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Protease inhibitors acids

Extraction of hGH from pituitary glands has been accompHshed by a variety of procedures with or without protease inhibitors. One of the first commercial procedures used glacial acetic acid at 70°C to extract the hGH from the glands (39). [Pg.197]

Permeation enhancers are used to improve absorption through the gastric mucosa. Eor example, oral dehvery of insulin (mol wt = 6000) has been reported from a water-in-oH- emulsion containing lecithin, nonesterified fatty acids, cholesterol [57-88-5], and the protease inhibitor aprotinin [9087-70-1] (23). [Pg.141]

In the rosary pea Abrus precatorius L. Trigollenine as well as its gallic acid ester Precatorine (209) is found (71P195) (Scheme 69). 1-Carboxymethyl-nicotinic acid (210) was isolated as a colorless solid from the marine sponge Anthosigmella cf. raromicrosclera as a cysteine protease inhibitor (98JNP671). This compound was first synthesized in 1991. The sodium... [Pg.127]

Uiastereoselecdve catalydc nitro-aldol reacdons of opdcally acdve iV-phthaloyl-c-phenyl-alanal with nitromethanein the presence of LLB proceed with high diastereoselecdvityfruirdryii = 99 11 as shown in Eq. 3.76. The product is converted via the Nef teacdon into f3S,35 -3-amino-3-hydroxy-4-phenylbutanoic acid, which is a subunit of the HIV-protease inhibitor... [Pg.58]

Other types of HIV-1 protease inhibitors have also been prepared using microwave-promoted Suzuki reaction [37]. The symmetric cyclic sulfamide (3K,4S,5S,6it)-3,6-bis(phenoxymethyl)-2,7-bis[4-(2-thienyl)benzyl]-l,2,7-thi-adiazepane-4,5-diol 1,1-dioxide, for instance, was synthesized via cross-couphng of (3aS,4R,8it,8aS) - 5,7 - bis(4 - bromobenzyl) - 2,2 - dimethyl - 4,8 - bis-(phenoxymethyl) hexahydro [1,3] dioxolo [4,5 - d] [ 1,2,7 ] - thiadiazepine 6,6 - dioxide with 2-thienylboronic acid for 3 min at 45 W (Scheme 19). [Pg.165]

The cis P-lactams 57 are shown to act as cholesterol absorption inhibitors <96BMCL1947> and 58, an analogue of the dipeptide Phe-Gly methyl ester, is a protease inhibitor <96BMCL983>. A straightforward synthesis of proclavaminic acid 59, a biosynthetic precursor of clavulanic acid, is reported <96TA2277>. [Pg.72]

Jones K, Hoggard PC, Khoo S, Maher B, Back DJ (2001) Effect of alphal-acid glycoprotein on the intracellular accumulation of the HIV protease inhibitors saquinavir, ritonavir and indinavir in vitro, Br J Chn Pharmacol 51 99-102... [Pg.48]

Other topical bleaching agents include arbu-tin, licorice, unsaturated fatty acids, soy extracts, serine protease inhibitors, ellagic acid and resveratrol. [Pg.153]

Further, Wasserman and coworkers developed a direct acylation of stabilized phosphonium ylides by carboxylic acids in presence of the EDCI/DMAP (way c). This last method allows the introduction of a-aminoacid structures into the resulting P-oxo phosphorus ylides [19-25],opening the way to the total synthesis of depsipeptide elastase inhibitors [22,24] or cyclic peptidic protease inhibitor EurystatinA [20]. [Pg.44]

Davies and Reider (1996) have given some details of the HIV protease inhibitor CRDCIVAN (INDINAVIR) for which (lS,2R)-c -amino indanol is required. Indene is epoxidized enantioselectively, using the lacobsen strategy (SS-salen Mn catalyst, aqueous NaOH and PiNO), to (lS,2/ )-indene oxide in a two-phase system, in which the OH concentration is controlled. Indene oxide was subjected to the Ritter reaction with MeCN, in the presence of oleum, and subsequent hydrolysis and crystallization in the presence of tartaric acid gives the desired amino indanol. [Pg.178]

