JP2018511631A5 - - Google Patents
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- JP2018511631A5 JP2018511631A5 JP2017553933A JP2017553933A JP2018511631A5 JP 2018511631 A5 JP2018511631 A5 JP 2018511631A5 JP 2017553933 A JP2017553933 A JP 2017553933A JP 2017553933 A JP2017553933 A JP 2017553933A JP 2018511631 A5 JP2018511631 A5 JP 2018511631A5
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- cancer
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- 150000001875 compounds Chemical class 0.000 claims description 80
- 125000000217 alkyl group Chemical group 0.000 claims description 30
- 239000008194 pharmaceutical composition Substances 0.000 claims description 21
- 125000005843 halogen group Chemical group 0.000 claims description 20
- 102100009283 HRAS Human genes 0.000 claims description 18
- 101710033925 HRAS Proteins 0.000 claims description 18
- 102100009279 KRAS Human genes 0.000 claims description 17
- 101710033922 KRAS Proteins 0.000 claims description 17
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims description 16
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 16
- 125000001072 heteroaryl group Chemical group 0.000 claims description 16
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 16
- 239000000203 mixture Substances 0.000 claims description 16
- -1 C 1 -C 6 alkylaminyl Chemical group 0.000 claims description 15
- 230000035772 mutation Effects 0.000 claims description 15
- 125000004181 carboxyalkyl group Chemical group 0.000 claims description 14
- 125000004966 cyanoalkyl group Chemical group 0.000 claims description 14
- 125000000623 heterocyclic group Chemical group 0.000 claims description 14
- 125000004415 heterocyclylalkyl group Chemical group 0.000 claims description 14
- 102100001119 NRAS Human genes 0.000 claims description 13
- 101710033916 NRAS Proteins 0.000 claims description 13
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims description 12
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims description 12
- 125000002837 carbocyclic group Chemical group 0.000 claims description 12
- 201000011510 cancer Diseases 0.000 claims description 11
- 125000006728 (C1-C6) alkynyl group Chemical group 0.000 claims description 10
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims description 10
- 125000003118 aryl group Chemical group 0.000 claims description 10
- 102200006538 KRAS G12C Human genes 0.000 claims description 7
- 102200124918 NRAS G12C Human genes 0.000 claims description 6
- 125000003545 alkoxy group Chemical group 0.000 claims description 6
- 125000001153 fluoro group Chemical group F* 0.000 claims description 6
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims description 6
- 201000010099 disease Diseases 0.000 claims description 5
- 230000002401 inhibitory effect Effects 0.000 claims description 5
- 235000018102 proteins Nutrition 0.000 claims description 5
- 102000004169 proteins and genes Human genes 0.000 claims description 5
- 108090000623 proteins and genes Proteins 0.000 claims description 5
- 206010058467 Lung neoplasm malignant Diseases 0.000 claims description 4
- 102000008300 Mutant Proteins Human genes 0.000 claims description 4
- 108010021466 Mutant Proteins Proteins 0.000 claims description 4
- 208000008443 Pancreatic Carcinoma Diseases 0.000 claims description 4
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 4
- 201000011231 colorectal cancer Diseases 0.000 claims description 4
- 201000005787 hematologic cancer Diseases 0.000 claims description 4
- 125000004446 heteroarylalkyl group Chemical group 0.000 claims description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 4
- 201000005202 lung cancer Diseases 0.000 claims description 4
- 230000001404 mediated Effects 0.000 claims description 4
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 4
- 201000002528 pancreatic cancer Diseases 0.000 claims description 4
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 4
- 125000001424 substituent group Chemical group 0.000 claims description 4
- 125000000151 cysteine group Chemical group N[C@@H](CS)C(=O)* 0.000 claims description 3
- 230000000051 modifying Effects 0.000 claims description 3
- 150000003839 salts Chemical class 0.000 claims description 3
- 239000011780 sodium chloride Substances 0.000 claims description 3
- 125000006727 (C1-C6) alkenyl group Chemical group 0.000 claims description 2
- 125000002373 5 membered heterocyclic group Chemical group 0.000 claims description 2
- 125000004070 6 membered heterocyclic group Chemical group 0.000 claims description 2
- 125000003341 7 membered heterocyclic group Chemical group 0.000 claims description 2
