SI9110025B - Novi ureido derivati poli-4-amino-2-karboksi-1-metilnih spojin - Google Patents

Novi ureido derivati poli-4-amino-2-karboksi-1-metilnih spojin Download PDF

Info

Publication number
SI9110025B
SI9110025B SI9110025A SI9110025A SI9110025B SI 9110025 B SI9110025 B SI 9110025B SI 9110025 A SI9110025 A SI 9110025A SI 9110025 A SI9110025 A SI 9110025A SI 9110025 B SI9110025 B SI 9110025B
Authority
SI
Slovenia
Prior art keywords
bis
methyl
imino
pyrrole
carbonyl
Prior art date
Application number
SI9110025A
Other languages
English (en)
Other versions
SI9110025A (en
Inventor
Nicola Mongelli
Giovanni Biasoli
Alfredo Paio
Maria Grandi
Marina Ciomei
Original Assignee
Pharmacia S.P.A.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Pharmacia S.P.A. filed Critical Pharmacia S.P.A.
Publication of SI9110025A publication Critical patent/SI9110025A/sl
Publication of SI9110025B publication Critical patent/SI9110025B/sl

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D207/00Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/30Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
    • C07D207/34Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00Drugs for disorders of the senses
    • A61P27/02Ophthalmic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Diabetes (AREA)
  • Emergency Medicine (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Ophthalmology & Optometry (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Endocrinology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Pyrrole Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Polyamides (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Peptides Or Proteins (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Claims (6)

  1. PATENTNI ZAHTEVKI Spojina s formulo (I)
    v kateri je vsak od m in n, ki sta enaka, celo število od 1 do 3; W je kisik ali žveplo; vsaka od skupin B, ki sta enaki, je fenilna ali naftilna skupina, substituirana z eno ali več kislinskimi skupinami; nasičen ali nenasičen, heteromonocikličen ali heterobicikličen obroč, ki vsebuje enega ali več heteroatomov, izbranih med dušikom, kisikom in žveplom, ki je substituiran z eno ali več kislinskimi skupinami; 2-deoksi-D-glukozna skupina, substituirana z eno ali več kislinskimi skupinami; ali skupina -CH2 (CHA)r CH2A, v kateri je vsaka skupina A, ki sta enaki ali različni, kislinska skupina, in rje 0,1 ali 2; in kjer je vsaka od zgornjih kislinskih skupin neodvisno izbrana izmed skupin sul-fonske, žveplove, sulfaminske, sulfinske, fosforjeve, fosfonske, fosfaminske ter karboksilne kisline, in njene farmacevtsko sprejemljive soli. Spojina s formulo (I) po zahtevku 1, v kateri je vsak od m in n, ki sta enaka,
  2. 2: W je kisik; vsaka od skupin B, ki sta enaki, je a’) fenilna ali naftilna skupina, substituirana z 1 do 3 kislinskimi skupinami; b’) tetrahidropiranilni ali tetrahidrofuranilni obroč, substituiran z 1 do 3 kislinskimi skupinami; ali c’) 2-deoksi-D-glukozna skupina, substituirana z 1 do 3 kislinskimi skupinami, in njene farmacevtsko sprejemljive soli.
