FI112211B - Menetelmä terapeuttisesti käyttökelpoisten 15-deoksispergualiinianalogien valmistamiseksi sekä menetelmässä käytettävät välituotteet - Google Patents

Menetelmä terapeuttisesti käyttökelpoisten 15-deoksispergualiinianalogien valmistamiseksi sekä menetelmässä käytettävät välituotteet Download PDF

Info

Publication number: FI112211B
Authority: FI; Finland
Prior art keywords: formula; compound; amino; group; och
Prior art date: 1992-12-02

Application number

FI935318A

Other languages

English (en)

Finnish (fi)

Swedish (sv)

Other versions

FI935318A0 (fi

FI935318L (fi

Inventor

Soth Samreth

Patrice Renaut

Luc Lebreton

Patrick Dutartre

Philippe Derrepas

Original Assignee

Fournier Ind & Sante

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.)

1992-12-02

Filing date

1993-11-29

Publication date

2003-11-14

1993-11-29 Application filed by Fournier Ind & Sante filed Critical Fournier Ind & Sante

1993-11-29 Publication of FI935318A0 publication Critical patent/FI935318A0/fi

1994-06-03 Publication of FI935318L publication Critical patent/FI935318L/fi

2003-11-14 Application granted granted Critical

2003-11-14 Publication of FI112211B publication Critical patent/FI112211B/fi

Links

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239000013543 active substance Substances 0.000 description 1
230000010933 acylation Effects 0.000 description 1
238000005917 acylation reaction Methods 0.000 description 1
125000005076 adamantyloxycarbonyl group Chemical group C12(CC3CC(CC(C1)C3)C2)OC(=O)* 0.000 description 1
239000011717 all-trans-retinol Substances 0.000 description 1
235000019169 all-trans-retinol Nutrition 0.000 description 1
230000000735 allogeneic effect Effects 0.000 description 1
238000010976 amide bond formation reaction Methods 0.000 description 1
150000001413 amino acids Chemical class 0.000 description 1
238000007098 aminolysis reaction Methods 0.000 description 1
QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
150000008064 anhydrides Chemical class 0.000 description 1
ZRALSGWEFCBTJO-UHFFFAOYSA-N anhydrous guanidine Natural products NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 description 1
230000000259 anti-tumor effect Effects 0.000 description 1
229940088710 antibiotic agent Drugs 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
239000012298 atmosphere Substances 0.000 description 1
125000001584 benzyloxycarbonyl group Chemical group C(=O)(OCC1=CC=CC=C1)* 0.000 description 1
230000003115 biocidal effect Effects 0.000 description 1
230000004071 biological effect Effects 0.000 description 1
208000037976 chronic inflammation Diseases 0.000 description 1
208000037893 chronic inflammatory disorder Diseases 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
229940125898 compound 5 Drugs 0.000 description 1
229960004397 cyclophosphamide Drugs 0.000 description 1
229930182912 cyclosporin Natural products 0.000 description 1
UQHKFADEQIVWID-UHFFFAOYSA-N cytokinin Natural products C1=NC=2C(NCC=C(CO)C)=NC=NC=2N1C1CC(O)C(CO)O1 UQHKFADEQIVWID-UHFFFAOYSA-N 0.000 description 1
239000004062 cytokinin Substances 0.000 description 1
229940043239 cytotoxic antineoplastic drug Drugs 0.000 description 1
230000006866 deterioration Effects 0.000 description 1
SOCTUWSJJQCPFX-UHFFFAOYSA-N dichromate(2-) Chemical compound [O-][Cr](=O)(=O)O[Cr]([O-])(=O)=O SOCTUWSJJQCPFX-UHFFFAOYSA-N 0.000 description 1
150000005690 diesters Chemical class 0.000 description 1
SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
239000003889 eye drop Substances 0.000 description 1
229940012356 eye drops Drugs 0.000 description 1
QEWYKACRFQMRMB-UHFFFAOYSA-N fluoroacetic acid Chemical compound OC(=O)CF QEWYKACRFQMRMB-UHFFFAOYSA-N 0.000 description 1
238000004108 freeze drying Methods 0.000 description 1
229960002706 gusperimus Drugs 0.000 description 1
230000035876 healing Effects 0.000 description 1
NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
239000001257 hydrogen Substances 0.000 description 1
125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
229910000041 hydrogen chloride Inorganic materials 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
230000001031 immunopharmacological effect Effects 0.000 description 1
