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Water molecules urea molecule

Polymerisation may occur as a result of dehydration of these compounds to methylene and dimethylene urea or more probably by a stepwise loss of water between the molecules of methylol and dimethylol-urea. [Pg.1017]

Urea has the remarkable property of forming crystalline complexes or adducts with straight-chain organic compounds. These crystalline complexes consist of a hoUow channel, formed by the crystallized urea molecules, in which the hydrocarbon is completely occluded. Such compounds are known as clathrates. The type of hydrocarbon occluded, on the basis of its chain length, is determined by the temperature at which the clathrate is formed. This property of urea clathrates is widely used in the petroleum-refining industry for the production of jet aviation fuels (see Aviation and other gas-TURBINE fuels) and for dewaxing of lubricant oils (see also Petroleum, refinery processes). The clathrates are broken down by simply dissolving urea in water or in alcohol. [Pg.310]

Incorporation of the position of water molecules that are firmly bound to the protein can impart affinity and novelty to the designed ligand. A prime example is the design of a class of HIV protease cyclic urea inhibitors by DuPont scientists that incorporated a water molecule bound to both flaps of the enzyme into their ligand [32]. The crystal structure of the HIV protease-cyclic urea complex [32] shows the urea carbonyl oxygen substituting for the position of the water molecule. [Pg.27]

If the metallisable dye is insoluble in water, a miscible solvent such as ethanol or ethylene glycol may be added. Polar solvents such as formamide or molten urea have sometimes been preferred. It is likely that such solvents will preferentially displace water molecules and coordinate with the chromium (III) ion as the first step in the reaction. If colourless organic chelates of chromium, such as those derived from oxalic or tartaric acid, are used instead of or in addition to hydrated chromium (III) salts, the difficulty of replacing the strongly coordinated water molecules in the first stage of the reaction is eliminated. In this way the initial reaction can be carried out at high pH without contamination by the precipitation of chromium hydroxide. Use of the complex ammonium chromisalicylate (5.12) in this connection should also be noted (section 5.4-1). [Pg.250]

Figure 15.2 Reaction mechanism of urease. Ni 1 binds urea and acts as a Lewis acid to polarise the carbonyl group, making its carbon more electrophilic, while Ni 2 facilitates deprotonation of a bound water molecule to generate a nucleophilic hydroxyl species. (From Ragsdale, 1998. Copyright 1998, with permission from Elsevier.)... Figure 15.2 Reaction mechanism of urease. Ni 1 binds urea and acts as a Lewis acid to polarise the carbonyl group, making its carbon more electrophilic, while Ni 2 facilitates deprotonation of a bound water molecule to generate a nucleophilic hydroxyl species. (From Ragsdale, 1998. Copyright 1998, with permission from Elsevier.)...
Urea increases the water content of the stratum corneum, presumably as a result of the hygroscopic characteristics of this naturally occurring molecule. Urea is also keratolytic. The mechanism of action appears to involve alterations in prekeratin and keratin, leading to increased solubilization. In addition, urea may break hydrogen bonds that keep the stratum... [Pg.1303]

The buried water molecule noticed in the crystal structure of this and many other inhibitor complexes is tetrahedrally coordinated to both the inhibitor and the flaps of the enzyme. Randad et al. (1993) have used molecular modelling based on the crystal structures to incorporate the water oxygen atom as the carbonyl oxygen of novel, cyclic ureas (67). They reasoned that displacement of the water should be energetically favourable... [Pg.107]

Lam et al. (1994) have also used this trick of both mimicking and displacing the water molecule. They designed a series of 7-membered ring cyclic ureas, including 68, which is a potent enzyme = 0.27 nM) and virus inhibitor, and also has significant oral bioavailability. This compound is currently under clinical investigation. Crystal structures of 10 of these cyclic urea complexes with protease have been determined, and show that, as the... [Pg.108]

Pure urea is manufactured commercially by pumping ammonia and carbon dioxide into an autoclave where they are heated together under pressure while more of each gas is pumped in. Ammonium carbamate is formed at first, this loses water from its molecule to form urea, and the autoclave finally becomes... [Pg.372]


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See also in sourсe #XX -- [ Pg.4 , Pg.5 ]




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