OA12047A - Arylmethyl-carbonylamino-thiazole derivatives and their use as antitumor agents. - Google Patents

Info

Publication number

OA12047A

OA12047A OA1200200052A OA1200200052A OA12047A OA 12047 A OA12047 A OA 12047A OA 1200200052 A OA1200200052 A OA 1200200052A OA 1200200052 A OA1200200052 A OA 1200200052A OA 12047 A OA12047 A OA 12047A

Authority

OA

OAPI

Prior art keywords

thiazol

amino

isopropyl

oxoethyl

acetamide

Prior art date

1999-08-12

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• 239000002246 antineoplastic agent Substances 0.000 title description 10
• 206010028980 Neoplasm Diseases 0.000 claims abstract description 23
• 201000011510 cancer Diseases 0.000 claims abstract description 11
• 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 10
• 238000011282 treatment Methods 0.000 claims abstract description 10
• 208000035475 disorder Diseases 0.000 claims abstract description 9
• 150000003839 salts Chemical class 0.000 claims abstract description 9
• 208000024827 Alzheimer disease Diseases 0.000 claims abstract description 5
• 208000023275 Autoimmune disease Diseases 0.000 claims abstract description 4
• 208000036142 Viral infection Diseases 0.000 claims abstract description 4
• 230000009385 viral infection Effects 0.000 claims abstract description 4
• DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 claims description 268
• 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 245
• -1 morpholino, piperazino Chemical group 0.000 claims description 123
• 150000001875 compounds Chemical class 0.000 claims description 101
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 44
• 125000000217 alkyl group Chemical group 0.000 claims description 42
• 238000000034 method Methods 0.000 claims description 40
• UPUWMQZUXFAUCJ-UHFFFAOYSA-N 2,5-dihydro-1,2-thiazole Chemical compound C1SNC=C1 UPUWMQZUXFAUCJ-UHFFFAOYSA-N 0.000 claims description 27
• BKIMMITUMNQMOS-UHFFFAOYSA-N nonane Chemical compound CCCCCCCCC BKIMMITUMNQMOS-UHFFFAOYSA-N 0.000 claims description 26
• 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 25
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 25
• KXDAEFPNCMNJSK-UHFFFAOYSA-N Benzamide Chemical compound NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 claims description 21
• 125000003545 alkoxy group Chemical group 0.000 claims description 21
• 125000003282 alkyl amino group Chemical group 0.000 claims description 21
• 125000003118 aryl group Chemical group 0.000 claims description 20
• QLNJFJADRCOGBJ-UHFFFAOYSA-N propionamide Chemical compound CCC(N)=O QLNJFJADRCOGBJ-UHFFFAOYSA-N 0.000 claims description 20
• 125000004663 dialkyl amino group Chemical group 0.000 claims description 19
• 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 16
• 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 14
• 125000004448 alkyl carbonyl group Chemical group 0.000 claims description 13
• 125000004390 alkyl sulfonyl group Chemical group 0.000 claims description 13
• 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 13
• JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 12
