AU2015235944B2 - Substituted indole Mcl-1 inhibitors - Google Patents
Substituted indole Mcl-1 inhibitors Download PDFInfo
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- AU2015235944B2 AU2015235944B2 AU2015235944A AU2015235944A AU2015235944B2 AU 2015235944 B2 AU2015235944 B2 AU 2015235944B2 AU 2015235944 A AU2015235944 A AU 2015235944A AU 2015235944 A AU2015235944 A AU 2015235944A AU 2015235944 B2 AU2015235944 B2 AU 2015235944B2
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- VAWQUIBIKZPMNL-UHFFFAOYSA-N Cc([n](C)nc1C)c1-c1c2[n](CCCNC3=O)c3c(CCCOc(cc3C)cc(C)c3Cl)c2ccc1Cl Chemical compound Cc([n](C)nc1C)c1-c1c2[n](CCCNC3=O)c3c(CCCOc(cc3C)cc(C)c3Cl)c2ccc1Cl VAWQUIBIKZPMNL-UHFFFAOYSA-N 0.000 description 1
- IWUUBOKMPIMVGE-UHFFFAOYSA-N Cc([n](C)nc1C)c1-c1c2[n](CCN(Cc(cc3)ccc3C(O)=O)C3=O)c3c(CCCOc(cc3C)cc(C)c3Cl)c2ccc1Cl Chemical compound Cc([n](C)nc1C)c1-c1c2[n](CCN(Cc(cc3)ccc3C(O)=O)C3=O)c3c(CCCOc(cc3C)cc(C)c3Cl)c2ccc1Cl IWUUBOKMPIMVGE-UHFFFAOYSA-N 0.000 description 1
- AGYYLBNJWUTFIM-UHFFFAOYSA-N Cc([n](C)nc1C)c1-c1c2[n](CCN(Cc(nc3)ccc3C(O)=O)C3=O)c3c(CCCOc(cc3C)cc(C)c3Cl)c2ccc1Cl Chemical compound Cc([n](C)nc1C)c1-c1c2[n](CCN(Cc(nc3)ccc3C(O)=O)C3=O)c3c(CCCOc(cc3C)cc(C)c3Cl)c2ccc1Cl AGYYLBNJWUTFIM-UHFFFAOYSA-N 0.000 description 1
- PSQKGRLAYSSXPH-UHFFFAOYSA-N Cc([n](C)nc1C)c1-c1c2[n](CCN(Cc3ccc(C)cc3)C3=O)c3c(CCCOc3cc(C)c(C)c(C)c3)c2ccc1Cl Chemical compound Cc([n](C)nc1C)c1-c1c2[n](CCN(Cc3ccc(C)cc3)C3=O)c3c(CCCOc3cc(C)c(C)c(C)c3)c2ccc1Cl PSQKGRLAYSSXPH-UHFFFAOYSA-N 0.000 description 1
- FADBVKGBAMQCQR-UHFFFAOYSA-N Cc([n](C)nc1C)c1-c1c2[n](CCN(c3cc(C(O)=O)cnc3)C3=O)c3c(CCCOc(cc3C)cc(C)c3Cl)c2ccc1Cl Chemical compound Cc([n](C)nc1C)c1-c1c2[n](CCN(c3cc(C(O)=O)cnc3)C3=O)c3c(CCCOc(cc3C)cc(C)c3Cl)c2ccc1Cl FADBVKGBAMQCQR-UHFFFAOYSA-N 0.000 description 1
- KBLWWKTYSLEKSG-UHFFFAOYSA-N Cc([n](C)nc1C)c1-c1c2[n](CCN(c3cc(NC4CCOCC4)cc(C(O)=O)c3)C3=O)c3c(CCCOc3cc(C)c(C)c(C)c3)c2ccc1Cl Chemical compound Cc([n](C)nc1C)c1-c1c2[n](CCN(c3cc(NC4CCOCC4)cc(C(O)=O)c3)C3=O)c3c(CCCOc3cc(C)c(C)c(C)c3)c2ccc1Cl KBLWWKTYSLEKSG-UHFFFAOYSA-N 0.000 description 1
- SKZRLKLCHRPYDV-UHFFFAOYSA-N Cc([n](C)nc1C)c1-c1c2[n](CCNC3=O)c3c(CCCOc(cc3C)cc(C)c3Cl)c2ccc1Cl Chemical compound Cc([n](C)nc1C)c1-c1c2[n](CCNC3=O)c3c(CCCOc(cc3C)cc(C)c3Cl)c2ccc1Cl SKZRLKLCHRPYDV-UHFFFAOYSA-N 0.000 description 1
- DLUVTGUNUNLWAN-UHFFFAOYSA-N Cc([n](C)nc1C)c1-c1cccc2c1[nH]c(C(Nc1cc(C(O)=O)cnc1)=O)c2CCCOc1c(cccc2)c2ccc1 Chemical compound Cc([n](C)nc1C)c1-c1cccc2c1[nH]c(C(Nc1cc(C(O)=O)cnc1)=O)c2CCCOc1c(cccc2)c2ccc1 DLUVTGUNUNLWAN-UHFFFAOYSA-N 0.000 description 1
- XKGXCDUPWMROJX-UHFFFAOYSA-N Cc(cc(cc1C)OCCCc2c(C(N(CC3)CCN3c3cc(C(OC)=O)ccc3)=O)[nH]c3cc(Cl)ccc23)c1Cl Chemical compound Cc(cc(cc1C)OCCCc2c(C(N(CC3)CCN3c3cc(C(OC)=O)ccc3)=O)[nH]c3cc(Cl)ccc23)c1Cl XKGXCDUPWMROJX-UHFFFAOYSA-N 0.000 description 1
- ZHQRUHLRFVMUKA-UHFFFAOYSA-N Cc(cc(cc1C)OCCCc2c(C(N(Cc3ccc(C(F)(F)F)cc3)c(cc3)ncc3S(N)(=O)=O)=O)[nH]c3ccccc23)c1Cl Chemical compound Cc(cc(cc1C)OCCCc2c(C(N(Cc3ccc(C(F)(F)F)cc3)c(cc3)ncc3S(N)(=O)=O)=O)[nH]c3ccccc23)c1Cl ZHQRUHLRFVMUKA-UHFFFAOYSA-N 0.000 description 1
- UCGUDMIMRDUMLQ-UHFFFAOYSA-N Cc1c(C2NN2)cccn1 Chemical compound Cc1c(C2NN2)cccn1 UCGUDMIMRDUMLQ-UHFFFAOYSA-N 0.000 description 1
- NHAVMIQJZFSDHL-UHFFFAOYSA-N Cc1cc(OCCCc2c(C(N(CC3)CCN3c(cc3)ccc3C(O)=O)=O)[nH]c3cc(Cl)ccc23)cc(C)c1Cl Chemical compound Cc1cc(OCCCc2c(C(N(CC3)CCN3c(cc3)ccc3C(O)=O)=O)[nH]c3cc(Cl)ccc23)cc(C)c1Cl NHAVMIQJZFSDHL-UHFFFAOYSA-N 0.000 description 1
- DOTMJBYEJSWBJL-UHFFFAOYSA-N Cc1cc(OCCCc2c(C(NCc3ccccc3)=O)[nH]c3ccccc23)cc(C)c1Cl Chemical compound Cc1cc(OCCCc2c(C(NCc3ccccc3)=O)[nH]c3ccccc23)cc(C)c1Cl DOTMJBYEJSWBJL-UHFFFAOYSA-N 0.000 description 1
- PBTLSCQMVLRIRH-KTAJNNJTSA-N NOC(/N=C\I)=O Chemical compound NOC(/N=C\I)=O PBTLSCQMVLRIRH-KTAJNNJTSA-N 0.000 description 1
- JSZAZZQHDRHICK-UHFFFAOYSA-N O=C(CN1)NS1(=O)=O Chemical compound O=C(CN1)NS1(=O)=O JSZAZZQHDRHICK-UHFFFAOYSA-N 0.000 description 1
