JPWO2021170109A5 - - Google Patents
Download PDFInfo
- Publication number
- JPWO2021170109A5 JPWO2021170109A5 JP2022551553A JP2022551553A JPWO2021170109A5 JP WO2021170109 A5 JPWO2021170109 A5 JP WO2021170109A5 JP 2022551553 A JP2022551553 A JP 2022551553A JP 2022551553 A JP2022551553 A JP 2022551553A JP WO2021170109 A5 JPWO2021170109 A5 JP WO2021170109A5
- Authority
- JP
- Japan
- Prior art keywords
- amino
- difluorobenzyl
- indazol
- benzamide
- piperazin
- 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
- -1 N-(5-(3,5-difluorobenzyl)-1H-indazol-3-yl)-4-(4-((1-((2-(2,6-dioxopiperidin-3-yl)- 1,3-dioxoisoindolin-5-yl)methyl)azetidin-3-yl)methyl)piperazin-1-yl)-2-((tetrahydro-2H-pyran-4-yl)amino)benzamide Chemical compound 0.000 claims 22
- KXDAEFPNCMNJSK-UHFFFAOYSA-N Benzamide Chemical compound NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 claims 18
- 150000003839 salts Chemical class 0.000 claims 13
- 150000001875 compounds Chemical class 0.000 claims 8
- 125000006716 (C1-C6) heteroalkyl group Chemical group 0.000 claims 4
- 201000010099 disease Diseases 0.000 claims 4
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 4
- 230000001404 mediated effect Effects 0.000 claims 4
- 206010028980 Neoplasm Diseases 0.000 claims 3
- 201000011510 cancer Diseases 0.000 claims 3
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims 2
- 125000006714 (C3-C10) heterocyclyl group Chemical group 0.000 claims 2
- 125000001313 C5-C10 heteroaryl group Chemical group 0.000 claims 2
- 208000002193 Pain Diseases 0.000 claims 2
- 125000003545 alkoxy group Chemical group 0.000 claims 2
- 125000000217 alkyl group Chemical group 0.000 claims 2
- 125000004452 carbocyclyl group Chemical group 0.000 claims 2
- QFJRNHWITCOYTM-UHFFFAOYSA-N C(C1=CC=2C(=O)N(C(=O)C=2C=C1)C1C(=O)NC(=O)CC1)N1CCC(CC1)N1CCN(CC1)C1=CC=C(C(=O)NC=2C3=CC(CC4=CC(=CC(=C4)F)F)=CC=C3NN=2)C(NC2CCOCC2)=C1 Chemical compound C(C1=CC=2C(=O)N(C(=O)C=2C=C1)C1C(=O)NC(=O)CC1)N1CCC(CC1)N1CCN(CC1)C1=CC=C(C(=O)NC=2C3=CC(CC4=CC(=CC(=C4)F)F)=CC=C3NN=2)C(NC2CCOCC2)=C1 QFJRNHWITCOYTM-UHFFFAOYSA-N 0.000 claims 1
- 208000000094 Chronic Pain Diseases 0.000 claims 1
- QRPAHVGMUMOIKN-UHFFFAOYSA-N O=C(C(C(NC1CCOCC1)=C1)=CC=C1N(CC1)CCN1C(C1)CC1(CC1)CN1C(C=C1)=CC(C(N2C(CCC(N3)=O)C3=O)=O)=C1C2=O)NC1=NNC2=CC=C(CC3=CC(F)=CC(F)=C3)C=C12 Chemical compound O=C(C(C(NC1CCOCC1)=C1)=CC=C1N(CC1)CCN1C(C1)CC1(CC1)CN1C(C=C1)=CC(C(N2C(CCC(N3)=O)C3=O)=O)=C1C2=O)NC1=NNC2=CC=C(CC3=CC(F)=CC(F)=C3)C=C12 QRPAHVGMUMOIKN-UHFFFAOYSA-N 0.000 claims 1
- KMSVJJXKUAZDSE-UHFFFAOYSA-N O=C(C(C(NC1CCOCC1)=C1)=CC=C1N(CC1)CCN1C(CC1)CCN1C(C=C1)=CC(C(N2C(CCC(N3)=O)C3=O)=O)=C1C2=O)NC1=NNC2=CC=C(CC3=CC(F)=CC(F)=C3)C=C12 Chemical compound O=C(C(C(NC1CCOCC1)=C1)=CC=C1N(CC1)CCN1C(CC1)CCN1C(C=C1)=CC(C(N2C(CCC(N3)=O)C3=O)=O)=C1C2=O)NC1=NNC2=CC=C(CC3=CC(F)=CC(F)=C3)C=C12 KMSVJJXKUAZDSE-UHFFFAOYSA-N 0.000 claims 1
- YCPLUHIVFNQIAA-UHFFFAOYSA-N O=C(C(C(NC1CCOCC1)=C1)=CC=C1N(CC1)CCN1C1CN(CC(C=C2C(N3C(CCC(N4)=O)C4=O)=O)=CC=C2C3=O)CCC1)NC1=NNC2=CC=C(CC3=CC(F)=CC(F)=C3)C=C12 Chemical compound O=C(C(C(NC1CCOCC1)=C1)=CC=C1N(CC1)CCN1C1CN(CC(C=C2C(N3C(CCC(N4)=O)C4=O)=O)=CC=C2C3=O)CCC1)NC1=NNC2=CC=C(CC3=CC(F)=CC(F)=C3)C=C12 YCPLUHIVFNQIAA-UHFFFAOYSA-N 0.000 claims 1
- IOEDKYXHTFGJII-UHFFFAOYSA-N O=C(C(C(NC1CCOCC1)=C1)=CC=C1N1CCN(CC(C2)OCCN2C(C=C2C(N3C(CCC(N4)=O)C4=O)=O)=CC=C2C3=O)CC1)NC1=NNC2=CC=C(CC3=CC(F)=CC(F)=C3)C=C12 Chemical compound O=C(C(C(NC1CCOCC1)=C1)=CC=C1N1CCN(CC(C2)OCCN2C(C=C2C(N3C(CCC(N4)=O)C4=O)=O)=CC=C2C3=O)CC1)NC1=NNC2=CC=C(CC3=CC(F)=CC(F)=C3)C=C12 IOEDKYXHTFGJII-UHFFFAOYSA-N 0.000 claims 1
