DE1793746B2 - O-ß-Hydroxyäthylderivate des Rutins - Google Patents
O-ß-Hydroxyäthylderivate des RutinsInfo
- Publication number
- DE1793746B2 DE1793746B2 DE1793746A DE1793746A DE1793746B2 DE 1793746 B2 DE1793746 B2 DE 1793746B2 DE 1793746 A DE1793746 A DE 1793746A DE 1793746 A DE1793746 A DE 1793746A DE 1793746 B2 DE1793746 B2 DE 1793746B2
- Authority
- DE
- Germany
- Prior art keywords
- rutin
- hydroxyethyl
- hours
- derivatives
- beta
- 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.)
- Withdrawn
Links
- JMGZEFIQIZZSBH-UHFFFAOYSA-N Bioquercetin Natural products CC1OC(OCC(O)C2OC(OC3=C(Oc4cc(O)cc(O)c4C3=O)c5ccc(O)c(O)c5)C(O)C2O)C(O)C(O)C1O JMGZEFIQIZZSBH-UHFFFAOYSA-N 0.000 title claims description 14
- IVTMALDHFAHOGL-UHFFFAOYSA-N eriodictyol 7-O-rutinoside Natural products OC1C(O)C(O)C(C)OC1OCC1C(O)C(O)C(O)C(OC=2C=C3C(C(C(O)=C(O3)C=3C=C(O)C(O)=CC=3)=O)=C(O)C=2)O1 IVTMALDHFAHOGL-UHFFFAOYSA-N 0.000 title claims description 14
- FDRQPMVGJOQVTL-UHFFFAOYSA-N quercetin rutinoside Natural products OC1C(O)C(O)C(CO)OC1OCC1C(O)C(O)C(O)C(OC=2C(C3=C(O)C=C(O)C=C3OC=2C=2C=C(O)C(O)=CC=2)=O)O1 FDRQPMVGJOQVTL-UHFFFAOYSA-N 0.000 title claims description 14
- 235000005493 rutin Nutrition 0.000 title claims description 14
- ALABRVAAKCSLSC-UHFFFAOYSA-N rutin Natural products CC1OC(OCC2OC(O)C(O)C(O)C2O)C(O)C(O)C1OC3=C(Oc4cc(O)cc(O)c4C3=O)c5ccc(O)c(O)c5 ALABRVAAKCSLSC-UHFFFAOYSA-N 0.000 title claims description 14
- 229960004555 rutoside Drugs 0.000 title claims description 14
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 29
- 150000001875 compounds Chemical class 0.000 description 13
- IKGXIBQEEMLURG-NVPNHPEKSA-N rutin Chemical compound O[C@@H]1[C@H](O)[C@@H](O)[C@H](C)O[C@H]1OC[C@@H]1[C@@H](O)[C@H](O)[C@@H](O)[C@H](OC=2C(C3=C(O)C=C(O)C=C3OC=2C=2C=C(O)C(O)=CC=2)=O)O1 IKGXIBQEEMLURG-NVPNHPEKSA-N 0.000 description 10
- 239000000203 mixture Substances 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 239000012153 distilled water Substances 0.000 description 4
- 238000002211 ultraviolet spectrum Methods 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 238000010521 absorption reaction Methods 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- 239000000155 melt Substances 0.000 description 3
- 230000001225 therapeutic effect Effects 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- REFJWTPEDVJJIY-UHFFFAOYSA-N Quercetin Chemical compound C=1C(O)=CC(O)=C(C(C=2O)=O)C=1OC=2C1=CC=C(O)C(O)=C1 REFJWTPEDVJJIY-UHFFFAOYSA-N 0.000 description 2
- 230000004856 capillary permeability Effects 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 235000005875 quercetin Nutrition 0.000 description 2
- 150000003305 rutin Chemical class 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- KIUKXJAPPMFGSW-DNGZLQJQSA-N (2S,3S,4S,5R,6R)-6-[(2S,3R,4R,5S,6R)-3-Acetamido-2-[(2S,3S,4R,5R,6R)-6-[(2R,3R,4R,5S,6R)-3-acetamido-2,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-2-carboxy-4,5-dihydroxyoxan-3-yl]oxy-5-hydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid Chemical compound CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@H](O[C@H]2[C@@H]([C@@H](O[C@H]3[C@@H]([C@@H](O)[C@H](O)[C@H](O3)C(O)=O)O)[C@H](O)[C@@H](CO)O2)NC(C)=O)[C@@H](C(O)=O)O1 KIUKXJAPPMFGSW-DNGZLQJQSA-N 0.000 description 1
- 108010003272 Hyaluronate lyase Proteins 0.000 description 1
- 102000001974 Hyaluronidases Human genes 0.000 description 1
- 206010061218 Inflammation Diseases 0.000 description 1
- ZVOLCUVKHLEPEV-UHFFFAOYSA-N Quercetagetin Natural products C1=C(O)C(O)=CC=C1C1=C(O)C(=O)C2=C(O)C(O)=C(O)C=C2O1 ZVOLCUVKHLEPEV-UHFFFAOYSA-N 0.000 description 1
- HWTZYBCRDDUBJY-UHFFFAOYSA-N Rhynchosin Natural products C1=C(O)C(O)=CC=C1C1=C(O)C(=O)C2=CC(O)=C(O)C=C2O1 HWTZYBCRDDUBJY-UHFFFAOYSA-N 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 230000003110 anti-inflammatory effect Effects 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 210000000941 bile Anatomy 0.000 description 1
- 210000004204 blood vessel Anatomy 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000007857 degradation product Substances 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 230000000593 degrading effect Effects 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 208000035475 disorder Diseases 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 235000019441 ethanol Nutrition 0.000 description 1
