LY294002-geldanamycin heterodimers as selective inhibitors of the PI3K and PI3K-related family
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作者:
Chiosis, G
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Mem Sloan Kettering Canc Ctr, Dept Mol Oncogenesis, New York, NY 10021 USAMem Sloan Kettering Canc Ctr, Dept Mol Oncogenesis, New York, NY 10021 USA
Chiosis, G
[1
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Rosen, N
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Mem Sloan Kettering Canc Ctr, Dept Mol Oncogenesis, New York, NY 10021 USAMem Sloan Kettering Canc Ctr, Dept Mol Oncogenesis, New York, NY 10021 USA
Rosen, N
[1
]
Sepp-Lorenzino, L
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Mem Sloan Kettering Canc Ctr, Dept Mol Oncogenesis, New York, NY 10021 USAMem Sloan Kettering Canc Ctr, Dept Mol Oncogenesis, New York, NY 10021 USA
Sepp-Lorenzino, L
[1
]
机构:
[1] Mem Sloan Kettering Canc Ctr, Dept Mol Oncogenesis, New York, NY 10021 USA
Several LY294002-GM heterodimers were synthesized with the intent of modulating their activity in the presence of hsp90 and thereby creating selective inhibitors of PI3K and PI3K-related family. (C) 2001 Elsevier Science Ltd. All rights reserved.
机构:
Harvard Univ, Howard Hughes Med Inst, Dept Chem & Biol Chem, Cambridge, MA 02138 USAHarvard Univ, Howard Hughes Med Inst, Dept Chem & Biol Chem, Cambridge, MA 02138 USA
Kuruvilla, FG
Schreiber, SL
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Harvard Univ, Howard Hughes Med Inst, Dept Chem & Biol Chem, Cambridge, MA 02138 USAHarvard Univ, Howard Hughes Med Inst, Dept Chem & Biol Chem, Cambridge, MA 02138 USA
机构:
Harvard Univ, Howard Hughes Med Inst, Dept Chem & Biol Chem, Cambridge, MA 02138 USAHarvard Univ, Howard Hughes Med Inst, Dept Chem & Biol Chem, Cambridge, MA 02138 USA
Kuruvilla, FG
Schreiber, SL
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Harvard Univ, Howard Hughes Med Inst, Dept Chem & Biol Chem, Cambridge, MA 02138 USAHarvard Univ, Howard Hughes Med Inst, Dept Chem & Biol Chem, Cambridge, MA 02138 USA