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1-(1-Phenethylpiperidin-4-yl)-1-phenylethanols as Potent and Highly Selective 5-HT2A Antagonists
1-(1-Phenethylpiperidin-4-yl)-1-phenylethanols as Potent and Highly Selective 5-HT2A Antagonists
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1-(1-Phenethylpiperidin-4-yl)-1-phenylethanols as Potent and Highly Selective 5-HT2A Antagonists

Heinrich, Timo ; Böttcher, Henning ; Prücher, Helmut ; Gottschlich, Rudolf ; Ackermann, Karl-August ; van Amsterdam, Christoph

ChemMedChem, 2006-02, Vol.1 (2), p.245-255 [Periódico revisado por pares]

Weinheim: WILEY-VCH Verlag

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2
[1-13C]Galactose Breath Test for Quantitative Measurement of Liver Function in a Short Period
[1-13C]Galactose Breath Test for Quantitative Measurement of Liver Function in a Short Period
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[1-13C]Galactose Breath Test for Quantitative Measurement of Liver Function in a Short Period

Suzuki, Shigeru ; Ishii, Yukimoto ; Asai, Satoshi ; Kohno, Tadashi ; Mazaki, Takerou ; Takahashi, Yasuo ; Iwai, Shigetomi ; Ishikawa, Koichi

Digestion, 2000, Vol.62 (2-3), p.194-199 [Periódico revisado por pares]

Basel, Switzerland: Karger

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3
1-[2-(1-Cyclobutylpiperidin-4-yloxy)-6,7-dihydro-4H-thiazolo[5,4-c]pyridin-5-yl]propan-1-one: a Histamine H 3 Receptor Inverse Agonist with Efficacy in Animal Models of Cognition
1-[2-(1-Cyclobutylpiperidin-4-yloxy)-6,7-dihydro-4H-thiazolo[5,4-c]pyridin-5-yl]propan-1-one: a Histamine H 3 Receptor Inverse Agonist with Efficacy in Animal Models of Cognition
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1-[2-(1-Cyclobutylpiperidin-4-yloxy)-6,7-dihydro-4H-thiazolo[5,4-c]pyridin-5-yl]propan-1-one: a Histamine H 3 Receptor Inverse Agonist with Efficacy in Animal Models of Cognition

Shinde, Anil Karbhari ; Badange, Rajesh Kumar ; Reballi, Veena ; Achanta, Pramod Kumar ; Bojja, Kumar ; Manchineella, Sravanthi ; Rao Muddana, Nageswara ; Subramanian, Ramkumar ; Choudary Palacharla, Raghava ; Benade, Vijay ; Jayarajan, Pradeep ; Thentu, Jagadeesh Babu ; Lingavarapu, Bujji Babu ; Yarra, Sivasekhar ; Kagita, Narendra ; Rao Doguparthi, Mallikarjuna ; Mohammed, Abdul Rasheed ; Nirogi, Ramakrishna

ChemMedChem, 2022-02, Vol.17 (3), p.e202100583 [Periódico revisado por pares]

Germany

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1-[2-(4-Benzyloxyphenoxy)Ethyl]Imidazole inhibits monoamine oxidase B and protects against neuronal loss and behavioral impairment in rodent models of Parkinson's disease
1-[2-(4-Benzyloxyphenoxy)Ethyl]Imidazole inhibits monoamine oxidase B and protects against neuronal loss and behavioral impairment in rodent models of Parkinson's disease
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1-[2-(4-Benzyloxyphenoxy)Ethyl]Imidazole inhibits monoamine oxidase B and protects against neuronal loss and behavioral impairment in rodent models of Parkinson's disease

Chung, Jin Yong ; Lee, Ji Won ; Ryu, Choon Ho ; Min, Hye Kyung ; Yoon, Yeo Jin ; Lim, Mi Jung ; Park, Cheol Hyoung

Journal of neuroscience research, 2015-08, Vol.93 (8), p.1267-1278 [Periódico revisado por pares]