- JYZIHLWOWKMNNX-UHFFFAOYSA-N Benzimidazole Chemical compound C1=C[CH]C2=NC=NC2=C1 JYZIHLWOWKMNNX-UHFFFAOYSA-N 0.000 claims description 2
- 206010027476 Metastasis Diseases 0.000 claims description 2
- 206010028980 Neoplasm Diseases 0.000 claims description 2
- ZADPBFCGQRWHPN-UHFFFAOYSA-N OBO Chemical compound OBO ZADPBFCGQRWHPN-UHFFFAOYSA-N 0.000 claims description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K [O-]P([O-])([O-])=O Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 2
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 2
- 125000000278 alkyl amino alkyl group Chemical group 0.000 claims description 2
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 claims description 2
- 125000002947 alkylene group Chemical group 0.000 claims description 2
- 125000004103 aminoalkyl group Chemical group 0.000 claims description 2
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 2
- 125000005418 aryl aryl group Chemical group 0.000 claims description 2
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 claims description 2
- 230000003833 cell viability Effects 0.000 claims description 2
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 2
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 2
- 239000003937 drug carrier Substances 0.000 claims description 2
- 230000000694 effects Effects 0.000 claims description 2
- 125000001188 haloalkyl group Chemical group 0.000 claims description 2
- 125000003453 indazolyl group Chemical group N1N=C(C2=C1C=CC=C2)* 0.000 claims description 2
- 125000001041 indolyl group Chemical group 0.000 claims description 2
- 238000002347 injection Methods 0.000 claims description 2
- 239000007924 injection Substances 0.000 claims description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- 125000001624 naphthyl group Chemical group 0.000 claims description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
- 239000010452 phosphate Substances 0.000 claims description 2
- 239000000651 prodrug Substances 0.000 claims description 2
- 229940002612 prodrugs Drugs 0.000 claims description 2
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 claims description 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 2
- 230000017066 negative regulation of growth Effects 0.000 claims 1
- 150000002830 nitrogen compounds Chemical class 0.000 claims 1
- 0 NC(C=CC*1CCC1)=O Chemical compound NC(C=CC*1CCC1)=O 0.000 description 6
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- NQVHELJXYAFNRV-ONEGZZNKSA-N CCOC(/C=C/C(N)=O)=O Chemical compound CCOC(/C=C/C(N)=O)=O NQVHELJXYAFNRV-ONEGZZNKSA-N 0.000 description 1
- KNVRBEGQERGQRP-UHFFFAOYSA-O C[NH+](C)C(CN)=O Chemical compound C[NH+](C)C(CN)=O KNVRBEGQERGQRP-UHFFFAOYSA-O 0.000 description 1
- 102200006614 HRAS G12C Human genes 0.000 description 1
- 101700053022 VGC Proteins 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drugs Drugs 0.000 description 1
- 239000012039 electrophile Substances 0.000 description 1
- 238000002372 labelling Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 230000035755 proliferation Effects 0.000 description 1
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201562147955P | 2015-04-15 | 2015-04-15 | |
US62/147,955 | 2015-04-15 | ||
PCT/US2016/027673 WO2016168540A1 (en) | 2015-04-15 | 2016-04-15 | Fused-tricyclic inhibitors of kras and methods of use thereof |
Publications (3)
Publication Number | Publication Date |
---|---|
JP2018511631A JP2018511631A (ja) | 2018-04-26 |
JP2018511631A5 true JP2018511631A5 (US20040106767A1-20040603-C00005.png) | 2019-05-09 |
JP6789239B2 JP6789239B2 (ja) | 2020-11-25 |
Family
ID=55806883
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2017553933A Active JP6789239B2 (ja) | 2015-04-15 | 2016-04-15 | Krasの縮合三環系インヒビターおよびその使用の方法 |
Country Status (8)
Families Citing this family (115)
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JO3805B1 (ar) | 2013-10-10 | 2021-01-31 | Araxes Pharma Llc | مثبطات كراس جي12سي |
JO3556B1 (ar) | 2014-09-18 | 2020-07-05 | Araxes Pharma Llc | علاجات مدمجة لمعالجة السرطان |
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2016
- 2016-04-15 EP EP16718179.1A patent/EP3283462B1/en active Active
- 2016-04-15 US US15/566,648 patent/US10428064B2/en active Active
- 2016-04-15 JP JP2017553933A patent/JP6789239B2/ja active Active
- 2016-04-15 MX MX2017013275A patent/MX2017013275A/es unknown
- 2016-04-15 WO PCT/US2016/027673 patent/WO2016168540A1/en active Application Filing
- 2016-04-15 ES ES16718179T patent/ES2856880T3/es active Active
- 2016-04-15 CA CA2982360A patent/CA2982360A1/en not_active Abandoned
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2018
- 2018-07-13 HK HK18109098.2A patent/HK1249513A1/zh unknown