GB1017960A - Therapeutically useful triterpene saponin preparations and the production thereof - Google Patents
Therapeutically useful triterpene saponin preparations and the production thereofInfo
- Publication number
- GB1017960A GB1017960A GB49629/63A GB4962963A GB1017960A GB 1017960 A GB1017960 A GB 1017960A GB 49629/63 A GB49629/63 A GB 49629/63A GB 4962963 A GB4962963 A GB 4962963A GB 1017960 A GB1017960 A GB 1017960A
- Authority
- GB
- United Kingdom
- Prior art keywords
- aescin
- primulic
- acid
- shearing forces
- hesperidin
- 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.)
- Expired
Links
- 238000002360 preparation method Methods 0.000 title abstract 4
- 238000004519 manufacturing process Methods 0.000 title 1
- 229930182493 triterpene saponin Natural products 0.000 title 1
- YFESOSRPNPYODN-RSMWSHJLSA-N (2s,3s,4s,5r,6r)-6-[[(4s,6ar,6bs,8r,8ar,9r,10r,14br)-9-acetyloxy-8-hydroxy-4,8a-bis(hydroxymethyl)-4,6a,6b,11,11,14b-hexamethyl-10-[(z)-2-methylbut-2-enoyl]oxy-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-4-hydroxy-3,5-bis[[(2s,3r,4s, Chemical compound O([C@@H]1[C@H](O[C@H]([C@@H]([C@H]1O)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)OC1CC[C@]2(C)C3CC=C4[C@@]([C@@]3(CCC2[C@]1(CO)C)C)(C)C[C@@H](O)[C@@]1(CO)[C@@H](OC(C)=O)[C@@H](C(CC14)(C)C)OC(=O)C(\C)=C/C)C(O)=O)[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O.O([C@@H]1[C@H](O[C@H]([C@@H]([C@H]1O)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)OC1CC[C@]2(C)C3CC=C4[C@@]([C@@]3(CCC2[C@]1(CO)C)C)(C)C[C@@H](O)[C@@]1(CO)[C@@H](OC(C)=O)[C@@H](C(CC14)(C)C)OC(=O)C(/C)=C/C)C(O)=O)[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O YFESOSRPNPYODN-RSMWSHJLSA-N 0.000 abstract 9
- AXNVHPCVMSNXNP-GKTCLTPXSA-N Aescin Natural products O=C(O[C@H]1[C@@H](OC(=O)C)[C@]2(CO)[C@@H](O)C[C@@]3(C)[C@@]4(C)[C@@H]([C@]5(C)[C@H]([C@](CO)(C)[C@@H](O[C@@H]6[C@@H](O[C@H]7[C@@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O7)[C@@H](O)[C@H](O[C@H]7[C@H](O)[C@@H](O)[C@H](O)[C@H](CO)O7)[C@@H](C(=O)O)O6)CC5)CC4)CC=C3[C@@H]2CC1(C)C)/C(=C/C)/C AXNVHPCVMSNXNP-GKTCLTPXSA-N 0.000 abstract 8
- LDPKDIVFHXKSCE-PCVCHNHVSA-N (2S,3R,4S,5R,6R)-6-[[(3S,4aR,6aR,6bS,8R,8aS,12aS,14aR,14bR)-8-hydroxy-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-4-hydroxy-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-3-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxyoxane-2-carboxylic acid Chemical compound O[C@@H]1[C@H](O)[C@@H](O)[C@H](C)O[C@H]1O[C@H]1[C@H](O[C@@H]2C([C@H]3[C@]([C@@H]4[C@@]([C@@]5(C[C@@H](O)[C@@]6(CO)CCC(C)(C)C[C@H]6C5=CC4)C)(C)CC3)(C)CC2)(C)C)O[C@H](C(O)=O)[C@H](O[C@H]2[C@@H]([C@@H](O)[C@@H](O)[C@@H](CO[C@H]3[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O3)O)O2)O)[C@@H]1O LDPKDIVFHXKSCE-PCVCHNHVSA-N 0.000 abstract 7
- 238000010008 shearing Methods 0.000 abstract 5
- 229930182490 saponin Natural products 0.000 abstract 4
- 150000007949 saponins Chemical class 0.000 abstract 4
- 235000017709 saponins Nutrition 0.000 abstract 4
- 239000001100 (2S)-5,7-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)chroman-4-one Substances 0.000 abstract 3
- QUQPHWDTPGMPEX-UHFFFAOYSA-N Hesperidine Natural products C1=C(O)C(OC)=CC=C1C1OC2=CC(OC3C(C(O)C(O)C(COC4C(C(O)C(O)C(C)O4)O)O3)O)=CC(O)=C2C(=O)C1 QUQPHWDTPGMPEX-UHFFFAOYSA-N 0.000 abstract 3
