JP6994767B2 - Cxcr4阻害剤およびその使用 - Google Patents
Cxcr4阻害剤およびその使用 Download PDFInfo
- Publication number
- JP6994767B2 JP6994767B2 JP2018566976A JP2018566976A JP6994767B2 JP 6994767 B2 JP6994767 B2 JP 6994767B2 JP 2018566976 A JP2018566976 A JP 2018566976A JP 2018566976 A JP2018566976 A JP 2018566976A JP 6994767 B2 JP6994767 B2 JP 6994767B2
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- Prior art keywords
- cancer
- tumor
- minutes
- compound
- compounds
- 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.)
- Expired - Fee Related
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- 0 C*1c2cccc(*3CC*(C)CC3)c2*=C1C*(CC[C@@]1N)[C@@]1C1=C(C)C=CC*1 Chemical compound C*1c2cccc(*3CC*(C)CC3)c2*=C1C*(CC[C@@]1N)[C@@]1C1=C(C)C=CC*1 0.000 description 35
- FTTATHOUSOIFOQ-UHFFFAOYSA-N C(C1)CN2C1CNCC2 Chemical compound C(C1)CN2C1CNCC2 FTTATHOUSOIFOQ-UHFFFAOYSA-N 0.000 description 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N C1NCCOC1 Chemical compound C1NCCOC1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
- ICFHDYFCVQPVHM-UHFFFAOYSA-N CN(CC1)CCN1c1cccc2nc(C=O)c[n]12 Chemical compound CN(CC1)CCN1c1cccc2nc(C=O)c[n]12 ICFHDYFCVQPVHM-UHFFFAOYSA-N 0.000 description 2
- QIQHWGGROIBWSH-UHFFFAOYSA-N Cc1c(C2NCCC2)nccc1 Chemical compound Cc1c(C2NCCC2)nccc1 QIQHWGGROIBWSH-UHFFFAOYSA-N 0.000 description 2
- MKPYXJBRSQWUJN-UHFFFAOYSA-N O=Cc1c[n]2c(Br)cccc2n1 Chemical compound O=Cc1c[n]2c(Br)cccc2n1 MKPYXJBRSQWUJN-UHFFFAOYSA-N 0.000 description 2
- UZURTQHPMXADGG-UHFFFAOYSA-N C(C1)CC2C1CC=CC2 Chemical compound C(C1)CC2C1CC=CC2 UZURTQHPMXADGG-UHFFFAOYSA-N 0.000 description 1
- WDIPXZLUVMBREE-UHFFFAOYSA-N C(C1)CN=C1c1c(cccc2)c2ccn1 Chemical compound C(C1)CN=C1c1c(cccc2)c2ccn1 WDIPXZLUVMBREE-UHFFFAOYSA-N 0.000 description 1
- LCWDOUVKPFFLAE-UHFFFAOYSA-N C(C1)CNC1c1c(cccc2)c2ccn1 Chemical compound C(C1)CNC1c1c(cccc2)c2ccn1 LCWDOUVKPFFLAE-UHFFFAOYSA-N 0.000 description 1
- CTDQAGUNKPRERK-UHFFFAOYSA-N C(CC1)CC11CCCCC1 Chemical compound C(CC1)CC11CCCCC1 CTDQAGUNKPRERK-UHFFFAOYSA-N 0.000 description 1
- NINJAJLCZUYDGV-UHFFFAOYSA-N C(CC1)CC11CNCC1 Chemical compound C(CC1)CC11CNCC1 NINJAJLCZUYDGV-UHFFFAOYSA-N 0.000 description 1
- GBCQLGDTLMHVHU-UHFFFAOYSA-N C(CC1)CC2C1CCCCC2 Chemical compound C(CC1)CC2C1CCCCC2 GBCQLGDTLMHVHU-UHFFFAOYSA-N 0.000 description 1
- YZHNMQSXBJPVKI-UHFFFAOYSA-N C(c(nc1[n]2cccc1)c2N(CC1)CCN1c1cnccc1)N(CCC1)C1c1ccccn1 Chemical compound C(c(nc1[n]2cccc1)c2N(CC1)CCN1c1cnccc1)N(CCC1)C1c1ccccn1 YZHNMQSXBJPVKI-UHFFFAOYSA-N 0.000 description 1
- MHKUMNZKLPFALZ-UHFFFAOYSA-N C1C2=CNC1CN2 Chemical compound C1C2=CNC1CN2 MHKUMNZKLPFALZ-UHFFFAOYSA-N 0.000 description 1
- WPHGSKGZRAQSGP-UHFFFAOYSA-N C1C2C1CCCC2 Chemical compound C1C2C1CCCC2 WPHGSKGZRAQSGP-UHFFFAOYSA-N 0.000 description 1
- DENNCEQUAZKJGC-UHFFFAOYSA-N C1C2NC1CCC2 Chemical compound C1C2NC1CCC2 DENNCEQUAZKJGC-UHFFFAOYSA-N 0.000 description 1
- NQRYJNQNLNOLGT-UHFFFAOYSA-N C1CCNCC1 Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 1
- DHXVGJBLRPWPCS-UHFFFAOYSA-N C1CCOCC1 Chemical compound C1CCOCC1 DHXVGJBLRPWPCS-UHFFFAOYSA-N 0.000 description 1
- GLUUGHFHXGJENI-UHFFFAOYSA-N C1NCCNC1 Chemical compound C1NCCNC1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 1
- RECARUFTCUAFPV-UHFFFAOYSA-N C1OCC11CCNCC1 Chemical compound C1OCC11CCNCC1 RECARUFTCUAFPV-UHFFFAOYSA-N 0.000 description 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N C=CN(CCC1)C1=O Chemical compound C=CN(CCC1)C1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
- RYTMGWKJWXKEQD-UHFFFAOYSA-N CC(C)(C)CC(C)(C)C1NCCOC1 Chemical compound CC(C)(C)CC(C)(C)C1NCCOC1 RYTMGWKJWXKEQD-UHFFFAOYSA-N 0.000 description 1
- AHDNCBFMVVKVJN-UHFFFAOYSA-N CC(C)(C1)CNCCC1(F)F Chemical compound CC(C)(C1)CNCCC1(F)F AHDNCBFMVVKVJN-UHFFFAOYSA-N 0.000 description 1
- WDAXTTCRUMJYDA-UHFFFAOYSA-N CC(C)CC1C2NCC1NC2 Chemical compound CC(C)CC1C2NCC1NC2 WDAXTTCRUMJYDA-UHFFFAOYSA-N 0.000 description 1
- CFEUAONHKPSKAG-UHFFFAOYSA-N CC(C)CC1NCC(C)NC1 Chemical compound CC(C)CC1NCC(C)NC1 CFEUAONHKPSKAG-UHFFFAOYSA-N 0.000 description 1
- BQQBIGFIVKSEIR-UHFFFAOYSA-N CC(C)c1c(C2N(Cc3c(COC(C)C)[n]4c(N5CCN(C)CC5)cccc4n3)CCC2)nccc1 Chemical compound CC(C)c1c(C2N(Cc3c(COC(C)C)[n]4c(N5CCN(C)CC5)cccc4n3)CCC2)nccc1 BQQBIGFIVKSEIR-UHFFFAOYSA-N 0.000 description 1
