WO1995019974A2 - Composes a base de calixarene presentant une activite antibacterienne, antifongique, anticancereuse et anti-vih - Google Patents
Composes a base de calixarene presentant une activite antibacterienne, antifongique, anticancereuse et anti-vih Download PDFInfo
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- WO1995019974A2 WO1995019974A2 PCT/IE1995/000008 IE9500008W WO9519974A2 WO 1995019974 A2 WO1995019974 A2 WO 1995019974A2 IE 9500008 W IE9500008 W IE 9500008W WO 9519974 A2 WO9519974 A2 WO 9519974A2
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- 150000001875 compounds Chemical class 0.000 title claims abstract description 397
- VTJUKNSKBAOEHE-UHFFFAOYSA-N calixarene Chemical compound COC(=O)COC1=C(CC=2C(=C(CC=3C(=C(C4)C=C(C=3)C(C)(C)C)OCC(=O)OC)C=C(C=2)C(C)(C)C)OCC(=O)OC)C=C(C(C)(C)C)C=C1CC1=C(OCC(=O)OC)C4=CC(C(C)(C)C)=C1 VTJUKNSKBAOEHE-UHFFFAOYSA-N 0.000 title claims abstract description 27
- 230000000843 anti-fungal effect Effects 0.000 title claims abstract description 15
- 230000000844 anti-bacterial effect Effects 0.000 title claims abstract description 11
- 229940121375 antifungal agent Drugs 0.000 title claims description 9
- 230000000694 effects Effects 0.000 title abstract description 24
- 125000004122 cyclic group Chemical group 0.000 claims abstract description 16
- 230000001093 anti-cancer Effects 0.000 claims abstract description 7
- YECHEDVCXXVLIY-UHFFFAOYSA-N cyclotriveratrylene Chemical group C1C2=CC(OC)=C(OC)C=C2CC2=CC(OC)=C(OC)C=C2CC2=C1C=C(OC)C(OC)=C2 YECHEDVCXXVLIY-UHFFFAOYSA-N 0.000 claims abstract description 6
- CRPNQSVBEWWHIJ-UHFFFAOYSA-N 2,3,4-trihydroxybenzaldehyde Chemical class OC1=CC=C(C=O)C(O)=C1O CRPNQSVBEWWHIJ-UHFFFAOYSA-N 0.000 claims abstract description 5
- 230000000840 anti-viral effect Effects 0.000 claims abstract description 5
- DGXAGETVRDOQFP-UHFFFAOYSA-N 2,6-dihydroxybenzaldehyde Chemical class OC1=CC=CC(O)=C1C=O DGXAGETVRDOQFP-UHFFFAOYSA-N 0.000 claims abstract description 3
- 238000000034 method Methods 0.000 claims description 287
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims description 138
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 123
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- VQOXZBDYSJBXMA-RKEBNKJGSA-N nystatin a1 Chemical compound O[C@H]1[C@@H](N)[C@H](O)[C@@H](C)O[C@@H]1OC1/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)CC(O)CC(O)CC(O)CCC(O)C(O)C[C@](O)(CC(O)C2C(O)=O)OC2C1 VQOXZBDYSJBXMA-RKEBNKJGSA-N 0.000 description 1
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- OXCMYAYHXIHQOA-UHFFFAOYSA-N potassium;[2-butyl-5-chloro-3-[[4-[2-(1,2,4-triaza-3-azanidacyclopenta-1,4-dien-5-yl)phenyl]phenyl]methyl]imidazol-4-yl]methanol Chemical compound [K+].CCCCC1=NC(Cl)=C(CO)N1CC1=CC=C(C=2C(=CC=CC=2)C2=N[N-]N=N2)C=C1 OXCMYAYHXIHQOA-UHFFFAOYSA-N 0.000 description 1
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- KSAVQLQVUXSOCR-UHFFFAOYSA-M sodium lauroyl sarcosinate Chemical compound [Na+].CCCCCCCCCCCC(=O)N(C)CC([O-])=O KSAVQLQVUXSOCR-UHFFFAOYSA-M 0.000 description 1
- 229960005322 streptomycin Drugs 0.000 description 1
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- VACCAVUAMIDAGB-UHFFFAOYSA-N sulfamethizole Chemical class S1C(C)=NN=C1NS(=O)(=O)C1=CC=C(N)C=C1 VACCAVUAMIDAGB-UHFFFAOYSA-N 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 description 1
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- FRACPXUHUTXLCX-BELIEFIBSA-N tert-butyl N-{1-[(1S)-1-{[(1R,2S)-1-(benzylcarbamoyl)-1-hydroxy-3-[(3S)-2-oxopyrrolidin-3-yl]propan-2-yl]carbamoyl}-2-cyclopropylethyl]-2-oxopyridin-3-yl}carbamate Chemical compound CC(C)(C)OC(=O)NC1=CC=CN(C1=O)[C@@H](CC2CC2)C(=O)N[C@@H](C[C@@H]3CCNC3=O)[C@H](C(=O)NCC4=CC=CC=C4)O FRACPXUHUTXLCX-BELIEFIBSA-N 0.000 description 1