- QUQPHWDTPGMPEX-UTWYECKDSA-N aurantiamarin Natural products COc1ccc(cc1O)[C@H]1CC(=O)c2c(O)cc(O[C@@H]3O[C@H](CO[C@@H]4O[C@@H](C)[C@H](O)[C@@H](O)[C@H]4O)[C@@H](O)[C@H](O)[C@H]3O)cc2O1 QUQPHWDTPGMPEX-UTWYECKDSA-N 0.000 abstract 3
- APSNPMVGBGZYAJ-GLOOOPAXSA-N clematine Natural products COc1cc(ccc1O)[C@@H]2CC(=O)c3c(O)cc(O[C@@H]4O[C@H](CO[C@H]5O[C@@H](C)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)cc3O2 APSNPMVGBGZYAJ-GLOOOPAXSA-N 0.000 abstract 3
- 229940025878 hesperidin Drugs 0.000 abstract 3
- VUYDGVRIQRPHFX-UHFFFAOYSA-N hesperidin Natural products COc1cc(ccc1O)C2CC(=O)c3c(O)cc(OC4OC(COC5OC(O)C(O)C(O)C5O)C(O)C(O)C4O)cc3O2 VUYDGVRIQRPHFX-UHFFFAOYSA-N 0.000 abstract 3
- QUQPHWDTPGMPEX-QJBIFVCTSA-N hesperidin Chemical compound C1=C(O)C(OC)=CC=C1[C@H]1OC2=CC(O[C@H]3[C@@H]([C@@H](O)[C@H](O)[C@@H](CO[C@H]4[C@@H]([C@H](O)[C@@H](O)[C@H](C)O4)O)O3)O)=CC(O)=C2C(=O)C1 QUQPHWDTPGMPEX-QJBIFVCTSA-N 0.000 abstract 3
- ARGKVCXINMKCAZ-UHFFFAOYSA-N neohesperidine Natural products C1=C(O)C(OC)=CC=C1C1OC2=CC(OC3C(C(O)C(O)C(CO)O3)OC3C(C(O)C(O)C(C)O3)O)=CC(O)=C2C(=O)C1 ARGKVCXINMKCAZ-UHFFFAOYSA-N 0.000 abstract 3
- 239000001397 quillaja saponaria molina bark Substances 0.000 abstract 3
- 239000013078 crystal Substances 0.000 abstract 2
- 229930003935 flavonoid Natural products 0.000 abstract 2
- -1 flavonoid glucoside Chemical class 0.000 abstract 2
- 235000017173 flavonoids Nutrition 0.000 abstract 2
- 229930182478 glucoside Natural products 0.000 abstract 2
- 239000004570 mortar (masonry) Substances 0.000 abstract 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract 1
- 239000008298 dragée Substances 0.000 abstract 1
- 210000001035 gastrointestinal tract Anatomy 0.000 abstract 1
- 229940069352 hesperidin complex Drugs 0.000 abstract 1
- 229910052573 porcelain Inorganic materials 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H15/00—Compounds containing hydrocarbon or substituted hydrocarbon radicals directly attached to hetero atoms of saccharide radicals
- C07H15/20—Carbocyclic rings
- C07H15/24—Condensed ring systems having three or more rings
- C07H15/256—Polyterpene radicals
-
- 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
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/22—Heterocyclic compounds, e.g. ascorbic acid, tocopherol or pyrrolidones
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Public Health (AREA)
- Organic Chemistry (AREA)
- Molecular Biology (AREA)
- General Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biochemistry (AREA)
- Biotechnology (AREA)
- Genetics & Genomics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Saccharide Compounds (AREA)
- Steroid Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEM55118A DE1282852B (de) | 1962-12-14 | 1962-12-14 | Peroral anwendbares aescinhaltiges Arzneimittel |
| CH1488763 | 1963-12-06 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1017960A true GB1017960A (en) | 1966-01-26 |
Family
ID=25715271
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB49629/63A Expired GB1017960A (en) | 1962-12-14 | 1963-12-16 | Therapeutically useful triterpene saponin preparations and the production thereof |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US3238104A (cg-RX-API-DMAC7.html) |