• 230000000694 effects Effects 0.000 claims description 12
• RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims description 12
• 125000000587 piperidin-1-yl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 claims description 12
• 125000006656 (C2-C4) alkenyl group Chemical group 0.000 claims description 11
• 125000003277 amino group Chemical group 0.000 claims description 11
• 125000003710 aryl alkyl group Chemical group 0.000 claims description 11
• 125000004391 aryl sulfonyl group Chemical group 0.000 claims description 11
• 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 11
• 229910052739 hydrogen Inorganic materials 0.000 claims description 11
• 239000001257 hydrogen Substances 0.000 claims description 11
• 230000005764 inhibitory process Effects 0.000 claims description 11
• 125000003806 alkyl carbonyl amino group Chemical group 0.000 claims description 10
• 125000004414 alkyl thio group Chemical group 0.000 claims description 10
• 125000001769 aryl amino group Chemical group 0.000 claims description 10
• 125000005129 aryl carbonyl group Chemical group 0.000 claims description 10
• 125000004473 dialkylaminocarbonyl group Chemical group 0.000 claims description 10
• 229910052757 nitrogen Inorganic materials 0.000 claims description 10
• 125000006650 (C2-C4) alkynyl group Chemical group 0.000 claims description 9
• 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 9
• 125000004457 alkyl amino carbonyl group Chemical group 0.000 claims description 9
• METKIMKYRPQLGS-UHFFFAOYSA-N atenolol Chemical compound CC(C)NCC(O)COC1=CC=C(CC(N)=O)C=C1 METKIMKYRPQLGS-UHFFFAOYSA-N 0.000 claims description 9
• 239000003795 chemical substances by application Substances 0.000 claims description 9
• 125000000753 cycloalkyl group Chemical group 0.000 claims description 9
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 9
• 108091000080 Phosphotransferase Proteins 0.000 claims description 8
• 125000004694 alkoxyaminocarbonyl group Chemical group 0.000 claims description 8
• 125000005125 aryl alkyl amino carbonyl group Chemical group 0.000 claims description 8
• 125000001691 aryl alkyl amino group Chemical group 0.000 claims description 8
• 125000005099 aryl alkyl carbonyl group Chemical group 0.000 claims description 8
• 125000005161 aryl oxy carbonyl group Chemical group 0.000 claims description 8
• 125000005110 aryl thio group Chemical group 0.000 claims description 8
• SNCZNSNPXMPCGN-UHFFFAOYSA-N butanediamide Chemical compound NC(=O)CCC(N)=O SNCZNSNPXMPCGN-UHFFFAOYSA-N 0.000 claims description 8
• 229910052736 halogen Inorganic materials 0.000 claims description 8
• 125000005843 halogen group Chemical group 0.000 claims description 8
• 150000002367 halogens Chemical class 0.000 claims description 8
• 102000020233 phosphotransferase Human genes 0.000 claims description 8
• 125000003386 piperidinyl group Chemical group 0.000 claims description 8
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 7
• 125000005126 aryl alkyl carbonyl amino group Chemical group 0.000 claims description 7
• 125000005100 aryl amino carbonyl group Chemical group 0.000 claims description 7