  3. 3. Spojina izbrana iz skupine, ki sestoji iz : 8,8’-(karbonil-bis(imino-N-metil-4,2-pirolkarbonil-imino(N-metil-4,2-pirol)karb-onilamino))bis( 1,3-naftalendisulfonske kisline); 8,8’-(karbonil-bis(imino-N-metil-4,2-pirolkarbonil-imino(N-metil-4,2-pirol)karb-onilimino))bis(3,5-naftalendisulfonske kisline); 8,8’-(karbonil-bis(imino-N-metil-4,2-pirolkarbonil-imino(N-metil-4,2-pirol)karb-onilimino))bis(2,5-naftalendisulfonske kisline); 8,8’-(karbonil-bis(imino-N-metil-4,2-pirolkarbonil-imino(N-metil-4,2-pirol)karb-onilimino))bis(2,4-naftalendisulfonske kisline); 8,8'-(karboniI-bis(imino-N-metil-4,2-piroIkarbonil-imino(N-metil-4,2-pirol)karb-onilimino))bis(l,6-naftalendisulfonske kisline); 8,8’-(karbonil-bis(imino-N-metil-4,2-pirolkarbonil-imino(N-metil-4,2-pirol)karb-onilimino))bis(2,4,6-naftalentrisulfonske kisline); 24 8,8’-(karbonil-bis(imino-N-meti]-4,2-piroIkarbonil-imino(N-metil-4,2-pirol)karb-onilimino))bis( 1,3,6-naftalentrisulfonske kisline); 8,8’-(karbonil-bis(imino-N-metil-4,2-pirolkarbonil-imino(N-nietil-4,2-pirol)karb-onilimino))bis(2,3,5-naftalensulfonske kisline); 2,2’-(karbonil-bis(imino-N-metil-4,2-pirolkarbonil-iraino(N-metil-4,2-pirol)karb-onilimino))bis(2-deoksi-D-glukoze-6-sulfata) in 2,2’-(karbonil-bis(imino-N-metil-4,2-pirolkarbonil-imino(N-metil-4,2-pirol)karb- onilimino))bis(2-deoksi-D-glukoze-6-fosfata) in njihovih farmacevtsko sprejemljivih soli.
  4. 4. Farmacevtsko sprejemljiva sol spojine po zahtevku 3, kjer je ta sol natrijeva ali kalijeva sol.
  5. 5. Postopek za pripravo spojine s formulo (I) ali njene farmacevtsko sprejemljive soli po kateremkoli od zahtevkov 1 do 4, označen s tem, da presnovimo spojino s formulo (II)
    (II) 25 v kateri sta n in B definirana kot v zahtevku 1, ali njeno sol s spojino s formulo (III) X-C-X II (III) w v kateri je W definiran kot v zahtevku 1 in je vsaka od skupin X, ki sta lahko enaki ali različni, dobra odhodna skupina, in po želji pretvorimo tako dobljeno spojino s formulo (I) v sol in/ali po želji dobimo prosto spojino s formulo (I) iz njene soli.
  6. 6. Farmacetvski pripravek, ki vsebuje farmacevtsko sprejemljiv nosilec in/ali razredčilo in kot aktivno snov spojino s formulo (I) ali njeno farmacevtsko sprejemljivo sol po kateremkoli od zahtevkov 1 do 4. Za: FARMITALIA CARLO ERBA S.R.L. v'PISARNA, 4.0.0. j/i - > ; \x;p ,ΪΝΑ. ČOPOVA 14 ...... - '· · 26
SI9110025A 1990-01-11 1991-01-10 Novi ureido derivati poli-4-amino-2-karboksi-1-metilnih spojin SI9110025B (sl)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB909000644A GB9000644D0 (en) 1990-01-11 1990-01-11 New ureido derivatives of poly-4-amino-2-carboxy-1-methyl compounds
YU2591A YU48548B (sh) 1990-01-11 1991-01-10 Novi ureido derivati poli-4-amino-2-karboksi-1-metilnih jedinjenja

