JP2011518194A5 - - Google Patents
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- Publication number
- JP2011518194A5 JP2011518194A5 JP2011505263A JP2011505263A JP2011518194A5 JP 2011518194 A5 JP2011518194 A5 JP 2011518194A5 JP 2011505263 A JP2011505263 A JP 2011505263A JP 2011505263 A JP2011505263 A JP 2011505263A JP 2011518194 A5 JP2011518194 A5 JP 2011518194A5
- Authority
- JP
- Japan
- Prior art keywords
- shal
- linker
- ligand
- phenoxy
- chloro
- 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.)
- Granted
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- 239000003446 ligand Substances 0.000 claims description 71
- -1 (3-chloro-5 (trifluoromethyl) pyridin-2-yloxy) phenoxy Chemical group 0.000 claims description 27
- 206010028980 Neoplasm Diseases 0.000 claims description 26
- 210000004027 cell Anatomy 0.000 claims description 26
- 201000011510 cancer Diseases 0.000 claims description 24
- 239000012636 effector Substances 0.000 claims description 24
- 239000000203 mixture Substances 0.000 claims description 23
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims description 20
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 18
- 108090000765 processed proteins & peptides Proteins 0.000 claims description 18
- 235000019260 propionic acid Nutrition 0.000 claims description 18
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 15
- YBJHBAHKTGYVGT-ZKWXMUAHSA-N biotin Natural products N1C(=O)N[C@@H]2[C@H](CCCCC(=O)O)SC[C@@H]21 YBJHBAHKTGYVGT-ZKWXMUAHSA-N 0.000 claims description 14
- 239000013522 chelant Substances 0.000 claims description 14
- 229920001223 polyethylene glycol Polymers 0.000 claims description 13
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 12
- 239000002202 Polyethylene glycol Substances 0.000 claims description 12
- 229910052799 carbon Inorganic materials 0.000 claims description 12
- 239000003550 marker Substances 0.000 claims description 12
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 12
- 108090001008 Avidin Proteins 0.000 claims description 10
- 229960002685 biotin Drugs 0.000 claims description 10
- 235000020958 biotin Nutrition 0.000 claims description 10
- 239000011616 biotin Substances 0.000 claims description 10
- DUWWHGPELOTTOE-UHFFFAOYSA-N n-(5-chloro-2,4-dimethoxyphenyl)-3-oxobutanamide Chemical compound COC1=CC(OC)=C(NC(=O)CC(C)=O)C=C1Cl DUWWHGPELOTTOE-UHFFFAOYSA-N 0.000 claims description 10
- SIEKBQPWGCCNGS-UHFFFAOYSA-N 3-[2-[3-chloro-5-(trifluoromethyl)pyridin-2-yl]oxyanilino]-3-oxopropanoic acid Chemical compound OC(=O)CC(=O)NC1=CC=CC=C1OC1=NC=C(C(F)(F)F)C=C1Cl SIEKBQPWGCCNGS-UHFFFAOYSA-N 0.000 claims description 8
- KSDVAPCASJRMAD-UHFFFAOYSA-N 4-[4-[(4-chlorophenyl)methyl]piperazin-1-yl]-3-nitrobenzoic acid Chemical compound [O-][N+](=O)C1=CC(C(=O)O)=CC=C1N1CCN(CC=2C=CC(Cl)=CC=2)CC1 KSDVAPCASJRMAD-UHFFFAOYSA-N 0.000 claims description 8
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 8
- YUVKUEAFAVKILW-UHFFFAOYSA-N 2-(4-{[5-(trifluoromethyl)pyridin-2-yl]oxy}phenoxy)propanoic acid Chemical compound C1=CC(OC(C)C(O)=O)=CC=C1OC1=CC=C(C(F)(F)F)C=N1 YUVKUEAFAVKILW-UHFFFAOYSA-N 0.000 claims description 6
