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. .: , 2007. 608 c.
ISBN 5-98657-009-
( ): pharmazeutischewirkstoffe1982.djvu
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Teejel® (Napp)-Komb.
I: Salicol® (Sais)
J: Satibon® (Grelan)
USA: Arthropan® (Purdue Frederick) Trilisate® (Purdue Frederick)
Ciclacillin
(Cyclacillin)
3485-14-1
Antibioticum
(l-aminocyclohexyl)penicillin or 6-(l-aminocyclohexanecarboxamido)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid
H
1-Ammo-cyclohexan-carbonsaure-N-carbonsaure-anhydrid
,CH3
'CH3
COOH
н H
,—. co-NH-j-4'sw.CH3 COOH
6-Amino-
pentcillansaure
NH2 Ciclacillin
DOT8,167 (1972).
USP 3 194 802 (American Home; ert. 13.7.1965; Anm. 7.2.1963; Prior. 26.2.1962). USP 3 553 201 (American Home; ert. 5.1.1971; Anm. 3.10.1967; Prior. 13.5.1966).
206 С Ciclacillin - Ciclonium-bromid - Ciclopirox Oiamin
Altemativ-Verfahren:
DOS 2 755 903 (Dobfar; Anm. 15.12.1977; I-Prior. 16.12.1976). Enzymatisch:
DAS 2 050982 (Kyowa Hakko; Anm. 16.10.1970; J-Prior. 24.10.1969). Uber Silyl-Derivate:
USP 3 478018 (American Home; ert. J 1.11.1969; Anm. 2.10.1967).
D: Ultracillin® (Griinenthal) J: Bionacillin-C® (Takaia) Citosarin® (Toyo Jozo)
Vastcillin® (Takeda) Wybital® (Wyeth)
Ciclonium-bromid
29546-59-6
Spasmolyticum;
Anticholinergicum
[diethylmethyl]2-[(a-methyl-a-5-norbornen-2-ylbenzyI)-oxy]ethyl]ammonium bromide
CH3
Aeetophenon
Ci
MgCI
5-Chtor- bzw.
Chlormagnesium
bicyclo[2.2.l]
hepten -(2)
(2-Norbornen-
5-yl-chlorid bzw.
-magnesiumchlorid
CH3
|^^>—C-OH
1 NaNH2
2. CI“CHj-CH2-N|C2H5)2 t Natriumamid 2. 2 - Diethylaminoethyi -chlond
,_v СНз C2H5
@-j-0-CH,-CH2-N
C2H5 bromid
CH3
C2H5
Ciclonium-bromid
Br'
DBP 1 052 982 (Asta; Anm. 29.6.1957). D: Dolo-Adamon® (Asta)-Komb.
Tranquo-Adamon® (Asta)-Komb.
Ciclopirox Oiamin
41621-49-2
29342-05-0 Ciclopirox
Fungicid
6-cyclohexyl-1 -hydroxy-4-methyl-2( 1 f/)-pyndone salt with ethanolamine
Ciclopirox Olamin - Cicloxilsaure С 207
a
СООСНз НзС^СН
I
CH3
5-Cyclohexyl-3-methyl-
5-oxo-2-pentensaure-methytester im Gemisch mit dem 3-Pentensaure-Derivat
laus /3,/9-Dimetl>ylacrytsaure-methylester)
NH2OH * HCI
Hydroxylamin-
Hydrochlorid
Cl^h
СООСНз
I i H2Cv. ^CH
I
CH3
5-Cyclohexyl-3-methyl-
5-oximino - 2 -pentensaure-methylester
1 NaCH/H20
2, H2N — CH; —CH?~OH __
2. Ethanolamm
• h2n-ch2-ch2-oh
Ciclopirox Olamin
NH20H
Hydroxyl-
amm
U
2-Amino-
pyridm
Ciclopirox
DOF 4, 795 (1979).
DOT 10,35 (1974).
a SA-P 696 039 (Hoechst AG; Anm. 12.8.1969; D-Prior. 31.8.1968).
DBP 1 795 270 (Hoechst AG; Anm. 31.8.1968).