- WVCMDDNYBQWYHE-UHFFFAOYSA-N O=C(C(C(NCCF)=C1)=CC=C1N1CCN(CC(C2)CN2C(C=C2)=CC(C(N3C(CCC(N4)=O)C4=O)=O)=C2C3=O)CC1)NC1=NNC2=CC=C(CC3=CC(F)=CC(F)=C3)C=C12 Chemical compound O=C(C(C(NCCF)=C1)=CC=C1N1CCN(CC(C2)CN2C(C=C2)=CC(C(N3C(CCC(N4)=O)C4=O)=O)=C2C3=O)CC1)NC1=NNC2=CC=C(CC3=CC(F)=CC(F)=C3)C=C12 WVCMDDNYBQWYHE-UHFFFAOYSA-N 0.000 claims 1
- WWZSCXKSVMAKTD-UHFFFAOYSA-N O=C(C(C=C1)=CC=C1N1CCN(CC(C2)CN2C(C=C2C(N3C(CCC(N4)=O)C4=O)=O)=CC=C2C3=O)CC1)NC1=NNC2=CC=C(CC3=CC(F)=CC(F)=C3)C=C12 Chemical compound O=C(C(C=C1)=CC=C1N1CCN(CC(C2)CN2C(C=C2C(N3C(CCC(N4)=O)C4=O)=O)=CC=C2C3=O)CC1)NC1=NNC2=CC=C(CC3=CC(F)=CC(F)=C3)C=C12 WWZSCXKSVMAKTD-UHFFFAOYSA-N 0.000 claims 1
- CIGKQAWSXVQMGA-UHFFFAOYSA-N O=C(C(C=C1)=CC=C1N1CCN(CCNC(C=C2)=CC(C(N3C(CCC(N4)=O)C4=O)=O)=C2C3=O)CC1)NC1=NNC2=CC=C(CC3=CC(F)=CC(F)=C3)C=C12 Chemical compound O=C(C(C=C1)=CC=C1N1CCN(CCNC(C=C2)=CC(C(N3C(CCC(N4)=O)C4=O)=O)=C2C3=O)CC1)NC1=NNC2=CC=C(CC3=CC(F)=CC(F)=C3)C=C12 CIGKQAWSXVQMGA-UHFFFAOYSA-N 0.000 claims 1
- DGQYLRDJYAWVJG-UHFFFAOYSA-N O=C(CNC(C=C1)=CC(C(N2C(CCC(N3)=O)C3=O)=O)=C1C2=O)N(CC1)CCN1C(C=C1)=CC=C1C(NC1=NNC2=CC=C(CC3=CC(F)=CC(F)=C3)C=C12)=O Chemical compound O=C(CNC(C=C1)=CC(C(N2C(CCC(N3)=O)C3=O)=O)=C1C2=O)N(CC1)CCN1C(C=C1)=CC=C1C(NC1=NNC2=CC=C(CC3=CC(F)=CC(F)=C3)C=C12)=O DGQYLRDJYAWVJG-UHFFFAOYSA-N 0.000 claims 1
- PHJNHVUVPFJGMV-UHFFFAOYSA-N O=C(CNC(C=C1)=CC(C(N2C(CCC(N3)=O)C3=O)=O)=C1C2=O)N(CC1)CCN1C1=CC=C(C(NC2=NNC3=CC=C(CC4=CC(F)=CC(F)=C4)C=C23)=O)C(NCCF)=C1 Chemical compound O=C(CNC(C=C1)=CC(C(N2C(CCC(N3)=O)C3=O)=O)=C1C2=O)N(CC1)CCN1C1=CC=C(C(NC2=NNC3=CC=C(CC4=CC(F)=CC(F)=C4)C=C23)=O)C(NCCF)=C1 PHJNHVUVPFJGMV-UHFFFAOYSA-N 0.000 claims 1
- 208000003251 Pruritus Diseases 0.000 claims 1
- 108091005682 Receptor kinases Proteins 0.000 claims 1
- DHXVGJBLRPWPCS-UHFFFAOYSA-N Tetrahydropyran Chemical compound C1CCOCC1 DHXVGJBLRPWPCS-UHFFFAOYSA-N 0.000 claims 1
- 102000005937 Tropomyosin Human genes 0.000 claims 1
- 108010030743 Tropomyosin Proteins 0.000 claims 1
- 208000005298 acute pain Diseases 0.000 claims 1
- 125000004567 azetidin-3-yl group Chemical group N1CC(C1)* 0.000 claims 1
- 238000002512 chemotherapy Methods 0.000 claims 1
- 239000003085 diluting agent Substances 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 230000004927 fusion Effects 0.000 claims 1
- 229910052736 halogen Inorganic materials 0.000 claims 1
- 150000002367 halogens Chemical class 0.000 claims 1
- 238000001794 hormone therapy Methods 0.000 claims 1
- 238000009169 immunotherapy Methods 0.000 claims 1
- 208000027866 inflammatory disease Diseases 0.000 claims 1
- 230000035772 mutation Effects 0.000 claims 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 1
- 238000001959 radiotherapy Methods 0.000 claims 1
- 125000003107 substituted aryl group Chemical group 0.000 claims 1
- 238000011285 therapeutic regimen Methods 0.000 claims 1
- 238000011282 treatment Methods 0.000 claims 1
- 238000011269 treatment regimen Methods 0.000 claims 1
Claims (15)
X1とX2は、独立してCHおよびNから選択され、
X3とX4は、独立してC(O)およびCR4R5から選択され、
R1は、H、-NR2R3、ハロゲン、任意選択で置換されたC1-6アルキル、任意選択で置換されたC1-C6ヘテロアルキル、任意選択で置換されたC3-10カルボシクリル、任意選択で置換された3~10員ヘテロシクリル、任意選択で置換された5~10員ヘテロアリール、任意選択で置換されたアリール、任意選択で置換されたC1-6ヘテロアルキル、任意選択で置換されたC1-6ハロアルキル、および任意選択で置換されたC1-6アルコキシから選択され、
R2、R3、R4、およびR5は、独立してH、任意選択で置換されたC1-6アルキル、任意選択で置換されたC1-C6ヘテロアルキル、任意選択で置換されたC3-10カルボシクリル、任意選択で置換された3~10員ヘテロシクリル、任意選択で置換された5~10員ヘテロアリール、任意選択で置換されたC1-6ヘテロアルキル、任意選択で置換されたC1-6ハロアルキル、および任意選択で置換されたC1-6アルコキシから選択され、ならびに
Lは、単結合、
X3とX4のうち一方はC(O)であり、他方はCR4R5であり、ならびに
Lは、
