Атлас лекарственных расний СССР - Цицин Н.В.
Скачать (прямая ссылка):
D: MasteridВ® Spritzamp. (Griinentlial) J: MastisolВ® (Shionogi)
F: PermastrilВ® (Cassenne) USA: DrolbanВ®(Lilly)
GB: MasterilВ® (Synthex) MasteroneВ® (Syntex)
I: MasteronВ® (Recordati)
Dyclonin
586-60-7
536-43-6
Hydrochtorid
Lokalanastheticum (nur topisch)
4'-butoxy-3-piperidinopropiophenone
h9cso
CH3
4-Butyloxy-
acetophenon
Pipendin Paraform-aldehyd
| НэСаО'
-Gr
CH2-CH2
0
Dyclonin
USP 2 771 391 (Allied Laboratories; ert. 1956; Prior. 1953).
USP 2 868 689 (Allied Labs.; ert. 1959; Anm. 1956).
J: Epicain AceВ® (SS PharmaceuticaI)-Komb. USA: DycloneВ® (Dow)
EpirocainВ® (Eisai)
Dydrogesteron 152-62-5
9/j,10a-pregna-4,6-diene-3,20-dione
Gestagen
344 D/E Dydrogesteron - Eburnamonin
Retroprogesteron Chloranil
{aus lumis?erol2)
USP 3 198 792 (North American Philips; ert 3.8.1965; Prior. 8.4.1959,12.6.1962).
P. Westerhof, E. H. Reerink, Red. Trav. Chim. Pays-Bas 79В» 771 (1960) (auch Ausgangsverbindung). Weiteres Verfahren:
M. P. Rappoldt, P. Westerhof, Reel. Trav. Chim. Pays-Bas 80,43 (1961).
D: DuphastonВ® (Thomae, Duphar)
F: DuphastonВ® (Duphar)
GB: DuphastonВ® (Duphar)
I: DufastonВ® (ISF)
DufastonВ® Depot. (ISF)
J: DuphastonВ® (Daiichi)
USA: DuphastonВ® (Philips-Roxane) GynorestВ® (Mead Johnson)
Eburnamonin
(Vincamon)
474-00-0
28645-79-1
Cerebraler Vasodilatator
' eburnamonine
Mn02-CeHtte/Toiu<ri
H5C2OOC OH CzHs
c/s-l-Ethyl-H2-hydroxy-2-ethoxycarbonyl-ethyl)-1,2,3, ДД 7,12,12b-octahydroindolo[2,3-ajcht-nolizin
(s. Vtncamin, S. 944)
Vgl. DOF 3,232 (1978).
DOT 14,160(1978).
GB-P 1440634 (Richter Gedeon; Laufzeit ab 7.12.1973; H-Prior. 8.12.1972). Ausgangsverbindung:
DOS 2 931295 (Richter Gedeon; Anm. 1.8.1979; H-Prior. 1.8.1978).
Weitere Verfahren:
DOS 2 323423 (Richter Gedeon; Anm. 9.5.1973; H-Prior. 17.5.1972).
USP 3 888 865 (Richter Gedeon; ert. 10.6.1975; Anm. 14.3.1973).
FP 2 268 016 (Omnium; Anm. 17.4.1974).
Isolierung aus Hunteria eburnea:
DOS 1932 245 (L. Olivier; Anm. 25.6.1969; F-Prior. 25.6.1968). Totalsynthese:
M. F. Bartlett, W. I. Taylor, J. Am. Chem. Soc. 82,5941 (1960).
E. Werkert, B. Wickberg,). Am. Chem. Soc. 87,1580 (1965),
Belg-P 776 337 (Roussel-Uclaf; Anm. 7.12.1971; F-Prior. 6.1.1971).
Belg-P 802 913 (Roussel-Uclaf; Anm. 27.7.1973; F-Prior. 31.7.1972).
G, Hugel et al, Tetrahedron Lett. 1974,1597.
Eburnamonin-Echothiopate-jodid-Econazol E 345
Kombination mit Glucose- 1-phosphat:
Belg-P 874154 (E. Corvi Mora; Anm. 14.2.1979).
Quarternare Ammonium-Salze:
DBP 1 244 794 (Richter Gedeon; Anm. 16.12.1963; H-Prior. 19.12.1962).
