A synthetic amide of all-trans retinoic acid (RA) that displays reduced toxicity relative to RA while maintaining significant biological activity. Active in the prevention and treatment of a variety of neoplasms in animals. Inhibits proliferation in cell lines of human breast cancer, prostate adenocarcinoma, and ovarian carcinoma. Inhibits angiogenesis, as well as endothelial cell motility and tubule formation. Induces apoptosis in malignant hemopoietic cell lines.
生化/生理作用
Cell permeable: no
Primary Target Active in the prevention and treatment of a variety of neoplasms in animals.
Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.
其他說明
Formelli, F., et al. 1996. FASEB J. 10, 1014. Naik, H.R., et al. 1995. Adv. Pharmacol. 33, 315. Delia, D., et al. 1993. Cancer Res. 53, 6036. Pienta, K.J., et al. 1993. Cancer Res. 53, 224. Grubbs, C.J., et al. 1990. Anticancer Res. 10, 661. McCarthy, D.J., et al. 1987. Cancer Res.47, 5014. Moon, R.C., et al. 1979. Cancer Res.39, 1339.
法律資訊
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany