P. J. Ham - Concepedia

Author

P. J. Ham

London School of Hygiene & Tropical Medicine

Also Known As

J Franklin, P J Ham, P. HAM, P. Ham, P. J. HAM, P. J. Ham, P.J. HAM, P.J. Ham, PETER J. HAM, Peter Ham

Publications

1.7K

Citations

H-Index

Concepts

All Affiliations

London School of Hygiene & Tropical Medicine University of London New Frontier Keele University Molecular Discovery (United Kingdom)

About

P. J. Ham is an author at London School of Hygiene & Tropical Medicine specializing in natural sciences, medicine, and biochemistry.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	15	20	766
2	Natural Sciences	15	16	616
3	Engineering	5	5	98
4	Education	1	1	25
5	Health Sciences	1	1	11

P. J. Ham

Publications

1.6K

Citations

H-Index

Page 1

	Year	Citations
<i>In vitro</i>and<i>in vivo</i>profile of SB 206553, a potent 5‐HT<sub>2C</sub>/5‐HT<sub>2B</sub>receptor antagonist with anxiolytic‐like properties G.A. Kennett, Martyn Wood, Fiona Bright, British Journal of Pharmacology	1996	240
Purification of an insect defensin from the mosquito, Aedes aegypti R. Chalk, H. Townson, Shunji Natori, Insect Biochemistry and Molecular Biology BiologyInsect VirusMedicineEntomologyMalaria	1994	85
6-Chloro-5-methyl-1-[[2-[(2-methyl-3- pyridyl)oxy]-5-pyridyl]carbamoyl]indoline (SB-242084): The First Selective and Brain Penetrant 5-HT<sub>2C</sub> Receptor Antagonist Steven M. Bromidge, Malcolm Duckworth, Ian T. Forbes, Journal of Medicinal Chemistry Altmetric Attention ScorePharmacotherapyChemical BiologyExperimental PharmacologyPharmaceutical Chemistry	1997	84
The Selective 5-HT<sub>1B</sub>Receptor Inverse Agonist 1‘-Methyl-5-[[2‘-methyl-4‘- (5-methyl-1,2,4-oxadiazol-3-yl)biphenyl-4-yl]carbonyl]-2,3,6,7-tetrahydro- spiro[furo[2,3-<i>f</i>]indole-3,4‘-piperidine] (SB-224289) Potently Blocks Terminal 5-HT Autoreceptor Function Both in Vitro and in Vivo Laramie M. Gaster, Frank E. Blaney, Susannah Davies, Journal of Medicinal Chemistry	1998	81
Biarylcarbamoylindolines Are Novel and Selective 5-HT<sub>2C</sub> Receptor Inverse Agonists: Identification of 5-Methyl-1-[[2-[(2-methyl-3-pyridyl)oxy]- 5-pyridyl]carbamoyl]-6-trifluoromethylindoline (SB-243213) as a Potential Antidepressant/Anxiolytic Agent Steven M. Bromidge, Steven Dabbs, David T. Davies, Journal of Medicinal Chemistry Potential Antidepressant/anxiolytic AgentPsychotropic MedicationInverse AgonistsPharmacotherapyNew Series	2000	79
N-(1-Methyl-5-indolyl)-N'-(3-pyridyl)urea hydrochloride: the first selective 5-HT1C receptor antagonist Ian T. Forbes, G.A. Kennett, Angela Gadre, Journal of Medicinal Chemistry Drug TargetAltmetric Attention ScorePeptide SciencePharmacotherapyPharmaceutical Chemistry	1993	67
Brugia pahangi: The Effects of Cecropins on Microfilariae in Vitro and in Aedes aegypti R. Chalk, H. Townson, P. J. Ham Experimental Parasitology BiologyBrugia PahangiAedes AegyptiMicrobiologyMedicine	1995	66
Novel and Selective 5-HT<sub>2C/2B</sub> Receptor Antagonists as Potential Anxiolytic Agents: Synthesis, Quantitative Structure−Activity Relationships, and Molecular Modeling of Substituted 1-(3-Pyridylcarbamoyl)indolines Steven M. Bromidge, Steven Dabbs, David T. Davies, Journal of Medicinal Chemistry Biological ActivityMolecular PharmacologyMedicinal ChemistryPotential Anxiolytic AgentsBiochemistry	1998	64
5-Methyl-1-(3-pyridylcarbamoyl)-1,2,3,5-tetrahydropyrrolo[2,3-f]indole: A Novel 5-HT2C/5-HT2B Receptor Antagonist with Improved Affinity, Selectivity, and Oral Activity Ian T. Forbes, P. J. Ham, Deborah H. Booth, Journal of Medicinal Chemistry Medicinal ChemistryBiochemistryImproved AffinityMedicineDrug Discovery	1995	61
An improved technique for the cryopreservation of <i>Onchocerca</i> microfilariae P. J. Ham, Simon Townson, Eric R. James, Parasitology	1981	58

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