- 238000012956 testing procedure Methods 0.000 description 1
- DPKBAXPHAYBPRL-UHFFFAOYSA-M tetrabutylazanium;iodide Chemical compound [I-].CCCC[N+](CCCC)(CCCC)CCCC DPKBAXPHAYBPRL-UHFFFAOYSA-M 0.000 description 1
- CVICLPSVRORJKL-UHFFFAOYSA-J tetrapotassium tetraacetate Chemical class [K+].[K+].[K+].[K+].CC([O-])=O.CC([O-])=O.CC([O-])=O.CC([O-])=O CVICLPSVRORJKL-UHFFFAOYSA-J 0.000 description 1
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- 238000005809 transesterification reaction Methods 0.000 description 1
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- GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical group [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 1
- 239000012137 tryptone Substances 0.000 description 1
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- HGBOYTHUEUWSSQ-UHFFFAOYSA-N valeric aldehyde Natural products CCCCC=O HGBOYTHUEUWSSQ-UHFFFAOYSA-N 0.000 description 1
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/64—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms, e.g. histidine
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- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C205/00—Compounds containing nitro groups bound to a carbon skeleton
- C07C205/27—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by etherified hydroxy groups
- C07C205/35—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by etherified hydroxy groups having nitro groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
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- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C205/00—Compounds containing nitro groups bound to a carbon skeleton
- C07C205/27—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by etherified hydroxy groups
- C07C205/35—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by etherified hydroxy groups having nitro groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
- C07C205/36—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by etherified hydroxy groups having nitro groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton to carbon atoms of the same non-condensed six-membered aromatic ring or to carbon atoms of six-membered aromatic rings being part of the same condensed ring system
- C07C205/37—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by etherified hydroxy groups having nitro groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton to carbon atoms of the same non-condensed six-membered aromatic ring or to carbon atoms of six-membered aromatic rings being part of the same condensed ring system the oxygen atom of at least one of the etherified hydroxy groups being further bound to an acyclic carbon atom
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- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C215/00—Compounds containing amino and hydroxy groups bound to the same carbon skeleton
- C07C215/74—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton
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- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C217/00—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton
- C07C217/78—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton
- C07C217/80—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of non-condensed six-membered aromatic rings
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- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C235/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms
- C07C235/02—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton
- C07C235/04—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton the carbon skeleton being acyclic and saturated
- C07C235/08—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton the carbon skeleton being acyclic and saturated having the nitrogen atom of at least one of the carboxamide groups bound to an acyclic carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms
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- C07C235/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms
- C07C235/02—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton
- C07C235/04—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton the carbon skeleton being acyclic and saturated
- C07C235/12—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton the carbon skeleton being acyclic and saturated having the nitrogen atom of at least one of the carboxamide groups bound to an acyclic carbon atom of a hydrocarbon radical substituted by carboxyl groups
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- C07C235/02—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton
- C07C235/04—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton the carbon skeleton being acyclic and saturated
- C07C235/16—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton the carbon skeleton being acyclic and saturated having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a six-membered aromatic ring
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- C07C237/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
- C07C237/28—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atom of at least one of the carboxamide groups bound to a carbon atom of a non-condensed six-membered aromatic ring of the carbon skeleton
- C07C237/36—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atom of at least one of the carboxamide groups bound to a carbon atom of a non-condensed six-membered aromatic ring of the carbon skeleton having the nitrogen atom of the carboxamide group bound to an acyclic carbon atom of a hydrocarbon radical substituted by carboxyl groups
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- C07C245/00—Compounds containing chains of at least two nitrogen atoms with at least one nitrogen-to-nitrogen multiple bond
- C07C245/02—Azo compounds, i.e. compounds having the free valencies of —N=N— groups attached to different atoms, e.g. diazohydroxides
- C07C245/06—Azo compounds, i.e. compounds having the free valencies of —N=N— groups attached to different atoms, e.g. diazohydroxides with nitrogen atoms of azo groups bound to carbon atoms of six-membered aromatic rings
- C07C245/08—Azo compounds, i.e. compounds having the free valencies of —N=N— groups attached to different atoms, e.g. diazohydroxides with nitrogen atoms of azo groups bound to carbon atoms of six-membered aromatic rings with the two nitrogen atoms of azo groups bound to carbon atoms of six-membered aromatic rings, e.g. azobenzene
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- C—CHEMISTRY; METALLURGY
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- C07C255/00—Carboxylic acid nitriles
- C07C255/49—Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
- C07C255/54—Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing cyano groups and etherified hydroxy groups bound to the carbon skeleton
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- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
- C07C323/10—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and singly-bound oxygen atoms bound to the same carbon skeleton
- C07C323/11—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and singly-bound oxygen atoms bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton
- C07C323/16—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and singly-bound oxygen atoms bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton containing six-membered aromatic rings
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- C07C69/66—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety
- C07C69/67—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety of saturated acids
- C07C69/708—Ethers
- C07C69/712—Ethers the hydroxy group of the ester being etherified with a hydroxy compound having the hydroxy group bound to a carbon atom of a six-membered aromatic ring
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- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
- C07D249/10—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D249/14—Nitrogen atoms
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- C07D257/02—Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D257/04—Five-membered rings
- C07D257/06—Five-membered rings with nitrogen atoms directly attached to the ring carbon atom
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- 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
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- C—CHEMISTRY; METALLURGY
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- 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 System
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/08—Esters of oxyacids of phosphorus
- C07F9/09—Esters of phosphoric acids
- C07F9/091—Esters of phosphoric acids with hydroxyalkyl compounds with further substituents on alkyl
-
- 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 System
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids RP(=O)(OH)2; Thiophosphonic acids, i.e. RP(=X)(XH)2 (X = S, Se)
- C07F9/40—Esters thereof
- C07F9/4003—Esters thereof the acid moiety containing a substituent or a structure which is considered as characteristic
- C07F9/4006—Esters of acyclic acids which can have further substituents on alkyl
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H13/00—Compounds containing saccharide radicals esterified by carbonic acid or derivatives thereof, or by organic acids, e.g. phosphonic acids
- C07H13/02—Compounds containing saccharide radicals esterified by carbonic acid or derivatives thereof, or by organic acids, e.g. phosphonic acids by carboxylic acids
- C07H13/04—Compounds containing saccharide radicals esterified by carbonic acid or derivatives thereof, or by organic acids, e.g. phosphonic acids by carboxylic acids having the esterifying carboxyl radicals attached to acyclic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H17/00—Compounds containing heterocyclic radicals directly attached to hetero atoms of saccharide radicals
- C07H17/04—Heterocyclic radicals containing only oxygen as ring hetero atoms
- C07H17/08—Hetero rings containing eight or more ring members, e.g. erythromycins
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
- C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
- C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
- C07H19/16—Purine radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2603/00—Systems containing at least three condensed rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2603/00—Systems containing at least three condensed rings
- C07C2603/92—Systems containing at least three condensed rings with a condensed ring system consisting of at least two mutually uncondensed aromatic ring systems, linked by an annular structure formed by carbon chains on non-adjacent positions of the aromatic system, e.g. cyclophanes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Engineering & Computer Science (AREA)
- Biotechnology (AREA)
- Genetics & Genomics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU15453/95A AU1545395A (en) | 1994-01-24 | 1995-01-24 | Calixarene-based compounds having antibacterial, antifungal, anticancer-hiv activity |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IE940057 | 1994-01-24 | ||
IES940057 | 1994-01-24 |
