists & inhibitors | Cell Survival - drug effects | Glycoside Hydrolase Inhibitors | Diabetes Mellitus, Experimental - drug therapy | Blood Glucose - analysis | Area Under Curve | Heterocyclic Compounds, 3-Ring - pharmacology | Plant Extracts - pharmacology | Humans | Hyperglycemia - drug therapy | Phaeophyta - chemistry | Hypoglycemic Agents - pharmacology | Animals | Heterocyclic Compounds, 3-Ring - isolation & purification | Heterocyclic Compounds, 3-Ring - therapeutic use | Postprandial Period | Mice | Phytotherapy | In Vitro Techniques | Plant Extracts - therapeutic use | Umbilical Veins - cytology | Endothelial Cells - drug effects | Index Medicus
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4. Full Text Electrochemical assay of α-glucosidase activity and the inhibitor screening in cell medium
by Zhang, Juan and Liu, Ying and Wang, Xiaonan and Chen, Yangyang and Li, Genxi
Biosensors and Bioelectronics, ISSN 0956-5663, 12/2015, Volume 74, pp. 666 - 672
An electrochemical method is established in this work for the assay of α-glucosidase activity and the inhibitor screening through one-step displacement... 
α-Glucosidase | Magnetic separation | Electrochemical method | Inhibitor | Cell | One-step displacement reaction | Pyrene boric acid | GOLD NANOPARTICLES | ELECTROCHEMISTRY | CHEMISTRY, ANALYTICAL | ACID | RATS | NANOSCIENCE & NANOTECHNOLOGY | IN-VITRO | BIOPHYSICS | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | SUCROSE | alpha-Glucosidase | DOPAMINE | BIOSENSOR | Cell Line | Reproducibility of Results | Epithelial Cells - metabolism | Magnetite Nanoparticles - ultrastructure | Glycoside Hydrolase Inhibitors - analysis | Equipment Design | Culture Media - metabolism | Magnetite Nanoparticles - chemistry | Animals | Conductometry - instrumentation | Swine | Sensitivity and Specificity | Biosensing Techniques - instrumentation | Enzyme Activation | Equipment Failure Analysis | alpha-Glucosidases - metabolism | alpha-Glucosidases - chemistry | Index Medicus | Nanoparticles | Binding | Screening | Enzymes | Corrosion inhibitors | Inhibition | Assaying | Displacement
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5. Full Text Transition Metal Substituted Polyoxometalates as α‐Glucosidase Inhibitors
by Hu, Jing‐Jing and Wang, Li and Chen, Bing‐Nian and Chi, Guo‐Xiang and Zhao, Mei‐Juan and Li, Yue
European Journal of Inorganic Chemistry, ISSN 1434-1948, 07/2019, Volume 2019, Issue 28, pp. 3270 - 3276
α‐Glucosidase inhibitors slow the digestion of carbohydrates and reduce blood sugar levels after meals. Recently, our experimental team found that... 
Polyoxometalates | Inhibitors | Enzyme kinetics | Molecular docking | α‐Glucosidase | DESIGN | MIMICS | ACIDS | TYROSINASE | CHEMISTRY, INORGANIC & NUCLEAR | CLUSTERS | alpha-Glucosidase | ACTIVITY IN-VITRO | COMPLICATIONS | PROTEINS | Carbohydrates | Transition metals | Phosphomolybdic acid | Glucosidase | Polyoxometallates | Substitutes | Hydrogen bonds | Chemical bonds | Docking | Inhibition | Meals
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6. Full Text Rapid screening and identification of α‐glucosidase inhibitors from mulberry leaves using enzyme‐immobilized magnetic beads coupled with HPLC/MS and NMR
by Tao, Yi and Zhang, Yufeng and Cheng, Yiyu and Wang, Yi
Biomedical Chromatography, ISSN 0269-3879, 02/2013, Volume 27, Issue 2, pp. 148 - 155
α ‐Glucosidase plays important roles in the digestion and absorption of carbohydrates in the small intestine. The inhibition of α ‐glucosidase is regarded as a... 
