Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Active Ligands

Bismuth nitrate ( magisterium bismuti ), a white pigment, was used in beauty care, painting, and as a medicant in the seventeenth century, and staggering amounts of bismuth compounds have been administered for therapeutic purposes in the past, for example, over a [Pg.29]

A striking feature of the cellular effects of bismuth compounds in animals (and one shared only by lead) is the production of intranuclear inclusion bodies of up to 5 ixm in diameter (87), for example, in the tubular epithelial cells of the kidney. Electron probe microanalysis shows that these contain both Bi and S, and so could be a complex with a Cys-rich protein such as metallothionein. Bismuth is known to be a potent inducer of renal metallothionein synthesis, and pretreatment of animals with bismuth salts can prevent some of the toxic side effects induced by cisplatin (88). The role of metallothionein in the pharmacology of bismuth remains to be established, but the strong involvement of zinc, also an inducer of metallothionein synthesis, in the metabolism of skin cells, for example, may be related. Like several other elements of Group V, the development of the biological chemistiy of Bi is hampered by the lack of good physical properties, in particular of a well-behaved NMR isotope. [Pg.30]

Antihypertensive Agents Nitric Oxide as a Muscle Relaxant [Pg.30]

Sodium nitroprusside, Na2[Fe(CN)sNO] (21), is a potent hypotensive agent widely used to control blood flow after myocardial infarction and [Pg.30]

Perhaps there are also enzymes that catalyze the formation and breakdown of N—N bonds in man. [Pg.32]


Benzoyl-2,3-dihydro-lH-pyrrolizine-l-cai boxylic acid (ketorolac, L ) and 2-(3-benzoyl-phenyl)propionic acid (ketoprofen, L ) ai e biologically activ ligands used in medicine as non-steroidal anti-inflammatory dmgs. [Pg.394]

The most widely studied interactions between biologically active ligands and organotin(lV) cations relate to the amino acids and their derivatives (N- or S-protected amino acids and peptides), though new data on several of the most commonly occurring amino acids are still being published. This is specially true for aqueous speciation studies. Nice and very detailed reviews were published in this area by Molloy and Nath. ... [Pg.365]

This survey of the literature data on the interactions of organotin(IV) cations with biologically active ligands demonstrates that this is still a very open field. Above all, it is necessary to emphasize that usage of such complexes to treat humans is not permitted at present. Consequently, all compounds examined and discussed here (although with promising anticancer activity) are in the exploratory research stage. [Pg.431]

High ee values have also been obtained with organometallics," including organotitanium compounds (methyl, aryl, allylic) in which an optically active ligand is coordinated to the titanium," allylic boron compounds, and organozinc compounds. [Pg.1210]

Catalytically active ligands can also be deliberately introduced after synthesis. [Pg.83]

The coordination of redox-active ligands such as 1,2-bis-dithiolates, to the M03Q7 cluster unit, results in oxidation-active complexes in sharp contrast with the electrochemical behavior found for the [Mo3S7Br6] di-anion for which no oxidation process is observed by cyclic voltammetry in acetonitrile within the allowed solvent window [38]. The oxidation potentials are easily accessible and this property can be used to obtain a new family of single-component molecular conductors as will be presented in the next section. Upon reduction, [M03S7 (dithiolate)3] type-11 complexes transform into [Mo3S4(dithiolate)3] type-I dianions, as represented in Eq. (7). [Pg.114]

Chebib, M and Johnston, GA (2000) GABA-Activated ligand gated ion channels medicinal chemistry and molecular biology. J. Med. Chem. 43 1427-1447. [Pg.248]

Enzymatic activity, ligand binding or transport capacity Cleavage C3 Leu Control... [Pg.21]

In addition, Bryce and Chesney have developed chiral oxazolines linked to tetrathiafulvalene in order to use these ligands as redox-active ligands. When applied to the test reaction, these ligands gave only low enantioselec-tivities (<21% ee), as shown in Scheme 1.32. [Pg.32]

In addition, Bryce et al. have studied the binding of palladium to other S/N-ferrocenyloxazoline ligands by cyclic voltammetry and proved that it was reversible.These redox-active liganding systems were successfully used in the test reaction, providing the product in both high yield and enantioselectivity of up to 93% ee, as shown in Scheme 1.70. [Pg.55]

Although the number of actinides is the same as that of the lanthanides, their availability and chemical characteristics have so far largely restricted the study of their ligand substitution mechanisms to dioxouranium(VI), which is the ionic form of uranium most amenable to such studies in solution. In the solid state, the oxo ligands occupy axial sites above and below the U(VI) center, and four (328), five (329, 330), and six (331, 332) oxygen donor atoms have been reported to occupy equatorial positions. From a mechanistic point of view, this variability of the occupancy of the equatorial plane suggests the possibility of both d- and a-activated ligand substitution pro-... [Pg.67]


