KR960701881A - 나프탈렌포스폰산의 우레이도 유도체 및 이의 제조 방법(Ureido derivatives of naphtha1enephosphonic acids and process for their preparation) - Google Patents
나프탈렌포스폰산의 우레이도 유도체 및 이의 제조 방법(Ureido derivatives of naphtha1enephosphonic acids and process for their preparation) Download PDFInfo
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- KR960701881A KR960701881A KR1019950704791A KR19950704791A KR960701881A KR 960701881 A KR960701881 A KR 960701881A KR 1019950704791 A KR1019950704791 A KR 1019950704791A KR 19950704791 A KR19950704791 A KR 19950704791A KR 960701881 A KR960701881 A KR 960701881A
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- aminopyrrole
- methylpyrrole
- naphthalene
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- 239000002253 acid Substances 0.000 title claims abstract 9
- 238000000034 method Methods 0.000 title claims 2
- 125000001951 carbamoylamino group Chemical group C(N)(=O)N* 0.000 title abstract 2
- 150000007513 acids Chemical class 0.000 title 1
- 150000003839 salts Chemical class 0.000 claims abstract 16
- ABLZXFCXXLZCGV-UHFFFAOYSA-N phosphonic acid group Chemical group P(O)(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 claims abstract 11
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 26
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 24
- 150000001875 compounds Chemical class 0.000 claims 21
- 150000002148 esters Chemical class 0.000 claims 3
- 238000004519 manufacturing process Methods 0.000 claims 2
- VEEGZPWAAPPXRB-BJMVGYQFSA-N (3e)-3-(1h-imidazol-5-ylmethylidene)-1h-indol-2-one Chemical compound O=C1NC2=CC=CC=C2\C1=C/C1=CN=CN1 VEEGZPWAAPPXRB-BJMVGYQFSA-N 0.000 claims 1
- MZOFCQQQCNRIBI-VMXHOPILSA-N (3s)-4-[[(2s)-1-[[(2s)-1-[[(1s)-1-carboxy-2-hydroxyethyl]amino]-4-methyl-1-oxopentan-2-yl]amino]-5-(diaminomethylideneamino)-1-oxopentan-2-yl]amino]-3-[[2-[[(2s)-2,6-diaminohexanoyl]amino]acetyl]amino]-4-oxobutanoic acid Chemical compound OC[C@@H](C(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(O)=O)NC(=O)CNC(=O)[C@@H](N)CCCCN MZOFCQQQCNRIBI-VMXHOPILSA-N 0.000 claims 1
- 108060008682 Tumor Necrosis Factor Proteins 0.000 claims 1
- 102000000852 Tumor Necrosis Factor-alpha Human genes 0.000 claims 1
- 239000012190 activator Substances 0.000 claims 1
- 229940121369 angiogenesis inhibitor Drugs 0.000 claims 1
- 239000004037 angiogenesis inhibitor Substances 0.000 claims 1
- 230000000852 anti-lentiviral effect Effects 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 239000003085 diluting agent Substances 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 230000003472 neutralizing effect Effects 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/553—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having one nitrogen atom as the only ring hetero atom
- C07F9/572—Five-membered rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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- 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
- A61P31/12—Antivirals
-
- 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
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
-
- 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
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
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- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Molecular Biology (AREA)
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- Engineering & Computer Science (AREA)
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- Bioinformatics & Cheminformatics (AREA)
- Immunology (AREA)
- Tropical Medicine & Parasitology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- AIDS & HIV (AREA)
- Heart & Thoracic Surgery (AREA)
- Transplantation (AREA)
- Cardiology (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Luminescent Compositions (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
Abstract
Description
Claims (13)
- 일반식(I)의 화합물 및 약제학적으로 허용되는 이의 염.상기 식에서, m과 n은 각각 동일하며 1 내지 4의 정수이고, p와 q는 각각 동일하며 1 내지 3의 정수이며, R 그룹은 각각 동일하며 유리 포스폰산 그룹 또는 에스테르화된 포스폰산 그룹이다.
- 제1항에 있어서, 에스테르가 C1-C6알킬 또는 페닐-C1-C6알킬 에스테르인 일반식(I)의 화합물의 에스테르.
