CN102863345A - 胺基丙二醇类衍生物、其制备方法和其药物组合物与用途 - Google Patents
胺基丙二醇类衍生物、其制备方法和其药物组合物与用途 Download PDFInfo
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- CN102863345A CN102863345A CN2011101882551A CN201110188255A CN102863345A CN 102863345 A CN102863345 A CN 102863345A CN 2011101882551 A CN2011101882551 A CN 2011101882551A CN 201110188255 A CN201110188255 A CN 201110188255A CN 102863345 A CN102863345 A CN 102863345A
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- 0 *C(CC(CO)(CO)N)c1ccc(*c2ccc(*)cc2)cc1 Chemical compound *C(CC(CO)(CO)N)c1ccc(*c2ccc(*)cc2)cc1 0.000 description 16
- DHCGEMXILWSOSE-UHFFFAOYSA-N CC(C)c1nc(-c(cc2)ccc2Oc2ccc(CCC(CO)(CO)N)cc2)c[o]1 Chemical compound CC(C)c1nc(-c(cc2)ccc2Oc2ccc(CCC(CO)(CO)N)cc2)c[o]1 DHCGEMXILWSOSE-UHFFFAOYSA-N 0.000 description 1
- RETIZUJJKZKQFC-UHFFFAOYSA-N CC(C)c1nc(-c(cc2)ccc2Sc2ccc(C(CC(CO)(CO)N)O)cc2)c[o]1 Chemical compound CC(C)c1nc(-c(cc2)ccc2Sc2ccc(C(CC(CO)(CO)N)O)cc2)c[o]1 RETIZUJJKZKQFC-UHFFFAOYSA-N 0.000 description 1
- CEEJTQJMQKTADT-UHFFFAOYSA-N CCC(OCC(c(cc1)ccc1Nc1ccc(CCC(C(OCC)=O)(C(OCC)=O)NC(C)=O)cc1)=O)=O Chemical compound CCC(OCC(c(cc1)ccc1Nc1ccc(CCC(C(OCC)=O)(C(OCC)=O)NC(C)=O)cc1)=O)=O CEEJTQJMQKTADT-UHFFFAOYSA-N 0.000 description 1
- CUNVFZMMGGMKIE-UHFFFAOYSA-N CCC(OCC(c(cc1)ccc1Oc1ccc(CCC(C(OCC)=O)(C(OCC)=O)NC(C)=O)cc1)=O)=O Chemical compound CCC(OCC(c(cc1)ccc1Oc1ccc(CCC(C(OCC)=O)(C(OCC)=O)NC(C)=O)cc1)=O)=O CUNVFZMMGGMKIE-UHFFFAOYSA-N 0.000 description 1
- NTRVEVBLGKYZOW-UHFFFAOYSA-O CCCc1nc(-c(cc2)ccc2Oc2ccc(CCC(CO)(CO)[NH3+])cc2)c[o]1 Chemical compound CCCc1nc(-c(cc2)ccc2Oc2ccc(CCC(CO)(CO)[NH3+])cc2)c[o]1 NTRVEVBLGKYZOW-UHFFFAOYSA-O 0.000 description 1
- ARCYZSIPSDCYEM-UHFFFAOYSA-N CCOC(C(CCc(cc1)ccc1Oc(cc1)ccc1-c1ccc(C)[o]1)(C(OCC)=O)NC(C)=O)=O Chemical compound CCOC(C(CCc(cc1)ccc1Oc(cc1)ccc1-c1ccc(C)[o]1)(C(OCC)=O)NC(C)=O)=O ARCYZSIPSDCYEM-UHFFFAOYSA-N 0.000 description 1
- WJEWRTFEZKMXAV-UHFFFAOYSA-N CCOC(C(CCc(cc1)ccc1Oc(cc1)ccc1C(COC(C1CC1)=O)=O)(C(OCC)=O)NC(C)=O)=O Chemical compound CCOC(C(CCc(cc1)ccc1Oc(cc1)ccc1C(COC(C1CC1)=O)=O)(C(OCC)=O)NC(C)=O)=O WJEWRTFEZKMXAV-UHFFFAOYSA-N 0.000 description 1
- QDAQRPILSLZOCB-UHFFFAOYSA-N CCOC(C(CCc(cc1)ccc1Sc(cc1)ccc1-c1c[o]c(C2CC2)n1)(C(OCC)=O)NC(C)=O)=O Chemical compound CCOC(C(CCc(cc1)ccc1Sc(cc1)ccc1-c1c[o]c(C2CC2)n1)(C(OCC)=O)NC(C)=O)=O QDAQRPILSLZOCB-UHFFFAOYSA-N 0.000 description 1
- PNXYMNANIHMCIU-UHFFFAOYSA-N CCOC(C(CCc(cc1)ccc1Sc(cc1)ccc1C(COC(C)=O)=O)(C(OCC)=O)NC(C)=O)=O Chemical compound CCOC(C(CCc(cc1)ccc1Sc(cc1)ccc1C(COC(C)=O)=O)(C(OCC)=O)NC(C)=O)=O PNXYMNANIHMCIU-UHFFFAOYSA-N 0.000 description 1
- OSYBUFSDHSFMDG-UHFFFAOYSA-O CCc1nc(-c(cc2)ccc2Oc2ccc(CCC(CO)(CO)[NH3+])cc2)c[o]1 Chemical compound CCc1nc(-c(cc2)ccc2Oc2ccc(CCC(CO)(CO)[NH3+])cc2)c[o]1 OSYBUFSDHSFMDG-UHFFFAOYSA-O 0.000 description 1