- 230000029142 excretion Effects 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 229930003935 flavonoid Natural products 0.000 description 1
- 150000002215 flavonoids Chemical class 0.000 description 1
- 235000017173 flavonoids Nutrition 0.000 description 1
- 210000001035 gastrointestinal tract Anatomy 0.000 description 1
- 230000002439 hemostatic effect Effects 0.000 description 1
- 229920002674 hyaluronan Polymers 0.000 description 1
- 229960003160 hyaluronic acid Drugs 0.000 description 1
- 229960002773 hyaluronidase Drugs 0.000 description 1
- 230000004054 inflammatory process Effects 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 210000000936 intestine Anatomy 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- MWDZOUNAPSSOEL-UHFFFAOYSA-N kaempferol Natural products OC1=C(C(=O)c2cc(O)cc(O)c2O1)c3ccc(O)cc3 MWDZOUNAPSSOEL-UHFFFAOYSA-N 0.000 description 1
- 210000003734 kidney Anatomy 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 244000005706 microflora Species 0.000 description 1
- 238000010606 normalization Methods 0.000 description 1
- 238000007911 parenteral administration Methods 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 229960001285 quercetin Drugs 0.000 description 1
- 150000003244 quercetin derivatives Chemical class 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 150000003306 rutin derivatives Chemical class 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
Classifications
-
- 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
- C07H17/06—Benzopyran radicals
- C07H17/065—Benzo[b]pyrans
- C07H17/07—Benzo[b]pyran-4-ones
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
- C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D311/04—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
- C07D311/22—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 4
- C07D311/26—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 4 with aromatic rings attached in position 2 or 3
- C07D311/28—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 4 with aromatic rings attached in position 2 or 3 with aromatic rings attached in position 2 only
- C07D311/30—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 4 with aromatic rings attached in position 2 or 3 with aromatic rings attached in position 2 only not hydrogenated in the hetero ring, e.g. flavones
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Biochemistry (AREA)
- Biotechnology (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Molecular Biology (AREA)
- Saccharide Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR36051A FR5072M (OSRAM) | 1965-10-25 | 1965-10-25 | |
| CH336266A CH458389A (fr) | 1965-10-25 | 1966-03-09 | Procédé de préparation de dérivés de la quercétine ou de ses glycosides |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE1793746A1 DE1793746A1 (de) | 1973-05-30 |
| DE1793746B2 true DE1793746B2 (de) | 1978-06-22 |
Family
ID=25692836
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE1543974A Withdrawn DE1543974B2 (de) | 1965-10-25 | 1966-10-08 | 09.03.66 Schweiz 3362-66 Verfahren zur Herstellung von reinen Mono-, Di-, Tri-, Tetra- oder Penta-O-beta-hydroxyäthylderivatendes Quercetins oder Rutins bzw. von Gemischen aus dem betreffenden Mono- und Di-, oder Di- und Tri-, oder Tri- und Tetra-, oder Tetra- und Pentaderivat |
| DE1793746A Withdrawn DE1793746B2 (de) | 1965-10-25 | 1966-10-08 | O-ß-Hydroxyäthylderivate des Rutins |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE1543974A Withdrawn DE1543974B2 (de) | 1965-10-25 | 1966-10-08 | 09.03.66 Schweiz 3362-66 Verfahren zur Herstellung von reinen Mono-, Di-, Tri-, Tetra- oder Penta-O-beta-hydroxyäthylderivatendes Quercetins oder Rutins bzw. von Gemischen aus dem betreffenden Mono- und Di-, oder Di- und Tri-, oder Tri- und Tetra-, oder Tetra- und Pentaderivat |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US3420815A (OSRAM) |
| BE (1) | BE688577A (OSRAM) |
| CH (1) | CH458389A (OSRAM) |
| DE (2) | DE1543974B2 (OSRAM) |
| ES (1) | ES333026A1 (OSRAM) |
| FR (1) | FR5072M (OSRAM) |
