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Steroids cholesterol and

Measurements. We weighed patients dally. Each morning we collected blood after a 10-hr fast and measured the serum total cholesterol, triglycerides and glucose. On the last three days of each diet we measured serum high density lipoprotein (HOL) cholesterol concentrations and calculated low density lipoprotein (LDL) cholesterol values. We collected all stools and measured frequency, wet and dry weights. Selected stool samples will be analyzed later for neutral steroids, cholesterol and bile acids. We used the paired T-test for statistical comparisons. [Pg.53]

The molecularly imprinted copolymer of 2-hydroxyethyl methacrylate (HEMA) and p-CyD-coupled HEMA was synthesized in chloroform to study its interaction with a pair of steroids cholesterol and testosterone [42]. The molecularly imprinted copolymer was found to absorb the print molecule several times better than an imprinted poly HEMA. Asanuma et al. [44] concluded that cholesterol binding by the HEMA polymer was not due to CyD inclusion because no inclusion of CyD to cholesterol can form in chloroform. Another strategy developed for imprinting using CyD elements is the vinyl CyD (Table 1 and 10.3(A)), which has been successfully applied for imprinting antibodies, oligo-peptides [45], and vancomycin [46[. [Pg.292]

Lanolin, wool fat, wool wax the fatty or more correctly waxy substance secreted by the skin of the sheep, m-p. 36-42°C. L constitutes up to 50% of the wei t of raw wool. It is a complicated mixture of fatty adds, alcohols, fats and waxy substances. The latter are chiefly esters of steroids (cholesterol and lanoster-ol) and long chain aliphatic alcohols with higher fatty acids, which are 6-hydroxylated or carry a terminal isopropyl or isobutyl residue. L. is obtained from raw wool by extraction with organic solvents or soap solutions. It forms water-in-oil suspensions, and is used widely in the pharmaceutical and cosmetics industries (as Adeps Lanae) as an ointment base. [Pg.352]

Other constituents present in musk include steroids (cholesterol and its esters, cholest-4-en-3-one, and possibly the bufadienolides re-sibufogenin and cinobufagin, and others) paraffins (long chain and branched) triglycerides (oleodipalmitin, palmitodiolein, and triolein methyl palmitate and methyl oleate wax protein (musk protein MP-1, MW ca. 35,000 Da) muscopyridine, hydroxymus-copyridine A and B, and other nitrogenous substances (e.g., urea and ammonium... [Pg.455]

Progesterone can be manufactured from cholesterol, from certain steroid sapogenins and from stigmasierol. [Pg.327]

Cholesterol is biosynthesized in the liver trans ported throughout the body to be used in a va riety of ways and returned to the liver where it serves as the biosynthetic precursor to other steroids But cholesterol is a lipid and isn t soluble in water How can it move through the blood if it doesn t dis solve in if The answer is that it doesn t dissolve but IS instead carried through the blood and tissues as part of a lipoprotein (lipid + protein = lipoprotein) The proteins that carry cholesterol from the liver are called low density lipoproteins or LDLs those that return it to the liver are the high-density lipoproteins or HDLs If too much cholesterol is being transported by LDL or too little by HDL the extra cholesterol builds up on the walls of the arteries caus mg atherosclerosis A thorough physical examination nowadays measures not only total cholesterol con centration but also the distribution between LDL and HDL cholesterol An elevated level of LDL cholesterol IS a risk factor for heart disease LDL cholesterol is bad cholesterol HDLs on the other hand remove excess cholesterol and are protective HDL cholesterol IS good cholesterol... [Pg.1096]

A steroid very closely related structurally to cholesterol is its 7 dehydro derivative 7 Dehydrocholesterol is formed by enzymatic oxidation of cholesterol and has a conju gated diene unit m its B ring 7 Dehydrocholesterol is present m the tissues of the skin where it is transformed to vitamin D3 by a sunlight induced photochemical reaction... [Pg.1096]

Bde salts, cholesterol, phosphoHpids, and other minor components are secreted by the Hver. Bile salts serve three significant physiological functions. The hydrophilic carboxylate group, which is attached via an alkyl chain to the hydrophobic steroid skeleton, allows the bile salts to form water-soluble micelles with cholesterol and phosphoHpids in the bile. These micelles assist in the solvation of cholesterol. By solvating cholesterol, bile salts contribute to the homeostatic regulation of the amount of cholesterol in the whole body. Bile salts are also necessary for the intestinal absorption of dietary fats and fat-soluble vitamins (24—26). [Pg.415]