- FMCXQMOIZYWCED-UHFFFAOYSA-N CC(c1c[n]2c(N3CCN(C)CC3)cccc2n1)Cl Chemical compound CC(c1c[n]2c(N3CCN(C)CC3)cccc2n1)Cl FMCXQMOIZYWCED-UHFFFAOYSA-N 0.000 description 1
- XNGCUBPOCIXWRJ-UHFFFAOYSA-N CC(c1c[n]2c(N3CCN(C)CC3)cccc2n1)O Chemical compound CC(c1c[n]2c(N3CCN(C)CC3)cccc2n1)O XNGCUBPOCIXWRJ-UHFFFAOYSA-N 0.000 description 1
- PIPWSBOFSUJCCO-UHFFFAOYSA-N CC1(C)NCCNC1 Chemical compound CC1(C)NCCNC1 PIPWSBOFSUJCCO-UHFFFAOYSA-N 0.000 description 1
- UXTQZCHTAUSBMK-UHFFFAOYSA-N CC1NC(C)C(C)(C)CNC1 Chemical compound CC1NC(C)C(C)(C)CNC1 UXTQZCHTAUSBMK-UHFFFAOYSA-N 0.000 description 1
- AETQPNPBVHZWJM-UHFFFAOYSA-N CCOCC(c1c[n]2c(N3CCN(C)CC3)cccc2n1)N(CCC1)C1c1c(C)c(-c(ccc2nc(C(/C=[O]/C)N(CCC3)C3c3nccc(-c(ccc4nc(C(CO)N(CCC5)C5c5c(C)cccn5)c[n]44)c4N4CCN(C)CC4)c3C)c[n]22)c2N2CCN(C)CC2)ccn1 Chemical compound CCOCC(c1c[n]2c(N3CCN(C)CC3)cccc2n1)N(CCC1)C1c1c(C)c(-c(ccc2nc(C(/C=[O]/C)N(CCC3)C3c3nccc(-c(ccc4nc(C(CO)N(CCC5)C5c5c(C)cccn5)c[n]44)c4N4CCN(C)CC4)c3C)c[n]22)c2N2CCN(C)CC2)ccn1 AETQPNPBVHZWJM-UHFFFAOYSA-N 0.000 description 1
- VJODBUYMBZPJTL-UHFFFAOYSA-N CCOCc1c(CN(CCC2)C2c2c(C(C)C)c(-c(ccc3nc(CN(CCC4)C4c4c(C(C)C)cccn4)c(COC)[n]33)c3N(CC3)CCN3C(C)C)ccn2)nc2[n]1c(N1CCN(C)CC1)ccc2 Chemical compound CCOCc1c(CN(CCC2)C2c2c(C(C)C)c(-c(ccc3nc(CN(CCC4)C4c4c(C(C)C)cccn4)c(COC)[n]33)c3N(CC3)CCN3C(C)C)ccn2)nc2[n]1c(N1CCN(C)CC1)ccc2 VJODBUYMBZPJTL-UHFFFAOYSA-N 0.000 description 1
- TXHDPGWNYNBNFW-UHFFFAOYSA-N CN(CC1)CCN1c1cccc2c1[nH]c(C=O)n2 Chemical compound CN(CC1)CCN1c1cccc2c1[nH]c(C=O)n2 TXHDPGWNYNBNFW-UHFFFAOYSA-N 0.000 description 1
- XQQXZCVNDASAAK-UHFFFAOYSA-N CN(CC1)CCN1c1cccc2nc(CN(CCC3)C3c3c(cccc4)c4ccn3)c[n]12 Chemical compound CN(CC1)CCN1c1cccc2nc(CN(CCC3)C3c3c(cccc4)c4ccn3)c[n]12 XQQXZCVNDASAAK-UHFFFAOYSA-N 0.000 description 1
- YEYNSKKMCKMPCF-UHFFFAOYSA-N CN1CC=NCC1 Chemical compound CN1CC=NCC1 YEYNSKKMCKMPCF-UHFFFAOYSA-N 0.000 description 1
- WJHGJDGITRCZLH-UHFFFAOYSA-N COC(c1nccc2ccccc12)=O Chemical compound COC(c1nccc2ccccc12)=O WJHGJDGITRCZLH-UHFFFAOYSA-N 0.000 description 1
- HOGMGTXLFFPPOQ-UHFFFAOYSA-N Cc1c(C(CCC2)N2C(c2c[n]3c(N4C=CN(C)CC4)cccc3n2)=O)nccc1 Chemical compound Cc1c(C(CCC2)N2C(c2c[n]3c(N4C=CN(C)CC4)cccc3n2)=O)nccc1 HOGMGTXLFFPPOQ-UHFFFAOYSA-N 0.000 description 1
- NNDRYIWNMBEAAQ-UHFFFAOYSA-N Cc1c(C2N(Cc3nc(CC(N4CC5(CC5)N(C)CC4)=C(C=C4)c5ccnc(C6N(Cc7c[n]8c(N9CC%10(CC%10)N(C)CC9)cccc8n7)CCC6)c5C)c4[nH]3)CCC2)nccc1C(Cc1nc(CN(CCC2)C2c(nccc2)c2Cl)c[n]11)C=C1N1CCN(C)CC1 Chemical compound Cc1c(C2N(Cc3nc(CC(N4CC5(CC5)N(C)CC4)=C(C=C4)c5ccnc(C6N(Cc7c[n]8c(N9CC%10(CC%10)N(C)CC9)cccc8n7)CCC6)c5C)c4[nH]3)CCC2)nccc1C(Cc1nc(CN(CCC2)C2c(nccc2)c2Cl)c[n]11)C=C1N1CCN(C)CC1 NNDRYIWNMBEAAQ-UHFFFAOYSA-N 0.000 description 1
- UWASFIYLKQRAJO-UHFFFAOYSA-N Cc1c(C2N(Cc3nc(cccc4N5CCN(C)CC5)c4[nH]3)CCC2)nccc1 Chemical compound Cc1c(C2N(Cc3nc(cccc4N5CCN(C)CC5)c4[nH]3)CCC2)nccc1 UWASFIYLKQRAJO-UHFFFAOYSA-N 0.000 description 1
- OGWNBCUQGQQCBH-UHFFFAOYSA-N Cc1cccnc1C(CCC1)N1C1(CC1)c1c[n]2c(N3CCN(C)CC3)cc(-c3cccc(C4N(Cc(nc(cc5)[n]6cc5-c5nc(C7N(Cc(nc8[n]9cccc8)c9N(CC8)CCN8C8=CC=NCC8)CCC7)ccc5)c6N(CC5)CCN5c5ccccn5)CCC4)n3)cc2n1 Chemical compound Cc1cccnc1C(CCC1)N1C1(CC1)c1c[n]2c(N3CCN(C)CC3)cc(-c3cccc(C4N(Cc(nc(cc5)[n]6cc5-c5nc(C7N(Cc(nc8[n]9cccc8)c9N(CC8)CCN8C8=CC=NCC8)CCC7)ccc5)c6N(CC5)CCN5c5ccccn5)CCC4)n3)cc2n1 OGWNBCUQGQQCBH-UHFFFAOYSA-N 0.000 description 1
- ONRDOXZIWWKPHY-UHFFFAOYSA-N Clc1c(C2NCCC2)nccc1 Chemical compound Clc1c(C2NCCC2)nccc1 ONRDOXZIWWKPHY-UHFFFAOYSA-N 0.000 description 1
- YADOEPHJIBKBCN-UHFFFAOYSA-N Nc1cccc(Cl)c1[N+]([O-])=O Chemical compound Nc1cccc(Cl)c1[N+]([O-])=O YADOEPHJIBKBCN-UHFFFAOYSA-N 0.000 description 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N c1ccccc1 Chemical compound c1ccccc1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 1
- UTCSSFWDNNEEBH-UHFFFAOYSA-N c1cnc2[n]1cccc2 Chemical compound c1cnc2[n]1cccc2 UTCSSFWDNNEEBH-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D407/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
- C07D407/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2021145599A JP2021185195A (ja) | 2016-06-21 | 2021-09-07 | Cxcr4阻害剤およびその使用 |
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201662352825P | 2016-06-21 | 2016-06-21 | |