- WDFDGBBBGDHDSU-UHFFFAOYSA-N CCc1nc(-c(cc2)ccc2Sc2ccc(C(CC(CO)(CO)N)O)cc2)c[o]1 Chemical compound CCc1nc(-c(cc2)ccc2Sc2ccc(C(CC(CO)(CO)N)O)cc2)c[o]1 WDFDGBBBGDHDSU-UHFFFAOYSA-N 0.000 description 1
- XXRQDYDLSZMMDW-UHFFFAOYSA-N Cc1cnc(-c(cc2)ccc2Oc2ccccc2)[s]1 Chemical compound Cc1cnc(-c(cc2)ccc2Oc2ccccc2)[s]1 XXRQDYDLSZMMDW-UHFFFAOYSA-N 0.000 description 1
- XXYBOBSZRFIKRU-UHFFFAOYSA-N Cc1nc(-c(cc2)ccc2Oc2ccc(CCC(C(CO)CO)N)cc2)c[o]1 Chemical compound Cc1nc(-c(cc2)ccc2Oc2ccc(CCC(C(CO)CO)N)cc2)c[o]1 XXYBOBSZRFIKRU-UHFFFAOYSA-N 0.000 description 1
- MENUPTURPLTOPX-UHFFFAOYSA-N Cc1nc(-c(cc2)ccc2Sc2ccc(C(CC(CO)(CO)N)O)cc2)c[o]1 Chemical compound Cc1nc(-c(cc2)ccc2Sc2ccc(C(CC(CO)(CO)N)O)cc2)c[o]1 MENUPTURPLTOPX-UHFFFAOYSA-N 0.000 description 1
- UPVAPBFTBPNLBS-UHFFFAOYSA-N NC(CCc(cc1)ccc1Sc(cc1)ccc1-c1c[o]cn1)(CO)CO Chemical compound NC(CCc(cc1)ccc1Sc(cc1)ccc1-c1c[o]cn1)(CO)CO UPVAPBFTBPNLBS-UHFFFAOYSA-N 0.000 description 1
- QPRKUNGRYAQYQV-UHFFFAOYSA-N NC(CCc(cc1)ccc1Sc(cc1)ccc1-c1ccc[nH]1)(CO)CO Chemical compound NC(CCc(cc1)ccc1Sc(cc1)ccc1-c1ccc[nH]1)(CO)CO QPRKUNGRYAQYQV-UHFFFAOYSA-N 0.000 description 1
- DPQABZYXTNPNKD-UHFFFAOYSA-O [NH3+]C(CCc(cc1)ccc1Oc(cc1)ccc1-c1c[o]c(C2CC2)n1)(CO)CO Chemical compound [NH3+]C(CCc(cc1)ccc1Oc(cc1)ccc1-c1c[o]c(C2CC2)n1)(CO)CO DPQABZYXTNPNKD-UHFFFAOYSA-O 0.000 description 1
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- C07D263/32—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
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- C—CHEMISTRY; METALLURGY
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- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/22—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C07D277/24—Radicals substituted by oxygen atoms
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- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/22—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C07D277/26—Radicals substituted by sulfur atoms
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- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/22—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C07D277/28—Radicals substituted by nitrogen atoms
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- C—CHEMISTRY; METALLURGY
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- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D307/38—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
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- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D307/38—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D307/40—Radicals substituted by oxygen atoms
- C07D307/42—Singly bound oxygen atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/02—Systems containing only non-condensed rings with a three-membered ring
