SK29999A3 - Antifungal combination therapy - Google Patents
Antifungal combination therapy Download PDFInfo
- Publication number
- SK29999A3 SK29999A3 SK299-99A SK29999A SK29999A3 SK 29999 A3 SK29999 A3 SK 29999A3 SK 29999 A SK29999 A SK 29999A SK 29999 A3 SK29999 A3 SK 29999A3
- Authority
- SK
- Slovakia
- Prior art keywords
- spp
- cryptococcus
- candida
- aspergillus
- inhibitor
- Prior art date
Links
- 238000002648 combination therapy Methods 0.000 title abstract description 6
- 229940121375 antifungal agent Drugs 0.000 title abstract 6
- 230000000843 anti-fungal effect Effects 0.000 title abstract 3
- 239000003112 inhibitor Substances 0.000 claims abstract description 15
- APKFDSVGJQXUKY-INPOYWNPSA-N amphotericin B Chemical compound O[C@H]1[C@@H](N)[C@H](O)[C@@H](C)O[C@H]1O[C@H]1/C=C/C=C/C=C/C=C/C=C/C=C/C=C/[C@H](C)[C@@H](O)[C@@H](C)[C@H](C)OC(=O)C[C@H](O)C[C@H](O)CC[C@@H](O)[C@H](O)C[C@H](O)C[C@](O)(C[C@H](O)[C@H]2C(O)=O)O[C@H]2C1 APKFDSVGJQXUKY-INPOYWNPSA-N 0.000 claims abstract description 14
- OXVVQYCKEAJWFA-QVCGFCSKSA-N 10,12-dimethyl-tetradecanoic acid [3-(3-amino-1-hydroxy-propyl)-6-[1,2-dihydroxy-2-(4-hydroxy-phenyl)-ethyl]-11,20,21,25-tetrahydroxy-15-(1-hydroxy-ethyl)-2,5,8,14,17,23-hexaoxo-1,4,7,13,16,22-hexaaza-tricyclo[22.3.0.09,13]heptacos-18-yl]-amide Chemical compound C1([C@H](O)[C@@H](O)[C@H]2C(=O)N[C@H](C(=O)N3CC[C@H](O)[C@H]3C(=O)N[C@H](O)[C@H](O)C[C@@H](C(N[C@H](C(=O)N3C[C@H](O)C[C@H]3C(=O)N2)[C@@H](C)O)=O)NC(=O)CCCCCCCCC(C)CC(C)CC)[C@H](O)CCN)=CC=C(O)C=C1 OXVVQYCKEAJWFA-QVCGFCSKSA-N 0.000 claims abstract description 13
- 150000004291 polyenes Chemical class 0.000 claims abstract description 12
- 229960003942 amphotericin b Drugs 0.000 claims abstract description 11
- KDCGOANMDULRCW-UHFFFAOYSA-N 7H-purine Chemical compound N1=CNC2=NC=NC2=C1 KDCGOANMDULRCW-UHFFFAOYSA-N 0.000 claims abstract description 8
- APKFDSVGJQXUKY-KKGHZKTASA-N Amphotericin-B Natural products O[C@H]1[C@@H](N)[C@H](O)[C@@H](C)O[C@H]1O[C@H]1C=CC=CC=CC=CC=CC=CC=C[C@H](C)[C@@H](O)[C@@H](C)[C@H](C)OC(=O)C[C@H](O)C[C@H](O)CC[C@@H](O)[C@H](O)C[C@H](O)C[C@](O)(C[C@H](O)[C@H]2C(O)=O)O[C@H]2C1 APKFDSVGJQXUKY-KKGHZKTASA-N 0.000 claims abstract description 8
- 229960004884 fluconazole Drugs 0.000 claims abstract description 8
- RFHAOTPXVQNOHP-UHFFFAOYSA-N fluconazole Chemical compound C1=NC=NN1CC(C=1C(=CC(F)=CC=1)F)(O)CN1C=NC=N1 RFHAOTPXVQNOHP-UHFFFAOYSA-N 0.000 claims abstract description 8
- 229920000057 Mannan Polymers 0.000 claims abstract description 5
- 239000002213 purine nucleotide Substances 0.000 claims abstract description 5
- 239000002719 pyrimidine nucleotide Substances 0.000 claims abstract description 5
- 150000003230 pyrimidines Chemical class 0.000 claims abstract description 5
- XMAYWYJOQHXEEK-OZXSUGGESA-N (2R,4S)-ketoconazole Chemical compound C1CN(C(=O)C)CCN1C(C=C1)=CC=C1OC[C@@H]1O[C@@](CN2C=NC=C2)(C=2C(=CC(Cl)=CC=2)Cl)OC1 XMAYWYJOQHXEEK-OZXSUGGESA-N 0.000 claims abstract description 4
