메뉴 건너뛰기




Volumn 16, Issue 2, 2008, Pages 783-793

Synthesis, in vitro characterization, and radiolabeling of reboxetine analogs as potential PET radioligands for imaging the norepinephrine transporter

Author keywords

(S, S)Reboxetine analogs; Carbon 11; Fluorine 18; Norepinephrine transporter; Positron Emission Tomography

Indexed keywords

2 [ALPHA(2 METHOXYPHENYLTHIO)PHENYLMETHYL]MORPHOLINE C 11; 2 [ALPHA[2 (2 FLUOROETHOXY)PHENYLTHIO]BENZYL]MORPHOLINE F 18; 2 [ALPHA[2 (3 FLUOROPROPOXY)PHENYLTHIO]BENZYL]MORPHOLINE F 18; 2 [ALPHA[2 (CARBOMETHOXY)PHENOXY]BENZYL]MORPHOLINE C 11; 2 [ALPHA[2 (CARBOMETHOXY)PHENYLTHIO]BENZYL]MORPHOLINE C 11; 2 [ALPHA[2 (METHYLTHIO)PHENOXY]BENZYL]MORPHOLINE C 11; 3BETA (4 IODOPHENYL) 2BETA TROPANECARBOXYLIC ACID METHYL ESTER; CARBON 11; CITALOPRAM; DOPAMINE TRANSPORTER; FLUORINE 18; FLUORINE DERIVATIVE; FLUOROETHYLBROSYLATE F 18; FLUOROPROPYLBROSYLATE F 18; IODINE 125; NISOXETINE; NORADRENALIN TRANSPORTER; RADIOLIGAND; REBOXETINE; SEROTONIN TRANSPORTER; TRITIUM; UNCLASSIFIED DRUG;

EID: 38549120307     PISSN: 09680896     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmc.2007.10.025     Document Type: Article
Times cited : (17)

References (33)
  • 22
    • 38549140214 scopus 로고    scopus 로고
    • note
    • In a paper, see Ref. 25, J. Boot et al., reported that the racemic mixture of compound 3 containing (S, S) and (R,R) enantiomers was prepared and resolved using chiral HPLC. One enantiomer was found to be potent and selective toward NET, whereas the opposite enantiomer was potent for both the NET and SERT. However, the assignment of absolute stereochemistry of resolved enantiomers was not reported in this paper.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.