- OOLBCHYXZDXLDS-UHFFFAOYSA-N 2-[4-(2,4-dichlorophenoxy)phenoxy]propanoic acid Chemical compound C1=CC(OC(C)C(O)=O)=CC=C1OC1=CC=C(Cl)C=C1Cl OOLBCHYXZDXLDS-UHFFFAOYSA-N 0.000 claims description 6
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims description 6
- 150000001412 amines Chemical class 0.000 claims description 6
- 235000014633 carbohydrates Nutrition 0.000 claims description 6
- 239000000412 dendrimer Substances 0.000 claims description 6
- 229920000736 dendritic polymer Polymers 0.000 claims description 6
- DCOPUUMXTXDBNB-UHFFFAOYSA-N diclofenac Chemical compound OC(=O)CC1=CC=CC=C1NC1=C(Cl)C=CC=C1Cl DCOPUUMXTXDBNB-UHFFFAOYSA-N 0.000 claims description 6
- XKHPEMKBJGUYCM-UHFFFAOYSA-N ethyl 2-oxochromene-3-carboxylate Chemical compound C1=CC=C2OC(=O)C(C(=O)OCC)=CC2=C1 XKHPEMKBJGUYCM-UHFFFAOYSA-N 0.000 claims description 6
- 108020004707 nucleic acids Proteins 0.000 claims description 6
- 102000039446 nucleic acids Human genes 0.000 claims description 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 6
- PWXJULSLLONQHY-UHFFFAOYSA-N phenylcarbamic acid Chemical compound OC(=O)NC1=CC=CC=C1 PWXJULSLLONQHY-UHFFFAOYSA-N 0.000 claims description 6
- 238000001514 detection method Methods 0.000 claims description 5
- MPPOHAUSNPTFAJ-UHFFFAOYSA-N 2-[4-[(6-chloro-1,3-benzoxazol-2-yl)oxy]phenoxy]propanoic acid Chemical compound C1=CC(OC(C)C(O)=O)=CC=C1OC1=NC2=CC=C(Cl)C=C2O1 MPPOHAUSNPTFAJ-UHFFFAOYSA-N 0.000 claims description 4
- 101710112752 Cytotoxin Proteins 0.000 claims description 4
- KDXKERNSBIXSRK-YFKPBYRVSA-N L-lysine Chemical compound NCCCC[C@H](N)C(O)=O KDXKERNSBIXSRK-YFKPBYRVSA-N 0.000 claims description 4
- COLNVLDHVKWLRT-QMMMGPOBSA-N L-phenylalanine Chemical compound OC(=O)[C@@H](N)CC1=CC=CC=C1 COLNVLDHVKWLRT-QMMMGPOBSA-N 0.000 claims description 4
- 239000004472 Lysine Substances 0.000 claims description 4
- KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Natural products NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 claims description 4
- QIAFMBKCNZACKA-UHFFFAOYSA-N N-benzoylglycine Chemical compound OC(=O)CNC(=O)C1=CC=CC=C1 QIAFMBKCNZACKA-UHFFFAOYSA-N 0.000 claims description 4
- WDLRUFUQRNWCPK-UHFFFAOYSA-N Tetraxetan Chemical compound OC(=O)CN1CCN(CC(O)=O)CCN(CC(O)=O)CCN(CC(O)=O)CC1 WDLRUFUQRNWCPK-UHFFFAOYSA-N 0.000 claims description 4
- 210000003719 b-lymphocyte Anatomy 0.000 claims description 4
- YUIKUTLBPMDDNQ-MRVPVSSYSA-N clodinafop Chemical compound C1=CC(O[C@H](C)C(O)=O)=CC=C1OC1=NC=C(Cl)C=C1F YUIKUTLBPMDDNQ-MRVPVSSYSA-N 0.000 claims description 4
- 238000010276 construction Methods 0.000 claims description 4
- 231100000599 cytotoxic agent Toxicity 0.000 claims description 4
- 239000002619 cytotoxin Substances 0.000 claims description 4
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 claims description 4
- 238000009472 formulation Methods 0.000 claims description 4
- 238000003384 imaging method Methods 0.000 claims description 4
- 239000002502 liposome Substances 0.000 claims description 4