- VHVPQPYKVGDNFY-DFMJLFEVSA-N 2-[(2r)-butan-2-yl]-4-[4-[4-[4-[[(2r,4s)-2-(2,4-dichlorophenyl)-2-(1,2,4-triazol-1-ylmethyl)-1,3-dioxolan-4-yl]methoxy]phenyl]piperazin-1-yl]phenyl]-1,2,4-triazol-3-one Chemical compound O=C1N([C@H](C)CC)N=CN1C1=CC=C(N2CCN(CC2)C=2C=CC(OC[C@@H]3O[C@](CN4N=CN=C4)(OC3)C=3C(=CC(Cl)=CC=3)Cl)=CC=2)C=C1 VHVPQPYKVGDNFY-DFMJLFEVSA-N 0.000 claims abstract description 4
- 229940123047 Elongation factor inhibitor Drugs 0.000 claims abstract description 4
- BYBLEWFAAKGYCD-UHFFFAOYSA-N Miconazole Chemical compound ClC1=CC(Cl)=CC=C1COC(C=1C(=CC(Cl)=CC=1)Cl)CN1C=NC=C1 BYBLEWFAAKGYCD-UHFFFAOYSA-N 0.000 claims abstract description 4
- 229930182764 Polyoxin Natural products 0.000 claims abstract description 4
- 230000000844 anti-bacterial effect Effects 0.000 claims abstract description 4
- XRECTZIEBJDKEO-UHFFFAOYSA-N flucytosine Chemical compound NC1=NC(=O)NC=C1F XRECTZIEBJDKEO-UHFFFAOYSA-N 0.000 claims abstract description 4
- 229960004413 flucytosine Drugs 0.000 claims abstract description 4
- 230000001939 inductive effect Effects 0.000 claims abstract description 4
- 229960004130 itraconazole Drugs 0.000 claims abstract description 4
- 229960004125 ketoconazole Drugs 0.000 claims abstract description 4
- 150000002632 lipids Chemical group 0.000 claims abstract description 4
- 229960002509 miconazole Drugs 0.000 claims abstract description 4
- 229960000988 nystatin Drugs 0.000 claims abstract description 4
- VQOXZBDYSJBXMA-NQTDYLQESA-N nystatin A1 Chemical compound O[C@H]1[C@@H](N)[C@H](O)[C@@H](C)O[C@H]1O[C@H]1/C=C/C=C/C=C/C=C/CC/C=C/C=C/[C@H](C)[C@@H](O)[C@@H](C)[C@H](C)OC(=O)C[C@H](O)C[C@H](O)C[C@H](O)CC[C@@H](O)[C@H](O)C[C@](O)(C[C@H](O)[C@H]2C(O)=O)O[C@H]2C1 VQOXZBDYSJBXMA-NQTDYLQESA-N 0.000 claims abstract description 4
- 230000035699 permeability Effects 0.000 claims abstract description 4
- 229960001589 posaconazole Drugs 0.000 claims abstract description 4
- RAGOYPUPXAKGKH-XAKZXMRKSA-N posaconazole Chemical compound O=C1N([C@H]([C@H](C)O)CC)N=CN1C1=CC=C(N2CCN(CC2)C=2C=CC(OC[C@H]3C[C@@](CN4N=CN=C4)(OC3)C=3C(=CC(F)=CC=3)F)=CC=2)C=C1 RAGOYPUPXAKGKH-XAKZXMRKSA-N 0.000 claims abstract description 4
- OPAHEYNNJWPQPX-RCDICMHDSA-N ravuconazole Chemical compound C=1SC([C@H](C)[C@](O)(CN2N=CN=C2)C=2C(=CC(F)=CC=2)F)=NC=1C1=CC=C(C#N)C=C1 OPAHEYNNJWPQPX-RCDICMHDSA-N 0.000 claims abstract description 4
- OGGVRVMISBQNMQ-MDGIRFSOSA-N sordarin Chemical compound O[C@H]1[C@H](O)[C@H](OC)[C@@H](C)O[C@H]1OC[C@]1([C@@]2(C(C(C)C)=C3)C(O)=O)[C@H]3C[C@]2(C=O)[C@@H]2CC[C@@H](C)[C@H]2C1 OGGVRVMISBQNMQ-MDGIRFSOSA-N 0.000 claims abstract description 4
- OGGVRVMISBQNMQ-UHFFFAOYSA-N sordarin Natural products OC1C(O)C(OC)C(C)OC1OCC1(C2(C(C(C)C)=C3)C(O)=O)C3CC2(C=O)C2CCC(C)C2C1 OGGVRVMISBQNMQ-UHFFFAOYSA-N 0.000 claims abstract description 4