230000001861 immunosuppressant effect Effects 0.000 description 1
238000010255 intramuscular injection Methods 0.000 description 1
238000010253 intravenous injection Methods 0.000 description 1
231100000518 lethal Toxicity 0.000 description 1
230000001665 lethal effect Effects 0.000 description 1
238000004811 liquid chromatography Methods 0.000 description 1
238000001325 log-rank test Methods 0.000 description 1
WRIRWRKPLXCTFD-UHFFFAOYSA-N malonamide Chemical compound NC(=O)CC(N)=O WRIRWRKPLXCTFD-UHFFFAOYSA-N 0.000 description 1
230000007246 mechanism Effects 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
150000007522 mineralic acids Chemical class 0.000 description 1
IDINUJSAMVOPCM-INIZCTEOSA-N n-[(1s)-2-[4-(3-aminopropylamino)butylamino]-1-hydroxy-2-oxoethyl]-7-(diaminomethylideneamino)heptanamide Chemical compound NCCCNCCCCNC(=O)[C@H](O)NC(=O)CCCCCCN=C(N)N IDINUJSAMVOPCM-INIZCTEOSA-N 0.000 description 1
210000000056 organ Anatomy 0.000 description 1
235000005985 organic acids Nutrition 0.000 description 1
150000007530 organic bases Chemical class 0.000 description 1
235000011837 pasties Nutrition 0.000 description 1
230000001575 pathological effect Effects 0.000 description 1
230000000144 pharmacologic effect Effects 0.000 description 1
239000012071 phase Substances 0.000 description 1
UYWQUFXKFGHYNT-UHFFFAOYSA-N phenylmethyl ester of formic acid Natural products O=COCC1=CC=CC=C1 UYWQUFXKFGHYNT-UHFFFAOYSA-N 0.000 description 1
235000011007 phosphoric acid Nutrition 0.000 description 1
150000003016 phosphoric acids Chemical class 0.000 description 1
230000003449 preventive effect Effects 0.000 description 1
230000001681 protective effect Effects 0.000 description 1
230000002441 reversible effect Effects 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
239000000344 soap Substances 0.000 description 1
239000007787 solid Substances 0.000 description 1
210000004989 spleen cell Anatomy 0.000 description 1
239000000829 suppository Substances 0.000 description 1
230000001629 suppression Effects 0.000 description 1
BQKPZRONQZKFSZ-UHFFFAOYSA-N tert-butyl n-[n'-(6-aminohexyl)-n-[(2-methylpropan-2-yl)oxycarbonyl]carbamimidoyl]carbamate Chemical compound CC(C)(C)OC(=O)NC(NC(=O)OC(C)(C)C)=NCCCCCCN BQKPZRONQZKFSZ-UHFFFAOYSA-N 0.000 description 1
FQPCRESDVNTGEN-UHFFFAOYSA-N tert-butyl n-[n'-(8-aminooctyl)-n-[(2-methylpropan-2-yl)oxycarbonyl]carbamimidoyl]carbamate Chemical compound CC(C)(C)OC(=O)NC(NC(=O)OC(C)(C)C)=NCCCCCCCCN FQPCRESDVNTGEN-UHFFFAOYSA-N 0.000 description 1
229940100615 topical ointment Drugs 0.000 description 1
238000006257 total synthesis reaction Methods 0.000 description 1
LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C279/00—Derivatives of guanidine, i.e. compounds containing the group, the singly-bound nitrogen atoms not being part of nitro or nitroso groups
- C07C279/04—Derivatives of guanidine, i.e. compounds containing the group, the singly-bound nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of guanidine groups bound to acyclic carbon atoms of a carbon skeleton
- C07C279/12—Derivatives of guanidine, i.e. compounds containing the group, the singly-bound nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of guanidine groups bound to acyclic carbon atoms of a carbon skeleton being further substituted by nitrogen atoms not being part of nitro or nitroso groups
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/13—Amines
- A61K31/155—Amidines (), e.g. guanidine (H2N—C(=NH)—NH2), isourea (N=C(OH)—NH2), isothiourea (—N=C(SH)—NH2)
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/16—Amides, e.g. hydroxamic acids
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/02—Antiprotozoals, e.g. for leishmaniasis, trichomoniasis, toxoplasmosis
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C279/00—Derivatives of guanidine, i.e. compounds containing the group, the singly-bound nitrogen atoms not being part of nitro or nitroso groups
- C07C279/20—Derivatives of guanidine, i.e. compounds containing the group, the singly-bound nitrogen atoms not being part of nitro or nitroso groups containing any of the groups, X being a hetero atom, Y being any atom, e.g. acylguanidines
- C07C279/24—Y being a hetero atom

