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10010428-100A selective antagonist of EP4 (Ki = 3.2 nM) that less potently binds EP2 (Ki = 630 nM) and has no affinity for EP1 or EP3 delays the healing of gastric ulcers, suppressing the upregulation of VEGF expression and angiogenesis blocks pain and
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10010428-250A selective antagonist of EP4 (Ki = 3.2 nM) that less potently binds EP2 (Ki = 630 nM) and has no affinity for EP1 or EP3 delays the healing of gastric ulcers, suppressing the upregulation of VEGF expression and angiogenesis blocks pain and
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10010428-50A selective antagonist of EP4 (Ki = 3.2 nM) that less potently binds EP2 (Ki = 630 nM) and has no affinity for EP1 or EP3 delays the healing of gastric ulcers, suppressing the upregulation of VEGF expression and angiogenesis blocks pain and
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16243-10A cell-permeable inhibitor of Arp2/3 complex action that inhibits actin polymerization in vitro, using human, bovine and fission yeast proteins (IC<sub>50</sub>s = 4, 32, and 24 µM, respectively) prevents the formation of actin filament comet
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16243-25A cell-permeable inhibitor of Arp2/3 complex action that inhibits actin polymerization in vitro, using human, bovine and fission yeast proteins (IC<sub>50</sub>s = 4, 32, and 24 µM, respectively) prevents the formation of actin filament comet
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16243-5A cell-permeable inhibitor of Arp2/3 complex action that inhibits actin polymerization in vitro, using human, bovine and fission yeast proteins (IC<sub>50</sub>s = 4, 32, and 24 µM, respectively) prevents the formation of actin filament comet
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17499-1A &beta3-adrenoceptor agonist (EC<sub>50</sub> = 3 nM) that is >10,000-fold selective over &beta1 and &beta2 causes a rapid decrease in blood glucose level in mice and has been used to study the induction of brown adipocytes and to increase
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17499-10A &beta3-adrenoceptor agonist (EC<sub>50</sub> = 3 nM) that is >10,000-fold selective over &beta1 and &beta2 causes a rapid decrease in blood glucose level in mice and has been used to study the induction of brown adipocytes and to increase
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17499-5A &beta3-adrenoceptor agonist (EC<sub>50</sub> = 3 nM) that is >10,000-fold selective over &beta1 and &beta2 causes a rapid decrease in blood glucose level in mice and has been used to study the induction of brown adipocytes and to increase
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17499-500A &beta3-adrenoceptor agonist (EC<sub>50</sub> = 3 nM) that is >10,000-fold selective over &beta1 and &beta2 causes a rapid decrease in blood glucose level in mice and has been used to study the induction of brown adipocytes and to increase
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19081-1A potent, irreversible inhibitor of EGFR kinase activity (IC<sub>50</sub> = 370 pM) halts cell cycling in cells that overexpress EGFR or c-ErbB2 (IC<sub>50</sub>s = 31-125 nM) profoundly blocks the growth of EGFR-overexpressing tumors in nude mice
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19081-10A potent, irreversible inhibitor of EGFR kinase activity (IC<sub>50</sub> = 370 pM) halts cell cycling in cells that overexpress EGFR or c-ErbB2 (IC<sub>50</sub>s = 31-125 nM) profoundly blocks the growth of EGFR-overexpressing tumors in nude mice