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THRO-005A
RGD-4C
Ala-Cys-Asp-Cys-Arg-Gly-Asp-Cys-Phe-Cys-Gly (Disulfide bridge: 2-10 and 4-8)
Ala-Cys-Asp-Cys-Arg-Gly-Asp-Cys-Phe-Cys-Gly (Disulfide bridge: 2-10 and 4-8)
Size：1
P1(RMB)：1070
MW：1145.3
One letter sequence：ACDCRGDCFCG (Disulfide bridge: 2-10 and 4-8)
Molecular Formula：C42H60N14O16S4
Description： This peptide, a double cyclic peptide, binds preferentially to integrins at sites of tumor angiogenesis and inflammed synovium in-vivo, and can be internalized into targeted cells.\n RGD-4C is a double cyclic peptide that can bind preferentially to integrins at sites of tumor angiogenesis and inflamed synovium in vivo, and can be internalized into targeted cells. Novel applications include the coupling of RGD-4C to proapoptotic domains to treat tumors and inflammatory arthritis, and to radioactive labels for the broad spectrum imaging of tumor tissue.
Literature Reference：Curnis, F. et al. Cancer Res. 64, 565 (2004)\nSu, Z. et al. Bioconjug. Chem. 13, 561 (2002)\nGerlag, M. et al. Arthritis Res. 3, 357 (2001)\nEllerby, H. et al. Nature Med. 5, 1032 (1999);
Cas：
P1(RMB)：1070
MW：1145.3
One letter sequence：ACDCRGDCFCG (Disulfide bridge: 2-10 and 4-8)
Molecular Formula：C42H60N14O16S4
Description： This peptide, a double cyclic peptide, binds preferentially to integrins at sites of tumor angiogenesis and inflammed synovium in-vivo, and can be internalized into targeted cells.\n RGD-4C is a double cyclic peptide that can bind preferentially to integrins at sites of tumor angiogenesis and inflamed synovium in vivo, and can be internalized into targeted cells. Novel applications include the coupling of RGD-4C to proapoptotic domains to treat tumors and inflammatory arthritis, and to radioactive labels for the broad spectrum imaging of tumor tissue.
Literature Reference：Curnis, F. et al. Cancer Res. 64, 565 (2004)\nSu, Z. et al. Bioconjug. Chem. 13, 561 (2002)\nGerlag, M. et al. Arthritis Res. 3, 357 (2001)\nEllerby, H. et al. Nature Med. 5, 1032 (1999);
Cas：
