JPWO2019217591A5 - - Google Patents
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- JPWO2019217591A5 JPWO2019217591A5 JP2020562649A JP2020562649A JPWO2019217591A5 JP WO2019217591 A5 JPWO2019217591 A5 JP WO2019217591A5 JP 2020562649 A JP2020562649 A JP 2020562649A JP 2020562649 A JP2020562649 A JP 2020562649A JP WO2019217591 A5 JPWO2019217591 A5 JP WO2019217591A5
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- Prior art keywords
- antibody
- alkyl
- amino acid
- seq
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- 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.)
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- 239000000126 substance Substances 0.000 description 66
- 125000000217 alkyl group Chemical group 0.000 description 52
- 230000027455 binding Effects 0.000 description 46
- 108090001123 antibodies Proteins 0.000 description 41
- 102000004965 antibodies Human genes 0.000 description 41
- 239000000611 antibody drug conjugate Substances 0.000 description 41
- 108091008116 antibody drug conjugates Proteins 0.000 description 41
- 239000000427 antigen Substances 0.000 description 36
- 108091007172 antigens Proteins 0.000 description 36
- 102000038129 antigens Human genes 0.000 description 36
- 125000005647 linker group Chemical group 0.000 description 28
- 125000000592 heterocycloalkyl group Chemical group 0.000 description 18
- 239000000562 conjugate Substances 0.000 description 14
- 102100004660 MSR1 Human genes 0.000 description 13
- 101700001066 MSR1 Proteins 0.000 description 13
- 229910052739 hydrogen Inorganic materials 0.000 description 13
- 239000001257 hydrogen Substances 0.000 description 13
- 229910052757 nitrogen Inorganic materials 0.000 description 13
- 125000003275 alpha amino acid group Chemical group 0.000 description 12
- 150000001875 compounds Chemical group 0.000 description 11
- 150000003839 salts Chemical class 0.000 description 10
- 239000011780 sodium chloride Substances 0.000 description 10
- 239000012453 solvate Substances 0.000 description 10
- 239000000203 mixture Substances 0.000 description 9
- HJYYPODYNSCCOU-ODRIEIDWSA-N MDL-62769 Chemical group OC1=C(C(O)=C2C)C3=C(O)C=C1NC(=O)\C(C)=C/C=C/[C@H](C)[C@H](O)[C@@H](C)[C@@H](O)[C@@H](C)[C@H](OC(C)=O)[C@H](C)[C@@H](OC)\C=C\O[C@@]1(C)OC2=C3C1=O HJYYPODYNSCCOU-ODRIEIDWSA-N 0.000 description 8
- 125000003118 aryl group Chemical group 0.000 description 7
- 201000010099 disease Diseases 0.000 description 7
- UFHFLCQGNIYNRP-UHFFFAOYSA-N hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 7
- 230000000051 modifying Effects 0.000 description 7
- 239000008194 pharmaceutical composition Substances 0.000 description 7
- 125000003710 aryl alkyl group Chemical group 0.000 description 6
- 125000004429 atoms Chemical group 0.000 description 6
- 125000005843 halogen group Chemical group 0.000 description 6
- 150000002431 hydrogen Chemical class 0.000 description 6
- 229910052760 oxygen Inorganic materials 0.000 description 6
- 150000003431 steroids Chemical group 0.000 description 6
- 108010047041 Complementarity Determining Regions Proteins 0.000 description 5
- 125000000539 amino acid group Chemical group 0.000 description 5
- 201000009910 diseases by infectious agent Diseases 0.000 description 5
- 125000005842 heteroatoms Chemical group 0.000 description 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 5
- 229910052717 sulfur Inorganic materials 0.000 description 5
- 241000191967 Staphylococcus aureus Species 0.000 description 4
- 229940076185 Staphylococcus aureus Drugs 0.000 description 4
- 125000003545 alkoxy group Chemical group 0.000 description 4
