A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, Application In Synthesis of 2-(6-Chloro-1H-indol-3-yl)acetic acid, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 1912-44-3, Name is 2-(6-Chloro-1H-indol-3-yl)acetic acid, molecular formula is C10H8ClNO2. In a Patent, authors is £¬once mentioned of 1912-44-3
Compounds exhibiting thrombopoietin-like activities
The compounds of the invention are compounds represented by the following general formula (1): 1wherein E represents one selected from the group consisting of a methylidyne group and a nitrilo group, R1 represents one selected from the group consisting of optionally substituted aryl groups and optionally substituted heteroaryl groups, R2 represents one selected from the group consisting of a hydrogen atom and alkyl groups, W1 represents an amino acid residue, A represents one selected from the group consisting of a carbonyl group and a sulfonyl group, X1 represents one selected from the group consisting of optionally substituted alkylene groups and optionally substituted alkenylene groups, and p represents 0 or 1; and their pharmacologically acceptable salts, which exhibit thrombopoietin-like activity.
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 1912-44-3, help many people in the next few years.Application In Synthesis of 2-(6-Chloro-1H-indol-3-yl)acetic acid
Reference£º
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