JP2019507179A - Wdr5タンパク質−タンパク質結合の阻害剤 - Google Patents
Wdr5タンパク質−タンパク質結合の阻害剤 Download PDFInfo
- Publication number
- JP2019507179A JP2019507179A JP2018546584A JP2018546584A JP2019507179A JP 2019507179 A JP2019507179 A JP 2019507179A JP 2018546584 A JP2018546584 A JP 2018546584A JP 2018546584 A JP2018546584 A JP 2018546584A JP 2019507179 A JP2019507179 A JP 2019507179A
- Authority
- JP
- Japan
- Prior art keywords
- alkylene
- alkyl
- phenyl
- carboxamide
- trifluoromethyl
- 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.)
- Pending
Links
- 0 CC(C)(C)C(*CC1N(C)CCN(C)C1)=* Chemical compound CC(C)(C)C(*CC1N(C)CCN(C)C1)=* 0.000 description 25
- CQESJDGMFKMMRE-UHFFFAOYSA-N CC(C)N(CC1)CC1N(C)C Chemical compound CC(C)N(CC1)CC1N(C)C CQESJDGMFKMMRE-UHFFFAOYSA-N 0.000 description 2
- CQESJDGMFKMMRE-VIFPVBQESA-N CC(C)N(CC1)C[C@H]1N(C)C Chemical compound CC(C)N(CC1)C[C@H]1N(C)C CQESJDGMFKMMRE-VIFPVBQESA-N 0.000 description 2
- UAIVFDJJMVMUGY-UHFFFAOYSA-N CC1N(C)CCN(C)C1 Chemical compound CC1N(C)CCN(C)C1 UAIVFDJJMVMUGY-UHFFFAOYSA-N 0.000 description 2
- UFOZYPFQCJEYTP-QMMMGPOBSA-N CCN1[C@@H](C)CN(C)CC1 Chemical compound CCN1[C@@H](C)CN(C)CC1 UFOZYPFQCJEYTP-QMMMGPOBSA-N 0.000 description 2
- TZEGGLAQRXWSCY-UHFFFAOYSA-N CN(C1)CC2C1CN(C)C2 Chemical compound CN(C1)CC2C1CN(C)C2 TZEGGLAQRXWSCY-UHFFFAOYSA-N 0.000 description 2
- RYAFIZYASRHWBM-UHFFFAOYSA-N CN(CC1)CC11N(C)CCC1 Chemical compound CN(CC1)CC11N(C)CCC1 RYAFIZYASRHWBM-UHFFFAOYSA-N 0.000 description 2
- ZEHZRJZZIYNPKU-UHFFFAOYSA-N CN1CC(CO)N(C)CC1 Chemical compound CN1CC(CO)N(C)CC1 ZEHZRJZZIYNPKU-UHFFFAOYSA-N 0.000 description 2
- RXYPXQSKLGGKOL-UHFFFAOYSA-N CN1CCN(C)CC1 Chemical compound CN1CCN(C)CC1 RXYPXQSKLGGKOL-UHFFFAOYSA-N 0.000 description 2
- GZOFLJABJGNWKH-LEDWDTFISA-N C/C=C(\C(\F)=C(\N1CCOCC1)/N=C)/c(cc1NC(C(C(C(F)(F)F)=C2)=CNC2=O)=O)ccc1N1CCN(C)CC1 Chemical compound C/C=C(\C(\F)=C(\N1CCOCC1)/N=C)/c(cc1NC(C(C(C(F)(F)F)=C2)=CNC2=O)=O)ccc1N1CCN(C)CC1 GZOFLJABJGNWKH-LEDWDTFISA-N 0.000 description 1
- YJDHOHIVOLFFBU-UHFFFAOYSA-N CC(C(C(F)(F)F)=C1)=CNC1=O Chemical compound CC(C(C(F)(F)F)=C1)=CNC1=O YJDHOHIVOLFFBU-UHFFFAOYSA-N 0.000 description 1
- OFSYGBOYTIOVRO-UHFFFAOYSA-N CC(C)N1CC(CO)N(C)CC1 Chemical compound CC(C)N1CC(CO)N(C)CC1 OFSYGBOYTIOVRO-UHFFFAOYSA-N 0.000 description 1
- OUGANWSTVHXQBG-UHFFFAOYSA-N CC(C1)N(C)CCN1c(c([N+]([O-])=O)c1)ccc1[Br]=C Chemical compound CC(C1)N(C)CCN1c(c([N+]([O-])=O)c1)ccc1[Br]=C OUGANWSTVHXQBG-UHFFFAOYSA-N 0.000 description 1
- HFVRIZUVLXIFHQ-UHFFFAOYSA-N CC(C1c(cc2NC(C(C(C(F)(F)F)=C3)=CNC3=O)=O)ccc2N2CCN(C)CC2)C(CN2CCNCC2)=CC=C1F Chemical compound CC(C1c(cc2NC(C(C(C(F)(F)F)=C3)=CNC3=O)=O)ccc2N2CCN(C)CC2)C(CN2CCNCC2)=CC=C1F HFVRIZUVLXIFHQ-UHFFFAOYSA-N 0.000 description 1
- NMZCIWVFVPOFHJ-UHFFFAOYSA-N CC1=NNC2OC2C=C1C(F)(F)F Chemical compound CC1=NNC2OC2C=C1C(F)(F)F NMZCIWVFVPOFHJ-UHFFFAOYSA-N 0.000 description 1
- ZMOFUPQDQLIJKR-UHFFFAOYSA-N CCC(C(C(F)(F)F)=C1)=CN(C)C1=O Chemical compound CCC(C(C(F)(F)F)=C1)=CN(C)C1=O ZMOFUPQDQLIJKR-UHFFFAOYSA-N 0.000 description 1
- PAOOGVCBFBNTMC-UHFFFAOYSA-N CCCc(ccc(CN1CC[U]CC1)c1)c1-c(cc1NC(C(C=C2)=NNC2=O)=O)ccc1N1CCN(C)CC1 Chemical compound CCCc(ccc(CN1CC[U]CC1)c1)c1-c(cc1NC(C(C=C2)=NNC2=O)=O)ccc1N1CCN(C)CC1 PAOOGVCBFBNTMC-UHFFFAOYSA-N 0.000 description 1
- TXIOGJHPPVXTOY-UHFFFAOYSA-N CCN1CCN(C)CC1 Chemical compound CCN1CCN(C)CC1 TXIOGJHPPVXTOY-UHFFFAOYSA-N 0.000 description 1
- LGTLXDJOAJDFLR-UHFFFAOYSA-N CCOP(OCC)(Cl)=O Chemical compound CCOP(OCC)(Cl)=O LGTLXDJOAJDFLR-UHFFFAOYSA-N 0.000 description 1
- BORFGFHEWSBJEX-UHFFFAOYSA-N CCOc1nnc(C(O)=O)c(C(F)(F)F)c1 Chemical compound CCOc1nnc(C(O)=O)c(C(F)(F)F)c1 BORFGFHEWSBJEX-UHFFFAOYSA-N 0.000 description 1
- ZTRGJVYOKMWOJB-UHFFFAOYSA-N CN(CC1)CCN1c(c(N)c1)ccc1-c(cc(CN1CCOCC1)cc1)c1F Chemical compound CN(CC1)CCN1c(c(N)c1)ccc1-c(cc(CN1CCOCC1)cc1)c1F ZTRGJVYOKMWOJB-UHFFFAOYSA-N 0.000 description 1
- NXANRMPZLDQPRU-UHFFFAOYSA-N CN(CC1)CCN1c(c(N)cc(Br)c1)c1F Chemical compound CN(CC1)CCN1c(c(N)cc(Br)c1)c1F NXANRMPZLDQPRU-UHFFFAOYSA-N 0.000 description 1
- SUKAIFXEIYXZHH-UHFFFAOYSA-N CN(CC1)CCN1c(c(NC(C(C(C(F)(F)F)=C1)=CNC1=O)=O)c1)ccc1-c1cc(CNC(CC2)CCC2(F)F)ccc1F Chemical compound CN(CC1)CCN1c(c(NC(C(C(C(F)(F)F)=C1)=CNC1=O)=O)c1)ccc1-c1cc(CNC(CC2)CCC2(F)F)ccc1F SUKAIFXEIYXZHH-UHFFFAOYSA-N 0.000 description 1
- MGQFUFPRTPQGCE-UHFFFAOYSA-N CN(CC1)CCN1c(c(NC(C(C(C(F)(F)F)=C1)=NNC1=O)=O)c1)ccc1-c(cc(CN1CCOCC1)cc1)c1F Chemical compound CN(CC1)CCN1c(c(NC(C(C(C(F)(F)F)=C1)=NNC1=O)=O)c1)ccc1-c(cc(CN1CCOCC1)cc1)c1F MGQFUFPRTPQGCE-UHFFFAOYSA-N 0.000 description 1
- HWTLFOPXWFNIAJ-UHFFFAOYSA-N CN1C2CN(C)CC1CC2 Chemical compound CN1C2CN(C)CC1CC2 HWTLFOPXWFNIAJ-UHFFFAOYSA-N 0.000 description 1
- ZFWWWWCAJVNZPE-UHFFFAOYSA-N CN1CC(CC2)N2CC1 Chemical compound CN1CC(CC2)N2CC1 ZFWWWWCAJVNZPE-UHFFFAOYSA-N 0.000 description 1
- ATZWXDWXCISHBE-UHFFFAOYSA-N CN1CC(CCC2)N2CC1 Chemical compound CN1CC(CCC2)N2CC1 ATZWXDWXCISHBE-UHFFFAOYSA-N 0.000 description 1
- ONSOPKHJBVLVLA-UHFFFAOYSA-N CN1CC2(COC2)N(C)CC1 Chemical compound CN1CC2(COC2)N(C)CC1 ONSOPKHJBVLVLA-UHFFFAOYSA-N 0.000 description 1
- MFARBWYPQHXEEK-UHFFFAOYSA-N CN1CC2N(C)CCC2C1 Chemical compound CN1CC2N(C)CCC2C1 MFARBWYPQHXEEK-UHFFFAOYSA-N 0.000 description 1
