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Атлас лекарственных расний СССР - Цицин Н.В.

Цицин Н.В. Атлас лекарственных расний СССР — Медлит, 1962. — 711 c.
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---Mep-Tyr-Phe-OMe —-► Mep-Tyr-Phe-NH-NH2 3 ЦТ
Desmopressin-Desonid D 275
1. HBr/CH3COOH
2. DMF/NEtj/pH 8,0/ -15В°C
3. РЁ * Isoamyirntrit
Bzl Bzl Tos
I I I
Mep-Tyr -Phe -Gin - Asn -Cys- Pro - □ - Arg-Gly — NH2
1. Na^./NHs,, /-40В«C
2. CHjCOOH/СЂР™ $.8
3. K3Fe(CNI6
U R*inigung an Sephaflex
Mep-Tyr-Phe-Gtn-Asn-Cys-Pro- D- Arg-Gly^NHj
Desmopressin
Abkiirzungen:
Biz = Benzyi-Rest
ET = Ethyl-Rest
Мер = 2-Mercaptopropionyl-Rest
Me = Methyi-Rest
Np = 4-Nitrophenyl-Rest
Tos = 4-Toluolsulfonyl-Rest
Z = Benzyloxycarbonyl-Rest
DOT 12, 23 (1976).
USP 3 454549 (Sandoz; ert. 8.7.1969; CH-Prior. 17.7.1964).
USP 3 497491 (Ceskoslovenska Akad.; ert. 24.2.1970; CS-Prior. 15.9.1966). R. L. Huguenin u. R. A. Boissonas, Helv. Chim. Acta 49, 695 (1966).
DOS 2 723453 (Ferring; Anm. 24.5.1977; S-Prior. 24.5.1976).
DOS 2 749 932 (Ferring; Anm. 8.11.1977; S-Prior. 12.11.1976).
GB-P 1 539317 (Ferring; Anm. 20.5.1977; S-Prior. 24.5.1976).
GB-P 1 539 318 (Ferring; Anm. 4.11.1977; S-Prior. 12.11.1976).
D: Minirin (Ferring) I: Minirin (Valeas)
GB: DDA VP (Ferring) USA; DDA VP (Ferring)
Desonid 638-94-8 Glucocorticoid
11/3,16a.l7,21-tetrahydroxypregna-l,4-diene-3,20-dione cyclic 16,17-acetal with acetone
0
16a-Hydroxyprednisolon
[-0H
V-OH
Hydrocortison (S. S. 470)
H0-CH2.
Desonid
a USP 3 536 586 (Squibb; ert. 27.10.1970; Prior. 25.1.1968). b USP 2 990401 (American Cyanamid; ert. 27.6.1961; Prior. 18.6.1958,11.3.1958). S. Bernstein et al., J. Am. Chem. Soc. 81,4573 (1959).
276 D Desonid - Desoxycortonacetat
Ausgangsverbindung:
siehe auch W. S. Allen, S. Bernstein, J. Am. Chem. Soc. 78, 1909 (1956). S. Bernstein, Recent Prog. Horm. Res. 14,1 (1958).
Weitere Verfahren:
USP 3 549498 (Squibb; ert. 22.12.1970; Prior. 2.4.1968).
D: TridesilonВ® (Klinge)
F: LocapredВ® (Fabre-Fimex)
GB: TridesilonВ® (Dome)
I: PrenacidВ® (Sifi)
ReticusВ® (Farmila)
Reticus Antimicotico (Farmila)-Komb.
