Matches in SemOpenAlex for { <https://semopenalex.org/work/W2027489671> ?p ?o ?g. }
- W2027489671 endingPage "4265" @default.
- W2027489671 startingPage "4254" @default.
- W2027489671 abstract "A series of N,N-dimethylated and N-monomethylated analogues of N,N-dimethyl-2-(2‘-amino-4‘-iodophenylthio)benzylamine substituted at the 4‘-phenyl position have been prepared and evaluated in vitro for serotonin transporter (SERT) selectivity. Several derivatives were prepared where the 4‘-position was either unsubstituted 13 and 33a or substituted with methyl 14a and 33b, ethenyl 14b and 34, ethyl 16 and 35, hydroxymethyl 20 and 41, hydroxyethyl 22, fluoroethyl 23, hydroxypropyl 27, and fluoropropyl 28. Competition binding in cells stably expressing the transfected human SERT, dopamine transporter (DAT), and norepinephrine transporter (NET) using [3H]citalopram, [3H]WIN 35,428 or [125I]RTI-55, and [3H]nisoxetine, respectively, demonstrated the following order of SERT affinity (Ki (nM)): 14a (0.25) > 16 (0.49) > 20 (0.57) > 14b (1.12) > 13 (1.59) > 33b (1.94) = 35 (2.04) ≫ 23 (8.50) = 28 (8.55) > 41 (15.11) ≫ 22 (51) > 33a (83.43) > 27 (92). The Ki values revealed that most of these derivatives displayed a high affinity for the SERT and a high selectivity over the DAT and NET. Moreover, substitution at the 4‘-position of the dimethylated and monomethylated benzylamines differently influenced SERT binding: (i) the dimethylated benzylamines exhibited higher SERT affinity than the monomethylated ones, (ii) alkyl, alkenyl, or hydroxymethyl functions at the 4‘-position afford compounds with high SERT affinity, and (iii) ω-hydroxy and fluoro-substituted ethyl and propyl groups at the 4‘-position decrease the SERT affinity. From this series, the dimethylated derivatives 13, 14a, 14b, 16, and 20 were radiolabeled with carbon-11 and their log P7.4 was calculated as a measure of their potential brain penetrance as positron emission tomography SERT imaging agents." @default.
- W2027489671 created "2016-06-24" @default.
- W2027489671 creator A5036023937 @default.
- W2027489671 creator A5059332651 @default.
- W2027489671 creator A5061471861 @default.
- W2027489671 creator A5086662895 @default.
- W2027489671 date "2005-06-01" @default.
- W2027489671 modified "2023-10-03" @default.
- W2027489671 title "Synthesis, in Vitro Characterization, and Radiolabeling of <i>N</i>,<i>N</i>-Dimethyl-2-(2‘-amino-4‘-substituted-phenylthio)benzylamines: Potential Candidates as Selective Serotonin Transporter Radioligands" @default.
- W2027489671 cites W1894736765 @default.
- W2027489671 cites W1982062983 @default.
- W2027489671 cites W1983638695 @default.
- W2027489671 cites W1986191934 @default.
- W2027489671 cites W1987330182 @default.
- W2027489671 cites W1990463755 @default.
- W2027489671 cites W1994406190 @default.
- W2027489671 cites W2000773787 @default.
- W2027489671 cites W2015793090 @default.
- W2027489671 cites W2018345883 @default.
- W2027489671 cites W2024308090 @default.
- W2027489671 cites W2035920757 @default.
- W2027489671 cites W2040844577 @default.
- W2027489671 cites W2041158481 @default.
- W2027489671 cites W2050448984 @default.
- W2027489671 cites W2051541361 @default.
- W2027489671 cites W2063089234 @default.
- W2027489671 cites W2076823265 @default.
- W2027489671 cites W2082916779 @default.
- W2027489671 cites W2094566937 @default.
- W2027489671 cites W2106193331 @default.
- W2027489671 cites W2133746049 @default.
- W2027489671 cites W2169396775 @default.
