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19480-5CWHM12 is an analog of RGD peptide (Item No. 14501), a tripeptide that inhibits integrin-ligand interactions in studies related to cell adhesion, migration, growth, and differentiation.
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16779-1A potent, orally bioavailable inhibitor of casein kinase 2 (CK2 Ki = 0.38 nM) inhibits proliferation in a panel of cancer cell lines that overexpress CK2 and prevents tumor growth of breast and pancreatic cancer cell xenografts in mice.
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16779-10A potent, orally bioavailable inhibitor of casein kinase 2 (CK2 Ki = 0.38 nM) inhibits proliferation in a panel of cancer cell lines that overexpress CK2 and prevents tumor growth of breast and pancreatic cancer cell xenografts in mice.
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16779-5A potent, orally bioavailable inhibitor of casein kinase 2 (CK2 Ki = 0.38 nM) inhibits proliferation in a panel of cancer cell lines that overexpress CK2 and prevents tumor growth of breast and pancreatic cancer cell xenografts in mice.
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16779-500A potent, orally bioavailable inhibitor of casein kinase 2 (CK2 Ki = 0.38 nM) inhibits proliferation in a panel of cancer cell lines that overexpress CK2 and prevents tumor growth of breast and pancreatic cancer cell xenografts in mice.
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18392-1A selective inhibitor of RNA polymerase I-driven transcription of rRNA (IC<sub>50</sub>s = 142, 113, and 54 nM in HCT116, A375, and MIA PaCa-2 tumor cells, respectively) demonstrates in vivo antitumor activity against human solid tumors in mouse
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18392-10A selective inhibitor of RNA polymerase I-driven transcription of rRNA (IC<sub>50</sub>s = 142, 113, and 54 nM in HCT116, A375, and MIA PaCa-2 tumor cells, respectively) demonstrates in vivo antitumor activity against human solid tumors in mouse
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18392-5A selective inhibitor of RNA polymerase I-driven transcription of rRNA (IC<sub>50</sub>s = 142, 113, and 54 nM in HCT116, A375, and MIA PaCa-2 tumor cells, respectively) demonstrates in vivo antitumor activity against human solid tumors in mouse
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18392-50A selective inhibitor of RNA polymerase I-driven transcription of rRNA (IC<sub>50</sub>s = 142, 113, and 54 nM in HCT116, A375, and MIA PaCa-2 tumor cells, respectively) demonstrates in vivo antitumor activity against human solid tumors in mouse
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16245-1A potent, reversible, orally bioavailable inhibitor of Pim-1, -2, and -3 (IC<sub>50</sub>s = 5, 25, and 16 nM, respectively) dose-dependently blocks the phosphorylation of the Pim targets Bad, 4E-BP1, and NKX3.1 acts synergistically with
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16245-10A potent, reversible, orally bioavailable inhibitor of Pim-1, -2, and -3 (IC<sub>50</sub>s = 5, 25, and 16 nM, respectively) dose-dependently blocks the phosphorylation of the Pim targets Bad, 4E-BP1, and NKX3.1 acts synergistically with
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16245-25A potent, reversible, orally bioavailable inhibitor of Pim-1, -2, and -3 (IC<sub>50</sub>s = 5, 25, and 16 nM, respectively) dose-dependently blocks the phosphorylation of the Pim targets Bad, 4E-BP1, and NKX3.1 acts synergistically with