- 229910052799 carbon Inorganic materials 0.000 description 4
- 239000003814 drug Substances 0.000 description 4
- 108010016626 Dipeptides Proteins 0.000 description 3
- 125000002947 alkylene group Chemical group 0.000 description 3
- 235000001014 amino acid Nutrition 0.000 description 3
- 239000008103 glucose Substances 0.000 description 3
- 230000002401 inhibitory effect Effects 0.000 description 3
- 150000002829 nitrogen Chemical group 0.000 description 3
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 3
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 description 2
- 206010060945 Bacterial infection Diseases 0.000 description 2
- 102000003676 Glucocorticoid Receptors Human genes 0.000 description 2
- 108090000079 Glucocorticoid Receptors Proteins 0.000 description 2
- 206010061218 Inflammation Diseases 0.000 description 2
- KZSNJWFQEVHDMF-BYPYZUCNSA-N L-valine Chemical compound CC(C)[C@H](N)C(O)=O KZSNJWFQEVHDMF-BYPYZUCNSA-N 0.000 description 2
- 125000006620 amino-(C1-C6) alkyl group Chemical group 0.000 description 2
- 125000000732 arylene group Chemical group 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 238000004166 bioassay Methods 0.000 description 2
- -1 but not limited to Chemical group 0.000 description 2
- 210000004027 cells Anatomy 0.000 description 2
- 239000003937 drug carrier Substances 0.000 description 2
- DHMQDGOQFOQNFH-UHFFFAOYSA-N glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 2
- 125000004474 heteroalkylene group Chemical group 0.000 description 2
- 125000005549 heteroarylene group Chemical group 0.000 description 2
- 200000000018 inflammatory disease Diseases 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000006011 modification reaction Methods 0.000 description 2
- 125000004043 oxo group Chemical group O=* 0.000 description 2
- 239000001301 oxygen Chemical group 0.000 description 2
- MYMOFIZGZYHOMD-UHFFFAOYSA-N oxygen Chemical group O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 230000011664 signaling Effects 0.000 description 2
- 125000000547 substituted alkyl group Chemical group 0.000 description 2
- 238000006467 substitution reaction Methods 0.000 description 2
- 238000002198 surface plasmon resonance spectroscopy Methods 0.000 description 2
- 201000010874 syndrome Diseases 0.000 description 2
- 239000004474 valine Substances 0.000 description 2
- 235000014393 valine Nutrition 0.000 description 2
- 125000000143 2-carboxyethyl group Chemical group [H]OC(=O)C([H])([H])C([H])([H])* 0.000 description 1
- 125000000981 3-amino-3-oxopropyl group Chemical group [H]C([*])([H])C([H])([H])C(=O)N([H])[H] 0.000 description 1
- 125000004042 4-aminobutyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])N([H])[H] 0.000 description 1
- 206010003210 Arteriosclerosis Diseases 0.000 description 1
- 206010003246 Arthritis Diseases 0.000 description 1
- 206010053555 Arthritis bacterial Diseases 0.000 description 1
- 241000894006 Bacteria Species 0.000 description 1
- MTCFGRXMJLQNBG-UWTATZPHSA-N D-serine Chemical compound OC[C@@H](N)C(O)=O MTCFGRXMJLQNBG-UWTATZPHSA-N 0.000 description 1
- 206010064687 Device related infection Diseases 0.000 description 1
- 206010058108 Dyslipidaemia Diseases 0.000 description 1
- 238000002965 ELISA Methods 0.000 description 1
- 206010014665 Endocarditis Diseases 0.000 description 1
- 208000001860 Eye Infections Diseases 0.000 description 1
- 206010015988 Eyelid infection Diseases 0.000 description 1
- 241000192125 Firmicutes Species 0.000 description 1
- 206010016952 Food poisoning Diseases 0.000 description 1
- 239000004471 Glycine Substances 0.000 description 1
