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Volumn 55, Issue 10, 2007, Pages 1489-1493

Catalytic aerobic oxidation of nor-binaltorphimine (nor-BNI) analogs without 4,5-epoxy bridge affords a more selective ligand for κ opioid receptor than the representative κ antagonist nor-BNI

Author keywords

receptor; Aerobic oxidation; Morphinan; Opioid; Platinum catalyst

Indexed keywords

6,6',7,7' TETRAHYDRO 6,6' IMINO 14 BETA, 14' ALPHA DIHYDROXY 3,3' DIMETHOXY 7,7' BIMORPHINAN; BINALTORPHIMINE; KAPPA OPIATE RECEPTOR; KAPPA OPIATE RECEPTOR ANTAGONIST; MORPHINAN DERIVATIVE; OXYGEN; PLATINUM; UNCLASSIFIED DRUG;

EID: 35648994814     PISSN: 00092363     EISSN: 13475223     Source Type: Journal    
DOI: 10.1248/cpb.55.1489     Document Type: Article
Times cited : (9)

References (40)
  • 13
    • 0002399140 scopus 로고
    • ed. by Tseng L. F, Harwood Academic Publishers, Singapore
    • Nock B., "The Pharmacology of Opioid Peptides," ed. by Tseng L. F., Harwood Academic Publishers, Singapore, 1995, pp. 29-56.
    • (1995) The Pharmacology of Opioid Peptides , pp. 29-56
    • Nock, B.1
  • 37
    • 35648959139 scopus 로고    scopus 로고
    • A radical process might also be taken into account. Two molecules of hydroperoxy radicals corresponding to hydroperoxide 14 could produce ketone, alcohol, and oxygen via an unstable tetraoxide. (Chemical Equation Presented) Lowry T. H., Richardson K. S., Mechanism and Theory in Organic Chemistry, 3rd ed., Harper & Row, Publishers, New York, 1987, pp. 779-782.
    • A radical process might also be taken into account. Two molecules of hydroperoxy radicals corresponding to hydroperoxide 14 could produce ketone, alcohol, and oxygen via an unstable tetraoxide. (Chemical Equation Presented) Lowry T. H., Richardson K. S., "Mechanism and Theory in Organic Chemistry," 3rd ed., Harper & Row, Publishers, New York, 1987, pp. 779-782.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.