- BCEHBSKCWLPMDN-MGPLVRAMSA-N voriconazole Chemical compound C1([C@H](C)[C@](O)(CN2N=CN=C2)C=2C(=CC(F)=CC=2)F)=NC=NC=C1F BCEHBSKCWLPMDN-MGPLVRAMSA-N 0.000 claims abstract description 4
- 229960004740 voriconazole Drugs 0.000 claims abstract description 4
- 241001527609 Cryptococcus Species 0.000 claims description 11
- 241000228212 Aspergillus Species 0.000 claims description 10
- 241000222120 Candida <Saccharomycetales> Species 0.000 claims description 10
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 claims description 10
- 244000053095 fungal pathogen Species 0.000 claims description 9
- 241000223682 Exophiala Species 0.000 claims description 8
- 239000000203 mixture Substances 0.000 claims description 8
- 241001480043 Arthrodermataceae Species 0.000 claims description 6
- 241000335423 Blastomyces Species 0.000 claims description 6
- 241000223203 Coccidioides Species 0.000 claims description 6
- 241000228402 Histoplasma Species 0.000 claims description 6
- 241001537205 Paracoccidioides Species 0.000 claims description 6
- 241000228143 Penicillium Species 0.000 claims description 6
- 241000223596 Pseudallescheria Species 0.000 claims description 6
- 241000235527 Rhizopus Species 0.000 claims description 6
- 230000037304 dermatophytes Effects 0.000 claims description 6
- UHPMCKVQTMMPCG-UHFFFAOYSA-N 5,8-dihydroxy-2-methoxy-6-methyl-7-(2-oxopropyl)naphthalene-1,4-dione Chemical compound CC1=C(CC(C)=O)C(O)=C2C(=O)C(OC)=CC(=O)C2=C1O UHPMCKVQTMMPCG-UHFFFAOYSA-N 0.000 claims description 5
- 241000223208 Curvularia Species 0.000 claims description 5
- 241000223218 Fusarium Species 0.000 claims description 5
- 241001149962 Sporothrix Species 0.000 claims description 5
- 241000223230 Trichosporon Species 0.000 claims description 5
- 150000003839 salts Chemical class 0.000 claims description 5
- 241000223600 Alternaria Species 0.000 claims description 4
- 241000233866 Fungi Species 0.000 claims description 4
- 241000235070 Saccharomyces Species 0.000 claims description 4
- 229940079593 drug Drugs 0.000 claims description 4
- 239000003814 drug Substances 0.000 claims description 4
- 208000015181 infectious disease Diseases 0.000 claims description 4
- 241000233872 Pneumocystis carinii Species 0.000 claims description 3
- 239000003899 bactericide agent Substances 0.000 claims 1
- 229940126534 drug product Drugs 0.000 claims 1
- 239000000825 pharmaceutical preparation Substances 0.000 claims 1
- YEBIHIICWDDQOL-YBHNRIQQSA-N polyoxin Polymers O[C@@H]1[C@H](O)[C@@H](C(C=O)N)O[C@H]1N1C(=O)NC(=O)C(C(O)=O)=C1 YEBIHIICWDDQOL-YBHNRIQQSA-N 0.000 claims 1
- 150000003212 purines Chemical class 0.000 claims 1
- 150000003851 azoles Chemical class 0.000 abstract description 7
- -1 nikkomycins Natural products 0.000 abstract description 4
