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Selective activities

Mobil MTG and MTO Process. Methanol from any source can be converted to gasoline range hydrocarbons using the Mobil MTG process. This process takes advantage of the shape selective activity of ZSM-5 zeoHte catalyst to limit the size of hydrocarbons in the product. The pore size and cavity dimensions favor the production of C-5—C-10 hydrocarbons. The first step in the conversion is the acid-catalyzed dehydration of methanol to form dimethyl ether. The ether subsequendy is converted to light olefins, then heavier olefins, paraffins, and aromatics. In practice the ether formation and hydrocarbon formation reactions may be performed in separate stages to faciHtate heat removal. [Pg.165]

Newel experimental approaches to anxiety therapy include ligands interacting with the ligand-gated ion channels that are selectively activated by nicotine, C qH 4N2 (87), the well-known active ingredient of cigarettes which has anxiolytic actions (42). Cholecystokinin B receptor ligands, specifically the dipeptoid, CI-988 [130404-91 -0] 02 1142 40 (88) have demonstrated anxiolytic activity ia preclinical models (43). [Pg.542]

NMD A receptors are selectively activated by A/-methyl-D-aspartate (NMD A) (182). NMD A receptor activation also requires glycine or other co-agonist occupation of an allosteric site. NMDAR-1, -2A, -2B, -2C, and -2D are the five NMD A receptor subunits known. Two forms of NMDAR-1 are generated by alternative splicing. NMDAR-1 proteins form homomeric ionotropic receptors in expression systems and may do so m situ in the CNS. Functional responses, however, are markedly augmented by co-expression of a NMDAR-2 and NMDAR-1 subunits. The kinetic and pharmacological properties of the NMD A receptor are influenced by the particular subunit composition. [Pg.551]

This selective activity is due in large part to the HSV-encoded thymidine kinase. Clinical studies... [Pg.306]

FIAC also strongly inhibits HCMV and Epstein-Barr vims (EBV) in vitro the two vimses known not to induce a specific viral thymidine kinase for their repHcation. However, HCMV may stimulate cellular kinases that can anabolize FIAC to its 5 -triphosphate, which specifically inhibits the HCMV-encoded DNA polymerase. This selective activity suggests that FIAC should be evaluated against HCMV infections. FIAC-ttiphosphate incorporated into DNA has shown strong in vitro activity against the DNA polymerases of human hepatitis B vims (HBV) and of woodchuck hepatitis vims (WHV) (37). [Pg.306]

Betazole (683) has been used as a chemical control substance for pharmacological characterization of histamine receptors (B-80MI40406), and shows a relative selective activity towards the H2-receptor. Betazole hydrochloride is used to diagnose impairment of the acid-producing cells of the stomach. [Pg.291]

Table 4. Properties of selected activated carbon products. Reprinted from [11], copyright (c) 1992 John Willey Sons, Inc., with permission. Table 4. Properties of selected activated carbon products. Reprinted from [11], copyright (c) 1992 John Willey Sons, Inc., with permission.
The selective activation of the methyl group in the 5-position is of considerable importance. This may be compared with the preceding activation of the nucleophilic substitution at C-5 by the substituent at C-4 (Section IV,B). [Pg.397]

Tiazofurine (142) is an antimetabolite with antineoplastic activity. It preferentially affects leukemic lymphocytes over normal cells due to selective activation by formation of its adenine dinucleotide by transformed cells. Of the syntheses available, one starts by conversion of iniidate 138 to methyl 2,5-anhydroallonothioate (139). Next, condensation with ethyl 2-amino-2-cyanoac-etate leads to the thioamide which undergoes thiol addition to the nitrile function to produce the amminothiazolecarboxyester system of 140 directly. Sodium nitrite in aqueous hypophosphorus acid eliminates the superfluous amino group via the diazonium transformation to give 141. This synthesis of tiazofurine (142) concludes by ester amide exchange in methanolic ammonia [48]. [Pg.96]

At present, no diugs exist that can selectively activate a2-receptor subtypes. Clonidine stimulates all three a2-subtypes with similar potency. Clonidine lowers blood pressure in patients with hypertension and it decreases sympathetic overactivity during opioid withdrawal. In intensive and postoperative care, clonidine is a potent sedative and analgesic and can prevent postoperative shivering. Clonidine and its derivative brimonidine lower... [Pg.45]