See other pages where Active Ligands is mentioned: [Pg.60]    [Pg.175]    [Pg.190]    [Pg.191]    [Pg.295]    [Pg.299]    [Pg.69]    [Pg.560]    [Pg.797]    [Pg.915]    [Pg.915]    [Pg.1035]    [Pg.1127]    [Pg.1237]    [Pg.1254]    [Pg.1254]    [Pg.426]    [Pg.112]    [Pg.212]    [Pg.231]    [Pg.3]    [Pg.193]    [Pg.349]    [Pg.116]    [Pg.354]    [Pg.496]    [Pg.436]    [Pg.181]    [Pg.62]    [Pg.775]    [Pg.233]    [Pg.243]    [Pg.235]    [Pg.47]    [Pg.549]    [Pg.31]    [Pg.239]    [Pg.45]    [Pg.53]    [Pg.179]   


SEARCH



Activation of C—H Bonds in Ligands

Activation of Polysaccharides for Covalently Attaching Ligands and Proteins

Activation of ligands

Active targeting ligands

Activity ligand-binding

Agonistic and Antagonistic Activities of Viral Chemokine Ligands

Ambiphilic metal-ligand activation (AMLA

Aminophosphines, optically active ligands

Bond Activation by Metal-Ligand Cooperation

Catechol ligands, redox activity

Chloride ligands activation

Complexes Containing Redox-active Ligands

Complexes with Optical Activity Due to Unidentate Ligands

Copper catalysts high-activity ligands

Copper catalyzed reactions active ligand development

Cytotoxicity and Antitumour Activity of Diphosphine Ligands

Energy: activation ligand field stabilization

High-Throughput Screening of Chiral Ligands and Activators

Highly Active Ethene Polymerization Catalysts with Unusual Imine Ligands

Less Known Redox-active Ligands in Metal Complexes

Ligand Binding and Activation

Ligand Binding and Activation of CAR

Ligand Binding, Activation and Corepression of the RXR-Heterodimers

Ligand activated

Ligand activated

Ligand at the active site

Ligand bimetallic activation

Ligand binding activation step

Ligand exchange reactions activation parameters

Ligand exchange reactions dissociatively activated reaction mechanism

Ligand field activation energy (LFAE

Ligand optical activity

Ligand, additivity redox-active

Ligand-activated nuclear receptor

Ligand-activated transcription

Ligand-activated transcription factors

Ligand-activated transcriptional regulator

Ligand-active site interactions

Ligand-dependent Activators

Ligand-field activation energy

Ligand-independent activity

Ligands optically active phosphine

Ligands peroxisome proliferator-activated receptor

Ligands surface active

Metal as a Carrier for Active Ligands

Myrtenal optically active ligand from

Nitrosylmetal complexes with additional redox-active ligands

Nitrosylmetal complexes without additional redox-active ligands

Octahedral complexes optically active ligands

Optically active ligand

Organoaluminum Complexes Incorporating Redox-Active Ligands

Oxidative activation tridentate ligands

Palladium chemistry high-activity ligands

Peroxisome Proliferator-Activated Receptor y Ligands

Peroxisome proliferator-activated receptors PPARs), fatty acid ligands

Phosphines high-activity ligands

Phosphoinositides ligand-activated hydrolysis

Polymerization on activated ligands

Potassium channel activators ligand binding

Prostaglandin selective ligands and structure-activity relationhips

Prostaglandin selective ligands and structure-activity relationships

Prostanoid receptors selective ligands and structure-activity relationships

Quantitative structure-activity relationship ligands

Receptor activator of NF-kB ligand

Receptor activator of nuclear factor-kB ligand

Receptors activated solely by synthetic ligands

Redox active bridging ligands

Redox-active ligands

Redox-active ligands dithiolenes

Redox-active ligands ferrocenes

Redox-active ligands polypyridines

Redox-active ligands porphyrins

Sandwich ligands, catalytic activity

Sonogashira coupling reaction ligand activity

Sonogashira reaction ligand activity

Steroid ligand-independent activation

Structural Determinants of Ligand Binding and Receptor Activation by CC Chemokines

Structure-Activity Relationships in Modeling Nucleic Acid Ligand Interactions

Structure-activity relationship nucleic acid ligand interactions

Structure-activity relationships three-dimensional-ligand-based

Structure-activity relationships, opioid ligands

Sulfido ligands activation

Three-dimensional ligand-based models structure-activity relationships

Transcriptional Regulators Ligand-dependent Activators

Transition metals ligand activation

© 2024 chempedia.info