- PCTMTFRHKVHKIS-BMFZQQSSSA-N (1s,3r,4e,6e,8e,10e,12e,14e,16e,18s,19r,20r,21s,25r,27r,30r,31r,33s,35r,37s,38r)-3-[(2r,3s,4s,5s,6r)-4-amino-3,5-dihydroxy-6-methyloxan-2-yl]oxy-19,25,27,30,31,33,35,37-octahydroxy-18,20,21-trimethyl-23-oxo-22,39-dioxabicyclo[33.3.1]nonatriaconta-4,6,8,10 Chemical compound C1C=C2C[C@@H](OS(O)(=O)=O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2.O[C@H]1[C@@H](N)[C@H](O)[C@@H](C)O[C@H]1O[C@H]1/C=C/C=C/C=C/C=C/C=C/C=C/C=C/[C@H](C)[C@@H](O)[C@@H](C)[C@H](C)OC(=O)C[C@H](O)C[C@H](O)CC[C@@H](O)[C@H](O)C[C@H](O)C[C@](O)(C[C@H](O)[C@H]2C(O)=O)O[C@H]2C1 PCTMTFRHKVHKIS-BMFZQQSSSA-N 0.000 abstract description 3
- 229920002101 Chitin Polymers 0.000 abstract description 3
- 229940098178 ambisome Drugs 0.000 abstract description 3
- 150000001720 carbohydrates Chemical class 0.000 abstract description 3
- 239000003429 antifungal agent Substances 0.000 abstract 3
- WWJFFVUVFNBJTN-UIBIZFFUSA-N (2S)-2-[[(2S,3S,4S)-2-amino-4-hydroxy-4-(5-hydroxypyridin-2-yl)-3-methylbutanoyl]amino]-2-[(2R,3S,4S,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]acetic acid Chemical class C[C@@H]([C@H](N)C(=O)N[C@@H]([C@H]1O[C@H]([C@@H](O)[C@@H]1O)n1ccc(=O)[nH]c1=O)C(O)=O)[C@H](O)c1ccc(O)cn1 WWJFFVUVFNBJTN-UIBIZFFUSA-N 0.000 abstract 1
- 229930184499 Nikkomycin Natural products 0.000 abstract 1
- WWJFFVUVFNBJTN-UHFFFAOYSA-N neopolyoxin C Natural products C=1C=C(O)C=NC=1C(O)C(C)C(N)C(=O)NC(C(O)=O)C(C(C1O)O)OC1N1C=CC(=O)NC1=O WWJFFVUVFNBJTN-UHFFFAOYSA-N 0.000 abstract 1
- WWJFFVUVFNBJTN-VHDFTHOZSA-N nikkomycin Z Chemical compound N1([C@@H]2O[C@@H]([C@H]([C@H]2O)O)[C@H](NC(=O)[C@@H](N)[C@H](C)[C@H](O)C=2N=CC(O)=CC=2)C(O)=O)C=CC(=O)NC1=O WWJFFVUVFNBJTN-VHDFTHOZSA-N 0.000 abstract 1
- 102000004169 proteins and genes Human genes 0.000 abstract 1
- 108090000623 proteins and genes Proteins 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 description 26
- 230000000855 fungicidal effect Effects 0.000 description 8
- 241000221204 Cryptococcus neoformans Species 0.000 description 7
- 108010049047 Echinocandins Proteins 0.000 description 7
- 230000000694 effects Effects 0.000 description 7
- 239000000417 fungicide Substances 0.000 description 7
- 239000003795 chemical substances by application Substances 0.000 description 5
- 238000000338 in vitro Methods 0.000 description 5
- 241001225321 Aspergillus fumigatus Species 0.000 description 4
- 241000222122 Candida albicans Species 0.000 description 4
- 201000007336 Cryptococcosis Diseases 0.000 description 3
- 230000008485 antagonism Effects 0.000 description 3
- 238000001727 in vivo Methods 0.000 description 3
- 230000001965 increasing effect Effects 0.000 description 3
- 230000002401 inhibitory effect Effects 0.000 description 3
- 238000002560 therapeutic procedure Methods 0.000 description 3
- 206010017533 Fungal infection Diseases 0.000 description 2
- 208000031888 Mycoses Diseases 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 238000002512 chemotherapy Methods 0.000 description 2
