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.., .. .: , 2008. 224 c.
ISBN 978-5-9704-0578-9
( ): pharmazeutischewirkstoffe1982.djvu
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476 H Hydroxocobalamin - Hydroxycarbamid - Hydroxychloroquin
Novobedouze (Bouchara) zahlreiche Komb.-Praparate GB: Neo-Cytamen® (Glaxo)
zahlreiche Komb.-Praparate I: Biocobal® V.C.A. (Esterfarm)
Bradirubra® (Ibim)
Cobalidrina® (Ital. Suisse)
Cobalvit® (Tosi-NO)
Fravit-B 12® (Francia Farm.)
Idro-Apavit® (LocateHi)
Idrobamina® (Tiber)
Idrocobalmin® 1000 (Panther-Osfa Chemie) Idrospes-B12® (Ausonia)
Idrozima-1000® (Labif)
Longicobal® (Farber-REF)
Longirubrin® (Donatello)
Natur-B12® (Panthox & Burck) Neo-Cytamen® (Glaxo)
Oh-B12 Pierrel® (Pierrel)
Red® (Neopharmed)
Rossobivit-1000® (Medici)
Rubitard-B 12® (Proter) zahlreiche Komb.-Praparate J; AnemisoJ® (Tobishi)
Aquo B® (Nippon Zoki)
Bistin® (Yamanouchi)
В-Red® S (Kyorin)
B-Valet® BJ2 (Tokyo Tanabe)
Cobalamin H (Otsuka)
Colsamine® (Kanto)
Dasvit® H (Tanabe)
Docelan® (Nippon Roussel-Chugai) Dolevern® (Seiko)
Fresmin®-S (Takeda) Funacomin-F® (Funai)
Hicobala® (Mitaka)
Hicobalan® (Maruko) Hydocobamin® (Hishiyama) Hydocomin® (Sanwa)
Hydroxomin® (Tokyo Hosei) Laseramin® (Choseido) Masblon®H (Fuso)
Nichicoba® (Nichiiko)
OH-B[2® (Morishita)
Rasedon® (Sawai)
Red-В® (Kowa)
Redisol® H (Merck-Banyu) Runova® (Squibb-Sankyo)
Solco H® (Tobishi)
Tsuerumin®S (Mohan)
Twelvmin® (Mohan)
Vigolatin® (Kowa)
USA: Neo-Betalin® (Lilly)
Rubramin PC® (Squibb) zahlreiche Komb.-Praparate
Hydroxycarbamid 127-07-1 Cytostaticum
(Hydroxyurea)
hydroxyurea
Amberfite
IRA-410
H2Nv.c^NH-0H I
0 I
Hydroxycarbamid I
Natrium- Hydroxylamin-cyanat Hydrochlorid
USP 2705 727 (DuPont; ert. 1955;Prior. 1952).
D: Litahr® (Heyden) I: Hydrea® (Squibb)
F: Hydrea® (Squibb) Onco-Carbide® (Simes)
GB: Hydrea®(Squibb) USA: Hydrea®(Squibb)
Hydroxychloroquin 118-42-3 Antirheumaticum;
747-36-4 Sulfat Antimalaria-Mittel 6168-85-0 Phosphat
7-chloro-4-[4-[ethyl(2-hydroxyethyl)amino]-l-methylbutylamino]quinoline
Hydroxychloroquin - p-Hydroxyephedrin H 477
H,C
/2Н5
SCH2-CH;-OH
1-Chlor-4 ~oxo- Ethy! -12-hydroxy-
pentan ethyU-amin
(l-Chlor-4-pentanon) (2-Ethyiaminoethanol)
H3C-CH-(CH2)3-N
ch2-ch2-oh
H-jC
//
C-{CH2)3-N
ch2—ch2—OH
NHj , H2 /Raney-Ni
C2H5
HN-CH-(CH2]3-N
CH3 CH2 —сн2—OH
Hydroxychloroquin
USP 2 546 658 (Sterling Drug; ert. 1951; Prior. 1949).
