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Solubility activity

Synthesized by soluble guanylyl cyclase and particulate guanylyl cyclase from guanosine triphosphate (GTP). Nitric oxide activates soluble guanylyl cyclase to enhance cyclic GMP production that contributes to various NO actions. Cyclic GMP is hydrolyzed by phosphodiesterases. Cyclic GMP binds to and activates cGMP-dependent protein kinase, phosphodiesterases, and Cyclic Nucleotide-regulated Cation Channels. [Pg.399]

Bis-hydrazide-containing molecules also can be used to activate soluble polymeric sub-stances-containing aldehyde groups. For instance, dextran may be periodate oxidized to create numerous formyl functionalities on each molecule. Subsequent reaction with a homobifunctional hydrazide in large excess results in a hydrazide-activated polymer having multivalent-binding capability toward aldehydes or ketones (Chapter 25, Section 2.2). Insoluble support matrices suitable for affinity chromatography have been activated in a similar fashion to create the hydrazide derivative (O Shannessy and Wilchek, 1990). [Pg.270]

This expression has been written in terms of concentration if activity coefficients sue known or estimated, then a thermodynamically ideal solubility product may be obtained from the Emalogous product of ionic activities. As the concentration of ions in solutions of lanthanide fluorides is low, the concentration and activity solubility products will not differ markedly, although activity coefficients for these salts of 3 + cations are significantly less than unity even in such dilute solutions (4a). [Pg.93]

The enzyme urease was discovered in soybeans by Takeuchi in 1909 it catalyzed the conversion of urea to ammonium carbonate. Jack beans were another excellent source of the enzyme. Jack bean powder could be stored for considerable periods and very active, soluble, urease extracted. After the action of urease, the ammonia could be estimated colorimetrically by Nesslerisation or titrimetrically. The Conway diffusion apparatus was specially developed for the estimation of urea titrimetrically and remained in use into the 1950s. [Pg.103]

Effect Activates soluble guanylate Activates soluble guanylate... [Pg.61]

Nickel carbonyl charged, or formed in the carbonylation reaction mixture, can catalyze the carbonylation of methanol (11). To maintain the activity of the nickel carbonyl catalyst high temperature and pressure are required (12-14). However, certain promoters can maintain an active, soluble, nickel carbonyl species under much milder conditions. The most reactive promoters are phosphines, alkali metal salts, tin compounds, and 2-hydroxypyridine. Reaction rates of 2 to 7 X 10-3(mol/1.sec) can be achieved without the use of high concentration of iodine (Table II). in addition, high reaction rates... [Pg.63]

NO released by GTN activates soluble, cytosolic form of guanylyl cyclase in vascular smooth muscles by interacting with haem group in the enzyme. This converts GTP to cGMP. cGMP dephosphorylates myosin light chain kinase and prevent myosin interaction with actin leading to relaxation. [Pg.185]

Rodent KC and HC, as well as human HC, express an inducible NO synthase under septic or inflammatory conditions. In vivo in endotoxemia, this expression is transient. Our in vivo data indicate that this induced -NO serves a protective role in the liver and reduces hepatic injury in endotoxemia. This protective action may be mediated by the capacity of NO to neutralize oxygen radicals and prevent platelet adherence and aggregation. Our in vitro studies show that HC-derived -NO can activate soluble guanylate cyclase. Other in vitro effects include the nonspecific suppression of protein synthesis and a small reduction in mitochondrial aconitase activity. The relevance of these in vitro actions to hepatic function in vivo remains to be determined. [Pg.233]

NO activates soluble guanylyl cyclase to elevate cGMP levels in vascular smooth muscle Vasodilator relaxes other smooth muscle inhalation of NO leads to increased blood flow to parts of the lung exposed to NO and decreased pulmonary vascular resistance Hypoxic respiratory failure and pulmonary hypertension Inhaled gas Toxicity Methemoglobinemia... [Pg.424]

Once IL-1 is released into the extracellular fluid, the following molecules can be employed to manipulate its activity soluble receptors, IL-IRa, IL-1 neutralizing antibodies, IL-l-specific binding proteins, high-affinity small molecules (Figure 10). [Pg.420]

Eukaryotic cells have six general types of signaling mechanisms gated ion channels receptor enzymes membrane proteins that act through G proteins nuclear proteins that bind steroids and act as transcription factors membrane proteins that attract and activate soluble protein kinases and adhesion receptors that carry information between the extracellular matrix and the cytoslceleton. [Pg.425]

