TY - JOUR
T1 - Characterization of Two Taxol Photoaffinity Analogues Bearing Azide and Benzophenone-Related Photoreactive Substituents in the A-Ring Side Chain
AU - Swindell, Charles S.
AU - Heerding, Julia M.
AU - Krauss, Nancy E.
AU - Horwitz, Susan Band
AU - Rao, Srinivasa
AU - Ringel, Israel
PY - 1994/5/1
Y1 - 1994/5/1
N2 - Taxol is a structurally novel and clinically effective antitumor drug, which, unlike other antimitotic agents, induces the assembly of tubulin into microtubules. To characterize the binding site(s) of taxol on the microtubule, taxol-based photoaffinity reagents 1 and 2 bearing photoreactive groups on the A-ring side chain were prepared and evaluated. Taxol analogue 1 exhibits better microtubule assembly activity, greater cytotoxicity toward J774.2 cells, and more specific and efficient photolabeling of the β-subunit of tubulin than does analogue 2. Therefore, it would appear that 1 is the better candidate for further studies aimed at the characterization of the taxol binding site on the microtubule.
AB - Taxol is a structurally novel and clinically effective antitumor drug, which, unlike other antimitotic agents, induces the assembly of tubulin into microtubules. To characterize the binding site(s) of taxol on the microtubule, taxol-based photoaffinity reagents 1 and 2 bearing photoreactive groups on the A-ring side chain were prepared and evaluated. Taxol analogue 1 exhibits better microtubule assembly activity, greater cytotoxicity toward J774.2 cells, and more specific and efficient photolabeling of the β-subunit of tubulin than does analogue 2. Therefore, it would appear that 1 is the better candidate for further studies aimed at the characterization of the taxol binding site on the microtubule.
UR - http://www.scopus.com/inward/record.url?scp=0028200190&partnerID=8YFLogxK
U2 - 10.1021/jm00036a009
DO - 10.1021/jm00036a009
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C2 - 7910216
AN - SCOPUS:0028200190
SN - 0022-2623
VL - 37
SP - 1446
EP - 1449
JO - Journal of Medicinal Chemistry
JF - Journal of Medicinal Chemistry
IS - 10
ER -