glucosidase inhibitor | α | magnetic beads | Morus alba | α-glucosidase inhibitor | Magnetic beads | 5-HT1A LIGANDS | CHEMISTRY, ANALYTICAL | ASSAY | CELL EXTRACTION | BIOCHEMISTRY & MOLECULAR BIOLOGY | BIOCHEMICAL RESEARCH METHODS | MASS-SPECTROMETRY | ONLINE | a-glucosidase inhibitor | PERFORMANCE LIQUID-CHROMATOGRAPHY | NANOPARTICLES | ANTIOXIDANT | POTENTIAL BIOACTIVE COMPONENTS | PHARMACOLOGY & PHARMACY | TLC STATIONARY PHASES | Enzymes, Immobilized - metabolism | Glycoside Hydrolase Inhibitors | Plant Extracts - chemistry | Chromatography, High Pressure Liquid - methods | Plant Extracts - pharmacology | Magnets | Quercetin - isolation & purification | Enzyme Inhibitors - chemistry | Kaempferols - isolation & purification | Kaempferols - analysis | Methanol - chemistry | Plant Leaves - chemistry | Quercetin - analogs & derivatives | Quercetin - chemistry | Kaempferols - chemistry | Quercetin - analysis | Enzyme Inhibitors - pharmacology | Enzyme Inhibitors - analysis | Drug Discovery | Enzyme Inhibitors - isolation & purification | Quercetin - pharmacology | Nuclear Magnetic Resonance, Biomolecular - methods | Magnetics - methods | Enzymes, Immobilized - antagonists & inhibitors | Kaempferols - pharmacology | Mass Spectrometry - methods | alpha-Glucosidases - metabolism | Morus - chemistry | Index Medicus
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7. Full Text New novel α–glucosidase inhibitors produced by microbial conversion
by Nguyen, Van Bon and Wang, San-Lang
Process Biochemistry, ISSN 1359-5113, 02/2018, Volume 65, pp. 228 - 232
Fermented Nutrient Broth (FNB) was found to be a potential source of antidiabetic drugs in the previous report. Thus, FNB was employed to isolate the active... 
α–glucosidase inhibitor | Diabetes | Microbial conversion | Paenibacillus sp | ENGINEERING, CHEMICAL | NEWLY ISOLATED STRAIN | 1-DEOXYNOJIRIMYCIN | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | alpha-glucosidase inhibitor | BIOCHEMISTRY & MOLECULAR BIOLOGY | PURIFICATION | FERMENTATION | IDENTIFICATION
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8. Full Text α- and β-Glucosidase inhibitors: chemical structure and biological activity
by Borges de Melo, Eduardo and da Silveira Gomes, Adriane and Carvalho, Ivone
Tetrahedron, ISSN 0040-4020, 2006, Volume 62, Issue 44, pp. 10277 - 10302
Glycoside trimming enzymes are crucially important in a broad range of metabolic pathways, including glycoprotein and glycolipid processing and carbohydrate... 
β-Glucosidase | Iminosugar | Carbasugar | α-Glucosidase | Non-glycosidic bond | Disaccharide | Thiosugar | Glucosidase inhibitor | LONG-TERM | CONDURITOL-A | GYMNEMA-SYLVESTRE | glucosidase inhibitor | CHEMISTRY, ORGANIC | TRANSITION-STATE | beta-glucosidase | carbasugar | iminosugar | alpha-glucosidase | non-glycosidic bond | POTENT GLYCOSIDASE INHIBITORS | SULFONIUM SULFATE STRUCTURE | MEDICINE SALACIA-RETICULATA | disaccharide | CONFORMATIONAL-ANALYSIS | thiosugar | TYPE-2 DIABETES-MELLITUS | SPONGE PENARES SP
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9. Full Text α-Glucosidase inhibitor from Buthus martensi Karsch
by Kim, Shin-Duk
Food Chemistry, ISSN 0308-8146, 01/2013, Volume 136, Issue 2, pp. 297 - 300
► An α-glucosidase inhibitor (compound S) was isolated from Karsch. ► The structure of compound S was elucidated as harmanyl β- -glucopyranoside. ► Compound S... 