- 229910052751 metal Inorganic materials 0.000 claims description 4
- 239000002184 metal Substances 0.000 claims description 4
- 239000008194 pharmaceutical composition Substances 0.000 claims description 4
- SIOXPEMLGUPBBT-UHFFFAOYSA-N picolinic acid Chemical compound OC(=O)C1=CC=CC=N1 SIOXPEMLGUPBBT-UHFFFAOYSA-N 0.000 claims description 4
- 230000026683 transduction Effects 0.000 claims description 4
- 238000010361 transduction Methods 0.000 claims description 4
- 229960004295 valine Drugs 0.000 claims description 4
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims description 3
- CZKNFPFWQYDPKT-UHFFFAOYSA-N ClC1=CC(C(F)(F)F)=CN=C1OC1=CC=CC=C1CC(=C)C#N Chemical compound ClC1=CC(C(F)(F)F)=CN=C1OC1=CC=CC=C1CC(=C)C#N CZKNFPFWQYDPKT-UHFFFAOYSA-N 0.000 claims description 3
- QVVDVENEPNODSI-BTNSXGMBSA-N (2s)-2-[[(2s)-2-[[(2s)-2-[[(2s)-2-[[(2s)-2-[[(2s)-2-amino-5-(diaminomethylideneamino)pentanoyl]amino]-5-(diaminomethylideneamino)pentanoyl]amino]-5-(diaminomethylideneamino)pentanoyl]amino]-5-(diaminomethylideneamino)pentanoyl]amino]-5-(diaminomethylidene Chemical group NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CCCN=C(N)N)C(O)=O QVVDVENEPNODSI-BTNSXGMBSA-N 0.000 claims description 2
- OZRPKALPSGYEHX-UHFFFAOYSA-N 2-methyl-1-(3-morpholin-4-ylpropyl)-5-phenylpyrrole-3-carboxylic acid Chemical compound C1COCCN1CCCN1C(C)=C(C(O)=O)C=C1C1=CC=CC=C1 OZRPKALPSGYEHX-UHFFFAOYSA-N 0.000 claims description 2
- ABOOPXYCKNFDNJ-UHFFFAOYSA-N 2-{4-[(6-chloroquinoxalin-2-yl)oxy]phenoxy}propanoic acid Chemical compound C1=CC(OC(C)C(O)=O)=CC=C1OC1=CN=C(C=C(Cl)C=C2)C2=N1 ABOOPXYCKNFDNJ-UHFFFAOYSA-N 0.000 claims description 2
- JEFTWCWADIIOMX-UHFFFAOYSA-N 3-[3-chloro-2-[5-(trifluoromethyl)pyridin-2-yl]oxyanilino]-3-oxopropanoic acid Chemical compound ClC=1C(=C(NC(CC(=O)O)=O)C=CC1)OC1=NC=C(C=C1)C(F)(F)F JEFTWCWADIIOMX-UHFFFAOYSA-N 0.000 claims description 2
- PHFMKISCNCBYKA-UHFFFAOYSA-N 3-[3-chloro-4-[5-(trifluoromethyl)pyridin-2-yl]oxyanilino]-2-oxopropanoic acid Chemical compound ClC=1C=C(NCC(C(=O)O)=O)C=CC1OC1=NC=C(C=C1)C(F)(F)F PHFMKISCNCBYKA-UHFFFAOYSA-N 0.000 claims description 2
- AQOIAODAHOWPFY-UHFFFAOYSA-N 3-[3-chloro-4-[5-(trifluoromethyl)pyridin-2-yl]oxyanilino]-3-oxopropanoic acid Chemical compound ClC1=CC(NC(=O)CC(=O)O)=CC=C1OC1=CC=C(C(F)(F)F)C=N1 AQOIAODAHOWPFY-UHFFFAOYSA-N 0.000 claims description 2
- XWLSXRYHLGGUGB-WCCKRBBISA-N 3-aminopropanoic acid;(2s)-2,5-diaminopentanoic acid Chemical compound NCCC(O)=O.NCCC[C@H](N)C(O)=O XWLSXRYHLGGUGB-WCCKRBBISA-N 0.000 claims description 2
- CZRCFAOMWRAFIC-UHFFFAOYSA-N 5-(tetradecyloxy)-2-furoic acid Chemical compound CCCCCCCCCCCCCCOC1=CC=C(C(O)=O)O1 CZRCFAOMWRAFIC-UHFFFAOYSA-N 0.000 claims description 2
- TZGKHPXUAULWOC-UHFFFAOYSA-N 6-[(4,6-dichloro-1,3,5-triazin-2-yl)amino]-3',6'-dihydroxyspiro[2-benzofuran-3,9'-xanthene]-1-one;hydron;chloride Chemical compound Cl.C=1C(O)=CC=C2C=1OC1=CC(O)=CC=C1C2(C1=CC=2)OC(=O)C1=CC=2NC1=NC(Cl)=NC(Cl)=N1 TZGKHPXUAULWOC-UHFFFAOYSA-N 0.000 claims description 2
- 108010066676 Abrin Proteins 0.000 claims description 2