Classifications
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- 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
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- A61K31/38—Heterocyclic compounds having sulfur as a ring hetero atom
- A61K31/381—Heterocyclic compounds having sulfur as a ring hetero atom having five-membered rings
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- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
- A61K31/404—Indoles, e.g. pindolol
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- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
- A61K31/404—Indoles, e.g. pindolol
- A61K31/4045—Indole-alkylamines; Amides thereof, e.g. serotonin, melatonin
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- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/415—1,2-Diazoles
- A61K31/4155—1,2-Diazoles non condensed and containing further heterocyclic rings
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- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
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- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/454—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
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- A61K31/47—Quinolines; Isoquinolines
- A61K31/472—Non-condensed isoquinolines, e.g. papaverine
- A61K31/4725—Non-condensed isoquinolines, e.g. papaverine containing further heterocyclic rings
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- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
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- A61K31/498—Pyrazines or piperazines ortho- and peri-condensed with carbocyclic ring systems, e.g. quinoxaline, phenazine
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- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
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- A61K31/551—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
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- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
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- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/30—Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
- C07D209/42—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
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- 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
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- C07D401/04—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 two hetero rings directly linked by a ring-member-to-ring-member bond
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- 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
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- 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
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- 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
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- 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
- C07D405/02—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 two hetero rings
- C07D405/12—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 two hetero rings linked by a chain containing hetero atoms as chain links
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- 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
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- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
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- 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
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| WO2015148854A1 (en) | 2014-03-27 | 2015-10-01 | Vanderbilt University | Substituted indole mcl-1 inhibitors |
| US9949965B2 (en) | 2014-10-17 | 2018-04-24 | Vanderbilt University | Tricyclic indole Mcl-1 inhibitors and uses thereof |