D: Quensyl® (Winthrop)
F: Plaquenil® (Winthrop)
GB: Plaquenil® (Winthrop)
I: Plaquenil® (Winthrop)
J: Eroquin® (Shionogi)
Plaquenil® (Yamanouchi) RhyumapirineS:Q (Nichiiko) Toremonil® (Iwaki)
USA: Plaquenil® (Winthrop)
p-Hydroxyephedri n
(Methylsynephrin,
Oxyephedrin,
Oxilofrin)
365-26-4
942-51-8
Hydrochlorid
' benzenemethanol, 4-hydroxy-a[l-(methylamino)ethyl]-
Kreislaulanalepticum; Sympathomimeticum
OH 0 I II
СН-С-СНз
1 -1L - Hydroxypheny t) - 2 -oxopropanol
h3c-nh2
Methytamin
I OH CH3 ;
; HO——CH—CH—NH —СНз
p-Hydroxyephednn___
о
о
CH2—О—ft ^—С~СНг~"СНз + Вгг 4-Benzyloxypropiophenon В rom
O'
CH2-0
4 ^—C —CH—Br CH3
CH3
N
NCH2‘
/V-B&nzyi-
m&lhyiarnin
(>ch2-c
О СНз СНз
II ! /
C-CH-N .
^-0
a DRP 571229 (IG-Farben; Anm. 1930).
Ausgangsverbindung:
DRP 555 404 (IG-Farben; Anm. 1930). b USP 1 877756 (M. Bockmiihl eta)., ert. 1932; D-Prior. 1929).
USP 1 878 021 (Winthrop; ert. 1932; D-Prior. 1928).
Weitere Verfahren:
DRP 526 393 (IG-Farben; Anm. 1928).
DRP 597 123 (IG-Farben; Anm. 1928).
Obersicht:
Ehrhart, Ruschig, Bd. 2,154.
p-Hydroxyephedrm
478 H p-Hydroyxephedrin - Hydroxymethylnitrofurantoin - Hydroxyprogesteron
D: Carnigen® (Albert-Roussel)-Komb. Dtben®-amid (Heumann)-Komb. Stimulol® (Thilo) Ticarda® (Hoechsr)-Komb.
Hydroxymethyl- 1088-92-2 Chemotherapeuticum
nitrofurantoin
* hydantoin, 3-(hydroxymethyl)-l-[(5-nitrofurfurylidene)amino]-
0 02N__^°v_CH=N-N $_// '^'o + CH20 ! ^ ^.снг-он — [°^устЛ0
l-(5-Nitrofurfurylidenamino)- Form-hydantoin (Nitrofurantoin) aidehyd Hydroxymethylnitrofurantoin
GB-P 988 374 (Norwich; Anm. 6.12.1961; USA-Prior. 27.12.1960).
D: Urfadyne® (Inpharzam) F: Urfadyn (Arsac)
Hydroxyprogesteron 68-96-2 302-23-8 Acetat Gestagen
17cf'hydroxypregn~4-ene-3,20-dione
3 НзС чс^° /\Ы-Р
1 1 H 1 V NaOH , 1 H f V Нвг/СНзСООН
s' -w ♦ H2U2 I н j rt Г ТйТ^
16-Dehydropregnenolon Wasserstoft-(s. S. 759) peroxyd
H3C V° , HC00H i I ^ L r-Br 2. h2 (Pa H3V°
1 )i| [ 1 Ameiser- f J Й

! !СН3СО]гС/[ HiC -^SC3H ' 2. Оо/дцоснсснл!, H3CNC.0 ^jJ.-О'-СО-СНз Г4 L /
I Acetanbydnc! j I Cyclohexanon /Aluminium iso p ropyiat rt]rt
Hydroxyprogesteronacetat
Hydroxyprogesteron-Hydroxyprogesteroncaproat H 479
О
Phenylsuifin-
saurechlorid
MCjHsta /СН?С:2
CH3ONa /СН3ОН
•ОСНз
а Н. J. Ringold et al., J. Am. Chem. Soc. 78,816 (1956).
USP 2 802 839 (Syntex; ert. 1957; Anm. 1953; MEX-Prior. 1953). b USP 4 041055 (Upjohn; ert. 9.8.1977; Anm. 17.11.1975). Weitere Verfahren:
USP 2648 662 (Glidden; ert. 1953; Anm. 1949).
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