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- Cephalosporin Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
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Priority Applications (8)
| Application Number | Priority Date | Filing Date | Title |
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| CN2011101882551A CN102863345A (zh) | 2011-07-06 | 2011-07-06 | 胺基丙二醇类衍生物、其制备方法和其药物组合物与用途 |
| KR1020147003101A KR20140048239A (ko) | 2011-07-06 | 2012-07-05 | 아미노 프로판디올 유도체, 제조방법 및 약제학적 조성물 및 사용 |
| EP12808109.8A EP2786982A4 (en) | 2011-07-06 | 2012-07-05 | AMINO-PROPYLENE GLYCOL DERIVATIVES, METHOD OF MANUFACTURING THEREOF, PHARMACEUTICAL COMPOSITION THEREFOR AND USE THEREOF |
| PCT/CN2012/078244 WO2013004190A1 (zh) | 2011-07-06 | 2012-07-05 | 胺基丙二醇类衍生物、其制备方法和其药物组合物与用途 |
| EA201490221A EA201490221A1 (ru) | 2011-07-06 | 2012-07-05 | Производные аминопропандиола, получение и фармацевтические композиции и применение |
| CN201280032727.7A CN103702973B (zh) | 2011-07-06 | 2012-07-05 | 胺基丙二醇类衍生物、其制备方法和其药物组合物与用途 |
| US14/130,861 US20140323501A1 (en) | 2011-07-06 | 2012-07-05 | Amino-propylene-glycol derivatives, preparation method and pharmaceutical composition and use thereof |
| JP2014517431A JP2014523887A (ja) | 2011-07-06 | 2012-07-05 | アミノプロパンジオール誘導体、準備、および医薬品組成物および用途 |
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| CN2011101882551A CN102863345A (zh) | 2011-07-06 | 2011-07-06 | 胺基丙二醇类衍生物、其制备方法和其药物组合物与用途 |
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| CN201280032727.7A Active CN103702973B (zh) | 2011-07-06 | 2012-07-05 | 胺基丙二醇类衍生物、其制备方法和其药物组合物与用途 |
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| CN201280032727.7A Active CN103702973B (zh) | 2011-07-06 | 2012-07-05 | 胺基丙二醇类衍生物、其制备方法和其药物组合物与用途 |
Country Status (7)
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| JP (1) | JP2014523887A (cg-RX-API-DMAC7.html) |
| KR (1) | KR20140048239A (cg-RX-API-DMAC7.html) |
| CN (2) | CN102863345A (cg-RX-API-DMAC7.html) |
| EA (1) | EA201490221A1 (cg-RX-API-DMAC7.html) |
| WO (1) | WO2013004190A1 (cg-RX-API-DMAC7.html) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN104844533A (zh) * | 2014-02-17 | 2015-08-19 | 中国医学科学院药物研究所 | 含五元芳杂环的氨基丙二醇类化合物、其制备方法及其医药用途 |
| CN111087356A (zh) * | 2018-10-24 | 2020-05-01 | 中国医学科学院药物研究所 | 一种艾托莫德的制备方法 |
| CN112930337A (zh) * | 2018-08-24 | 2021-06-08 | 赛尼欧普罗有限责任公司 | 抗增殖活性的苯氧基(杂)芳基醚 |
| CN115974803A (zh) * | 2022-12-12 | 2023-04-18 | 渐宽(苏州)生物科技有限公司 | 一种普赛莫德的晶型及其制备方法和用途 |
| WO2024131863A1 (zh) * | 2022-12-22 | 2024-06-27 | 渐宽(苏州)生物科技有限公司 | 一种艾托莫德的晶型及其制备方法和应用 |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2014175287A1 (ja) | 2013-04-26 | 2014-10-30 | 国立大学法人 京都大学 | 脳動脈瘤の形成および/または増大の抑制若しくは縮小用医薬組成物 |
| IL315313A (en) * | 2018-08-24 | 2024-10-01 | Xeniopro GmbH | Aromatic molecules for use in the treatment of pathological conditions |