- 239000000890 drug combination Substances 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 244000052769 pathogen Species 0.000 description 2
- 230000002195 synergetic effect Effects 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 201000002909 Aspergillosis Diseases 0.000 description 1
- 208000036641 Aspergillus infections Diseases 0.000 description 1
- 206010013710 Drug interaction Diseases 0.000 description 1
- 229920001503 Glucan Polymers 0.000 description 1
- 241000699670 Mus sp. Species 0.000 description 1
- 206010067482 No adverse event Diseases 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 210000002421 cell wall Anatomy 0.000 description 1
- 230000001332 colony forming effect Effects 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 230000001408 fungistatic effect Effects 0.000 description 1
- 239000001963 growth medium Substances 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 238000007918 intramuscular administration Methods 0.000 description 1
- 230000000670 limiting effect Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000003389 potentiating effect Effects 0.000 description 1
- 230000002829 reductive effect Effects 0.000 description 1
- 238000007920 subcutaneous administration Methods 0.000 description 1
- 230000004083 survival effect Effects 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/04—Peptides having up to 20 amino acids in a fully defined sequence; Derivatives thereof
- A61K38/12—Cyclic peptides, e.g. bacitracins; Polymyxins; Gramicidins S, C; Tyrocidins A, B or C
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- A61K38/1703—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
- A61K38/1709—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- A61K38/1703—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
- A61K38/1709—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals
- A61K38/1751—Bactericidal/permeability-increasing protein [BPI]
-
- 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
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Gastroenterology & Hepatology (AREA)
- Immunology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Marine Sciences & Fisheries (AREA)
- Zoology (AREA)
- Molecular Biology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US2632796P | 1996-09-12 | 1996-09-12 | |
| GBGB9620739.4A GB9620739D0 (en) | 1996-10-04 | 1996-10-04 | Antifungal combination therapy |
| PCT/US1997/015987 WO1998010782A1 (fr) | 1996-09-12 | 1997-09-09 | Therapie antifongique combinee |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SK29999A3 true SK29999A3 (en) | 2000-02-14 |
Family
ID=26310166
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SK299-99A SK29999A3 (en) | 1996-09-12 | 1997-09-09 | Antifungal combination therapy |
Country Status (21)
| Country | Link |
|---|---|
| EP (1) | EP0925070B1 (fr) |
| JP (1) | JP3288051B2 (fr) |
| KR (1) | KR100380871B1 (fr) |
