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1. Morin: A promising natural drug
by Caselli, Anna and Cirri, Paolo and Santi, Alice and Paoli, Paolo
Current Medicinal Chemistry, ISSN 0929-8673, 03/2016, Volume 23, Issue 8, pp. 774 - 791
Morin is a natural polyphenol, originally isolated from members of the Moraceae family that can be extracted from leaves, fruits, stems and branches of... 
Natural drug | Polyphenol | Morin | Anti-oxidant | Anti-diabetic | Anti-inflammatory | Flavonoid | OXIDATIVE STRESS | CHEMISTRY, MEDICINAL | BIOCHEMISTRY & MOLECULAR BIOLOGY | anti-oxidant | polyphenol | PSIDIUM-GUAJAVA | ANTIOXIDANT ACTIVITY RELATIONSHIPS | P-GLYCOPROTEIN | IN-VITRO | INDUCED DIABETIC-RATS | anti-inflammatory | NITRIC-OXIDE | PHARMACOLOGY & PHARMACY | flavonoid | anti-diabetic | NATURALLY-OCCURRING FLAVONOIDS | HUMAN MAST-CELLS | natural drug | QUANTITATIVE STRUCTURE | Antihypertensive Agents - pharmacology | Antioxidants - chemistry | Hypoglycemic Agents - metabolism | Antioxidants - metabolism | Humans | Anti-Inflammatory Agents, Non-Steroidal - chemistry | Biological Products - pharmacology | Antihypertensive Agents - metabolism | Neuroprotective Agents - metabolism | Anti-Inflammatory Agents, Non-Steroidal - pharmacology | Antineoplastic Agents - metabolism | Neuroprotective Agents - pharmacology | Anti-Bacterial Agents - chemistry | Antineoplastic Agents - pharmacology | Flavonoids - pharmacology | Anti-Inflammatory Agents, Non-Steroidal - metabolism | Neuroprotective Agents - chemistry | Anti-Bacterial Agents - metabolism | Hypoglycemic Agents - chemistry | Antioxidants - pharmacology | Antineoplastic Agents - chemistry | Hypoglycemic Agents - pharmacology | Antihypertensive Agents - chemistry | Biological Products - chemistry | Animals | Flavonoids - metabolism | Biological Products - metabolism | Anti-Bacterial Agents - pharmacology | Flavonoids - chemistry
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2. Full Text Endogenous and exogenous cardiac glycosides: their roles in hypertension, salt metabolism, and cell growth
by Wilhelm Schoner and Georgios Scheiner-Bobis
American Journal of Physiology - Cell Physiology, ISSN 0363-6143, 08/2007, Volume 293, Issue 2, pp. 509 - 536
Cardiotonic steroids (CTS), long used to treat heart failure, are endogenously produced in mammals. Among them are the hydrophilic cardenolide ouabain and the... 
Cell proliferation | Arterial hypertension | Endogenous cardiotonic steroids | Rostafuroxin | Sodium/potassium-adenosinetriphosphatase | Cancer therapy | Ouabain | Marinobufagenin | Sodium pump | Oleandrin | Bufalin | Sodium metabolism | ouabain | PROTEIN-KINASE-C | PHYSIOLOGY | BOVINE ADRENOCORTICAL-CELLS | BUFALIN INDUCES APOPTOSIS | PLASMALEMMAL NA/K-ATPASE | cell proliferation | SIGNAL-TRANSDUCING FUNCTION | endogenous cardiotonic steroids | FACTOR-KAPPA-B | oleandrin | sodium/potassium-adenosinetriphosphatase | VASCULAR SMOOTH-MUSCLE | NA+-K+-ATPASE | CELL BIOLOGY | arterial hypertension | cancer therapy | OUABAIN-LIKE COMPOUND | sodium pump | DIGITALIS-LIKE COMPOUNDS | bufalin | rostafuroxin | sodium metabolism | marinobufagenin | Cardiac Glycosides - pharmacology | Neoplasms - metabolism | Antihypertensive Agents - pharmacology | Digoxin - metabolism | Calcium - metabolism | Humans | Myocardial Contraction - drug effects | Hypertension - drug therapy | Antineoplastic Agents - therapeutic use | Structure-Activity Relationship | Antihypertensive Agents - metabolism | Ouabain - metabolism | Antineoplastic Agents - metabolism | Bufanolides - metabolism | Antineoplastic Agents - pharmacology | Blood Pressure - drug effects | Molecular Structure | Cell Death - drug effects | Sodium Chloride - metabolism | Ouabain - pharmacology | Sodium-Potassium-Exchanging ATPase - antagonists & inhibitors | Diabetes Mellitus - metabolism | Cardiovascular System - drug effects | Antihypertensive Agents - therapeutic use | Antineoplastic Agents - chemistry | Digoxin - pharmacology | Hypertension - physiopathology | Hypertension - metabolism | Neoplasms - drug therapy | Antihypertensive Agents - chemistry | Sodium-Potassium-Exchanging ATPase - metabolism | Animals | Myocytes, Cardiac - drug effects | Cardiovascular System - metabolism | Diabetes Mellitus - physiopathology | Cardiac Glycosides - chemistry | Myocytes, Cardiac - metabolism | Bufanolides - pharmacology | Cardiac Glycosides - metabolism | Cardiac Glycosides - therapeutic use | Cell Proliferation - drug effects | Neoplasms - pathology
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3. Full Text Relevance of UDP-glucuronosyltransferase polymorphisms for drug dosing: A quantitative systematic review
by Stingl, J.C and Bartels, H and Viviani, R and Lehmann, M.L and Brockmöller, J
Pharmacology and Therapeutics, ISSN 0163-7258, 01/2014, Volume 141, Issue 1, pp. 92 - 116
UDP-glucuronosyltransferases (UGT) catalyze the biotransformation of many endobiotics and xenobiotics, and are coded by polymorphic genes. However, knowledge... 
Drug metabolism | UDP-glucuronosyltransferases | Pharmacogenetics | Pharmacogenetics-based dose adjustments | UGT1A1 | Polymorphism | UGT2B7 GENETIC POLYMORPHISMS | MYCOPHENOLIC-ACID PHARMACOKINETICS | HUMAN LIVER-MICROSOMES | GLUCURONIDATION POTENTIAL ROLE | METASTATIC COLORECTAL-CANCER | RENAL-TRANSPLANT RECIPIENTS | CELL LUNG-CANCER | NONSTEROIDAL ANTIINFLAMMATORY DRUGS | IN-VITRO CHARACTERIZATION | IRINOTECAN-INDUCED NEUTROPENIA | PHARMACOLOGY & PHARMACY | Psychotropic Drugs - pharmacokinetics | Humans | Analgesics - metabolism | Analgesics - pharmacokinetics | Antihypertensive Agents - metabolism | Antihypertensive Agents - pharmacokinetics | Uridine Diphosphate - metabolism | Polymorphism, Genetic | Antineoplastic Agents - metabolism | Glucuronosyltransferase - genetics | Pharmaceutical Preparations - metabolism | Glucuronosyltransferase - metabolism | Anti-HIV Agents - pharmacokinetics | Antineoplastic Agents - pharmacokinetics | Psychotropic Drugs - metabolism | Anti-HIV Agents - metabolism | Pharmaceutical Preparations - administration & dosage | Pharmacokinetics | Physiological aspects | Xenobiotics | Index Medicus
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4. Full Text Use of mechanistic modeling to assess interindividual variability and interspecies differences in active uptake in human and rat hepatocytes
by Ménochet, Karelle and Kenworthy, Kathryn E and Houston, J. Brian and Galetin, Aleksandra
Drug Metabolism and Disposition, ISSN 0090-9556, 09/2012, Volume 40, Issue 9, pp. 1744 - 1756
Interindividual variability in activity of uptake transporters is evident in vivo, yet limited data exist in vitro, confounding in vitro-in vivo extrapolation.... 
DRUG TRANSPORTERS | IN-VITRO CLEARANCE | CRYOPRESERVED HUMAN HEPATOCYTES | HMG-COA REDUCTASE | PHARMACOLOGY & PHARMACY | ANION TRANSPORTING POLYPEPTIDES | HEPATIC-UPTAKE | HEALTHY-VOLUNTEERS | METABOLIC ENZYMES | RECEPTOR ANTAGONIST | PREDICTION | Antihypertensive Agents - pharmacology | Tetrazoles - pharmacology | Species Specificity | Valsartan | Hypoglycemic Agents - metabolism | Benzoates - metabolism | Humans | Antihypertensive Agents - metabolism | Hepatocytes - metabolism | Angiotensin II Type 1 Receptor Blockers - pharmacology | Angiotensin II Type 1 Receptor Blockers - metabolism | Organic Anion Transporters - metabolism | Pyrimidines - metabolism | Quinolines - pharmacology | Tetrazoles - metabolism | Carbamates - metabolism | Dose-Response Relationship, Drug | Fluorobenzenes - pharmacology | Drug Interactions | Hydroxymethylglutaryl-CoA Reductase Inhibitors - metabolism | Biological Transport | Piperidines - pharmacology | Hepatocytes - drug effects | Carbamates - pharmacology | Pravastatin - pharmacology | Fluorobenzenes - metabolism | Piperidines - metabolism | Pravastatin - metabolism | Valine - analogs & derivatives | Rats | Rosuvastatin Calcium | Pyrimidines - pharmacology | Sulfonamides - pharmacology | Hypoglycemic Agents - pharmacology | Quinolines - metabolism | Animals | Hydroxymethylglutaryl-CoA Reductase Inhibitors - pharmacology | Valine - metabolism | Models, Biological | Benzimidazoles - metabolism | Sulfonamides - metabolism | Benzoates - pharmacology | Benzimidazoles - pharmacology | Kinetics | Valine - pharmacology | Organic Anion Transporters - drug effects
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5. Bioactive peptides
by Shahidi, Fereidoon and Zhong, Ying
Journal of AOAC International, ISSN 1060-3271, 07/2008, Volume 91, Issue 4, pp. 914 - 931
Peptides with biological activities, released during gastrointestinal digestion or food processing, play an important role in metabolic regulation and... 
CHEMISTRY, ANALYTICAL | IONIZATION-MASS-SPECTROMETRY | CLASS IIA BACTERIOCINS | BOWMAN-BIRK INHIBITOR | SPONTANEOUSLY HYPERTENSIVE-RATS | I-CONVERTING-ENZYME | RADICAL-SCAVENGING ACTIVITIES | FOOD SCIENCE & TECHNOLOGY | LACTIC-ACID BACTERIA | PROTEIN-DERIVED PEPTIDES | CORE HISTONE ACETYLATION | SOYBEAN BETA-CONGLYCININ | Antihypertensive Agents - pharmacology | Antioxidants - metabolism | Humans | Anti-Bacterial Agents - metabolism | Antihypertensive Agents - metabolism | Antioxidants - pharmacology | Peptides - pharmacology | Antineoplastic Agents - metabolism | Animals | Peptides - metabolism | Anticholesteremic Agents - metabolism | Anti-Bacterial Agents - pharmacology | Antineoplastic Agents - pharmacology | Immunologic Factors - metabolism | Anticholesteremic Agents - pharmacology | Immunologic Factors - pharmacology
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6. Full Text L-citrulline supplementation: Impact on cardiometabolic health
by Allerton, Timothy D and Proctor, David N and Stephens, Jacqueline M and Dugas, Tammy R and Spielmann, Guillaume and Irving, Brian A
Nutrients, ISSN 2072-6643, 07/2018, Volume 10, Issue 7, p. 921
Diminished bioavailability of nitric oxide (NO), the gaseous signaling molecule involved in the regulation of numerous vital biological functions, contributes... 
