JP2021530507A - 神経細胞に抗がん剤を送達するためのコンジュゲート、その使用方法及び製造方法 - Google Patents
神経細胞に抗がん剤を送達するためのコンジュゲート、その使用方法及び製造方法 Download PDFInfo
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- JP2021530507A JP2021530507A JP2021501277A JP2021501277A JP2021530507A JP 2021530507 A JP2021530507 A JP 2021530507A JP 2021501277 A JP2021501277 A JP 2021501277A JP 2021501277 A JP2021501277 A JP 2021501277A JP 2021530507 A JP2021530507 A JP 2021530507A
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- 0 C(C1)C2*C1*C2 Chemical compound C(C1)C2*C1*C2 0.000 description 9
- ZXGGCBQORXDVTE-UMCMBGNQSA-N Nc1c2nc(NCc(cc3)cc(Cl)c3Cl)[n]([C@@H]([C@@H]3O)O[C@H](COCc(cc4)ccc4C#N)[C@H]3O)c2ncn1 Chemical compound Nc1c2nc(NCc(cc3)cc(Cl)c3Cl)[n]([C@@H]([C@@H]3O)O[C@H](COCc(cc4)ccc4C#N)[C@H]3O)c2ncn1 ZXGGCBQORXDVTE-UMCMBGNQSA-N 0.000 description 2
- CWJJHESJXJQCJA-UHFFFAOYSA-N C(c1ccc(CN2CCNCCCNCCNCCC2)cc1)NCc1ncccc1 Chemical compound C(c1ccc(CN2CCNCCCNCCNCCC2)cc1)NCc1ncccc1 CWJJHESJXJQCJA-UHFFFAOYSA-N 0.000 description 1
- RVAQIUULWULRNW-UHFFFAOYSA-N CC(C)c(cc(C(N1c(cc2)cc3c2[n](C)cc3)=NNC1=O)c(O)c1)c1O Chemical compound CC(C)c(cc(C(N1c(cc2)cc3c2[n](C)cc3)=NNC1=O)c(O)c1)c1O RVAQIUULWULRNW-UHFFFAOYSA-N 0.000 description 1
- JEDPSOYOYVELLZ-UHFFFAOYSA-N CC(NCCNCc(ccc(OCc1c(C)c(-c2ccccc2)ccc1)n1)c1OC)=O Chemical compound CC(NCCNCc(ccc(OCc1c(C)c(-c2ccccc2)ccc1)n1)c1OC)=O JEDPSOYOYVELLZ-UHFFFAOYSA-N 0.000 description 1
- MEIAIUMBXGGUHK-OZOFXUPYSA-N CCCNC(C(C=C1CC(/C(/C)=C/C=C\[C@@H]([C@H](/C(/C)=C/[C@H](C)[C@@H](C)[C@H](C[C@H](C)C2)OC)OC(N)=C)OC)O)=O)=C2C1=O Chemical compound CCCNC(C(C=C1CC(/C(/C)=C/C=C\[C@@H]([C@H](/C(/C)=C/[C@H](C)[C@@H](C)[C@H](C[C@H](C)C2)OC)OC(N)=C)OC)O)=O)=C2C1=O MEIAIUMBXGGUHK-OZOFXUPYSA-N 0.000 description 1
- LNAHXUFSBJYSSF-APJHNWBZSA-N CCCNC(C(C=C1CC(/C(/C)=C/C=C\[C@@H]([C@H](/C(/C)=C/[C@H](C)[C@@H](C2OC2)[C@H](C[C@H](C)C2)OC)OC(N)=O)OC)=O)=O)=C2C1=O Chemical compound CCCNC(C(C=C1CC(/C(/C)=C/C=C\[C@@H]([C@H](/C(/C)=C/[C@H](C)[C@@H](C2OC2)[C@H](C[C@H](C)C2)OC)OC(N)=O)OC)=O)=O)=C2C1=O LNAHXUFSBJYSSF-APJHNWBZSA-N 0.000 description 1
- WJUNQSYQHHIVFX-UHFFFAOYSA-N CCNC(c1cc2c(-c(cc(c(Cl)c3)OCCN4CCCC4)c3Cl)nc(N)nc2[s]1)=O Chemical compound CCNC(c1cc2c(-c(cc(c(Cl)c3)OCCN4CCCC4)c3Cl)nc(N)nc2[s]1)=O WJUNQSYQHHIVFX-UHFFFAOYSA-N 0.000 description 1
- YLQODGGPIHWTHR-UHFFFAOYSA-N CN(CC1)CCC1NC(c1n[o]c(-c(c(O)cc(O)c2)c2Oc(cc2)ccc2[N+]([O-])=O)c1)=O Chemical compound CN(CC1)CCC1NC(c1n[o]c(-c(c(O)cc(O)c2)c2Oc(cc2)ccc2[N+]([O-])=O)c1)=O YLQODGGPIHWTHR-UHFFFAOYSA-N 0.000 description 1
- QULDDKSCVCJTPV-UHFFFAOYSA-N Cc(cnc(C[n]1c2nc(N)nc(Cl)c2nc1)c1C)c1OC Chemical compound Cc(cnc(C[n]1c2nc(N)nc(Cl)c2nc1)c1C)c1OC QULDDKSCVCJTPV-UHFFFAOYSA-N 0.000 description 1
- ZMSVFJWGYKIQDD-UHFFFAOYSA-N Cc1c(COc2cc(OC)c(CN(CCCC3)C3(CNC)C=O)c(OC)c2)cccc1-c1ccccc1 Chemical compound Cc1c(COc2cc(OC)c(CN(CCCC3)C3(CNC)C=O)c(OC)c2)cccc1-c1ccccc1 ZMSVFJWGYKIQDD-UHFFFAOYSA-N 0.000 description 1
- WAIDUHWTEYSBGW-SANMLTNESA-N Cc1c(COc2cc(OC)c(CN(CCCC3)[C@@H]3C(N)=O)c(OC)c2)cccc1-c1ccccc1 Chemical compound Cc1c(COc2cc(OC)c(CN(CCCC3)[C@@H]3C(N)=O)c(OC)c2)cccc1-c1ccccc1 WAIDUHWTEYSBGW-SANMLTNESA-N 0.000 description 1
- VIGHQZSTZWNWFA-UHFFFAOYSA-N NC(CCCSc1nc(-c2c(cccc3COC4)c3c4cc2Cl)nc(N)n1)=O Chemical compound NC(CCCSc1nc(-c2c(cccc3COC4)c3c4cc2Cl)nc(N)n1)=O VIGHQZSTZWNWFA-UHFFFAOYSA-N 0.000 description 1
Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
- A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
- A61K47/62—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being a protein, peptide or polyamino acid
- A61K47/64—Drug-peptide, drug-protein or drug-polyamino acid conjugates, i.e. the modifying agent being a peptide, protein or polyamino acid which is covalently bonded or complexed to a therapeutically active agent