MAPK cascades are composed of three cytoplasmic kinases, the MAPKKK, MAPKK, and MAPK, that are regulated by phosphorylation (Fig. 1) [1, 2]. The MAPKKK, also called MEKK for MEK kinase, is a serine/threonine kinase. Selective activation of MAPKKKs by upstream cellular stimuli results in the phosphorylation of MAPKK, also called MEK for MAP/ERK kinase by the MAPKKK. MAPKKK members are structurally diverse and are differentially regulated by specific upstream stimuli. The MAPKK is phosphorylated by the MAPKKK on two specific serine/ threonine residues in its activation loop. The MAPKK family members are dual specificity kinases capable of phosphorylating critical threonine and tyrosine residues in the activation loop of the MAPKs. MAPKKs have the fewest members in the MAPK signaling module. MAPKs are a family of serine/threonine kinases that upon activation by their respective MAPKKs, are capable of phosphorylating cytoplasmic substrates as well as... [Pg.741]

Molecnlar Mechanisms of SERM Action as a Means of Understanding their Tissue-Selective Activities... [Pg.1114]

Sensory receptors expressed in particular in taste receptor cells of the taste buds that sense the five basic tastes salt, sour, sweet, bitter and umami (glutamate taste). Sodium type ion channels sense salty taste whereas sour taste is transduced by potassium type ion channels. The underlying cause of sweet, bitter, and umami tastes is the selective activation of different groups of G protein coupled receptors that discriminate between sweet, bitter, and umami tasting molecules. [Pg.1195]

Selective active immunization against rubella Same as for BOG vaccine Total volume of reconstituted vial SC... [Pg.570]

Selective active immunization against mumps Same as for BCG vaccine 0.5 ml. 9C (total volume of reconstituted vaccine)... [Pg.570]

Kroes, R.A., Abravaya, K., Seidenfeld, J., Morimoto, R.l. (1991). Selective activation of human heat shock gene transcription by nitrosurea antitumor drugs mediated by isocyanate-induced damage and activation of heat shock transcription factor. Proc. Natl. Acad. Sci. USA 88,4825-4829. [Pg.456]

One of the most important phenomena in material science is the reinforcement of mbber by rigid entities, such as carbon black, clays, silicates, calcium carbonate, zinc oxide, MH, and metal oxide [45 7]. Thus, these fillers or reinforcement aids are added to mbber formulations to optimize properties that meet a given service application or sets of performance parameters [48-53]. Although the original purpose is to lower the cost of the molding compounds, prime importance is now attached to the selective active fillers and their quantity that produce specific improvements in mbber physical properties. [Pg.95]

Rh(TMP)- under these conditions, and in fact the selective activation of methane in benzene solution is a distinctive and unusual feature of this system, given that aryl C—H activation ought to be thermodynamically favored over alkyl C—H activation. The proposed linear transition state proposed in Fig. 8 is the key to this different reactivity. The corresponding trimolecular transition state for an arene would be expected to be bent, and this would be precluded by the bulky TMP... [Pg.303]

As a general rule, the optimal immobilization method is found empirically by a process of trial and error, where the selectivity, activity, and operational stability of the enzyme after immobilization are taken into account. The immobilization process is very sensitive to different parameters and is treated as a kind of art [16]. [Pg.100]

The use of molecular biology methods, described in Section 5.3 seems to be especially worthwhile as it offers novel possibilities of optimization on process adjustment. Directed evolution leads to the formation of new biocatalysts with improved characteristics (selectivity, activity, stability, etc.). Incorporation ofnon-proteinogenic amino acids makes it possible to reach beyond the repertoire of building blocks used by nature. The prospect of bioconjugate preparation offers the possibility to form functional clusters of enzymes and to perform multiple synthetic steps in one pot. [Pg.116]

Kojima T, Obata K. Mukai K. Sato S, Takai T. Minegishi Y, Karasuyama H Mast cells and basophils are selectively activated in vitro and in vivo through CD200R3 in an IgE-independent manner. J Immunol 2007 179 7093-7100. [Pg.95]

We examined the effects of selective activation of histamine Hj receptors on coronary hemodynamics in two groups patients with atypical chest pain and normal coronary arteries, and patients with vasospastic angina [48]. Selective Hj receptor stimulation was achieved by infusing histamine intravenously (0.5 pg/kg/min) for 5 min after pretreatment with cimetidine to antagonize the H2 receptors. Heart rate was kept constant (100 beats/min) by coronary sinus pacing. [Pg.104]

TAFs. It is conceivable that different combinations of TAFs with TBP—or one of several recently discovered TBP-like factors (TLFs)—may bind to different promoters, and recent reports suggest that this may account for selective activation noted in various promoters and for the different strengths of certain promoters. TAFs, since they are required for the action of activators, are often called coactivators. There are thus three classes of transcription factors involved in the regulation of class II genes basal factors, coactivators, and activator-repressors (Table 37-A). How these classes of proteins interact to govern both the site and frequency of transcription is a question of central importance. [Pg.351]