| US62/352,825 | 2016-06-21 | ||
| US201762456513P | 2017-02-08 | 2017-02-08 | |
| US62/456,513 | 2017-02-08 | ||
| PCT/US2017/038613 WO2017223243A1 (en) | 2016-06-21 | 2017-06-21 | Cxcr4 inhibitors and uses thereof |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2021145599A Division JP2021185195A (ja) | 2016-06-21 | 2021-09-07 | Cxcr4阻害剤およびその使用 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2019518768A JP2019518768A (ja) | 2019-07-04 |
| JP2019518768A5 JP2019518768A5 (https=) | 2020-06-11 |
| JP6994767B2 true JP6994767B2 (ja) | 2022-01-14 |
Family
ID=60783546
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2018566976A Expired - Fee Related JP6994767B2 (ja) | 2016-06-21 | 2017-06-21 | Cxcr4阻害剤およびその使用 |
| JP2021145599A Pending JP2021185195A (ja) | 2016-06-21 | 2021-09-07 | Cxcr4阻害剤およびその使用 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2021145599A Pending JP2021185195A (ja) | 2016-06-21 | 2021-09-07 | Cxcr4阻害剤およびその使用 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US11332470B2 (https=) |
| EP (1) | EP3472129A4 (https=) |
| JP (2) | JP6994767B2 (https=) |
| CN (1) | CN109641838A (https=) |
| CA (1) | CA3027500A1 (https=) |
| WO (1) | WO2017223243A1 (https=) |
Families Citing this family (29)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR102043337B1 (ko) | 2014-08-28 | 2019-11-11 | 아셰뉴론 에스아 | 글리코시다제 저해제 |
| CN109069426B (zh) | 2015-12-14 | 2021-10-29 | X4 制药有限公司 | 治疗癌症的方法 |
| WO2017106332A1 (en) | 2015-12-14 | 2017-06-22 | X4 Pharmaceuticals, Inc. | Methods for treating cancer |
| PL3393468T3 (pl) | 2015-12-22 | 2023-01-23 | X4 Pharmaceuticals, Inc. | Metody leczenia niedoboru odporności |
| US11261183B2 (en) | 2016-02-25 | 2022-03-01 | Asceneuron Sa | Sulfoximine glycosidase inhibitors |
| CA3014572C (en) | 2016-02-25 | 2023-10-03 | Asceneuron S.A. | Acid addition salts of piperazine derivatives |
| KR20180132629A (ko) | 2016-02-25 | 2018-12-12 | 아셰뉴론 에스아 | 글리코시다제 저해제 |
| US11337969B2 (en) | 2016-04-08 | 2022-05-24 | X4 Pharmaceuticals, Inc. | Methods for treating cancer |
| WO2017223243A1 (en) | 2016-06-21 | 2017-12-28 | X4 Pharmaceuticals, Inc. | Cxcr4 inhibitors and uses thereof |
| ES2870920T3 (es) | 2016-06-21 | 2021-10-28 | X4 Pharmaceuticals Inc | Inhibidores de CXCR4 y usos de los mismos |
| CN109640988A (zh) | 2016-06-21 | 2019-04-16 | X4 制药有限公司 | Cxcr4抑制剂及其用途 |
| GB201617630D0 (en) | 2016-10-18 | 2016-11-30 | Cellcentric Ltd | Pharmaceutical compounds |
| EP3585387A4 (en) | 2017-02-21 | 2020-08-12 | Emory University | CHEMIOKIN CXCR4 RECEIVER MODULATORS AND THEIR USES |
| JP6945199B2 (ja) * | 2017-05-19 | 2021-10-06 | 国立大学法人山口大学 | アキシチニブの薬物動態判定方法及びアキシチニブの薬物動態に基づくアキシチニブによる治療効果予測方法 |
| US11213525B2 (en) | 2017-08-24 | 2022-01-04 | Asceneuron Sa | Linear glycosidase inhibitors |
| JP7282786B2 (ja) * | 2017-09-25 | 2023-05-29 | シージーンテック (スーチョウ, チャイナ) カンパニー リミテッド | Cxcr4阻害剤としてのヘテロアリール化合物、それを用いた組成物及び方法 |
| KR102678977B1 (ko) * | 2017-09-25 | 2024-06-28 | 씨젠테크 (쑤저우, 차이나) 컴퍼니 리미티드 | Cxcr4 저해제로서 헤테로아릴 화합물, 그 조성물 및 이용 방법 |
| CN110317191B (zh) * | 2018-03-28 | 2021-09-21 | 盛世泰科生物医药技术(苏州)有限公司 | 一种吡啶杂环化合物及其作为cxcr4抑制剂的应用 |
| US11649235B2 (en) | 2018-03-19 | 2023-05-16 | Emory University | Pan-tropic entry inhibitors |
| GB201806320D0 (en) | 2018-04-18 | 2018-05-30 | Cellcentric Ltd | Process |
| WO2020010451A1 (en) * | 2018-07-10 | 2020-01-16 | Trillium Therapeutics Inc. | Heteroaromatic-fused imidazolyl amides, compositions and uses thereof as sting agonists |
| WO2020039027A1 (en) * | 2018-08-22 | 2020-02-27 | Asceneuron S. A. | Pyrrolidine glycosidase inhibitors |
| WO2020039028A1 (en) | 2018-08-22 | 2020-02-27 | Asceneuron S. A. | Tetrahydro-benzoazepine glycosidase inhibitors |
| WO2020039029A1 (en) | 2018-08-22 | 2020-02-27 | Asceneuron S. A. | Spiro compounds as glycosidase inhibitors |
| JP7407171B2 (ja) | 2018-08-22 | 2023-12-28 | エースニューロン・ソシエテ・アノニム | グリコシダーゼ阻害剤として有用なピペラジン誘導体のコハク酸付加塩及びフマル酸付加塩 |
| US10548889B1 (en) | 2018-08-31 | 2020-02-04 | X4 Pharmaceuticals, Inc. | Compositions of CXCR4 inhibitors and methods of preparation and use |
| JP7623943B2 (ja) * | 2018-11-30 | 2025-01-29 | カイメラ セラピューティクス, インコーポレイテッド | Irak分解剤およびそれらの使用 |
