Browsing by Author Yamamoto, Izumi

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Issue DateTitleAuthor(s)Citation
2011Agonist responses of (R)- and (S)-3-fluoro-??-aminobutyric acids suggest an enantiomeric fold for GABA binding to GABA(C) receptorsCollins (Chebib), Mary; Gavande, Navnath; Johnston, Graham; Yamamoto, Izumi; Deniau, Gildas; O'Hagan, David; Pharmacy; Pharmacy; School of Medical Sciences: Pharmacology; PharmacyAgonist responses of (R)- and (S)-3-fluoro-??-aminobutyric acids suggest an enantiomeric fold for GABA binding to GABA(C) receptors, Chemical Communications, vol.47, 28, 2011,pp 7956-7958
2012Differentiating Enantioselective Actions of GABOB: A Possible Role for Threonine 244 in the Binding Site of GABAC rho1 ReceptorsAbsalom, Nathan Luke; Carland, Jane; Collins, Mary; Doddareddy, Munikumar; Gavande, Navnath; Hanrahan, Jane; Johnston, Graham; Yamamoto, Izumi; Pharmacy; School of Medical Sciences: Pharmacology; Pharmacy; School of Medical Sciences: Brain and Mind Centre; Pharmacy; Pharmacy; School of Medical Sciences: Pharmacology; PharmacyDifferentiating Enantioselective Actions of GABOB: A Possible Role for Threonine 244 in the Binding Site of GABAC rho1 Receptors, ACS Chemical Neuroscience, vol.3, 9, 2012,pp 665-673
2012The enantiomers of syn-2,3-difluoro-4-aminobutyric acid elicit opposite responses at the GABA(C) receptorCollins (Chebib), Mary; Doddareddy, Munikumar; Gavande, Navnath; Hunter, Luke; Jordan, Meredith; Yamamoto, Izumi; Pharmacy; Brand Management; Pharmacy; Chemistry; Chemistry; PharmacyThe enantiomers of syn-2,3-difluoro-4-aminobutyric acid elicit opposite responses at the GABA(C) receptor, Chemical Communications, vol.48, 6, 2012,pp 829-831
2011Medicinal Chemistry of p GABAc ReceptorsCollins (Chebib), Mary; Gavande, Navnath; Hanrahan, Jane; Johnston, Graham; Kim, Hye-Lim; Kumar, Rohan; Mewett, Kenneth; Ng, Clarissa; Yamamoto, Izumi; Pharmacy; Pharmacy; Pharmacy; School of Medical Sciences: Pharmacology; Pharmacy; Pharmacy; School of Medical Sciences: Pharmacology; Pharmacy; PharmacyMedicinal Chemistry of p GABAc Receptors, Future Medicinal Chemistry, vol.3, 2, 2011,pp 197-209
2011Novel Cyclic Phosphinic Acids as GABAC F Receptor Antagonists: Design, Synthesis, and PharmacologyBurden, Peter; Collins (Chebib), Mary; Gavande, Navnath; Hanrahan, Jane; Johnston, Graham; Tu-Hoa, Ai; Yamamoto, Izumi; Salam, Noeris; School of Medical Sciences: Pharmacology; Pharmacy; Pharmacy; Pharmacy; School of Medical Sciences: Pharmacology; School of Medical Sciences: Pharmacology; PharmacyNovel Cyclic Phosphinic Acids as GABAC F Receptor Antagonists: Design, Synthesis, and Pharmacology, A C S Medicinal Chemistry Letters, vol.2, N/A, 2011,pp 11-16
2015Probing the Mode of Neurotransmitter Binding to GABA Receptors Using Selectively Fluorinated GABA AnaloguesAbsalom, Nathan Luke; Collins, Mary; Yamamoto, Izumi; Hunter, Luke; O'Hagan, David; Pharmacy; Pharmacy; PharmacyProbing the Mode of Neurotransmitter Binding to GABA Receptors Using Selectively Fluorinated GABA Analogues, Australian Journal of Chemistry: an international journal for chemical science, vol.68, 1, 2015,pp 23-30
2012Structurally Diverse GABA Antagonists Interact Differently with Open and Closed Conformational States of the p1 ReceptorAbsalom, Nathan; Allan, Robin; Carland, Jane; Collins (Chebib), Mary; Gavande, Navnath; Hanrahan, Jane; Johnston, Graham; Locock, Katherine; Yamamoto, Izumi; Pharmacy; School of Medical Sciences: Pharmacology; Pharmacy; Pharmacy; Pharmacy; Pharmacy; School of Medical Sciences: Pharmacology; School of Medical Sciences: Pharmacology; PharmacyStructurally Diverse GABA Antagonists Interact Differently with Open and Closed Conformational States of the p1 Receptor, ACS Chemical Neuroscience, vol.3, 4, 2012,pp 293-301
2013γ-Aminobutyric Acid(C) (GABAC) Selective Antagonists Derived from the Bioisosteric Modification of 4-Aminocyclopent-1-enecarboxylic Acid: Amides and HydroxamatesAllan, Robin; Collins (Chebib), Mary; Hanrahan, Jane; Johnston, Graham; Locock, Katherine; Tran, Priscilla; Yamamoto, Izumi; School of Medical Sciences: Pharmacology; Pharmacy; Pharmacy; School of Medical Sciences: Pharmacology; School of Medical Sciences: Pharmacology; School of Medical Sciences: Pharmacology; Pharmacyγ-Aminobutyric Acid(C) (GABAC) Selective Antagonists Derived from the Bioisosteric Modification of 4-Aminocyclopent-1-enecarboxylic Acid: Amides and Hydroxamates, Journal of Medicinal Chemistry, vol.56, 13, 2013,pp 5626-5630