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1. Full Text Dual targeting DNA gyrase B (GyrB) and topoisomerse IV (ParE) inhibitors: A review
by Azam, Mohammed Afzal and Thathan, Janarthanan and Jubie, Selvaraj
Bioorganic Chemistry, ISSN 0045-2068, 10/2015, Volume 62, pp. 41 - 63
GyrB and ParE are type IIA topoisomerases and found in most bacteria. Its function is vital for DNA replication, repair and decatenation. The highly conserved... 
GyrB | Pyrrolopyrimidines | ParE | ATPase inhibitors | BROAD-SPECTRUM | BIOCHEMISTRY & MOLECULAR BIOLOGY | ESCHERICHIA-COLI | VIVO ANTIBACTERIAL ACTIVITIES | CHEMISTRY, ORGANIC | PYRROLOPYRIMIDINE INHIBITORS | STREPTOCOCCUS-PNEUMONIAE | BIOLOGICAL EVALUATION | NEISSERIA-GONORRHOEAE | STAPHYLOCOCCUS-AUREUS | ANTISTAPHYLOCOCCAL ACTIVITIES | IN-VITRO ACTIVITY | DNA Topoisomerase IV - drug effects | Amino Acid Sequence | DNA Gyrase - drug effects | Topoisomerase II Inhibitors - pharmacology | Quinolines - pharmacology | Pyrrolidines - pharmacology | Indazoles - pharmacology | Organophosphates - pharmacology | Topoisomerase Inhibitors - pharmacology | Pyrroles - pharmacology | Barbiturates - pharmacology | Aminopyridines - pharmacology | Fluoroquinolones - pharmacology | Pyrrolidinones - pharmacology | Urea - analogs & derivatives | Benzimidazoles - pharmacology | Anti-Bacterial Agents - pharmacology | Prodrugs - pharmacology | Quinazolinones - pharmacology | Spiro Compounds - pharmacology | Urea - pharmacology | Pyrazoles - pharmacology | DNA
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2. Full Text A novel GABA A receptor pharmacology: Drugs interacting with the α +β - interface
by Sieghart, Werner and Ramerstorfer, Joachim and Sarto-Jackson, Isabella and Varagic, Zdravko and Ernst, Margot
British Journal of Pharmacology, ISSN 0007-1188, 05/2012, Volume 166, Issue 2, pp. 476 - 485
GABAA receptors are ligand-gated chloride channels composed of five subunits that can belong to different subunit classes. The existence of 19 different... 
barbiturates | benzodiazepines | allosteric binding sites | receptors | CGS 9895 | anesthetics | pharmacology | GABA | steroids | receptor subtypes | structure | SINGLE AMINO-ACID | GATED ION-CHANNEL | GENERAL ANESTHETIC ETOMIDATE | SELECTIVE PARTIAL AGONIST | EPSILON-SUBUNIT | A RECEPTOR | ALPHA-5 SUBUNIT | PHARMACOLOGY & PHARMACY | GAMMA-AMINOBUTYRIC-ACID | RAT-BRAIN | BENZODIAZEPINE BINDING-SITE | GABAA receptors | Pharmaceutical Preparations - metabolism | Animals | Humans | Protein Subunits - chemistry | Receptors, GABA-A - metabolism | Receptors, GABA-A - chemistry | Benzodiazepines - metabolism | Protein Subunits - metabolism
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3. Full Text GABA- receptors: distinctive functions and molecular pharmacology
by Naffaa, MM and Hung, S and Chebib, M and Johnston, GAR and Hanrahan, JR
BRITISH JOURNAL OF PHARMACOLOGY, ISSN 0007-1188, 07/2017, Volume 174, Issue 13, pp. 1881 - 1894
The homomeric GABA- ligand-gated ion channels (also known as GABA(C) or GABA(A)- receptors) are similar to heteromeric GABA(A) receptors in structure, function... 