- JNQDOBIXZRXNIQ-VYRBHSGPSA-N C[C@@H](C1)N(C)C(C)CN1C(CC(C(c(c(F)c1)ccc1C(N)=O)=C1)=C)=C1NC(C(C(C(F)(F)F)=C1)=CNC1=O)=O Chemical compound C[C@@H](C1)N(C)C(C)CN1C(CC(C(c(c(F)c1)ccc1C(N)=O)=C1)=C)=C1NC(C(C(C(F)(F)F)=C1)=CNC1=O)=O JNQDOBIXZRXNIQ-VYRBHSGPSA-N 0.000 description 1
- PPWOZUZOUBSKMC-DTWKUNHWSA-N C[C@@H](CN(C)C1)N(C)[C@@H]1C#C Chemical compound C[C@@H](CN(C)C1)N(C)[C@@H]1C#C PPWOZUZOUBSKMC-DTWKUNHWSA-N 0.000 description 1
- JFHIBLVJVBDEMD-FYZYNONXSA-N C[C@@H](CN(C)CC1)N1c(c(NC(C(C(C(F)(F)[Fm])=C1)=CNC1=O)=O)c1)ccc1-c1cc(CN2CCOCC2)ccc1F Chemical compound C[C@@H](CN(C)CC1)N1c(c(NC(C(C(C(F)(F)[Fm])=C1)=CNC1=O)=O)c1)ccc1-c1cc(CN2CCOCC2)ccc1F JFHIBLVJVBDEMD-FYZYNONXSA-N 0.000 description 1
- XVJRVYONDJGSLX-JAMMHHFISA-N C[C@@H]1N(C)C(C)CN(C)C1 Chemical compound C[C@@H]1N(C)C(C)CN(C)C1 XVJRVYONDJGSLX-JAMMHHFISA-N 0.000 description 1
- GTMHTXCHHZKEHH-CALCHBBNSA-N C[C@H](C1)N(C)[C@@H](C)CN1c(c(NC(C(C(C(F)(F)F)=C1)=CNC1=O)=O)c1)ccc1-c(cc(nc1)OCC2CC2)c1F Chemical compound C[C@H](C1)N(C)[C@@H](C)CN1c(c(NC(C(C(C(F)(F)F)=C1)=CNC1=O)=O)c1)ccc1-c(cc(nc1)OCC2CC2)c1F GTMHTXCHHZKEHH-CALCHBBNSA-N 0.000 description 1
- LJNXBBXOOOEVBP-AOOOYVTPSA-N C[C@H](C1)N(C)[C@@H](C)CN1c(c([N+]([O-])=O)c1)ccc1Br Chemical compound C[C@H](C1)N(C)[C@@H](C)CN1c(c([N+]([O-])=O)c1)ccc1Br LJNXBBXOOOEVBP-AOOOYVTPSA-N 0.000 description 1
- CRJVRDBFAYGWJT-UHFFFAOYSA-N Cc1cc(C(Nc2cc(-c(cc(CN3CCOCC3)cc3)c3F)ccc2N2CCN(C)CC2)=O)cc(C)c1F Chemical compound Cc1cc(C(Nc2cc(-c(cc(CN3CCOCC3)cc3)c3F)ccc2N2CCN(C)CC2)=O)cc(C)c1F CRJVRDBFAYGWJT-UHFFFAOYSA-N 0.000 description 1
- MEOHLGIHUVTTHK-UHFFFAOYSA-N Cc1ncc(C(O)=O)c(C(F)(F)F)c1 Chemical compound Cc1ncc(C(O)=O)c(C(F)(F)F)c1 MEOHLGIHUVTTHK-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
-
- 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
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/81—Amides; Imides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/81—Amides; Imides
- C07D213/82—Amides; Imides in position 3
-
- 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
- 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
- C07D235/24—Benzimidazoles; Hydrogenated benzimidazoles 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 in position 2
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
- C07D237/02—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings
- C07D237/06—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D237/10—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three 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
- C07D237/14—Oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
