WO2003033491A1 - Medicinal composition for prevention or alleviation of side effect of antitumor and medicinal antitumor composition - Google Patents
Medicinal composition for prevention or alleviation of side effect of antitumor and medicinal antitumor composition Download PDFInfo
- Publication number
- WO2003033491A1 WO2003033491A1 PCT/JP2002/010676 JP0210676W WO03033491A1 WO 2003033491 A1 WO2003033491 A1 WO 2003033491A1 JP 0210676 W JP0210676 W JP 0210676W WO 03033491 A1 WO03033491 A1 WO 03033491A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- antitumor
- medicinal
- composition
- alleviation
- prevention
- Prior art date
- Legal status (The legal status 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 status listed.)
- Ceased
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D407/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
- C07D407/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing three or more hetero rings
-
- 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
- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/34—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide
- A61K31/341—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide not condensed with another ring, e.g. ranitidine, furosemide, bufetolol, muscarine
-
- 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
- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/35—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom
- A61K31/351—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom not condensed with another ring
-
- 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
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4433—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with oxygen as a ring hetero atom
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
- C07D493/02—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
- C07D493/08—Bridged systems
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Medicines Containing Plant Substances (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
Physiologically active substances NK34896A and NK34896B, which each is represented by the general formula (1) (1) or the general formula (2) (2) (wherein X represents hydrogen or an optionally substituted, C1-8, linear or branched, aliphatic hydrocarbon group or optionally substituted, C3-8 alicyclic hydrocarbon group, and Y represents C1-4 alkyl) and analogues of these. They are usable as a preventive or alleviator for side effects of an antitumor and as an antitumor medicine.
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2001318445A JP2003128671A (en) | 2001-10-16 | 2001-10-16 | Ester derivatives of bioactive substance nk34896a or nk34896 b, production method therefor and use thereof |
| JP2001-318445 | 2001-10-16 | ||
| JP2001-327075 | 2001-10-25 | ||
| JP2001327075A JP2003128581A (en) | 2001-10-25 | 2001-10-25 | Prophylactic or alleviating medicine against adverse effect |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2003033491A1 true WO2003033491A1 (en) | 2003-04-24 |
Family
ID=26623929
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/JP2002/010676 Ceased WO2003033491A1 (en) | 2001-10-16 | 2002-10-15 | Medicinal composition for prevention or alleviation of side effect of antitumor and medicinal antitumor composition |
Country Status (1)
| Country | Link |
|---|---|
| WO (1) | WO2003033491A1 (en) |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4537965A (en) * | 1984-08-03 | 1985-08-27 | Eli Lilly And Company | Method of preparing 4aR,8aR-5-permissibly substituted-6-oxo-octahydro-1H(and 2H)-pyrazolo[3,4-g]quinolines, useful as intermediates |
| JPH02229189A (en) * | 1989-03-02 | 1990-09-11 | Microbial Chem Res Found | New substance inostamicin, its use and manufacture |
| WO1999015500A1 (en) * | 1997-09-05 | 1999-04-01 | Glaxo Group Limited | Substituted oxindole derivatives as protein tyrosine kinase and as protein serine/threonine kinase inhibitors |
| JP2002069075A (en) * | 2000-08-30 | 2002-03-08 | Nippon Kayaku Co Ltd | New physiologically active substance nk34896b and method for producing the same |
| JP2002068980A (en) * | 2000-08-30 | 2002-03-08 | Nippon Kayaku Co Ltd | Usage of biologically active material, nk34896 analog |
-
2002
- 2002-10-15 WO PCT/JP2002/010676 patent/WO2003033491A1/en not_active Ceased
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4537965A (en) * | 1984-08-03 | 1985-08-27 | Eli Lilly And Company | Method of preparing 4aR,8aR-5-permissibly substituted-6-oxo-octahydro-1H(and 2H)-pyrazolo[3,4-g]quinolines, useful as intermediates |
| JPH02229189A (en) * | 1989-03-02 | 1990-09-11 | Microbial Chem Res Found | New substance inostamicin, its use and manufacture |
| WO1999015500A1 (en) * | 1997-09-05 | 1999-04-01 | Glaxo Group Limited | Substituted oxindole derivatives as protein tyrosine kinase and as protein serine/threonine kinase inhibitors |
| JP2002069075A (en) * | 2000-08-30 | 2002-03-08 | Nippon Kayaku Co Ltd | New physiologically active substance nk34896b and method for producing the same |
| JP2002068980A (en) * | 2000-08-30 | 2002-03-08 | Nippon Kayaku Co Ltd | Usage of biologically active material, nk34896 analog |
Non-Patent Citations (4)
| Title |
|---|
| EVANS DAVID A. ET AL.: "Synthetic studies in the lysocellin family of polyether antibiotics. The total synthesis of ferensimyc in B", JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, vol. 113, no. 20, 1991, pages 7613 - 7630, XP002962307 * |
| SIMIZU SIRO ET AL.: "Potentiation of paclitaxel cytotoxicity by inostamycin in human small cell lung carcinoma, Ms-1 cells", JOURNAL OF CANCER RESEARCH, vol. 89, no. 9, 1998, pages 970 - 976, XP002962304 * |
| WESTLEY JOHN W. ET AL.: "Isolation and characterization of four polyether antibiotics, X-14889A, B, C and D, closely related tolysocellin and the ferensimycins", THE JOURNAL OF ANTIBIOTICS, vol. 46, no. 2, 1993, pages 280 - 286, XP002962306 * |
| YOSHINORI ITO: "Paclitaxel", JAPANESE JOURNAL OF CLINICAL MEDICINE, vol. 58, 2000, pages 259 - 264, XP002962305 * |
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Legal Events
| Date | Code | Title | Description |
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| AK | Designated states |
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| 121 | Ep: the epo has been informed by wipo that ep was designated in this application | ||
| 122 | Ep: pct application non-entry in european phase |