F: CervoxanВ® (Sobio) I: EburnalВ® (Chiesi)
EburnalВ® Fiale (Chiesi)
Echothiopate-jodid 513-10-0 Cholinesterase-inhibitor
(Ecothiopate)
5-(2-dimethylaminoethyl)-0,0-diethylphosphorothioate mcthiodide
H5C2O y0 p'
H5c20/ Nci
РЎРќР·
hs-ch2-ch2-n
CH3
H5c2os 0
X /
H5C2O S—CH2 —CH2 —N
Phosphorsaure- 2-Dimethylammo-
CH3
CH3
diethylester-chtorid
ethyimercaptan
CH3I
Methyl-
jodid
H5C'В°S y? rH
A ,l 3
HsC20 s-ch2-ch2-n-ch3 CH3
Echothiopate-jodid
USP 2 911 430 (Campbell Pharmaceuticals; ert. 3.11.1959; Prior. 15.1.1958).
D: Phospholinjodid Augentropfen (Dr. Winzer) J: Phospholin Jodide (Santen, Tobishi)
F: PhospholineВ® (Promedica) USA: EchodideВ® (Alcon)
GB: Phospoline Jodide (Ayerst) Phospholine JodideВ® (Ayerst)
I: Phospholine JodideВ® (Chinoin)
ECOnaZOl 27220-47-9 Fungicid; 24169-02-6 Nitrat Antimykoticum
l-[2,4-dichloro-/?-[0>chlorobenzyl)oxy]phenethyl]imidazole
I. NaH
Cl 2. С1-СНг—C
Cl
1-(2,4-Dichlorphenyl)-
2-H-imidazolyl)-ethanol (vgl. Miconazol-Synthese,
S.601)
1. Natriumhydnd
2. i-Chlorbensylchtorid
N-СНг-СН —0-CH2 .C!
Рѕ
346 E Econazol - Edrophonium-chlorid - Enfluran
DOT 11,308 (1975).
DAS 1 940388 (Janssen; Anm. 8.8.1969; USA-Prior. 19.8.1968). USP 3 717 655 (Janssen; ert. 20.2.1973; Prior. 19.8.1968).
E. F. Godefroi et al., J. Med. Chem. 12, 784 (1969).
D: Epi PevarylВ® (Cilag-Chemie) Gyno-PevarylВ® (Cilag-Chemie) F; Gyno-PevarylВ® (Cilag-Chimie) PevarylВ® (Cilag-Chimie)
GB: EcostatinВ® (Fair)
Gyno PevarylВ® (Ortho) PevarylВ® (Ortho)
I: PevarylВ® (Cilag)
SkilarВ® (Italchemie)
Edrophonium-chlorid
116-38-1
473-37-0
302-83-0
Hydroxid
Bromid
Curare-Antagonist
ethyl (m-hydroxyphenyl)dimethylammonium chloride
_ /РЎРќР·
<fjV~N + C2H5B(
J 4CH3 HO
3-Dimethylamino- Ethyl-pherol bromid
/^-^N-РЎРќР·
н«Г ^
Edrophonium-bromtd
AgCl^
__, ?2H5
cr
РќРµ/ РЎРќСЌ Edrophonium-chlorid
USP 2 647 924 (Hoffmann-LaRoche; ert. 1953; Prior. 1950).
GB: TensilonВ® (Roche) J: AntirexВ® (Kyorin)
USA; TensilonВ® (Roche)
Enfluran
13838-16-9
Inhaiationsanastheticum
2-chloro-l,l,2-trifluoroethyl difluoromethy! ether
Cl F I ! F-CH-C-O-CH Р·
F
2-СМог-1Д,2-ЫМиог-
ethyl-methylether
Cl F Cl I I I F-CH-C-0-CH I I F Cl
2-Chlor-1,1,2-tnf luor-ethyl-dichlormethylether
HjFj/SbCls Oder SbFj/SbCts
Cl F F I 1 I F-CH-C-O-CH I I F F
Enfluran
USP 3 469 011 (Air Reduction Comp.; ert. 23.9.1969; Anm. Р—Рђ0Р›966).
USP 3 527 813 (Air Reduction Comp.; ert. 8.9.1970; Prior. 3.10.1966,4.9.196S).
