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With the increasing proportion of cancer in the world year by year, cancer has become the main cause of death and a major public health problem in the world. Anticancer peptides can destroy the structure of tumor cell membrane or inhibit the proliferation and migration of cancer cells and the formation of tumor blood vessels, almost no hemolysis and no damage to normal human cells, which has become a hot spot in the research of new anti-tumor drugs. Because of the need to constantly find new therapeutic drugs, especially those that can escape drug resistance, inhibit metastasis and have no other important side effects, anticancer peptides have become one of the goals of new research. Anticancer peptides are a new type of anticancer drugs with small molecular peptides, which kill cancer cells by destroying the structure of tumor cell membrane or inhibiting the proliferation and migration of cancer cells and the formation of tumor blood vessels, but have low toxicity to normal cells. It is a hot spot in the research of new anti-tumor drugs at present.
Cancer kills millions of people every year. As a traditional means of cancer treatment, chemotherapy has some defects, such as low selectivity, great side effects, and multi-drug resistance and so on. Compared with traditional chemotherapeutic drugs, peptides as anti-cancer compounds have high selectivity and low toxicity. The modification of anticancer peptides and the combination of anticancer peptides with traditional drugs can give better play to the effect of anticancer peptides, which will become an important direction of the development of anticancer peptides.
References
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Basic Fibroblast Growth Factor, Human, called basic fibroblast growth factor (bFGF/FGF-b/FGF-2), is a single cha ...
Teriparatide is a human parathyroid hormone analog with the same structure as the N-terminal 34 amino acid seque ...
APC 366 [N-(1-hydroxy-2-naphthoyl)-L-arginyl-L-prolinamide], is a novel selective inhibitor of mast cell tryptas ...
Jingzhaotoxin-III (β-TRTX-Cj1α) is a kind of sodium channel gating modifier which is from the tarantula Chilobra ...
Trimetazidine is a partial fatty acid oxidation inhibitor that inhibits 3-ketoacyl CoA thiolase, one of the enzymes of fatty ...