Hypertension | Obesity | Watermelon | Liver | Cardiovascular disease | Inflammation | Adipocytes | Endothelial function | Supplements | Enterocytes | Mitochondria | Interventions | Arginine | Nitric oxide | Flow mediated dilation | Therapeutics | Aging | Insulin resistance | Muscle | Diabetes | Immune cells | DEPENDENT DIABETES-MELLITUS | therapeutics | NITRIC-OXIDE SYNTHESIS | L-ARGININE SUPPLEMENTATION | PRESERVED EJECTION FRACTION | enterocytes | HUMAN SKELETAL-MUSCLE | NUTRITION & DIETETICS | arginine | inflammation | muscle | CULTURED ENDOTHELIAL-CELLS | MUSCLE PROTEIN ANABOLISM | watermelon | adipocytes | insulin resistance | obesity | endothelial function | cardiovascular disease | nitric oxide | ORAL L-CITRULLINE | liver | SPONTANEOUSLY HYPERTENSIVE-RATS | mitochondria | immune cells | CHAIN AMINO-ACIDS | supplements | interventions | aging | hypertension | diabetes | flow mediated dilation | Vasodilator Agents - therapeutic use | Hypoglycemic Agents - metabolism | Antioxidants - metabolism | Humans | Citrulline - metabolism | Metabolic Syndrome - metabolism | Antihypertensive Agents - metabolism | Diabetic Angiopathies - physiopathology | Vasodilator Agents - metabolism | Metabolic Syndrome - physiopathology | Hypertension - prevention & control | Metabolic Syndrome - immunology | Anti-Inflammatory Agents, Non-Steroidal - metabolism | Diabetic Angiopathies - prevention & control | Dietary Supplements - adverse effects | Vascular Stiffness | Sarcopenia - metabolism | Endothelium, Vascular - immunology | Hypoglycemic Agents - therapeutic use | Diabetic Angiopathies - metabolism | Sarcopenia - immunology | Endothelium, Vascular - physiopathology | Insulin Resistance | Metabolic Syndrome - therapy | Hypertension - immunology | Citrulline - therapeutic use | Antihypertensive Agents - therapeutic use | Evidence-Based Medicine | Citrulline - adverse effects | Hypertension - physiopathology | Antihypertensive Agents - adverse effects | Hypertension - metabolism | Antioxidants - therapeutic use | Sarcopenia - physiopathology | Animals | Anti-Inflammatory Agents, Non-Steroidal - adverse effects | Anti-Inflammatory Agents, Non-Steroidal - therapeutic use | Endothelium, Vascular - metabolism | Models, Biological | Sarcopenia - prevention & control | Diabetic Angiopathies - immunology | Antioxidants - adverse effects | Vasodilator Agents - adverse effects | Hypoglycemic Agents - adverse effects | Health | Dietary supplements | Muscles | Amino acids | Gastrointestinal tract | Bioavailability | Citrulline | Metabolism | Nitric-oxide synthase | Substrates | Urea | L-citrulline | Synthesis | Gastrointestinal system | Blood pressure | Adults | Supplementation | Age
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7. Full Text L‐Theanine: properties, synthesis and isolation from tea
by Vuong, Quan V and Bowyer, Michael C and Roach, Paul D
Journal of the Science of Food and Agriculture, ISSN 0022-5142, 08/2011, Volume 91, Issue 11, pp. 1931 - 1939
Theanine is a non‐protein amino acid that occurs naturally in the tea plant ( Camellia sinensis ) and contributes to the favourable taste of tea. It is also... 
synthesis | tea | isolation | health benefits | theanine | properties | Tea | Isolation | Synthesis | Properties | Theanine | Health benefits | GAMMA-GLUTAMYLMETHYLAMIDE | FOOD SCIENCE & TECHNOLOGY | CAFFEINE | CATECHINS | GREEN TEA | ENZYMATIC PRODUCTION | AMINO-ACIDS | L-CYSTINE | AGRICULTURE, MULTIDISCIPLINARY | GLUTAMINE-SYNTHETASE | FERMENTATION | CHEMISTRY, APPLIED | UMAMI TASTE | Anti-Anxiety Agents - metabolism | Camellia sinensis - chemistry | Plant Leaves - chemistry | Glutamates - therapeutic use | Camellia sinensis - metabolism | Plant Roots - metabolism | Humans | Antineoplastic Agents, Phytogenic - chemistry | Glutamates - metabolism | Anti-Anxiety Agents - isolation & purification | Antihypertensive Agents - metabolism | Antihypertensive Agents - therapeutic use | Glutamates - isolation & purification | Glutamates - chemistry | Antihypertensive Agents - chemistry | Animals | Antihypertensive Agents - isolation & purification | Anti-Anxiety Agents - chemistry | Antineoplastic Agents, Phytogenic - metabolism | Anti-Anxiety Agents - therapeutic use | Antineoplastic Agents, Phytogenic - therapeutic use | Tea - chemistry | Antineoplastic Agents, Phytogenic - isolation & purification | Learning | Immune systems | Health | Amino acids | Foods | Promotion
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8. Full Text Effects of aliskiren on blood pressure, albuminuria, and (Pro)renin receptor expression in diabetic TG(mRen-2)27 Rats
by Feldman, David and Jin, Li and Xuan, Hong and Contrepas, Aurelie and Zhou, Yinong and Webb, Randy and Mueller, Dominik and Feldt, Sana and Cumin, Frederick and Maniara, Wieslawa and Persohn, Elke and Schuetz, Helmut and Danser, Jan and Nguyen, Genevieve
Hypertension, ISSN 0194-911X, 07/2008, Volume 52, Issue 1, pp. 130 - 136
textabstractThe aim of this study was to explore the effects of the renin inhibitor aliskiren in streptozotocin-diabetic TG(mRen-2)27 rats. Furthermore, we... 