- 제1항에 있어서, m과 n이 각각 2이고, p와 q가 각각 2이며, R 그룹이 각각 동일하며 유리 포스폰산그룹, C1-C6알킬 에스테르화된 포스폰산 그룹 또는 페닐-C1-C6알킬 에스테르화된 포스폰산 그룹인 일반식(I)의 화합물 및 약제학적으로 허용되는 이의 염.
- 카보닐 비스-3-({4-[(4-아미노피롤-1-메틸-2-카보닐)아미노]-1-메틸피롤-2-카보닐}아미노)-나프탈렌-1,5-디포스폰산; 카보닐 비스-4-({4-[(4-아미노피롤-1-메틸-2-카보닐)아미노]-1-메틸피롤-2-카보닐}아미노)-나프탈렌-1,7-디포스폰산; 카보닐 비스-3-({4-[(4-아미노피롤-1-메틸-2-카보닐)아미노]-1-메틸피롤-2-카보닐}아미노)-나프탈렌-1,6-디포스폰산; 카보닐 비스-4-({4-[(4-아미노피롤-1-메틸-2-카보닐)아미노]-1-메틸피롤-2-카보닐}아미노)-나프탈렌-1,6-디포스폰산; 카보닐 비스-3-({4-[(4-아미노피롤-1-메틸-2-카보닐)아미노]-1-메틸피롤-2-카보닐}아미노)-나프탈렌-5,7-디포스폰산; 카보닐 비스-2-({4-[(4-아미노피롤-1-메틸-2-카보닐)아미노]-1-메틸피롤-2-카보닐}아미노)-나프탈렌-1,5-디포스폰산; 카보닐비스-1-({4-[(4-아미노피롤-1-메틸-2-카보닐)아미노]-1-메틸피롤-2-카보닐}아미노)-나프탈렌-5,7-디포스폰산; 카보닐 비스-4-({4-[(4-아미노피롤-1-메틸-2-카보닐)아미노]-1-메틸피롤-2-카보닐}아미노)-나프탈렌-5,7-디포스폰산; 카보닐 비스-1-({4-[(4-아미노피롤-1-메틸-2-카보닐)아미노]-1-메틸피롤-2-카보닐}아미노)-나프탈렌-5,6-디포스폰산; 카보닐 비스-4-({4-[(4-아미노피롤-1-에틸-2-카보닐)아미노]-1-메틸피롤-2-카보닐}아미노)-나프탈렌-5,6-디포스폰산; 카보닐 비스-4-({4-[(4-아미노피롤-1-메틸-2-카보닐)아미노]-1-메틸피롤-2-카보닐}아미노)-나프탈렌-2,5-디포스폰산; 카보닐 비스-4-({4-[(4-아미노피롤-1-메틸-2-카보닐)아미노]-1-메틸피롤-2-카보닐}아미노)-나프탈렌-6,7-디포스폰산; 카보닐비스-4-({4-[(4-아미노피롤-1-메틸-2-카보닐)아미노]-1-메틸피롤-2-카보닐}아미노)-나프탈렌-2,6-디포스폰산; 카보닐 비스-4-({4-[(4-아미노피롤-1-메틸-2-카보닐)아미노]-1-메틸피롤-2-카보닐}아미노)-나프탈렌-2,7-디포스폰산; 카보닐 비스-1-({4-[(4-아미노피롤-1-메틸-2-카보닐)아미노]-1-메틸피롤-2-카보닐}아미노)-나프탈렌-5-포스폰산; 카보닐 비스-4-({4-[(4-아미노피롤-1-메틸-2-카보닐)아미노]-1-메틸피롤-2-카보닐}아미노)-나프탈렌-5-포스폰산; 카보닐 비스-4-({4-[(4-아미노피롤-1-메틸-2-카보닐)아미노]-1-메틸피롤-2-카보닐}아미노)-나프탈렌-6-프스폰산; 카보닐 비스-1-({4-[(4-아미노피롤-1-메틸-2-카보닐)아미노]-1-메틸피롤-2-카보닐}아미노)-나프탈렌-6-포스폰산; 카보닐 비스-4-({4-[(4-아미노피롤-1-메틸-2-카보닐)아미노]-1-메틸피롤-2-카보닐}아미노)-나프탈렌-2,5,6-트리포스폰산; 