| CN (1) | CN1235554A (fr) |
| AT (1) | ATE248625T1 (fr) |
| AU (1) | AU721334B2 (fr) |
| CA (1) | CA2265824C (fr) |
| CY (1) | CY2481B1 (fr) |
| CZ (1) | CZ88499A3 (fr) |
| DE (1) | DE69724626T2 (fr) |
| DK (1) | DK0925070T3 (fr) |
| EA (1) | EA002469B1 (fr) |
| EE (1) | EE03748B1 (fr) |
| ES (1) | ES2203819T3 (fr) |
| IL (1) | IL128870A0 (fr) |
| NO (1) | NO991207L (fr) |
| NZ (1) | NZ334446A (fr) |
| PL (1) | PL333282A1 (fr) |
| PT (1) | PT925070E (fr) |
| SK (1) | SK29999A3 (fr) |
| WO (1) | WO1998010782A1 (fr) |
Families Citing this family (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1056849C (zh) * | 1994-11-08 | 2000-09-27 | 葛兰素惠尔康有限公司 | 抗真菌的粪壳菌素衍生物及其制备方法和其在制药中的应用 |
| US6069126A (en) * | 1996-09-12 | 2000-05-30 | Merck & Co., Inc. | Antifungal combination therapy |
| AUPQ066399A0 (en) | 1999-05-31 | 1999-06-24 | Fujisawa Pharmaceutical Co., Ltd. | Antifungal combination use |
| AUPQ462399A0 (en) * | 1999-12-13 | 2000-01-13 | Fujisawa Pharmaceutical Co., Ltd. | New use |
| KR100680464B1 (ko) * | 2000-06-28 | 2007-02-08 | 주식회사 하이닉스반도체 | 반도체 소자의 캐패시터 제조 방법 |
| WO2002098463A1 (fr) * | 2001-06-05 | 2002-12-12 | The New Industry Research Organization | Compositions antifongiques |
| NZ561675A (en) * | 2005-04-07 | 2010-07-30 | Toyama Chemical Co Ltd | Pharmaceutical composition and method using antifungal agent in combination |
| TWI385169B (zh) | 2005-10-31 | 2013-02-11 | Eisai R&D Man Co Ltd | 經雜環取代之吡啶衍生物及含有彼之抗真菌劑 |
| PT2070536E (pt) * | 2006-10-06 | 2012-03-06 | Toyama Chemical Co Ltd | Composição farmacêutica que contém um derivado de fenilamidina e processo para utilização dessa composição farmacêutica em associação com um agente antifúngico |
| TWI426918B (zh) * | 2007-02-12 | 2014-02-21 | Merck Sharp & Dohme | Il-23拮抗劑於治療感染之用途 |
| WO2009129525A2 (fr) * | 2008-04-18 | 2009-10-22 | Board Of Supervisors Of Louisiana State University And Agricultural And Mechanical College | Cellobio-oligosaccharides antifongiques et anti-carie produits par la dextransucrase |
| CN102274215B (zh) * | 2010-06-10 | 2013-04-10 | 吉林大学 | 一种具有与氟康唑协同抗真菌作用的增效剂 |
| CN102274217B (zh) * | 2010-06-10 | 2013-04-10 | 吉林大学 | 三氯生作为抗真菌药物氟康唑增效剂的新用途 |
| CN102274216B (zh) * | 2010-06-10 | 2013-04-10 | 吉林大学 | 一种提高氟康唑抗真菌作用的增效剂 |
| WO2012060448A1 (fr) | 2010-11-05 | 2012-05-10 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | Composition pharmaceutique combinée en tant qu'agent antifongique |
| WO2012162412A2 (fr) * | 2011-05-24 | 2012-11-29 | Agraquest, Inc., A Delaware Corporation | Combinaisons synergiques de fongicides de type polyène et de peptides non ribosomaux et procédés d'utilisation associés |
| CN102319326A (zh) * | 2011-07-23 | 2012-01-18 | 李玮 | 一种治疗脚癣的浸药卫生纸 |
| CN114052029A (zh) * | 2021-11-25 | 2022-02-18 | 兰州大学 | 具哌嗪和哌啶骨架的医用化合物在防治植物真菌病害中的用途 |
| CN114652836B (zh) * | 2022-03-25 | 2023-06-20 | 山东大学 | T3ss小分子抑制剂及其筛选方法和应用 |