Publications (2)

Publication Number Publication Date
SI9110025A SI9110025A (en) 1996-10-31
SI9110025B true SI9110025B (sl) 1998-06-30

Family

ID=10669147

Family Applications (1)

Application Number Title Priority Date Filing Date
SI9110025A SI9110025B (sl) 1990-01-11 1991-01-10 Novi ureido derivati poli-4-amino-2-karboksi-1-metilnih spojin

Country Status (33)

Country Link
US (3) US5260329A (sl)
EP (1) EP0462258B1 (sl)
JP (1) JP3121343B2 (sl)
KR (1) KR0176258B1 (sl)
CN (1) CN1032750C (sl)
AT (1) ATE131810T1 (sl)
AU (1) AU647446B2 (sl)
BG (1) BG60534B2 (sl)
CA (1) CA2050331C (sl)
CZ (1) CZ285251B6 (sl)
DE (1) DE69115570T2 (sl)
DK (1) DK0462258T3 (sl)
ES (1) ES2084153T3 (sl)
FI (1) FI99011C (sl)
GB (1) GB9000644D0 (sl)
GR (1) GR3018767T3 (sl)
HK (1) HK1006455A1 (sl)
HR (1) HRP930311B1 (sl)
HU (2) HUT61280A (sl)
IE (1) IE69462B1 (sl)
IL (1) IL96875A (sl)
MX (1) MX9203119A (sl)
MY (1) MY107890A (sl)
NO (1) NO176274C (sl)
NZ (1) NZ236707A (sl)
PT (1) PT96455B (sl)
RU (1) RU2078079C1 (sl)
SI (1) SI9110025B (sl)
SK (1) SK280190B6 (sl)
UA (1) UA32513A (sl)
WO (1) WO1991010649A1 (sl)
YU (1) YU48548B (sl)
ZA (1) ZA91177B (sl)