- W2027489671 cites W4236296817 @default.
- W2027489671 doi "https://doi.org/10.1021/jm050079o" @default.
- W2027489671 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/15974579" @default.
- W2027489671 hasPublicationYear "2005" @default.
- W2027489671 type Work @default.
- W2027489671 sameAs 2027489671 @default.
- W2027489671 citedByCount "24" @default.
- W2027489671 countsByYear W20274896712012 @default.
- W2027489671 countsByYear W20274896712013 @default.
- W2027489671 countsByYear W20274896712015 @default.
- W2027489671 countsByYear W20274896712017 @default.
- W2027489671 countsByYear W20274896712018 @default.
- W2027489671 countsByYear W20274896712019 @default.
- W2027489671 countsByYear W20274896712020 @default.
- W2027489671 countsByYear W20274896712022 @default.
- W2027489671 countsByYear W20274896712023 @default.
- W2027489671 crossrefType "journal-article" @default.
- W2027489671 hasAuthorship W2027489671A5036023937 @default.
- W2027489671 hasAuthorship W2027489671A5059332651 @default.
- W2027489671 hasAuthorship W2027489671A5061471861 @default.
- W2027489671 hasAuthorship W2027489671A5086662895 @default.
- W2027489671 hasConcept C104317684 @default.
- W2027489671 hasConcept C118792377 @default.
- W2027489671 hasConcept C149011108 @default.
- W2027489671 hasConcept C155647269 @default.
- W2027489671 hasConcept C161790260 @default.
- W2027489671 hasConcept C170493617 @default.
- W2027489671 hasConcept C176233148 @default.
- W2027489671 hasConcept C185592680 @default.
- W2027489671 hasConcept C2775864247 @default.
- W2027489671 hasConcept C2776276205 @default.
- W2027489671 hasConcept C2776755682 @default.
- W2027489671 hasConcept C2778897192 @default.
- W2027489671 hasConcept C2780591741 @default.
- W2027489671 hasConcept C55493867 @default.
- W2027489671 hasConcept C71240020 @default.
- W2027489671 hasConceptScore W2027489671C104317684 @default.
- W2027489671 hasConceptScore W2027489671C118792377 @default.
- W2027489671 hasConceptScore W2027489671C149011108 @default.
- W2027489671 hasConceptScore W2027489671C155647269 @default.
- W2027489671 hasConceptScore W2027489671C161790260 @default.
- W2027489671 hasConceptScore W2027489671C170493617 @default.
- W2027489671 hasConceptScore W2027489671C176233148 @default.
- W2027489671 hasConceptScore W2027489671C185592680 @default.
- W2027489671 hasConceptScore W2027489671C2775864247 @default.
- W2027489671 hasConceptScore W2027489671C2776276205 @default.
- W2027489671 hasConceptScore W2027489671C2776755682 @default.
- W2027489671 hasConceptScore W2027489671C2778897192 @default.
- W2027489671 hasConceptScore W2027489671C2780591741 @default.
- W2027489671 hasConceptScore W2027489671C55493867 @default.
- W2027489671 hasConceptScore W2027489671C71240020 @default.
- W2027489671 hasIssue "13" @default.
- W2027489671 hasLocation W20274896711 @default.
- W2027489671 hasLocation W20274896712 @default.
- W2027489671 hasOpenAccess W2027489671 @default.
- W2027489671 hasPrimaryLocation W20274896711 @default.
- W2027489671 hasRelatedWork W118528465 @default.
- W2027489671 hasRelatedWork W1965493970 @default.
- W2027489671 hasRelatedWork W1986443065 @default.
- W2027489671 hasRelatedWork W2019719355 @default.
- W2027489671 hasRelatedWork W2033548057 @default.
- W2027489671 hasRelatedWork W2039765983 @default.
- W2027489671 hasRelatedWork W2078892911 @default.
- W2027489671 hasRelatedWork W2079507733 @default.
- W2027489671 hasRelatedWork W2174099922 @default.
- W2027489671 hasRelatedWork W2950644251 @default.