Reticus GynoJetus (Farmila)-Komb. Reticus Tape (Farmila)-Komb. SterodermВ® (De Angeli)
J: TridesonitВ® (Miles)
USA: TridesilonВ® (Dome)
Desoxycortonacetat
(Deoxycorticosterone acetate)
56-47-3
Mineralcorticoid
21-hydroxypregn-4-ene-3,20-dione-acetate
C=0 H,c
'c-0-CO-CH,/|7osOH) РќРў\) HjC
Isoprcpenylacetat
H3C-C0-0-CH2
OHC-0
,-Diox an 2. KHCO3/CH3COOH
1 N-Jodsuccmimid 0HC“0
H2/Pd-<
H3C-CO-O-CH2
=0
<^>=0/AI!0CHICH,yj
Cycto- / Aluminium-hexaron / tfiisopropanciat
H3C-CO-O-CH2
c=0
Desoxycortonacetat
c^o
CaC03/
CH30H/THF
I-CH2
sc*o
CHjCOOK/
РќСЌРЎ-РЎРћ-РЎРќ,
Desoxycortonacetat
Progesteron
Jod
Desoxycortonacetat - Desoximetason D 277
HcC-,OOC
Pregnenolon Oxalsaure-
diethylester
I
/Р”[[РћРЎРќ(РЎРќСЌ lab -в–є Desoxycortonacetat
Cycto- I Aluminium-hnaron I triisopropanolat
a F. Sondheimer et al., J. Am. Chem. Soc. 79,5034 (1957). Ausgangsverbindung:
Рњ. E. Wall, J. Am. Chem. Soc. 77,5665 (1955). b H. J. Ringold, G. Stork, J. Am. Chem. Soc. 80,250 (1958). СЃ H. Ruschig, Angew. Chem. 60,247 (1948).
H. Ruschig, Chem. Ber. 88, 878 (1955).
Weitere Verfahren:
DBP 871 153 (Hoechst; Anm. 1937).
DBP 875 353 (Schering AG; Anm. 1938).
USP 2 312 480 (Roche-Organon; ert. 1943, CH-Prior. 1937). USP 2 409043 (Schering Corp.;ert. 1946, D-Prior. 1939). USP 2 470 903 (W. C. Ross; ert. 1949; GB-Prior. 1945).
A. Serini et al., Ber. Dtsch. Chem. Ges. 72,391 (1939).
A. L. Wilds, РЎ. H. Shunk, J. Am. Chem. Soc. 70,2427 (1948). Obersicht:
Ullmann, 4. Auflage, Bd. 13, 52.
D: CortironВ® (Schering)
DocabolinВ® (Nourypharma)-Phenylpropionat-Komb.
PercortenВ® M(Ciba)-21-(2,2'Dimethyl-propionat)
Percorten® „wasserloslich“ (Ciba)-Glucosid F: Syncortyl® (Roussel)
GB: Deoxycortone Acetate Implants (Organon)
PercortenВ® M Crystals (Ciba)-21-(2,2-Dimethyl-propionat)
I: Corticosterone (Mitim)
DeSOXimetaSOn 382-67-2 Glucocorticoid
(Desoximethasone)
9-fluoro-ll/J,21-dihydroxy-16a-methylpregna-l,4-diene-3,20-dione
CortironВ® (Schering)
CortisterilВ® (Ital Suisse)
J: SyncortaВ® (Takeda)
USA: Artho-SteroneВ® (Philips-Roxane)-Komb. Cortate PelletsВ® (Schering)
CortinaqВ® (Central)
Deoxycortone Acetate (Christina)
Doca AcetateВ® (Organon)
PercortenВ® (Ciba)
PercortenВ® Pivaiat (Ciba)-21В«(2,2-Dimethyl-propionat)
278 D Desoximetason - Dexamethason
H3C-C0-0-CH2
*СЃРЅР·
21 - Acetoxy - 3,20 -dioxo-11/?- Methan -hydroxy-1Ba-methyl-1,4- sulfonyi-
pregnadien chlorid
H3C-CO-O-CH2.
+ РќР·РЎ-SO2CI
Рћ
i-ar/HCio4/[oMFj
N-Srom- /Perchloc-succmimid I saure
h3c-co-o-ch2n ohc-o^
-CH3
NaHC0a/CH30H
HO—CH2
-•CH3
1 (НзС — COl20/[pyridir]
2 h2f2/|dmf]
3 NaHCQ3 /РЎРќ3РћРќ__
1 Acetanhydrid
2 Ftuorwasserstoff
USP 3 099654 (Roussel-Uclaf; ert. 30.6.1963; F-Prior. 17.8.1^60).
DOS 1 159441 (Roussel-Uclaf; Anm. 4.8.1961; F-Prior. 17.8.1960).
FP 1 296 544 (Roussel-Uclaf; Anm. 17.8.1960).
R. Joly et al., Arzneim. Forsch. 24,1 (1974).
Ausgangsverbindung:
DOS 1205 096 (Roussel-Uctaf; Anm. 12.5.1961; F-Prior. 14.5.1960,16.5.1960). Weitere Verfahren:
Belg-P 614 196 (Schering AG, Anm. 21.2.1962; D-Prior. 22.2.1961).
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