Families Citing this family (38)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9000644D0 (en) * 1990-01-11 1990-03-14 Erba Carlo Spa New ureido derivatives of poly-4-amino-2-carboxy-1-methyl compounds
AU1224392A (en) * 1991-02-06 1992-09-07 Synphar Laboratories, Inc. Oligopeptide antiretroviral agents
GB2261661A (en) * 1991-11-21 1993-05-26 Erba Carlo Spa Derivatives of poly-4-amino-2-carboxy-1-methyl pyrroles
GB9216962D0 (en) * 1992-08-11 1992-09-23 Erba Carlo Spa Therapeutically active naphthalenesulfonic-pyrrolecarboxamido derivatives
GB9225475D0 (en) * 1992-12-05 1993-01-27 Imp Cancer Res Tech Compounds to combat angiogenesis
US5629327A (en) * 1993-03-01 1997-05-13 Childrens Hospital Medical Center Corp. Methods and compositions for inhibition of angiogenesis
US6114355A (en) * 1993-03-01 2000-09-05 D'amato; Robert Methods and compositions for inhibition of angiogenesis
US8143283B1 (en) 1993-03-01 2012-03-27 The Children's Medical Center Corporation Methods for treating blood-born tumors with thalidomide
GB9304589D0 (en) * 1993-03-05 1993-04-21 Erba Carlo Spa Biologically active ureido derivatives useful as antimetastic agents
GB9307948D0 (en) * 1993-04-16 1993-06-02 Erba Carlo Spa Biologically active ureido derivatives useful in the treatment of lentivirus-induced disease
DE4320157A1 (de) * 1993-06-18 1994-12-22 Bayer Ag Verwendung von 1,2,4-Dithiazolium-Salzen als Chemotherapeutica
US5463063A (en) * 1993-07-02 1995-10-31 Celgene Corporation Ring closure of N-phthaloylglutamines
GB9403909D0 (en) * 1994-03-01 1994-04-20 Erba Carlo Spa Ureido derivatives of naphthalenephosphonic acids and process for their preparation
GB9504065D0 (en) * 1995-03-01 1995-04-19 Pharmacia Spa Poly-pyrrolecarboxamidonaphthalenic acid derivatives
US6346510B1 (en) 1995-10-23 2002-02-12 The Children's Medical Center Corporation Therapeutic antiangiogenic endostatin compositions
GB2310207A (en) * 1996-02-15 1997-08-20 Pharmacia Spa Antiviral ureido derivatives of substituted heterocyclic compounds
JP2002513391A (ja) * 1996-11-05 2002-05-08 ザ チルドレンズ メディカル センター コーポレイション 血管形成の抑制のための方法と組成物
GB9713733D0 (en) * 1997-06-27 1997-09-03 Pharmacia & Upjohn Spa Poly-branched polycarboxamido compounds
GB9713732D0 (en) * 1997-06-27 1997-09-03 Pharmacia & Upjohn Spa Substituted triazinic compounds
AU1711499A (en) 1997-12-04 1999-06-16 Government Of The United States Of America, As Represented By The Secretary Of The Department Of Health And Human Services, The Ureido derivatives of poly-4-amino-2-carboxy-1-methyl pyrrole compounds or inhibition of inflammation
GB9727524D0 (en) 1997-12-31 1998-02-25 Pharmacia & Upjohn Spa Synergistic antitumor composition containing a biologically active ureido compound
US6232297B1 (en) * 1999-02-01 2001-05-15 University Of Virginia Patent Foundation Methods and compositions for treating inflammatory response
US7427606B2 (en) * 1999-02-01 2008-09-23 University Of Virginia Patent Foundation Method to reduce inflammatory response in transplanted tissue
US7378400B2 (en) * 1999-02-01 2008-05-27 University Of Virginia Patent Foundation Method to reduce an inflammatory response from arthritis
GB0015447D0 (en) * 2000-06-23 2000-08-16 Pharmacia & Upjohn Spa Combined therapy against tumors comprising substituted acryloyl derivates and alkylating agents
DE60130799T2 (de) 2000-11-30 2008-07-17 Children's Medical Center Corp., Boston Synthese von 4-aminothalidomid enantiomeren
US6825228B2 (en) * 2001-06-13 2004-11-30 Genesoft Pharmaceuticals, Inc. Benzothiophene compounds having antiinfective activity
AU2002323063B2 (en) * 2001-08-06 2007-11-08 Entremed, Inc. Synthesis and anti-tumor activity of nitrogen substituted thalidomide analogs
CA2460911C (en) * 2001-10-01 2011-08-30 University Of Virginia Patent Foundation 2-propynyl adenosine analogs having a2a agonist activity and compositions thereof
PT1471054E (pt) 2002-01-11 2009-09-23 Daiichi Sankyo Co Ltd Derivado de aminoálcool ou derivado de ácido fosfónico e composição medicinal que os contém
KR20110136901A (ko) 2004-02-24 2011-12-21 상꾜 가부시키가이샤 아미노 알코올 화합물
US7605143B2 (en) * 2004-08-02 2009-10-20 University Of Virginia Patent Foundation 2-propynyl adenosine analogs with modified 5′-ribose groups having A2A agonist activity
WO2006028618A1 (en) * 2004-08-02 2006-03-16 University Of Virginia Patent Foundation 2-polycyclic propynyl adenosine analogs with modified 5'-ribose groups having a2a agonist activity
US7442687B2 (en) * 2004-08-02 2008-10-28 The University Of Virginia Patent Foundation 2-polycyclic propynyl adenosine analogs having A2A agonist activity
WO2007120972A2 (en) * 2006-02-10 2007-10-25 University Of Virginia Patent Foundation Method to treat sickle cell disease
US8188063B2 (en) * 2006-06-19 2012-05-29 University Of Virginia Patent Foundation Use of adenosine A2A modulators to treat spinal cord injury
US8058259B2 (en) * 2007-12-20 2011-11-15 University Of Virginia Patent Foundation Substituted 4-{3-[6-amino-9-(3,4-dihydroxy-tetrahydro-furan-2-yl)-9H-purin-2-yl]-prop-2-ynyl}-piperidine-1-carboxylic acid esters as A2AR agonists
EP3381897A1 (en) 2017-03-27 2018-10-03 Leadiant Biosciences SA Derivatives of the disodium 2,2'-{carbonylbis[imino-3,1-phenylenecarbonylimino(1-methyl-1h-pyrrole-4,2-diyl)carbonylimino]}dinaphthalene-1,5-disulfonate salt and related compounds as heparanase inhibitors for the treatment of cancer