• 125000004104 aryloxy group Chemical group 0.000 claims description 7
• 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 claims description 7
• IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 7
• 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims description 6
• QOXOZONBQWIKDA-UHFFFAOYSA-N 3-hydroxypropyl Chemical group [CH2]CCO QOXOZONBQWIKDA-UHFFFAOYSA-N 0.000 claims description 6
• DFPAKSUCGFBDDF-UHFFFAOYSA-N Nicotinamide Chemical compound NC(=O)C1=CC=CN=C1 DFPAKSUCGFBDDF-UHFFFAOYSA-N 0.000 claims description 6
• FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 claims description 6
• YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 claims description 6
• 125000004656 alkyl sulfonylamino group Chemical group 0.000 claims description 6
• DNSISZSEWVHGLH-UHFFFAOYSA-N butanamide Chemical compound CCCC(N)=O DNSISZSEWVHGLH-UHFFFAOYSA-N 0.000 claims description 6
• 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 6
• 125000004356 hydroxy functional group Chemical group O* 0.000 claims description 6
• 238000004519 manufacturing process Methods 0.000 claims description 6
• UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 6
• 125000002112 pyrrolidino group Chemical group [*]N1C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 claims description 6
• 125000000979 2-amino-2-oxoethyl group Chemical group [H]C([*])([H])C(=O)N([H])[H] 0.000 claims description 5
• WNWVKZTYMQWFHE-UHFFFAOYSA-N 4-ethylmorpholine Chemical group [CH2]CN1CCOCC1 WNWVKZTYMQWFHE-UHFFFAOYSA-N 0.000 claims description 5
• NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 5
• 125000000304 alkynyl group Chemical group 0.000 claims description 5
• 125000004658 aryl carbonyl amino group Chemical group 0.000 claims description 5
• QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 5
• 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 claims description 5
• 125000002883 imidazolyl group Chemical group 0.000 claims description 5
• 125000004433 nitrogen atom Chemical group N* 0.000 claims description 5
• 229910052760 oxygen Inorganic materials 0.000 claims description 5
• 239000001301 oxygen Substances 0.000 claims description 5
• 239000008194 pharmaceutical composition Substances 0.000 claims description 5
• 125000000719 pyrrolidinyl group Chemical group 0.000 claims description 5
• OTDNZOGQKZNOHQ-UHFFFAOYSA-N 2-methyl-n-[4-[2-oxo-2-[(5-propan-2-yl-1,3-thiazol-2-yl)amino]ethyl]-1,3-thiazol-2-yl]propanamide Chemical compound S1C(NC(=O)C(C)C)=NC(CC(=O)NC=2SC(=CN=2)C(C)C)=C1 OTDNZOGQKZNOHQ-UHFFFAOYSA-N 0.000 claims description 4
• NUZDYTKXGWBRIE-UHFFFAOYSA-N 4-acetamido-n-[4-[2-oxo-2-[(5-propan-2-yl-1,3-thiazol-2-yl)amino]ethyl]phenyl]benzamide Chemical compound S1C(C(C)C)=CN=C1NC(=O)CC(C=C1)=CC=C1NC(=O)C1=CC=C(NC(C)=O)C=C1 NUZDYTKXGWBRIE-UHFFFAOYSA-N 0.000 claims description 4
• 201000001320 Atherosclerosis Diseases 0.000 claims description 4
• 241000124008 Mammalia Species 0.000 claims description 4
• 208000031481 Pathologic Constriction Diseases 0.000 claims description 4
• 201000004681 Psoriasis Diseases 0.000 claims description 4