- IYMAXBFPHPZYIK-BQBZGAKWSA-N Arg-Gly-Asp Chemical compound NC(N)=NCCC[C@H](N)C(=O)NCC(=O)N[C@@H](CC(O)=O)C(O)=O IYMAXBFPHPZYIK-BQBZGAKWSA-N 0.000 claims description 2
- 108090000695 Cytokines Proteins 0.000 claims description 2
- 102000004127 Cytokines Human genes 0.000 claims description 2
- 102000016607 Diphtheria Toxin Human genes 0.000 claims description 2
- 108010053187 Diphtheria Toxin Proteins 0.000 claims description 2
- 108700006830 Drosophila Antp Proteins 0.000 claims description 2
- 108090000790 Enzymes Proteins 0.000 claims description 2
- 102000004190 Enzymes Human genes 0.000 claims description 2
- 108010058597 HLA-DR Antigens Proteins 0.000 claims description 2
- 102000006354 HLA-DR Antigens Human genes 0.000 claims description 2
- 108010036449 HLA-DR10 antigen Proteins 0.000 claims description 2
- HTTJABKRGRZYRN-UHFFFAOYSA-N Heparin Chemical compound OC1C(NC(=O)C)C(O)OC(COS(O)(=O)=O)C1OC1C(OS(O)(=O)=O)C(O)C(OC2C(C(OS(O)(=O)=O)C(OC3C(C(O)C(O)C(O3)C(O)=O)OS(O)(=O)=O)C(CO)O2)NS(O)(=O)=O)C(C(O)=O)O1 HTTJABKRGRZYRN-UHFFFAOYSA-N 0.000 claims description 2
- 108010070875 Human Immunodeficiency Virus tat Gene Products Proteins 0.000 claims description 2
- 208000015914 Non-Hodgkin lymphomas Diseases 0.000 claims description 2
- 108010077850 Nuclear Localization Signals Proteins 0.000 claims description 2
- 101710160107 Outer membrane protein A Proteins 0.000 claims description 2
- 101000762949 Pseudomonas aeruginosa (strain ATCC 15692 / DSM 22644 / CIP 104116 / JCM 14847 / LMG 12228 / 1C / PRS 101 / PAO1) Exotoxin A Proteins 0.000 claims description 2
- 108010039491 Ricin Proteins 0.000 claims description 2
- 101710192266 Tegument protein VP22 Proteins 0.000 claims description 2
- 102000006601 Thymidine Kinase Human genes 0.000 claims description 2
- 108020004440 Thymidine kinase Proteins 0.000 claims description 2
- 108010031318 Vitronectin Proteins 0.000 claims description 2
- 102100035140 Vitronectin Human genes 0.000 claims description 2
- 239000002253 acid Substances 0.000 claims description 2
- 108010072041 arginyl-glycyl-aspartic acid Proteins 0.000 claims description 2
- JCXGWMGPZLAOME-RNFDNDRNSA-N bismuth-213 Chemical group [213Bi] JCXGWMGPZLAOME-RNFDNDRNSA-N 0.000 claims description 2
- 229940079593 drug Drugs 0.000 claims description 2
- 239000003814 drug Substances 0.000 claims description 2
- 239000002532 enzyme inhibitor Substances 0.000 claims description 2
- 229940125532 enzyme inhibitor Drugs 0.000 claims description 2
- 229960002897 heparin Drugs 0.000 claims description 2
- 229920000669 heparin Polymers 0.000 claims description 2
- 230000002401 inhibitory effect Effects 0.000 claims description 2
- 102000006495 integrins Human genes 0.000 claims description 2
- 108010044426 integrins Proteins 0.000 claims description 2
- 208000032839 leukemia Diseases 0.000 claims description 2
- 150000002632 lipids Chemical group 0.000 claims description 2
- 230000036210 malignancy Effects 0.000 claims description 2
- 230000003211 malignant effect Effects 0.000 claims description 2