- A61K47/642—Drug-peptide, drug-protein or drug-polyamino acid conjugates, i.e. the modifying agent being a peptide, protein or polyamino acid which is covalently bonded or complexed to a therapeutically active agent the peptide or protein in the drug conjugate being a cytokine, e.g. IL2, chemokine, growth factors or interferons being the inactive part of the conjugate
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D211/60—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D225/00—Heterocyclic compounds containing rings of more than seven members having one nitrogen atom as the only ring hetero atom
- C07D225/04—Heterocyclic compounds containing rings of more than seven members having one nitrogen atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/06—Benzimidazoles; Hydrogenated benzimidazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
- C07D235/08—Radicals containing only hydrogen and carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D265/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom and one oxygen atom as the only ring hetero atoms
- C07D265/28—1,4-Oxazines; Hydrogenated 1,4-oxazines
- C07D265/30—1,4-Oxazines; Hydrogenated 1,4-oxazines not condensed with other rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/12—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains three hetero rings
- C07D498/18—Bridged systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/475—Growth factors; Growth regulators
- C07K14/48—Nerve growth factor [NGF]
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/705—Receptors; Cell surface antigens; Cell surface determinants
- C07K14/70575—NGF/TNF-superfamily, e.g. CD70, CD95L, CD153, CD154
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Molecular Biology (AREA)
- Animal Behavior & Ethology (AREA)
- Biochemistry (AREA)
- Biophysics (AREA)
- Zoology (AREA)
- Genetics & Genomics (AREA)
- Toxicology (AREA)
- Gastroenterology & Hepatology (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Epidemiology (AREA)
- Cell Biology (AREA)
- Immunology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicinal Preparation (AREA)
- Peptides Or Proteins (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201862700131P | 2018-07-18 | 2018-07-18 | |
| US62/700,131 | 2018-07-18 | ||
| PCT/US2019/042253 WO2020018700A1 (en) | 2018-07-18 | 2019-07-17 | Conjugates for delivering an anti-cancer agent to nerve cells, methods of use and methods of making thereof |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2021530507A true JP2021530507A (ja) | 2021-11-11 |
| JPWO2020018700A5 JPWO2020018700A5 (https=) | 2022-07-25 |
| JP2021530507A5 JP2021530507A5 (https=) | 2022-07-25 |
Family
ID=69165153
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2021501277A Pending JP2021530507A (ja) | 2018-07-18 | 2019-07-17 | 神経細胞に抗がん剤を送達するためのコンジュゲート、その使用方法及び製造方法 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US11897928B2 (https=) |
| EP (1) | EP3823674A4 (https=) |
| JP (1) | JP2021530507A (https=) |
| CA (1) | CA3105879A1 (https=) |
| MX (1) | MX2021000644A (https=) |
| WO (1) | WO2020018700A1 (https=) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA3200359A1 (en) * | 2020-11-30 | 2022-06-02 | Constance A. Mckee | Methods for using neurotrophin receptor binding conjugate compositions in the treatment of a neurological condition |
| WO2025218761A1 (zh) * | 2024-04-17 | 2025-10-23 | 晶核生物医药科技(上海)有限公司 | 环状肽类化合物、其药物组合物及其应用 |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2002532560A (ja) * | 1998-12-21 | 2002-10-02 | ザヴォス | 治療成分を神経細胞に細胞内送達するための化合物 |
| JP2015501315A (ja) * | 2011-11-01 | 2015-01-15 | アステックス セラピューティックス リミテッド | 置換ベンジルアミン化合物および医療、特にc型肝炎ウイルス(hcv)感染症の治療におけるその使用 |
| WO2016155670A1 (zh) * | 2015-04-01 | 2016-10-06 | 苏州晶云药物科技有限公司 | 一种cdk抑制剂和mek抑制剂的共晶及其制备方法 |
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| MX2021000644A (es) | 2021-08-19 |
| US11897928B2 (en) | 2024-02-13 |
| WO2020018700A1 (en) | 2020-01-23 |
| CA3105879A1 (en) | 2020-01-23 |
| EP3823674A1 (en) | 2021-05-26 |
| EP3823674A4 (en) | 2022-12-28 |
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