X 1 and X 2 are independently selected from CH and N;
X3 and X4 are independently selected from C(O) and CR4R5 ,
R 1 is H, -NR 2 R 3 , halogen, optionally substituted C 1-6 alkyl, optionally substituted C 1 -C 6 heteroalkyl, optionally substituted C 3-10 carbocyclyl, optionally substituted 3-10 membered heterocyclyl, optionally substituted 5-10 membered heteroaryl, optionally substituted aryl, optionally substituted C 1-6 heteroalkyl, optionally substituted selected from C 1-6 haloalkyl substituted with, and C 1-6 alkoxy optionally substituted with
R 2 , R 3 , R 4 , and R 5 are independently H, optionally substituted C 1-6 alkyl, optionally substituted C 1 -C 6 heteroalkyl, optionally substituted optionally substituted C 3-10 carbocyclyl, optionally substituted 3-10 membered heterocyclyl, optionally substituted 5-10 membered heteroaryl, optionally substituted C 1-6 heteroalkyl, optionally substituted selected from C 1-6 haloalkyl, and optionally substituted C 1-6 alkoxy, and L is a single bond,
N-(5-(3,5-ジフルオロベンジル)-1H-インダゾール-3-イル)-4-(4-((1-((2-(2,6-ジオキソピペリジン-3-イル)-1,3-ジオキソイソインドリン-5-イル)メチル)アゼチジン-3-イル)ピペラジン-1-イル)-2-((テトラヒドロ-2H-ピラン-4-イル)アミノ)ベンズアミド、
N-(5-(3,5-ジフルオロベンジル)-1H-インダゾール-3-イル)-4-(4-(2-((2-(2,6-ジオキソピペリジン-3-イル)-1,3-ジオキソイソインドリン-5-イル)アミノ)エチル)ピペラジン-1-イル)ベンズアミド、
N-(5-(3,5-ジフルオロベンジル)-1H-インダゾール-3-イル)-4-(4-((2-(2,6-ジオキソピペリジン-3-イル)-1,3-ジオキソイソインドリン-5-イル)グリシル)ピペラジン-1-イル)ベンズアミド、
N-(5-(3,5-ジフルオロベンジル)-1H-インダゾール-3-イル)-4-(4-((1-(2-(2,6-ジオキソピペリジン-3-イル)-1,3-ジオキソイソインドリン-5-イル)アゼチジン-3-イル)メチル)ピペラジン-1-イル)ベンズアミド、
N-(5-(3,5-ジフルオロベンジル)-1H-インダゾール-3-イル)-4-(4-((2-(2,6-ジオキソピペリジン-3-イル)-1,3-ジオキソイソインドリン-5-イル)グリシル)ピペラジン-1-イル)-2-((2-フルオロエチル)アミノ)ベンズアミド、
N-(5-(3,5-ジフルオロベンジル)-1H-インダゾール-3-イル)-4-(4-((1-(2-(2,6-ジオキソピペリジン-3-イル)-1,3-ジオキソイソインドリン-5-イル)アゼチジン-3-イル)メチル)ピペラジン-1-イル)-2-((2-フルオロエチル)アミノ)ベンズアミド、
N-(5-(3,5-ジフルオロベンジル)-1H-インダゾール-3-イル)-4-(4-((1-(2-(2,6-ジオキソピペリジン-3-イル)-1,3-ジオキソイソインドリン-5-イル)ピロリジン-3-イル)メチル)ピペラジン-1-イル)-2-((テトラヒドロ-2H-ピラン-4-イル)アミノ)ベンズアミド、
N-(5-(3,5-ジフルオロベンジル)-1H-インダゾール-3-イル)-4-(4-(1-(2-(2,6-ジオキソピペリジン-3-イル)-1,3-ジオキソイソインドリン-5-イル)アゼチジン-3-イル)ピペラジン-1-イル)-2-((テトラヒドロ-2H-ピラン-4-イル)アミノ)ベンズアミド、
N-(5-(3,5-ジフルオロベンジル)-1H-インダゾール-3-イル)-4-(4-(3-(2-(2,6-ジオキソピペリジン-3-イル)-1,3-ジオキソイソインドリン-5-イル)プロピル)ピペラジン-1-イル)-2-((テトラヒドロ-2H-ピラン-4-イル)アミノ)ベンズアミド、
N-(5-(3,5-ジフルオロベンジル)-1H-インダゾール-3-イル)-4-(4-(1-((2-(2,6-ジオキソピペリジン-3-イル)-1,3-ジオキソイソインドリン-5-イル)メチル)ピペリジン-3-イル)ピペラジン-1-イル)-2-((テトラヒドロ-2H-ピラン-4-イル)アミノ)ベンズアミド、
N-(5-(3,5-ジフルオロベンジル)-1H-インダゾール-3-イル)-4-(4-(1-(2-(2,6-ジオキソピペリジン-3-イル)-1,3-ジオキソイソインドリン-5-イル)ピペリジン-4-イル)ピペラジン-1-イル)-2-((テトラヒドロ-2H-ピラン-4-イル)アミノ)ベンズアミド、
N-(5-(3,5-ジフルオロベンジル)-1H-インダゾール-3-イル)-4-(4-(1-((2-(2,6-ジオキソピペリジン-3-イル)-1,3-ジオキソイソインドリン-5-イル)メチル)ピペリジン-4-イル)ピペラジン-1-イル)-2-((テトラヒドロ-2H-ピラン-4-イル)アミノ)ベンズアミド、
N-(5-(3,5-ジフルオロベンジル)-1H-インダゾール-3-イル)-4-(4-((4-(2-(2,6-ジオキソピペリジン-3-イル)-1,3-ジオキソイソインドリン-5-イル)モルホリン-2-イル)メチル)ピペラジン-1-イル)-2-((テトラヒドロ-2H-ピラン-4-イル)アミノ)ベンズアミド、
N-(5-(3,5-ジフルオロベンジル)-1H-インダゾール-3-イル)-4-(4-(1-(2-(2,6-ジオキソピペリジン-3-イル)-1,3-ジオキソイソインドリン-5-イル)ピロリジン-3-イル)ピペラジン-1-イル)-2-((テトラヒドロ-2H-ピラン-4-イル)アミノ)ベンズアミド、
N-(5-(3,5-ジフルオロベンジル)-1H-インダゾール-3-イル)-4-(4-(1-((2-(2,6-ジオキソピペリジン-3-イル)-1,3-ジオキソイソインドリン-5-イル)メチル)ピロリジン-3-イル)ピペラジン-1-イル)-2-((テトラヒドロ-2H-ピラン-4-イル)アミノ)ベンズアミド、
N-(5-(3,5-ジフルオロベンジル)-1H-インダゾール-3-イル)-4-(4-(6-(2-(2,6-ジオキソピペリジン-3-イル)-1,3-ジオキソイソインドリン-5-イル)-6-アザスピロ[3.4]オクタン-2-イル)ピペラジン-1-イル)-2-((テトラヒドロ-2H-ピラン-4-イル)アミノ)ベンズアミド、
N-(5-(3,5-ジフルオロベンジル)-1H-インダゾール-3-イル)-4-(4-(1-(1-(2-(2,6-ジオキソピペリジン-3-イル)-1,3-ジオキソイソインドリン-5-イル)アゼチジン-3-イル)エチル)ピペラジン-1-イル)-2-((テトラヒドロ-2H-ピラン-4-イル)アミノ)ベンズアミド、
