摘要:
In one aspect, the present invention provides a contrast enhancement agent comprising an iron chelate having structure I and salts thereof wherein R1 is independently at each occurrence a hydroxy group, a C1-C3 hydroxyalkyl group, or a C1-C3 alkyl group, and b is 0-4; R2-R7 are independently at each occurrence hydrogen, a C1-C3 hydroxyalkyl group, or a C1-C3 alkyl group, with the proviso that at least one of R1-R7 is a hydroxy group or a C1-C3 hydroxyalkyl group; and wherein Q is one or more charge balancing counterions. Also provided are a metal chelating ligand having structure IX and medical formulations comprising the contrast enhancement agent I.
摘要:
Methods for introducing fluorine atom onto a polypeptide are provided. Also provided are linkers, bioconjugates, and bifunctional compound agents made using the methods, linkers, and bioconjugates. The methods comprise: (i) providing a linker comprising a thiol-reactive terminus and an aldehyde-reactive terminus; (ii) reacting the thiol-reactive terminus of the linker with a polypeptide comprising at least one thiol group or a reactive derivative thereof; and (iii) subsequently reacting the aldehyde-reactive terminus of the linker with a fluorine-substituted aldehyde.
摘要:
Compounds effective in inhibiting replication of Hepatitis C virus (“HCV”) or other viruses are disclosed. This invention is also directed to compositions comprising such compounds, co-formulation or co-administration of such compounds with other anti-viral or therapeutic agents, processes and intermediates for the syntheses of such compounds, and methods of using such compounds for the treatment of HCV or other viral infections.
摘要:
An isolated polypeptide, Z domain, derived from B domain of Staphylococcal protein A, comprising a pair of anti-parallel alpha helices that are capable of binding a target, is provided herein. Introduction of an engineered disulfide bridge between two natural or un-natural amino acids in the polypeptide is provided here. Also provided are methods of using the two-helix binders.
摘要:
An isolated polypeptide, Z domain, derived from B domain of Staphylococcal protein A, comprising a pair of anti-parallel alpha helices that are capable of binding a target, is provided herein. Introduction of an un-natural amino acid in the polypeptide is provided here. Also provided are methods of using the two-helix binders.
摘要:
A method of automatically detecting and tracking successive frames in a region of interesting by an electronic imaging device includes: decomposing a frame into intensity, color and direction features according to human perceptions; filtering an input image by a Gaussian pyramid to obtain levels of pyramid representations by down sampling; calculating the features of pyramid representations; using a linear center-surround operator similar to a biological perception to expedite the calculation of a mean value of the peripheral region; using the difference of each feature between a small central region and the peripheral region as a measured value; overlaying the pyramid feature maps to obtain a conspicuity map and unify the conspicuity maps of the three features; obtaining a saliency map of the frames by linear combination; and using the saliency map for a segmentation to mark an interesting region of a frame in the large region of the conspicuity maps.
摘要:
A method and system for calculating a customer value is provided. At least one relationship type for at least one pair of customers which are selected from a plurality of customers is determined. A first customer from the plurality of customers is selected. At least one second customer having a direct relationship or an indirect relationship with the first customer based on the at least one relationship type which is selected from the relationship types is determined. The first customer value based on the first predetermined calculation rule by using first values and base values is calculated.
摘要:
The present invention provides a system and method for enabling the synchronization of a switch and an interface device. Based on a comparison of cell sequence numbers included in cells received from the interface device to a current cell time within the switch, cell time adjustment information can be transmitted to the interface device. The cell time adjustment information is used by the interface device to determine the cell sequence number that is included in cells transmitted to the switch.
摘要:
The present invention provides an HCV polymerase inhibiting compound having the formula (I) and a composition comprising a therapeutically effective amount of said compound. The present invention also provides a method for inhibiting hepatitis C virus (HCV) polymerase, a method for inhibiting HCV viral replication, and a method for treating or preventing HCV infection. Processes for making said compounds, and synthetic intermediates employed in said processes, are also provided.