카보닐 비스-4-({4-[(4-아미노피롤-1-메틸-2-카보닐)아미노]-1-메틸피롤-2-카보닐}아미노)-나프탈렌-1,5,7-트리포스폰산; 카보닐 비스-3-({4-[(4-아미노피롤-1-메틸-2-카보닐)아미노]-1-메틸피롤-2-카보닐}아미노)-나프탈렌-1,5,7-트리포스폰산; 카보닐 비스-3-{[4-({4-[(4-아미노피롤-1-메틸-2-카보닐)아미노]-1-메틸피롤-2-카보닐}아미노)-나프탈렌-1,5-디포스폰산; 카보닐 비스-4-{[4-({4-[(4-아미노피롤-1-메틸-2-카보닐)아미노]-1-메틸피롤-2-카보닐}아미노)-나프탈렌-1,7-디포스폰산; 카보닐 비스-1-{[4-({4-[(4-아미노피롤-1-메틸-2-카보닐)아미노]-1-메틸피롤-2-카보닐}아미노)-나프탈렌-5,7-디포스폰산; 카보닐 비스-4-{[4-({4-[(4-아미노피롤-1-메틸-2-카보닐)아미노]-1-메틸피롤-2-카보닐}아미노)-나프탈렌-5,7-디포스폰산; 카보닐 비스-3-{[4-({4-[(4-아미노피롤-1-메틸-2-카보닐)아미노]-1-메틸피롤-2-카보닐}아미노)-나프탈렌-1,5,7-트리포스폰산 및 이들의 C1-C6알킬 에스테르, 페닐-C1-C6알킬 에스테르 및 약제학적으로 허용되는 이의 염으로 이루어지는 그룹으로부터 선택되는 화합물.
- 일반식(Ⅱ)의 화합물 또는 이의 염을 일반식(Ⅲ)의 화합물과 반응시키고, 필요한 경우, 일반식(I)의 화합물을 일반식(I)의 또 다른 화합물로 전환시키며/시키거나, 필요한 경우, 이렇게 하여 수득한 일반식(I)의 화합물을 염화시키고/거나, 필요한 경우, 이의 에스테르 또는 염으로부터 일반식(I)의 유리산을 수득하며/하거나, 필요한 경우, 일반식(I)의 산을 에스테르화시킴을 포함하는 제1항에서 정의한 일반식(I)의 화합물의 제조방법.상기 식에서, n, p와 R은 제1항에서 정의한 바와 같고, X 그룹은 각각 동일하거나 상이하며 우수한 이탈그룹이다.
- 약제학적으로 허용되는 담체 및/또는 희석제와 활성 화합물로서의 제1항 내지 제4항 중의 어느 한 항에 따르는 일반식(I)의 화합물 또는 약제학적으로 허용되는 이의 염을 포함하는 약제학적 조성물.
- 맥관 형성 억제제로서 사용하기 위한, 제1항 내지 제4항 중의 어느 한 항에 따르는 일반식(I)의 화합물 또는 약제학적으로 허용되는 이의 염.
- TNF-α 중화 활성화제로서 사용하기 위한, 제1항 내지 제4항 중의 어느 한 항에 따르는 일반식(I)의 화합물 또는 약제학적으로 허용되는 이의 염.
- 항렌티바이러스제로서 사용하기 위한, 제1항 내지 제4항 중의 어느 한 항에 따르는 일반식(I)의 화합물 또는 약제학적으로 허용되는 이의 염.
- 일반식(Ⅱ)의 화합물 및 이의 염.상기 식에서, n은 1 내지 4의 정수이고, p는 1 내지 3의 정수이며, R 그룹은 유리 포스폰산 그룹 또는 에스테르화된 포스폰산 그룹이다.
- 일반식(Ⅳ)의 화합물 또는 이의 염을 환원시킴을 포함하여, 제10항에서 정의한 일반식(Ⅱ)의 화합물 또는 이의 염을 제조하는 방범.상기 식에서, n, p와 R은 제10항에서 정의한 바와 같다.
