摘要:
A group of functionalized amine chelants having ortho ligating functionality that form complexes with rare-earth type metal ions are disclosed. The complexes can be covalently attached to an antibody or antibody fragment and used for therapeutic and/or diagnostic purposes. In addition certain of the chelant-radionuclide complexes can be effectively employed in compositions useful as therapeutic and/or diagnostic agents for calcific tumors and/or relief of bone pain.
摘要:
Prodrugs of 3-hydroxy-3-methylglutarylcoenzyme A (HMG-CoA) reductase inhibitors which are useful as antihypercholesterolemic agents and are represented by the following general structural formula (I): the amido ester moiety of which is in the L-configuration, and pharmaceutically acceptable salts thereof are disclosed.
摘要:
The present invention relates to a compound having the structure of formula (III):
wherein the C 2 - 4 alkyl is selected from the group consisting of ethyl, isopropyl, n-propyl, butyl, and t-butyl, or an N-oxide, crystalline form, hydrate, or pharmaceutically acceptable salt thereof.
摘要:
An object of the invention is to develop a group of new compounds with inhibitory activity against the function of Pinl as candidate compounds for drugs. The present invention provides compounds represented by the following Formula (I) or salts thereof, as well as Pin1 inhibitors, pharmaceutical compositions, therapeutic or prophylactic agents for inflammatory diseases, for cancer, and for obesity, which are prepared using the above compounds or salts thereof.
摘要:
Nanostructures are formed from alkylated derivatives of aromatic acids of the formula:
wherein at least one of R 1 to R 6 represents a carboxylic acid group, a primary amide group, an ester group, an amidine group, or a salt thereof, at least one other of R 1 to R 6 is X-R c , and the remaining of R 1 to R 6 independently represent H or substituted or unsubstituted organic groups; X represents a linking group; and R c represents a substituted or unsubstituted alkyl group.
摘要:
The present invention relates to substituted N-biphenyl-3-acetylamino-benzamides and N-[3-(acetylamino)phenyl]-biphenyl-carboxamides of general formula (I) as described and defined herein, to methods of preparing said compounds, to intermediate compounds useful for preparing said compounds, to pharmaceutical compositions and combinations comprising said compounds and to the use of said compounds for manufacturing a pharmaceutical composition for the treatment or prophylaxis of a disease, in particular of a hyperproliferative disorder, as a sole agent or in combination with other active ingredients.
摘要:
The present invention relates to novel compounds corresponding to the general formula (I) below: to compositions containing them, to processes for preparing them and to their use in pharmaceutical compositions intended for use in human or veterinary medicine, or alternatively in cosmetic compositions.