| CN111087358B (zh) * | 2018-10-24 | 2022-06-21 | 中国医学科学院药物研究所 | 普赛莫德的制备方法 |
| CN111087359B (zh) * | 2018-10-24 | 2022-06-21 | 中国医学科学院药物研究所 | 艾托莫德的制备方法 |
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-
2012
- 2012-07-05 CN CN201280032727.7A patent/CN103702973B/zh active Active
- 2012-07-05 US US14/130,861 patent/US20140323501A1/en not_active Abandoned
- 2012-07-05 WO PCT/CN2012/078244 patent/WO2013004190A1/zh not_active Ceased
- 2012-07-05 JP JP2014517431A patent/JP2014523887A/ja active Pending
- 2012-07-05 EP EP12808109.8A patent/EP2786982A4/en not_active Withdrawn
- 2012-07-05 EA EA201490221A patent/EA201490221A1/ru unknown
- 2012-07-05 KR KR1020147003101A patent/KR20140048239A/ko not_active Ceased
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| US6963012B2 (en) * | 2001-09-27 | 2005-11-08 | Kyorin Pharmaceutical Co., Ltd. | Diaryl ether derivative, addition salt thereof, and immunosuppressant |
| CN100351244C (zh) * | 2002-05-27 | 2007-11-28 | 诺瓦提斯公司 | 双芳族链烷醇 |
| WO2005014525A2 (en) * | 2003-08-12 | 2005-02-17 | Mitsubishi Pharma Corporation | Bi-aryl compound having immunosuppressive activity |
| WO2005044780A1 (ja) * | 2003-11-10 | 2005-05-19 | Kyorin Pharmaceutical Co., Ltd. | アミノカルボン酸誘導体とその付加塩及びs1p受容体調節剤 |
| WO2006041015A1 (ja) * | 2004-10-12 | 2006-04-20 | Kyorin Pharmaceutical Co., Ltd. | アミノアルコール誘導体とその付加塩及び免疫抑制剤 |
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Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN104844533A (zh) * | 2014-02-17 | 2015-08-19 | 中国医学科学院药物研究所 | 含五元芳杂环的氨基丙二醇类化合物、其制备方法及其医药用途 |
| CN104844533B (zh) * | 2014-02-17 | 2019-04-09 | 中国医学科学院药物研究所 | 含五元芳杂环的氨基丙二醇类化合物、其制备方法及其医药用途 |
| CN112930337A (zh) * | 2018-08-24 | 2021-06-08 | 赛尼欧普罗有限责任公司 | 抗增殖活性的苯氧基(杂)芳基醚 |
| CN112930337B (zh) * | 2018-08-24 | 2025-07-04 | 赛尼欧普罗有限责任公司 | 抗增殖活性的苯氧基(杂)芳基醚 |
| CN111087356A (zh) * | 2018-10-24 | 2020-05-01 | 中国医学科学院药物研究所 | 一种艾托莫德的制备方法 |
| CN111087356B (zh) * | 2018-10-24 | 2022-06-21 | 中国医学科学院药物研究所 | 一种艾托莫德的制备方法 |
| CN115974803A (zh) * | 2022-12-12 | 2023-04-18 | 渐宽(苏州)生物科技有限公司 | 一种普赛莫德的晶型及其制备方法和用途 |
| CN115974803B (zh) * | 2022-12-12 | 2024-04-09 | 渐宽(苏州)生物科技有限公司 | 一种普赛莫德的晶型及其制备方法和用途 |
| WO2024125412A1 (zh) * | 2022-12-12 | 2024-06-20 | 渐宽(苏州)生物科技有限公司 | 一种普赛莫德的晶型及其制备方法和用途 |
| WO2024131863A1 (zh) * | 2022-12-22 | 2024-06-27 | 渐宽(苏州)生物科技有限公司 | 一种艾托莫德的晶型及其制备方法和应用 |
Also Published As
| Publication number | Publication date |
|---|---|
| CN103702973A (zh) | 2014-04-02 |
| US20140323501A1 (en) | 2014-10-30 |
| WO2013004190A1 (zh) | 2013-01-10 |
| CN103702973B (zh) | 2016-01-20 |
| EP2786982A4 (en) | 2015-04-15 |
| EA201490221A1 (ru) | 2014-12-30 |
| KR20140048239A (ko) | 2014-04-23 |
| JP2014523887A (ja) | 2014-09-18 |
| EP2786982A1 (en) | 2014-10-08 |
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