JP2018501261A5 - - Google Patents
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- Publication number
- JP2018501261A5 JP2018501261A5 JP2017533503A JP2017533503A JP2018501261A5 JP 2018501261 A5 JP2018501261 A5 JP 2018501261A5 JP 2017533503 A JP2017533503 A JP 2017533503A JP 2017533503 A JP2017533503 A JP 2017533503A JP 2018501261 A5 JP2018501261 A5 JP 2018501261A5
- Authority
- JP
- Japan
- Prior art keywords
- methyl
- acetamide
- inden
- hydroxy
- dimethoxybenzylidene
- 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
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- -1 nitro, hydroxyl Chemical group 0.000 claims description 154
- 150000001875 compounds Chemical class 0.000 claims description 37
- 150000003839 salts Chemical class 0.000 claims description 37
- 239000011780 sodium chloride Substances 0.000 claims description 37
- 239000000651 prodrug Substances 0.000 claims description 36
- 229940002612 prodrugs Drugs 0.000 claims description 36
- 108020004532 RAS Proteins 0.000 claims description 27
- 125000000217 alkyl group Chemical group 0.000 claims description 27
- 239000000203 mixture Substances 0.000 claims description 27
- 108020001180 rasD Proteins 0.000 claims description 27
- 125000003545 alkoxy group Chemical group 0.000 claims description 22
- 230000000875 corresponding Effects 0.000 claims description 20
- 229910052736 halogen Inorganic materials 0.000 claims description 20
- 150000002367 halogens Chemical class 0.000 claims description 20
- 229910052739 hydrogen Inorganic materials 0.000 claims description 20
- 239000001257 hydrogen Substances 0.000 claims description 20
- UFHFLCQGNIYNRP-UHFFFAOYSA-N hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 18
- 230000031018 biological processes and functions Effects 0.000 claims description 16
- 230000001404 mediated Effects 0.000 claims description 16
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims description 15
- 230000002401 inhibitory effect Effects 0.000 claims description 15
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 14
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 claims description 14
- 125000004644 alkyl sulfinyl group Chemical group 0.000 claims description 14
- KXDHJXZQYSOELW-UHFFFAOYSA-M carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 claims description 14
- 239000004202 carbamide Substances 0.000 claims description 14
- 229960000539 carbamide Drugs 0.000 claims description 14
- 235000013877 carbamide Nutrition 0.000 claims description 14
- XSQUKJJJFZCRTK-UHFFFAOYSA-N urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 14
- 125000003282 alkyl amino group Chemical group 0.000 claims description 13
- 125000005278 alkyl sulfonyloxy group Chemical group 0.000 claims description 13
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 13
- 239000003814 drug Substances 0.000 claims description 13
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 13
- KFJCFMUEEDXYBN-FMCGGJTJSA-N CS(=O)(=O)OC1=C(C=C(C=C1OC)\C=C/1\C(=C(C2=CC(=CC=C\12)F)CC(NC=1C=C(C=CC=1)C)=O)C)OC Chemical compound CS(=O)(=O)OC1=C(C=C(C=C1OC)\C=C/1\C(=C(C2=CC(=CC=C\12)F)CC(NC=1C=C(C=CC=1)C)=O)C)OC KFJCFMUEEDXYBN-FMCGGJTJSA-N 0.000 claims description 12
- DLFVBJFMPXGRIB-UHFFFAOYSA-N acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 claims description 12
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 claims description 12
- 125000004414 alkyl thio group Chemical group 0.000 claims description 12
- 125000004103 aminoalkyl group Chemical group 0.000 claims description 12
- 201000011510 cancer Diseases 0.000 claims description 12
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 12
- 125000004966 cyanoalkyl group Chemical group 0.000 claims description 12
- 125000004663 dialkyl amino group Chemical group 0.000 claims description 12
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 claims description 12
- 125000001188 haloalkyl group Chemical group 0.000 claims description 12
