Synthesis of a radoilabeled type A cholecystokinin receptor antagonist, (R)-N-pentyl-N-(4,5-di[3H]pentyl)N(α)-(3-quinolinoyl)glutamic acid amide

Journal of Labelled Compounds and Radiopharmaceuticals

Volumn 43, Issue 1, 2000, Pages 77-90

  Malone, Justin A ^a   Reidelberger, Roger D ^b,c   Hulce, Martin ^a,b  

^a CREIGHTON UNIVERSITY   (United States)

^b CREIGHTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c VA NEBRASKA WESTERN IOWA HEALTH CARE SYSTEM   (United States)

Author keywords

3H; Amide coupling; Benzodiazepinone; CCK(A) antagonist; Cholecystokinin

Indexed keywords

AMINO ACIDS; DICHLOROMETHANE;

3H; AMIDE COUPLINGS; AMINO MOIETY; BENZODIAZEPINONE; CCK(A) ANTAGONIST; CHOLECYSTOKININ; DEPROTECTION; GLUTAMIC ACID; RECEPTOR ANTAGONISTS; TRITIATION;

AMIDES;

CARBOXYLIC ACID DERIVATIVE; CHOLECYSTOKININ RECEPTOR BLOCKING AGENT; DICHLOROMETHANE; GLUTAMIC ACID DERIVATIVE; N (3 QUINOLYLCARBONYL) DEXTRO GLUTAMIC ACID ALPHA DIPENTYLAMIDE; PENTYLAMINE;

ARTICLE; DRUG SYNTHESIS; TITRIMETRY;

EID: 0033966323     PISSN: 03624803     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1099-1344(200001)43:1<77::AID-JLCR292>3.0.CO;2-V     Document Type: Article

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