| EP4525994A1 (en) * | 2022-05-18 | 2025-03-26 | The Regents Of The University Of Michigan | Combination therapies for treatment of cancer |
| KR20260029377A (ko) * | 2023-06-29 | 2026-03-04 | 테라닙 인코포레이티드 | 암 및 염증성 질환 치료에 사용하기 위한 이미다조[1,2-α]피리딘 화합물 및 그 화합물의 제조 방법 |
Citations (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2006502134A (ja) | 2002-08-09 | 2006-01-19 | アストラゼネカ アクチボラグ | 代謝調節型グルタミン酸受容体において活性を有する化合物 |
| JP2008511669A (ja) | 2004-09-02 | 2008-04-17 | スミスクライン ビーチャム コーポレーション | 化合物 |
| US20100028299A1 (en) | 2007-09-18 | 2010-02-04 | Shirit Einav | Methods and compositions of treating a flaviviridae family viral infection |
| JP2010535773A (ja) | 2007-08-10 | 2010-11-25 | グラクソスミスクライン エルエルシー | ウイルス感染を治療するための窒素含有二環式化学物質 |
| WO2011050245A1 (en) | 2009-10-23 | 2011-04-28 | Yangbo Feng | Bicyclic heteroaryls as kinase inhibitors |
| JP2013530237A (ja) | 2010-07-07 | 2013-07-25 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | Rhoキナーゼインヒビター |
| JP2013545744A (ja) | 2010-11-10 | 2013-12-26 | アクテリオン ファーマシューティカルズ リミテッド | オレキシン受容体拮抗薬として有用なラクタム誘導体 |
| JP2014526526A (ja) | 2011-09-26 | 2014-10-06 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツング | リゾホスファチジン酸(lpa)受容体アンタゴニストとしてのベンジルピペリジン化合物 |
| WO2015009616A1 (en) | 2013-07-15 | 2015-01-22 | Novartis Ag | Piperidinyl indole derivatives and their use as complement factor b inhibitors |
Family Cites Families (140)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4810643A (en) | 1985-08-23 | 1989-03-07 | Kirin- Amgen Inc. | Production of pluripotent granulocyte colony-stimulating factor |
| US4933447A (en) | 1987-09-24 | 1990-06-12 | Ss Pharmaceutical Co., Ltd. | Quinoline derivatives |
| US6001826A (en) | 1989-12-21 | 1999-12-14 | Anormed, Inc. | Chemical compounds |
| US5021409A (en) | 1989-12-21 | 1991-06-04 | Johnson Matthey Plc | Antiviral cyclic polyamines |
| GB9126677D0 (en) | 1991-12-16 | 1992-02-12 | Johnson Matthey Plc | Improvements in chemical compounds |
| GB9200245D0 (en) | 1992-01-07 | 1992-02-26 | British Bio Technology | Compounds |
| US5235056A (en) | 1992-04-22 | 1993-08-10 | Ciba-Geigy Corporation | Substituted 1-hydroxy-2,6-diaryl-4-piperidone ketals and polymer compositions stabilized therewith |
| GB9400411D0 (en) | 1994-01-11 | 1994-03-09 | Johnson Matthey Plc | Improvements in chemical compounds |
| US6506770B1 (en) | 1996-06-06 | 2003-01-14 | Anormed, Inc. | Antiviral compounds |
| GB9511357D0 (en) | 1995-06-06 | 1995-08-02 | Johnson Matthey Plc | Improved antiviral compounds |
| WO1997009976A2 (en) | 1995-09-01 | 1997-03-20 | Washington University | Method of reducing neurotoxic injury with zinc chelators |
| PL329070A1 (en) | 1996-03-22 | 1999-03-15 | Du Pont Pharm Co | Novel dissymetrical synthesis of r-alpha-propylpiperonylamine and its analoques |
| CN100525766C (zh) | 1997-06-02 | 2009-08-12 | 詹森药业有限公司 | 用作平滑肌细胞增殖抑制剂的(咪唑-5-基)甲基-2-喹啉酮衍生物 |
| WO1999004794A1 (en) | 1997-07-25 | 1999-02-04 | Merck & Co., Inc. | Cyclic amine modulators of chemokine receptor activity |
| EP1031563B1 (en) | 1997-09-30 | 2005-12-28 | Daiichi Pharmaceutical Co., Ltd. | Sulfonyl derivatives |
| GB9726229D0 (en) | 1997-12-12 | 1998-02-11 | Zeneca Ltd | Resolution of chiral amines |
| US6172061B1 (en) | 1997-12-19 | 2001-01-09 | Takeda Chemical Industries, Ltd. | Pharmaceutical composition for antagonizing CCR5 comprising anilide derivative |
| US6607799B1 (en) | 1998-10-15 | 2003-08-19 | 3M Innovative Properties Company | Surgical dressing with delivery system and method of manufacture |
| US6635278B1 (en) | 1998-12-15 | 2003-10-21 | Gilead Sciences, Inc. | Pharmaceutical formulations |
| US6365583B1 (en) | 1999-02-02 | 2002-04-02 | Anormed, Inc. | Methods to enhance white blood cell count |
| BR0010655A (pt) | 1999-03-24 | 2002-02-13 | Anormed Inc | Compostos heterocìclicos para ligação ao receptor de quimiocina |
| US6245799B1 (en) * | 1999-11-08 | 2001-06-12 | American Home Products Corp | [(Indol-3-yl)-cycloalkyl]-3-substituted azetidines for the treatment of central nervous system disorders |
| EP1228065A1 (en) * | 1999-11-08 | 2002-08-07 | Wyeth | (indol-3-yl)-cycloalkyl]-3-substituted azetidines for the treatment of central nervous system disorders |
