RU2019144960A - Мультибиотические средства и способы их применения - Google Patents
Мультибиотические средства и способы их применения Download PDFInfo
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- RU2019144960A RU2019144960A RU2019144960A RU2019144960A RU2019144960A RU 2019144960 A RU2019144960 A RU 2019144960A RU 2019144960 A RU2019144960 A RU 2019144960A RU 2019144960 A RU2019144960 A RU 2019144960A RU 2019144960 A RU2019144960 A RU 2019144960A
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- RU
- Russia
- Prior art keywords
- multibiotic
- agent
- compound
- following structure
- salt
- Prior art date
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- 239000003814 drug Substances 0.000 title 1
- 229940079593 drug Drugs 0.000 title 1
- 239000003795 chemical substances by application Substances 0.000 claims 25
- 150000001875 compounds Chemical class 0.000 claims 9
- 150000003839 salts Chemical class 0.000 claims 8
- KWGRBVOPPLSCSI-WPRPVWTQSA-N (-)-ephedrine Chemical compound CN[C@@H](C)[C@H](O)C1=CC=CC=C1 KWGRBVOPPLSCSI-WPRPVWTQSA-N 0.000 claims 2
- SRBFZHDQGSBBOR-IOVATXLUSA-N D-xylopyranose Chemical compound O[C@@H]1COC(O)[C@H](O)[C@H]1O SRBFZHDQGSBBOR-IOVATXLUSA-N 0.000 claims 2
- 125000002252 acyl group Chemical group 0.000 claims 2
- PYMYPHUHKUWMLA-UHFFFAOYSA-N arabinose Natural products OCC(O)C(O)C(O)C=O PYMYPHUHKUWMLA-UHFFFAOYSA-N 0.000 claims 2
- SRBFZHDQGSBBOR-UHFFFAOYSA-N beta-D-Pyranose-Lyxose Natural products OC1COC(O)C(O)C1O SRBFZHDQGSBBOR-UHFFFAOYSA-N 0.000 claims 2
- 150000001720 carbohydrates Chemical class 0.000 claims 2
- 239000000546 pharmaceutical excipient Substances 0.000 claims 2
- HDTRYLNUVZCQOY-UHFFFAOYSA-N α-D-glucopyranosyl-α-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OC1C(O)C(O)C(O)C(CO)O1 HDTRYLNUVZCQOY-UHFFFAOYSA-N 0.000 claims 1
- 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 claims 1
- HMFHBZSHGGEWLO-SOOFDHNKSA-N D-ribofuranose Chemical compound OC[C@H]1OC(O)[C@H](O)[C@@H]1O HMFHBZSHGGEWLO-SOOFDHNKSA-N 0.000 claims 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 1
- 229930091371 Fructose Natural products 0.000 claims 1
- 239000005715 Fructose Substances 0.000 claims 1
- RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 0.000 claims 1
- SEOVTRFCIGRIMH-UHFFFAOYSA-N Indole-3-acetic acid Natural products C1=CC=C2C(CC(=O)O)=CNC2=C1 SEOVTRFCIGRIMH-UHFFFAOYSA-N 0.000 claims 1
- GOLXRNDWAUTYKT-UHFFFAOYSA-N Indole-3-propionic acid Natural products C1=CC=C2C(CCC(=O)O)=CNC2=C1 GOLXRNDWAUTYKT-UHFFFAOYSA-N 0.000 claims 1
- 241000736262 Microbiota Species 0.000 claims 1
- PYMYPHUHKUWMLA-LMVFSUKVSA-N Ribose Natural products OC[C@@H](O)[C@@H](O)[C@@H](O)C=O PYMYPHUHKUWMLA-LMVFSUKVSA-N 0.000 claims 1
- HDTRYLNUVZCQOY-WSWWMNSNSA-N Trehalose Natural products O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 HDTRYLNUVZCQOY-WSWWMNSNSA-N 0.000 claims 1
- 125000003158 alcohol group Chemical group 0.000 claims 1
- HDTRYLNUVZCQOY-LIZSDCNHSA-N alpha,alpha-trehalose Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 HDTRYLNUVZCQOY-LIZSDCNHSA-N 0.000 claims 1
- HMFHBZSHGGEWLO-UHFFFAOYSA-N alpha-D-Furanose-Ribose Natural products OCC1OC(O)C(O)C1O HMFHBZSHGGEWLO-UHFFFAOYSA-N 0.000 claims 1
- WQZGKKKJIJFFOK-PHYPRBDBSA-N alpha-D-galactose Chemical compound OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@H]1O WQZGKKKJIJFFOK-PHYPRBDBSA-N 0.000 claims 1
- PYMYPHUHKUWMLA-WDCZJNDASA-N arabinose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)C=O PYMYPHUHKUWMLA-WDCZJNDASA-N 0.000 claims 1
- OEYIOHPDSNJKLS-UHFFFAOYSA-N choline Chemical compound C[N+](C)(C)CCO OEYIOHPDSNJKLS-UHFFFAOYSA-N 0.000 claims 1
- 229960001231 choline Drugs 0.000 claims 1
- KWGRBVOPPLSCSI-UHFFFAOYSA-N d-ephedrine Natural products CNC(C)C(O)C1=CC=CC=C1 KWGRBVOPPLSCSI-UHFFFAOYSA-N 0.000 claims 1
