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Target, targets clusters

At the target, clusters are broken up and sample molecular ions, accompanied by some remaining solvent ions, are extracted by an electrical potential through a small hole into the mass spectrometer analyzer (Figure 11.1), where their mass-to-charge (m/z) ratios are measured in the usual way. The mass spectrometer may be of any type. [Pg.72]

Sample. This source places no restrictions on target material. Clusters of metals, produced. For example, polyethylene and alumina have been studied as well as refractory metals like tungsten and niobium. Molecular solids, liquids, and solutions could also be used. However the complexity of the vaporization process and plasma chemistry makes for even more complex mixtures in the gas phase. To date the transition metals(1-3) and early members of group 13 (IIIA) and 14 (IVA)( 11-16) have been the most actively studied. [Pg.49]

Briinig, I., Scotti, E Sidler, C and Fritschy, J. M. (2002) Intact sorting, targeting, and clustering of y-aminobutyric acid A receptor subtypes in hippocampal neurons in vitro. J. Comp. Neurol. 443,43—45. [Pg.107]

Figure 2.18 Chemogenomic analysis of targets BioPrint targets clustered in chemical space by fingerprint of activities against the consistent BioPrint compound set. Figure 2.18 Chemogenomic analysis of targets BioPrint targets clustered in chemical space by fingerprint of activities against the consistent BioPrint compound set.
Target Clustering as Strategy in Drug Discovery 4.1. Target clustering... [Pg.66]

Target clustering based on structural and functional similarity... [Pg.67]

Figure 3. Approaches to cluster protein targets for screening of small molecule libraries. Currently, protein targets are clustered based on functional or amino acid sequence similarity (left). We propose to cluster proteins purely based on structural similarity of protein cores and to apply this clustering to compound library design (right). Figure 3. Approaches to cluster protein targets for screening of small molecule libraries. Currently, protein targets are clustered based on functional or amino acid sequence similarity (left). We propose to cluster proteins purely based on structural similarity of protein cores and to apply this clustering to compound library design (right).
The examples from literature and the hrst application of PSSC clustering in the discovery of inhibitors for proteins from the Cdc25A, AChE and 1 lfdTDSi/2 cluster convincingly demonstrates that application of target clustering based on protein structure similarity in conjunction with natural... [Pg.79]

Nitrogenase is another big target of cluster synthesis. The X-ray elucidation of the active center of the Fe-Mo cofactor and P-cluster... [Pg.46]

H)N-NDR systems DL activator accelerated waves, inhomogeneous (BF unstable) oscillations stationary domains, standing waves, anti-phase oscillations with n = 1 pulses, target patterns, clusters enhanced acceleration of potential fronts, mainly homogenizing effect cluster formation in the oscillatory region... [Pg.200]

Database Mining 6.500 compounds in target-clustered subsets... [Pg.238]

Predominantly, the book covers systematic elaborations on pharmaceutically relevant target families with clear focus centred around systematic medicinal chemistry access routes towards the distinct members of those target clusters. Contributions by R. Buijsman and B. Klebl and colleagues provide detailed insights into the world of protein kinase inhibitors. While R. Buij sman systematically focuses on the detailed structural requirements of protein kinase binding sites that... [Pg.482]

Starting from the X-ray structures of one bacterial and one human DHFR, the GRID/PCA analysis shows that PG 1 distinguishes between the two target proteins, clustering the objects into two groups, while PG 2 ranks the probes. [Pg.61]

It has been proposed that cardiac Na channels may be targeted and clustered to specific locations in a similar manner to that observed for Na channels in brain (Cohen 1996). The presence of j subunits in cardiac myocytes may facilitate Na channel locahzation and clustering to discrete functional domains via homophilic or heterophihc cell adhesion interactions. Interestingly, treatment of inside-out patches of ventricular cells with cytochalasin-D induced Na channels to enter a mode characterized by lower peak open probability with a greater persistent activity, consistent with a decrease in the rate of inactivation (Undrovinas et al... [Pg.135]


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See also in sourсe #XX -- [ Pg.97 ]




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