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Organic Chemistry (AREA)
Veterinary Medicine (AREA)
Pharmacology & Pharmacy (AREA)
Public Health (AREA)
General Health & Medical Sciences (AREA)
Animal Behavior & Ethology (AREA)
Life Sciences & Earth Sciences (AREA)
Medicinal Chemistry (AREA)
General Chemical & Material Sciences (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Chemical Kinetics & Catalysis (AREA)
Immunology (AREA)
Bioinformatics & Cheminformatics (AREA)
Engineering & Computer Science (AREA)
Epidemiology (AREA)
Oncology (AREA)
Tropical Medicine & Parasitology (AREA)
Transplantation (AREA)
Communicable Diseases (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Steroid Compounds (AREA)
Medicines Containing Plant Substances (AREA)
Medicines Containing Material From Animals Or Micro-Organisms (AREA)
Preparation Of Compounds By Using Micro-Organisms (AREA)
Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
Soil Conditioners And Soil-Stabilizing Materials (AREA)
Curing Cements, Concrete, And Artificial Stone (AREA)
Peptides Or Proteins (AREA)
Polysaccharides And Polysaccharide Derivatives (AREA)
Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)

FI935318A 1992-12-02 1993-11-29 Menetelmä terapeuttisesti käyttökelpoisten 15-deoksispergualiinianalogien valmistamiseksi sekä menetelmässä käytettävät välituotteet FI112211B (fi)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
FR9214517A FR2698628B1 (fr)	1992-12-02	1992-12-02	Analogues de 15-déoxyspergualine, leur procédé de préparation et leur utilisation en thérapeutique.
FR9214517		1992-12-02

Publications (3)

Publication Number	Publication Date
FI935318A0 FI935318A0 (fi)	1993-11-29
FI935318L FI935318L (fi)	1994-06-03
FI112211B true FI112211B (fi)	2003-11-14

Family

ID=9436147

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
FI935318A FI112211B (fi)	1992-12-02	1993-11-29	Menetelmä terapeuttisesti käyttökelpoisten 15-deoksispergualiinianalogien valmistamiseksi sekä menetelmässä käytettävät välituotteet

Country Status (24)

