MXPA04007918A - Derivados de fenalenona, procedimientos para su preparacion y utilizacion de los mismos. - Google Patents
Derivados de fenalenona, procedimientos para su preparacion y utilizacion de los mismos.Info
- Publication number
- MXPA04007918A MXPA04007918A MXPA04007918A MXPA04007918A MXPA04007918A MX PA04007918 A MXPA04007918 A MX PA04007918A MX PA04007918 A MXPA04007918 A MX PA04007918A MX PA04007918 A MXPA04007918 A MX PA04007918A MX PA04007918 A MXPA04007918 A MX PA04007918A
- Authority
- MX
- Mexico
- Prior art keywords
- formula
- compound
- alkyl
- preparation
- alkenyl
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 23
- WWBGWPHHLRSTFI-UHFFFAOYSA-N phenalen-1-one Chemical class C1=CC(C(=O)C=C2)=C3C2=CC=CC3=C1 WWBGWPHHLRSTFI-UHFFFAOYSA-N 0.000 title abstract description 8
- 238000004519 manufacturing process Methods 0.000 title abstract description 5
- 241000985529 Penicillium herquei Species 0.000 claims abstract description 21
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 12
- 244000005700 microbiome Species 0.000 claims abstract description 8
- 208000035143 Bacterial infection Diseases 0.000 claims abstract description 4
- 208000031888 Mycoses Diseases 0.000 claims abstract description 4
- 150000001875 compounds Chemical class 0.000 claims description 106
- 235000015097 nutrients Nutrition 0.000 claims description 23
- 238000002360 preparation method Methods 0.000 claims description 17
- 150000003839 salts Chemical class 0.000 claims description 17
- 239000000203 mixture Substances 0.000 claims description 12
- 239000003963 antioxidant agent Substances 0.000 claims description 10
- 201000010099 disease Diseases 0.000 claims description 10
- 239000000825 pharmaceutical preparation Substances 0.000 claims description 10
- 229940127557 pharmaceutical product Drugs 0.000 claims description 10
- 230000008569 process Effects 0.000 claims description 10
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 9
- 125000000217 alkyl group Chemical group 0.000 claims description 9
- 238000011282 treatment Methods 0.000 claims description 8
- 125000003342 alkenyl group Chemical group 0.000 claims description 6
- 238000011321 prophylaxis Methods 0.000 claims description 6
- 230000005764 inhibitory process Effects 0.000 claims description 5
- 239000002168 alkylating agent Substances 0.000 claims description 4
- 229940100198 alkylating agent Drugs 0.000 claims description 4
- 238000012258 culturing Methods 0.000 claims description 4
- YXHKONLOYHBTNS-UHFFFAOYSA-N Diazomethane Chemical class C=[N+]=[N-] YXHKONLOYHBTNS-UHFFFAOYSA-N 0.000 claims description 3
- 230000003078 antioxidant effect Effects 0.000 claims description 3
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 3
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 2
- 125000000304 alkynyl group Chemical group 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 150000002367 halogens Chemical class 0.000 claims description 2
- 125000001424 substituent group Chemical group 0.000 claims description 2
- 230000001173 tumoral effect Effects 0.000 claims description 2
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- 108010000684 Matrix Metalloproteinases Proteins 0.000 claims 1
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- 208000025747 Rheumatic disease Diseases 0.000 abstract description 3
- 208000022362 bacterial infectious disease Diseases 0.000 abstract description 3
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 21
- 239000000243 solution Substances 0.000 description 21
- 239000000126 substance Substances 0.000 description 17
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 15
- 239000002609 medium Substances 0.000 description 12
- 238000002955 isolation Methods 0.000 description 11
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- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 8
- 238000000746 purification Methods 0.000 description 8
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- ONDSBJMLAHVLMI-UHFFFAOYSA-N trimethylsilyldiazomethane Chemical compound C[Si](C)(C)[CH-][N+]#N ONDSBJMLAHVLMI-UHFFFAOYSA-N 0.000 description 6
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- 229910052784 alkaline earth metal Inorganic materials 0.000 description 3
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- BTQBPLOITIIODY-SSDOTTSWSA-N (9r)-4,5,6,7-tetrahydroxy-1,8,8,9-tetramethyl-9h-phenaleno[1,2-b]furan-3-one Chemical compound OC1=C(O)C(O)=C2C(=O)C=C(C)C3=C2C1=C(O)C1=C3O[C@H](C)C1(C)C BTQBPLOITIIODY-SSDOTTSWSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
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- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 1
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- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
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- OGWKCGZFUXNPDA-XQKSVPLYSA-N vincristine Chemical compound C([N@]1C[C@@H](C[C@]2(C(=O)OC)C=3C(=CC4=C([C@]56[C@H]([C@@]([C@H](OC(C)=O)[C@]7(CC)C=CCN([C@H]67)CC5)(O)C(=O)OC)N4C=O)C=3)OC)C[C@@](C1)(O)CC)CC1=C2NC2=CC=CC=C12 OGWKCGZFUXNPDA-XQKSVPLYSA-N 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D307/92—Naphthofurans; Hydrogenated naphthofurans
-
- 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]
-
- 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
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/10—Antimycotics
-
