Disclosed is a novel pharmacophore and novel inotropic compositions created from the novel pharmacophore.
Finally, this invention also relates to compounds having the features of the pharmacophore.
A pharmacophore having a spatial arrangement of atoms defined by the binding pocket identified in the model, along with a compound defined by the pharmacophore is also disclosed.
The pharmacophore of vitamin C is the ascorbate ion .
A method of increasing the concentration of a pharmacophore in a cell is further encompassed by the invention.
Disclosed herein is a pharmacophore model for antimalarial activity and methods of making and using thereof.
The pharmacophore comprises two hydrophobic aliphatic functions, one aromatic function and one hydrogen bond acceptor function.
Molecular field information for these structures is clustered to determine a consensus field pharmacophore.
Thus, the method of the present invention is able to efficiently screen very large numbers of molecular entities for the presence of a desired pharmacophore.
The therapeutic moiety can be a quinolone, an oxazolidinone, a macrolide, an aminoglycoside, a tetracycline core or a structure/pharmacophore associated with an antibacterial agent.
The invention relates to an anti-inflammatory oligopeptides which contain the terminal pharmacophore Cys-Asn-Ser which is capable of inhibiting the NF-κβ signaling pathway.
The pharmacophore model was made using a test set of tryptanthrin compounds which exhibit antimalarial activity.
Multiple spatially related pharmacophores define small molecule inhibitors of OLIG2 in glioblastoma.
Also disclosed are arthropod repellent compounds identified by screening databases with the pharmacophore model.
Suitable methods include de novo compound design, use of a pharmacophore, and automated docking algorithms.
Improved competitive inhibitors of FAAH employ an α-keto heterocyclic pharmacophore and a binding subunit having a ?-unsaturation.
The compatible scaffolds and corresponding substituents are combined to represent one or more molecule or molecules containing the desired pharmacophore.
The present invention provides molecules, designed using the estrogen pharmacophore, that possess predicted and demonstrated estrogenic and/or estrogenic modulatory biological activity.
A method for constructing a potentially pharmaceutically useful molecule that displays a predefined pharmacophore associated with a desired biological activity is disclosed.
Multiple spatially related pharmacophores define small molecule inhibitors of OLIG2 in glioblastoma
Requêtes fréquentes français :1-200, -1k, -2k, -3k, -4k, -5k, -7k, -10k, -20k, -40k, -100k, -200k, -500k, -1000k,
Requêtes fréquentes anglais :1-200, -1k, -2k, -3k, -4k, -5k, -7k, -10k, -20k, -40k, -100k, -200k, -500k, -1000k,
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