Rao et. al recently published another method for the quantitation of the MB fraction. The method is based on the selective activating capacity of dithiothreitol on CR isoenzyme MB, after isoenzyme MM is activated by glutathione (51). Apparently the MB isoenzyme is not activated by glutathione" Eut is activated by dithiothreitol. The difference between CR activities obtained in the presence of glutathione alone and those obtained with both glutathione and dithiothreitol represent MB activity. The correlation is excellent (r 0.998) between the activity of MB in the isoenzyme mixture determined by this method, and the activity of isolated MB. [Pg.198]

Aston-Jones, G, Rajkowski, J, Kubiak, P and Alexinsky, T (1994) Locus coeruleus neurons in monkey are selectively activated by attended cues in a vigilance task. J. Neurosci. 14 4467 480. [Pg.184]

Lowry, CA, Odda, JE, Lightman, SL and Ingram, CD (2000) Corticotropin-releasing factor (CRF) increases the in vitro firing rates of serotonergic neurones in the rat dorsal raphe nucleus evidence for selective activation of a topographically organised mesolimbocortical system. J. Psychopharmacol. 14 (Suppl 2) All. [Pg.208]


See other pages where Selective activities is mentioned: [Pg.95]    [Pg.351]    [Pg.551]    [Pg.41]    [Pg.332]    [Pg.127]    [Pg.222]    [Pg.162]    [Pg.369]    [Pg.121]    [Pg.256]    [Pg.285]    [Pg.12]    [Pg.794]    [Pg.798]    [Pg.912]    [Pg.931]    [Pg.1037]    [Pg.189]    [Pg.151]    [Pg.160]    [Pg.68]    [Pg.248]    [Pg.274]    [Pg.71]   
See also in sourсe #XX -- [ Pg.398 ]




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Activation, selective phosphonium salts

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Activator selection

Activator selection

Active Ensemble Structures for Selective Oxidation Catalyses at Surfaces

Active ingredient design/selection

Active ingredients selective

Active site atomic arrangement, selectivity

Active space selection

Active-site selective reagents

Active-site selective reagents properties

Activity and Selectivity Maps

Activity and selectivity

Activity, selectivity, and stability

Activity-based compound selection

Activity/selectivity

Aldehydes activation, selective

Basic Performance Criteria for a Catalyst Activity, Selectivity and Stability of Enzymes

Bond-selective activation

Boronic acid-Nucleophile Complex Formed in the Enzyme Active Site as a way to Improve Potency and Selectivity

CH Activation is a Selective, Coordination Reaction

Cascade Reactions for Assaying Transketolase Activity by In Vivo Selection

Catalyst Activity Down-selection

Catalysts activity and selectivity

Catalytic activity olefin selectivity

Catalytic activity product selectivity

Catalytic activity selectivity

Compound selection structure-activity relationship models

Correlations of the catalyst microstructure with catalytic activity and selectivity

Enantiomer-Selective Activation of Racemic Catalysts

Flubendiamide selectively activating insect

In Vitro Profiling Drug Activity, Selectivity and Liability

Laser induced selective activation

Leaving group selective activation

Oligosaccharide synthesis by selective anomeric activation

Oligosaccharide synthesis by selective two-stage activation

Optically selective activation

Optimization of the Activity Profile and Wider Selectivity

Oxides selectivity and activity

Polymer-capped Bimetallic Nanoclusters as Active and Selective Catalysts

Predicted coke-conversion selectivity catalyst activity

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 relationships selective drug design

Quantitative structure-activity variable selection

Reference to the Active Cell or a Selected Range of Cells

SELECT VOLUNTEER ACTIVITIES WITH CARE

Selected Novel Glucokinase Activator Structures from Recent Patent Literatur

Selection Rules for IR and Raman-Active Vibrational Modes

Selection activity

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Selection for catalytic activity

Selection of reactive active site residues by affinity labeling

Selection rule for an infrared active mode of vibration

Selection rules for an infrared or Raman active mode of vibration

Selective Oxidative Activation of Methane

Selective activation

Selective activation

Selective activation three step sequential

Selective activation with three leaving groups

Selective activity meter

Selective adsorption of phenanthrene on activated carbons for surfactant

Selective antitumor activity

Selective drugs, activity toward

Selective drugs, activity toward receptors

Selective heat inactivation activities

Selective heating of active sites

Selective optimization of side activities

Selective optimization of side activities SOSA)

Selective oxygen activation

Selective peroxisome proliferator activated

Selective radical activation

Selective serotonin reuptake activation effects

Selectivity active carbon content dependence

Selectivity in C-H Activation

Selectivity of catalytic activity

Selectivity-activity relationships

Side activities, selective optimization

State-selective active-space methods

Synthesis through selective activation

The ORR Activity on Selected Cases

The Selective Activation of Alternative Reaction Sites in Substrates

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Tutorial Selection of Relevant Descriptors in a Structure-Activity Study

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