Aliskiren | Diabetic nephropathy | Renin inhibitor | (pro)renin receptor | TG(mRen-2)rat | RENIN/PRORENIN RECEPTOR | NONPROTEOLYTIC ACTIVATION | aliskiren | TRANSGENIC RATS | ANGIOTENSIN-II | NEPHROPATHY | MESANGIAL CELLS | PERIPHERAL VASCULAR DISEASE | renin inhibitor | HEART-RATE | PRORENIN | HYPERTENSION | diabetic nephropathy | Renin - metabolism | Antihypertensive Agents - pharmacology | Gene Expression - drug effects | Diabetic Nephropathies - etiology | Humans | Collagen Type III - metabolism | Male | Antihypertensive Agents - metabolism | Receptors, Cell Surface - antagonists & inhibitors | Albuminuria - physiopathology | Collagen Type I - genetics | Diabetic Nephropathies - physiopathology | Amides - pharmacokinetics | Albuminuria - metabolism | Blood Pressure - drug effects | Diabetes Mellitus, Experimental - complications | Diabetes Mellitus, Experimental - metabolism | Diabetes Mellitus, Experimental - physiopathology | Amides - pharmacology | Collagen Type IV - metabolism | Collagen Type I - metabolism | Albuminuria - etiology | Diabetic Nephropathies - metabolism | Rats | Receptors, Cell Surface - metabolism | Antihypertensive Agents - pharmacokinetics | Collagen Type III - genetics | Rats, Sprague-Dawley | Animals | Renin - antagonists & inhibitors | Transforming Growth Factor beta - genetics | Fumarates - pharmacokinetics | Fumarates - pharmacology | Collagen Type IV - genetics | Transforming Growth Factor beta - metabolism | Receptors, Cell Surface - genetics
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9. Full Text Therapeutic role of nitric oxide as emerging molecule
by Kumar, Sahil and Singh, Rajesh K and Bhardwaj, T.R
Biomedicine & Pharmacotherapy, ISSN 0753-3322, 2016, Volume 85, pp. 182 - 201
Abstract NO has many physiological roles; in inflammation, pain, rheumatoid arthritis, immune system, gastroprotection, as antioxidant and reported to be a... 
Internal Medicine | Medical Education | Nitric Oxide(NO) | Antimalarial | Antihypertensive | NO-donors | Non steroidal anti-inflammatory Drugs(NSAIDs) | MEDICINE, RESEARCH & EXPERIMENTAL | III LONG-TERM | NIPRADILOL OPHTHALMIC SOLUTION | INFLAMMATORY RESPONSES | THROMBUS FORMATION | NO-DONOR | NITROXYL ANION | OPEN-ANGLE GLAUCOMA | Non steroidal anti-inflammatory Drugs (NSAIDs) | NONSTEROIDAL ANTIINFLAMMATORY DRUGS | IN-VIVO | PHARMACOLOGY & PHARMACY | ACTIVE ULCERATIVE-COLITIS | Antimalarials - metabolism | Nitric Oxide Donors - chemistry | Anti-Infective Agents - metabolism | Humans | Nitric Oxide Donors - metabolism | Anti-Infective Agents - therapeutic use | Antimalarials - therapeutic use | Antineoplastic Agents - therapeutic use | Structure-Activity Relationship | Antihypertensive Agents - metabolism | Antihypertensive Agents - therapeutic use | Antineoplastic Agents - chemistry | Antineoplastic Agents - metabolism | Antihypertensive Agents - chemistry | Animals | Anti-Infective Agents - chemistry | Antimalarials - chemistry | Platelet Aggregation Inhibitors - chemistry | Molecular Structure | Nitric Oxide Donors - therapeutic use | Platelet Aggregation Inhibitors - metabolism | Nitric Oxide - metabolism | Platelet Aggregation Inhibitors - therapeutic use | Antioxidants | Glaucoma | Rheumatoid factor | Animal behavior | Nitric oxide | Pharmacy | Drugstores | Nitrates | Arthritis | Health aspects | Transdermal medication | Fluocinolone acetonide
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10. Full Text Investigation of the impact of substrate selection on in vitro organic anion transporting polypeptide 1B1 inhibition profiles for the prediction of drug-drug interactions
by Izumi, Saki and Nozaki, Yoshitane and Maeda, Kazuya and Komori, Takafumi and Takenaka, Osamu and Kusuhara, Hiroyuki and Sugiyama, Yuichi
Drug Metabolism and Disposition, ISSN 0090-9556, 01/2015, Volume 43, Issue 2, pp. 235 - 247
The risk assessment of organic anion transporting polypeptide (OATP) 1B1-mediated drug-drug interactions (DDIs) is an indispensable part of drug development.... 
