PT1912972E - Compostos de imidazole substituídos como inibidores de ksp - Google Patents

Info

Publication number

PT1912972E

PT1912972E PT06789653T PT06789653T PT1912972E PT 1912972 E PT1912972 E PT 1912972E PT 06789653 T PT06789653 T PT 06789653T PT 06789653 T PT06789653 T PT 06789653T PT 1912972 E PT1912972 E PT 1912972E

Authority

PT

Portugal

Prior art keywords

benzyl

phenyl

imidazol

amino

fluoro

Prior art date

2005-08-09

Links

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• 239000003112 inhibitor Substances 0.000 title description 10
• 150000002460 imidazoles Chemical class 0.000 title description 4
• -1 amino, substituted amino Chemical group 0.000 claims description 372
• 150000001875 compounds Chemical class 0.000 claims description 199
• 125000000623 heterocyclic group Chemical group 0.000 claims description 130
• 239000000203 mixture Substances 0.000 claims description 102
• 125000001072 heteroaryl group Chemical group 0.000 claims description 82
• 125000003118 aryl group Chemical group 0.000 claims description 52
• 125000000217 alkyl group Chemical group 0.000 claims description 51
• 125000003107 substituted aryl group Chemical group 0.000 claims description 47
• 125000000753 cycloalkyl group Chemical group 0.000 claims description 39
• 229910052739 hydrogen Inorganic materials 0.000 claims description 39
• WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical group CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 claims description 39
• 239000001257 hydrogen Substances 0.000 claims description 35
• 206010028980 Neoplasm Diseases 0.000 claims description 34
• 125000000547 substituted alkyl group Chemical group 0.000 claims description 33
• 125000005346 substituted cycloalkyl group Chemical group 0.000 claims description 29
• 125000004180 3-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(F)=C1[H] 0.000 claims description 27
• 125000003342 alkenyl group Chemical group 0.000 claims description 24
• 201000011510 cancer Diseases 0.000 claims description 22
• 229910052757 nitrogen Inorganic materials 0.000 claims description 22
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 20
• XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 19
• 125000000304 alkynyl group Chemical group 0.000 claims description 19
• 125000004433 nitrogen atom Chemical group N* 0.000 claims description 19
• 239000003795 chemical substances by application Substances 0.000 claims description 18
• 125000005843 halogen group Chemical group 0.000 claims description 17
• 150000003839 salts Chemical class 0.000 claims description 17
• 125000001424 substituent group Chemical group 0.000 claims description 17
• 229910052799 carbon Inorganic materials 0.000 claims description 16
• 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 16
• 125000004426 substituted alkynyl group Chemical group 0.000 claims description 16
• 125000005017 substituted alkenyl group Chemical group 0.000 claims description 15