| CN116473985B (zh) * | 2023-03-29 | 2024-12-10 | 暨南大学 | 一种多烯类抗真菌药物组合物及其应用 |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5378804A (en) * | 1993-03-16 | 1995-01-03 | Merck & Co., Inc. | Aza cyclohexapeptide compounds |
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1997
- 1997-09-09 EP EP97941495A patent/EP0925070B1/fr not_active Expired - Lifetime
- 1997-09-09 IL IL12887097A patent/IL128870A0/xx unknown
- 1997-09-09 PL PL97333282A patent/PL333282A1/xx unknown
- 1997-09-09 DE DE69724626T patent/DE69724626T2/de not_active Expired - Lifetime
- 1997-09-09 AU AU43392/97A patent/AU721334B2/en not_active Ceased
- 1997-09-09 EA EA199900283A patent/EA002469B1/ru not_active IP Right Cessation
- 1997-09-09 DK DK97941495T patent/DK0925070T3/da active
- 1997-09-09 CN CN97199420A patent/CN1235554A/zh active Pending
- 1997-09-09 SK SK299-99A patent/SK29999A3/sk unknown
- 1997-09-09 ES ES97941495T patent/ES2203819T3/es not_active Expired - Lifetime
- 1997-09-09 CZ CZ99884A patent/CZ88499A3/cs unknown
- 1997-09-09 JP JP51380898A patent/JP3288051B2/ja not_active Expired - Fee Related
- 1997-09-09 WO PCT/US1997/015987 patent/WO1998010782A1/fr not_active Ceased
- 1997-09-09 AT AT97941495T patent/ATE248625T1/de active
- 1997-09-09 KR KR10-1999-7002052A patent/KR100380871B1/ko not_active Expired - Fee Related
- 1997-09-09 PT PT97941495T patent/PT925070E/pt unknown
- 1997-09-09 EE EEP199900088A patent/EE03748B1/xx not_active IP Right Cessation
- 1997-09-09 CA CA002265824A patent/CA2265824C/fr not_active Expired - Fee Related
- 1997-09-09 NZ NZ334446A patent/NZ334446A/xx unknown
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1999
- 1999-03-11 NO NO991207A patent/NO991207L/no not_active Application Discontinuation
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Also Published As
| Publication number | Publication date |
|---|---|
| CY2481B1 (en) | 2005-06-03 |
| DE69724626T2 (de) | 2004-07-29 |
| PL333282A1 (en) | 1999-11-22 |
| NO991207D0 (no) | 1999-03-11 |
| JP3288051B2 (ja) | 2002-06-04 |
| EE9900088A (et) | 1999-10-15 |
| EA199900283A1 (ru) | 1999-08-26 |
| ES2203819T3 (es) | 2004-04-16 |
| ATE248625T1 (de) | 2003-09-15 |
| CA2265824A1 (fr) | 1998-03-19 |
| DK0925070T3 (da) | 2003-12-01 |
| EP0925070A1 (fr) | 1999-06-30 |
| NO991207L (no) | 1999-05-11 |
| JP2000503675A (ja) | 2000-03-28 |
| CZ88499A3 (cs) | 1999-10-13 |
| WO1998010782A1 (fr) | 1998-03-19 |
| KR20000036054A (ko) | 2000-06-26 |
| DE69724626D1 (de) | 2003-10-09 |
| NZ334446A (en) | 2000-11-24 |
| EP0925070B1 (fr) | 2003-09-03 |
| KR100380871B1 (ko) | 2003-04-18 |
| EE03748B1 (et) | 2002-06-17 |
| AU4339297A (en) | 1998-04-02 |
| IL128870A0 (en) | 2000-06-01 |
| EA002469B1 (ru) | 2002-06-27 |
| AU721334B2 (en) | 2000-06-29 |
| CN1235554A (zh) | 1999-11-17 |
| PT925070E (pt) | 2003-12-31 |
| CA2265824C (fr) | 2004-11-09 |
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