In addition, there is now epidemiological evidence that dietary antioxidants, such as vitamins A, C, D and E, phytic acid, and protease inhibitors can prevent carcinogenesis, including that of the gastrointestinal (GI) tract (Graf and Eaton, 1990 Block, 1991 Malone, 1991 Troll, 1991 Weisburger, 1991). [Pg.159]

Several aryl esters of 6-chloromethyl-2-oxo-2//-l -benzopyran-3-carboxylic acid act as human Lon protease inhibitors (alternate substrate inhibitors)46 without having any effect on the 20S proteasome. Proteasomes are the major agents of protein turnover and the breakdown of oxidized proteins in the cytosol and nucleus of eukaryotic cells,47 whereas Lon protease seems to play a major role in the elimination of oxidatively modified proteins in the mitochondrial matrix. The coumarin derivatives are potentially useful tools for investigating the various biological roles of Lon protease without interfering with the proteasome inhibition. [Pg.368]

Specific concomitant medications or consumptions (check specific statin package insert for warnings) fibrates (especially gemfibrozil, but other fibrates too), nicotinic acid (rarely), cyclosporine, azole antifungals such as itraconazole and ketoconazole, macrolide antibiotics such as erythromycin and clarithromycin, protease inhibitors used to treat Acquired Immune Deficiency Syndrome, nefazodone (antidepressant), verapamil, amiodarone, large quantities of grapefruit juice (usually more than 1 quart per day), and alcohol abuse (independently predisposes to myopathy)... [Pg.188]

When diabetic rabbits (24) were treated with 50 IU of bovine insulin imbibed at 50 mg/g poly (acrylic acid) (Figure 14) no reduction in serum glucose over that achieved by the dry blend control could be detected. Pretreatment of the animals with oral doses of either a penetration enhancer, sodium taurocholate, or a protease inhibitor, aproteinin, failed to improve the insulin activity. One possible explanation for this unexpected lack of activity might be that the diseased animals exhibit impaired ileal absorption of fluids (25). [Pg.232]

Fig. 7.3 Binding of the HIV protease inhibitor ritonavir. Amino acids highlighted in cyan are mutated in resistant strains of the virus and tend to occur at the extremities of the inhibitor (see color plates, p. XXXIII). Fig. 7.3 Binding of the HIV protease inhibitor ritonavir. Amino acids highlighted in cyan are mutated in resistant strains of the virus and tend to occur at the extremities of the inhibitor (see color plates, p. XXXIII).
From Sigma 3-aminoethylcarbazole (AEC) acrylamide/bis-acrylamide (30%) 37.5 1 amino acids alumina bentonite benzamidine bovine fiver tRNA bovine serum albumin (BSA) creatine phosphate (CP) diethyl pyrocarbonate (DEPC) dithiothreitol (DTT) Escherichia coli MRE600 tRNA pyrophosphatase (Ppase) Ca++ salt of folinic acid, (5-formyl THF) IIHPHS K salt of phospho-enol pyruvic acid, (PEP) creatine phospho kinase (CPK) protease inhibitor cocktail for fungal and yeast extracts phenylmethylsulfonyl fluoride (PMSF) spermidine trihydrochloride Tween 20. [Pg.262]


See other pages where Protease inhibitors acids is mentioned: [Pg.317]    [Pg.317]    [Pg.206]    [Pg.113]    [Pg.314]    [Pg.893]    [Pg.12]    [Pg.28]    [Pg.44]    [Pg.86]    [Pg.156]    [Pg.160]    [Pg.310]    [Pg.319]    [Pg.257]    [Pg.40]    [Pg.589]    [Pg.160]    [Pg.208]    [Pg.73]    [Pg.73]    [Pg.341]    [Pg.105]    [Pg.168]    [Pg.95]    [Pg.264]    [Pg.260]    [Pg.494]   
See also in sourсe #XX -- [ Pg.71 ]




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Acid inhibitors

Protease acidic

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