Publications (3)
Publication Number | Publication Date |
---|---|
WO1995019974A2 true WO1995019974A2 (fr) | 1995-07-27 |
WO1995019974A3 WO1995019974A3 (fr) | 1995-09-21 |
WO1995019974B1 WO1995019974B1 (fr) | 1995-11-16 |
Family
ID=11040267
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/IE1995/000008 WO1995019974A2 (fr) | 1994-01-24 | 1995-01-24 | Composes a base de calixarene presentant une activite antibacterienne, antifongique, anticancereuse et anti-vih |
Country Status (2)
Country | Link |
---|---|
AU (1) | AU1545395A (fr) |
WO (1) | WO1995019974A2 (fr) |
Cited By (26)
Publication number | Priority date | Publication date | Assignee | Title |
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WO1997015566A1 (fr) * | 1994-04-28 | 1997-05-01 | Georghiou Paris E | Oligomeres nouveaux, procede de preparation et procedes d'utilisation |
NL1008988C2 (nl) * | 1998-04-24 | 1999-10-26 | Stichting Tech Wetenschapp | Calixareenverbinding en een selectief molecuul voorzien van een dergelijke verbinding. |
EP1005356A1 (fr) * | 1998-06-08 | 2000-06-07 | Advanced Medicine, Inc. | Agents antibacteriens |
EP1038871A1 (fr) * | 1997-12-09 | 2000-09-27 | Cosmo Research Institute | Derives sulfones de sulfures phenoles cycliques, leur procede de preparation, agents de separation et de recuperation contenant des sulfures phenoles cycliques, procedes de separation et de recuperation utilisant ces agents, et compositions de medicaments contenant lesdits sulfures |
WO2002044121A1 (fr) * | 2000-12-01 | 2002-06-06 | Aids Care Pharma Limited | Composes antiviraux |
EP1367044A1 (fr) * | 2002-05-31 | 2003-12-03 | Aids Care Pharma Limited | Dérivés du calixarène à activité antivirale |
DE10226099A1 (de) * | 2002-06-12 | 2004-01-08 | Jörg Martin Dipl.-Chem. Dormann | Filtermaterial für Toxine, Bakterien, Viren und andere physiologische Schadstoffe |
WO2004085442A2 (fr) * | 2003-03-24 | 2004-10-07 | Centre National De La Recherche Scientifique | Nouveaux composes calix arenes, leur procede de preparation et leur utilisation, en particulier comme mimes de sites enzymatiques |
WO2006042104A2 (fr) * | 2004-10-04 | 2006-04-20 | Regents Of The University Of Minnesota | Mimetiques a conformation peptidique a base de calixarene, procedes d'utilisation, et procedes d'elaboration |
US7338977B2 (en) * | 2003-11-25 | 2008-03-04 | Aids Care Pharma Limited | Anti-viral compounds |
WO2009025335A1 (fr) * | 2007-08-23 | 2009-02-26 | Jsr Corporation | Composition et composé sensibles au rayonnement |
FR2939666A1 (fr) * | 2008-12-17 | 2010-06-18 | Inst Radioprot Et De Surete Nu | Formulations cosmetiques et pharmaceutiques de molecules de calix[6]arenes |
AU2005208771B2 (en) * | 2004-01-23 | 2011-11-24 | The Trustees Of The University Of Pennsylvania | Facially amphiphilic polyaryl and polyarylalkynyl polymers and oligomers and uses thereof |
US8236800B2 (en) | 2003-03-17 | 2012-08-07 | The Trustees Of The University Of Pennsylvania | Facially amphiphilic polymers and oligomers and uses thereof |
WO2012140364A1 (fr) * | 2011-04-12 | 2012-10-18 | Universite De Lorraine | Utilisation de calixarenes dans le traitement des infections bacteriennes |
WO2012140365A1 (fr) * | 2011-04-12 | 2012-10-18 | Universite De Lorraine | Utilisation de calixarenes associes avec un antibiotique dans le traitement des infections bacteriennes |
WO2013024777A1 (fr) * | 2011-08-12 | 2013-02-21 | 三菱瓦斯化学株式会社 | Composé cyclique ainsi que procédé de fabrication de celui-ci, composition, et procédé de formation de motif de réserve |
KR20140093239A (ko) * | 2011-11-18 | 2014-07-25 | 미쯔비시 가스 케미칼 컴파니, 인코포레이티드 | 환상 화합물, 그 제조 방법, 감방사선성 조성물 및 레지스트 패턴 형성 방법 |
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US8889163B2 (en) | 2001-03-08 | 2014-11-18 | The Trustees Of The University Of Pennsylvania | Facially amphiphilic polymers as anti-infective agents |