| US6602872B1 (en) | 1999-12-13 | 2003-08-05 | Merck & Co., Inc. | Substituted pyridazines having cytokine inhibitory activity |
| US6683192B2 (en) | 2000-03-30 | 2004-01-27 | Curis, Inc. | Small organic molecule regulators of cell proliferation |
| PE20020354A1 (es) | 2000-09-01 | 2002-06-12 | Novartis Ag | Compuestos de hidroxamato como inhibidores de histona-desacetilasa (hda) |
| CA2419224A1 (en) | 2000-09-15 | 2002-03-21 | Anormed Inc. | Chemokine receptor binding heterocyclic compounds |
| PT1317451E (pt) | 2000-09-15 | 2006-12-29 | Anormed Inc | Compostos heterocíclicos que se ligam a receptores de quimioquinas |
| US6835731B2 (en) | 2000-09-15 | 2004-12-28 | Anormed, Inc. | Chemokine receptor binding heterocyclic compounds |
| MXPA03005152A (es) | 2000-12-11 | 2004-10-14 | Tularik Inc | Antogonista de cxcr3. |
| US6878714B2 (en) | 2001-01-12 | 2005-04-12 | Amgen Inc. | Substituted alkylamine derivatives and methods of use |
| GB0107228D0 (en) | 2001-03-22 | 2001-05-16 | Astrazeneca Ab | Chemical compounds |
| EP1389617B1 (en) | 2001-04-27 | 2007-01-03 | Zenyaku Kogyo Kabushiki Kaisha | Heterocyclic compound and antitumor agent containing the same as active ingredient |
| US6794379B2 (en) | 2001-06-06 | 2004-09-21 | Tularik Inc. | CXCR3 antagonists |
| ES2380009T3 (es) | 2001-07-31 | 2012-05-07 | Genzyme Global S.A.R.L. | Métodos para movilizar las células madre/progenitoras |
| US7169750B2 (en) | 2001-07-31 | 2007-01-30 | Anormed, Inc. | Methods to mobilize progenitor/stem cells |
| US8178123B2 (en) | 2001-08-29 | 2012-05-15 | Femina Pharma Incorporated | Method for augmentation of intraepithelial and systemic exposure of therapeutic agents having substrate activity for cytochrome P450 enzymes and membrane efflux systems following vaginal and oral cavity administration |
| WO2003022785A2 (en) | 2001-09-12 | 2003-03-20 | Anormed Inc. | Synthesis of enantiomerically pure amino-substituted fused bicyclic rings |
| US7354932B2 (en) | 2001-12-21 | 2008-04-08 | Anormed, Inc. | Chemokine receptor binding heterocyclic compounds with enhanced efficacy |
| CA2467718C (en) | 2001-12-21 | 2011-04-26 | Anormed Inc. | Chemokine receptor binding heterocyclic compounds with enhanced efficacy |
| TWI329105B (en) | 2002-02-01 | 2010-08-21 | Rigel Pharmaceuticals Inc | 2,4-pyrimidinediamine compounds and their uses |
| US7491544B2 (en) | 2002-05-20 | 2009-02-17 | New York University | Chiral piperidine and quinucledine ligands |
| WO2004019973A1 (en) | 2002-08-14 | 2004-03-11 | Atugen Ag | Use of protein kinase n beta |
| WO2004052862A1 (ja) | 2002-12-10 | 2004-06-24 | Ono Pharmaceutical Co., Ltd. | 含窒素複素環化合物およびその医薬用途 |
| KR20070087266A (ko) | 2003-04-03 | 2007-08-28 | 세마포르 파머슈티컬즈, 아이엔씨. | 피아이-3 키나아제 억제제 프로드러그 |
| EP1613613B1 (en) | 2003-04-11 | 2021-06-02 | Genzyme Corporation | Cxcr4 chemokine receptor binding compounds |
| AU2004232361A1 (en) | 2003-04-22 | 2004-11-04 | Anormed Inc. | Chemokine receptor binding heterocyclic compounds with enhanced efficacy |
| US7501518B2 (en) * | 2003-04-22 | 2009-03-10 | Genzyme Corporation | Methods of making 2,6-diaryl piperidine derivatives |
| US7173015B2 (en) | 2003-07-03 | 2007-02-06 | The Trustees Of The University Of Pennsylvania | Inhibition of Syk kinase expression |
| US7498346B2 (en) | 2003-12-11 | 2009-03-03 | Genzyme Corporation | Chemokine receptor binding compounds |
| CN1930127B (zh) | 2004-03-15 | 2012-11-21 | 阿诺麦德股份有限公司 | 用于合成cxcr4拮抗剂的方法 |
| EP1742936A2 (en) | 2004-04-13 | 2007-01-17 | Icagen, Inc. | Polycyclic pyridines as potassium ion channel modulators |
| DE102004021716A1 (de) | 2004-04-30 | 2005-12-01 | Grünenthal GmbH | Substituierte Imidazo[1,2-a]pyridin-Verbindungen und Arzneimittel enthaltend substituierte Imidazo[1,2-a]pyridin-Verbindungen |
| SI2612862T1 (sl) | 2004-05-13 | 2017-04-26 | Icos Corporation | Kinazolini kot inhibitorji humane fosfatidilinozitol 3-kinaze delta |
| US20080096861A1 (en) | 2004-08-02 | 2008-04-24 | Smithkline Beecham Corporation | Chemical Compounds |
| CA2577100A1 (en) | 2004-08-16 | 2006-03-02 | Smithkline Beecham Corporation | Chemical compounds |
| WO2006036816A2 (en) | 2004-09-24 | 2006-04-06 | Smithkline Beecham Corporation | Chemical compounds |