• 125000004442 acylamino group Chemical group 0.000 claims description 14
• 239000004202 carbamide Substances 0.000 claims description 14
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 12
• 125000003545 alkoxy group Chemical group 0.000 claims description 12
• 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 12
• 238000011282 treatment Methods 0.000 claims description 12
• OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 11
• 125000004093 cyano group Chemical group *C#N 0.000 claims description 11
• 125000005415 substituted alkoxy group Chemical group 0.000 claims description 11
• 125000006284 3-fluorobenzyl group Chemical group [H]C1=C([H])C(=C([H])C(F)=C1[H])C([H])([H])* 0.000 claims description 10
• RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 claims description 9
• 125000004429 atom Chemical group 0.000 claims description 9
• 150000001733 carboxylic acid esters Chemical group 0.000 claims description 9
• 150000002148 esters Chemical class 0.000 claims description 9
• 239000008194 pharmaceutical composition Substances 0.000 claims description 9
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 9
• 125000000266 alpha-aminoacyl group Chemical group 0.000 claims description 7
• 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 7
• UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 6
• 125000002947 alkylene group Chemical group 0.000 claims description 6
• 201000010099 disease Diseases 0.000 claims description 6
• 229960001330 hydroxycarbamide Drugs 0.000 claims description 6
• 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims description 5
• 239000003937 drug carrier Substances 0.000 claims description 5
• 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 5
• IVXQBCUBSIPQGU-UHFFFAOYSA-N piperazine-1-carboxamide Chemical compound NC(=O)N1CCNCC1 IVXQBCUBSIPQGU-UHFFFAOYSA-N 0.000 claims description 5
• 210000004556 brain Anatomy 0.000 claims description 4
• 210000001072 colon Anatomy 0.000 claims description 4
• 210000000244 kidney pelvis Anatomy 0.000 claims description 4
• 230000002062 proliferating effect Effects 0.000 claims description 4
• 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 4
• 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 4
• GEBYXLCXSRCDDD-RSXGOPAZSA-N (3r)-n-(3-aminopropyl)-n-[(1r)-1-(1-benzyl-4-phenylimidazol-2-yl)-2,2-dimethylpropyl]-3-hydroxypyrrolidine-1-carboxamide Chemical compound NCCCN([C@H](C(C)(C)C)C=1N(C=C(N=1)C=1C=CC=CC=1)CC=1C=CC=CC=1)C(=O)N1CC[C@@H](O)C1 GEBYXLCXSRCDDD-RSXGOPAZSA-N 0.000 claims description 3
• MYELFCBDZMZCFZ-QFIPXVFZSA-N 1-[(1r)-1-(1-benzyl-4-phenylimidazol-2-yl)-2,2-dimethylpropyl]-1,3-diazinan-2-one Chemical compound N1([C@H](C(C)(C)C)C=2N(C=C(N=2)C=2C=CC=CC=2)CC=2C=CC=CC=2)CCCNC1=O MYELFCBDZMZCFZ-QFIPXVFZSA-N 0.000 claims description 3
• 125000004179 3-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(Cl)=C1[H] 0.000 claims description 3
• 125000006291 3-hydroxybenzyl group Chemical group [H]OC1=C([H])C([H])=C([H])C(=C1[H])C([H])([H])* 0.000 claims description 3
