RU2644554C2 - Амин-функциональные полиамиды - Google Patents
Амин-функциональные полиамиды Download PDFInfo
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- RU2644554C2 RU2644554C2 RU2015144224A RU2015144224A RU2644554C2 RU 2644554 C2 RU2644554 C2 RU 2644554C2 RU 2015144224 A RU2015144224 A RU 2015144224A RU 2015144224 A RU2015144224 A RU 2015144224A RU 2644554 C2 RU2644554 C2 RU 2644554C2
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- RU
- Russia
- Prior art keywords
- compound
- alkyl
- formula
- poly
- acid
- Prior art date
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- 239000004952 Polyamide Substances 0.000 title description 133
- 229920002647 polyamide Polymers 0.000 title description 133
- 150000001875 compounds Chemical class 0.000 claims abstract description 130
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 claims abstract description 99
- 239000008194 pharmaceutical composition Substances 0.000 claims abstract description 70
- 208000015181 infectious disease Diseases 0.000 claims abstract description 68
- 125000005915 C6-C14 aryl group Chemical group 0.000 claims abstract description 63
- 125000001072 heteroaryl group Chemical group 0.000 claims abstract description 55
- 206010028116 Mucosal inflammation Diseases 0.000 claims abstract description 53
- 201000010927 Mucositis Diseases 0.000 claims abstract description 53
- 125000004404 heteroalkyl group Chemical group 0.000 claims abstract description 50
- 230000002685 pulmonary effect Effects 0.000 claims abstract description 34
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims abstract description 33
- 201000003883 Cystic fibrosis Diseases 0.000 claims abstract description 32
- 125000006376 (C3-C10) cycloalkyl group Chemical group 0.000 claims abstract description 31
- 238000011282 treatment Methods 0.000 claims abstract description 28
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- 208000031650 Surgical Wound Infection Diseases 0.000 claims abstract description 11
- 206010036410 Postoperative wound infection Diseases 0.000 claims abstract description 9
- 229920000642 polymer Polymers 0.000 claims description 36
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 30
- 229920001577 copolymer Polymers 0.000 claims description 19
- 229920001223 polyethylene glycol Polymers 0.000 claims description 19
- 239000002202 Polyethylene glycol Substances 0.000 claims description 17
- 150000003973 alkyl amines Chemical class 0.000 claims description 15
- 241000589517 Pseudomonas aeruginosa Species 0.000 claims description 14
- 125000003827 glycol group Chemical group 0.000 claims description 14
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- QRJZGVVKGFIGLI-UHFFFAOYSA-N 2-phenylguanidine Chemical group NC(=N)NC1=CC=CC=C1 QRJZGVVKGFIGLI-UHFFFAOYSA-N 0.000 claims description 12
- PJJJBBJSCAKJQF-UHFFFAOYSA-N guanidinium chloride Chemical group [Cl-].NC(N)=[NH2+] PJJJBBJSCAKJQF-UHFFFAOYSA-N 0.000 claims description 12
- 125000000217 alkyl group Chemical group 0.000 claims description 11
- 150000001450 anions Chemical class 0.000 claims description 11
- 125000002795 guanidino group Chemical group C(N)(=N)N* 0.000 claims description 11
- 125000001424 substituent group Chemical group 0.000 claims description 11
- 229910052736 halogen Inorganic materials 0.000 claims description 9
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- 230000000694 effects Effects 0.000 abstract description 7
- 239000008177 pharmaceutical agent Substances 0.000 abstract description 2
- 239000000126 substance Substances 0.000 abstract description 2
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- 239000000243 solution Substances 0.000 description 158
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 117