| GB (1) | GB1159317A (OSRAM) |
| NL (1) | NL148894B (OSRAM) |
| SE (1) | SE351847B (OSRAM) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2827935A1 (de) * | 1978-06-26 | 1980-01-10 | Helm Chemiewerk Gmbh & Co Kg | Verfahren zur herstellung von trishydroxyaethylrutin |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3890298A (en) * | 1972-05-23 | 1975-06-17 | Us Agriculture | Dihydrochalcone xylosides and their use as sweetening agents |
| US4153788A (en) * | 1974-04-09 | 1979-05-08 | Zyma S.A. | Process of preparing mono-O-β-hydroxyethyl-7 rutoside |
| PT68117A (fr) * | 1977-06-02 | 1978-06-01 | Sarget Lab | Nouveau procede de preparation de derives de glycosides benzopyranniques |
| JPS60147224A (ja) * | 1984-01-10 | 1985-08-03 | ジユゼツペ カネストリ | ポリマ−分散剤、その製造方法およびその分散剤を含有する分散体 |
| US5478579A (en) * | 1991-02-06 | 1995-12-26 | Biodyn Medical Research, Inc. | Method for treatment of osteoporosis |
| DE19850282A1 (de) * | 1998-10-30 | 2000-05-04 | Merck Patent Gmbh | Verfahren zur Herstellung von Quercetin und Isoquercetin-Derivaten |
| BR9914811A (pt) * | 1998-10-30 | 2001-07-03 | Merck Patent Gmbh | Processo para a preparação de derivados de quercetina e isoquercetina |
| FR2787111B1 (fr) * | 1998-12-11 | 2001-02-23 | Negma Lab | Troxerutine a forte teneur en trihydroxy-ethyl-rutoside, a mouillabilite elevee, et procede de preparation |
| US7166640B2 (en) * | 2000-07-28 | 2007-01-23 | Immupharm Aps | Method of treating symptoms of common cold, allergic rhinitis and infections relating to the respiratory tract |
| EP2468741A1 (en) | 2010-12-16 | 2012-06-27 | Bel/Novamann International s.r.o. | Novel quercetin derivatives, their preparation, pharmaceutical compositions containing them and their use |
| CN102924546A (zh) * | 2012-11-08 | 2013-02-13 | 兰亚朝 | 曲克芦丁的制备方法 |
| CN104177461B (zh) * | 2013-05-21 | 2016-11-09 | 济南新力特科技有限公司 | 三羟乙基芦丁的制备方法 |
| KR101809943B1 (ko) * | 2014-05-23 | 2017-12-18 | 지난 신라이트 테크놀로지 컴퍼니 리미티드 | 트리하이드록시에틸 루토사이드의 제조방법 |
| CN106589017B (zh) * | 2016-11-14 | 2019-10-29 | 重庆市碚圣医药科技股份有限公司 | 3’,4’,7-三羟乙基芦丁的制备方法 |
| JP2022511400A (ja) | 2018-10-02 | 2022-01-31 | ヤンセン ファーマシューティカ エヌ．ベー． | ヒドロキシエチルケルセチングルクロニドを含む医薬組成物 |
| US11304968B2 (en) | 2018-11-16 | 2022-04-19 | Janssen Pharmaceutica Nv | Pharmaceutical compositions comprising a hydroxyethylquercetin glucuronide |
| US10639294B2 (en) | 2018-10-02 | 2020-05-05 | Janssen Pharmaceutica Nv | Pharmaceutical compositions comprising a hydroxyethylquercetin glucuronide metabolite |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3042666A (en) * | 1958-02-26 | 1962-07-03 | Ici Ltd | Polyether derivatives |
| US3167538A (en) * | 1962-05-24 | 1965-01-26 | Olin Mathieson | Process for alkoxylating a mixture of methyl glucoside and a hydroxy compound, and the product of that process |
-
1965
- 1965-10-25 FR FR36051A patent/FR5072M/fr not_active Expired
-
1966
- 1966-03-09 CH CH336266A patent/CH458389A/fr unknown
- 1966-10-08 DE DE1543974A patent/DE1543974B2/de not_active Withdrawn
- 1966-10-08 DE DE1793746A patent/DE1793746B2/de not_active Withdrawn
- 1966-10-20 BE BE688577D patent/BE688577A/xx unknown
- 1966-10-24 ES ES0333026A patent/ES333026A1/es not_active Expired
- 1966-10-24 US US588746A patent/US3420815A/en not_active Expired - Lifetime
- 1966-10-24 GB GB47639/66A patent/GB1159317A/en not_active Expired
- 1966-10-25 SE SE14600/66A patent/SE351847B/xx unknown
- 1966-10-25 NL NL666615071A patent/NL148894B/xx not_active IP Right Cessation
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2827935A1 (de) * | 1978-06-26 | 1980-01-10 | Helm Chemiewerk Gmbh & Co Kg | Verfahren zur herstellung von trishydroxyaethylrutin |
Also Published As
| Publication number | Publication date |
|---|---|
| GB1159317A (en) | 1969-07-23 |
| NL148894B (nl) | 1976-03-15 |
| US3420815A (en) | 1969-01-07 |
| DE1543974A1 (de) | 1970-02-12 |
| NL6615071A (OSRAM) | 1967-04-26 |
| CH458389A (fr) | 1968-06-30 |
| SE351847B (OSRAM) | 1972-12-11 |
| DE1793746A1 (de) | 1973-05-30 |
| BE688577A (OSRAM) | 1967-04-20 |
| DE1543974B2 (de) | 1975-06-05 |
| ES333026A1 (es) | 1967-12-01 |
| FR5072M (OSRAM) | 1967-05-16 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8230 | Patent withdrawn |