• 125000004801 4-cyanophenyl group Chemical group [H]C1=C([H])C(C#N)=C([H])C([H])=C1* 0.000 claims description 3
• 208000015914 Non-Hodgkin lymphomas Diseases 0.000 claims description 3
• 229940122803 Vinca alkaloid Drugs 0.000 claims description 3
• ZNKDSAAYZDEZAY-ZVPJJTBRSA-N n-[(1r)-1-(1-benzyl-4-phenylimidazol-2-yl)-2,2-dimethylpropyl]-n-[[(3s,4s)-4-hydroxypyrrolidin-3-yl]methyl]-4-piperidin-1-ylpiperidine-1-carboxamide Chemical compound C1CC(N2CCCCC2)CCN1C(=O)N([C@H](C(C)(C)C)C=1N(C=C(N=1)C=1C=CC=CC=1)CC=1C=CC=CC=1)C[C@@H]1CNC[C@H]1O ZNKDSAAYZDEZAY-ZVPJJTBRSA-N 0.000 claims description 3
• NYCVCXMSZNOGDH-UHFFFAOYSA-N pyrrolidine-1-carboxylic acid Chemical compound OC(=O)N1CCCC1 NYCVCXMSZNOGDH-UHFFFAOYSA-N 0.000 claims description 3
• 210000002784 stomach Anatomy 0.000 claims description 3
• 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 3
• JHYXLHFINQYNSP-CVWIZFJUSA-N (3r)-n-(3-amino-2-fluoropropyl)-n-[(1r)-1-(1-benzyl-4-phenylimidazol-2-yl)-2,2-dimethylpropyl]-3-hydroxypiperidine-1-carboxamide Chemical compound NCC(F)CN([C@H](C(C)(C)C)C=1N(C=C(N=1)C=1C=CC=CC=1)CC=1C=CC=CC=1)C(=O)N1CCC[C@@H](O)C1 JHYXLHFINQYNSP-CVWIZFJUSA-N 0.000 claims description 2
• RQRGEDRGKIMIJF-SANMLTNESA-N 1-(3-aminopropyl)-1-[(1r)-1-(1-benzyl-4-phenylimidazol-2-yl)-2,2-dimethylpropyl]-3-thiophen-2-ylurea Chemical compound NCCCN([C@H](C(C)(C)C)C=1N(C=C(N=1)C=1C=CC=CC=1)CC=1C=CC=CC=1)C(=O)NC1=CC=CS1 RQRGEDRGKIMIJF-SANMLTNESA-N 0.000 claims description 2
• PRXTZIHOAREPRY-UNMCSNQZSA-N 1-[(2s)-3-amino-2-fluoropropyl]-1-[(1r)-1-[4-(3-fluorophenyl)-1-[(3-fluorophenyl)methyl]imidazol-2-yl]-2,2-dimethylpropyl]urea Chemical compound NC[C@H](F)CN(C(N)=O)[C@H](C(C)(C)C)C1=NC(C=2C=C(F)C=CC=2)=CN1CC1=CC=CC(F)=C1 PRXTZIHOAREPRY-UNMCSNQZSA-N 0.000 claims description 2
• RVDLTNPIDXTVSV-RDPSFJRHSA-N 1-[(3s)-3-amino-4-fluorobutyl]-1-[(1r)-1-[1-benzyl-4-(2,5-difluorophenyl)imidazol-2-yl]-2,2-dimethylpropyl]-3-methylurea Chemical compound FC[C@@H](N)CCN(C(=O)NC)[C@H](C(C)(C)C)C1=NC(C=2C(=CC=C(F)C=2)F)=CN1CC1=CC=CC=C1 RVDLTNPIDXTVSV-RDPSFJRHSA-N 0.000 claims description 2
• QASIFHDHOVFUCD-NVQXNPDNSA-N 1-[(3s)-3-amino-4-fluorobutyl]-1-[(1r)-1-[1-benzyl-4-(2,5-difluorophenyl)imidazol-2-yl]-2,2-dimethylpropyl]-3-propan-2-ylurea Chemical compound FC[C@@H](N)CCN(C(=O)NC(C)C)[C@H](C(C)(C)C)C1=NC(C=2C(=CC=C(F)C=2)F)=CN1CC1=CC=CC=C1 QASIFHDHOVFUCD-NVQXNPDNSA-N 0.000 claims description 2
• PAYFEVPWKCEPQP-OFVILXPXSA-N 1-[(3s)-3-amino-4-methoxybutyl]-1-[(1r)-1-[1-benzyl-4-(2,5-difluorophenyl)imidazol-2-yl]-2,2-dimethylpropyl]-3-methylurea Chemical compound COC[C@@H](N)CCN(C(=O)NC)[C@H](C(C)(C)C)C1=NC(C=2C(=CC=C(F)C=2)F)=CN1CC1=CC=CC=C1 PAYFEVPWKCEPQP-OFVILXPXSA-N 0.000 claims description 2
• 125000000175 2-thienyl group Chemical group S1C([*])=C([H])C([H])=C1[H] 0.000 claims description 2
• 125000004208 3-hydroxyphenyl group Chemical group [H]OC1=C([H])C([H])=C([H])C(*)=C1[H] 0.000 claims description 2