- 230000001394 metastastic effect Effects 0.000 claims description 2
- 206010061289 metastatic neoplasm Diseases 0.000 claims description 2
- 239000002245 particle Substances 0.000 claims description 2
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 2
- 229960005190 phenylalanine Drugs 0.000 claims description 2
- 229920000729 poly(L-lysine) polymer Polymers 0.000 claims description 2
- 108010011110 polyarginine Proteins 0.000 claims description 2
- 229940002612 prodrug Drugs 0.000 claims description 2
- 239000000651 prodrug Substances 0.000 claims description 2
- 230000035755 proliferation Effects 0.000 claims description 2
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 claims description 2
- 230000005945 translocation Effects 0.000 claims description 2
- 210000004881 tumor cell Anatomy 0.000 claims description 2
- 230000003612 virological effect Effects 0.000 claims 1
- 238000000034 method Methods 0.000 description 15
- 241000700605 Viruses Species 0.000 description 1
- 239000002771 cell marker Substances 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US4671208P | 2008-04-21 | 2008-04-21 | |
| US61/046,712 | 2008-04-21 | ||
| PCT/US2009/041276 WO2009132020A2 (en) | 2008-04-21 | 2009-04-21 | Selective high-affinity polydentate ligands and methods of making such |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2014043517A Division JP2014122234A (ja) | 2008-04-21 | 2014-03-06 | 選択的高親和性リガンドおよびこれらを作製する方法 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2011518194A JP2011518194A (ja) | 2011-06-23 |
| JP2011518194A5 true JP2011518194A5 (https=) | 2013-05-02 |
| JP5623384B2 JP5623384B2 (ja) | 2014-11-12 |
Family
ID=41217391
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2011505263A Expired - Fee Related JP5623384B2 (ja) | 2008-04-21 | 2009-04-21 | 選択的高親和性リガンドおよびこれらを作製する方法 |
| JP2014043517A Withdrawn JP2014122234A (ja) | 2008-04-21 | 2014-03-06 | 選択的高親和性リガンドおよびこれらを作製する方法 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2014043517A Withdrawn JP2014122234A (ja) | 2008-04-21 | 2014-03-06 | 選択的高親和性リガンドおよびこれらを作製する方法 |
Country Status (8)
| Country | Link |
|---|---|
| US (5) | US9884070B2 (https=) |
| EP (1) | EP2268654B1 (https=) |
| JP (2) | JP5623384B2 (https=) |
| CN (1) | CN102083850B (https=) |
| AU (1) | AU2009239491B2 (https=) |
| CA (1) | CA2721980C (https=) |
| ES (1) | ES2613844T3 (https=) |
| WO (1) | WO2009132020A2 (https=) |
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| WO2011057078A2 (en) | 2009-11-05 | 2011-05-12 | University Of Virginia Patent Foundation | Compositions and methods for detecting plectin-1 as a biomarker for cancer |
| BR112014015197A8 (pt) * | 2011-12-21 | 2017-06-13 | Novira Therapeutics Inc | agentes antivirais de hepatite b |
| JP6103832B2 (ja) * | 2012-06-25 | 2017-03-29 | Hoya株式会社 | Ｅｇｆｒ結合性ペプチド |
| EP3019559A4 (en) | 2013-08-22 | 2017-04-05 | Sony Corporation | Water soluble fluorescent or colored dyes and methods for their use |
| JP2017525678A (ja) * | 2014-07-14 | 2017-09-07 | ピーイージー バイオサイエンシーズ インコーポレイテッド | 重合エンケファリンプロドラッグ |
