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. .: , 2007. 608 c.
ISBN 5-98657-009-
( ): pharmazeutischewirkstoffe1982.djvu
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GB-P 1 339605 (Beecham; Anm. 1.4.1971; Laufzeit ab 28.3.1972). b DAS 2 611286 (Bristol-Myers; Anm. 17.3.1976; USA Prior. 17.3.1975).
Altemativ-Synthesen:
USP 4053 360 (Bristol-Myers; ert. 11.10.1977; GB-Prior. 5.6.1974,19.3.1975).
DOS 2 454 841 (Archifar; Anm. 19.11.1974; I-Prior. 17.5.1974).
DOS 2 755 903 (Dobfar;Anm. 15.12.1977; I-Prior. 16.12.1976).
GB-P 1535 291 (Bristol-Myers; Anm. 5.3.1976; USA-Prior. 17.3.1975).
USP 4098 796 (Novo; ert. 4.7.1978; Anm. 7.6.1976),
Belg-P 867414 (Antibioticos S.A.; Anm. 24.5.1978; E-Prior. 4.6.1977).
Mikrobiologische Acylierung von 6-APA mit D-a-(4-Hydroxyphenyl)-glycinmethylester-Hydrochlorid mittels Aphanocladium aranearum ATCC20453:
USP 4073 687 (Shionogi; ert. 14.2.1978; J-Prior. 14.5.1975).
Amoxicillin - Amphetaminil A 49
•Na-Salz:
GB-P 1543317 (Beecham; Laufzeit ab 4Я.1976; Prior. 27.9.1975). DOS 2 729 112 (Beecham; Anm. 28.6.1977; GB-Prior. 7.7.1976).
Trihydrat:
DAS 2 611286 (Bristol-Myers; Anm. 17.3.1976; USA-Prior. 17.3.1975). DOS 2 732 528 (Bristol-Myers; Anm. 19.7,1977; GB-Prior. 20.7.1976). Wasserlosliche Salze mit Arginin oder Lysin: GB-P 1 504 767 (Beecham; Laufzeit ab 23.8.1976; Prior. 2.7.1975, 30.9.1975; 3.11.1975). GB-P 1539510 (Beecham; Laufzeit ab 23.8.1976; Prior. 23.8.1975, 30.9.1975, 3.11.1975). ^Amorphes41 Amoxicillin: DAS 2112 634 (Beecham; Anm. 16.3.1971; GB-Prior. 16.3.1970). Formulierung fur Injektionslosungen: GB-P 1 532 993 (Beecham; Anm. 7.3.1975; Laufzeit ab 9.2.1976). O-Acetylamoxicillin: USP4053 360 (Bristol-Myers; ert. 11.10.1977; GB-Prior. 5.6.1974,19.3.1975).
D:
GB:
1:
Amoxypen® (Grunenthal) Clamoxyl® (Wiilfing)
□amoxyi® (Beecham-Sevigne) Hiconcil® (Allard)
Amoxil® (Bencard)
Alfamox® (Alfa Farm.)
Am-73 (Medici)
Amoxillin (Esscti)
Isimoxin® (Isi)
Moxal® (Roger Bellon)
Piramox® (Pharmax)
Veiamox® (2^ambeletti) Amplimox® (Iton)-Tribydrat Ibiamox® (Ibi)-Trihydrat Majurpen® (Cyanamid)-Trihydrat Pamocil® (Lancet)-Trihydrat Paradroxil® (Bristol)-Trihydrat Simplamox® (ISF)-Trihydrat Sintoplus® (Aesculapius)-Trihydrat Zimox® (Farmalabor)-Tnhydrat Ibiamox Iniett.® (Ibi)-Na-Salz
USA;
Sintoplus Inett.® (Aesculapius)-Na-Salz zahlreiche Komb.-Praparate Amolin® (Takeda)
Amoxycillin (Mohan; Toho) Chitacillin® (Banyu)
Clamoxyl® (Beecham)
Delacillin® (Sankyo)
Efpenix® (Toyo Jozo)
Hiconcil® (Bristol)
Himinomax® (Kaken)
Pacetocin® (Kyowa)
Sawacillin® (Fujisawa)
WideciJIin® (Meiji)
Amoxicillin (Parke Davis)
Amoxil® (Beecham-Massengill) Larotid® (Roche)
Polymox® (Bristol)
Robamox Robicaps® (Robins)
Sumox® (Reid Provident)
Trimox® (Squibb)
Utimox® (Parke Davis)
Wymox® (Wyeth)
Amphetaminil
17590-01-1
Psychotonicum
[(a-methy]phenethyl)amino]pbenylacetonitrile
o-
CH3
CH2-CH-NH2
2-Amino-1-phenyi-
propan
Natrium-
cyamd
>0
Benzaldehyd
CH3
Amphetamine
Oe-P 223 606 (Dr. H. Voigt; Anm. 25.4.1961; Laufzeit ab 15.3.1962). Klosa, J. Prakt. Chem. 20,275 (1963).
D: AN I® (Voigt)
50 A Amphotericin В - Ampicillin
Amphotericin В 1397-89-3 fungicides Antibioticum
polyene antibiotic
Fermentativ aus Streptomyces nodosus.
DOT7,192 (1971).
USP 2908611 (Olin Mathieson; ert. 1959; Prior. 1954).
D: Ampho-Moronal® (Heyden)
Amphotericin В zur Infusion (Heyden) Mysteclin® (Heyden)-Komb.
F: Amphocycline® (Squibb)-Komb. Fungizone® (Squibb)
GB: FungiIin®/-TP (Squibb)
1: Fimgiliri® (Squibb) Fungizone® (Squibb)
J: Fungizone® (Squibb-Sankyo) USA: Fungizone® (Squibb)
Ampicillin 69-53-4 Antibioticum
7177-48-2 Tribydrat 69-52-3 Na-Salz
23277-71-6 K-Salz
d-(—)-(,Cf-aminobenzyl)penicillin om-( — )-6-(2'amino-2-phenylacetamido)-3,3-dimethyi-7-oxo-4-thia-1 -azabicycio[3.2.0jheptane-2-carboxyIic add 3
/_V-CH-C00H ClCTOC;H;tMtC^H,)i CH-CO-O-COOC2H5
\_/ 1 CMorameisen- /Triethyl- \—/ |
NH — CO — 0— CHz-” CeHs aaureethyi- amin NH —CO — 0 — CHj —CgHs
ester
D-M-CbO-Phenytglycin
ТЯС'""*
h. fYcH-CO-NH-H-V3
6-.m,no- w'fH40'NHt[X
pMicillansaure NH 0 ' \ CH3
C0-0-CH2-C6H5 t00H CbO-Ampicillin [Na-Salz)
Hz/Pd-BaC03
i-\ 4
(I yj-ch-co-nhH-rS4/CHs
_ NHZ 0W>/cH3
COOH
Ampicillin
Ampicillin A 51
/“V-CH-CO-CI
NH2-HCI
HzN-j-j-S СИ3
i-N~/vCH3
COOH
Ampicillin
0.(-)-*-Phenyi-
glycinciilorid-
Hydrochlond
6-Ammo-
penicillansaure
CH-CoONa
NH2
0-(-)-Phenylglycm
(Na-Salz)
HiC-CO-CH;-COOCH3
Acetessigsauremethylester
o- CH-COONa
~~ NH
t
НзС-С = СН-СООСНз
A/-(1-Methoxycarbonyt-propen-2-yi)-o-(-}-phenyiglycin-Natrium (0 -!->-Phertylglycin-Dane-Salz)
t. CICOOC2H5/Pyridir
COOH
1. Chlorameisen-saureeth/lesier
2. 5-Amino-penicillansaure
a GB-P 893049 (Beecham; Anm. 6.10.1958,12.5.1959).
GB-P 902 703 (Beecham; Laufzeit ab 19.5.1961; Prior. 25.8.1960).
USP 2985 648 (Beecham; ert. 23.5.1961; GB-Prior. 6.10.1958).
DAS 1 139844 (Beecham; Anm. 6.10.1959; GB-Prior. 6.10.1958, 12.5.1960).
DBP 1 156 078 (Beecham; Anm. 29.5.1961; GB-Prior. 25.8.1960). b USP 3 140282 (Bristol-Myers; ert. 7.7.1964; Anm. 5.3.1962). с GB-P 991 586 (Beecham; Anm. 28.2.1963, 3.12.1963; Laufzeit ab 13.2.1964). Weitere Verfahren:
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