Results 291 to 300 of about 1,747,583 (341)
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Nuclear-Receptor Ligands and Ligand-Binding Domains
Annual Review of Biochemistry, 1999▪ Abstract The determination of several structures of nuclear receptor ligand binding domains (LBD) has led to new insights into the mechanism of action of this very important class of receptors. This review describes and compares the different LBD structures and their relationship to the function of the nuclear receptors.
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Dalton Transactions, 2019
This special web collection of Dalton Transactions focuses on nitrogen ligands, as a tribute to the 150th anniversary of the development of the periodic table.
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This special web collection of Dalton Transactions focuses on nitrogen ligands, as a tribute to the 150th anniversary of the development of the periodic table.
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Intramolecular ligandligand interactions in mixed ligand complexes
Inorganica Chimica Acta, 1983Abstract One of the most important properties of mixed ligand complexes is direct and metal ion-mediated ligandligand interactions, the latter being known as π-acidπ-base interactions around the central metal ion. Examples of direct intramolecular ligandligand interactions are ionic and hydrogen bonds between charged and/or polar side groups and ...
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Intramolecular ligand-ligand interactions in mixed ligand complexes
Journal of Molecular Catalysis, 1984Abstract Intramolecular ligand-ligand interactions in the ternary Cu(II)- and Pd(II)- amino acid systems have been investigated by synthetic, spectroscopic and potentiometric methods. Various ternary Cu(II)- and Pd(II)- complexes containing amino acids with charged and/or polar side groups were isolated as crystals. Electrostatic interactions between
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Cannabinoid Receptors and Their Ligands: Ligand—Ligand and Ligand—Receptor Modeling Approaches
2005The cannabinoid CB1 and CB2 receptors belong to the class A, rhodopsin-like family of GPCRs. Antagonists for each receptor sub-type, as well as four structural classes of agonists that bind to both receptors, have been identified. An extensive amount of structure-activity relationship information (SAR) has been developed for agonists and antagonists ...
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