- 229960002179 ephedrine Drugs 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- 229930182830 galactose Natural products 0.000 claims 1
- 125000004383 glucosinolate group Chemical group 0.000 claims 1
- 229920002674 hyaluronan Polymers 0.000 claims 1
- 229960003160 hyaluronic acid Drugs 0.000 claims 1
- 239000003290 indole 3-propionic acid Substances 0.000 claims 1
- 239000003617 indole-3-acetic acid Substances 0.000 claims 1
- JCQLYHFGKNRPGE-FCVZTGTOSA-N lactulose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 JCQLYHFGKNRPGE-FCVZTGTOSA-N 0.000 claims 1
- 229960000511 lactulose Drugs 0.000 claims 1
- PFCRQPBOOFTZGQ-UHFFFAOYSA-N lactulose keto form Natural products OCC(=O)C(O)C(C(O)CO)OC1OC(CO)C(O)C(O)C1O PFCRQPBOOFTZGQ-UHFFFAOYSA-N 0.000 claims 1
- KBOPZPXVLCULAV-UHFFFAOYSA-N mesalamine Chemical compound NC1=CC=C(O)C(C(O)=O)=C1 KBOPZPXVLCULAV-UHFFFAOYSA-N 0.000 claims 1
- 229960004963 mesalazine Drugs 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- 239000002417 nutraceutical Substances 0.000 claims 1
- 235000021436 nutraceutical agent Nutrition 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
Classifications
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Claims (32)
1. Мультибиотическое средство, содержащее три или более фрагментов, которые независимо представляют собой спиртовые ядра или ацилы, при условии, что мультибиотическое средство содержит по меньшей мере три различных фрагмента и что фрагменты связаны одной или несколькими сложноэфирными или гликозидными связями,
причем каждое спиртовое ядро независимо представляет собой углевод или его олигомер, месаламин, холин или эфедрин, причем каждый углевод или его олигомер представляет собой ксилозу, арабинозу, фруктозу, галактозу, глюкозинолат, рибозу или ее олигомер; трегалозу; лактулозу; или гиалуроновую кислоту;
причем каждый ацил независимо представляет собой ацил короткоцепочечной жирной кислоты, ацил β-гидроксибутирата, ацил ацетоацетата, ацил индол-3-уксусной кислоты, ацил индол-3-пропионовой кислоты или ацил 3-(индол-3-ил)-акриловой кислоты.
2. Мультибиотическое средство по п. 1, где мультибиотическое средство выбрано из группы, состоящей из соединений со следующей структурой:
3. Мультибиотическое средство по п. 1, где мультибиотическое средство представляет собой соединение со следующей структурой:
или его соль.
4. Мультибиотическое средство по п. 1, где мультибиотическое средство представляет собой соединение со следующей структурой:
или его соль.
5. Мультибиотическое средство по п. 1, где мультибиотическое средство представляет собой соединение со следующей структурой:
или его соль.
6. Мультибиотическое средство по п. 1, где мультибиотическое средство представляет собой соединение со следующей структурой:
или его соль.
7. Мультибиотическое средство по п. 1, где мультибиотическое средство представляет собой соединение со следующей структурой:
или его соль.
8. Мультибиотическое средство по п. 1, где мультибиотическое средство представляет собой соединение со следующей структурой:
или его соль.
9. Мультибиотическое средство по п. 1, где мультибиотическое средство представляет собой соединение со следующей структурой:
или его соль.
10. Фармацевтическая композиция, содержащая мультибиотическое средство по любому из пп.1-9 и фармацевтически приемлемое вспомогательное вещество.
11. Нутрицевтическая композиция, содержащая мультибиотическое средство по любому из пп.1-9 и физиологически приемлемое вспомогательное вещество.
12. Мультибиотическое средство по любому из пп.1-9 для применения в доставке биологически активного соединения к целевому участку у субъекта.
13. Мультибиотическое средство для применения по п.12, где мультибиотическое средство вводят перорально.
14. Мультибиотическое средство для применения по п.12, где мультибиотическое средство по существу активируется микробиотой субъекта.