- C07D237/02—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings
- C07D237/06—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D237/10—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three 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
- C07D237/24—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/12—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms
- C07D295/135—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms with the ring nitrogen atoms and the substituent nitrogen atoms separated by carbocyclic rings or by carbon chains interrupted by carbocyclic rings
-
- 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
- C07D401/02—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
- C07D401/12—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 linked by a chain containing hetero atoms as chain links
-
- 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
- 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
-
- 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
- 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
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/10—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing aromatic 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/08—Bridged systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Epidemiology (AREA)
- Hematology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Oncology (AREA)
- Diabetes (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyrrole Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pyridine Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201662301678P | 2016-03-01 | 2016-03-01 | |
| US62/301,678 | 2016-03-01 | ||
| PCT/CA2017/050271 WO2017147701A1 (en) | 2016-03-01 | 2017-03-01 | Inhibitors of wdr5 protein-protein binding |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2019507179A true JP2019507179A (ja) | 2019-03-14 |
| JP2019507179A5 JP2019507179A5 (https=) | 2020-04-09 |
Family
ID=59743040
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2018546584A Pending JP2019507179A (ja) | 2016-03-01 | 2017-03-01 | Wdr5タンパク質−タンパク質結合の阻害剤 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US11174250B2 (https=) |
| EP (1) | EP3423437A4 (https=) |
| JP (1) | JP2019507179A (https=) |
| AU (1) | AU2017226005A1 (https=) |
| CA (1) | CA3015417A1 (https=) |
| WO (1) | WO2017147701A1 (https=) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2020532561A (ja) * | 2017-09-06 | 2020-11-12 | プロペロン セラピューティクス インコーポレイテッド | Wdr5タンパク質−タンパク質結合の阻害剤 |