Glucopyranoside | Uncompetitive inhibitor | Buthus martensi Karsch | α-Glucosidase inhibitor | β-Carboline | NUTRITION & DIETETICS | FOOD SCIENCE & TECHNOLOGY | alpha-Glucosidase inhibitor | LEAVES | AGENTS | beta-Carboline | CHEMISTRY, APPLIED | Glycoside Hydrolase Inhibitors | Animals | Enzyme Inhibitors - metabolism | Magnetic Resonance Spectroscopy | Enzyme Inhibitors - chemistry | Scorpions - chemistry | Molecular Structure | Kinetics | Scorpions - metabolism | alpha-Glucosidases - chemistry | Index Medicus
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10. Full Text Grape skin phenolics as inhibitors of mammalian α-glucosidase and α-amylase - effect of food matrix and processing on efficacy
by Lavelli, V and Sri Harsha, P. S. C and Ferranti, P and Scarafoni, A and Iametti, S
Food and Function, ISSN 2042-6496, 3/2016, Volume 7, Issue 3, pp. 1655 - 1663
Type-2 diabetes is continuously increasing worldwide. Hence, there is a need to develop functional foods that efficiently alleviate damage due to... 
DIGESTION | FRUITS | PROANTHOCYANIDINS | QUALITY | PROTEIN | DIETARY FIBER | STABILITY | BIOCHEMISTRY & MOLECULAR BIOLOGY | FOOD SCIENCE & TECHNOLOGY | EXTRACTS | COCOA | BY-PRODUCTS | Food, Fortified - analysis | alpha-Amylases - antagonists & inhibitors | Phenols - isolation & purification | Plant Extracts - chemistry | Vitis - chemistry | Fruit - chemistry | Rats | Food Additives - chemistry | Glycoside Hydrolase Inhibitors - chemistry | Proanthocyanidins - chemistry | Animals | Swine | alpha-Amylases - chemistry | Phenols - chemistry | Food Handling | Kinetics | alpha-Glucosidases - chemistry | Index Medicus
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11. Full Text Isolation of a new phlorotannin, a potent inhibitor of carbohydrate- hydrolyzing enzymes, from the brown alga Sargassum patens
by Kawamura-Konishi, Yasuko and Watanabe, Natsuko and Saito, Miki and Nakajima, Noriyuki and Sakaki, Toshiyuki and Katayama, Takane and Enomoto, Toshiki
Journal of Agricultural and Food Chemistry, ISSN 0021-8561, 06/2012, Volume 60, Issue 22, pp. 5565 - 5570
Ethanol extracts from 15 kinds of marine algae collected from the coast of the Noto Peninsula in Japan were examined for their inhibitory effects on human... 
α-amylase inhibitor | Phloroglucinol derivative | α-glucosidase inhibitor | Sargassum patens | ANTIPLASMIN INHIBITOR | ECKLONIA-KUROME OKAMURA | alpha-amylase inhibitor | alpha-glucosidase inhibitor | FOOD SCIENCE & TECHNOLOGY | AGENT | ANGSTROM RESOLUTION | GLUCOSIDASE | CAVA | ANTIOXIDANT | GENES | AGRICULTURE, MULTIDISCIPLINARY | STOLONIFERA | CHEMISTRY, APPLIED | Salivary alpha-Amylases - chemistry | Humans | Japan | Enzyme Inhibitors - pharmacology | Rats | Pancreatic alpha-Amylases - antagonists & inhibitors | Phaeophyta - chemistry | Enzyme Inhibitors - isolation & purification | Animals | Enzyme Inhibitors - chemistry | Sargassum - chemistry | Kinetics | Pancreatic alpha-Amylases - chemistry | Salivary alpha-Amylases - antagonists & inhibitors | Index Medicus
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12. Full Text Comparative evaluation of quercetin, isoquercetin and rutin as inhibitors of α-glucosidase
by Li, Yan Qin and Zhou, Feng Chao and Gao, Fei and Bian, Jun Sheng and Shan, Fang
Journal of Agricultural and Food Chemistry, ISSN 0021-8561, 12/2009, Volume 57, Issue 24, pp. 11463 - 11468
Three flavonoids from tartary buckwheat bran, namely, quercetin (Que), isoquercetin (Iso) and rutin (Rut), have been evaluated as alpha-glucosidase inhibitors... 