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 12
- 125000000278 alkyl amino alkyl group Chemical group 0.000 claims description 11
- 125000003396 thiol group Chemical group [H]S* 0.000 claims description 11
- FDDDEECHVMSUSB-UHFFFAOYSA-N Sulfanilamide Chemical compound NC1=CC=C(S(N)(=O)=O)C=C1 FDDDEECHVMSUSB-UHFFFAOYSA-N 0.000 claims description 10
- 125000005530 alkylenedioxy group Chemical group 0.000 claims description 10
- IVRMZWNICZWHMI-UHFFFAOYSA-N azide Chemical compound [N-]=[N+]=[N-] IVRMZWNICZWHMI-UHFFFAOYSA-N 0.000 claims description 10
- 229960001663 sulfanilamide Drugs 0.000 claims description 10
- 230000002159 abnormal effect Effects 0.000 claims description 8
- 239000008194 pharmaceutical composition Substances 0.000 claims description 5
- 125000004189 3,4-dichlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(Cl)C([H])=C1* 0.000 claims description 4
- 125000006275 3-bromophenyl group Chemical group [H]C1=C([H])C(Br)=C([H])C(*)=C1[H] 0.000 claims description 4
- 125000004800 4-bromophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Br 0.000 claims description 4
- 210000004369 Blood Anatomy 0.000 claims description 4
- 206010058467 Lung neoplasm malignant Diseases 0.000 claims description 4
- 206010028980 Neoplasm Diseases 0.000 claims description 4
- 208000008443 Pancreatic Carcinoma Diseases 0.000 claims description 4
- 239000008280 blood Substances 0.000 claims description 4
- 201000011231 colorectal cancer Diseases 0.000 claims description 4
- 201000010099 disease Diseases 0.000 claims description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 4
- 201000007270 liver cancer Diseases 0.000 claims description 4
- 201000005202 lung cancer Diseases 0.000 claims description 4
- 229910052760 oxygen Inorganic materials 0.000 claims description 4
- 239000001301 oxygen Substances 0.000 claims description 4
- MYMOFIZGZYHOMD-UHFFFAOYSA-N oxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims description 4
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims description 4
- 201000002528 pancreatic cancer Diseases 0.000 claims description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
- 108010014186 ras Proteins Proteins 0.000 claims description 4
- 102000016914 ras Proteins Human genes 0.000 claims description 4
- 125000003107 substituted aryl group Chemical group 0.000 claims description 4
- 210000001519 tissues Anatomy 0.000 claims description 4
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 3
- 239000003937 drug carrier Substances 0.000 claims description 3
- 229940079593 drugs Drugs 0.000 claims description 3
- 238000000338 in vitro Methods 0.000 claims description 3
- 206010006187 Breast cancer Diseases 0.000 claims description 2
- 206010059866 Drug resistance Diseases 0.000 claims description 2
- 206010017758 Gastric cancer Diseases 0.000 claims description 2
- 206010024324 Leukaemias Diseases 0.000 claims description 2
- 206010025323 Lymphomas Diseases 0.000 claims description 2
- 206010025650 Malignant melanoma Diseases 0.000 claims description 2
- 206010027476 Metastasis Diseases 0.000 claims description 2
- 206010030155 Oesophageal carcinoma Diseases 0.000 claims description 2
- 206010025310 Other lymphomas Diseases 0.000 claims description 2
- 206010033128 Ovarian cancer Diseases 0.000 claims description 2
- 206010060862 Prostate cancer Diseases 0.000 claims description 2
- 206010038389 Renal cancer Diseases 0.000 claims description 2
- 206010039491 Sarcoma Diseases 0.000 claims description 2
- 206010046766 Uterine cancer Diseases 0.000 claims description 2
- 150000001408 amides Chemical class 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
- 150000001540 azides Chemical class 0.000 claims description 2
- 238000004166 bioassay Methods 0.000 claims description 2
- 239000004305 biphenyl Chemical group 0.000 claims description 2
- 235000010290 biphenyl Nutrition 0.000 claims description 2