United States: Blackwell Publishing Ltd

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5
1, 2-Dihydroisoquinoline-N-acetic Acid Derivatives as New Carriers for Brain-specific Delivery II: Delivery of Phenethylamine as Model Drug
1, 2-Dihydroisoquinoline-N-acetic Acid Derivatives as New Carriers for Brain-specific Delivery II: Delivery of Phenethylamine as Model Drug
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1, 2-Dihydroisoquinoline-N-acetic Acid Derivatives as New Carriers for Brain-specific Delivery II: Delivery of Phenethylamine as Model Drug

Mahmoud, Sahar ; Sheha, Mahmoud ; Aboul-Fadl, Tarek ; Farag, Hassan

Archiv der Pharmazie (Weinheim), 2003-07, Vol.336 (4-5), p.258-263 [Periódico revisado por pares]

Weinheim: WILEY-VCH Verlag

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6
(+/-)-1-(2,5-Dimethoxy-4-ethylthiophenyl)-2-aminopropane (ALEPH-2), a novel putative anxiolytic agent lacking affinity for benzodiazepine sites and serotonin-1A receptors
(+/-)-1-(2,5-Dimethoxy-4-ethylthiophenyl)-2-aminopropane (ALEPH-2), a novel putative anxiolytic agent lacking affinity for benzodiazepine sites and serotonin-1A receptors
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(+/-)-1-(2,5-Dimethoxy-4-ethylthiophenyl)-2-aminopropane (ALEPH-2), a novel putative anxiolytic agent lacking affinity for benzodiazepine sites and serotonin-1A receptors

Reyes-Parada, M ; Scorza, C ; Romero, V ; Silveira, R ; Medina, J H ; Andrus, D ; Nichols, D E ; Cassels, B K

Naunyn-Schmiedeberg's archives of pharmacology, 1996-11, Vol.354 (5), p.579 [Periódico revisado por pares]

Germany

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7
1,1-Dichloroethylene: An Apoptotic Hepatotoxin?
1,1-Dichloroethylene: An Apoptotic Hepatotoxin?
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1,1-Dichloroethylene: An Apoptotic Hepatotoxin?

Reynolds, Edward S. ; Kanz, Mary Faggard ; Chieco, Pasquale ; Moslen, Mary Treinen

Environmental health perspectives, 1984-08, Vol.57, p.313-320 [Periódico revisado por pares]

United States: National Institute of Environmental Health Sciences. National Institutes of Health. Department of Health, Education and Welfare

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8
1,1-Dichloroethylene hepatotoxicity: proposed mechanism of action and distribution and binding of 14C radioactivity following inhalation exposure in rats
1,1-Dichloroethylene hepatotoxicity: proposed mechanism of action and distribution and binding of 14C radioactivity following inhalation exposure in rats
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1,1-Dichloroethylene hepatotoxicity: proposed mechanism of action and distribution and binding of 14C radioactivity following inhalation exposure in rats

Jaeger, R J ; Shoner, L G ; Coffman, L

Environmental health perspectives, 1977-12, Vol.21, p.113-119 [Periódico revisado por pares]

United States

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9
1,10-Phenanthroline stimulates internucleosomal DNA fragmentation in isolated rat-liver nuclei by promoting the redox activity of endogenous copper ions
1,10-Phenanthroline stimulates internucleosomal DNA fragmentation in isolated rat-liver nuclei by promoting the redox activity of endogenous copper ions
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1,10-Phenanthroline stimulates internucleosomal DNA fragmentation in isolated rat-liver nuclei by promoting the redox activity of endogenous copper ions

Burkitt, M J ; Milne, L ; Nicotera, P ; Orrenius, S

Biochemical journal, 1996-01, Vol.313 ( Pt 1) (1), p.163-169 [Periódico revisado por pares]

England

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10
1,1,1,2,3,4,4,5,5,5-Decafluoropentane (HFC-4310mee)
1,1,1,2,3,4,4,5,5,5-Decafluoropentane (HFC-4310mee)
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1,1,1,2,3,4,4,5,5,5-Decafluoropentane (HFC-4310mee)

Toxicology and industrial health, 2021-08, Vol.37 (8), p.441-450 [Periódico revisado por pares]

London, England: SAGE Publications

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