- 일반식(V)의 화합물 및 이의 염.상기 식에서, p는 1 내지 3의 정수이고, R 그룹은 유리 포스폰산 그룹 또는 에스테르화된 포스폰산 그룹이다.
- 일반식(X)의 화합물 또는 이의 염을 환원시킴을 포함하여, 제12항에서 정의한 일반식(V)의 화합물 또는 이의 염을 제조하는 방법.상기 식에서, R과 p는 제12항에서 정의한 바와 같다.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB9403909A GB9403909D0 (en) | 1994-03-01 | 1994-03-01 | Ureido derivatives of naphthalenephosphonic acids and process for their preparation |
GB9403909.6 | 1994-03-01 | ||
PCT/EP1995/000444 WO1995023806A2 (en) | 1994-03-01 | 1995-02-08 | Ureido derivatives of naphthalenephosphonic acids and process for their preparation |
Publications (1)
Publication Number | Publication Date |
---|---|
KR960701881A true KR960701881A (ko) | 1996-03-28 |
Family
ID=10751089
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019950704791A Ceased KR960701881A (ko) | 1994-03-01 | 1995-02-08 | 나프탈렌포스폰산의 우레이도 유도체 및 이의 제조 방법(Ureido derivatives of naphtha1enephosphonic acids and process for their preparation) |
Country Status (26)
Country | Link |
---|---|
US (1) | US5700788A (ko) |
EP (1) | EP0696287B1 (ko) |
JP (1) | JPH08509992A (ko) |
KR (1) | KR960701881A (ko) |
CN (1) | CN1061050C (ko) |
AT (1) | ATE190312T1 (ko) |
AU (1) | AU678704B2 (ko) |
CA (1) | CA2160250A1 (ko) |
DE (1) | DE69515390T2 (ko) |
DK (1) | DK0696287T3 (ko) |
ES (1) | ES2145268T3 (ko) |
FI (1) | FI955180A0 (ko) |
GB (1) | GB9403909D0 (ko) |
GR (1) | GR3033356T3 (ko) |
HU (1) | HUT74987A (ko) |
IL (1) | IL112716A0 (ko) |
MX (1) | MX9504381A (ko) |
MY (1) | MY130125A (ko) |
NO (1) | NO308005B1 (ko) |
NZ (1) | NZ281205A (ko) |
PL (1) | PL311339A1 (ko) |
PT (1) | PT696287E (ko) |
RU (1) | RU2136692C1 (ko) |
TW (1) | TW290547B (ko) |
WO (1) | WO1995023806A2 (ko) |
ZA (1) | ZA951653B (ko) |
Families Citing this family (29)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0486526B2 (en) | 1989-08-07 | 2001-03-07 | Peptech Limited | Tumour necrosis factor binding ligands |
US5959087A (en) * | 1989-08-07 | 1999-09-28 | Peptide Technology, Ltd. | Tumour necrosis factor binding ligands |
US20030225254A1 (en) | 1989-08-07 | 2003-12-04 | Rathjen Deborah Ann | Tumour necrosis factor binding ligands |
US20040120952A1 (en) * | 2000-08-07 | 2004-06-24 | Centocor, Inc | Anti-TNF antibodies and peptides of human tumor necrosis factor |
US6284471B1 (en) * | 1991-03-18 | 2001-09-04 | New York University Medical Center | Anti-TNFa antibodies and assays employing anti-TNFa antibodies |
US6277969B1 (en) * | 1991-03-18 | 2001-08-21 | New York University | Anti-TNF antibodies and peptides of human tumor necrosis factor |
US7192584B2 (en) * | 1991-03-18 | 2007-03-20 | Centocor, Inc. | Methods of treating psoriasis with anti-TNF antibodies |
US20050255104A1 (en) * | 1993-01-29 | 2005-11-17 | Centocor, Inc. | Methods of treating psoriasis using anti-TNF receptor fusion proteins |
GB9504065D0 (en) * | 1995-03-01 | 1995-04-19 | Pharmacia Spa | Poly-pyrrolecarboxamidonaphthalenic acid derivatives |
FR2736914B1 (fr) * | 1995-07-21 | 1997-08-22 | Adir | Nouveaux derives d'acide aminophenylphosphonique, leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