• 125000004575 3-pyrrolidinyl group Chemical group [H]N1C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 2
• 208000031261 Acute myeloid leukaemia Diseases 0.000 claims description 2
• 208000003200 Adenoma Diseases 0.000 claims description 2
• 206010001233 Adenoma benign Diseases 0.000 claims description 2
• 208000032791 BCR-ABL1 positive chronic myelogenous leukemia Diseases 0.000 claims description 2
• 208000010833 Chronic myeloid leukaemia Diseases 0.000 claims description 2
• 208000028018 Lymphocytic leukaemia Diseases 0.000 claims description 2
• 208000034578 Multiple myelomas Diseases 0.000 claims description 2
• 208000033761 Myelogenous Chronic BCR-ABL Positive Leukemia Diseases 0.000 claims description 2
• 208000033776 Myeloid Acute Leukemia Diseases 0.000 claims description 2
• 206010035226 Plasma cell myeloma Diseases 0.000 claims description 2
• 125000004202 aminomethyl group Chemical group [H]N([H])C([H])([H])* 0.000 claims description 2
• 210000000481 breast Anatomy 0.000 claims description 2
• 210000000621 bronchi Anatomy 0.000 claims description 2
• 230000001413 cellular effect Effects 0.000 claims description 2
• 210000003679 cervix uteri Anatomy 0.000 claims description 2
• 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 2
• 210000003238 esophagus Anatomy 0.000 claims description 2
• 210000003228 intrahepatic bile duct Anatomy 0.000 claims description 2
• 210000000867 larynx Anatomy 0.000 claims description 2
• 210000004185 liver Anatomy 0.000 claims description 2
• 210000004072 lung Anatomy 0.000 claims description 2
• 208000003747 lymphoid leukemia Diseases 0.000 claims description 2
• 201000001441 melanoma Diseases 0.000 claims description 2
• STUHQDIOZQUPGP-UHFFFAOYSA-N morpholin-4-ium-4-carboxylate Chemical compound OC(=O)N1CCOCC1 STUHQDIOZQUPGP-UHFFFAOYSA-N 0.000 claims description 2
• 210000000214 mouth Anatomy 0.000 claims description 2
• 208000025113 myeloid leukemia Diseases 0.000 claims description 2
• 210000001672 ovary Anatomy 0.000 claims description 2
• 210000000496 pancreas Anatomy 0.000 claims description 2
• 210000003800 pharynx Anatomy 0.000 claims description 2
• 210000002307 prostate Anatomy 0.000 claims description 2
• 210000000664 rectum Anatomy 0.000 claims description 2
• 210000000813 small intestine Anatomy 0.000 claims description 2
• 210000001685 thyroid gland Anatomy 0.000 claims description 2
• 210000003932 urinary bladder Anatomy 0.000 claims description 2
• 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 9
• 150000002431 hydrogen Chemical class 0.000 claims 7
• 229960000575 trastuzumab Drugs 0.000 claims 4
• VVIAGPKUTFNRDU-UHFFFAOYSA-N 6S-folinic acid Natural products C1NC=2NC(N)=NC(=O)C=2N(C=O)C1CNC1=CC=C(C(=O)NC(CCC(O)=O)C(O)=O)C=C1 VVIAGPKUTFNRDU-UHFFFAOYSA-N 0.000 claims 2
• CMSMOCZEIVJLDB-UHFFFAOYSA-N Cyclophosphamide Chemical compound ClCCN(CCCl)P1(=O)NCCCO1 CMSMOCZEIVJLDB-UHFFFAOYSA-N 0.000 claims 2
• GHASVSINZRGABV-UHFFFAOYSA-N Fluorouracil Chemical compound FC1=CNC(=O)NC1=O GHASVSINZRGABV-UHFFFAOYSA-N 0.000 claims 2