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AU2019282691A1 (en) | 2018-06-05 | 2020-12-24 | Flagship Pioneering Innovations V, Inc. | Active agents and methods of their use for the treatment of metabolic disorders and nonalcoholic fatty liver disease |
WO2019236772A1 (en) * | 2018-06-05 | 2019-12-12 | Flagship Pioneering Innovations V, Inc. | Acylated active agents and methods of their use for the treatment of autoimmune disorders |
WO2020037009A1 (en) | 2018-08-13 | 2020-02-20 | Flagship Pioneering Innovations V, Inc. | Conjugates and methods of using the same |
WO2020106454A2 (en) * | 2018-11-07 | 2020-05-28 | Regents Of The University Of Minnesota | Analgesic and anti-addictive compositions for treatment of chronic pain and opioid addiction |
MX2021006684A (es) * | 2018-12-06 | 2021-09-10 | Flagship Pioneering Innovations V Inc | Conjugados portadores de monometil fumarato y métodos para su uso. |
WO2020249197A1 (de) * | 2019-06-12 | 2020-12-17 | Ioi Oleo Gmbh | Verfahren zur herstellung von acylverkappten 3-hydroxycarbonsäuren sowie deren salzen und estern |
WO2021132235A1 (ja) * | 2019-12-26 | 2021-07-01 | 住友化学株式会社 | 粘着剤組成物 |
CN115515581A (zh) | 2020-01-10 | 2022-12-23 | 帕西拉制药股份有限公司 | 通过给予缓释脂质体麻醉组合物治疗疼痛 |
WO2021141963A1 (en) | 2020-01-10 | 2021-07-15 | Pacira Pharmaceuticals, Inc. | Treatment of pain by subarachnoid administration of sustained-release liposomal anesthetic compositions |
US10738077B1 (en) * | 2020-04-09 | 2020-08-11 | Shaanxi University Of Science And Technology | Hydroxytyrosol ursodeoxycholic acid ester with antioxidant activity and a method of preparing the same |
MY198026A (en) * | 2020-11-06 | 2023-07-26 | Stellar Biomolecular Res Gmbh | Parenteral nutrition formulation and methods of preparation thereof |
WO2022140580A1 (en) * | 2020-12-24 | 2022-06-30 | Orn Almarsson | Xanthophyll derivatives |
CN112979464B (zh) * | 2020-12-28 | 2022-02-11 | 中国农业科学院农产品加工研究所 | 白藜芦醇共轭亚油酸酯及其制备方法 |
US11918688B2 (en) | 2021-01-11 | 2024-03-05 | Pacira Pharmaceuticals, Inc. | Treatment of hip pain with sustained-release liposomal anesthetic compositions |
WO2022197899A2 (en) | 2021-03-19 | 2022-09-22 | Pacira Pharmaceuticals, Inc. | Treatment of pain in pediatric patients by administration of sustained-release liposomal anesthetic compositions |
CN113045416B (zh) * | 2021-03-23 | 2023-08-18 | 南京纽邦生物科技有限公司 | 一种(r)-3-羟基丁酰-(r)-3-羟基丁酯的制备方法 |
CA3238205A1 (en) * | 2021-11-12 | 2023-05-19 | Rajaram Samant | A synergistic composition for activating intracellular secondary messenger(camp) pathway |
CN114957004A (zh) * | 2022-05-20 | 2022-08-30 | 上海远志昌浦生物科技有限公司 | 一种(r)-3-羟基丁酸-(r)-羟基丁酯及其中间体的合成方法和应用 |
US11918565B1 (en) | 2022-11-03 | 2024-03-05 | Pacira Pharmaceuticals, Inc. | Treatment of post-operative pain via sciatic nerve block with sustained-release liposomal anesthetic compositions |
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DE19709787A1 (de) * | 1997-03-11 | 1998-09-17 | Bayer Ag | Oligosaccaride und deren Derivate sowie ein chemo-enzymatisches Verfahren zu deren Herstellung |
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EP2323669B2 (en) * | 2008-08-18 | 2018-07-18 | BioActor B.V. | Arabinoxylan for modulating the barrier function of the intestinal surface |
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CN105407718B (zh) * | 2013-06-04 | 2019-01-04 | 维奥姆生物科学有限公司 | 涂布的颗粒和包括其的组合物 |
EP3180023B1 (en) | 2014-08-13 | 2020-02-19 | The Regents of The University of California | Biodegradable trehalose glycopolymers |
US9492473B2 (en) * | 2015-01-26 | 2016-11-15 | Kaleido Biosciences, Inc. | Glycan therapeutics and related methods thereof |
JP2016222612A (ja) * | 2015-06-01 | 2016-12-28 | 昭和電工株式会社 | 化粧料または皮膚外用剤 |
WO2017091544A1 (en) * | 2015-11-24 | 2017-06-01 | Theravance Biopharma R&D Ip, Llc | Prodrugs of a jak inhibitor compound for treatment of gastrointestinal inflammatory disease |
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SG11201910198UA (en) | 2019-11-28 |
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KR20200011972A (ko) | 2020-02-04 |
WO2018226732A1 (en) | 2018-12-13 |
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