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US11319299B2 (en) | 2016-03-01 | 2022-05-03 | Propellon Therapeutics Inc. | Substituted carboxamides as inhibitors of WDR5 protein-protein binding |
| KR20190084063A (ko) | 2016-10-28 | 2019-07-15 | 이칸 스쿨 오브 메디슨 엣 마운트 시나이 | Ezh2-매개성 암 치료용 조성물 및 방법 |
| WO2018106870A1 (en) | 2016-12-08 | 2018-06-14 | Icahn School Of Medicine At Mount Sinai | Compositions and methods for treating cdk4/6-mediated cancer |
| US10501466B2 (en) | 2017-09-19 | 2019-12-10 | Vanderbilt University | WDR5 inhibitors and modulators |
| JP2021515013A (ja) | 2018-03-06 | 2021-06-17 | アイカーン スクール オブ メディスン アット マウント シナイ | セリンスレオニンキナーゼ(akt)分解/破壊化合物および使用方法 |
| CN108715585A (zh) * | 2018-04-23 | 2018-10-30 | 中国药科大学 | 苯基联三氮唑类mll1-wdr5蛋白-蛋白相互作用抑制剂 |
| US10844044B2 (en) | 2018-06-14 | 2020-11-24 | Vanderbilt University | WDR5 inhibitors and modulators |
| EP3810145A4 (en) * | 2018-06-21 | 2022-06-01 | Icahn School of Medicine at Mount Sinai | Wd40 repeat domain protein 5 (wdr5) degradation / disruption compounds and methods of use |
| US10807959B2 (en) | 2018-08-16 | 2020-10-20 | Vanderbilt University | WDR5-MLL1 inhibitors and modulators |
| CN109734674B (zh) | 2019-02-26 | 2022-08-26 | 中国药科大学 | 苯胺类wdr5蛋白-蛋白相互作用抑制剂及其制法和用途 |
| JP7503851B2 (ja) | 2019-05-06 | 2024-06-21 | アイカーン スクール オブ メディスン アット マウント シナイ | Hpk1の分解剤としてのヘテロ二官能性化合物 |
| US12103924B2 (en) | 2020-06-01 | 2024-10-01 | Icahn School Of Medicine At Mount Sinai | Mitogen-activated protein kinase kinase (MEK) degradation compounds and methods of use |
| US20230286948A1 (en) * | 2022-03-14 | 2023-09-14 | Huyabio International, Llc | Haloalkylpyridyl triazole mll1-wdr5 protein-protein interaction inhibitor |
| CN119365449A (zh) * | 2022-07-01 | 2025-01-24 | 甘李药业股份有限公司 | 一种用作wdr5抑制剂的化合物或其可药用盐及其应用 |
| CN117486791A (zh) * | 2023-10-18 | 2024-02-02 | 南通敏言生物医药科技有限公司 | 一种5-甲氧基-4-(三氟甲基)吡啶-2-甲酸甲酯的合成方法 |
| WO2026058961A1 (en) | 2024-09-13 | 2026-03-19 | Alivexis, Inc. | Wdr5 inhibitors, compounds, pharmaceutical compositions, and methods of use thereof |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2014003124A1 (ja) * | 2012-06-28 | 2014-01-03 | 富士フイルム株式会社 | 新規なアミド誘導体またはその塩 |
| CN105175284A (zh) * | 2015-07-21 | 2015-12-23 | 中国药科大学 | 酰胺类化合物、制备方法及其医药用途 |
Family Cites Families (45)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR100354309B1 (ko) | 1993-11-12 | 2003-01-06 | 파마시아 앤드 업존 캄파니 | 피리미딘-티오알킬및알킬에테르화합물 |
| JPH0959236A (ja) | 1995-08-23 | 1997-03-04 | Dai Ichi Seiyaku Co Ltd | ベンズアミド化合物 |
| US20010051719A1 (en) | 1996-12-19 | 2001-12-13 | Smithkline Beecham P.L.C. | Novel compounds |
