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Journal of pharmaceutical sciences, ISSN 0022-3549, 09/2017, Volume 106, Issue 9, pp. 2566 - 2575
blood-brain barrier | P-glycoprotein | MRP | ABC transporters | cerebrospinal fluid | Physical Sciences | Chemistry | Life Sciences & Biomedicine | Pharmacology & Pharmacy | Chemistry, Medicinal | Chemistry, Multidisciplinary | Science & Technology | Central Nervous System - metabolism | Humans | 2,4-Dichlorophenoxyacetic Acid - chemistry | Ochratoxins - chemistry | Male | Thiophenes - metabolism | Ochratoxins - metabolism | Pravastatin - chemistry | Brain - metabolism | Uric Acid - chemistry | Biological Transport | Quinazolines - metabolism | Tetrahydroisoquinolines - chemistry | Adenosine Triphosphate - metabolism | Cyclic GMP - chemistry | Multidrug Resistance-Associated Proteins - genetics | Quinazolines - chemistry | Methotrexate - chemistry | 2,4-Dichlorophenoxyacetic Acid - metabolism | Acridines - chemistry | Methotrexate - metabolism | Uric Acid - metabolism | Acridines - metabolism | Pravastatin - metabolism | Mice, Inbred C57BL | Quinolines - chemistry | Blood-Brain Barrier - metabolism | Quinolines - metabolism | Animals | Cyclic GMP - metabolism | Tetrahydroisoquinolines - metabolism | Kinetics | Adenosine Triphosphate - chemistry | Thiophenes - chemistry | Multidrug Resistance-Associated Proteins - metabolism | Index Medicus | Blood–brain barrier
Journal Article
Nature (London), ISSN 0028-0836, 05/2012, Volume 485, Issue 7398, pp. 327 - 332
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Structure of solids and liquids; crystallography | Structure of specific crystalline solids | Physics | Exact sciences and technology | Condensed matter: structure, mechanical and thermal properties | Organic compounds | Naltrexone - analogs & derivatives | Humans | Naltrexone - chemistry | Crystallography, X-Ray | Structure-Activity Relationship | Diterpenes, Clerodane - chemistry | Receptors, Adrenergic, beta-2 - chemistry | Piperidines - pharmacology | Tetrahydroisoquinolines - chemistry | Receptors, Opioid, kappa - chemistry | Binding Sites | Receptors, Opioid, kappa - genetics | Naltrexone - metabolism | Morphinans - chemistry | Tetrahydroisoquinolines - pharmacology | Piperidines - chemistry | Receptors, Opioid, kappa - antagonists & inhibitors | Mutagenesis, Site-Directed | Receptors, Opioid, kappa - metabolism | Models, Molecular | Receptors, CXCR4 - metabolism | Guanidines - chemistry | Diterpenes, Clerodane - metabolism | Diterpenes, Clerodane - pharmacology | Protein Conformation | Receptors, CXCR4 - chemistry | Index Medicus
Journal Article
Molecules (Basel, Switzerland), ISSN 1420-3049, 05/2020, Volume 25, Issue 9, p. 2049
Biochemistry & Molecular Biology | Physical Sciences | Chemistry | Life Sciences & Biomedicine | Chemistry, Multidisciplinary | Science & Technology | Magnetic Resonance Spectroscopy | Quinolines - chemistry | Sulfides - chemistry | Hydroxamic Acids - chemistry | Lactams | Chemistry, Pharmaceutical | Isoquinolines - chemistry | Chemistry, Organic | Cyclization | Tetrahydroisoquinolines - chemistry | Nitrogen Compounds - chemistry | Drug Design | Molecular Structure | Indole Alkaloids - chemistry | Indoles - chemistry | Sulfide | Solvents | Reduction | Ammonium | Acids | Dehydrogenation | Decarboxylation | Tetrahydroisoquinoline | Carboxylic acids | Sulfur | Sodium sulfide | Index Medicus | tetrahydroisoquinolonic acid | cryptolepine | nitroarene reduction | hydroxamic acid | indoloisoquinoline | Castagnoli–Cushman reaction | Communication | heteroannulation | dibenzonaphthyridine
Journal Article