• 230000022131 cell cycle Effects 0.000 claims description 4
• 239000003085 diluting agent Substances 0.000 claims description 4
• 239000003937 drug carrier Substances 0.000 claims description 4
• 150000002431 hydrogen Chemical class 0.000 claims description 4
• QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 4
• 125000005476 oxopyrrolidinyl group Chemical group 0.000 claims description 4
• 208000037803 restenosis Diseases 0.000 claims description 4
• 230000036262 stenosis Effects 0.000 claims description 4
• 208000037804 stenosis Diseases 0.000 claims description 4
• 229910052717 sulfur Inorganic materials 0.000 claims description 4
• 239000011593 sulfur Substances 0.000 claims description 4
• 230000002792 vascular Effects 0.000 claims description 4
• ITXDTLFHXZMTLP-UHFFFAOYSA-N 2-[2-[(2-chloroacetyl)amino]-1,3-thiazol-4-yl]-n-(5-propan-2-yl-1,3-thiazol-2-yl)acetamide Chemical compound S1C(C(C)C)=CN=C1NC(=O)CC1=CSC(NC(=O)CCl)=N1 ITXDTLFHXZMTLP-UHFFFAOYSA-N 0.000 claims description 3
• OTPSCVPEDTYBCE-UHFFFAOYSA-N 2-[2-[[2-(4-methylpiperazin-1-yl)acetyl]amino]-1,3-thiazol-4-yl]-n-(5-propan-2-yl-1,3-thiazol-2-yl)acetamide Chemical compound S1C(C(C)C)=CN=C1NC(=O)CC1=CSC(NC(=O)CN2CCN(C)CC2)=N1 OTPSCVPEDTYBCE-UHFFFAOYSA-N 0.000 claims description 3
• ZEYSLZVCVAIGKV-UHFFFAOYSA-N 2-[4-[(2-methoxyacetyl)amino]phenyl]-n-(5-propan-2-yl-1,3-thiazol-2-yl)acetamide Chemical compound C1=CC(NC(=O)COC)=CC=C1CC(=O)NC1=NC=C(C(C)C)S1 ZEYSLZVCVAIGKV-UHFFFAOYSA-N 0.000 claims description 3
• LGEPXMXHJWNJLH-UHFFFAOYSA-N 4-hydroxy-n-[4-[2-oxo-2-[(5-propan-2-yl-1,3-thiazol-2-yl)amino]ethyl]-1,3-thiazol-2-yl]butanamide Chemical compound S1C(C(C)C)=CN=C1NC(=O)CC1=CSC(NC(=O)CCCO)=N1 LGEPXMXHJWNJLH-UHFFFAOYSA-N 0.000 claims description 3
• HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims description 3
• 206010018364 Glomerulonephritis Diseases 0.000 claims description 3
• 208000007766 Kaposi sarcoma Diseases 0.000 claims description 3
• 208000009905 Neurofibromatoses Diseases 0.000 claims description 3
• 102100026379 Neurofibromin Human genes 0.000 claims description 3
• ZCQWOFVYLHDMMC-UHFFFAOYSA-N Oxazole Chemical compound C1=COC=N1 ZCQWOFVYLHDMMC-UHFFFAOYSA-N 0.000 claims description 3
• WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 claims description 3
• CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 claims description 3
• 201000010208 Seminoma Diseases 0.000 claims description 3
• 206010003246 arthritis Diseases 0.000 claims description 3
• 210000003169 central nervous system Anatomy 0.000 claims description 3
• 201000005787 hematologic cancer Diseases 0.000 claims description 3
• 208000024200 hematopoietic and lymphoid system neoplasm Diseases 0.000 claims description 3
• 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 3
• CTAPFRYPJLPFDF-UHFFFAOYSA-N isoxazole Chemical compound C=1C=NOC=1 CTAPFRYPJLPFDF-UHFFFAOYSA-N 0.000 claims description 3
• WRIRWRKPLXCTFD-UHFFFAOYSA-N malonamide Chemical compound NC(=O)CC(N)=O WRIRWRKPLXCTFD-UHFFFAOYSA-N 0.000 claims description 3
• 201000001441 melanoma Diseases 0.000 claims description 3