| US6541669B1 (en) | 1998-06-08 | 2003-04-01 | Theravance, Inc. | β2-adrenergic receptor agonists |
| DE19952146A1 (de) | 1999-10-29 | 2001-06-07 | Boehringer Ingelheim Pharma | Arylalkane, Arylalkene und Aryl-azaalkane, diese Verbindungen enthaltende Arzneimittel und Verfahren zu ihrer Herstellung |
| CN100355751C (zh) | 2000-03-29 | 2007-12-19 | 西克拉塞尔有限公司 | 2-取代的4-杂芳基-嘧啶、其组合物及其用途 |
| JP2002193938A (ja) * | 2000-12-01 | 2002-07-10 | Bayer Ag | 4−アリールピリジン誘導体 |
| EP1389194A2 (en) | 2001-04-27 | 2004-02-18 | Vertex Pharmaceuticals Incorporated | Inhibitors of bace |
| GB0215676D0 (en) | 2002-07-05 | 2002-08-14 | Novartis Ag | Organic compounds |
| CN1681487A (zh) | 2002-07-15 | 2005-10-12 | 美瑞德生物工程公司 | 化合物、组合物及其使用方法 |
| AU2003270489A1 (en) | 2002-09-09 | 2004-03-29 | Cellular Genomics, Inc. | 6-ARYL-IMIDAZO(1,2-a)PYRAZIN-8-YLAMINES, METHOD OF MAKING, AND METHOD OF USE THEREOF |
| GB0412072D0 (en) | 2004-05-28 | 2004-06-30 | Syngenta Participations Ag | Chemical compounds |
| RU2401265C2 (ru) | 2004-06-10 | 2010-10-10 | Айрм Ллк | Соединения и композиции в качестве ингибиторов протеинкиназы |
| WO2006081172A2 (en) | 2005-01-26 | 2006-08-03 | Irm Llc | Compounds and compositions as protein kinase inhibitors |
| WO2006124731A2 (en) | 2005-05-12 | 2006-11-23 | Irm Llc | Compounds and compositions as protein kinase inhibitors |
| DE102005022977A1 (de) | 2005-05-19 | 2006-12-07 | Merck Patent Gmbh | Phenylchinazolinderivate |
| US20070254894A1 (en) | 2006-01-10 | 2007-11-01 | Kane John L Jr | Novel small molecules with selective cytotoxicity against human microvascular endothelial cell proliferation |
| KR20080092412A (ko) | 2006-02-06 | 2008-10-15 | 아이알엠 엘엘씨 | 단백질 키나제 억제제로서의 화합물 및 조성물 |
| CA2644143C (en) | 2006-04-05 | 2013-10-01 | Novartis Ag | Combinations comprising bcr-abl/c-kit/pdgf-r tk inhibitors for treating cancer |
| CA2679659C (en) | 2007-03-01 | 2016-01-19 | Novartis Ag | Pim kinase inhibitors and methods of their use |
| BRPI0813356A2 (pt) | 2007-06-15 | 2014-12-30 | Irm Llc | Inibidores de proteína quinase e métodos para uso dos mesmos |
| CN101875617B (zh) | 2009-03-23 | 2015-05-20 | 中国医学科学院药物研究所 | 烷氧基取代芳环的氨甲酰基类芳酸化合物及其制法和用途 |
| MX2011011661A (es) | 2009-05-07 | 2011-11-18 | Astrazeneca Ab | Compuestos 1-cianoetilheterociclilcarboxamida sustituidos 750. |
| WO2011129936A2 (en) | 2010-04-16 | 2011-10-20 | Kinex Pharmaceuticals, Llc | Compositions and methods for the prevention and treatment of cancer |
| WO2011149874A2 (en) | 2010-05-26 | 2011-12-01 | Schering Corporation | N-phenyl imidazole carboxamide inhibitors of 3-phosphoinositide-dependent protein kinase-1 |