Anilinonaphthalenesulfonic acid ammonia salt (ANS reagent) fatty acids [112,113] lecithin/sphingomyelin [114, 115] cholesterol and its esters [116, 117] steroids, detergents, hydrocarbons [118,119] prenol, prenylquinones [120]... [Pg.44]

In the early 1930 s, when the prime research aim was the commercial synthesis of the sex hormones (whose structures had just been elucidated), the principal raw material available was cholesterol extracted from the spinal cord or brain of cattle or from sheep wool grease. This sterol (as its 3-acetate 5,6-dibromide) was subjected to a rather drastic chromic acid oxidation, which produced a variety of acidic, ketonic and hydroxylated products derived mainly by attack on the alkyl side-chain. The principal ketonic material, 3j -hydroxyandrost-5-en-17-one, was obtained in yields of only about 7% another useful ketone, 3 -hydroxypregn-5-en-20-one (pregnenolone) was obtained in much lower yield. The chief acidic product was 3j -hydroxy-androst-5-ene-17j -carboxylic acid. All three of these materials were then further converted by various chemical transformations into steroid hormones and synthetic analogs ... [Pg.127]

Lipids are classified into two broad types those like fats and waxes, which contain ester linkages and can be hydrolyzed, and those like cholesterol and other steroids, which don t have ester linkages and can t be hydrolyzed. [Pg.1060]

BCRP (ABCG2) Cisplatin, folate, methotrexate, mitoxantrone, topotecan, irinotecan, steroids (cholesterol, testosterone, progesterone), certain chlorophyll metabolites, and others... [Pg.7]

The breast cancer resistance protein (BCRP) belongs to the G-branch of the ABC-transporter family (ABCG2). In contrast to most other ABC-proteins, BCRP consists of only one transmembrane domain (TDM) with one nucleotide binding fold (NBF) at its C-terminus. Because of this structural characteristic BCRP as well as other ABC-transporters with only one TMD are termed half transporters. To achieve functional activity these transporters have to form hetero- or homodimers. BCRP is involved in the multidrug resistance of certain tumors and transports endogenous compounds like cholesterol and steroid hormones. [Pg.250]

Cholesterol is a widely distributed sterol found free or esterified to fatty acids. It is an important intermediate in the biosynthesis of steroid hormones and the principal component of cell plasma membranes and the membranes of intracellular organelles. [Pg.356]

The lipids of major physiologic significance are fatty acids and their esters, together with cholesterol and other steroids. [Pg.121]

Acetyl-CoA is also used as the precursor for biosynthesis of long-chain fatty acids steroids, including cholesterol and ketone bodies. [Pg.129]

Step 5—Formation of Cholesterol The formation of cholesterol from lanosterol takes place in the membranes of the endoplasmic reticulum and involves changes in the steroid nucleus and side chain (Figure 26-3). The methyl groups on C,4 and C4 are removed to form 14-desmethyl lanosterol and then zymosterol. The double bond at 03—C9 is subsequently moved to Cj-Cg in two steps, forming desmosterol. Finally, the double bond of the side chain is reduced, producing cholesterol. The exact order in which the steps described actually take place is not known with certainty. [Pg.220]

Figure 26-3. Biosynthesis of cholesterol. The numbered positions are those of the steroid nucleus and the open and solid circles indicate the fate of each of the carbons in the acetyl moiety of acetyl-CoA. Asterisks Refer to labeling of squalene in Figure 26-2. Figure 26-3. Biosynthesis of cholesterol. The numbered positions are those of the steroid nucleus and the open and solid circles indicate the fate of each of the carbons in the acetyl moiety of acetyl-CoA. Asterisks Refer to labeling of squalene in Figure 26-2.

See other pages where Steroids cholesterol and is mentioned: [Pg.411]    [Pg.171]    [Pg.203]    [Pg.6]    [Pg.134]    [Pg.4]    [Pg.199]    [Pg.85]    [Pg.4]    [Pg.659]    [Pg.411]    [Pg.171]    [Pg.203]    [Pg.6]    [Pg.134]    [Pg.4]    [Pg.199]    [Pg.85]    [Pg.4]    [Pg.659]    [Pg.685]    [Pg.1094]    [Pg.414]    [Pg.68]    [Pg.63]    [Pg.191]    [Pg.685]    [Pg.1094]    [Pg.251]    [Pg.847]    [Pg.305]    [Pg.705]    [Pg.1127]    [Pg.123]    [Pg.124]    [Pg.219]    [Pg.627]    [Pg.632]    [Pg.273]    [Pg.274]    [Pg.218]   
See also in sourсe #XX -- [ Pg.156 ]




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Steroids Cholesterol, Bile Salts, and Steroid Hormones

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