| TW200619206A (en) | 2004-09-29 | 2006-06-16 | Anormed Inc | Chemokine-binding heterocyclic compound salts, and methods of use thereof |
| DE602006010979D1 (de) | 2005-01-19 | 2010-01-21 | Rigel Pharmaceuticals Inc | Prodrugs aus 2,4-pyrimidindiamin-verbindungen und ihre verwendungen |
| US20090093454A1 (en) * | 2005-03-04 | 2009-04-09 | Kristjan Gudmundsson | Chemical Compounds |
| EP1888550B1 (en) | 2005-05-12 | 2014-06-25 | AbbVie Bahamas Ltd. | Apoptosis promoters |
| GB0510390D0 (en) | 2005-05-20 | 2005-06-29 | Novartis Ag | Organic compounds |
| US20090203533A1 (en) | 2005-07-08 | 2009-08-13 | Siemens Medicals Solutions Diagnositcs Gmbh | Methods and Kits for Predicting and Monitoring Direct Response to Cancer Therapy |
| US20080214562A1 (en) | 2005-07-11 | 2008-09-04 | Kristjan Gudmundsson | Chemical Compounds |
| US7402325B2 (en) | 2005-07-28 | 2008-07-22 | Phoenix Biotechnology, Inc. | Supercritical carbon dioxide extract of pharmacologically active components from Nerium oleander |
| WO2007015074A1 (en) | 2005-08-02 | 2007-02-08 | Ineos Europe Limited | Diene polymerisation |
| CA2619828A1 (en) | 2005-08-19 | 2007-02-22 | Genzyme Corporation | Methods to enhance chemotherapy |
| EP1919872A4 (en) | 2005-08-31 | 2009-08-05 | Smithkline Beecham Corp | CHEMICAL COMPOUNDS |
| BRPI0617162B8 (pt) | 2005-10-07 | 2021-05-25 | Exelixis Inc | compostos inibidores de fosfatidilinositol 3-quinase composições farmacêuticas que os contem e métodos de uso dos mesmos |
| CN103626742B (zh) | 2005-11-01 | 2017-04-26 | 塔格根公司 | 激酶的联-芳基间-嘧啶抑制剂 |
| WO2007058322A1 (ja) | 2005-11-18 | 2007-05-24 | Ono Pharmaceutical Co., Ltd. | 塩基性基を含有する化合物およびその用途 |
| US20070123538A1 (en) | 2005-11-30 | 2007-05-31 | Schering Corporation | Compositions comprising a combination of CCR5 and CXCR4 antagonists |
| EP2455382B1 (en) | 2005-12-13 | 2016-10-26 | Incyte Holdings Corporation | Heteroaryl substituted pyrrolo[2,3-b]pyridines and pyrrolo[2,3-b]pyrimidines as Janus kinase inhibitors |
| JO2660B1 (en) | 2006-01-20 | 2012-06-17 | نوفارتيس ايه جي | Pi-3 inhibitors and methods of use |
| JP2009524689A (ja) | 2006-01-25 | 2009-07-02 | スミスクライン ビーチャム コーポレーション | 化合物 |
| PE20070946A1 (es) | 2006-01-25 | 2007-10-16 | Smithkline Beecham Corp | COMPUESTOS DERIVADOS DE IMIDAZO[1,2-a]PIRIDINA COMO MODULADORES DEL RECEPTOR DE QUIMIOQUINA (CXCR4) |
| GB0605786D0 (en) | 2006-03-22 | 2006-05-03 | Glaxo Group Ltd | Compounds |
| MX2008013578A (es) | 2006-04-26 | 2009-03-23 | Hoffmann La Roche | Derivados de tieno [3,2-d]pirimidina utiles como inhibidores de fosfatidilinositol 3-cinasa(p13k). |
| CN101466376A (zh) | 2006-06-12 | 2009-06-24 | 辉瑞产品公司 | 用于提高免疫重建并治疗hiv患者的机会感染的ccr5拮抗剂 |
| TWI482772B (zh) | 2006-08-21 | 2015-05-01 | Astrazeneca Ab | 適合口服且包含三唑并[4,5-d]嘧啶衍生物之組合物 |
| BRPI0622054B8 (pt) | 2006-09-22 | 2021-05-25 | Oxford Amherst Llc | composto e composição farmacêutica |
| US20100298314A1 (en) | 2006-12-20 | 2010-11-25 | Schering Corporation | Novel jnk inhibitors |
| HRP20151386T1 (hr) | 2007-03-12 | 2016-02-26 | Ym Biosciences Australia Pty Ltd | Fenil aminopirimidinski spojevi i njihova primjena |
| WO2008118802A1 (en) | 2007-03-23 | 2008-10-02 | Regents Of The University Of Minnesota | Therapeutic compounds |
| EP1974729A1 (en) | 2007-03-28 | 2008-10-01 | Santhera Pharmaceuticals (Schweiz) AG | Substituted imidazopyridine derivates as melanocortin- 4 receptor antagonists |
| CN101855222A (zh) | 2007-05-10 | 2010-10-06 | 通用电气健康护理有限公司 | 对大麻素cb2受体具有活性的咪唑并(1,2-a)吡啶和相关化合物 |
| PE20090717A1 (es) | 2007-05-18 | 2009-07-18 | Smithkline Beecham Corp | Derivados de quinolina como inhibidores de la pi3 quinasa |
| US20110070657A1 (en) | 2007-08-17 | 2011-03-24 | The General Hospital Corporation | Detecting ions and measuring ion concentrations |
| CA2709883A1 (en) * | 2007-12-19 | 2009-06-25 | The Scripps Research Institute | Benzimidazoles and analogs as rho kinase inhibitors |
| US8158616B2 (en) | 2008-03-11 | 2012-04-17 | Incyte Corporation | Azetidine and cyclobutane derivatives as JAK inhibitors |
| CN102088993A (zh) | 2008-03-20 | 2011-06-08 | 卡罗勒斯治疗公司 | 炎症的治疗方法 |
| AU2009228034A1 (en) | 2008-03-28 | 2009-10-01 | Altiris Therapeutics | Chemokine receptor modulators |