α-glucosidase | Tartary buckwheat | Inhibitor | Diabetes | Flavonoid compound | SUBSTITUTION | BAICALEIN | FLUORESCENCE SPECTROSCOPY | FOOD SCIENCE & TECHNOLOGY | ACARBOSE | FLAVONOIDS | INSULIN SENSITIVITY | alpha-glucosidase | inhibitor | tartary buckwheat | 5,6,7-TRIHYDROXYFLAVONE | AMYLASE | AGRICULTURE, MULTIDISCIPLINARY | CHEMISTRY, APPLIED | PROTEINS | diabetes | BOVINE SERUM-ALBUMIN | Acarbose - pharmacology | Glycoside Hydrolase Inhibitors | Quercetin - analogs & derivatives | Fagopyrum - chemistry | Rutin - metabolism | Acarbose - metabolism | Enzyme Inhibitors - metabolism | Hypoglycemic Agents - metabolism | Saccharomyces cerevisiae Proteins - antagonists & inhibitors | Rutin - pharmacology | Enzyme Inhibitors - pharmacology | Spectrometry, Fluorescence | Hypoglycemic Agents - pharmacology | Quercetin - pharmacology | Saccharomyces cerevisiae Proteins - metabolism | Protein Binding | Seeds - chemistry | Kinetics | Quercetin - metabolism | alpha-Glucosidases - metabolism | Index Medicus
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13. Full Text Are the effects of α-glucosidase inhibitors on cardiovascular events related to elevated levels of hydrogen gas in the gastrointestinal tract?
by Suzuki, Yoshihiko and Sano, Motoaki and Hayashida, Kentaro and Ohsawa, Ikuroh and Ohta, Shigeo and Fukuda, Keiichi
FEBS Letters, ISSN 0014-5793, 2009, Volume 583, Issue 13, pp. 2157 - 2159
The major side-effect of treatment with -glucosidase inhibitors, flatulence, occurs when undigested carbohydrates are fermented by colonic bacteria, resulting... 
Type 2 diabetes | α-Glucosidase inhibitors | Antioxidant | Hydrogen gas | Glucosidase inhibitors | alpha-Glucosidase inhibitors | OXIDATIVE STRESS | TOLERANCE | BIOCHEMISTRY & MOLECULAR BIOLOGY | ATHEROSCLEROSIS | INJURY | RISK | ACARBOSE | CELL BIOLOGY | HYPERGLYCEMIA | BIOPHYSICS | DISEASE | HYPERTENSION | Acarbose - pharmacology | Glycoside Hydrolase Inhibitors | Acarbose - metabolism | Enzyme Inhibitors - metabolism | Antioxidants - metabolism | Cardiovascular Diseases - prevention & control | Humans | Enzyme Inhibitors - pharmacology | Gastrointestinal Tract - drug effects | Male | Flatulence - chemically induced | Gastrointestinal Tract - metabolism | Myocardium - metabolism | Female | Blood Glucose - metabolism | Hydrogen - metabolism | alpha-Glucosidases - metabolism | Index Medicus
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14. Full Text Synthesis of 3-acyloxyxanthone derivatives as α-glucosidase inhibitors: A further insight into the 3-substituents’ effect
by Li, Gai-Li and Cai, Chao-Yun and He, Jia-Yun and Rao, Li and Ma, Lin and Liu, Yan and Wang, Bo
Bioorganic & Medicinal Chemistry, ISSN 0968-0896, 04/2016, Volume 24, Issue 7, pp. 1431 - 1438
Considerable interest has been attracted in xanthone and its derivatives because of their important biological activities. In this paper, a series of novel... 
