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Volumn 15, Issue 6, 2005, Pages 1583-1586

Synthesis and in vitro biological evaluation of a carbon glycoside analogue of morphine-6-glucuronide

Author keywords

Morphine; Morphine 6 glucuronide; Pain

Indexed keywords

AMINE; BENZYL DERIVATIVE; CARBOHYDRATE DERIVATIVE; CARBON; DELTA OPIATE RECEPTOR AGONIST; GUANOSINE 5' O (3 THIOTRIPHOSPHATE); GUANOSINE TRIPHOSPHATE; KAPPA OPIATE RECEPTOR AGONIST; MORPHINE; MORPHINE 6 GLUCURONIDE DERIVATIVE; MORPHINE DERIVATIVE; MU OPIATE RECEPTOR AGONIST; NITROGEN; PARTIAL AGONIST; PROPANE; SILANE; SILANE DERIVATIVE; SULFUR 35; UNCLASSIFIED DRUG;

EID: 14644402967     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2005.01.072     Document Type: Article
Times cited : (11)

References (18)
  • 15
    • 85030813662 scopus 로고    scopus 로고
    • note
    • 3CN/MeOH (0.7 mL). The organic solvent was removed under a stream of argon. To the residue MeOH (0.2 mL) was added and the resulting material was analyzed by HPLC using the reverse phase conditions described above. The extraction efficiency was 45%. Selected metabolic extracts were also analyzed with an M-8000 ion trap mass spectrometer (Hitachi, San Jose, CA) equipped with an electrospray ionization source. Sample delivery was carried out in the flow injection analysis mode using a LaChrom separation module with an isocratic solvent system of MeOH/water/HCOOH (50:50:0.17, v/v) running at0.2 mL/min


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.