N-(5-(3,5-ジフルオロベンジル)-1H-インダゾール-3-イル)-4-(4-(4-(1-(2,6-ジオキソピペリジン-3-イル)-3-メチル-2-オキソ-2,3-ジヒドロ-1H-ベンゾ[d]イミダゾール-4-イル)ブチル)ピペラジン-1-イル)-2-((テトラヒドロ-2H-ピラン-4-イル)アミノ)ベンズアミド、
N-(5-(3,5-ジフルオロベンジル)-1H-インダゾール-3-イル)-4-(4-(4-(1-(2,6-ジオキソピペリジン-3-イル)-3-メチル-2-オキソ-2,3-ジヒドロ-1H-ベンゾ[d]イミダゾール-4-イル)ブタ-3-イン-1-イル)ピペラジン-1-イル)-2-((テトラヒドロ-2H-ピラン-4-イル)アミノ)ベンズアミド、
N-(5-(3,5-ジフルオロベンジル)-1H-インダゾール-3-イル)-4-(4-(3-((1-(2,6-ジオキソピペリジン-3-イル)-3-メチル-2-オキソ-2,3-ジヒドロ-1H-ベンゾ[d]イミダゾール-4-イル)アミノ)プロピル)ピペラジン-1-イル)-2-((テトラヒドロ-2H-ピラン-4-イル)アミノ)ベンズアミド、
N-(5-(3,5-ジフルオロベンジル)-1H-インダゾール-3-イル)-4-(4-(3-((1-(2,6-ジオキソピペリジン-3-イル)-3-メチル-2-オキソ-2,3-ジヒドロ-1H-ベンゾ[d]イミダゾール-5-イル)アミノ)プロピル)ピペラジン-1-イル)-2-((テトラヒドロ-2H-ピラン-4-イル)アミノ)ベンズアミド、
N-(5-(3,5-ジフルオロベンジル)-1H-インダゾール-3-イル)-4-(4-((1-(2-(2,6-ジオキソピペリジン-3-イル)-3-オキソイソインドリン-5-イル)アゼチジン-3-イル)メチル)ピペラジン-1-イル)-2-((テトラヒドロ-2H-ピラン-4-イル)アミノ)ベンズアミド、
N-(5-(3,5-ジフルオロベンジル)-1H-インダゾール-3-イル)-4-(4-(4-(1-(2,6-ジオキソピペリジン-3-イル)-3-メチル-2-オキソ-2,3-ジヒドロ-1H-ベンゾ[d]イミダゾール-5-イル)ブタ-3-イン-1-イル)ピペラジン-1-イル)-2-((テトラヒドロ-2H-ピラン-4-イル)アミノ)ベンズアミド、
N-(5-(3,5-ジフルオロベンジル)-1H-インダゾール-3-イル)-4-(4-(4-(1-(2,6-ジオキソピペリジン-3-イル)-3-メチル-2-オキソ-2,3-ジヒドロ-1H-ベンゾ[d]イミダゾール-5-イル)ブチル)ピペラジン-1-イル)-2-((テトラヒドロ-2H-ピラン-4-イル)アミノ)ベンズアミド、
N-(5-(3,5-ジフルオロベンジル)-1H-インダゾール-3-イル)-4-(4-((1-(1-(2,6-ジオキソピペリジン-3-イル)-3-メチル-2-オキソ-2,3-ジヒドロ-1H-ベンゾ[d]イミダゾール-5-イル)アゼチジン-3-イル)メチル)ピペラジン-1-イル)-2-((テトラヒドロ-2H-ピラン-4-イル)アミノ)ベンズアミド、
N-(5-(3,5-ジフルオロベンジル)-1H-インダゾール-3-イル)-4-(4-(2-((1-(2,6-ジオキソピペリジン-3-イル)-3-メチル-2-オキソ-2,3-ジヒドロ-1H-ベンゾ[d]イミダゾール-5-イル)アミノ)エチル)ピペラジン-1-イル)-2-((テトラヒドロ-2H-ピラン-4-イル)アミノ)ベンズアミド、
N-(5-(3,5-ジフルオロベンジル)-1H-インダゾール-3-イル)-4-(4-(2-((1-(2,6-ジオキソピペリジン-3-イル)-3-メチル-2-オキソ-2,3-ジヒドロ-1H-ベンゾ[d]イミダゾール-4-イル)アミノ)エチル)ピペラジン-1-イル)-2-((テトラヒドロ-2H-ピラン-4-イル)アミノ)ベンズアミド、
N-(5-(3,5-ジフルオロベンジル)-1H-インダゾール-3-イル)-4-(4-(1-(2-(2,6-ジオキソピペリジン-3-イル)-1-オキソイソインドリン-5-イル)アゼチジン-3-イル)ピペラジン-1-イル)-2-((テトラヒドロ-2H-ピラン-4-イル)アミノ)ベンズアミド、
N-(5-(3,5-ジフルオロベンジル)-1H-インダゾール-3-イル)-4-(4-(1-(2-(2,6-ジオキソピペリジン-3-イル)-3-オキソイソインドリン-5-イル)アゼチジン-3-イル)ピペラジン-1-イル)-2-((テトラヒドロ-2H-ピラン-4-イル)アミノ)ベンズアミド、
N-(5-(3,5-ジフルオロベンジル)-1H-インダゾール-3-イル)-4-(4-((1-(2-(2,6-ジオキソピペリジン-3-イル)-1,3-ジオキソイソインドリン-5-イル)アゼチジン-3-イル)アミノ)ピペリジン-1-イル)-2-((テトラヒドロ-2H-ピラン-4-イル)アミノ)ベンズアミド、
N-(5-(3,5-ジフルオロベンジル)-1H-インダゾール-3-イル)-4-(4-(3-(2-(2,6-ジオキソピペリジン-3-イル)-1-オキソイソインドリン-5-イル)アゼチジン-1-イル)ピペリジン-1-イル)-2-((テトラヒドロ-2H-ピラン-4-イル)アミノ)ベンズアミド、
N-(5-(3,5-ジフルオロベンジル)-1H-インダゾール-3-イル)-4-(4-(3-(2-(2,6-ジオキソピペリジン-3-イル)-1,3-ジオキソイソインドリン-5-イル)アゼチジン-1-イル)ピペリジン-1-イル)-2-((テトラヒドロ-2H-ピラン-4-イル)アミノ)ベンズアミド、
N-(5-(3,5-ジフルオロベンジル)-1H-インダゾール-3-イル)-4-(4-(6-(2-(2,6-ジオキソピペリジン-3-イル)-1,3-ジオキソイソインドリン-5-イル)-2,6-ジアザスピロ[3.3]ヘプタン-2-イル)ピペリジン-1-イル)-2-((テトラヒドロ-2H-ピラン-4-イル)アミノ)ベンズアミド、
(S)-N-(5-(3,5-ジフルオロベンジル)-1H-インダゾール-3-イル)-4-(4-((1-(2-(2,6-ジオキソピペリジン-3-イル)-1,3-ジオキソイソインドリン-5-イル)アゼチジン-3-イル)メチル)ピペラジン-1-イル)-2-((テトラヒドロ-2H-ピラン-4-イル)アミノ)ベンズアミド、
(R)-N-(5-(3,5-ジフルオロベンジル)-1H-インダゾール-3-イル)-4-(4-((1-(2-(2,6-ジオキソピペリジン-3-イル)-1,3-ジオキソイソインドリン-5-イル)アゼチジン-3-イル)メチル)ピペラジン-1-イル)-2-((テトラヒドロ-2H-ピラン-4-イル)アミノ)ベンズアミド、
(S)-N-(5-(3,5-ジフルオロベンジル)-1H-インダゾール-3-イル)-4-(4-(1-(2-(2,6-ジオキソピペリジン-3-イル)-1,3-ジオキソイソインドリン-5-イル)アゼチジン-3-イル)ピペラジン-1-イル)-2-((テトラヒドロ-2H-ピラン-4-イル)アミノ)ベンズアミド、および
(R)-N-(5-(3,5-ジフルオロベンジル)-1H-インダゾール-3-イル)-4-(4-(1-(2-(2,6-ジオキソピペリジン-3-イル)-1,3-ジオキソイソインドリン-5-イル)アゼチジン-3-イル)ピペラジン-1-イル)-2-((テトラヒドロ-2H-ピラン-4-イル)アミノ)ベンズアミド
からなる群から選択される二価化合物、またはその薬学的に許容可能な塩。 N-(5-(3,5-difluorobenzyl)-1H-indazol-3-yl)-4-(4-((1-((2-(2,6-dioxopiperidin-3-yl)- 1,3-dioxoisoindolin-5-yl)methyl)azetidin-3-yl)methyl)piperazin-1-yl)-2-((tetrahydro-2H-pyran-4-yl)amino)benzamide,
N-(5-(3,5-difluorobenzyl)-1H-indazol-3-yl)-4-(4-((1-((2-(2,6-dioxopiperidin-3-yl)- 1,3-dioxoisoindolin-5-yl)methyl)azetidin-3-yl)piperazin-1-yl)-2-((tetrahydro-2H-pyran-4-yl)amino)benzamide,