C RECEPTOR | CONFERS BARBITURATE SENSITIVITY | RETINAL BIPOLAR CELLS | BINDING-SITE | TRANSMEMBRANE DOMAIN | PHARMACOLOGY & PHARMACY | GATED ION CHANNELS | XENOPUS OOCYTES | GAMMA-AMINOBUTYRIC-ACID | AGONIST BINDING | BETA-SUBUNIT | Receptors | γ-Aminobutyric acid A receptors | Ion channels (ligand-gated) | Ligands | Pharmacology | Ion channels | Selectivity | Receptor mechanisms | γ-Aminobutyric acid C receptors | Structure-activity relationships | Binding sites | Structure-function relationships
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4. Full Text Pharmacological characterization of harmaline-induced tremor activity in mice
by Paterson, Neil E and Malekiani, Sam A and Foreman, Mark M and Olivier, Berend and Hanania, Taleen
European Journal of Pharmacology, ISSN 0014-2999, 2009, Volume 616, Issue 1, pp. 73 - 80
Harmaline-induced tremor in rodents is a model of essential tremor. We utilized a novel assay to quantify tremor activity in mice and found that tremor... 
Harmaline | Dopamine | Gabapentin | Primidone | Lithium | Glutamate | Carbamazepine | Valproate | Validity | D 1 receptor | GABA | Propranolol | Essential tremor | ICR mouse | D 2 receptor | γ-Hydroxy-butyrate | receptor | GAMMA-HYDROXYBUTYRIC ACID | NUCLEUS-ACCUMBENS DOPAMINE | D-2 receptor | SUBUNIT MESSENGER-RNAS | AMINO-ACIDS | SODIUM-VALPROATE | PHARMACOLOGY & PHARMACY | gamma-Hydroxy-butyrate | AMINOBUTYRIC-ACID | RECEPTOR SUBUNITS | NEUROTRANSMITTER RELEASE | INFERIOR OLIVE | D-1 receptor | DRUG-INDUCED TREMOR | Receptors, Glutamate - metabolism | Muscimol - pharmacology | gamma-Aminobutyric Acid - metabolism | Glutamates - metabolism | Male | Anticonvulsants - pharmacology | Dose-Response Relationship, Drug | Propranolol - pharmacology | Lithium Chloride - pharmacology | Neurotransmitter Agents - pharmacology | Tremor - chemically induced | Behavior, Animal - drug effects | Raclopride - pharmacology | Chlordiazepoxide - pharmacology | Dopamine - metabolism | Baclofen - pharmacology | Harmaline - pharmacology | Affect - drug effects | Benzazepines - pharmacology | Piperazines - pharmacology | Mice, Inbred ICR | Sodium Oxybate - pharmacology | Animals | Mice | Carbolines - pharmacology | Propranolol hydrochloride | Methyl aspartate | Pyridine | Analysis | Gamma-hydroxybutyrate | Chemical properties | Barbiturates | Index Medicus
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5. Full Text High in Vitro susceptibility to the novel spiropyrimidinetrione ETX0914 (AZD0914) among 873 contemporary clinical Neisseria gonorrhoeae Isolates from 21 European countries from 2012 to 2014
by Unemo, Magnus and Ringlander, Johan and Wiggins, Catherine and Fredlund, Hans and Jacobsson, Susanne and Cole, Michelle and Balla, Eszter and Barbara, Christopher and Jose Borrego, Maria and Brilene, Tatiana and Chisholm, Stephanie and Crucitti, Tania and van Dam, Alje and Hoffmann, Steen and Jeverica, Samo and Kohl, Peter and Maikanti, Panayiota and Mlynarczyk-Bonikowska, Beata and Pakarna, Gatis and Pavlik, Peter and Stary, Angelika and Stefanelli, Paola and Svanborg, Guðrún and Syversen, Gaute and Tzelepi, Eva and Vazquez, Julio and European Collaborative Grp and Örebro universitet and Institutionen för hälsovetenskap och medicin
Antimicrobial agents and chemotherapy, ISSN 0066-4804, 2015, Volume 59, Issue 9, pp. 5220 - 5225
Resistance in Neisseria gonorrhoeae against all antimicrobials available for the treatment of gonorrhea has emerged. The first gonococcal strains with... 