| AT (1) | AT245733B (cg-RX-API-DMAC7.html) |
| BE (1) | BE641151A (cg-RX-API-DMAC7.html) |
| CH (1) | CH474541A (cg-RX-API-DMAC7.html) |
| DE (2) | DE1282852B (cg-RX-API-DMAC7.html) |
| DK (1) | DK107183C (cg-RX-API-DMAC7.html) |
| FR (1) | FR3473M (cg-RX-API-DMAC7.html) |
| GB (1) | GB1017960A (cg-RX-API-DMAC7.html) |
| IT (1) | IT1150100B (cg-RX-API-DMAC7.html) |
| NL (2) | NL142595B (cg-RX-API-DMAC7.html) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS51139613A (en) * | 1975-05-24 | 1976-12-02 | Nippon Shinyaku Co Ltd | An absorbable non-crystalline sterol glycoside monopalmitate ester and a method for preparing its pharmaceutical |
| DE2530953C2 (de) * | 1975-07-11 | 1994-07-07 | Dr. Madaus & Co, 5000 Köln | Verfahren zur Herstellung von röntgenamorphem Aescin, nach diesem Verfahren erhältliches röntgenamorphes Aescin und dieses enthaltende Arzneimittel |
| JPS5948810B2 (ja) * | 1980-03-22 | 1984-11-29 | 山之内製薬株式会社 | ニカルジピン持続性製剤用組成物 |
| CN116115566B (zh) * | 2021-11-15 | 2025-02-14 | 上海维洱生物医药科技有限公司 | 一种七叶皂苷钠脂质体及其制备方法 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2123248A (en) * | 1937-01-14 | 1938-07-12 | Louis N Markwood | Insoluble reaction products of peat and process of making same |
| US2350804A (en) * | 1939-07-22 | 1944-06-06 | Ohta Masaki | Derivatives of hesperidin and process for preparing the same |
| US2691654A (en) * | 1952-06-11 | 1954-10-12 | Buroughs Wellcome & Co U S A I | Amino heterocycles and method of making |
| DE1134180B (de) * | 1954-01-22 | 1962-08-02 | Nitritfabrik Ges Mit Beschraen | Verfahren zur Umwandlung von therapeutisch anwendbaren, in Wasser praktisch unloeslichen organischen Stoffen in ein echt wasserloesliches Produkt |
| US2780620A (en) * | 1954-01-28 | 1957-02-05 | Merle M Krider | Partial acidic hydrolysis of steroidal saponins |
| US3110711A (en) * | 1960-06-14 | 1963-11-12 | Klinge Co Chem Pharm Fab | Process of producing two escin isomers from horse chestnut extracts, and products |
-
0
- NL NL301747D patent/NL301747A/xx unknown
-
1962
- 1962-12-14 DE DEM55118A patent/DE1282852B/de active Pending
-
1963
- 1963-12-04 CH CH1488663A patent/CH474541A/de not_active IP Right Cessation
- 1963-12-11 DK DK577663AA patent/DK107183C/da active
- 1963-12-12 FR FR957029A patent/FR3473M/fr not_active Expired
- 1963-12-12 IT IT25495/63A patent/IT1150100B/it active
- 1963-12-12 BE BE641151A patent/BE641151A/xx unknown
- 1963-12-12 AT AT997463A patent/AT245733B/de active
- 1963-12-12 NL NL63301747A patent/NL142595B/xx not_active IP Right Cessation
- 1963-12-13 US US330479A patent/US3238104A/en not_active Expired - Lifetime
- 1963-12-16 GB GB49629/63A patent/GB1017960A/en not_active Expired
-
1964
- 1964-12-05 DE DE19641493999 patent/DE1493999A1/de active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| NL142595B (nl) | 1974-07-15 |
| NL301747A (cg-RX-API-DMAC7.html) | |
| IT1150100B (it) | 1986-12-10 |
| DK107183C (da) | 1967-05-01 |
| AT245733B (de) | 1966-03-10 |
| US3238104A (en) | 1966-03-01 |
| FR3473M (fr) | 1965-08-09 |
| DE1282852B (de) | 1968-11-14 |
| DE1493999A1 (de) | 1970-02-05 |
| BE641151A (cg-RX-API-DMAC7.html) | 1964-04-01 |
| CH474541A (de) | 1969-06-30 |
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