• AMLGOMUQBFIHPF-UHFFFAOYSA-N n-[4-[2-oxo-2-[(5-propan-2-yl-1,3-thiazol-2-yl)amino]ethyl]-1,3-thiazol-2-yl]benzamide Chemical compound S1C(C(C)C)=CN=C1NC(=O)CC1=CSC(NC(=O)C=2C=CC=CC=2)=N1 AMLGOMUQBFIHPF-UHFFFAOYSA-N 0.000 claims description 3
• BYEFXUBTPUCHGJ-UHFFFAOYSA-N n-[4-[2-oxo-2-[(5-propan-2-yl-1,3-thiazol-2-yl)amino]ethyl]phenyl]-1,3-benzodioxole-5-carboxamide Chemical compound S1C(C(C)C)=CN=C1NC(=O)CC(C=C1)=CC=C1NC(=O)C1=CC=C(OCO2)C2=C1 BYEFXUBTPUCHGJ-UHFFFAOYSA-N 0.000 claims description 3
• 201000004931 neurofibromatosis Diseases 0.000 claims description 3
• 229960003966 nicotinamide Drugs 0.000 claims description 3
• 235000005152 nicotinamide Nutrition 0.000 claims description 3
• 239000011570 nicotinamide Substances 0.000 claims description 3
• 201000008968 osteosarcoma Diseases 0.000 claims description 3
• 210000001428 peripheral nervous system Anatomy 0.000 claims description 3
• 208000015768 polyposis Diseases 0.000 claims description 3
• 206010041823 squamous cell carcinoma Diseases 0.000 claims description 3
• 125000003107 substituted aryl group Chemical group 0.000 claims description 3
• 208000001608 teratocarcinoma Diseases 0.000 claims description 3
• 125000000437 thiazol-2-yl group Chemical group [H]C1=C([H])N=C(*)S1 0.000 claims description 3
• 229930192474 thiophene Natural products 0.000 claims description 3
• 210000001685 thyroid gland Anatomy 0.000 claims description 3
• JUYXRYAKOREOPH-UHFFFAOYSA-N 2-[2-[[2-(dimethylamino)acetyl]amino]-1,3-thiazol-4-yl]-n-(5-propan-2-yl-1,3-thiazol-2-yl)acetamide Chemical compound S1C(C(C)C)=CN=C1NC(=O)CC1=CSC(NC(=O)CN(C)C)=N1 JUYXRYAKOREOPH-UHFFFAOYSA-N 0.000 claims description 2
• BEXGHNAZEIPDFE-UHFFFAOYSA-N 2-[4-[(2-amino-2-oxoethyl)amino]phenyl]-n-(5-propan-2-yl-1,3-thiazol-2-yl)acetamide Chemical compound S1C(C(C)C)=CN=C1NC(=O)CC1=CC=C(NCC(N)=O)C=C1 BEXGHNAZEIPDFE-UHFFFAOYSA-N 0.000 claims description 2
• XPIHETDVVVKZJO-UHFFFAOYSA-N 2-[4-[methyl(2-morpholin-4-ylethyl)amino]phenyl]-n-(5-propan-2-yl-1,3-thiazol-2-yl)acetamide Chemical compound S1C(C(C)C)=CN=C1NC(=O)CC1=CC=C(N(C)CCN2CCOCC2)C=C1 XPIHETDVVVKZJO-UHFFFAOYSA-N 0.000 claims description 2
• RXRXQDZXKBXOOY-UHFFFAOYSA-N 3-amino-n-[4-[2-oxo-2-[(5-propan-2-yl-1,3-thiazol-2-yl)amino]ethyl]-1,3-thiazol-2-yl]propanamide Chemical compound S1C(C(C)C)=CN=C1NC(=O)CC1=CSC(NC(=O)CCN)=N1 RXRXQDZXKBXOOY-UHFFFAOYSA-N 0.000 claims description 2
• 206010004446 Benign prostatic hyperplasia Diseases 0.000 claims description 2
• LKJPYSCBVHEWIU-UHFFFAOYSA-N N-[4-cyano-3-(trifluoromethyl)phenyl]-3-[(4-fluorophenyl)sulfonyl]-2-hydroxy-2-methylpropanamide Chemical compound C=1C=C(C#N)C(C(F)(F)F)=CC=1NC(=O)C(O)(C)CS(=O)(=O)C1=CC=C(F)C=C1 LKJPYSCBVHEWIU-UHFFFAOYSA-N 0.000 claims description 2
• 239000000824 cytostatic agent Substances 0.000 claims description 2
• 230000001085 cytostatic effect Effects 0.000 claims description 2
• 230000003325 follicular Effects 0.000 claims description 2
• 230000002685 pulmonary effect Effects 0.000 claims description 2
• 238000001959 radiotherapy Methods 0.000 claims description 2
• 125000001424 substituent group Chemical group 0.000 claims description 2