MULTIDRUG-RESISTANT | CEFTRIAXONE TREATMENT | ANTIBACTERIAL ACTIVITY | PHARYNGEAL GONORRHEA | MICROBIOLOGY | PHARMACOLOGY & PHARMACY | FUTURE | UNTREATABLE GONORRHEA | ANTIMICROBIAL RESISTANCE | 500 MG | DNA GYRASE INHIBITOR | TREATMENT FAILURE | Neisseria gonorrhoeae - drug effects | Europe | Humans | Ciprofloxacin - pharmacology | Drug Resistance, Bacterial | Ceftriaxone - pharmacology | Azithromycin - pharmacology | Microbial Sensitivity Tests | Barbiturates - pharmacology | Fluoroquinolones - pharmacology | Anti-Bacterial Agents - pharmacology | Cefixime - pharmacology | Spiro Compounds - pharmacology | Susceptibility | Basic Medicine | Medical and Health Sciences | Microbiology in the medical area | Microbiology | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper | Mikrobiologi | Farmakologi och toxikologi | Mikrobiologi inom det medicinska området | Pharmacology and Toxicology
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6. The Neurobiology of opiate reward processes
by Lane, John D and Smith, James E., Jr
1983, ISBN 0444804307, xix, 475
Receptors, Endorphin | Receptors | Narcotics | Reinforcement (Psychology) | Endorphins | Reward (Psychology) | Neuroregulators | Metabolism | Physiological effect
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7. Opioid analgesics
: chemistry and receptors
by Casy, Alan F and Parfitt, Robert T
1986, ISBN 0306421305, xv, 518
Endorphins | Receptors | Analgesics | Narcotics | Opium
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8. Opiates
by Lenz, George R
1986, ISBN 9780124438309, xi, 560 p., [1] leaf of plates
Models | Narcotics | Structure-activity relationships | Pharmaceutical chemistry
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9. Full Text Brain protection by anesthetic agents
by Koerner, Ines P and Brambrink, Ansgar M
Current Opinion in Anaesthesiology, ISSN 0952-7907, 10/2006, Volume 19, Issue 5, pp. 481 - 486
Purpose of review Patients at risk for perioperative stroke, or those who have suffered recent cerebral injury, may benefit from neuroprotective properties of... 
Neuroprotection | Anesthesia | Neurotoxicity | Perioperative cerebral ischemia | Posttreatment | Preconditioning | neurotoxicity | perioperative cerebral ischemia | neuroprotection | ANESTHESIOLOGY | posttreatment | anesthesia | preconditioning | Anesthetics, Inhalation - pharmacology | Lidocaine - pharmacology | Xenon - pharmacology | Anesthetics, Dissociative - pharmacology | Isoflurane - pharmacology | Humans | Propofol - pharmacology | Anesthetics - pharmacology | Neuroprotective Agents - toxicity | Anesthetics, Local - pharmacology | Brain - drug effects | Anesthetics, Intravenous - pharmacology | Anesthetics - toxicity | Animals | Neuroprotective Agents - pharmacology | Cerebrovascular Disorders - prevention & control | Time Factors | Barbiturates - pharmacology | Brain - pathology | Neuroprotective Agents - adverse effects | Ketamine - pharmacology | Anesthetics - adverse effects
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10. Full Text Discriminative stimulus effects of pregnanolone in rhesus monkeys
by Gerak, Lisa R and Gerak, Lisa R and France, Charles P and France, Charles P
Psychopharmacology, ISSN 0033-3158, 1/2014, Volume 231, Issue 1, pp. 181 - 190
Neuroactive steroids and benzodiazepines can positively modulate GABA by acting at distinct binding sites on synaptic GABAA receptors. Although these receptors... 
Drug discrimination | Neurosciences | Biomedicine | Pharmacology/Toxicology | Psychiatry | Pregnanolone | Benzodiazepines | Rhesus monkeys | DIAZEPAM | PSYCHIATRY | NEUROSTEROIDS | RATS | ANTAGONISM | NEUROSCIENCES | GABA(A) RECEPTOR SUBTYPES | NEUROACTIVE STEROID PREGNANOLONE | AMINOBUTYRIC ACID(A) MODULATORS | ANTICONVULSANT TOLERANCE | PHARMACOLOGY & PHARMACY | MIDAZOLAM | Data Interpretation, Statistical | Gonadal Steroid Hormones - pharmacology | Male | Excitatory Amino Acid Antagonists - pharmacology | Macaca mulatta | Dose-Response Relationship, Drug | Isoxazoles - pharmacology | Flumazenil - pharmacology | Reinforcement Schedule | Animals | Pregnanolone - pharmacology | Conditioning, Operant - drug effects | GABA Modulators - pharmacology | Receptors, GABA-A - drug effects | Discrimination (Psychology) - drug effects | Hypnotics and Sedatives - pharmacology | Dizocilpine Maleate - pharmacology | Midazolam - pharmacology | Flunitrazepam - pharmacology | Complications and side effects | Rhesus monkey | Receptors | Physiological aspects | GABA | Dosage and administration | Genetic aspects | Research | Psychotropic drugs | Stimulants | Animal behavior | Monkeys & apes | Psychopharmacology | Barbiturates | benzodiazepines | rhesus monkeys | drug discrimination | pregnanolone
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11. Full Text In vitro antibacterial activity of AZD0914, a new spiropyrimidinetrione DNA gyrase/topoisomerase inhibitor with potent activity against gram-positive, fastidious gram-negative, and atypical bacteria
by Huband, Michael D and Bradford, Patricia A and Otterson, Linda G and Basarab, Gregory S and Kutschke, Amy C and Giacobbe, Robert A and Patey, Sara A and Alm, Richard A and Johnstone, Michele R and Potter, Marie E and Miller, Paul F and Mueller, John P
Antimicrobial Agents and Chemotherapy, ISSN 0066-4804, 01/2015, Volume 59, Issue 1, pp. 467 - 474
AZD0914 is a new spiropyrimidinetrione bacterial DNA gyrase/topoisomerase inhibitor with potent in vitro antibacterial activity against key Gram-positive... 
