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A Brossi

Showing results (101-110 of 118) with videos related to

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Journal of Medicinal Chemistry|June 20, 1998
Antitumor agents. 185. Synthesis and biological evaluation of tridemethylthiocolchicine analogues as novel topoisomerase II inhibitorsJ Guan, X K Zhu, Y Tachibana, et al.
Bioorganic & Medicinal Chemistry|January 9, 1999
Antitumor agents. Part 186: Synthesis and biological evaluation of demethylcolchiceinamide analogues as cytotoxic DNA topoisomerase II inhibitorsJ Guan, X K Zhu, Y Tachibana, et al.
Archiv Der Pharmazie|January 1, 1991
Oxoaporphine alkaloids: conversion of lysicamine into liriodendronine and its 2-O-methyl ether, and antifungal activityV Pabuccuoglu, M D Rozwadowska, A Brossi, et al.
The Journal of Biological Chemistry|September 27, 2000
Mapping the binding site of colchicinoids on beta -tubulin. 2-Chloroacetyl-2-demethylthiocolchicine covalently reacts predominantly with cysteine 239 and secondarily with cysteine 354R Bai, D G Covell, X F Pei, et al.
Journal of Medicinal Chemistry|June 1, 1980
Mammalian alkaloids. 8. Synthesis and biological effects of tetrahydropapaveroline related 1-benzyltetrahydroisoquinolinesA Brossi, K C Rice, C P Mak, et al.
Journal of Medicinal Chemistry|March 1, 1979
Paradoxical effects of N-cyanoalkyl substituents upon the activities of several classes of opioidsA E Jacobson, K C Rice, J Reden, et al.
Journal of Medicinal Chemistry|November 1, 1986
Comparison of (-)-eseroline with (+)-eseroline and dihydroseco analogues in antinociceptive assays: confirmation of rubreserine structure by X-ray analysisB Schönenberger, A E Jacobson, A Brossi, et al.
Journal of Medicinal Chemistry|March 1, 1979
Deoxymorphines: role of the phenolic hydroxyl in antinociception and opiate receptor interactionsJ Reden, M F Reich, K C Rice, et al.
Medicinal Research Reviews|January 1, 1988
Colchicine and its analogues: recent findingsA Brossi, H J Yeh, M Chrzanowska, et al.
Neuroreport|February 15, 1995
Maze learning in aged rats is enhanced by phenserine, a novel anticholinesteraseH Ikari, E L Spangler, N H Greig, et al.
Pageof 12

Showing results (101-110 of 118) with videos related to

Sort By:
Pageof 12
Journal of Medicinal Chemistry|June 20, 1998
Antitumor agents. 185. Synthesis and biological evaluation of tridemethylthiocolchicine analogues as novel topoisomerase II inhibitorsJ Guan, X K Zhu, Y Tachibana, et al.
Bioorganic & Medicinal Chemistry|January 9, 1999
Antitumor agents. Part 186: Synthesis and biological evaluation of demethylcolchiceinamide analogues as cytotoxic DNA topoisomerase II inhibitorsJ Guan, X K Zhu, Y Tachibana, et al.
Archiv Der Pharmazie|January 1, 1991
Oxoaporphine alkaloids: conversion of lysicamine into liriodendronine and its 2-O-methyl ether, and antifungal activityV Pabuccuoglu, M D Rozwadowska, A Brossi, et al.
The Journal of Biological Chemistry|September 27, 2000
Mapping the binding site of colchicinoids on beta -tubulin. 2-Chloroacetyl-2-demethylthiocolchicine covalently reacts predominantly with cysteine 239 and secondarily with cysteine 354R Bai, D G Covell, X F Pei, et al.
Journal of Medicinal Chemistry|June 1, 1980
Mammalian alkaloids. 8. Synthesis and biological effects of tetrahydropapaveroline related 1-benzyltetrahydroisoquinolinesA Brossi, K C Rice, C P Mak, et al.
Journal of Medicinal Chemistry|March 1, 1979
Paradoxical effects of N-cyanoalkyl substituents upon the activities of several classes of opioidsA E Jacobson, K C Rice, J Reden, et al.
Journal of Medicinal Chemistry|November 1, 1986
Comparison of (-)-eseroline with (+)-eseroline and dihydroseco analogues in antinociceptive assays: confirmation of rubreserine structure by X-ray analysisB Schönenberger, A E Jacobson, A Brossi, et al.
Journal of Medicinal Chemistry|March 1, 1979
Deoxymorphines: role of the phenolic hydroxyl in antinociception and opiate receptor interactionsJ Reden, M F Reich, K C Rice, et al.
Medicinal Research Reviews|January 1, 1988
Colchicine and its analogues: recent findingsA Brossi, H J Yeh, M Chrzanowska, et al.
Neuroreport|February 15, 1995
Maze learning in aged rats is enhanced by phenserine, a novel anticholinesteraseH Ikari, E L Spangler, N H Greig, et al.
Pageof 12