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Cholesterine

Reinitzer F 1888 Beitrage zur kenntnis des cholesterins Monatsh. Chem. 9 421-41... [Pg.2565]

Cholesterin, n. cholesterol, cholesterin. saure, /. cholesteric acid (cholesterol). [Pg.92]

Die Reduktion von 17/3-Nitro-3/3-acetoxy-androsten-(5) mit Chrom(II)-chlorid liefert in 70%iger Ausbeute 3(5-Acetoxy-17-hydroximino-androsten-(5) (F 178—1790)2. 6-Ni-tro-3/3-acetoxy-cholesterin wird in THF zum 5 a -1 Iydroxy-3 [i-acetoxy-6-hydroximino-cholestan3 (F 128—131°) reduziert ... [Pg.521]

Reinitzer, F. (1888) Beitrage zur Kenntniss des Cholesterins. Monatsheftefur Chemie, 9, 421-441. [Pg.392]

An impressive example for the successful use of domino reactions for the synthesis of pharmacological lead structures was described by Paulsen et al1241 Recently, the difluoro compound 57 has been identified as highly potent inhibitor of the cholesterin-ester-transferprotein (CETP), which is responsible for a transfer of cholesterin from high-density lipoprotein (HDL) to low-density lipoprotein (LDL). This clearly results in an increase of LDL and a decrease of HDL which raise the risk of coronary heart desea-ses. The core structure of 57 is now accessible efficiently by a combination of a Mukaiyama-MichaeL... [Pg.46]

Reinitzer, F., Beitrage zur Kermtnis des Cholesterins, A/onali/ . Cftem., 9 412-441 (1888). Lehmann, O., Uber flieBende Kristalle, Z. Physikal Chem., 4 462-471 (1889). [Pg.145]

Reinitzer, F. Beitrage zur Kenntnis des Cholesterins , Monatsh. 9, 421, 1888. The term liquid crystals was first used by O. Lehmann in Fluessige Kristalle . Engelmann, Leipzig, 1904. See also H. Kelker, History of liquid crystals. Mol. Cryst. Liq, Cryst. 21, 1 (1973). For a history of the discovery and recognition of plastic crystals see J. Timmermanns, Plastic crystals, a historical review. J. Phys. Chem. Solids 18,1 (1961)... [Pg.52]

Poly-substituted aromatic rings are difficult to synthesize—in a recent work, inhibitors of the cholesterine ester transfer protein (CETP) were synthesized, using a highly sophisticated assembly of basic organic reactions and comprising... [Pg.19]

Diethoxy-thiophosphoryloxy)- XII/2, 638 Cabonrs-Hoffmann-Spaltung E2, 51 Cholesterin... [Pg.1152]

Chlortalidone, 464 Chlortet, 463 Chlortetracycline, 463 Chlortetracycline calcium, 463 Chlortetracycline hydrochloride, 463 Chlorthal dimethyl, 82 Chlorthalidone, 464 Chlorthiamid, 82 Chlortoluron, 82 Chlor-Trimeton, 457 Chlortripelennamine, 648 Chlor-Tripolon, 457 Chlortritylimidazol, 487 Chlorzide, 663 Chlorzoxazone, 465 Chlosudimeprimyl, 483 Chlotride, 454 Cholecalciferol, 465 Choledyl, 1011 Cholestenol, 466 Cholesterin, 466 Cholesterol, 466 Choline, 466 (metabolite), 999 Choline acid tartrate, 466 Choline bitartrate, 466... [Pg.1265]

Stoltefuss J, Logers M, Schmidt G, Brandes A, Schmeck C, Bremm KD, Bischoff H, Schmidt D (1999) 4-heteroaryl-tetrahydroquinolines and their use as inhibitors of the cholesterin-ester transfer protein. PCX Int Appl. CODEN P1XXD2 WO 9914215 A1 19990325,p 107... [Pg.92]

CHOLESTERIN CHOLESTEROL BASE H CHOLESTERYL ALCOHOL CHOLESTRIN CHOLESTROL CORDULAN DUSOUNE DUSORAN DYTHOL HYDROCERIN 3-P-HYDROXYCHOLEST-5-ENE KATHRO LANOL ... [Pg.359]

Reinitzer, F. Beitrage zur Kenntniss des Cholesterins. [Contribution on the identification of cholesterol.] Sitzgsher. d. Akad. d. Wissensch. 94, 420-441 (1888)... [Pg.684]

Figure 4.21 Domain formation of phospholipids with different chain lengths, the standard motif of biological membranes, was evaluated with disulfides AA and BB. Domain formation was only detectable in the presence of large amounts of cholesterin. ... Figure 4.21 Domain formation of phospholipids with different chain lengths, the standard motif of biological membranes, was evaluated with disulfides AA and BB. Domain formation was only detectable in the presence of large amounts of cholesterin. ...

See other pages where Cholesterine is mentioned: [Pg.1077]    [Pg.394]    [Pg.983]    [Pg.35]    [Pg.90]    [Pg.414]    [Pg.415]    [Pg.155]    [Pg.156]    [Pg.186]    [Pg.191]    [Pg.50]    [Pg.64]    [Pg.64]    [Pg.69]    [Pg.81]    [Pg.426]    [Pg.203]    [Pg.183]    [Pg.126]    [Pg.127]    [Pg.138]    [Pg.387]    [Pg.1077]    [Pg.466]    [Pg.592]    [Pg.1583]    [Pg.426]    [Pg.451]    [Pg.1130]    [Pg.426]    [Pg.182]   
See also in sourсe #XX -- [ Pg.25 ]




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Cholesterin

Cholesterine ester transfer protein

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