N-(5-(3,5-difluorobenzyl)-1H-indazol-3-yl)-4-(4-(2-((2-(2,6-dioxopiperidin-3-yl)-1 ,3-dioxoisoindolin-5-yl)amino)ethyl)piperazin-1-yl)benzamide,
N-(5-(3,5-difluorobenzyl)-1H-indazol-3-yl)-4-(4-((2-(2,6-dioxopiperidin-3-yl)-1,3- dioxoisoindolin-5-yl)glycyl)piperazin-1-yl)benzamide,
N-(5-(3,5-difluorobenzyl)-1H-indazol-3-yl)-4-(4-((1-(2-(2,6-dioxopiperidin-3-yl)-1 , 3-dioxoisoindolin-5-yl)azetidin-3-yl)methyl)piperazin-1-yl)benzamide,
N-(5-(3,5-difluorobenzyl)-1H-indazol-3-yl)-4-(4-((2-(2,6-dioxopiperidin-3-yl)-1,3- dioxoisoindolin-5-yl)glycyl)piperazin-1-yl)-2-((2-fluoroethyl)amino)benzamide,
N-(5-(3,5-difluorobenzyl)-1H-indazol-3-yl)-4-(4-((1-(2-(2,6-dioxopiperidin-3-yl)-1 ,3-dioxoisoindolin-5-yl)azetidin-3-yl)methyl)piperazin-1-yl)-2-((2-fluoroethyl)amino)benzamide,
N-(5-(3,5-difluorobenzyl)-1H-indazol-3-yl)-4-(4-((1-(2-(2,6-dioxopiperidin-3-yl)-1 ,3-dioxoisoindolin-5-yl)pyrrolidin-3-yl)methyl)piperazin-1-yl)-2-((tetrahydro-2H-pyran-4-yl)amino)benzamide,
N-(5-(3,5-difluorobenzyl)-1H-indazol-3-yl)-4-(4-(1-(2-(2,6-dioxopiperidin-3-yl)-1, 3-dioxoisoindolin-5-yl)azetidin-3-yl)piperazin-1-yl)-2-((tetrahydro-2H-pyran-4-yl)amino)benzamide,
N-(5-(3,5-difluorobenzyl)-1H-indazol-3-yl)-4-(4-(3-(2-(2,6-dioxopiperidin-3-yl)-1, 3-dioxoisoindolin-5-yl)propyl)piperazin-1-yl)-2-((tetrahydro-2H-pyran-4-yl)amino)benzamide,
N-(5-(3,5-difluorobenzyl)-1H-indazol-3-yl)-4-(4-(1-((2-(2,6-dioxopiperidin-3-yl)-1 ,3-dioxoisoindolin-5-yl)methyl)piperidin-3-yl)piperazin-1-yl)-2-((tetrahydro-2H-pyran-4-yl)amino)benzamide,
N-(5-(3,5-difluorobenzyl)-1H-indazol-3-yl)-4-(4-(1-(2-(2,6-dioxopiperidin-3-yl)-1, 3-dioxoisoindolin-5-yl)piperidin-4-yl)piperazin-1-yl)-2-((tetrahydro-2H-pyran-4-yl)amino)benzamide,
N-(5-(3,5-difluorobenzyl)-1H-indazol-3-yl)-4-(4-(1-((2-(2,6-dioxopiperidin-3-yl)-1 ,3-dioxoisoindolin-5-yl)methyl)piperidin-4-yl)piperazin-1-yl)-2-((tetrahydro-2H-pyran-4-yl)amino)benzamide,
N-(5-(3,5-difluorobenzyl)-1H-indazol-3-yl)-4-(4-((4-(2-(2,6-dioxopiperidin-3-yl)-1 ,3-dioxoisoindolin-5-yl)morpholin-2-yl)methyl)piperazin-1-yl)-2-((tetrahydro-2H-pyran-4-yl)amino)benzamide,
N-(5-(3,5-difluorobenzyl)-1H-indazol-3-yl)-4-(4-(1-(2-(2,6-dioxopiperidin-3-yl)-1, 3-dioxoisoindolin-5-yl)pyrrolidin-3-yl)piperazin-1-yl)-2-((tetrahydro-2H-pyran-4-yl)amino)benzamide,
N-(5-(3,5-difluorobenzyl)-1H-indazol-3-yl)-4-(4-(1-((2-(2,6-dioxopiperidin-3-yl)-1 ,3-dioxoisoindolin-5-yl)methyl)pyrrolidin-3-yl)piperazin-1-yl)-2-((tetrahydro-2H-pyran-4-yl)amino)benzamide,
N-(5-(3,5-difluorobenzyl)-1H-indazol-3-yl)-4-(4-(6-(2-(2,6-dioxopiperidin-3-yl)-1, 3-dioxoisoindolin-5-yl)-6-azaspiro[3.4]octan-2-yl)piperazin-1-yl)-2-((tetrahydro-2H-pyran-4-yl)amino)benzamide ,
N-(5-(3,5-difluorobenzyl)-1H-indazol-3-yl)-4-(4-(1-(1-(2-(2,6-dioxopiperidin-3-yl) -1,3-dioxoisoindolin-5-yl)azetidin-3-yl)ethyl)piperazin-1-yl)-2-((tetrahydro-2H-pyran-4-yl)amino)benzamide,
N-(5-(3,5-difluorobenzyl)-1H-indazol-3-yl)-4-(4-(4-(1-(2,6-dioxopiperidin-3-yl)-3- Methyl-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-4-yl)butyl)piperazin-1-yl)-2-((tetrahydro-2H-pyran-4-yl)amino)benzamide ,
N-(5-(3,5-difluorobenzyl)-1H-indazol-3-yl)-4-(4-(4-(1-(2,6-dioxopiperidin-3-yl)-3- Methyl-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-4-yl)but-3-yn-1-yl)piperazin-1-yl)-2-((tetrahydro-2H-pyran) -4-yl)amino)benzamide,
N-(5-(3,5-difluorobenzyl)-1H-indazol-3-yl)-4-(4-(3-((1-(2,6-dioxopiperidin-3-yl)-3 -Methyl-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-4-yl)amino)propyl)piperazin-1-yl)-2-((tetrahydro-2H-pyran-4-yl) amino) benzamide,
