S 12363

Known as: S-12363, Vincaleukoblastine, O4-deacetyl-3-de(methoxycarbonyl)-3-(((1-(diethoxyphosphinyl)-2-methylpropyl)amino)carbonyl)-, (3(S))-, sulfate (salt) 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1990-1994
0119901994

Papers overview

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1994
1994
Two sensitive analytical methods for the analysis of S 12363 in plasma are described. A highly sensitive procedure for human and… (More)
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1993
1993
We have established a model of human renal cell carcinoma, Kgg2, transplanted into athymic nude mice which expressed P… (More)
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1993
1993
S 12363 is a new Vinca alkaloid derivative, characterized by the grafting of an alpha-aminophosphonate, onto the Vinca nucleus… (More)
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1993
1993
S 12363 is a new vinca alkaloid derivative obtained by appending an optically active alpha-aminophosphonate at the C23 position… (More)
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1992
1992
S 12363, a new vinca alkaloid derivative, was considerably more cytotoxic to murine L1210 cells and five human tumor cell lines… (More)
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1991
1991
S 12363 is a new Vinca alkaloid derivative obtained by appending an optically active alpha-aminophosphonate at the C23 position… (More)
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1991
1991
The action of two epimers of a new vinblastine derivative that differ in their in vivo antitumor activity and their cytotoxicity… (More)
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1991
1991
S 12363 is a new highly potent vinca alkaloid derivative characterized by the grafting of an a-aminophosphonate, bioisoster of… (More)
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1990
1990
S 12363 is a new vinca alkaloid derivative obtained by grafting an optically active alpha-aminophosphonate at the C23 position of… (More)
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