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Атлас Гематология - Андерсон Ш.

Андерсон Ш. Атлас Гематология — М.: Логосфера, 2007. — 608 c.
ISBN 5-98657-009-Х
Скачать (прямая ссылка): pharmazeutischewirkstoffe1982.djvu
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AldactoneВ® (Boehringer Mannh., Searle) AldactoneВ®-SaltutinВ® pro inj. (Boehringer Mannh., Searle)-Komb. OsyrolВ® pro inj. (Hoechst)
SincomenВ® (Schering)-Komb. AldatenseВ® (Searle)-Komb.
PhanuraneВ® (Specia) SoludactoneВ® (Searle) I: AldatenseВ® (Spa) SoldactoneВ® (Spa) VenactoneВ® (Lepetit) USA: SoldactoneВ® (Searle)
Kanamycin (A)
59-01-8
25389-94-0
Antibioticum
Sulfat
* D-streptamin, 0-3-amino-3-deoxy-a-u-glucopyranosyl-(l—>6)-0-|6-ammo6-deoxy-a-i> glucopyranosyl-(l-»4)]-2-deoxy-
Kanamycin (A)
Aus Fermentationslosungen von Streptomyces kanamyceticus USP 2 931798 (H. Umezawa, K. Maeda, M. Meda; ert. 5.4.1960; J-Prior. 5.9.1956). USP 2 936 307 (Bristol-Myers; ert. 1960; Anm. 1957). USP 2 967 177 (Bristol-Myers; ert. 1961; Anm. 1958). USP 3 032 547 (Merck & Co.; ert. 1962; Anm. 1958).
GB:
KanabristolВ® (Bristol)
Kanamycin ,,Griinentha)“ (Griinenthal) Kanamytrex® (Boehringer Ing.) Kamycine® (Bristol)
Kamypen (Bristol)-Komb.
Kanamycine Theraplix (Theraplix) KanamyloneВ® (Theraplix)-Komb. OphthalmokalixanВ® (Bristol) OtokalixanВ® (Bristol)
KannasynВ® (Winthrop)
KantrexВ® (Bristol)
EnterokanacinВ® (Labif)
KanacetВ® (Boniscontro & G.)
KanaceticВ® (Boniscontro & G.)
KanacillinaВ® (Morgan)
Kanamicina FirraaВ® (Firma)
Kanamirina Sulfa to FarmitaliaВ® (Farmitalia) Kanapiam OraleВ® (Piam)
KanoВ® (Pierrel)
KantrexВ® (Bristol)
KeimicinaВ® (Robin)
J: KanacillinВ® (Banyu; Meiji)-Komb.
KanacyclinВ® (Banyu; Meiji)-Komb.
KanafuracinВ® (Fujita)-Komb.
Kanamycin (Banyu; Meiji; Tanabe; Yamanouchi) USA: KantrexВ® (Bristol)
Kawain - Kebuzon Рљ 509
Kawain
(Kavain, Cavain)
500-64-1
Vasodilatator;
Antikonvulsivum;
Psychotonicum;
Endoanaestheticum
*2Я-ругап-2-опе, 5,6-dihydro-4-methoxy-6-(2-phenylethenyi)-, [/?-(£)]-
Рѕ
Рё
Рќ3РЎ~РЎ-РЎРќ2-РЎРћРћРЎ2Рќ5
Acetessigsaureethylester
0
2, Q-CH=CH-CH0 f^CH = CH 0 0
I. W-Bromsuccirvmid 2 Zimtaldebyd
0
!CH2C)2SQz/KzC03
Oimethylsulfal
Q-CH = CH_o^o
РћРЎРќР·
FP 1526 596 (Spezialchemie; Anm. 9.6.1967, D-Prior. 29.7.1966).
Weitere Verfahren:
E. M, Fowler, H. B. Henbest, J. Chem. Soc. 1950,3642 (Racemat).
D. G, F. R. Kostermans, Rec. Trav. Chim. Pays Bas 70,79 (1951) (Racemat). Isolierung von ( +)-Kawain:
W. Borsche, W. Peitzsch, Ber. Dtsch. Chem. Ges. 63, 2414 (1930).
Absolute Konfiguration:
G. Snatzke, R. Hansel, Tetrahedron Lett. 1968,1797.
Herstellung einer endoanasthetisch wirksamen Losung:
GB-P 1214936 (Spezialchemie; Laufzeit ab 5.6.1968; D-Prior. 5.6.1967). Ubersicht:
R. Kretzschmer, H. J. Teschendorf, Chem. Ztg. 98,24 (1974).
D:
durontВ® (Woelm)-Komb. KavaformВ® (Dr. Schwab)
NeuronikaВ® (Klinge)
Kebuzon
(Cetophenylbutazone;
Ketophenylbutazon)
853-34-9
Antiphlogisticum;
Antirheumaticum
4-(3-oxobutyl)-l,2-diphenyl-3,5-pyrazolidinedione
H3c
C-CH = CH2
Methylvinylkelon
C00C*HS
H2C
РЎРћРћРЎР·РќР±
Maiorsauredi-
ethylester
HjC
COOC2H5 \ I
C-CH2-CH2-CH--COOC2H5
HQ —CH?~ CH;~OH Elhylenglykoi
2-{ 3 - Oxobutyt) -malonsaurediethylester
510 Рљ Kebuzon - Ketamin
r-0 РЎРќР· COCCUS Q-HH-NH-Q/N.OCH, (fcArQ
^0 РЎРќ2-РЎРќ2-РЎРќ-РЎРћРћРЎРіРќ5 Hydrazobenzol ^
2-(3,3-Ethylendioxybutyt)-malcn- О—^СНг CHz
saurediethytester CH3
/CHj
0=C I TosOH CH3 AcetOn
РЅР·СЃ-СЃРѕ-СЃРЅРі-СЃРЅРі 0
p
-O
“A
1,2 -Diphenyl -
pyrazoiidm-3,5-
dion
{aus Hydrazobenzoi und Malonsauredi-•thyiester/
РЎРќСЌ
РЎ!-РЎРќРі-РЎРќ=РЎ
l.3-Dichlor-2’butea
Cl
\
C= CH-CHt
-0
H3C
1 HjSOt
2 h20
a R. Denss et al., Helv. Chim. Acta. 40,402 (1957). Ausgangsprodukt:
M. Kuhn, J. Prakt. Chem. (II) 156,103 (1940). b OE-P 198 263 (Synfarma; Anm. 1955).
D: Kebuzon (Steiner)
F: KetazoneВ® (Beytout) J: HichillosВ® (Kotani) KentanВ®-S (Sawai) KetazonВ® (Kyowa)
Ketobutan (Santen) Ketobutane (Yamagaia) KetobutazoneВ® (Sato, Toho) KetophezonВ® (Kissei) VintopВ® (Maruko)
Ketamifl 6740-88-1 Analgeticum;
1867-66-9 Hydrochloric! Anaestheticum
2-(o-chlorophenyl)-2-(methy\amino)cyc]ohexanone
.Cl
Cl
CN
2-Chlor-
benzo-
nitril
Р’РіРњРґ-С„
Cyciopentyl-bromid bzw. Cyclopentyl-magnesium-bromid
6
M2-Chior-
benzoyl)-
cyclopentan
Cl
6”
CH3NH? fl.
Ketamin - Ketoprofen Рљ 511
Ketamm
DOT2, 152 (1966); 6, 42 (1970).
USP 3254124 (Parke-Davis; ert. 31.5.1966; Prior. 31.7.1961, 29.6.1962).
Belg-P 634208 (Parke-Davis; Anm. 27.6.1963; USA-Prior. 29.6.1962).
D: KetanestВ® (Parke-Davis) J: KetalarВ® (Parke-Davis-Sankyo)
F: Ketalar (Parke-Davis) USA: KetajectВ® (Bristol)
GB: KetalarВ® (Parke-Davis) KetalarВ® (Parke-Davis)
I: KetalarВ® (Parke-Davis)
Ketoprofen
22071-15-4
Anaigeticum;
Antiphlogisticum
m-benzoylhydratropic acid
0-8-0
Bf2/Br-CH2-CH2-
РЎРќР·
3- Methylbenzophenon
РЎРќРі-* Br 3-Brommethylbenzophenori
Q-s^3
0 ch2-cn
(3-BenzoylpheriyD-aceto-
nitril)
NaQCzHs /C0(0C;Hs)?
Oiethylcar в– 
h5c2ooc'
РќРіРЎРіРћРћРЎ"' \
CN
lQ-!-Q
В° ^РЎРќ-РЎРќР·! HOOC
Ketoprofen
USP 3641 127 (Rhone-Poulenc; ert. 8.2.1972; F-Prior. 27.1.1967).
Alternativ-Verfahren:
DOS 2 646 792 (Mitsubishi Petrochemical; Anm. 16.10.1976; J-Prior. 23.10.1975, 31.7.1976). USP 4097 522 (Aziende Chim. Riun. Angelini Francesco; ert. 27.6.1978; I-Prior. 5.6.1975). DOS 2 744 832 (LEK; Anm. 5.10.1977; YU-Prior. 18.10.1976).
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