| WO2009151910A2 (en) | 2008-05-25 | 2009-12-17 | Wyeth | Combination product of receptor tyrosine kinase inhibitor and fatty acid synthase inhibitor for treating cancer |
| US8338439B2 (en) | 2008-06-27 | 2012-12-25 | Celgene Avilomics Research, Inc. | 2,4-disubstituted pyrimidines useful as kinase inhibitors |
| JP2010016628A (ja) | 2008-07-03 | 2010-01-21 | Canon Inc | 画像処理装置及び画像処理方法 |
| ES2467108T3 (es) | 2008-12-09 | 2014-06-11 | Gilead Sciences, Inc. | Moduladores de receptores tipo toll |
| EP2482805B1 (en) | 2009-09-28 | 2014-11-19 | Zenbury International Limited | Pharmaceutical composition |
| US20110293686A1 (en) | 2010-05-28 | 2011-12-01 | Searete Llc, A Limited Liability Corporation Of The State Of Delaware | Anti-viral compositions and methods for administration |
| CA2706292A1 (en) | 2010-05-28 | 2011-11-28 | Pharmascience Inc. | A stable pharmaceutical formulation comprising telmisartan and hydrochlorothiazide |
| US9155723B2 (en) | 2010-06-28 | 2015-10-13 | The General Hospital Corporation | Anti-CXCR4 as a sensitizer to cancer therapeutics |
| GB201017345D0 (en) | 2010-10-14 | 2010-11-24 | Proximagen Ltd | Receptor antagonists |
| US9267934B2 (en) | 2010-10-26 | 2016-02-23 | University Of South Alabama | Methods and compositions for ameliorating pancreatic cancer |
| EP3153510B1 (en) | 2010-12-03 | 2020-05-06 | Emory University | Fused azines as chemokine cxcr4 receptor modulators and uses related thereto |
| JP6076913B2 (ja) | 2010-12-07 | 2017-02-08 | ドレクセル ユニバーシティ | 癌からの転移を阻害する方法 |
| PH12013501201A1 (en) | 2010-12-09 | 2013-07-29 | Univ Pennsylvania | Use of chimeric antigen receptor-modified t cells to treat cancer |
| CN103476410B (zh) | 2011-01-11 | 2020-02-21 | 戴麦里克斯生物科学有限公司 | 联合疗法 |
| RU2638802C2 (ru) | 2011-05-16 | 2017-12-15 | Джензим Корпорейшн | Применение антагонистов cxcr4 |
| AR087364A1 (es) | 2011-07-29 | 2014-03-19 | Pf Medicament | Anticuerpo anti-cxcr4 y su uso para la deteccion y dianostico de canceres |
| US8889159B2 (en) | 2011-11-29 | 2014-11-18 | Gilead Pharmasset Llc | Compositions and methods for treating hepatitis C virus |
| JP2015503624A (ja) | 2012-01-12 | 2015-02-02 | ギリアード サイエンシーズ, インコーポレイテッド | 医薬組成物およびその調製方法 |
| EP2922861A4 (en) | 2012-11-26 | 2016-09-14 | Caris Life Sciences Switzerland Holdings Gmbh | BIOMARKER COMPOSITIONS AND METHODS |
| US10064826B2 (en) | 2013-03-15 | 2018-09-04 | Navinta, Llc | Direct compression and dry granulation processes for preparing carglumic acid tablets having less impurities than those produced by wet granulation process |
| WO2014197680A1 (en) | 2013-06-05 | 2014-12-11 | Salk Institute For Biological Studies | Vitamin d receptor agonists to treat diseases involving cxcl12 activity |
| CA2920377A1 (en) | 2013-08-05 | 2015-02-12 | Cambridge Enterprise Limited | Inhibition of cxcr4 signaling in cancer immunotherapy |
| EA201690473A1 (ru) | 2013-08-27 | 2017-03-31 | ГАЙЛИД ФАРМАССЕТ ЭлЭлСи | Комбинированный состав двух противовирусных соединений |
| CA3206628A1 (en) | 2013-09-12 | 2015-03-19 | Dana-Farber Cancer Institute, Inc. | Methods for evaluating and treating waldenstrom's macroglobulinemia |
| KR20160093012A (ko) | 2013-11-05 | 2016-08-05 | 코그네이트 바이오서비시즈, 인코포레이티드 | 암 치료를 위한 체크포인트 억제제 및 치료제의 배합물 |
| WO2015143092A1 (en) | 2014-03-18 | 2015-09-24 | The Research Foundation For The State University Of New York | Therapeutic agent for treating tumors |
| NZ724368A (en) | 2014-03-19 | 2023-07-28 | Infinity Pharmaceuticals Inc | Heterocyclic compounds for use in the treatment of pi3k-gamma mediated disorders |
| EP3157921A1 (en) | 2014-06-23 | 2017-04-26 | Dr. Reddy's Laboratories Ltd. | Substituted imidazo[1,2-a]pyridine compounds useful for the treatment of pain |
| DK3169341T3 (da) | 2014-07-16 | 2019-08-05 | Transgene Sa | Onkolytisk virus til ekspression af immun-checkpoint-modulatorer |
| SG11201704756YA (en) | 2014-12-12 | 2017-07-28 | Commw Scient Ind Res Org | Dislodgement and release of hsc using alpha 9 integrin antagonist and cxcr4 antagonist |
| US20180133327A1 (en) | 2015-03-16 | 2018-05-17 | Amal Therapeutics Sa | Cell Penetrating Peptides and Complexes Comprising the Same |
