Big Chemical Encyclopedia

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

Articles Figures Tables About

2- cleaved

Cleave the peptide into smaller fragments separate these fragments and determine the ammo acid composition of the fragments... [Pg.1130]

Phenacyl esters can be prepared from the phenacyl bromide, a carboxylic acid, and potassium fluoride as base. These phenacyl esters can be cleaved by irradiation (313 nm, dioxane or EtOH, 20°, 6 h, 80-95 % yield, R = amino acids > 300 nm, 30°, 8 h, R = a gibberellic acid, 36-62% yield ). Another phenacyl derivative, RC02CH(C0C6H5)C6H3 3,5-(0CH3)2, cleaved by irradiation, has also been reported. ... [Pg.239]

Table 2 depicts an approach to the modification of biomass with a view to effecting necessary changes, structural or otherwise, in natural polymers. Conventionally, modifications [54-63] are effected mainly by two ways (1) mechanical and/or chemical modifications without destroying the main structural backbone, and (2) cleav-... [Pg.415]

H2O2 The chemical symbol for hydrogen peroxide Hag Haemagglutinin Hag-1, Hag-2 Cleaved haemagglutinin subunits-1, -2 H E Haematoxylin and eosin hIL Human interleukin Hb Haemoglobin... [Pg.282]

FIGURE 4 Electropherogram of somatropin CRS (A) Electropherogram of the EP reference solution somatropin CRS I.Omg/ml (B) blank. The major peak corresponds to somatropin. The peaks 1—5 correspond to the impurities described by the Ph.Eur. (2) cleaved form (3) Gin-18 somatropin (4) deamidated forms. Temperature 30 C voltage program 0—l7.4kV. For more conditions see text. [Pg.253]

After DNA binds (step (T)), an active-site Tyr attacks a phosphodiester bond on one DNA strand in step (2), cleaving it, creating a covalent 5 - —Tyr protein-DNA linkage, and liberating the 3 -hydroxyl group... [Pg.936]

Cleave both strands of the DNA carrier with a restriction endonuclease. [Pg.416]

Selective cleavage of methoxythioanisoles. o-, rn-, and p-Methoxythioanisoles are selectively cleaved by sodium in HMPT to methoxythiophenols by cleavage of the CH3—S bond. Cleavage of the C—O bond occurs to a minor extent (less than 5%) in the case of o- and m-methoxythioanisoles. In contrast, sodium isopropanethiolate, (CH3)2CHSNa,2 cleaves the same substrates selectively to the sodium salts of (methylthio)phenols. Again, this process is not completely selective in the case of o-and m-methoxythioanisoles. Sodium isopropanethiolate also effects dealkylation of uryl alkyl sulfides when HMPT is used as solvent, and this reaction provides a convenient synthesis of aromatic thiols.3... [Pg.579]

Lin, X., Koelsch, G, Wu, S., Downs, D., Dashti, A., Tang, J. Human aspartic protease memapsin 2 cleaves the (3-secretase site of (3-amyloid precursor protein. Proc. Natl. Acad. Sci. USA 2000, 97, 1456-1460. [Pg.277]

Step 2 cleaves the silyl protecting group using a standard protocol with tetrabutylammonium fluoride (TBAF) in THF. [Pg.221]

Cleaving reagent trifluoroacetic acid (TFA Shanghai Fluoride Chemicals, Shanghai, China). [Pg.179]

Cleave the Dde group from the resin with 2% hydrazine and 1% allyl alcohol in DMF for 3 x 3 min (see Note 5). Wash the resin with DMF three times. Reagent needed hydrazine. [Pg.269]

The source of organic materials. Possible sources cited have included mineral-catalyzed hydrothermal synthesis, atmospheric syntheses driven by radiation or electrical discharges (see Section 5.1), and delivery from outer space (see Section 5.2). Cleaves and Chalmers have summarized the alternatives.61... [Pg.81]

Cleave several -fig aliquots of the DNA with different restriction endonucleases, following the manufacturer s recommendations. Fractionate the digested DNA by electrophoresis through 0.8% (w/v) agarose gels, then visualize the DNA by ethidium bromide staining and transillumination. [Pg.311]