Among the different peripheral cells expressing APP, platelets are particularly interesting because they show concentrations of its isoforms equivalent to those found in the brain [96]. Some differences between these two cellular populations are nevertheless present both at mRNA and at protein levels the isoform 695, lacking the Kuntiz Protease Inhibitor (KPI) domain, is by far the most abundant in neuronal tissue, whereas its expression is nearly undetectable in platelets in whom the major isoform is APP 770 [97]. After the platelets are activated, soluble forms of cleaved APP are released, analogous to processing in neurons. [Pg.120]

Bacterial signal peptidase is an example of a known enzyme that could serve as a target for new antibacterial agents [13], Recently, a catalytically active, soluble fragment of signal peptidase from E. coli has been crystallized as a complex with a P-lactam inhibitor [69], This represents a major step in the efforts toward the rational design of inhibitors that can be readily tested for their enzyme inhibition and bacterial growth-inhibition activities. [Pg.253]

Dowex AI (%) Activity Activity (soluble enzyme) (immobilized enzyme) (U/mL) (U/mL) IC (%) Retention after hydrolysis (%)... [Pg.149]

In these phase I studies, trastuzumab displayed dose-dependent pharmacokinetics, with a serum half-life ranging from 1 day at the 10-mg dose level to 14 days at the 500-mg dose level. Importantly, when administered at the higher dose levels, consistent serum trough concentrations of trastuzumab above 10 pg/ml were achieved, which was the target concentration based on the in vitro antiproliferative activity. Soluble HER ECD was detected in 24 of 28 patients and was correlated with altered trastuzumab pharmacokinetics. Also, in contrast to 4D5 therapy, no human antihuman antibodies (HAHA) were observed following trastuzumab administration. [Pg.397]

N. A. Robinson, N. H. Goss and H. G.Wood (1984). Polyphosphate kinase from Propionibaterium shermanii-. formation of an enzymatically active soluble complex with basic proteins and characterization of synthesed polyphosphate. Biochem. Int., 8, 757-769. [Pg.252]

The activation of Gs has been studied extensively both in native membranes and with purified Gs in solution. Non-hydrolyzable GTP analogs, but not GTP, activate soluble Gs. However, both the analogs and GTP elicit Gs activation in membranes,... [Pg.5]

Nitric oxide is synthesized from the amino acid arginine in a reaction catalysed by NOS I-arginine + 02 + NADPH — citrulline + NADP+ + NO (thiol, tetrahydrobiopterin, FMN and FAD being requisite cofactors in this process). NO subsequently acts by activating soluble GC, thereby successively causing elevation of cGMP and PKG activation. NO can also act by activating Ca2 1 -dependent K+ channels. [Pg.256]


See other pages where Solubility activity is mentioned: [Pg.249]    [Pg.564]    [Pg.1144]    [Pg.177]    [Pg.75]    [Pg.327]    [Pg.238]    [Pg.34]    [Pg.185]    [Pg.242]    [Pg.405]    [Pg.189]    [Pg.139]    [Pg.124]    [Pg.228]    [Pg.736]    [Pg.249]    [Pg.421]    [Pg.347]    [Pg.249]    [Pg.526]    [Pg.540]    [Pg.287]    [Pg.363]    [Pg.95]    [Pg.164]    [Pg.170]    [Pg.361]    [Pg.6]    [Pg.253]    [Pg.254]   
See also in sourсe #XX -- [ Pg.398 , Pg.399 , Pg.403 ]




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Activated water-soluble

Activators of Soluble Guanylyl Cyclase

Active pharmaceutical ingredient Solubility

Active pharmaceutical ingredients development solubility stability

Activity Coefficient and Solubility in Water

Activity coefficient from solubility

Activity coefficient from solubility measurement

Activity coefficient solubility parameter

Activity coefficient, and solubility

Activity coefficients calculation, from solubilities

Activity solubility equilibria

Activity solubility product

Activity solubility product constant

Activity, definition solubility product

Aqueous solubility and activity coefficient

Drug solubility and biological activity

Electrolytes, activity coefficients solubility

Electrolytes, soluble surface-active

Esters, active water-soluble

Organics, solubility activity)

Parenteral preparations active substance solubility

Preformulation, active solubility

Solubility Structure-activity relationships

Solubility group activity)

Solubility product— solvent activity coefficients from

Solubility surface activity measurements

Solubility transport activity

Solubility, Chemical Potential, and Ion Activities

Soluble enzyme activity

Soluble guanylate cyclase activation

Soluble guanylate cyclase activation mechanism

Soluble guanylate cyclase activation production

Soluble guanylate cyclase activation synthesis

Suppositories active substance solubility

Water Soluble Fullerenes with Antiviral Activity

Water-soluble activated ester

Water-soluble active ingredients

Water-soluble antimicrobial active

Water-soluble antimicrobial active components

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