| CN105985524A (zh) * | 2015-02-10 | 2016-10-05 | 北京师范大学 | 针对特定靶标具备指纹识别特征的多肽复合物分子的构建方法 |
| KR102646956B1 (ko) | 2015-02-26 | 2024-03-14 | 소니그룹주식회사 | 페닐에티닐나프탈렌 염료 및 이의 사용 방법 |
| US11827661B2 (en) | 2015-02-26 | 2023-11-28 | Sony Group Corporation | Water soluble fluorescent or colored dyes comprising conjugating groups |
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| CN105678112B (zh) * | 2016-02-03 | 2018-08-03 | 中国农业科学院北京畜牧兽医研究所 | 一种计算机辅助筛选小分子化合物靶标适配体的实现方法 |
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| WO2017177065A2 (en) | 2016-04-06 | 2017-10-12 | Sony Corporation | Ultra bright dimeric or polymeric dyes with spacing linker groups |
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| EP3464477A1 (en) | 2016-06-06 | 2019-04-10 | Sony Corporation | Ionic polymers comprising fluorescent or colored reporter groups |
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| US11524988B2 (en) | 2016-09-19 | 2022-12-13 | H. Lee Moffitt Cancer Center And Research Institute, Inc. | Artificial antigen presenting cells for genetic engineering of immune cells |
| WO2018098384A1 (en) * | 2016-11-22 | 2018-05-31 | Regents Of The University Of California | Segregation modulation for immunotherapy |
| WO2018152434A1 (en) * | 2017-02-17 | 2018-08-23 | The Regents Of The University Of California | Systems and methods for making assignments in isotope-labelled proteins using nuclear magnetic resonance data |
| WO2018156735A1 (en) * | 2017-02-22 | 2018-08-30 | H. Lee Moffitt Cancer Center And Research Institute, Inc. | Bispecific antibody for cancer immunotherapy |
| WO2019071153A1 (en) * | 2017-10-05 | 2019-04-11 | Sony Corporation | PROGRAMMABLE DENDRITIC MEDICINES |
| KR20260011205A (ko) | 2017-10-05 | 2026-01-22 | 소니그룹주식회사 | 프로그램가능한 중합체성 약물 |
| WO2019089765A1 (en) * | 2017-11-01 | 2019-05-09 | Arrowhead Pharmcaceuticals, Inc. | Integrin ligands and uses thereof |
| CN111836645A (zh) | 2017-11-16 | 2020-10-27 | 索尼公司 | 可编程的聚合药物 |
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2009
- 2009-04-21 CN CN200980122906.8A patent/CN102083850B/zh not_active Expired - Fee Related
- 2009-04-21 EP EP09734156.4A patent/EP2268654B1/en not_active Not-in-force
- 2009-04-21 US US12/988,801 patent/US9884070B2/en not_active Expired - Fee Related
- 2009-04-21 JP JP2011505263A patent/JP5623384B2/ja not_active Expired - Fee Related
- 2009-04-21 ES ES09734156.4T patent/ES2613844T3/es active Active
- 2009-04-21 WO PCT/US2009/041276 patent/WO2009132020A2/en not_active Ceased
- 2009-04-21 CA CA2721980A patent/CA2721980C/en active Active
- 2009-04-21 AU AU2009239491A patent/AU2009239491B2/en not_active Ceased
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2014
- 2014-03-06 JP JP2014043517A patent/JP2014122234A/ja not_active Withdrawn
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2017
- 2017-09-13 US US15/703,848 patent/US10646502B2/en not_active Expired - Fee Related
- 2017-09-13 US US15/703,809 patent/US10292992B2/en not_active Expired - Fee Related
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