- 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
- A61P39/00—General protective or antinoxious agents
- A61P39/06—Free radical scavengers or antioxidants
-
- 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
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N1/00—Microorganisms, e.g. protozoa; Compositions thereof; Processes of propagating, maintaining or preserving microorganisms or compositions thereof; Processes of preparing or isolating a composition containing a microorganism; Culture media therefor
- C12N1/14—Fungi; Culture media therefor
- C12N1/145—Fungal isolates
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P17/00—Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms
- C12P17/02—Oxygen as only ring hetero atoms
- C12P17/04—Oxygen as only ring hetero atoms containing a five-membered hetero ring, e.g. griseofulvin, vitamin C
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P7/00—Preparation of oxygen-containing organic compounds
- C12P7/02—Preparation of oxygen-containing organic compounds containing a hydroxy group
- C12P7/22—Preparation of oxygen-containing organic compounds containing a hydroxy group aromatic
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12R—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES C12C - C12Q, RELATING TO MICROORGANISMS
- C12R2001/00—Microorganisms ; Processes using microorganisms
- C12R2001/645—Fungi ; Processes using fungi
- C12R2001/80—Penicillium
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Animal Behavior & Ethology (AREA)
- Zoology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Wood Science & Technology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Genetics & Genomics (AREA)
- Biotechnology (AREA)
- Biochemistry (AREA)
- General Engineering & Computer Science (AREA)
- Microbiology (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Rheumatology (AREA)
- Biomedical Technology (AREA)
- Toxicology (AREA)
- Botany (AREA)
- Mycology (AREA)
- Tropical Medicine & Parasitology (AREA)
- Virology (AREA)
- Pain & Pain Management (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Hydrogenated Pyridines (AREA)
- Anti-Oxidant Or Stabilizer Compositions (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Furan Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10206849A DE10206849A1 (de) | 2002-02-18 | 2002-02-18 | Phenalenon-Derivate, Verfahren zur Herstellung und Verwendung derselben |
| PCT/EP2003/001060 WO2003068946A1 (de) | 2002-02-18 | 2003-02-04 | Phenalenon-derivative, verfahren zur herstellung und verwendung derselben |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MXPA04007918A true MXPA04007918A (es) | 2004-11-26 |
Family
ID=27674733
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MXPA04007918A MXPA04007918A (es) | 2002-02-18 | 2003-02-04 | Derivados de fenalenona, procedimientos para su preparacion y utilizacion de los mismos. |
Country Status (10)
| Country | Link |
|---|---|
| EP (1) | EP1478731A1 (enExample) |
| JP (1) | JP2005517710A (enExample) |
| AR (1) | AR038524A1 (enExample) |
| AU (1) | AU2003210205B2 (enExample) |
| BR (1) | BR0307733A (enExample) |
| CA (1) | CA2476618A1 (enExample) |
| DE (1) | DE10206849A1 (enExample) |
| MX (1) | MXPA04007918A (enExample) |
| PE (1) | PE20030904A1 (enExample) |
| WO (1) | WO2003068946A1 (enExample) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9376415B2 (en) | 2009-03-30 | 2016-06-28 | Nippon Suisan Kaisha, Ltd. | Tricyclic condensed heterocyclic compound, process of producing same, and use thereof |
| WO2011009899A2 (en) * | 2009-07-22 | 2011-01-27 | Instituto Biomar, S.A. | Phenalenones as antitumoral agents |
| FR2987622B1 (fr) * | 2012-03-02 | 2016-01-15 | Centre Nat Rech Scient | Composes oxo-phenalenes, leur preparation et utilisation dans les domaines des materiaux et therapeutique |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2812510B2 (ja) * | 1989-10-06 | 1998-10-22 | 日清製油株式会社 | アトロベネチンの用途 |
| AU2864100A (en) * | 1999-02-01 | 2000-08-18 | Cytovia, Inc. | Methods of identifying therapeutically effective antineoplastic agents with cultured cells having intact cell membranes and corresponding products |
-
2002
- 2002-02-18 DE DE10206849A patent/DE10206849A1/de not_active Withdrawn
-
2003
- 2003-02-04 BR BR0307733-0A patent/BR0307733A/pt not_active IP Right Cessation
- 2003-02-04 WO PCT/EP2003/001060 patent/WO2003068946A1/de not_active Ceased
- 2003-02-04 JP JP2003568061A patent/JP2005517710A/ja not_active Abandoned
- 2003-02-04 MX MXPA04007918A patent/MXPA04007918A/es unknown
- 2003-02-04 EP EP03739452A patent/EP1478731A1/de not_active Withdrawn
- 2003-02-04 CA CA002476618A patent/CA2476618A1/en not_active Abandoned
- 2003-02-04 AU AU2003210205A patent/AU2003210205B2/en not_active Expired - Fee Related
- 2003-02-06 PE PE2003000139A patent/PE20030904A1/es not_active Application Discontinuation
- 2003-02-14 AR ARP030100503A patent/AR038524A1/es not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| DE10206849A1 (de) | 2005-07-28 |
| JP2005517710A (ja) | 2005-06-16 |
| WO2003068946A1 (de) | 2003-08-21 |
| AU2003210205B2 (en) | 2007-06-14 |
| EP1478731A1 (de) | 2004-11-24 |
| CA2476618A1 (en) | 2003-08-21 |
| AR038524A1 (es) | 2005-01-19 |
| PE20030904A1 (es) | 2003-11-18 |
| AU2003210205A1 (en) | 2003-09-04 |
| BR0307733A (pt) | 2005-01-25 |
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