Nature (London), ISSN 0028-0836, 12/2020, Volume 588, Issue 7836, pp. 83 - 88
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Chemistry, Organic - methods | Artificial Intelligence - standards | Sesquiterpenes - chemical synthesis | Tetrahydroisoquinolines - chemical synthesis | Chemistry Techniques, Synthetic - standards | Chemistry Techniques, Synthetic - methods | Benzylisoquinolines - chemistry | Lactones - chemical synthesis | Indole Alkaloids - chemical synthesis | Macrolides - chemistry | Tetrahydroisoquinolines - chemistry | Automation - methods | Chemistry, Organic - standards | Indole Alkaloids - chemistry | Lactones - chemistry | Software - standards | Indans - chemistry | Knowledge Bases | Reproducibility of Results | Sesquiterpenes - chemistry | Automation - standards | Benzylisoquinolines - chemical synthesis | Biological Products - chemical synthesis | Macrolides - chemical synthesis | Indans - chemical synthesis | Design | Organic chemistry | Knowledge bases (artificial intelligence) | Algorithms | Cost estimates | Natural products | Computation | Chemists | Computer applications | Logic | Artificial intelligence | Optimization | Index Medicus
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 09/2011, Volume 50, Issue 37, pp. 8538 - 8564
tetrahydroisoquinoline | pictet‐spengler reaction | asymmetric synthesis | pictet‐spenglerase | tetrahydrocarboline | pictet-spengler reaction | pictet-spenglerase | Physical Sciences | Chemistry | Chemistry, Multidisciplinary | Science & Technology | Biological Products - chemical synthesis | Biological Products - chemistry | Chemistry, Organic | Humans | Molecular Conformation | Models, Molecular | Alkaloids - chemical synthesis | Alkaloids - therapeutic use | Drug Discovery | Alkaloids - chemistry | Biological Products - therapeutic use | Natural products | Corporate profiles | Index Medicus
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Effects of a detergent micelle environment on P-glycoprotein (ABCB1)-ligand interactions
The Journal of biological chemistry, ISSN 0021-9258, 04/2017, Volume 292, Issue 17, pp. 7066 - 7076
Life Sciences & Biomedicine | Biochemistry & Molecular Biology | Science & Technology | Acridines - chemistry | Dibenzocycloheptenes - chemistry | Baculoviridae - metabolism | Detergents - chemistry | Humans | Insecta | Quinolines - chemistry | ATP Binding Cassette Transporter, Subfamily B - chemistry | Peptides, Cyclic - chemistry | Drug Delivery Systems | Verapamil - chemistry | Hydrolysis | Animals | Tetrahydroisoquinolines - chemistry | Micelles | Glucosides - chemistry | Inhibitory Concentration 50 | Protein Binding | Ligands | Mice | Adenosine Triphosphate - chemistry | Drug Evaluation, Preclinical | Binding Sites | Index Medicus | P-glycoprotein | docking | ATP hydrolysis | molecular modeling | multidrug transporter | Membrane Biology | proteoliposomes | nanodiscs | drug resistance | ABC transporter | detergent micelles
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Natural product reports, ISSN 0265-0568, 1/2015, Volume 32, Issue 2, pp. 328 - 347
Biochemistry & Molecular Biology | Physical Sciences | Chemistry | Chemistry, Organic | Life Sciences & Biomedicine | Pharmacology & Pharmacy | Chemistry, Medicinal | Science & Technology | Marine Biology | Tetrahydroisoquinolines - pharmacology | Animals | Tetrahydroisoquinolines - chemistry | Dioxoles - pharmacology | Antineoplastic Agents - pharmacology | Molecular Structure | Antineoplastic Agents - chemistry | Trabectedin | Dioxoles - chemistry | Urochordata - chemistry | Index Medicus
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