Step [2] Cleave the three n bonds and use arrows to show where the new bonds will be formed. [Pg.588]

Other reactions include the apparent oxidative addition of the OH radical from water to [t -(Me3Si)2C5H3]2Ln (Ln = Sm, Yb) to give [)j -(Me3Si)2C5H3]2Ln( i-OH) 2 complexes, which have been structurally characterized . The complex (f] -Cp )2Sm(THF)2 cleaves the C-N bond of isonitriles to give the cyano complex, ( -Cp )2Sm(CN) (CNR), among other products . [Pg.391]

NH2NH2,H2O,MeOH,0°Ctort, l-2h Hg(OAc>2, 2-3horCu(OAc>2, 3-24b HSCH2CH2OH, 71-92% yield. These conditions return the free tbiol. Tbe use of Hg(OAc)2 cleaves tbe Acm (acetamidometbyl) group in the presence of the Pirn group. [Pg.677]

The configurations at C(4 ) of the hexahydroquinines were established62 by conversions1" (see also p. 213) to the corresponding N(l )—C(2 ) cleaved quinoli-zines in which the stereochemistry could be assigned by n.m.r. [Pg.236]

The reactive intermediate Fe(dmpe)2 cleaves the C—H bonds of other aromatic substrates, but the reactions are complex. The final products with anisole or methyl benzoate are methyl derivatives derived from cleavage of their respective O—CH3 bonds. Chlorobenzene gives a transient aryl hydride, but the ultimate product is the phenyliron chloro complex. Both Ru(dmpe)2H(CioH7) and Os(dmpe)2H(CioH7) are also in equilibrium with their respective M(dmpe)2 intermediates, but the equilibria are very sluggish and of little synthetic utility. An alternative approach to these species is photochemical activation of Fe(dmpe)H2 the products can be obtained more cleanly, and the intermediate Fe(dmpe)2 cleaves even aliphatic C—H bonds. [Pg.218]

EFEs have relatively broad substrate specificities, such as trypsin (cleavage site Lys-X and Arg-X, X represents an amino acid) and chymotrypsin (cleavage site Phe-X, Trp-X, Tyr-X and Leu-X), as shown in Fig. (9) [28]. F-III-2 cleaves [3-amyloid 1-40 at six sites, and oxidized insulin B-chain at five sites and F-II digested them at six and ten, respectively [28]. [Pg.837]

Uranyl Acetate. The complex U02(OAc)2 cleaves HIV mRNA upon photoactivation in a uniform fashion unless the nucleic acid is associated with protein (94). Recently, it has been shown that intense, specific cleavage occurs on RNA which is bound to HeLa cell nuclear protein. Rather an imprint than a footprint, this strong cleavage indicates that the structure of the RNA and its accessibility to metal complexes in solution is changed in the presence of protein. [Pg.468]


See other pages where 2- cleaved is mentioned: [Pg.395]    [Pg.478]    [Pg.592]    [Pg.343]    [Pg.1494]    [Pg.239]    [Pg.152]    [Pg.259]    [Pg.4233]    [Pg.165]    [Pg.570]    [Pg.149]    [Pg.15]    [Pg.102]    [Pg.96]    [Pg.71]    [Pg.581]    [Pg.449]    [Pg.386]    [Pg.4232]    [Pg.215]   
See also in sourсe #XX -- [ Pg.35 , Pg.51 , Pg.54 ]




