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Bioorganic & Medicinal Chemistry Letters|August 2, 2015
Re-exploring the N-phenylpicolinamide derivatives to develop mGlu4 ligands with improved affinity and in vitro microsomal stabilityZhaoda Zhang, Kun-Eek Kil, Pekka Poutiainen, et al.
Molecular Pharmacology|May 23, 2003
3,4-methylenedioxymethamphetamine (MDMA, "Ecstasy") induces fenfluramine-like proliferative actions on human cardiac valvular interstitial cells in vitroVincent Setola, Sandra J Hufeisen, K Jane Grande-Allen, et al.
Plos One|July 7, 2011
Securinine, a myeloid differentiation agent with therapeutic potential for AMLKalpana Gupta, Amitabha Chakrabarti, Sonia Rana, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|June 5, 2009
PSD-95 is essential for hallucinogen and atypical antipsychotic drug actions at serotonin receptorsAtheir I Abbas, Prem N Yadav, Wei-Dong Yao, et al.
Bioorganic & Medicinal Chemistry|July 4, 2008
Identification of a butyrophenone analog as a potential atypical antipsychotic agent: 4-[4-(4-chlorophenyl)-1,4-diazepan-1-yl]-1-(4-fluorophenyl)butan-1-oneSeth Y Ablordeppey, Ramazan Altundas, Barbara Bricker, et al.
Nature Structural & Molecular Biology|April 21, 2015
PRESTO-Tango as an open-source resource for interrogation of the druggable human GPCRomeWesley K Kroeze, Maria F Sassano, Xi-Ping Huang, et al.
Nature Neuroscience|December 7, 2010
Transient neuronal inhibition reveals opposing roles of indirect and direct pathways in sensitizationSusan M Ferguson, Daniel Eskenazi, Masago Ishikawa, et al.
ACS Medicinal Chemistry Letters|July 11, 2012
Rational Drug Design Leading to the Identification of a Potent 5-HT(2C) Agonist Lacking 5-HT(2B) ActivityGang Chen, Sung Jin Cho, Xi-Ping Huang, et al.
Biochemistry|June 15, 2005
Identification of the molecular mechanisms by which the diterpenoid salvinorin A binds to kappa-opioid receptorsFeng Yan, Philip D Mosier, Richard B Westkaemper, et al.
The Journal of Pharmacology and Experimental Therapeutics|March 22, 2003
L-homocysteine sulfinic acid and other acidic homocysteine derivatives are potent and selective metabotropic glutamate receptor agonistsQi Shi, Jason E Savage, Sandra J Hufeisen, et al.
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