DOS 2 214 608 (Hoechst AG; Anm. 25.3.1972). b USP 3 972 888 (Hoechst AG; ert. 3.8.1976; D-Prior. 25.3.1972).
D: Batrafen® (Cassella-Riede!) J: Batrafen® (Hoechst)
Cicloxilsaure 57808-63-6 Cholereticum;
(Cicloxilic acid) Lebertherapeuticum
m-2-hydroxy-2 phenylcvclohexanecarboxylic acid
1. CH20
2. NaOH
.снгон
Kaiium-
permanganat
l-Phenylcyclo-
hexen
c/s-2-Hydroxy-
methyl-l-pheryl-
cyclohexanol
DOT 15,165 (1979).
Belg-P 848 143 (Guidotti Int.; Anm. 9.12.1976; I-Prior. 12.11.1975). Anwendung als Cholereticum und weiteres Verfahren:
USP 3 700 775 (L. Turbanti; ert. 24.10.1972; I-Prior. 29.4.1966).
208 С Cicloxilsaure - Cicrotonsaure - Cimetidin
Stereochemie:
L. Turbanti et al., Arzneim. Forsch. 28 (II), 1449 (1978). I: Plecton® (Guidotti)
Cicrotonsaure
(Acide cicrotoique;
Cicrotoic acid)
/З-methylcyclohexaneacrylic acid СНз
СгЧ
Acetylcyclo-
hexan
ВГ-СН2-СООС2Н5
Bromessigsaure-
ethylester
25229-42-9
H3C OH
,c
a
Cholereticum
CH2-COOC2H5
3-Cyclohexyl-3-hydroxy-
buttersaureethylester
a'
CH3
4CH-COOC2H5
3-Cydohexyl-2-buten-
saureethylester
FP-M4 665 (A. H. C. Soc. de Chim. Organ, et Biol.; Anm. 3.5.1965). F: Accroibile® (Adrian-Marinier)
CH3
[^^SlH-COOH
Cicrotonsaure
Cimetidin
51481-61-9
Ulcustherapeuticum (H2-Rezeptorantagonist)
l-cyano-2-methyl-3-[2-[[(5-methylimidazol-4-yl)methyl]thiolethyl]-guanidine
НзС
^-CH-COOCzHs
o' Cl
2 - Chtoracetessigsaure-ethylester
2 H2N-CHO
Formamid
H3C*.
И
cvl'S
H5C2OOC
5-Methylimida-
zol-i-carbon-
saureethylester
H3C
HO-CH2
A-Hydroxymethyl-5-
methylimidazol-
Hydrochlond
HS-CHr~CH?~NHz • на
Cysteanmn - Hydrochlorid
НзС-
H2N-CH2-CH2-S-
•2H«
CH2
S-СНз
i-(2-AminoethylHhiomethyl-5-methyl-imidazol -Dihydrochlond
W-Cyanoimido-^S-difnethyl-dilhiocarbonat (aus Cyanamid, KOH, Schwefelkohlenstoff und DimethylsuHat)
Cimetidin - Cinchocain С 209
и н
НзС^С^ cH|NH;, нзс"Л
H3C-S-C-NH-CH2-CH2-S-CH2 НзС-NH“C-NH-CH?-CH2-S-CH2
н^сн I n-cn
I Cimetidin I
DOF 1, 13 (1976); 2, 71 (1977).
USP 3 894151 (Smith Kline + French; ert. 8.7.1975; GB-Prior. 20.4.1972).
USP 4000302 (Smith Kline + French; ert. 28.12.1976; GB-Prior. 20.4.1972).
DOS2320131 (Smith Kline + French; Anm. 19.4.1973; GB-Prior. 20.4.1972) - Med. Anw.
DOS 2 344779 (Smith Kline + French; Anm. 5.9.1973; GB-Prior. 5.9.1972 und 8.2.1973).
USP 3 950333 (Smith Kline + French; ert. 13.4.1976; Anm. 14.3.1974; Prior. 29.2.1972 und 20.9.1972). Cimetidin ,,A“:
DOS 2 742 531 (Smith Kline + French; Anm. 21.9.1977; GB-Prior. 21.9.1976, 24.1.1977).
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