N-(5-(3,5-difluorobenzyl)-1H-indazol-3-yl)-4-(4-(3-((1-(2,6-dioxopiperidin-3-yl)-3 -Methyl-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-5-yl)amino)propyl)piperazin-1-yl)-2-((tetrahydro-2H-pyran-4-yl) amino) benzamide,
N-(5-(3,5-difluorobenzyl)-1H-indazol-3-yl)-4-(4-((1-(2-(2,6-dioxopiperidin-3-yl)-3 -oxoisoindolin-5-yl)azetidin-3-yl)methyl)piperazin-1-yl)-2-((tetrahydro-2H-pyran-4-yl)amino)benzamide,
N-(5-(3,5-difluorobenzyl)-1H-indazol-3-yl)-4-(4-(4-(1-(2,6-dioxopiperidin-3-yl)-3- Methyl-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-5-yl)but-3-yn-1-yl)piperazin-1-yl)-2-((tetrahydro-2H-pyran -4-yl)amino)benzamide,
N-(5-(3,5-difluorobenzyl)-1H-indazol-3-yl)-4-(4-(4-(1-(2,6-dioxopiperidin-3-yl)-3- Methyl-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-5-yl)butyl)piperazin-1-yl)-2-((tetrahydro-2H-pyran-4-yl)amino)benzamide ,
N-(5-(3,5-difluorobenzyl)-1H-indazol-3-yl)-4-(4-((1-(1-(2,6-dioxopiperidin-3-yl)-3 -Methyl-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-5-yl)azetidin-3-yl)methyl)piperazin-1-yl)-2-((tetrahydro-2H-pyran- 4-yl)amino)benzamide,
N-(5-(3,5-difluorobenzyl)-1H-indazol-3-yl)-4-(4-(2-((1-(2,6-dioxopiperidin-3-yl)-3 -Methyl-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-5-yl)amino)ethyl)piperazin-1-yl)-2-((tetrahydro-2H-pyran-4-yl) amino) benzamide,
N-(5-(3,5-difluorobenzyl)-1H-indazol-3-yl)-4-(4-(2-((1-(2,6-dioxopiperidin-3-yl)-3 -Methyl-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-4-yl)amino)ethyl)piperazin-1-yl)-2-((tetrahydro-2H-pyran-4-yl) amino) benzamide,
N-(5-(3,5-difluorobenzyl)-1H-indazol-3-yl)-4-(4-(1-(2-(2,6-dioxopiperidin-3-yl)-1- oxoisoindolin-5-yl)azetidin-3-yl)piperazin-1-yl)-2-((tetrahydro-2H-pyran-4-yl)amino)benzamide,
N-(5-(3,5-difluorobenzyl)-1H-indazol-3-yl)-4-(4-(1-(2-(2,6-dioxopiperidin-3-yl)-3- oxoisoindolin-5-yl)azetidin-3-yl)piperazin-1-yl)-2-((tetrahydro-2H-pyran-4-yl)amino)benzamide,
N-(5-(3,5-difluorobenzyl)-1H-indazol-3-yl)-4-(4-((1-(2-(2,6-dioxopiperidin-3-yl)-1 ,3-dioxoisoindolin-5-yl)azetidin-3-yl)amino)piperidin-1-yl)-2-((tetrahydro-2H-pyran-4-yl)amino)benzamide,
N-(5-(3,5-difluorobenzyl)-1H-indazol-3-yl)-4-(4-(3-(2-(2,6-dioxopiperidin-3-yl)-1- oxoisoindolin-5-yl)azetidin-1-yl)piperidin-1-yl)-2-((tetrahydro-2H-pyran-4-yl)amino)benzamide,
N-(5-(3,5-difluorobenzyl)-1H-indazol-3-yl)-4-(4-(3-(2-(2,6-dioxopiperidin-3-yl)-1, 3-dioxoisoindolin-5-yl)azetidin-1-yl)piperidin-1-yl)-2-((tetrahydro-2H-pyran-4-yl)amino)benzamide,
N-(5-(3,5-difluorobenzyl)-1H-indazol-3-yl)-4-(4-(6-(2-(2,6-dioxopiperidin-3-yl)-1, 3-Dioxoisoindolin-5-yl)-2,6-diazaspiro[3.3]heptan-2-yl)piperidin-1-yl)-2-((tetrahydro-2H-pyran-4-yl)amino ) benzamide,
(S)-N-(5-(3,5-difluorobenzyl)-1H-indazol-3-yl)-4-(4-((1-(2-(2,6-dioxopiperidine-3- yl)-1,3-dioxoisoindolin-5-yl)azetidin-3-yl)methyl)piperazin-1-yl)-2-((tetrahydro-2H-pyran-4-yl)amino)benzamide,
(R)-N-(5-(3,5-difluorobenzyl)-1H-indazol-3-yl)-4-(4-((1-(2-(2,6-dioxopiperidine-3- yl)-1,3-dioxoisoindolin-5-yl)azetidin-3-yl)methyl)piperazin-1-yl)-2-((tetrahydro-2H-pyran-4-yl)amino)benzamide,
(S)-N-(5-(3,5-difluorobenzyl)-1H-indazol-3-yl)-4-(4-(1-(2-(2,6-dioxopiperidin-3-yl) )-1,3-dioxoisoindolin-5-yl)azetidin-3-yl)piperazin-1-yl)-2-((tetrahydro-2H-pyran-4-yl)amino)benzamide, and (R) -N-(5-(3,5-difluorobenzyl)-1H-indazol-3-yl)-4-(4-(1-(2-(2,6-dioxopiperidin-3-yl)-1 , 3-dioxoisoindolin-5-yl)azetidin-3-yl)piperazin-1-yl)-2-((tetrahydro-2H-pyran-4-yl)amino)benzamide. or a pharmaceutically acceptable salt thereof.