Country	Link
US (1)	US5476870A (cs)
EP (1)	EP0600762B1 (cs)
JP (1)	JP2945261B2 (cs)
KR (1)	KR100187328B1 (cs)
CN (1)	CN1045431C (cs)
AT (1)	ATE140215T1 (cs)
AU (1)	AU664124B2 (cs)
CA (1)	CA2110437C (cs)
CZ (1)	CZ284958B6 (cs)
DE (1)	DE69303583T2 (cs)
DK (1)	DK0600762T3 (cs)
ES (1)	ES2092263T3 (cs)
FI (1)	FI112211B (cs)
FR (1)	FR2698628B1 (cs)
GR (1)	GR3021269T3 (cs)
HK (1)	HK1000467A1 (cs)
HU (1)	HU218908B (cs)
NO (1)	NO180483C (cs)
NZ (1)	NZ250330A (cs)
RU (1)	RU2114823C1 (cs)
SK (1)	SK280286B6 (cs)
TW (1)	TW311132B (cs)
UA (1)	UA39920C2 (cs)
ZA (1)	ZA938821B (cs)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
WO1996024579A1 (fr) *	1995-02-10	1996-08-15	Fournier Industrie Et Sante	Analogues de la 15-deoxyspergualine, leur utilisation en therapeutique et leur procede de preparation
FR2734263B1 (fr) *	1995-05-17	1997-06-20	Fournier Ind & Sante	Analogues de la 15-deoxyspergualine, leur procede de preparation et leur utilisation en therapeutique
NZ332830A (en) *	1996-12-20	2000-04-28	Sueddeutsche Kalkstickstoff	Creatine pyruvates, method for their production and their use in medicaments for weight control, body fat control, increasing muscle strength, the treatment of oxygen deficiency conditions and as free radical scavengers
DE19728436A1 (de) *	1997-07-03	1999-01-07	Niels Franke	Niedrigdosierte 15-Desoxyspergualin-Präparate
EP1107998B1 (en) *	1998-08-28	2004-02-04	Gryphon Sciences	Method for the preparation of polyamide chains of precise length, their conjugates with proteins
DE19923961A1 (de) *	1999-05-25	2000-11-30	Euro Nippon Kayaku Gmbh	Verwendung von 15-Deoxyspergualin zur Behandlung von hyperreaktiven entzündlichen Erkrankungen und Autoimmunerkrankungen
WO2006069782A2 (en)	2004-12-27	2006-07-06	Silence Therapeutics Ag.	Lipid complexes coated with peg and their use
MXPA06012722A (es)	2004-05-05	2007-02-14	Atugen Ag	Lipidos, complejos de lipido y su uso.
WO2010074591A1 (ru)	2008-12-24	2010-07-01	Закрытое Акционерное Общество "Beptekc"	Амиды креатина, способ их получения, средство, обладающее нейропротекторным действием
RU2428414C2 (ru)	2009-11-03	2011-09-10	Закрытое Акционерное Общество "Вертекс"	Способ получения амидов креатина
FR2963238B1 (fr) *	2010-07-29	2012-12-28	Fournier Lab Sa	Derives de 15-desoxyspergualine pour le traitement et/ou la prevention des maladies inflammatoires oculaires
US20130190278A1 (en) *	2010-07-29	2013-07-25	Laboratoires Fournier Sa	Compounds for the Treatment/Prevention of Ocular Inflammatory Diseases
KR101695730B1 (ko)	2015-03-10	2017-01-12	하경훈	마늘꼭지 절단기의 절단장치
FR3050455B1 (fr) *	2016-04-26	2019-06-14	Temisis	Derives amides des acides polycafeoylquiniques, procede de preparation et utilisations

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS5942356A (ja) *	1982-09-02	1984-03-08	Microbial Chem Res Found	スパガリン関連化合物およびその製造法
EP0241797B1 (en) *	1986-04-04	1991-06-12	Microbial Chemistry Research Foundation	Novel spergualin-related compounds and process for producing the same
US5061787A (en) *	1988-06-24	1991-10-29	Nippon Kayaku Kabushiki Kaisha	Novel spergualin-related compounds and compositions

1992
- 1992-12-02 FR FR9214517A patent/FR2698628B1/fr not_active Expired - Fee Related
1993
- 1993-11-17 EP EP93402795A patent/EP0600762B1/fr not_active Expired - Lifetime
- 1993-11-17 DK DK93402795.4T patent/DK0600762T3/da active
- 1993-11-17 DE DE69303583T patent/DE69303583T2/de not_active Expired - Fee Related
- 1993-11-17 AT AT93402795T patent/ATE140215T1/de not_active IP Right Cessation
- 1993-11-17 ES ES93402795T patent/ES2092263T3/es not_active Expired - Lifetime
- 1993-11-19 TW TW082109707A patent/TW311132B/zh active
- 1993-11-24 AU AU51883/93A patent/AU664124B2/en not_active Ceased
- 1993-11-25 ZA ZA938821A patent/ZA938821B/xx unknown
- 1993-11-29 FI FI935318A patent/FI112211B/fi not_active IP Right Cessation
- 1993-11-30 NZ NZ250330A patent/NZ250330A/en unknown
- 1993-11-30 KR KR1019930025761A patent/KR100187328B1/ko not_active Expired - Fee Related
- 1993-11-30 NO NO934338A patent/NO180483C/no not_active IP Right Cessation
- 1993-12-01 RU RU93053038A patent/RU2114823C1/ru not_active IP Right Cessation
- 1993-12-01 HU HU9303406A patent/HU218908B/hu not_active IP Right Cessation
- 1993-12-01 CA CA002110437A patent/CA2110437C/en not_active Expired - Fee Related
- 1993-12-01 UA UA93003726A patent/UA39920C2/uk unknown
- 1993-12-02 JP JP5342673A patent/JP2945261B2/ja not_active Expired - Fee Related
- 1993-12-02 SK SK1357-93A patent/SK280286B6/sk unknown
- 1993-12-02 CZ CZ932622A patent/CZ284958B6/cs not_active IP Right Cessation
- 1993-12-02 CN CN93121647A patent/CN1045431C/zh not_active Expired - Fee Related
- 1993-12-02 US US08/161,773 patent/US5476870A/en not_active Expired - Fee Related
1996
- 1996-10-04 GR GR960402621T patent/GR3021269T3/el unknown
1997
- 1997-11-04 HK HK97102083A patent/HK1000467A1/xx not_active IP Right Cessation