SEARCH



1,3-Oxathiolanes cleaved

2-Methoxyethoxymethyl ethers cleaved

4- Methoxybenzyl ether cleaved

Acetate esters cleaved

Acetoacetate, cleaving enzyme,

Acetonides cleaved

Acid cleaving

Affinity cleaving

Aldolase Cleaves Fructose-1,6-bisphosphate

Anchors Cleaved by Reduction

Anchors cleaved by nucleophiles

Applications of RNA-Cleaving DNAzymes

Aryl ethers, cleaving

Benzyl ester cleaved

Benzyl ethers cleaved

Benzylidene acetals cleaved

Beta-site amyloid precursor protein cleaving

Beta-site amyloid precursor protein cleaving enzyme 1 (BACE

Bonds cleaving enzymes

Carbon-Heteroatom Bond-Forming or Cleaving Reactions

Chain cleaving agents

Chiral Auxiliary that is Cleaved off after the Reaction

Citrate cleaving enzymes

Clays cleaving

Cleave

Cleave

Cleave Cleaved

Cleave, Peter

Cleaved crystal faces

Cleaved from Individual Beads

Cleaved from the Solid Support

Cleaved mica

Cleaved-dimer model

Cleaving

Cleaving Genes - Restriction Enzymes

Cleaving RNA

Cleaving eggs

Cleaving reactions

Cleaving the Protein into Peptides

Cleaving transition-metal catalyzed

Cleaving, sample preparation

Crushing and cleaving

DNA Cleaving Drugs

DNA cleaving

DNA cleaving agents

Detection of Caspases, Cleaved Substrates, Regulators, and Inhibitors

Double bond cleaving dioxygenases

Double bonds cleaving reaction

Ene-diol Cleaving Dioxygenases

Enzyme-substrate complex extradiol cleaving

Esters Cleaved by -Elimination Reactions

Extradiol cleaving

Extradiol cleaving dioxygenases

Folic acid cleaving enzyme

Follicular small cleaved cell lymphoma

Freshly cleaved muscovite mica

Glucocerebroside cleaving enzyme

Glucosidase cleaves

Glycol-cleaving Reagents

Hydroxylamine cleaving ester bonds

Inositol-cleaving enzyme

Inositol-cleaving enzyme and

Intramembrane cleaving proteases

Linkages, cleaved

Linkers, oxidatively cleaved

Linkers, reductively cleaved

Lipoxygenase cleaving enzymes

Mechanical cleaving of polymer chains

Methoxymethyl ethers cleaved

Methylthiomethyl ethers cleaved

Nickel atom cleaves

Nickel double bonds cleaving reaction

Nucleophilic ring cleaving reactions

Oligopeptide-cleaving catalysts

Other Double Bond-Cleaving Dioxygenases

P-O bond-cleaving enzymes

Palladium double bonds cleaving reaction

Peptide cleaving

Peptide deformylase, protein cleaving catalyst

Peptides cleaving enzymes

Peptides protein cleaved into

Phosphates Cleaved by Cyclodeesterification

Phosphates cleaved

Phosphates cleaved photochemically

Proteases, protein cleaving agents

Protecting Groups Cleaved by Acid

Protecting Groups Cleaved by Dissolving Metal Reduction

Protecting Groups Cleaved by Fluoride Ions

Protecting Groups Cleaved by Light

Protecting Groups Cleaved by Nucleophilic Substitution

Protecting Groups Cleaved by Reductive Elimination

Protecting Groups Cleaved by Transition Metal Catalysis

Protein cleaving agents

Proteomics analysis cleave proteins

RNA-cleaving DNAzymes

RNA-cleaving agents

Reactions in which carbon-cobalt bonds are cleaved

Rhodium-Catalyzed Nucleophilic Ring Cleaving Reactions of Allylic Ethers and Amines

Ring-cleaving biaryl synthesis

Salt cleaving

Selective chemical methods for cleaving peptide bonds

Selective enzymic methods for cleaving peptide bonds

Single bond cleaving reaction

Sodium dithionite cleaving diazo bonds

Substituent-cleaving enzymes

Substituent-cleaving enzymes hydrolysis

TV-Benzylamines, to protect amines cleaved

Tetrahydropyranyl ethers cleaved

The Catalytic Strategy of P-O Bond-Cleaving Enzymes Comparing EcoRV and Myosin

Thiosulfate-cleaving enzyme

Trifluoroacetic acid cleaving with

Trimethylsilyl ethers cleaved

Use of DTT to Cleave Disulfide-Containing Crosslinking Agents

Vacuum-cleaved surfaces

Van Cleave

Von Willebrand factor cleaving protease

Wedge cleaving

© 2024 chempedia.info