| WO2011156557A2 (en) | 2010-06-11 | 2011-12-15 | Thomas James B | Compounds active at the neurotensin receptor |
| WO2011159685A2 (en) | 2010-06-16 | 2011-12-22 | The Regents Of The University Of Michigan | Inhibition of wdr5 interaction with its binding partners and therapeutic methods |
| CN201802360U (zh) | 2010-06-29 | 2011-04-20 | 中国石油化工股份有限公司胜利油田分公司采油工艺研究院 | 曲柄无游梁抽油机 |
| WO2012066065A1 (en) | 2010-11-17 | 2012-05-24 | Novartis Ag | Phenyl-heteroaryl amine compounds and their uses |
| WO2014048878A1 (en) | 2012-09-26 | 2014-04-03 | Evotec (Uk) Ltd. | Phenyl- or pyridyl- pyrrolo[2,3b]pyrazine derivatives useful in the treatment or prevention of proliferative disorders or dysplasia |
| CA2887598A1 (en) | 2012-10-12 | 2014-04-17 | Takeda Pharmaceutical Company Limited | Cyclopropanamine compound and use thereof |
| US9079866B2 (en) | 2013-02-04 | 2015-07-14 | Janssen Pharmaceutica Nv | Flap modulators |
| CA2932353A1 (en) | 2013-12-13 | 2015-06-18 | Steven P. Treon | Methods to treat lymphoplasmacytic lymphoma |
| EP3079683A4 (en) | 2013-12-13 | 2017-12-20 | Dana-Farber Cancer Institute, Inc. | Methods to treat lymphoplasmacytic lymphoma |
| CN104926801B (zh) | 2014-03-22 | 2019-06-04 | 浙江大学 | 取代氮杂环类衍生物、含其的药物组合物及其在抗肿瘤中的应用 |
| CN105585565B (zh) | 2014-10-23 | 2019-10-01 | 中国医学科学院药物研究所 | 含2-苯胺基-4-噻唑基吡啶衍生物及其制法和药物组合物与用途 |
| CN105837575B (zh) | 2015-01-13 | 2019-01-15 | 四川大学 | 3-乙炔基吡唑并嘧啶衍生物及其制备方法和用途 |
| US11319299B2 (en) | 2016-03-01 | 2022-05-03 | Propellon Therapeutics Inc. | Substituted carboxamides as inhibitors of WDR5 protein-protein binding |
| IL302705A (en) | 2016-03-01 | 2023-07-01 | Immatics Biotechnologies Gmbh | Peptides, combinations of peptides, cell-based drugs for use in immunotherapy against bladder cancer and other types of cancer |
| WO2017221092A1 (en) | 2016-06-20 | 2017-12-28 | Novartis Ag | Triazolopyridine compounds and uses thereof |
| US10160763B2 (en) | 2016-09-13 | 2018-12-25 | Vanderbilt University | WDR5 inhibitors and modulators |
| WO2019046944A1 (en) | 2017-09-06 | 2019-03-14 | Propellon Therapeutics Inc. | INHIBITORS OF PROTEIN BINDING WDR5-PROTEIN |
| US10501466B2 (en) | 2017-09-19 | 2019-12-10 | Vanderbilt University | WDR5 inhibitors and modulators |
| WO2020086857A1 (en) | 2018-10-24 | 2020-04-30 | Vanderbilt University | Wdr5 inhibitors and modulators |
| WO2021026672A1 (en) | 2019-08-09 | 2021-02-18 | Novartis Ag | Heterocyclic wdr5 inhibitors as anti-cancer compounds |
-
2017
- 2017-03-01 JP JP2018546584A patent/JP2019507179A/ja active Pending
- 2017-03-01 US US16/080,851 patent/US11174250B2/en not_active Expired - Fee Related