- 201000005216 brain cancer Diseases 0.000 claims description 2
- 239000011203 carbon fibre reinforced carbon Substances 0.000 claims description 2
- 201000007455 central nervous system cancer Diseases 0.000 claims description 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical group C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims description 2
- 230000002124 endocrine Effects 0.000 claims description 2
- 201000004101 esophageal cancer Diseases 0.000 claims description 2
- 201000003115 germ cell cancer Diseases 0.000 claims description 2
- 201000010536 head and neck cancer Diseases 0.000 claims description 2
- 201000010982 kidney cancer Diseases 0.000 claims description 2
- 201000001441 melanoma Diseases 0.000 claims description 2
- 230000035755 proliferation Effects 0.000 claims description 2
- 201000011549 stomach cancer Diseases 0.000 claims description 2
- 238000006467 substitution reaction Methods 0.000 claims description 2
- 150000003457 sulfones Chemical class 0.000 claims description 2
- 230000004083 survival Effects 0.000 claims description 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 2
- 230000004565 tumor cell growth Effects 0.000 claims description 2
- 230000001225 therapeutic Effects 0.000 claims 2
- IAVUPMFITXYVAF-HTRCEHHLSA-N (4R,6R)-4-(ethylamino)-6-methyl-7,7-dioxo-5,6-dihydro-4H-thieno[2,3-b]thiopyran-2-sulfonamide Chemical compound CCN[C@@H]1C[C@@H](C)S(=O)(=O)C2=C1C=C(S(N)(=O)=O)S2 IAVUPMFITXYVAF-HTRCEHHLSA-N 0.000 claims 1
- 239000003112 inhibitor Substances 0.000 claims 1
- 125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 claims 1
- 150000002431 hydrogen Chemical class 0.000 description 2
- 241000790917 Dioxys <bee> Species 0.000 description 1
- 229940093912 Gynecological Sulfonamides Drugs 0.000 description 1
- 229940079867 intestinal antiinfectives Sulfonamides Drugs 0.000 description 1
- 229940005938 ophthalmologic antiinfectives Sulfonamides Drugs 0.000 description 1
- 150000003456 sulfonamides Chemical class 0.000 description 1
- 229940026752 topical Sulfonamides Drugs 0.000 description 1
Description
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Claims (19)
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- åèšæ£è ããç°åžžãå€ç°åããããã¯é掻æ§ïœïœïœéºäŒåãããã¯ïŒ²ïœïœã¿ã³ãã¯è³ªããŸãã¯ç°åžžãªïŒ²ïœïœåªä»æ§çç©åŠçããã»ã¹ã«ã€ããŠã®åèšæ£è ã®çµç¹ãè¡æ¶²ããŸãã¯è «çã®ã¢ãã»ã€ãå©çšããããšã«ãã£ãŠäºãéžæããããè«æ±é ïŒããïŒïŒã®ããããäžé ã«èšèŒã®çµæç©ã
- åèšæ£è ã®çµç¹ãè¡æ¶²ããŸãã¯è «çããç°åžžãå€ç°åããããã¯é掻æ§ïœïœïœéºäŒåãããã¯ïŒ²ïœïœã¿ã³ãã¯è³ªããŸãã¯ç°åžžãªïŒ²ïœïœåªä»æ§çç©åŠçããã»ã¹ãå«æãããè«æ±é ïŒããïŒïŒã®ããããäžé ã«èšèŒã®çµæç©ã
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US9862698B2 (en) * | 2014-12-16 | 2018-01-09 | Adt Pharmaceuticals, Inc. | Indenyl compounds, pharmaceutical compositions, and medical uses thereof |
US20160168108A1 (en) | 2014-12-16 | 2016-06-16 | Adt Pharmaceuticals, Inc. | Method of treating or preventing ras-mediated diseases |
US20200138829A1 (en) * | 2017-05-24 | 2020-05-07 | Ferro Therapeutics, Inc. | Methods of cancer treatment |
CN112041301A (zh) | 2018-02-28 | 2020-12-04 | 莹çœæ²»çå ¬åž | å ·æéæ»äº¡è¯±å¯ŒæŽ»æ§çååç©åå ¶äœ¿çšæ¹æ³ |
CA3096700C (en) | 2018-04-26 | 2023-08-22 | Adt Pharmaceuticals, Llc | Anticancer indenes, indanes, azaindenes, azaindanes, pharmaceutical compositions and uses |
US11040964B2 (en) | 2019-02-27 | 2021-06-22 | Ferro Therapeutics, Inc. | Compounds and methods of use |
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US6063818A (en) * | 1996-06-13 | 2000-05-16 | Cell Pathways Inc. | Substituted benzylidene indenyl formamides, acetamides and propionamides |
JP2007534702A (ja) * | 2004-04-26 | 2007-11-29 | ãã³ããŒãã«ãã»ãŠãããŒã·ã㣠| èè žæ¯æ§ã®äœãæ²»çè¬ãšããŠã®ã€ã³ããŒã«é ¢é žãåã³ã€ã³ãã³é ¢é žèªå°äœ |
AU2007205208B2 (en) * | 2006-01-04 | 2012-11-01 | Southern Research Institute | Derivatives of sulindac, use thereof and preparation thereof |
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