WO2015196086A1 (fr) * | 2014-06-20 | 2015-12-23 | The University of Montana, Missoula, MT | Nouveaux inhibiteurs du système xc(-) |
CN107043364A (zh) * | 2016-02-05 | 2017-08-15 | 徐州医学院 | 氧杂杯[4]芳烃衍生物及其应用 |
CN107325810A (zh) * | 2017-06-29 | 2017-11-07 | 广东医科大学 | 一种穴状多羟基荧光化合物及其应用 |
WO2020074776A1 (fr) * | 2018-10-08 | 2020-04-16 | Aalto University Foundation Sr | Composés macrocycliques et leurs utilisations |
CN112771042A (zh) * | 2018-09-28 | 2021-05-07 | 重庆复创医药研究有限公司 | 作为蛋白激酶抑制剂的萘啶酮和吡啶基嘧啶酮类化合物 |
CN115252869A (zh) * | 2022-08-18 | 2022-11-01 | 南通大学 | 一种促进血管再生的纳米敷料及其制备方法 |
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US4604404A (en) * | 1985-04-03 | 1986-08-05 | A. H. Robins Company, Inc. | Antiviral sulfonated naphthalene formaldehyde condensation polymers |
EP0259016A1 (fr) * | 1986-08-29 | 1988-03-09 | LOCTITE (IRELAND) Ltd. | Dérivés de la calixarène et leur utilisation comme accélérateurs pour compositions adhésives instantanées |
EP0262910A2 (fr) * | 1986-09-29 | 1988-04-06 | LOCTITE (IRELAND) Ltd. | Compositions d'encapsulation |
EP0279521A1 (fr) * | 1987-01-21 | 1988-08-24 | LOCTITE (IRELAND) Ltd. | Oxacalixarènes fonctionnalisés, leur préparation et leur utilisation dans des compositions adhésives à prise rapide |
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WO1992013542A1 (fr) * | 1991-01-31 | 1992-08-20 | Rhone-Poulenc Rorer S.A. | Application de polymeres biologiquement actifs pour l'obtention d'un medicament pour le traitement d'infections a retrovirus |
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Cited By (56)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1997015566A1 (fr) * | 1994-04-28 | 1997-05-01 | Georghiou Paris E | Oligomeres nouveaux, procede de preparation et procedes d'utilisation |
EP1038871A1 (fr) * | 1997-12-09 | 2000-09-27 | Cosmo Research Institute | Derives sulfones de sulfures phenoles cycliques, leur procede de preparation, agents de separation et de recuperation contenant des sulfures phenoles cycliques, procedes de separation et de recuperation utilisant ces agents, et compositions de medicaments contenant lesdits sulfures |
EP1038871A4 (fr) * | 1997-12-09 | 2001-09-19 | Cosmo Res Inst | Derives sulfones de sulfures phenoles cycliques, leur procede de preparation, agents de separation et de recuperation contenant des sulfures phenoles cycliques, procedes de separation et de recuperation utilisant ces agents, et compositions de medicaments contenant lesdits sulfures |
US6355671B1 (en) | 1997-12-09 | 2002-03-12 | Cosmo Research Institute | Sulfonated derivatives of cyclic phenol sulfides, process for the preparation thereof, separating and recovering agents containing cyclic phenol sulfides, methods for separation and recovery therewith, and drug compositions containing the sulfides |
NL1008988C2 (nl) * | 1998-04-24 | 1999-10-26 | Stichting Tech Wetenschapp | Calixareenverbinding en een selectief molecuul voorzien van een dergelijke verbinding. |
EP1005356A1 (fr) * | 1998-06-08 | 2000-06-07 | Advanced Medicine, Inc. | Agents antibacteriens |
EP1005356A4 (fr) * | 1998-06-08 | 2001-08-22 | Advanced Medicine Inc | Agents antibacteriens |
WO2002044121A1 (fr) * | 2000-12-01 | 2002-06-06 | Aids Care Pharma Limited | Composes antiviraux |
US8889163B2 (en) | 2001-03-08 | 2014-11-18 | The Trustees Of The University Of Pennsylvania | Facially amphiphilic polymers as anti-infective agents |
EP1367044A1 (fr) * | 2002-05-31 | 2003-12-03 | Aids Care Pharma Limited | Dérivés du calixarène à activité antivirale |
DE10226099A1 (de) * | 2002-06-12 | 2004-01-08 | Jörg Martin Dipl.-Chem. Dormann | Filtermaterial für Toxine, Bakterien, Viren und andere physiologische Schadstoffe |
