Thomas M Keck

researcher

Thomas M Keck is …
instance of (P31):
humanQ5

External links are
P6178Dimensions author ID01360436762.35
P496ORCID iD0000-0003-1845-9373
P1053ResearcherIDG-9798-2012
P1153Scopus author ID14825230800

P69educated atUniversity of Southern CaliforniaQ4614
Oregon Health & Science UniversityQ282097
P108employerUCLA David Geffen School of MedicineQ842165
Rowan UniversityQ1799872
National Institute on Drug AbuseQ6973751
P735given nameThomasQ16428906
ThomasQ16428906
P106occupationresearcherQ1650915
P21sex or gendermaleQ6581097

Reverse relations

author (P50)
Q41444993A Novel Class of Dopamine D4 Receptor Ligands Bearing an Imidazoline Nucleus
Q37617118A novel mGluR5 antagonist, MFZ 10-7, inhibits cocaine-taking and cocaine-seeking behavior in rats
Q28828620Beyond small-molecule SAR: using the dopamine D3 receptor crystal structure to guide drug design
Q33768527Chiral Resolution and Serendipitous Fluorination Reaction for the Selective Dopamine D3 Receptor Antagonist BAK2-66
Q93333645Discovery, Optimization and Characterization of ML417: A Novel and Highly Selective D3 Dopamine Receptor Agonist
Q64080830Dopamine D Receptor-Selective Compounds Reveal Structure-Activity Relationships that Engender Agonist Efficacy
Q44805749Dopamine D4 receptor deficiency in mice alters behavioral responses to anxiogenic stimuli and the psychostimulant methylphenidate.
Q34314041Fenobam sulfate inhibits cocaine-taking and cocaine-seeking behavior in rats: implications for addiction treatment in humans.
Q37077658High Affinity Dopamine D3 Receptor (D3R)-Selective Antagonists Attenuate Heroin Self-Administration in Wild-Type but not D3R Knockout Mice.
Q40955120Highly Selective Dopamine D3 Receptor (D3R) Antagonists and Partial Agonists Based on Eticlopride and the D3R Crystal Structure: New Leads for Opioid Dependence Treatment.
Q90889342Multitarget 1,4-Dioxane Compounds Combining Favorable D2-like and 5-HT1A Receptor Interactions with Potential for the Treatment of Parkinson's Disease or Schizophrenia
Q37025051Novel Analogues of (R)-5-(Methylamino)-5,6-dihydro-4H-imidazo[4,5,1-ij]quinolin-2(1H)-one (Sumanirole) Provide Clues to Dopamine D2/D3 Receptor Agonist Selectivity
Q48252285Synthesis and Pharmacological Characterization of Novel trans-Cyclopropylmethyl-Linked Bivalent Ligands That Exhibit Selectivity and Allosteric Pharmacology at the Dopamine D3 Receptor (D3R).
Q47390221The replacement of the 2-methoxy substituent of N-((6,6-diphenyl-1,4-dioxan-2-yl)methyl)-2-(2-methoxyphenoxy)ethan-1-amine improves the selectivity for 5-HT1A receptor over α1-adrenoceptor and D2-like receptor subtypes
Q48145124Toward Understanding the Structural Basis of Partial Agonism at the Dopamine D3 Receptor
Q34435684Tranylcypromine substituted cis-hydroxycyclobutylnaphthamides as potent and selective dopamine D₃ receptor antagonists.
Q35554948Using click chemistry toward novel 1,2,3-triazole-linked dopamine D3 receptor ligands

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