(R)-N-(5-(3,5-ジフルオロベンジル)-1H-インダゾール-3-イル)-4-(4-((1-(2-(2,6-ジオキソピペリジン-3-イル)-1,3-ジオキソイソインドリン-5-イル)アゼチジン-3-イル)メチル)ピペラジン-1-イル)-2-((テトラヒドロ-2H-ピラン-4-イル)アミノ)ベンズアミド
からなる群から選択される、請求項5に記載の二価化合物、またはその薬学的に許容可能な塩。 (S)-N-(5-(3,5-difluorobenzyl)-1H-indazol-3-yl)-4-(4-((1-(2-(2,6-dioxopiperidine-3- yl)-1,3-dioxoisoindolin-5-yl)azetidin-3-yl)methyl)piperazin-1-yl)-2-((tetrahydro-2H-pyran-4-yl)amino)benzamide, and (R)-N-(5-(3,5-difluorobenzyl)-1H-indazol-3-yl)-4-(4-((1-(2-(2,6-dioxopiperidine-3- yl)-1,3-dioxoisoindolin-5-yl)azetidin-3-yl)methyl)piperazin-1-yl)-2-((tetrahydro-2H-pyran-4-yl)amino)benzamide 6. A divalent compound according to claim 5, or a pharmaceutically acceptable salt thereof, selected from the group.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CNPCT/CN2020/076748 | 2020-02-26 | ||
CN2020076748 | 2020-02-26 | ||
PCT/CN2021/078240 WO2021170109A1 (en) | 2020-02-26 | 2021-02-26 | Tropomyosin receptor kinase (trk) degradation compounds and methods of use |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2023514872A JP2023514872A (en) | 2023-04-11 |
JPWO2021170109A5 true JPWO2021170109A5 (en) | 2024-03-04 |
Family
ID=77490737
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2022551553A Pending JP2023514872A (en) | 2020-02-26 | 2021-02-26 | Tropomyosin receptor kinase (TRK) degrading compounds and methods of use thereof |
Country Status (11)
Country | Link |
---|---|
US (1) | US20230257380A1 (en) |
EP (1) | EP4110772A4 (en) |
JP (1) | JP2023514872A (en) |
KR (1) | KR20230010070A (en) |
CN (1) | CN115697989A (en) |
AU (1) | AU2021225981A1 (en) |
BR (1) | BR112022016901A2 (en) |
CA (1) | CA3173262A1 (en) |
IL (1) | IL295799A (en) |
MX (1) | MX2022010465A (en) |
WO (1) | WO2021170109A1 (en) |
Families Citing this family (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN118530239A (en) * | 2018-08-22 | 2024-08-23 | 上海睿跃生物科技有限公司 | Tropomyosin Receptor Kinase (TRK) degrading compounds and methods of use |
US11969472B2 (en) | 2018-08-22 | 2024-04-30 | Cullgen (Shanghai), Inc. | Tropomyosin receptor kinase (TRK) degradation compounds and methods of use |
WO2022161414A1 (en) * | 2021-01-26 | 2022-08-04 | 成都茵创园医药科技有限公司 | Aromatic compound, pharmaceutical composition containing same, and application thereof |
TW202309030A (en) | 2021-05-07 | 2023-03-01 | 美商凱麥拉醫療公司 | Cdk2 degraders and uses thereof |
CN115504963A (en) * | 2021-06-22 | 2022-12-23 | 苏州开拓药业股份有限公司 | C-Myc protein degradation agent |
TW202317097A (en) * | 2021-09-08 | 2023-05-01 | 大陸商南京明德新藥研發有限公司 | Glutarimide compounds and applications thereof |
WO2023055952A1 (en) * | 2021-09-29 | 2023-04-06 | C4 Therapeutics, Inc. | Neurotrophic tyrosine receptor kinase (ntrk) degrading compounds |
KR20240110576A (en) * | 2021-10-22 | 2024-07-15 | 글루탁스 테라퓨틱스 (상하이) 씨오., 엘티디. | CRBN E3 ligase ligand compounds, protein degraders developed based on the ligand compounds, and their applications |
EP4180428A1 (en) * | 2021-11-12 | 2023-05-17 | Genzyme Corporation | Crystalline imidazo[4,5-b]pyridine compound, pharmaceutical compositions, and their use in treating medical conditions |
CN118401512A (en) * | 2021-12-24 | 2024-07-26 | 苏州开拓药业股份有限公司 | Polyprotein degradation agent with imide skeleton |
TW202333670A (en) * | 2022-01-04 | 2023-09-01 | 大陸商海思科醫藥集團股份有限公司 | Compound for inhibiting and degrading irak4, and pharmaceutical composition and pharmaceutical application thereof |
WO2023193760A1 (en) * | 2022-04-06 | 2023-10-12 | Cullgen (Shanghai) , Inc. | Compounds and methods of treating cancers |