US9241917B2 (en) | 2003-03-17 | 2016-01-26 | The Trustees Of The University Of Pennsylvania | Facially amphiphilic polymers and oligomers and uses thereof |
US8455490B2 (en) | 2003-03-17 | 2013-06-04 | The Trustees Of The University Of Pennsylvania | Facially amphiphilic polymers and oligomers and uses thereof |
US8236800B2 (en) | 2003-03-17 | 2012-08-07 | The Trustees Of The University Of Pennsylvania | Facially amphiphilic polymers and oligomers and uses thereof |
WO2004085442A3 (fr) * | 2003-03-24 | 2004-12-16 | Centre Nat Rech Scient | Nouveaux composes calix arenes, leur procede de preparation et leur utilisation, en particulier comme mimes de sites enzymatiques |
WO2004085442A2 (fr) * | 2003-03-24 | 2004-10-07 | Centre National De La Recherche Scientifique | Nouveaux composes calix arenes, leur procede de preparation et leur utilisation, en particulier comme mimes de sites enzymatiques |
WO2004085441A1 (fr) * | 2003-03-24 | 2004-10-07 | Centre National De La Recherche Scientifique | Nouveaux composes de calix arenes, leur procede de preparation et leur utilisation, notamment en tant que mimes enzymatiques |
US7338977B2 (en) * | 2003-11-25 | 2008-03-04 | Aids Care Pharma Limited | Anti-viral compounds |
US8222456B2 (en) | 2004-01-23 | 2012-07-17 | The Trustees Of The University Of Pennsylvania | Facially amphiphilic polyaryl and polyarylalkynyl polymers and oligomers and uses thereof |
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US8716530B2 (en) | 2004-01-23 | 2014-05-06 | The Trustess Of The University Of Pennsylvania | Facially amphiphilic polyaryl and polyarylalkynyl polymers and oligomers and uses thereof |
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WO2009025335A1 (fr) * | 2007-08-23 | 2009-02-26 | Jsr Corporation | Composition et composé sensibles au rayonnement |
WO2010070049A1 (fr) * | 2008-12-17 | 2010-06-24 | Institut De Radioprotection Et De Surete Nucleaire | Formulations cosmetiques et pharmaceutiques de molecules de calixarenes |
US8987334B2 (en) | 2008-12-17 | 2015-03-24 | Institut De Radioprotection Et De Surete Nucleaire | Cosmetic and pharmaceutical formulations of calixarene molecules |
FR2939666A1 (fr) * | 2008-12-17 | 2010-06-18 | Inst Radioprot Et De Surete Nu | Formulations cosmetiques et pharmaceutiques de molecules de calix[6]arenes |
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KR20140104949A (ko) * | 2011-11-18 | 2014-08-29 | 미쯔비시 가스 케미칼 컴파니, 인코포레이티드 | 환상 화합물, 그 제조방법, 감방사선성 조성물 및 레지스트 패턴 형성방법 |
KR20140093239A (ko) * | 2011-11-18 | 2014-07-25 | 미쯔비시 가스 케미칼 컴파니, 인코포레이티드 | 환상 화합물, 그 제조 방법, 감방사선성 조성물 및 레지스트 패턴 형성 방법 |
KR101986544B1 (ko) | 2011-11-18 | 2019-06-07 | 미쯔비시 가스 케미칼 컴파니, 인코포레이티드 | 환상 화합물, 그 제조 방법, 감방사선성 조성물 및 레지스트 패턴 형성 방법 |
KR102004692B1 (ko) | 2011-11-18 | 2019-07-29 | 미쯔비시 가스 케미칼 컴파니, 인코포레이티드 | 환상 화합물, 그 제조방법, 감방사선성 조성물 및 레지스트 패턴 형성방법 |
WO2015196086A1 (fr) * | 2014-06-20 | 2015-12-23 | The University of Montana, Missoula, MT | Nouveaux inhibiteurs du système xc(-) |
CN107043364A (zh) * | 2016-02-05 | 2017-08-15 | 徐州医学院 | 氧杂杯[4]芳烃衍生物及其应用 |
CN107043364B (zh) * | 2016-02-05 | 2020-04-03 | 徐州医学院 | 氧杂杯[4]芳烃衍生物及其应用 |
CN107325810A (zh) * | 2017-06-29 | 2017-11-07 | 广东医科大学 | 一种穴状多羟基荧光化合物及其应用 |
CN112771042A (zh) * | 2018-09-28 | 2021-05-07 | 重庆复创医药研究有限公司 | 作为蛋白激酶抑制剂的萘啶酮和吡啶基嘧啶酮类化合物 |
WO2020074776A1 (fr) * | 2018-10-08 | 2020-04-16 | Aalto University Foundation Sr | Composés macrocycliques et leurs utilisations |
CN113164412A (zh) * | 2018-10-08 | 2021-07-23 | 阿尔托大学基金会 | 大环化合物及其用途 |
CN115252869A (zh) * | 2022-08-18 | 2022-11-01 | 南通大学 | 一种促进血管再生的纳米敷料及其制备方法 |
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AU1545395A (en) | 1995-08-08 |
WO1995019974A3 (fr) | 1995-09-21 |
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