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2785183A (en) * 1954-04-19 1957-03-12 American Cyanamid Co N [4-aminopyrrolyl-2-carbonyl] amino acids
US2785182A (en) * 1954-04-19 1957-03-12 American Cyanamid Co Substituted pyrrolecarboxamidopyroles
CA1308516C (en) * 1987-07-06 1992-10-06 J. William Lown Oligopeptide anticancer and antiviral agents
GB9000644D0 (en) * 1990-01-11 1990-03-14 Erba Carlo Spa New ureido derivatives of poly-4-amino-2-carboxy-1-methyl compounds
GB9028123D0 (en) * 1990-12-28 1991-02-13 Erba Carlo Spa Monoclonal antibodies against human tumor necrosis factor alpha

Also Published As

Publication number Publication date
WO1991010649A1 (en) 1991-07-25
NZ236707A (en) 1992-10-28
NO176274B (no) 1994-11-28
NO913572L (no) 1991-09-10
IE910074A1 (en) 1991-07-17
JPH04504426A (ja) 1992-08-06
IL96875A0 (en) 1992-03-29
ZA91177B (en) 1991-10-30
KR920701150A (ko) 1992-08-11
HU912923D0 (en) 1992-01-28
CS9100056A2 (en) 1991-10-15
MY107890A (en) 1996-06-29
FI99011C (fi) 1997-09-25
ES2084153T3 (es) 1996-05-01
PT96455A (pt) 1991-10-15
BG60534B2 (bg) 1995-07-28
HK1006455A1 (en) 1999-02-26
UA32513A (uk) 2001-02-15
HRP930311B1 (en) 2000-04-30
CZ285251B6 (cs) 1999-06-16
AU647446B2 (en) 1994-03-24
FI99011B (fi) 1997-06-13
AU7059991A (en) 1991-08-05
ATE131810T1 (de) 1996-01-15
FI914251A0 (fi) 1991-09-09
MX9203119A (es) 1992-07-01
US5260329A (en) 1993-11-09
RU2078079C1 (ru) 1997-04-27
HU211237A9 (en) 1995-11-28
US5420296A (en) 1995-05-30
IE69462B1 (en) 1996-09-18
JP3121343B2 (ja) 2000-12-25
GR3018767T3 (en) 1996-04-30
DE69115570T2 (de) 1996-05-02
EP0462258B1 (en) 1995-12-20
NO176274C (no) 1995-03-08
US5593976A (en) 1997-01-14
SI9110025A (en) 1996-10-31
DE69115570D1 (de) 1996-02-01
YU48548B (sh) 1998-11-05
CN1032750C (zh) 1996-09-11
NO913572D0 (no) 1991-09-10
EP0462258A1 (en) 1991-12-27
IL96875A (en) 1995-03-30
CA2050331C (en) 2002-03-19
HRP930311A2 (en) 1994-12-31
PT96455B (pt) 1998-06-30
HUT61280A (en) 1992-12-28
CA2050331A1 (en) 1991-07-12
YU2591A (sh) 1994-05-10
SK280190B6 (sk) 1999-09-10
DK0462258T3 (da) 1996-01-29
KR0176258B1 (ko) 1999-03-20
CN1053230A (zh) 1991-07-24
GB9000644D0 (en) 1990-03-14

Similar Documents

Publication Publication Date Title
SI9110025B (sl) Novi ureido derivati poli-4-amino-2-karboksi-1-metilnih spojin
TNSN88012A1 (fr) Procede de preparation de l'enantiomere dextrogyre de l'alpha (tetrahydro-4,5,6,7 thieno (3,2-c) pyridyl - 5) (chloro -2 phenyl) acetate de methyle
ATE40368T1 (de) Xanthin-derivate, verfahren zu ihrer herstellung und diese enthaltende pharmazeutische zusammensetzungen.
EA200200774A1 (ru) Новые соединения, обладающие гиполипидемической, гипохолестеринемической активностью, способ их получения и содержащие их композиции
EA200000792A3 (ru) Новые пиридиновые соединения, способ их получения и содержащие их фармацевтические композиции
FR2388044A1 (fr) Produit de lavage pour textiles exempt de phosphates et convenant en particulier pour les lavages a temperature elevee
NL7504631A (nl) Werkwijze voor het bereiden van een vloeibaar wasmiddel.
EP0351385A3 (en) New amidino and guanidino derivatives
EA200100969A1 (ru) Новые соединения циклобутендиона, способ их получения и содержащие их фармацевтические композиции
JPS5116306A (ja) Ekitaisenzaisoseibutsu
EA200100597A2 (ru) Новые 1,1- и 1,2-дизамещенные циклопропановые соединения, способ их получения и содержащие их фармацевтические композиции
JPS55100380A (en) 11imidazoll22ylidenee33heterocyclic urea derivative*its manufacture and pharmaceutic composition having antidepressive activity
SE8004079L (sv) Nya hydroxiaminoeburnanderivat jemte sett for deras framstellning
DE61397T1 (de) Loesliche, n2-substituierte derivate von 2,4-diamino-5-benzyl-pyrimidinen, verfahren zu deren herstellung und diese enthaltende arzneimittel.
HUT47398A (en) Antiparasitic compositions comprising 2,2-dimethyl-cyclopropanecarboxylic acid derivatives and process for producing the active ingredients and their intermediates
DE2460593B2 (de) U-Dithiolanyl(2)- und U-Dithianyl ©-verbindungen, Verfahren zu ihrer Herstellung und diese enthaltende pharmazeutische Präparate'
YU45758B (sh) Postopek za pripravo 12-amino-piridizino /4'5':3,4/-pirolo/2,1-a/ izokinolinov
SE7906089L (sv) Nya farmaceutiska beredningar med stegrade hypotensiva effekter
DE1670284C3 (de) Penicilline
DE3168174D1 (en) Cephalosporin derivatives, process for their preparation and pharmaceutical compositions containing them
IL45734A (en) S-(1,6-dihydropyridazin-(1)-ylmethyl)-thiol-phosphoric acid esters and ester -amides their preparation and their use as nematocides
DE1155785B (de) Verfahren zur Herstellung von neuen 2-Acyl-4-aminophenolaethern
CH596190A5 (en) Anti-bacterial benzyl-pyrimidines
TH17400EX (th) สารผสม