- QNAYBMKLOCPYGJ-REOHCLBHSA-N L-alanine Chemical compound C[C@H](N)C(O)=O QNAYBMKLOCPYGJ-REOHCLBHSA-N 0.000 description 1
- RHGKLRLOHDJJDR-BYPYZUCNSA-N L-citrulline zwitterion Chemical group NC(=O)NCCC[C@H]([NH3+])C([O-])=O RHGKLRLOHDJJDR-BYPYZUCNSA-N 0.000 description 1
- 206010061227 Lipid metabolism disease Diseases 0.000 description 1
- 210000002540 Macrophages Anatomy 0.000 description 1
- 210000002264 Mammary Glands, Animal Anatomy 0.000 description 1
- 210000004293 Mammary Glands, Human Anatomy 0.000 description 1
- 208000008466 Metabolic Disease Diseases 0.000 description 1
- RJQXTJLFIWVMTO-TYNCELHUSA-N Methicillin Chemical compound COC1=CC=CC(OC)=C1C(=O)N[C@@H]1C(=O)N2[C@@H](C(O)=O)C(C)(C)S[C@@H]21 RJQXTJLFIWVMTO-TYNCELHUSA-N 0.000 description 1
- 229940010383 Mycobacterium tuberculosis Drugs 0.000 description 1
- 241000187479 Mycobacterium tuberculosis Species 0.000 description 1
- 208000003926 Myelitis Diseases 0.000 description 1
- 206010030861 Ophthalmia neonatorum Diseases 0.000 description 1
- 206010035664 Pneumonia Diseases 0.000 description 1
- 102000014452 Scavenger Receptors Human genes 0.000 description 1
- 108010078070 Scavenger Receptors Proteins 0.000 description 1
- 206010040047 Sepsis Diseases 0.000 description 1
- 210000003491 Skin Anatomy 0.000 description 1
- 206010040893 Skin necrosis Diseases 0.000 description 1
- 231100000765 Toxin Toxicity 0.000 description 1
- 210000002700 Urine Anatomy 0.000 description 1
- MYPYJXKWCTUITO-LYRMYLQWSA-N VANCOMYCIN Chemical compound O([C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1OC1=C2C=C3C=C1OC1=CC=C(C=C1Cl)[C@@H](O)[C@H](C(N[C@@H](CC(N)=O)C(=O)N[C@H]3C(=O)N[C@H]1C(=O)N[C@H](C(N[C@@H](C3=CC(O)=CC(O)=C3C=3C(O)=CC=C1C=3)C(O)=O)=O)[C@H](O)C1=CC=C(C(=C1)Cl)O2)=O)NC(=O)[C@@H](CC(C)C)NC)[C@H]1C[C@](C)(N)[C@H](O)[C@H](C)O1 MYPYJXKWCTUITO-LYRMYLQWSA-N 0.000 description 1
- 229960003165 Vancomycin Drugs 0.000 description 1
- 108010059993 Vancomycin Proteins 0.000 description 1
- 235000004279 alanine Nutrition 0.000 description 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 201000001320 atherosclerosis Diseases 0.000 description 1
- 238000006065 biodegradation reaction Methods 0.000 description 1
- 230000000903 blocking Effects 0.000 description 1
- 125000002057 carboxymethyl group Chemical group [H]OC(=O)C([H])([H])[*] 0.000 description 1
- 230000002860 competitive Effects 0.000 description 1
- 201000010870 diseases of metabolism Diseases 0.000 description 1
- 229940079593 drugs Drugs 0.000 description 1
- 230000001747 exhibiting Effects 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- 125000001072 heteroaryl group Chemical group 0.000 description 1
- 125000004435 hydrogen atoms Chemical group [H]* 0.000 description 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 1
- 239000007943 implant Substances 0.000 description 1
- 230000002757 inflammatory Effects 0.000 description 1
- 230000004054 inflammatory process Effects 0.000 description 1
- 230000003834 intracellular Effects 0.000 description 1
- 239000003446 ligand Substances 0.000 description 1
- 201000009906 meningitis Diseases 0.000 description 1
- 230000002503 metabolic Effects 0.000 description 1
- 229960003085 meticillin Drugs 0.000 description 1
- 230000035772 mutation Effects 0.000 description 1
- 230000000626 neurodegenerative Effects 0.000 description 1
- 230000002062 proliferating Effects 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 231100000486 side effect Toxicity 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 125000003107 substituted aryl group Chemical group 0.000 description 1
- 239000003053 toxin Substances 0.000 description 1