| WO2017147410A1 (en) * | 2016-02-25 | 2017-08-31 | Amgen Inc. | Compounds that inhibit mcl-1 protein |
| CN109153643B (zh) * | 2016-03-04 | 2022-06-21 | 范德比尔特大学 | 取代的吲哚mcl-1抑制剂 |
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| CA3024482A1 (en) | 2016-05-19 | 2017-11-23 | Bayer Aktiengesellschaft | Macrocyclic indole derivatives |
| US10981932B2 (en) | 2016-05-19 | 2021-04-20 | Bayer Aktiengesellschaft | Macrocyclic indole derivatives |
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| JP6453507B2 (ja) * | 2017-03-30 | 2019-01-16 | アムジエン・インコーポレーテツド | Mcl−1タンパク質を阻害する化合物 |
| US20200062738A1 (en) * | 2017-04-30 | 2020-02-27 | Development Center For Biotechnology | Anti-cancer stemness drugs |
| WO2019040511A1 (en) * | 2017-08-22 | 2019-02-28 | University Of Maryland Batimore | DOUBLE INHIBITORS OF BCL-2 AND HDM2 FAMILIES BY CO-MIMETTISM OF ALPHA BH3 AND P53 PROPELLERS |
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| TWI810220B (zh) | 2017-11-17 | 2023-08-01 | 德商拜耳廠股份有限公司 | 經取代之巨環吲哚衍生物 |
| US11478451B1 (en) | 2017-11-17 | 2022-10-25 | Bayer Aktiengesellschaft | Macrocyclic chlorine substituted indole derivatives |
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| UY37973A (es) | 2017-11-17 | 2019-06-28 | Bayer Ag | Derivados de indol macrocíclicos |
| WO2019096907A1 (en) | 2017-11-17 | 2019-05-23 | Bayer Aktiengesellschaft | Aryl annulated macrocyclic indole derivatives |
| CN109988151B (zh) * | 2017-12-29 | 2021-04-23 | 北京赛特明强医药科技有限公司 | 一种炔类化合物、制备方法及其应用 |
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| CN108251104B (zh) * | 2018-02-27 | 2019-11-05 | 山东大学 | 一种取代吲哚-2-羧酸类Bcl-2小分子荧光探针及其应用 |
| DK3793565T3 (en) * | 2018-05-14 | 2022-03-07 | Gilead Sciences Inc | Mcl-1-inhibitorer |
| EP3810573A4 (en) | 2018-06-25 | 2021-12-08 | Suzhou Mednes Pharma Tech Co., Ltd. | COMPOUNDS AND METHODS FOR THE TREATMENT OF CONDITIONS ASSOCIATED WITH THE HEDGEHOG ROUTE |
| EP3856258B1 (en) * | 2018-09-27 | 2024-07-31 | Pierre Fabre Medicament | Sulfomaleimide-based linkers and corresponding conjugates |
| US11691989B2 (en) | 2018-11-22 | 2023-07-04 | Ascentage Pharma (Suzhou) Co., Ltd. | Macrocyclic indoles as Mcl-1 inhibitors |
| TWI745836B (zh) * | 2019-01-18 | 2021-11-11 | 大陸商蘇州亞盛藥業有限公司 | 作為mcl-1抑製劑的大螺環醚 |
| US12338250B2 (en) | 2019-05-17 | 2025-06-24 | The Broad Institute, Inc. | Methods of preparing macrocyclic indoles |
| WO2021092053A1 (en) * | 2019-11-08 | 2021-05-14 | Unity Biotechnology, Inc. | Mcl-1 inhibitor macrocycle compounds for use in clinical management of conditions caused or mediated by senescent cells and for treating cancer |
| WO2021092061A1 (en) * | 2019-11-08 | 2021-05-14 | Unity Biotechnology, Inc. | Combination treatment for senescence-associated diseases |
| WO2024123195A1 (en) * | 2022-12-06 | 2024-06-13 | Captor Therapeutics S.A. | Targeted protein degradation using prodrugs of bifunctional compounds that bind ubiquitin ligase and target mcl-1 protein |
| AU2023389065A1 (en) * | 2022-12-06 | 2025-06-19 | Captor Therapeutics S.A. | Targeted protein degradation using bifunctional compounds that bind ubiquitin ligase and target mcl-1 protein |
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| EP3122353A4 (en) | 2017-12-13 |
| CN106456602A (zh) | 2017-02-22 |
| CN106456602B (zh) | 2020-11-24 |
| US10533010B2 (en) | 2020-01-14 |
| US20200140447A1 (en) | 2020-05-07 |
| EP3122353A1 (en) | 2017-02-01 |
| JP2017510641A (ja) | 2017-04-13 |
| JP6757312B2 (ja) | 2020-09-16 |
| CA2943815C (en) | 2023-04-04 |
| US20230039309A1 (en) | 2023-02-09 |
| US12195472B2 (en) | 2025-01-14 |
| AU2015235944A1 (en) | 2016-10-13 |
| CA2943815A1 (en) | 2015-10-01 |
| US20170174689A1 (en) | 2017-06-22 |
| EP3122353B1 (en) | 2020-10-28 |
| US11208415B2 (en) | 2021-12-28 |
| WO2015148854A1 (en) | 2015-10-01 |
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