| EP3307778A1 (en) | 2015-06-12 | 2018-04-18 | Bristol-Myers Squibb Company | Treatment of cancer by combined blockade of the pd-1 and cxcr4 signaling pathways |
| EP4585268A3 (en) | 2015-09-14 | 2025-10-15 | Twelve Therapeutics, Inc. | Solid forms of isoquinolinone derivatives, process of making, compositions comprising, and methods of using the same |
| US10379661B2 (en) | 2015-09-25 | 2019-08-13 | Samsung Electronics Co., Ltd. | Coordinate measuring apparatus and coordinate measuring system having the same |
| CN109069426B (zh) | 2015-12-14 | 2021-10-29 | X4 制药有限公司 | 治疗癌症的方法 |
| WO2017106332A1 (en) | 2015-12-14 | 2017-06-22 | X4 Pharmaceuticals, Inc. | Methods for treating cancer |
| PL3393468T3 (pl) | 2015-12-22 | 2023-01-23 | X4 Pharmaceuticals, Inc. | Metody leczenia niedoboru odporności |
| CA3010617A1 (en) | 2016-01-22 | 2017-07-27 | X4 Pharmaceuticals, Inc. | Methods for treating cancer |
| US11337969B2 (en) | 2016-04-08 | 2022-05-24 | X4 Pharmaceuticals, Inc. | Methods for treating cancer |
| ES3014978T3 (en) | 2016-04-14 | 2025-04-28 | Creatv Microtech Inc | Methods of using pd-l1 expression in treatment decisions for cancer therapy |
| WO2017223243A1 (en) | 2016-06-21 | 2017-12-28 | X4 Pharmaceuticals, Inc. | Cxcr4 inhibitors and uses thereof |
| CN109640988A (zh) | 2016-06-21 | 2019-04-16 | X4 制药有限公司 | Cxcr4抑制剂及其用途 |
| ES2870920T3 (es) | 2016-06-21 | 2021-10-28 | X4 Pharmaceuticals Inc | Inhibidores de CXCR4 y usos de los mismos |
| JP2020525427A (ja) | 2017-06-21 | 2020-08-27 | エックス4 ファーマシューティカルズ, インコーポレイテッド | 癌を処置するための方法 |
| US20210349099A1 (en) | 2017-11-07 | 2021-11-11 | X4 Pharmaceuticals, Inc. | Cancer biomarkers and methods of use thereof |
| WO2019126106A1 (en) | 2017-12-19 | 2019-06-27 | X4 Pharmaceuticals, Inc. | Acyclic cxcr4 inhibitors and uses thereof |
| JP2021521439A (ja) | 2018-04-13 | 2021-08-26 | エックス4 ファーマシューティカルズ, インコーポレイテッド | がん血清バイオマーカーおよびその使用方法 |
| US10548889B1 (en) | 2018-08-31 | 2020-02-04 | X4 Pharmaceuticals, Inc. | Compositions of CXCR4 inhibitors and methods of preparation and use |
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2017
- 2017-06-21 WO PCT/US2017/038613 patent/WO2017223243A1/en not_active Ceased
- 2017-06-21 US US16/311,055 patent/US11332470B2/en active Active
- 2017-06-21 JP JP2018566976A patent/JP6994767B2/ja not_active Expired - Fee Related
- 2017-06-21 CA CA3027500A patent/CA3027500A1/en active Pending
- 2017-06-21 CN CN201780048907.7A patent/CN109641838A/zh active Pending
- 2017-06-21 EP EP17816166.7A patent/EP3472129A4/en not_active Withdrawn
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2021
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Patent Citations (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2006502134A (ja) | 2002-08-09 | 2006-01-19 | アストラゼネカ アクチボラグ | 代謝調節型グルタミン酸受容体において活性を有する化合物 |
| JP2008511669A (ja) | 2004-09-02 | 2008-04-17 | スミスクライン ビーチャム コーポレーション | 化合物 |
| JP2010535773A (ja) | 2007-08-10 | 2010-11-25 | グラクソスミスクライン エルエルシー | ウイルス感染を治療するための窒素含有二環式化学物質 |
| US20100028299A1 (en) | 2007-09-18 | 2010-02-04 | Shirit Einav | Methods and compositions of treating a flaviviridae family viral infection |
| WO2011050245A1 (en) | 2009-10-23 | 2011-04-28 | Yangbo Feng | Bicyclic heteroaryls as kinase inhibitors |
| JP2013530237A (ja) | 2010-07-07 | 2013-07-25 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | Rhoキナーゼインヒビター |
| JP2013545744A (ja) | 2010-11-10 | 2013-12-26 | アクテリオン ファーマシューティカルズ リミテッド | オレキシン受容体拮抗薬として有用なラクタム誘導体 |
| JP2014526526A (ja) | 2011-09-26 | 2014-10-06 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツング | リゾホスファチジン酸(lpa)受容体アンタゴニストとしてのベンジルピペリジン化合物 |
| WO2015009616A1 (en) | 2013-07-15 | 2015-01-22 | Novartis Ag | Piperidinyl indole derivatives and their use as complement factor b inhibitors |
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| US11332470B2 (en) | 2022-05-17 |
| CA3027500A1 (en) | 2017-12-28 |
| US20190322671A1 (en) | 2019-10-24 |
| EP3472129A4 (en) | 2019-12-04 |
| JP2019518768A (ja) | 2019-07-04 |
| EP3472129A1 (en) | 2019-04-24 |
| CN109641838A (zh) | 2019-04-16 |
| JP2021185195A (ja) | 2021-12-09 |
| WO2017223243A1 (en) | 2017-12-28 |
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