GB2310207A (en) * | 1996-02-15 | 1997-08-20 | Pharmacia Spa | Antiviral ureido derivatives of substituted heterocyclic compounds |
FR2758562B1 (fr) * | 1997-01-20 | 1999-02-19 | Adir | Nouveaux derives d'acides mixtes aminobenzyliques, leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
FR2758560B1 (fr) * | 1997-01-20 | 2000-02-04 | Adir | Nouveaux derives d'acides aminophenylboronique, leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
GB9713732D0 (en) * | 1997-06-27 | 1997-09-03 | Pharmacia & Upjohn Spa | Substituted triazinic compounds |
GB9713733D0 (en) * | 1997-06-27 | 1997-09-03 | Pharmacia & Upjohn Spa | Poly-branched polycarboxamido compounds |
AU739637B2 (en) * | 1997-07-24 | 2001-10-18 | University Of Kentucky Research Foundation, The | Phosphonated agents and their antiangiogenic and antitumorigenic use |
US6096730A (en) * | 1997-07-24 | 2000-08-01 | University Of Kentucky Research Foundation | Phosphonated agents and their antiangiogenic and antitumorigenic use |
US6562859B1 (en) | 1997-12-04 | 2003-05-13 | The United States Of America As Represented By The Department Of Health And Human Services | Ureido derivatives of poly-4-amino-2-carboxy-1-methyl pyrrole compounds for inhibition of inflammation |
US6395718B1 (en) | 1998-07-06 | 2002-05-28 | Guilford Pharmaceuticals Inc. | Pharmaceutical compositions and methods of inhibiting angiogenesis using naaladase inhibitors |
KR100672965B1 (ko) | 1998-07-06 | 2007-02-28 | 길포드 파마슈티컬스 인코포레이티드 | 약제학적 화합물로 유용한 나알라다제 억제제 및 그의조성물 |
WO2000051637A1 (en) * | 1999-03-02 | 2000-09-08 | Centocor, Inc. | ANTI-TNFα ANTIBODIES IN THERAPY OF ASTHMA |
US6348464B1 (en) * | 1999-11-12 | 2002-02-19 | Guilford Pharmaceuticals, Inc. | Pyrrolecarbonylimino derivatives as naaladase inhibitors |
US20110195063A1 (en) * | 2000-08-07 | 2011-08-11 | Centocor, Inc. | Methods of Treating Ankylosing Spondylitis Using Anti-TNF Antibodies and Peptides of Human Tumor Necrosis Factor |
US20050249735A1 (en) * | 2000-08-07 | 2005-11-10 | Centocor, Inc. | Methods of treating ankylosing spondylitis using anti-TNF antibodies and peptides of human tumor necrosis factor |
US20060018907A1 (en) * | 2000-08-07 | 2006-01-26 | Centocor, Inc. | Anti-TNF antibodies and peptides of human tumor necrosis factor |
TWI334439B (en) | 2001-08-01 | 2010-12-11 | Centocor Inc | Anti-tnf antibodies, compositions, methods and uses |
US20090038182A1 (en) * | 2007-08-09 | 2009-02-12 | Lans Maris J | Footwear with built-in scale |
US10465003B2 (en) | 2016-02-05 | 2019-11-05 | Janssen Biotech, Inc. | Anti-TNF antibodies, compositions, methods and use for the treatment or prevention of type 1 diabetes |
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)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5310752A (en) * | 1986-05-20 | 1994-05-10 | Farmitalia Carlo Erba Spa | Site specific alkylating agents |
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 |
IT1247878B (it) * | 1991-02-15 | 1995-01-05 | Menarini Farma Ind | Derivati poli-4-aminopirrol-2-carbossiamidici,processi di preparazione e composizioni farmaceutiche che li contengono |