GYRB MUTATIONS | RESISTANT | GRLA | CEFTRIAXONE | MICROBIOLOGY | PHARMACOLOGY & PHARMACY | STAPHYLOCOCCUS-AUREUS | Microbial Sensitivity Tests | Gram-Negative Bacteria - drug effects | Nucleic Acid Synthesis Inhibitors - pharmacology | Barbiturates - pharmacology | Gram-Positive Bacteria - drug effects | Atypical Bacterial Forms - drug effects | DNA Gyrase - drug effects | Fluoroquinolones - pharmacology | Drug Resistance, Bacterial | Anti-Bacterial Agents - pharmacology | Topoisomerase II Inhibitors - pharmacology | Spiro Compounds - pharmacology | Susceptibility
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12. Full Text Multidrug-resistant Neisseria gonorrhoeae isolates from Nanjing, China, are sensitive to killing by a novel DNA gyrase inhibitor, ETX0914 (AZD0914)
by Su, Xiao-Hong and Wang, Bao-Xi and Le, Wen-Jing and Liu, Yu-Rong and Wan, Chuan and Li, Sai and Alm, Richard A and Mueller, John P and Rice, Peter A
Antimicrobial Agents and Chemotherapy, ISSN 0066-4804, 01/2016, Volume 60, Issue 1, pp. 621 - 623
We tested the activity of ETX0914 against 187 Neisseria gonorrhoeae isolates from men with urethritis in Nanjing, China, in 2013. The MIC50, MIC90, and MIC... 
GUANGZHOU | SWEDEN | CEFTRIAXONE TREATMENT | CEFIXIME | SUSCEPTIBILITY | PHARYNGEAL GONORRHEA | MICROBIOLOGY | PHARMACOLOGY & PHARMACY | IN-VITRO ACTIVITY | TREATMENT FAILURE | Gene Expression | Gonorrhea - microbiology | Neisseria gonorrhoeae - drug effects | Humans | Tetracycline - pharmacology | Urethritis - microbiology | Ciprofloxacin - pharmacology | Ceftriaxone - pharmacology | Male | Topoisomerase II Inhibitors - pharmacology | Neisseria gonorrhoeae - enzymology | Azithromycin - pharmacology | Microbial Sensitivity Tests | DNA Gyrase - metabolism | Neisseria gonorrhoeae - isolation & purification | DNA Gyrase - genetics | Barbiturates - pharmacology | Anti-Bacterial Agents - pharmacology | Drug Resistance, Multiple, Bacterial - genetics | Neisseria gonorrhoeae - genetics | Drug Resistance, Multiple, Bacterial - drug effects | Spiro Compounds - pharmacology
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13. Full Text Discriminative stimulus effects of L-838,417 (7-tert-butyl-3-(2,5-difluoro-phenyl)-6-(2-methyl-2H-[1,2,4]triazol-3-ylmethoxy)-[1,2,4]triazolo[4,3-b]pyridazine): Role of GABA A receptor subtypes
by Licata, Stephanie C and Platt, Donna M and Rüedi-Bettschen, Daniela and Atack, John R and Dawson, Gerard R and Van Linn, Michael L and Cook, James M and Rowlett, James K
Neuropharmacology, ISSN 0028-3908, 2010, Volume 58, Issue 2, pp. 357 - 364
Previous reports suggest that γ-aminobutyric acid type A (GABA ) receptors containing α1 subunits may play a pivotal role in mediating the discriminative... 