Applications Claiming Priority (11)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201862669276P | 2018-05-09 | 2018-05-09 | |
US62/669,276 | 2018-05-09 | ||
US201862678200P | 2018-05-30 | 2018-05-30 | |
US62/678,200 | 2018-05-30 | ||
US201862769946P | 2018-11-20 | 2018-11-20 | |
US62/769,946 | 2018-11-20 | ||
US201962789987P | 2019-01-08 | 2019-01-08 | |
US62/789,987 | 2019-01-08 | ||
US201962821362P | 2019-03-20 | 2019-03-20 | |
US62/821,362 | 2019-03-20 | ||
PCT/US2019/031383 WO2019217591A1 (en) | 2018-05-09 | 2019-05-08 | Anti-msr1 antibodies and methods of use thereof |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2021523147A JP2021523147A (ja) | 2021-09-02 |
JPWO2019217591A5 true JPWO2019217591A5 (es) | 2022-06-02 |
Family
ID=66625372
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2020562649A Pending JP2021523147A (ja) | 2018-05-09 | 2019-05-08 | 抗msr1抗体及びその使用方法 |
Country Status (14)
Country | Link |
---|---|
US (2) | US11377502B2 (es) |
EP (1) | EP3790899A1 (es) |
JP (1) | JP2021523147A (es) |
KR (1) | KR20210008008A (es) |
CN (1) | CN112533951A (es) |
AU (1) | AU2019265703A1 (es) |
BR (1) | BR112020022400A2 (es) |
CA (1) | CA3098453A1 (es) |
CL (1) | CL2020002873A1 (es) |
CO (1) | CO2020015084A2 (es) |
MX (1) | MX2020011546A (es) |
PH (1) | PH12020551865A1 (es) |
SG (1) | SG11202010909RA (es) |
WO (1) | WO2019217591A1 (es) |
Families Citing this family (18)
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AU2017359043B2 (en) | 2016-11-08 | 2022-06-16 | Regeneron Pharmaceuticals, Inc. | Steroids and protein-conjugates thereof |
AU2018270784B2 (en) | 2017-05-18 | 2024-05-16 | Regeneron Pharmaceuticals, Inc. | Cyclodextrin protein drug conjugates |
WO2018213082A1 (en) * | 2017-05-18 | 2018-11-22 | Regeneron Pharmaceuticals, Inc. | Bis-octahydrophenanthrene carboxamides and protein conjugates thereof |
AU2019205542A1 (en) * | 2018-01-08 | 2020-07-16 | Regeneron Pharmaceuticals, Inc. | Steroids and antibody-conjugates thereof |
KR20210094568A (ko) | 2018-11-20 | 2021-07-29 | 리제너론 파마슈티칼스 인코포레이티드 | Lxr 작용물질로서 사용하기 위한 비스-옥타하이드로펜안트렌 카복스아미드 유도체 및 그의 단백질 접합체 |
US11666658B2 (en) * | 2018-12-21 | 2023-06-06 | Regeneran Pharmaceuticals, Inc. | Rifamycin analogs and antibody-drug conjugates thereof |
CN113905767A (zh) | 2019-01-08 | 2022-01-07 | 里珍纳龙药品有限公司 | 无痕连接体及其蛋白质偶联物 |
US20230220065A1 (en) * | 2020-06-16 | 2023-07-13 | Academia Sinica | Antibodies to interleukin-1beta and uses thereof |
IL299153A (en) * | 2020-07-13 | 2023-02-01 | Regeneron Pharma | Camptothecin analogs conjugated to a glutamine residue in protein, and their uses |
CN114605367B (zh) * | 2020-12-03 | 2023-06-27 | 中国人民解放军军事科学院军事医学研究院 | 含香豆素的连接子及含该连接子的抗体偶联药物 |
EP4308170A1 (en) | 2021-03-18 | 2024-01-24 | Seagen Inc. | Selective drug release from internalized conjugates of biologically active compounds |
CN117098540A (zh) * | 2021-03-26 | 2023-11-21 | 瑞泽恩制药公司 | 与万古霉素联合的利福霉素类似物及其用途 |
US11806405B1 (en) | 2021-07-19 | 2023-11-07 | Zeno Management, Inc. | Immunoconjugates and methods |
CN115671308A (zh) * | 2021-07-30 | 2023-02-03 | 北京键凯科技股份有限公司 | 一种靶向性的抗体-聚乙二醇-siRNA药物偶联物 |
CN115594766A (zh) * | 2021-12-30 | 2023-01-13 | 辽宁键凯科技有限公司(Cn) | 一种缀合物及用其制备的抗体偶联药物 |
CA3241734A1 (en) * | 2022-01-12 | 2023-07-20 | Amy Han | Camptothecin analogs conjugated to a glutamine residue in a protein, and their use |
US20240067640A1 (en) | 2022-03-11 | 2024-02-29 | Firefly Bio, Inc. | Phenyl maleimide linker agents |
WO2024059237A2 (en) * | 2022-09-15 | 2024-03-21 | Adcentrx Therapeutics Inc. | Novel glucocorticoid receptor agonists and immunoconjugates thereof |
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