GB9304589D0 (en) * | 1993-03-05 | 1993-04-21 | Erba Carlo Spa | Biologically active ureido derivatives useful as antimetastic agents |
-
1994
- 1994-03-01 GB GB9403909A patent/GB9403909D0/en active Pending
-
1995
- 1995-02-08 PT PT95909683T patent/PT696287E/pt unknown
- 1995-02-08 AT AT95909683T patent/ATE190312T1/de not_active IP Right Cessation
- 1995-02-08 NZ NZ281205A patent/NZ281205A/en unknown
- 1995-02-08 HU HU9503433A patent/HUT74987A/hu unknown
- 1995-02-08 EP EP95909683A patent/EP0696287B1/en not_active Expired - Lifetime
- 1995-02-08 US US08/535,056 patent/US5700788A/en not_active Expired - Fee Related
- 1995-02-08 KR KR1019950704791A patent/KR960701881A/ko not_active Ceased
- 1995-02-08 JP JP7522653A patent/JPH08509992A/ja active Pending
- 1995-02-08 PL PL95311339A patent/PL311339A1/xx unknown
- 1995-02-08 WO PCT/EP1995/000444 patent/WO1995023806A2/en active IP Right Grant
- 1995-02-08 RU RU95122243A patent/RU2136692C1/ru active
- 1995-02-08 MX MX9504381A patent/MX9504381A/es not_active IP Right Cessation
- 1995-02-08 CA CA002160250A patent/CA2160250A1/en not_active Abandoned
- 1995-02-08 CN CN95190139A patent/CN1061050C/zh not_active Expired - Fee Related
- 1995-02-08 ES ES95909683T patent/ES2145268T3/es not_active Expired - Lifetime
- 1995-02-08 DE DE69515390T patent/DE69515390T2/de not_active Expired - Fee Related
- 1995-02-08 DK DK95909683T patent/DK0696287T3/da active
- 1995-02-08 AU AU18488/95A patent/AU678704B2/en not_active Ceased
- 1995-02-21 IL IL11271695A patent/IL112716A0/xx unknown
- 1995-02-22 TW TW084101627A patent/TW290547B/zh active
- 1995-02-28 ZA ZA951653A patent/ZA951653B/xx unknown
- 1995-03-01 MY MYPI95000534A patent/MY130125A/en unknown
- 1995-10-30 NO NO954346A patent/NO308005B1/no unknown
- 1995-10-30 FI FI955180A patent/FI955180A0/fi unknown
-
2000
- 2000-05-05 GR GR20000401041T patent/GR3033356T3/el unknown
Also Published As
Publication number | Publication date |
---|---|
EP0696287A1 (en) | 1996-02-14 |
PT696287E (pt) | 2000-08-31 |
EP0696287B1 (en) | 2000-03-08 |
NO954346D0 (no) | 1995-10-30 |
RU2136692C1 (ru) | 1999-09-10 |
ATE190312T1 (de) | 2000-03-15 |
CA2160250A1 (en) | 1995-09-08 |
AU678704B2 (en) | 1997-06-05 |
NO308005B1 (no) | 2000-07-03 |
GB9403909D0 (en) | 1994-04-20 |
NZ281205A (en) | 1997-01-29 |
CN1124027A (zh) | 1996-06-05 |
JPH08509992A (ja) | 1996-10-22 |
AU1848895A (en) | 1995-09-18 |
ZA951653B (en) | 1995-12-08 |
FI955180L (fi) | 1995-10-30 |
FI955180A0 (fi) | 1995-10-30 |
HUT74987A (en) | 1997-03-28 |
PL311339A1 (en) | 1996-02-05 |
MX9504381A (es) | 1997-01-31 |
US5700788A (en) | 1997-12-23 |
WO1995023806A3 (en) | 1995-09-28 |
ES2145268T3 (es) | 2000-07-01 |
DE69515390T2 (de) | 2000-09-21 |
MY130125A (en) | 2007-06-29 |
CN1061050C (zh) | 2001-01-24 |
DE69515390D1 (de) | 2000-04-13 |
TW290547B (ko) | 1996-11-11 |
IL112716A0 (en) | 1995-05-26 |
DK0696287T3 (da) | 2000-07-31 |
GR3033356T3 (en) | 2000-09-29 |
WO1995023806A2 (en) | 1995-09-08 |
HU9503433D0 (en) | 1996-01-29 |
NO954346L (no) | 1995-10-30 |
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