• 239000005517 L01XE01 - Imatinib Substances 0.000 claims 2
• ZDZOTLJHXYCWBA-VCVYQWHSSA-N N-debenzoyl-N-(tert-butoxycarbonyl)-10-deacetyltaxol Chemical compound O([C@H]1[C@H]2[C@@](C([C@H](O)C3=C(C)[C@@H](OC(=O)[C@H](O)[C@@H](NC(=O)OC(C)(C)C)C=4C=CC=CC=4)C[C@]1(O)C3(C)C)=O)(C)[C@@H](O)C[C@H]1OC[C@]12OC(=O)C)C(=O)C1=CC=CC=C1 ZDZOTLJHXYCWBA-VCVYQWHSSA-N 0.000 claims 2
• 229940045799 anthracyclines and related substance Drugs 0.000 claims 2
• VSRXQHXAPYXROS-UHFFFAOYSA-N azanide;cyclobutane-1,1-dicarboxylic acid;platinum(2+) Chemical compound [NH2-].[NH2-].[Pt+2].OC(=O)C1(C(O)=O)CCC1 VSRXQHXAPYXROS-UHFFFAOYSA-N 0.000 claims 2
• 229960004562 carboplatin Drugs 0.000 claims 2
• DQLATGHUWYMOKM-UHFFFAOYSA-L cisplatin Chemical compound N[Pt](N)(Cl)Cl DQLATGHUWYMOKM-UHFFFAOYSA-L 0.000 claims 2
• 229960004316 cisplatin Drugs 0.000 claims 2
• 229960004397 cyclophosphamide Drugs 0.000 claims 2
• 229960003668 docetaxel Drugs 0.000 claims 2
• 229960002949 fluorouracil Drugs 0.000 claims 2
• VVIAGPKUTFNRDU-ABLWVSNPSA-N folinic acid Chemical compound C1NC=2NC(N)=NC(=O)C=2N(C=O)C1CNC1=CC=C(C(=O)N[C@@H](CCC(O)=O)C(O)=O)C=C1 VVIAGPKUTFNRDU-ABLWVSNPSA-N 0.000 claims 2
• 235000008191 folinic acid Nutrition 0.000 claims 2
• 239000011672 folinic acid Substances 0.000 claims 2
• SDUQYLNIPVEERB-QPPQHZFASA-N gemcitabine Chemical compound O=C1N=C(N)C=CN1[C@H]1C(F)(F)[C@H](O)[C@@H](CO)O1 SDUQYLNIPVEERB-QPPQHZFASA-N 0.000 claims 2
• 229960005277 gemcitabine Drugs 0.000 claims 2
• 229960002411 imatinib Drugs 0.000 claims 2
• KTUFNOKKBVMGRW-UHFFFAOYSA-N imatinib Chemical compound C1CN(C)CCN1CC1=CC=C(C(=O)NC=2C=C(NC=3N=C(C=CN=3)C=3C=NC=CC=3)C(C)=CC=2)C=C1 KTUFNOKKBVMGRW-UHFFFAOYSA-N 0.000 claims 2
• UWKQSNNFCGGAFS-XIFFEERXSA-N irinotecan Chemical compound C1=C2C(CC)=C3CN(C(C4=C([C@@](C(=O)OC4)(O)CC)C=4)=O)C=4C3=NC2=CC=C1OC(=O)N(CC1)CCC1N1CCCCC1 UWKQSNNFCGGAFS-XIFFEERXSA-N 0.000 claims 2
• 229960004768 irinotecan Drugs 0.000 claims 2
• 229960001691 leucovorin Drugs 0.000 claims 2
• RFIOZSIHFNEKFF-UHFFFAOYSA-M piperazine-1-carboxylate Chemical compound [O-]C(=O)N1CCNCC1 RFIOZSIHFNEKFF-UHFFFAOYSA-M 0.000 claims 2
• 229960004641 rituximab Drugs 0.000 claims 2
• GFFXZLZWLOBBLO-ASKVSEFXSA-N tezacitabine Chemical compound O=C1N=C(N)C=CN1[C@H]1C(=C/F)/[C@H](O)[C@@H](CO)O1 GFFXZLZWLOBBLO-ASKVSEFXSA-N 0.000 claims 2
• 229950006410 tezacitabine Drugs 0.000 claims 2
• DUSUPQUAQUSROW-ILRLXPBVSA-N (2S)-1-[(3-amino-4-fluorobutyl)-[(1R)-1-[1-benzyl-4-(2,5-difluorophenyl)imidazol-2-yl]-2,2-dimethylpropyl]carbamoyl]pyrrolidine-2-carboxylic acid Chemical compound NC(CCN(C(=O)N1[C@@H](CCC1)C(=O)O)[C@H](C(C)(C)C)C=1N(C=C(N=1)C1=C(C=CC(=C1)F)F)CC1=CC=CC=C1)CF DUSUPQUAQUSROW-ILRLXPBVSA-N 0.000 claims 1
• AXZRSNIRYBQWBV-VPUSJEBWSA-N (3r)-n-(3-aminopropyl)-n-[(1r)-1-(1-benzyl-4-phenylimidazol-2-yl)-2,2-dimethylpropyl]-3-hydroxypiperidine-1-carboxamide Chemical compound NCCCN([C@H](C(C)(C)C)C=1N(C=C(N=1)C=1C=CC=CC=1)CC=1C=CC=CC=1)C(=O)N1CCC[C@@H](O)C1 AXZRSNIRYBQWBV-VPUSJEBWSA-N 0.000 claims 1