- 239000000047 product Substances 0.000 description 107
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 105
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- 239000002253 acid Substances 0.000 description 25
- BHZOKUMUHVTPBX-UHFFFAOYSA-M sodium acetic acid acetate Chemical compound [Na+].CC(O)=O.CC([O-])=O BHZOKUMUHVTPBX-UHFFFAOYSA-M 0.000 description 25
- 239000002904 solvent Substances 0.000 description 24
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 21
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- 125000003118 aryl group Chemical group 0.000 description 19
- ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 description 18
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 17
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- 230000001225 therapeutic effect Effects 0.000 description 10
- OXEZLYIDQPBCBB-UHFFFAOYSA-N 4-(3-piperidin-4-ylpropyl)piperidine Chemical compound C1CNCCC1CCCC1CCNCC1 OXEZLYIDQPBCBB-UHFFFAOYSA-N 0.000 description 9
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- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 9
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- LDXJRKWFNNFDSA-UHFFFAOYSA-N 2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)-1-[4-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidin-5-yl]piperazin-1-yl]ethanone Chemical compound C1CN(CC2=NNN=C21)CC(=O)N3CCN(CC3)C4=CN=C(N=C4)NCC5=CC(=CC=C5)OC(F)(F)F LDXJRKWFNNFDSA-UHFFFAOYSA-N 0.000 description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 6
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- OTBHHUPVCYLGQO-UHFFFAOYSA-N bis(3-aminopropyl)amine Chemical compound NCCCNCCCN OTBHHUPVCYLGQO-UHFFFAOYSA-N 0.000 description 6
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- HMUNWXXNJPVALC-UHFFFAOYSA-N 1-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]-2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)C(CN1CC2=C(CC1)NN=N2)=O HMUNWXXNJPVALC-UHFFFAOYSA-N 0.000 description 4
- NQHVTVSAFRAXPA-UHFFFAOYSA-N 2-pyrrolidin-2-ylpyrrolidine Chemical compound C1CCNC1C1NCCC1 NQHVTVSAFRAXPA-UHFFFAOYSA-N 0.000 description 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical group N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
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- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 4
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- YLZOPXRUQYQQID-UHFFFAOYSA-N 3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)-1-[4-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidin-5-yl]piperazin-1-yl]propan-1-one Chemical compound N1N=NC=2CN(CCC=21)CCC(=O)N1CCN(CC1)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F YLZOPXRUQYQQID-UHFFFAOYSA-N 0.000 description 3
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| KR20170028979A (ko) * | 2014-07-11 | 2017-03-14 | 젠자임 코포레이션 | 주쇄 폴리아민 |
| CN104292148A (zh) * | 2014-09-22 | 2015-01-21 | 西南科技大学 | 一种橡胶或树脂光稳定剂的制备方法 |
| JP2018519404A (ja) * | 2015-07-09 | 2018-07-19 | ヘンケル アイピー アンド ホールディング ゲゼルシャフト ミット ベシュレンクテル ハフツング | 低粘度透明ポリアミド |
| CN108601723B (zh) * | 2015-11-03 | 2022-05-17 | 硕腾服务有限责任公司 | 溶胶-凝胶聚合物复合材料及其用途 |
| CN109310776B (zh) * | 2016-04-14 | 2022-02-11 | 勃林格殷格翰动物保健美国公司 | 含有抗微生物的聚酰胺或奥替尼啶防腐剂的多次剂量组合物 |
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| RU2732206C2 (ru) * | 2018-12-29 | 2020-09-14 | Вероника Андреевна Гусева | Способ лечения маститов у крупного рогатого скота |
| KR102052086B1 (ko) * | 2019-07-25 | 2019-12-04 | 복세원 | 젖소 유두 보호제 및 그 제조방법 |
| CN111471630B (zh) * | 2020-06-11 | 2021-11-02 | 鲁东大学 | 一株棒杆菌Ytld-phe09及其应用 |
| CN114796583B (zh) * | 2022-03-25 | 2023-02-10 | 浙江大学 | 一种基于聚硫辛酸的生物医用贴片材料及其制备方法 |
| CN115531518B (zh) * | 2022-09-22 | 2023-05-23 | 湖南科技学院 | 一种用于防治奶牛乳房炎的中药软膏及其制备方法 |
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