Inhibition kinetics | α-Glucosidase | Xanthone derivatives | Inhibitory activity | CELLS | CHEMISTRY, MEDICINAL | SYNERGETIC INHIBITION | BIOCHEMISTRY & MOLECULAR BIOLOGY | alpha-Glucosidase | CHEMISTRY, ORGANIC | GENISTEIN | DISCOVERY | Dose-Response Relationship, Drug | Glycoside Hydrolase Inhibitors - chemical synthesis | Xanthones - chemistry | Saccharomyces cerevisiae - enzymology | Molecular Structure | Structure-Activity Relationship | Glycoside Hydrolase Inhibitors - chemistry | Glycoside Hydrolase Inhibitors - pharmacology | Xanthones - pharmacology | alpha-Glucosidases - metabolism | Xanthones - chemical synthesis | Index Medicus
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15. Full Text Discovery of xanthine oxidase inhibitors and/or α-glucosidase inhibitors by carboxyalkyl derivatization based on the flavonoid of apigenin
by Su, Zhuo-Ran and Fan, Shi-Yong and Shi, Wei-Guo and Zhong, Bo-Hua
Bioorganic & Medicinal Chemistry Letters, ISSN 0960-894X, 07/2015, Volume 25, Issue 14, pp. 2778 - 2781
Three series of apigenin derivatives have been prepared by coupling the carboxyl alkyl group to 4′-, 5- or 7-hydroxyl groups of apigenin respectively.... 
Xanthine oxidase | Diabetes | α-Glucosidase | Apigenin | Gout | CHEMISTRY, MEDICINAL | ACID | STABILITY | OXIDOREDUCTASE | RATS | CHEMISTRY, ORGANIC | CHRYSIN DERIVATIVES | CANCER | INTESTINAL-ABSORPTION | alpha-Glucosidase | FLOWERS | Apigenin - therapeutic use | Hypoglycemic Agents - metabolism | Glycoside Hydrolase Inhibitors - metabolism | Glycoside Hydrolase Inhibitors - therapeutic use | Structure-Activity Relationship | Apigenin - chemistry | Uric Acid - blood | Drug Evaluation, Preclinical | Xanthine Oxidase - antagonists & inhibitors | Disease Models, Animal | Hypoglycemic Agents - therapeutic use | Xanthine Oxidase - metabolism | Glucose Tolerance Test | Infusions, Parenteral | Hypoglycemic Agents - chemistry | Glycoside Hydrolase Inhibitors - chemistry | Hyperuricemia - drug therapy | Animals | Protein Binding | Mice | Apigenin - metabolism | Flavonoids - chemistry | alpha-Glucosidases - metabolism | Hyperuricemia - chemically induced | alpha-Glucosidases - chemistry | Index Medicus
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16. Full Text Synthesis of new oxadiazole derivatives as α-glucosidase inhibitors
by Taha, Muhammad and Ismail, Nor Hadiani and Imran, Syahrul and Rokei, Muhammad Qamarruddin Bin and Saad, Syed Muhammad and Khan, Khalid Mohammed
Bioorganic & Medicinal Chemistry, ISSN 0968-0896, 08/2015, Volume 23, Issue 15, pp. 4155 - 4162
Oxadiazole derivatives ( – ) having hydrazone linkage, were synthesized through condensation reaction between benzohydrazide with various benzaldehydes. The... 
α-Glucosidase inhibitors | Oxadiazole | Benzohydrazone | Antidiabetic | alpha-Glucosidase inhibitors | DESIGN | CHEMISTRY, MEDICINAL | BIOCHEMISTRY & MOLECULAR BIOLOGY | REPLACEMENTS | CHEMISTRY, ORGANIC | THIADIAZOLES | DISCOVERY | Glycoside Hydrolase Inhibitors - chemical synthesis | Drug Evaluation, Preclinical - methods | Chemistry Techniques, Synthetic | Inhibitory Concentration 50 | Molecular Structure | Structure-Activity Relationship | Glycoside Hydrolase Inhibitors - pharmacology | Oxadiazoles - chemistry | alpha-Glucosidases - metabolism | Index Medicus
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