• GEBYXLCXSRCDDD-AHWVRZQESA-N (3s)-n-(3-aminopropyl)-n-[(1r)-1-(1-benzyl-4-phenylimidazol-2-yl)-2,2-dimethylpropyl]-3-hydroxypyrrolidine-1-carboxamide Chemical compound NCCCN([C@H](C(C)(C)C)C=1N(C=C(N=1)C=1C=CC=CC=1)CC=1C=CC=CC=1)C(=O)N1CC[C@H](O)C1 GEBYXLCXSRCDDD-AHWVRZQESA-N 0.000 claims 1
• JHYXLHFINQYNSP-OBDYRVMHSA-N (3s)-n-[(2r)-3-amino-2-fluoropropyl]-n-[(1r)-1-(1-benzyl-4-phenylimidazol-2-yl)-2,2-dimethylpropyl]-3-hydroxypiperidine-1-carboxamide Chemical compound NC[C@@H](F)CN([C@H](C(C)(C)C)C=1N(C=C(N=1)C=1C=CC=CC=1)CC=1C=CC=CC=1)C(=O)N1CCC[C@H](O)C1 JHYXLHFINQYNSP-OBDYRVMHSA-N 0.000 claims 1
• UBUFNHIDNFICAK-USZFVNFHSA-N (3s)-n-[(2r)-3-amino-2-fluoropropyl]-n-[(1r)-1-(1-benzyl-4-phenylimidazol-2-yl)-2,2-dimethylpropyl]-3-hydroxypyrrolidine-1-carboxamide Chemical compound NC[C@@H](F)CN([C@H](C(C)(C)C)C=1N(C=C(N=1)C=1C=CC=CC=1)CC=1C=CC=CC=1)C(=O)N1CC[C@H](O)C1 UBUFNHIDNFICAK-USZFVNFHSA-N 0.000 claims 1
• YJAJCWNCASSMCP-WKDCXCOVSA-N 1-(3-amino-2-fluoropropyl)-1-[(1r)-1-(1-benzyl-4-phenylimidazol-2-yl)-2,2-dimethylpropyl]-3-(oxan-4-yl)urea Chemical compound NCC(F)CN([C@H](C(C)(C)C)C=1N(C=C(N=1)C=1C=CC=CC=1)CC=1C=CC=CC=1)C(=O)NC1CCOCC1 YJAJCWNCASSMCP-WKDCXCOVSA-N 0.000 claims 1
• JHUBDJRPIBVVOT-DEOSSOPVSA-N 1-(3-aminopropyl)-1-[(1r)-1-(1-benzyl-4-phenylimidazol-2-yl)-2,2-dimethylpropyl]-3,3-dimethylurea Chemical compound NCCCN(C(=O)N(C)C)[C@H](C(C)(C)C)C1=NC(C=2C=CC=CC=2)=CN1CC1=CC=CC=C1 JHUBDJRPIBVVOT-DEOSSOPVSA-N 0.000 claims 1
• PVYDRBCTJXWSNM-DEOSSOPVSA-N 1-(3-aminopropyl)-1-[(1r)-1-[1-benzyl-4-(2,5-difluorophenyl)imidazol-2-yl]-2,2-dimethylpropyl]-3,3-dimethylurea Chemical compound NCCCN(C(=O)N(C)C)[C@H](C(C)(C)C)C1=NC(C=2C(=CC=C(F)C=2)F)=CN1CC1=CC=CC=C1 PVYDRBCTJXWSNM-DEOSSOPVSA-N 0.000 claims 1
• NESJORCGJBAFKO-MHZLTWQESA-N 1-(3-aminopropyl)-1-[(1r)-1-[1-benzyl-4-(2,5-difluorophenyl)imidazol-2-yl]-2,2-dimethylpropyl]-3-(3,5-dimethyl-1,2-oxazol-4-yl)urea Chemical compound CC1=NOC(C)=C1NC(=O)N(CCCN)[C@H](C(C)(C)C)C1=NC(C=2C(=CC=C(F)C=2)F)=CN1CC1=CC=CC=C1 NESJORCGJBAFKO-MHZLTWQESA-N 0.000 claims 1
• RVDVXHZKWMWYEP-QHCPKHFHSA-N 1-(3-aminopropyl)-1-[(1r)-1-[1-benzyl-4-(2,5-difluorophenyl)imidazol-2-yl]-2,2-dimethylpropyl]-3-methylurea Chemical compound NCCCN(C(=O)NC)[C@H](C(C)(C)C)C1=NC(C=2C(=CC=C(F)C=2)F)=CN1CC1=CC=CC=C1 RVDVXHZKWMWYEP-QHCPKHFHSA-N 0.000 claims 1
• PKAHTZGPEBWADF-NGQVCNFZSA-N 1-[(1r)-1-[1-benzyl-4-(2,5-difluorophenyl)imidazol-2-yl]-2,2-dimethylpropyl]-1-[(3s)-3-(1,3-dioxoisoindol-2-yl)-4-fluorobutyl]-3-methylurea Chemical compound C1([C@H](N(CC[C@@H](CF)N2C(C3=CC=CC=C3C2=O)=O)C(=O)NC)C(C)(C)C)=NC(C=2C(=CC=C(F)C=2)F)=CN1CC1=CC=CC=C1 PKAHTZGPEBWADF-NGQVCNFZSA-N 0.000 claims 1
• DWRXANOIMWBODT-NOZRDPDXSA-N 1-[(2r)-3-amino-2-fluoropropyl]-1-[(1r)-1-(1-benzyl-4-phenylimidazol-2-yl)-2,2-dimethylpropyl]-3-(2-methoxyethyl)urea Chemical compound COCCNC(=O)N(C[C@H](F)CN)[C@H](C(C)(C)C)C1=NC(C=2C=CC=CC=2)=CN1CC1=CC=CC=C1 DWRXANOIMWBODT-NOZRDPDXSA-N 0.000 claims 1
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