Also Published As

Publication number	Publication date
FI935318A0 (fi)	1993-11-29
DE69303583D1 (de)	1996-08-14
ZA938821B (en)	1994-06-30
NO934338D0 (no)	1993-11-30
SK280286B6 (sk)	1999-11-08
TW311132B (cs)	1997-07-21
SK135793A3 (en)	1994-06-08
DK0600762T3 (da)	1996-11-11
UA39920C2 (uk)	2001-07-16
HK1000467A1 (en)	1998-03-27
CA2110437C (en)	1999-04-13
NO934338L (no)	1994-06-03
FR2698628B1 (fr)	1995-02-17
ES2092263T3 (es)	1996-11-16
EP0600762A1 (fr)	1994-06-08
NO180483B (no)	1997-01-20
EP0600762B1 (fr)	1996-07-10
KR940014435A (ko)	1994-07-18
HUT65782A (en)	1994-07-28
FI935318L (fi)	1994-06-03
DE69303583T2 (de)	1996-11-21
CZ284958B6 (cs)	1999-04-14
AU664124B2 (en)	1995-11-02
JP2945261B2 (ja)	1999-09-06
NZ250330A (en)	1995-06-27
JPH06293728A (ja)	1994-10-21
US5476870A (en)	1995-12-19
GR3021269T3 (en)	1997-01-31
HU218908B (hu)	2000-12-28
CZ262293A3 (en)	1994-06-15
HU9303406D0 (en)	1994-03-28
RU2114823C1 (ru)	1998-07-10
CN1095709A (zh)	1994-11-30
FR2698628A1 (fr)	1994-06-03
CA2110437A1 (en)	1994-06-03
AU5188393A (en)	1994-06-16
KR100187328B1 (ko)	1999-05-15
ATE140215T1 (de)	1996-07-15
CN1045431C (zh)	1999-10-06
NO180483C (no)	1997-04-30

Legal Events

Date	Code	Title	Description
2006-05-31	MA	Patent expired

Publication	Publication Date	Title
FI112211B (fi)	2003-11-14	Menetelmä terapeuttisesti käyttökelpoisten 15-deoksispergualiinianalogien valmistamiseksi sekä menetelmässä käytettävät välituotteet
US20040063725A1 (en)	2004-04-01	Novel n(phenylsulphonyl)glycine derivatives and their therapeutic use
HK1000467B (en)	1998-03-27	Analogues of the 15-deoxyspergualin, process for their preparation and their use as immunosuppresants
RU2113431C1 (ru)	1998-06-20	Аналоги 15-дезоксиспергуалина, способ их получения, способ получения промежуточных соединений (варианты), аминозащищенные соединения в качестве промежуточных соединений и фармацевтическая композиция на основе аналогов 15-дезоксиспергуалина
JP2860778B2 (ja)	1999-02-24	１５−デオキシスペルグアリン類似体、その製造方法および治療薬
US6258976B1 (en)	2001-07-10	Process for the preparation of polyamines and polyamine derivatives
HK1000489B (en)	1998-03-27	Analogs of 15-deoxyspergualine, process for their preparation and their use as immunosuppressive agents