- 2017-03-01 CA CA3015417A patent/CA3015417A1/en active Pending
- 2017-03-01 WO PCT/CA2017/050271 patent/WO2017147701A1/en not_active Ceased
- 2017-03-01 EP EP17759040.3A patent/EP3423437A4/en not_active Withdrawn
- 2017-03-01 AU AU2017226005A patent/AU2017226005A1/en not_active Abandoned
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2014003124A1 (ja) * | 2012-06-28 | 2014-01-03 | 富士フイルム株式会社 | 新規なアミド誘導体またはその塩 |
| CN105175284A (zh) * | 2015-07-21 | 2015-12-23 | 中国药科大学 | 酰胺类化合物、制备方法及其医药用途 |
Non-Patent Citations (1)
| Title |
|---|
| 長瀬 博, 最新 創薬化学 上巻, vol. 株式会社 テクノミック, JPN6021003924, 15 August 1998 (1998-08-15), pages 259 - 262, ISSN: 0004786116 * |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2020532561A (ja) * | 2017-09-06 | 2020-11-12 | プロペロン セラピューティクス インコーポレイテッド | Wdr5タンパク質−タンパク質結合の阻害剤 |
Also Published As
| Publication number | Publication date |
|---|---|
| US20190119264A1 (en) | 2019-04-25 |
| EP3423437A1 (en) | 2019-01-09 |
| EP3423437A4 (en) | 2019-07-24 |
| WO2017147701A1 (en) | 2017-09-08 |
| AU2017226005A1 (en) | 2018-09-06 |
| US11174250B2 (en) | 2021-11-16 |
| CA3015417A1 (en) | 2017-09-08 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US12264147B2 (en) | Substituted carboxamides as inhibitors of WDR5 protein-protein binding | |
| JP2019507179A (ja) | Wdr5タンパク質−タンパク質結合の阻害剤 | |
| JP6959248B2 (ja) | 癌治療用の4,6−ジヒドロピロロ[3,4−c]ピラゾール−5(1H)−カルボニトリル誘導体 | |
| JP5976778B2 (ja) | キナーゼ阻害剤としてのピラゾリル−ピリミジン誘導体 | |
| RU2743074C2 (ru) | Соединения, активные по отношению к бромодоменам | |
| JP6750806B2 (ja) | Cdk阻害剤としての置換型ヘテロシクリル誘導体 | |
| JP2020532561A (ja) | Wdr5タンパク質−タンパク質結合の阻害剤 | |
| KR20190112000A (ko) | Rho-키나아제 억제제로서 티로신 아마이드 유도체 | |
| AU2016352813A1 (en) | Novel pyrazolo pyrimidine derivatives | |
| KR20240127909A (ko) | Sos1 억제제로서의 아졸릴피리딘 피리다지논 아미드 | |
| CN109641909B (zh) | 雷帕霉素信号通路抑制剂的机理靶标及其治疗应用 | |
| CN115894376B (zh) | 一种芳香族酰胺类化合物、药物组合物及其用途 | |
| NZ717556B2 (en) | Spirocyclic compounds as tryptophan hydroxylase inhibitors |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20200228 |
|
| A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20200228 |
|
| A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20210114 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20210209 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20210510 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20211026 |
|
| A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20220126 |
|
| A02 | Decision of refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A02 Effective date: 20220531 |