GEMFIBROZIL | CYCLOSPORINE-A | PHARMACOKINETICS | MECHANISM | HEALTHY-SUBJECTS | PHARMACOLOGY & PHARMACY | HEPATIC-UPTAKE | TRANSPLANT RECIPIENTS | OATP1B1 | ROSUVASTATIN | HEPATOBILIARY TRANSPORT | Estradiol - analogs & derivatives | Phenylalanine - analogs & derivatives | Cyclosporine - pharmacology | Hypoglycemic Agents - metabolism | Humans | Antihypertensive Agents - metabolism | Organic Anion Transporters - metabolism | Cyclohexanes - metabolism | Organic Anion Transporters - genetics | Drug Interactions | Hydroxymethylglutaryl-CoA Reductase Inhibitors - metabolism | Membrane Transport Modulators - pharmacology | HEK293 Cells | Biological Transport - drug effects | Drug Evaluation, Preclinical | Binding, Competitive | Recombinant Proteins - metabolism | Estradiol - metabolism | Organic Anion Transporters - antagonists & inhibitors | Phenylalanine - metabolism | Gemfibrozil - pharmacology | Models, Biological | Sulfonamides - metabolism | Kinetics | Rifampin - pharmacology | Solute Carrier Organic Anion Transporter Family Member 1b1
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11. Full Text Modeling the effects of commonly used drugs on human metabolism
by Sahoo, Swagatika and Haraldsdóttir, Hulda S and Fleming, Ronan M. T and Thiele, Ines
FEBS Journal, ISSN 1742-464X, 01/2015, Volume 282, Issue 2, pp. 297 - 317
Metabolism contributes significantly to the pharmacokinetics and pharmacodynamics of a drug. In addition, diet and genetics have a profound effect on cellular... 
inborn errors of metabolism | genome‐scale metabolic network reconstruction | constraint‐based modeling | reconstruction module | drug metabolism | genome-scale metabolic network reconstruction | constraint-based modeling | TRANSPLANT PATIENTS | GLOBAL RECONSTRUCTION | BIOCHEMISTRY & MOLECULAR BIOLOGY | HMG-COA REDUCTASE | IN-VITRO METABOLISM | HUMAN LIVER-MICROSOMES | CLINICAL PHARMACOKINETICS | CYTOCHROME-P450 3A4 | INBORN-ERRORS | INTESTINAL-ABSORPTION | PHARMACEUTICAL DRUGS | Analgesics - therapeutic use | Inactivation, Metabolic | Humans | Immunosuppressive Agents - therapeutic use | Analgesics - metabolism | Drug-Related Side Effects and Adverse Reactions - metabolism | Analgesics - pharmacokinetics | Antihypertensive Agents - metabolism | Antihypertensive Agents - therapeutic use | Antihypertensive Agents - adverse effects | Hydroxymethylglutaryl-CoA Reductase Inhibitors - pharmacokinetics | Hydroxymethylglutaryl-CoA Reductase Inhibitors - adverse effects | Hydroxymethylglutaryl-CoA Reductase Inhibitors - metabolism | Cytochrome P-450 CYP3A - metabolism | Hydroxymethylglutaryl-CoA Reductase Inhibitors - therapeutic use | Drug Design | Immunosuppressive Agents - metabolism | Immunosuppressive Agents - adverse effects | Analgesics - adverse effects | Hypertension | Drugs | Food habits | Genomics | Cytochrome P-450 | Immunosuppressive agents | Prescribing | Metabolites | Analgesics | Analysis | Physiological aspects | Models | Statins | Metabolism | Drug therapy | Pharmacology
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