US20230416240A1 (en) * | 2022-06-16 | 2023-12-28 | Prelude Therapeutics Incorporated | Kat6 targeting compounds |
TW202412851A (en) * | 2022-08-05 | 2024-04-01 | 大陸商深圳市新樾生物科技有限公司 | Protein kinase degrading agent, medicament and use |
WO2024149362A1 (en) * | 2023-01-13 | 2024-07-18 | Shenzhen Newdel Biotech Co., Ltd. | Use of compound 1 in treatment or prevention of atopic dermatitis |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20220101015A (en) * | 2014-04-14 | 2022-07-18 | 아비나스 오퍼레이션스, 인코포레이티드 | Imide-based modulators of proteolysis and associated methods of use |
WO2016096709A1 (en) * | 2014-12-16 | 2016-06-23 | Eudendron S.R.L. | Heterocyclic derivatives modulating activity of certain protein kinases |
KR20230175343A (en) * | 2015-03-18 | 2023-12-29 | 아비나스 오퍼레이션스, 인코포레이티드 | Compounds and methods for the enhanced degradation of targeted proteins |
EP3454856B1 (en) * | 2016-05-10 | 2024-09-11 | C4 Therapeutics, Inc. | Heterocyclic degronimers for target protein degradation |
EP3455219A4 (en) * | 2016-05-10 | 2019-12-18 | C4 Therapeutics, Inc. | Amine-linked c3-glutarimide degronimers for target protein degradation |
EP3455218A4 (en) * | 2016-05-10 | 2019-12-18 | C4 Therapeutics, Inc. | C3-carbon linked glutarimide degronimers for target protein degradation |
KR102538307B1 (en) * | 2017-12-13 | 2023-05-31 | 상하이테크 유니버시티 | ALK protein degraders and their use in cancer treatment |
CN118530239A (en) * | 2018-08-22 | 2024-08-23 | 上海睿跃生物科技有限公司 | Tropomyosin Receptor Kinase (TRK) degrading compounds and methods of use |
-
2021
- 2021-02-26 EP EP21760113.7A patent/EP4110772A4/en active Pending
- 2021-02-26 IL IL295799A patent/IL295799A/en unknown
- 2021-02-26 KR KR1020227033274A patent/KR20230010070A/en unknown
- 2021-02-26 MX MX2022010465A patent/MX2022010465A/en unknown
- 2021-02-26 BR BR112022016901A patent/BR112022016901A2/en unknown
- 2021-02-26 JP JP2022551553A patent/JP2023514872A/en active Pending
- 2021-02-26 AU AU2021225981A patent/AU2021225981A1/en active Pending
- 2021-02-26 US US17/904,822 patent/US20230257380A1/en active Pending
- 2021-02-26 CN CN202180031506.7A patent/CN115697989A/en active Pending
- 2021-02-26 CA CA3173262A patent/CA3173262A1/en active Pending
- 2021-02-26 WO PCT/CN2021/078240 patent/WO2021170109A1/en active Application Filing
Similar Documents
Publication | Publication Date | Title |
---|---|---|
IL295799A (en) | Tropomyosin receptor kinase (trk) degradation compounds and methods of use | |
JPWO2021170109A5 (en) | ||
JP2011515462A5 (en) | ||
JP2014511869A5 (en) | ||
RU2606497C2 (en) | Thiazolylphenyl-benzenesulfonamido derivatives as kinase inhibitors | |
RU2401265C2 (en) | Compounds and compositions as protein kinase inhibitors | |
JP2020503299A5 (en) | ||
JP2019077725A5 (en) | ||
JP2009541268A5 (en) | ||
JP2009526072A5 (en) | ||
JP5938038B2 (en) | Derivatives of pyrazolophenyl-benzenesulfonamide compounds and their use as antitumor agents | |
JP2014525444A5 (en) | ||
JP2009525978A5 (en) | ||
JP2017510555A5 (en) | ||
WO2014181287A1 (en) | Heterocyclyl compounds and uses thereof | |
JPWO2020038415A5 (en) | ||
JP2007519754A5 (en) | ||
JP2019505595A5 (en) | ||
JP2015531773A (en) | Sulfamoyl-arylamide and its use as a medicament for the treatment of hepatitis B | |
RU2010110640A (en) | COMPOUNDS AND COMPOSITIONS 5- (4- (HALOGENALCOXY) Phenyl) PYRIMIDIN-2-AMINE AS KINASE INHIBITORS | |
JP2008513500A5 (en) | ||
JP2013510876A5 (en) | ||
JP2012508223A5 (en) | ||
JP2013517283A5 (en) | ||
CA2628844A1 (en) | Pyrazole derivatives and their medical use |