Discriminative stimulus | Squirrel monkey | L-838,417 | GABAA receptor | Subjective effects | Benzodiazepine | SQUIRREL-MONKEYS | EFFICACY | RHESUS-MONKEYS | ANTAGONISM | TRIAZOLAM | NEUROSCIENCES | DRUG DISCRIMINATION | ZOLPIDEM | BENZODIAZEPINE SITE LIGANDS | ABUSE | PHARMACOLOGY & PHARMACY | SELECTIVITY | Triazoles - administration & dosage | Catheterization | GABA Modulators - administration & dosage | Saimiri | Fluorobenzenes - administration & dosage | Diazepam - pharmacology | GABA Antagonists - pharmacology | Central Nervous System Depressants - pharmacology | Dose-Response Relationship, Drug | Fluorobenzenes - pharmacology | Neuropsychological Tests | Triazoles - pharmacology | Flumazenil - pharmacology | Ethanol - pharmacology | Animals | Barbiturates - pharmacology | GABA Agonists - pharmacology | GABA Modulators - pharmacology | Discrimination (Psychology) - drug effects | Pyridines - pharmacology | Receptors, GABA-A - metabolism | Carbolines - pharmacology
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14. Full Text In vitro activity of AZD0914, a novel DNA gyrase inhibitor, against Chlamydia trachomatis and Chlamydia pneumoniae
by Kohlhoff, Stephan A and Hub, Michael D and Hammerschlaga, Margaret R
Antimicrobial Agents and Chemotherapy, ISSN 0066-4804, 12/2014, Volume 58, Issue 12, pp. 7595 - 7596
The in vitro activities of AZD0914, levofloxacin, azithromycin, and doxycycline against 10 isolates each of Chlamydia trachomatis and Chlamydia pneumoniae were... 
MICROBIOLOGY | PHARMACOLOGY & PHARMACY | COMMUNITY-ACQUIRED PNEUMONIA | EFFICACY | Chlamydophila pneumoniae - drug effects | Topoisomerase II Inhibitors - pharmacology | Chlamydophila pneumoniae - growth & development | Levofloxacin - pharmacology | Chlamydophila pneumoniae - enzymology | Azithromycin - pharmacology | Chlamydia trachomatis - growth & development | Microbial Sensitivity Tests | DNA Gyrase - metabolism | Barbiturates - pharmacology | Doxycycline - pharmacology | Anti-Bacterial Agents - pharmacology | Chlamydia trachomatis - drug effects | Chlamydia trachomatis - enzymology | Spiro Compounds - pharmacology | Susceptibility
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15. Full Text Numerous classes of general anesthetics inhibit etomidate binding to γ-aminobutyric acid type A (GABAA) receptors
by Li, Guo-Dong and Chiara, David C and Cohen, Jonathan B and Olsen, Richard W
Journal of Biological Chemistry, ISSN 0021-9258, 03/2010, Volume 285, Issue 12, pp. 8615 - 8620
Enhancement of gamma-aminobutyric acid type A receptor (GABA(A)R)-mediated inhibition is a property of most general anesthetics and a candidate for a molecular... 
GLYCINE RECEPTORS | ALCOHOL | SUBTYPES | ISOFLURANE | PHARMACOLOGY | BIOCHEMISTRY & MOLECULAR BIOLOGY | SITES | GATED ION CHANNELS | ACETYLCHOLINE-RECEPTOR | MODULATION | PROPOFOL | Isoflurane - pharmacology | Humans | Propofol - pharmacology | Octanols - pharmacology | Receptors, GABA-A - chemistry | Dose-Response Relationship, Drug | Anesthetics, General | Ethanol - pharmacology | Animals | Barbiturates - pharmacology | Cattle | Allosteric Site | Etomidate - pharmacology | Protein Binding | Binding Sites | Membrane Proteins | Protein Structure and Folding | Ethanol | Protein Drug Interactions | Protein Domains | GABA Receptors | Protein Conformation | Propofol | Barbiturates | Etomidate | Isoflurane
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16. Full Text GABAA receptor pharmacology
by Johnston, G.A.R
Pharmacology and Therapeutics, ISSN 0163-7258, 1996, Volume 69, Issue 3, pp. 173 - 198
γ-Aminobutyric acid (GABA) receptors for the inhibitory neurotransmitter GABA are likely to be found on most, if not all, neurons in the brain and spinal cord.... 
