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Felypressin

Therapeutic Function Choleretic agent Chemical Name 3-n-Butoxy-l-phenoxv-2-propanol Common Name — [Pg.619]

Initially, 4.5 g (0.08 mol) pulverized potassium hydroxide was dissolved in 300 ml isopropanol in a 500 ml four-neck flask equipped with stirrer, intensive cooler, dropping funnel and feed pipe for the gas treatment with nitrogen. [Pg.619]

0 g (0.4 mol) n-butylglycidyl ether and 41A g (0.44 mol) phenol was added thereto, whereafter the material was heated to boiling under nitrogen. The material was stirred, about 8.5 hours, until no glycidyl ether could be determined, e.g., by gas chromatography. [Pg.619]

After the suspension was cooled under nitrogen, the solvent was distilled off under vacuum. The residue was taken up in 200 ml water and the milky emulsion extracted exhaustively with ether. From the organic phase, the excess butylglycidyl ether was extracted with diluted potassium hydroxide solution. The ether phase was washed neutral with water and the solvent removed after drying with sodium sulfate. The remaining oily residue was distilled under vacuum there was obtained a colorless liquid of BP 123.5°C/0.07 mm. Yield 81.8 g (91.1% of the theory). [Pg.619]

Hoffmann, H., Wagner, J., Hofrichter, G. and Grill, H. U.S. Patent 3,839,587 October 1, 1974 assigned to Chemisch-Pharmazeutische Fabrik Adolf Klinge and Co. [Pg.619]

Chemical Abstracts Registry No. 3102-00-8 Trade Name Manufacturer [Pg.619]

5 hours, until no glycidyl ether could be determined, e.g., by gas chromatography. [Pg.619]


N-Carbobenzoxy-S-benzyl-L-cysteinyl-L-phenylalanyl azide Felypressin... [Pg.1620]

N-Carbobenzoxy-L-glutaminyi-L-aspara-ginyl-S-benzyl-L-cysteinyi azide Felypressin Ornipressin... [Pg.1620]

Polypetides of medicinal interest were reviewed earlier in this series [453] and developments have continued apace. Angiotensinamide, pentagastrin, tetra-cosactrin and felypressin are now either widely used or growing in importance and serve to illustrate how rapidly this branch of medicinal chemistry is expanding. [Pg.56]

Felypressin and ornipressin serve as adjunctive vasoconstrictors in infiltration local anesthesia (p. 206). [Pg.164]

Y. Azuma, K. Ohura (2004). Immunological modulation by lidocaine-epinephrine and prilocaine-felypressin on the functions related to natural immunity in neutrophils and macrophages. Curr. Drug Targ. Immune, Endocr. Metabol. Disord. 4 29-36. [Pg.405]


See other pages where Felypressin is mentioned: [Pg.619]    [Pg.619]    [Pg.621]    [Pg.1609]    [Pg.1614]    [Pg.1686]    [Pg.1725]    [Pg.835]    [Pg.835]    [Pg.2322]    [Pg.2342]    [Pg.2390]    [Pg.2437]    [Pg.165]    [Pg.206]    [Pg.339]    [Pg.362]    [Pg.350]    [Pg.350]    [Pg.101]    [Pg.104]    [Pg.215]    [Pg.520]    [Pg.1558]    [Pg.1558]    [Pg.1559]    [Pg.1559]    [Pg.835]    [Pg.835]    [Pg.2322]    [Pg.2342]    [Pg.2390]    [Pg.2437]   
See also in sourсe #XX -- [ Pg.164 , Pg.206 ]

See also in sourсe #XX -- [ Pg.350 ]

See also in sourсe #XX -- [ Pg.835 ]

See also in sourсe #XX -- [ Pg.168 , Pg.204 ]

See also in sourсe #XX -- [ Pg.380 , Pg.385 ]




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