• 230000005747 tumor angiogenesis Effects 0.000 claims description 2
• QCQWRTATHSYOGH-UHFFFAOYSA-N 2-[2-[(2-fluoroacetyl)amino]-1,3-thiazol-4-yl]-n-(5-propan-2-yl-1,3-thiazol-2-yl)acetamide Chemical compound S1C(C(C)C)=CN=C1NC(=O)CC1=CSC(NC(=O)CF)=N1 QCQWRTATHSYOGH-UHFFFAOYSA-N 0.000 claims 2
• XGKFCSOSNIHLTI-UHFFFAOYSA-N 2-[4-(2-morpholin-4-ylethylamino)phenyl]-n-(5-propan-2-yl-1,3-thiazol-2-yl)acetamide Chemical compound S1C(C(C)C)=CN=C1NC(=O)CC(C=C1)=CC=C1NCCN1CCOCC1 XGKFCSOSNIHLTI-UHFFFAOYSA-N 0.000 claims 2
• BCCWEQFYZCJLCE-UHFFFAOYSA-N 2-[4-[[3-(dimethylamino)-2-hydroxypropyl]amino]phenyl]-n-(5-propan-2-yl-1,3-thiazol-2-yl)acetamide Chemical compound S1C(C(C)C)=CN=C1NC(=O)CC1=CC=C(NCC(O)CN(C)C)C=C1 BCCWEQFYZCJLCE-UHFFFAOYSA-N 0.000 claims 2
• UGMDPLFPVDXIKU-UHFFFAOYSA-N 2-cyano-n-[4-[2-oxo-2-[(5-propan-2-yl-1,3-thiazol-2-yl)amino]ethyl]-1,3-thiazol-2-yl]acetamide Chemical compound S1C(C(C)C)=CN=C1NC(=O)CC1=CSC(NC(=O)CC#N)=N1 UGMDPLFPVDXIKU-UHFFFAOYSA-N 0.000 claims 2
• JUDSXZMOCRCDQM-UHFFFAOYSA-N 1-acetyl-n-[4-[2-oxo-2-[(5-propan-2-yl-1,3-thiazol-2-yl)amino]ethyl]-1,3-thiazol-2-yl]piperidine-4-carboxamide Chemical compound S1C(C(C)C)=CN=C1NC(=O)CC1=CSC(NC(=O)C2CCN(CC2)C(C)=O)=N1 JUDSXZMOCRCDQM-UHFFFAOYSA-N 0.000 claims 1
• OYFBZCDKJQUZIV-UHFFFAOYSA-N 2,2,2-trifluoro-n-[4-[2-oxo-2-[(5-propan-2-yl-1,3-thiazol-2-yl)amino]ethyl]-1,3-thiazol-2-yl]acetamide Chemical compound S1C(C(C)C)=CN=C1NC(=O)CC1=CSC(NC(=O)C(F)(F)F)=N1 OYFBZCDKJQUZIV-UHFFFAOYSA-N 0.000 claims 1
• FWDNBSRTVKBKBT-UHFFFAOYSA-N 2,2,3,3,3-pentafluoro-n-[4-[2-oxo-2-[(5-propan-2-yl-1,3-thiazol-2-yl)amino]ethyl]-1,3-thiazol-2-yl]propanamide Chemical compound S1C(C(C)C)=CN=C1NC(=O)CC1=CSC(NC(=O)C(F)(F)C(F)(F)F)=N1 FWDNBSRTVKBKBT-UHFFFAOYSA-N 0.000 claims 1
• HQCKPRAQBXUJBV-UHFFFAOYSA-N 2-[2-(2,3-dihydroxypropylamino)-1,3-thiazol-4-yl]-n-(5-propan-2-yl-1,3-thiazol-2-yl)acetamide Chemical compound S1C(C(C)C)=CN=C1NC(=O)CC1=CSC(NCC(O)CO)=N1 HQCKPRAQBXUJBV-UHFFFAOYSA-N 0.000 claims 1
• FRXQYJCXJZIVDE-UHFFFAOYSA-N 2-[2-(2-oxopyrrolidin-1-yl)-1,3-thiazol-4-yl]-n-(5-propan-2-yl-1,3-thiazol-2-yl)acetamide Chemical compound S1C(C(C)C)=CN=C1NC(=O)CC1=CSC(N2C(CCC2)=O)=N1 FRXQYJCXJZIVDE-UHFFFAOYSA-N 0.000 claims 1
• IOHLVTZUFQWZJS-UHFFFAOYSA-N 2-[2-[(2-amino-2-oxoethyl)amino]-1,3-thiazol-4-yl]-n-(5-propan-2-yl-1,3-thiazol-2-yl)acetamide Chemical compound S1C(C(C)C)=CN=C1NC(=O)CC1=CSC(NCC(N)=O)=N1 IOHLVTZUFQWZJS-UHFFFAOYSA-N 0.000 claims 1
• UDNSSCBKEKACHB-UHFFFAOYSA-N 2-[2-[[3-(dimethylamino)-2-hydroxypropyl]amino]-1,3-thiazol-4-yl]-n-(5-propan-2-yl-1,3-thiazol-2-yl)acetamide Chemical compound S1C(C(C)C)=CN=C1NC(=O)CC1=CSC(NCC(O)CN(C)C)=N1 UDNSSCBKEKACHB-UHFFFAOYSA-N 0.000 claims 1
• DJYPNPCYARISTG-UHFFFAOYSA-N 2-cyano-n-[4-[2-oxo-2-[(5-propan-2-yl-1,3-thiazol-2-yl)amino]ethyl]phenyl]acetamide Chemical compound S1C(C(C)C)=CN=C1NC(=O)CC1=CC=C(NC(=O)CC#N)C=C1 DJYPNPCYARISTG-UHFFFAOYSA-N 0.000 claims 1
• MTEZLAATISORQK-UHFFFAOYSA-N 2-methoxyacetamide Chemical compound COCC(N)=O MTEZLAATISORQK-UHFFFAOYSA-N 0.000 claims 1
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