Neuroactive steroids | Barbiturates | GABA receptors | Benzodiazepines | Bicuculline | Receptors, GABA - classification | Receptors, GABA - physiology | Humans | GABA Agonists - pharmacology | GABA Antagonists - pharmacology
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17. Full Text In Vitro antibacterial activity of AZD0914 against human mycoplasmas and ureaplasmas
by Waites, Ken B and Crabb, Donna M and Duffy, Lynn B and Huband, Michael D
Antimicrobial Agents and Chemotherapy, ISSN 0066-4804, 06/2015, Volume 59, Issue 6, pp. 3627 - 3629
In this study, susceptibilities were determined for AZD0914, a spiropyrimidinetrione DNA gyrase inhibitor, azithromycin, doxycycline, and levofloxacin against... 
RESISTANCE | MICROBIOLOGY | PHARMACOLOGY & PHARMACY | DNA GYRASE INHIBITOR | Microbial Sensitivity Tests | Mycoplasma pneumoniae - drug effects | Barbiturates - pharmacology | Humans | Doxycycline - pharmacology | Anti-Bacterial Agents - pharmacology | Ureaplasma - drug effects | Levofloxacin - pharmacology | Mycoplasma genitalium - drug effects | Mycoplasma - drug effects | Spiro Compounds - pharmacology | Azithromycin - pharmacology | Susceptibility
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18. Medicinal chemistry and molecular pharmacology of GABA(C) receptors
by Johnston, Graham A R
Current topics in medicinal chemistry, ISSN 1568-0266, 2002, Volume 2, Issue 8, pp. 903 - 913
GABA(C) receptors belong to the nicotinicoid superfamily of ionotropic receptors that include nicotinic acetylcholine receptors, bicuculline-sensitive GABA(A)... 
Muscimol - pharmacology | Amino Acids, Cyclic - pharmacology | Receptors, GABA - genetics | Crotonates - pharmacology | Imidazoles - pharmacology | GABA Antagonists - pharmacology | Isoxazoles - pharmacology | Animals | Barbiturates - pharmacology | Phosphinic Acids - pharmacology | Receptors, GABA-A - genetics | GABA Agonists - pharmacology | Receptors, GABA-A - drug effects | Organophosphorus Compounds - pharmacology | Pyridines - pharmacology | Receptors, GABA - drug effects
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19. Full Text Inhibition of matrix metalloproteinase‐9 by a barbiturate‐nitrate hybrid ameliorates dextran sulphate sodium‐induced colitis: effect on inflammation‐related genes
by O'Sullivan, Shane and Wang, Jun and Pigott, Maria T and Docherty, Neil and Boyle, Noreen and Lis, Samuel Kana and Gilmer, John F and Medina, Carlos
British Journal of Pharmacology, ISSN 0007-1188, 04/2017, Volume 174, Issue 7, pp. 512 - 524
Background and Purpose Matrix metalloproteinase‐9 (MMP‐9) is up‐regulated in ulcerative colitis and implicated in the pathology of the disease. In this study,... 
COLON-CANCER | CROHNS-DISEASE | CONCISE GUIDE | PHARMACOLOGY | ULCERATIVE-COLITIS | RECEPTOR | PHARMACOLOGY & PHARMACY | PHOSPHOLIPASE A | MICE | EXPRESSION | BOWEL-DISEASE | Dextran Sulfate - pharmacology | Inflammation - pathology | Rats, Wistar | Colitis - genetics | Enzyme Inhibitors - pharmacology | Nitrates - pharmacology | Rats | Anti-Inflammatory Agents, Non-Steroidal - chemistry | Male | Nitrates - administration & dosage | Anti-Inflammatory Agents, Non-Steroidal - pharmacology | Matrix Metalloproteinase 9 - metabolism | Animals | Barbiturates - pharmacology | Inflammation - drug therapy | Matrix Metalloproteinase 9 - genetics | Colitis - chemically induced | Enzyme Inhibitors - chemistry | Inflammation - genetics | Colitis - drug therapy | Dextran Sulfate - administration & dosage | Barbiturates - administration & dosage | Disease Models, Animal | Animal experimentation | Dextran | Nitric oxide | Analysis | Genes | Genetic research | Inflammation | Gene expression | Ulcerative colitis | Drugs | Inflammatory bowel disease | Colon | Rodents | Research Papers | Research Paper
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