Extended knowledge of 473257-60-2

I hope this article can help some friends in scientific research. I am very proud of our efforts over the past few months and hope to 473257-60-2, help many people in the next few years.Safety of Ethyl 5-chloro-6-fluoro-1H-indole-2-carboxylate

A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, SDS of cas: 473257-60-2, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 473257-60-2, Name is Ethyl 5-chloro-6-fluoro-1H-indole-2-carboxylate, molecular formula is C11H9ClFNO2. In a Article, authors is Salamone, Stephane,once mentioned of 473257-60-2

Breast cancer is the most prevalent cancer in women. The development of resistances to therapeutic agents and the absence of targeted therapy for triple negative breast cancer motivate the search for alternative treatments. With this aim in mind, we synthesised new derivatives of troglitazone, a compound which was formerly used as an anti-diabetic agent and which exhibits anti-proliferative activity on various cancer cell lines. Among the compounds prepared, some displayed micromolar activity against hormone-dependent and hormone-independent breast cancer cells. Furthermore, the influence of the compounds on the viability of primary cultures of human hepatocytes was evaluated. This enabled us to obtain for the first time interesting structure-toxicity relationships in this family of compounds, resulting in 6b and 8b, which show good anti-proliferative activities and poor toxicity towards hepatocytes, compared to troglitazone.

I hope this article can help some friends in scientific research. I am very proud of our efforts over the past few months and hope to 473257-60-2, help many people in the next few years.Safety of Ethyl 5-chloro-6-fluoro-1H-indole-2-carboxylate

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles