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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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USP 3 732 Р­40 (Asta-Werke; ert. 8.5.1973; Prior. 30.6.1967,11.9.1970,14.1.1971).
D: IxotenВ® (Asta) I: IxotenВ® (Schering)
Trolnitrat 7077-34-1 Coronardiiatator
588-42-1 Diphosphat
2,2' ,2'' -nitrilotrie thanol trinitrate CH2-CH2-OH
ho-ch2-ch2-n
СЃРЅРі-СЃРЅ2-РѕРЅ
Tnethanolarmn [Tris-(2-hydroxyethyl )-amin]
HN0,/H?SCt
ch2-ch2-o-no2 .
o2n-o-ch2-ch2-n
ch2-ch2-o-no2
Trolnitrat
FP 984 523 (J. Metadier; Anm. 1949).
D: AngitritВ® (Nordmark)
J: AmitolenВ® (Hokuriku)
EtaminВ® (Zeria)
SedaiisВ® (Kayaku) USA: MetamineВ® (Pfizer)
Tromantadin
53783-83-8
41544-24-5 Hydrochlorid
Virustaticum
iV-l-adamantyl-2-[2-(dimethylamino)ethoxy]acetamide
Tromantadin - Tropenzilin-bromid T 931
Cl-C-CH2-Cl
1-Amino- Chloracetyt-adamantan chlorid
kih-c-ch2-o
Na/ НО—CH2 —CHj—MCH3I2 2 -Oimethylaminoethanol
HChloracetamido)-
adamaatan
DOT 10, 105(1974).
DOS 1 941 218 (Merz & Co.; Anm. 13.8.1969).
D. Peteri u. W. Sterner, Arzneim.-Forsch. 23, 577 (1973).
D: Viru-„Merz“ Serol (Merz & Co.)
CH3
0
II /
nh-c-ch2-o-ch2-ch2-n
РЎ Hi
Tromantadin
T ropenzilin-bromid
143-92-0
Spasmolyticum
7-methoxy-8-methyltropinium bromide benzilate
CH2-CHO
I
H3CO-CH-CHO
2-Methoxy-
succindialdehyd
H3CO
S-Methoxy-
tropinon
CH2 -COOCH3
+ H2N-CH3 + 0=C^
COOCH3
NaOH
Methyl-
amin
Hj/Rarwy-Ni
CH2~COOCH3
Acetondicarbonsaure-
dimethyiester
H3CO 0CH3
РќР­РЎ
5-Methoxy-
tropin
OH
H5C,OOC-C-
'iNai
Benzilsaure-
ethyiester
H3CO
в–  6
CH3Br
Methyl -brom id
OH I
o-co-c
H3CO
Tropenzilin-bronvd
0
n
-a
CH-P 325 296 (Sandoz; Anm. 1954).
A. Stoll et al., Helv. Chim. Acta 37,495 (1954); 38, 571 (1955).
D: PelerofВ® (Sandoz)-Komb.
F: PaleroJВ® (Salvoxyl-Wander)
932 T Tropicamid - Trospium-chlorid - Troxerutin
Tropicamid
1508-75-4
Parasympathicolyticum;
Mydriaticum
' benzene acetamide, /V-ethyl-a-(hydroxymethyl)-/V-(4-pyridinyl-methyl)-
h2n-c2h5 ♦ ci-ch2-<^n
Ethylamin 4-Chiormethyl-pyridin (-Hydro-chiorid)
/2Рќ5 HNv
Рћ
H3C-CO-0-CH2
0
?H-C-N
ch2-\^n
OrK
H3C-CO—0—CH; ci
_/ fvj 0-AceВ»yllropasaure-
v h chlorid
Ethyl-K-pyridyl-
methyl)-amin
0
! L V-CH-C-N ,_. ,
I \L_y I \ /Р“^> \
CH2-OH CH2
Tropicamid
DOT 16,89(1980).
USP2726245 (Hoffmann-LaRoche; ert. 1955; CH-Prior. 1952).
D: Mydriaticum „Roche"® (Roche) J: Mydrin® (Santen)
F: Mydriaticum (Merck Sharp & Dohme-Chibret) USA: MydriacylВ® (Alcon)
GB: MydriacylВ® (Smith & Nephew) TryptarВ® (Armour)
f: VisurmdriaticВ® (Isf)
Trospium-chlorid
10405-02-4
Anticholinergicum;
Spasmolyticum
3 a-hydroxyspiro[l a,H5 aH-nortropane-8 Р”' -pyrrolidinium] chloride benzilate
H 1 Br-ICHjk-Br
N't—Л 2. HCI
V РѕРЅ
Nortropm
[bas. lonenaustauscher ] 1 U-Dibrombutan
Р“>
V QY
1 Q- C-CO-CI 6
1. В«-Chtordiphenyl-acetylchlorid
Ci
Trospium-chlorid
DBP 1 194422 (Pfleger; Anm. 5.3.1963). D: SpasmexВ® (Pfleger)
J; SpasmexВ® (Nikken)
TrOXerUtin 7085-55-4
3',4',7-tris(hydroxyethyl)rutin
Venenmittel
Troxerutin - L-Tryptophan T 933
<$> + C" ^pJ/oH OH OH
CH2-CH2-OH
OH Rutosid
2-Chlorethanol
[Ethylenchlorhydrinl
NaOH
DAS 1061 327 (Zyma; Anm. 30.12.1957; CH-Prior. 4.7.1957).
GB-P 833 174 (Zyma S.A.; Anm. 27.6.1958; CH-Prior. 4.7.1957).
Synthese mit Ethylenoxid:
DAS 1 543 974 (Zyma; Anm. 8.10.1966; F-Prior. 25.10.1965 u. CH-Prior. 9.3.1966). DAS 1 793 746 (Zyma; Anm. 8.10.1966; F-Prior. 25.10.1965).
PherarutinВ® (Kanoldt) Troxerutin-ratiopharm (ratiopharm) VenorutonВ® (Zyma-Blaes)
EscinoВ® (DOMS)-Komb.
FragiprelВ® (INAVA)-Komb. GinkorВ® (Beaufour)-Komb. GvnostatВ® (Bouchara)-Komb.
Hemor-Alpha (Synthemedica)-Komb. ParievalВ® (Negma)-Komb.
RelveneВ® (Pharmascience) Rutilemone (Pharmascience) RutovincineВ® (Joullie)-Komb. VenamitolВ® (Negma)
GB: ParovenВ® (Zyma)
L-Tryptophan 73-22-3 Antidepressivum;
essentieJJe Aminosaure
* tryptophan, l a
COOC2H5
H2C=CH-CH = 0 + HC-NH-C0-CH3
I
COOC2H5
Acrolein Acetamidomalon-
saurediethylester
u COOC2H5
\ I
^с-снг-снг-с-ын-со-снз
Рѕ COOC2H5
COOC2H5
I COOC2Hs
CH2-CH2—C-COOC2H5 I
Рі-V II CH2-C-COOC2H5
VMH-NH2 CH NH-CO-CH3 u 4n Р› I
II u-4n
aCH NH-CO-CH3 u 4f-|
Рё q-4,
H H
NH-C0-CH3
934 T L-Tryptophan - Tubocurarinchlorid
H
CHj— CH —COOH
NH-CO-CH3
[ Acyiase j
und Racemisierung von N- Acetyl-o-tryptopnan
A/-Acetyl- 0, l-tryptophan
CH2-CH-COOH
ii 4 NH2
N
H
l-Tryptophan
NC-CH2-CH2-*CHO
2-Cyanopropionaldehyd
NC-CH2-CH2
H2 /Rarwy-Ni (Р Р> /РЎРќ3РЎРћРћРќ
5-(2-Cyanoethyl)-hydantoin
Pherylhydrann
H 0
3-(5-Hydantoinyl)-propion-
aldehyd
РЎ Cl
ks
CH-CH2-CH2-\ 1 N^o H 0
CH2
H
'N-4,
5 -{3-Indolylmethyl) -hydantoin
oi
CH2-CH-COOH
I
nh2
H
в–Ў ,L-Tryptophan
Oc5
CH2-CH-COOH
1
NH-C0-CH3
[Acyiase]
l-Tryptophan
A/-Acetyl-0, L-tryptoDhan
Р° Рћ. T. Warner u. Рћ. Рђ. РњРѕРµ, J. Am. Chem. Soc. 70,2765 (1948). b Y. Komachiya et al., Nippon Kagaku Kaishi 86,856 (1965). Enzymatische Racematspaltung:
I. Chibata et al., Bull. Agric. Chem. Soc. Jpn. 21,58,304 (1957). Kombin. mit p -Blockern:
USP 4161 530 (Ciba-Geigy; ert. 17.7.1979; CH-Prior. 6.1,1975). GB-P 1 531091 (Ciba-Geigy; Anm. 5.1.1976; CH-Prior. 6.1.1975). W. Volk et al., Arzneim.-Forsch. 28 (II), 1798 (1978).
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