KR20100119773A - 소정의 화학물질, 조성물 및 방법 - Google Patents
소정의 화학물질, 조성물 및 방법 Download PDFInfo
- Publication number
- KR20100119773A KR20100119773A KR1020107018611A KR20107018611A KR20100119773A KR 20100119773 A KR20100119773 A KR 20100119773A KR 1020107018611 A KR1020107018611 A KR 1020107018611A KR 20107018611 A KR20107018611 A KR 20107018611A KR 20100119773 A KR20100119773 A KR 20100119773A
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- KR
- South Korea
- Prior art keywords
- chloro
- pyridin
- imidazo
- ethylpropyl
- optionally substituted
- 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.)
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- 238000000034 method Methods 0.000 title claims abstract description 51
- 239000000203 mixture Substances 0.000 title claims description 58
- 150000005829 chemical entities Chemical class 0.000 title claims 2
- 239000000126 substance Substances 0.000 claims abstract description 103
- 210000002027 skeletal muscle Anatomy 0.000 claims abstract description 59
- 102000003505 Myosin Human genes 0.000 claims abstract description 43
- 108060008487 Myosin Proteins 0.000 claims abstract description 41
- 102000007469 Actins Human genes 0.000 claims abstract description 37
- 108010085238 Actins Proteins 0.000 claims abstract description 37
- 108090000362 Lymphotoxin-beta Proteins 0.000 claims abstract description 17
- 102000013534 Troponin C Human genes 0.000 claims abstract description 17
- 102000013394 Troponin I Human genes 0.000 claims abstract description 17
- 108010065729 Troponin I Proteins 0.000 claims abstract description 17
- 206010049565 Muscle fatigue Diseases 0.000 claims abstract description 13
- 208000010428 Muscle Weakness Diseases 0.000 claims abstract description 12
- 206010028372 Muscular weakness Diseases 0.000 claims abstract description 12
- 102000005937 Tropomyosin Human genes 0.000 claims abstract description 12
- 108010030743 Tropomyosin Proteins 0.000 claims abstract description 12
- 201000006938 muscular dystrophy Diseases 0.000 claims abstract description 12
- 206010017577 Gait disturbance Diseases 0.000 claims abstract description 9
- 208000001145 Metabolic Syndrome Diseases 0.000 claims abstract description 9
- 201000000690 abdominal obesity-metabolic syndrome Diseases 0.000 claims abstract description 9
- 208000018360 neuromuscular disease Diseases 0.000 claims abstract description 9
- 206010039966 Senile dementia Diseases 0.000 claims abstract description 4
- 150000001875 compounds Chemical class 0.000 claims description 110
- -1 cyano, sulfonyl Chemical group 0.000 claims description 109
- 210000001087 myotubule Anatomy 0.000 claims description 62
- 125000001072 heteroaryl group Chemical group 0.000 claims description 54
- 239000001257 hydrogen Substances 0.000 claims description 54
- 229910052739 hydrogen Inorganic materials 0.000 claims description 54
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims description 49
- 125000000217 alkyl group Chemical group 0.000 claims description 48
- 125000005843 halogen group Chemical group 0.000 claims description 43
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 41
- 150000003839 salts Chemical class 0.000 claims description 36
- 125000003118 aryl group Chemical group 0.000 claims description 34
- 150000002431 hydrogen Chemical class 0.000 claims description 34
- 230000001965 increasing effect Effects 0.000 claims description 34
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 31
- 201000010099 disease Diseases 0.000 claims description 30
- 230000027455 binding Effects 0.000 claims description 25
- 102000004903 Troponin Human genes 0.000 claims description 23
- 108090001027 Troponin Proteins 0.000 claims description 23
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 23
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 21
- 125000000547 substituted alkyl group Chemical group 0.000 claims description 21
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 20
- 125000005346 substituted cycloalkyl group Chemical group 0.000 claims description 19
- 229910001424 calcium ion Inorganic materials 0.000 claims description 18
- 230000000694 effects Effects 0.000 claims description 18
- UBQKCCHYAOITMY-UHFFFAOYSA-N pyridin-2-ol Chemical compound OC1=CC=CC=N1 UBQKCCHYAOITMY-UHFFFAOYSA-N 0.000 claims description 18
- 125000003107 substituted aryl group Chemical group 0.000 claims description 18
- BHPQYMZQTOCNFJ-UHFFFAOYSA-N Calcium cation Chemical compound [Ca+2] BHPQYMZQTOCNFJ-UHFFFAOYSA-N 0.000 claims description 17
- 125000003545 alkoxy group Chemical group 0.000 claims description 17
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 16
- 239000000843 powder Substances 0.000 claims description 16
- 125000005415 substituted alkoxy group Chemical group 0.000 claims description 16
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 14
- 125000002252 acyl group Chemical group 0.000 claims description 13
- 125000001153 fluoro group Chemical group F* 0.000 claims description 12
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 12
- 239000008194 pharmaceutical composition Substances 0.000 claims description 11
- 125000004426 substituted alkynyl group Chemical group 0.000 claims description 11
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 11
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 10
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 10
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 claims description 10
- 125000003396 thiol group Chemical group [H]S* 0.000 claims description 10
- 125000005017 substituted alkenyl group Chemical group 0.000 claims description 9
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims description 9
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 8
- 229910019142 PO4 Inorganic materials 0.000 claims description 7
- 125000003342 alkenyl group Chemical group 0.000 claims description 7
- 239000007788 liquid Substances 0.000 claims description 7
- 125000003538 pentan-3-yl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])[H] 0.000 claims description 7
- 239000010452 phosphate Substances 0.000 claims description 7
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 7
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 claims description 6
- 125000004076 pyridyl group Chemical group 0.000 claims description 6
- 230000004044 response Effects 0.000 claims description 6
- 230000001235 sensitizing effect Effects 0.000 claims description 6
- 239000000725 suspension Substances 0.000 claims description 6
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims description 5
- 125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 claims description 5
- 125000003226 pyrazolyl group Chemical group 0.000 claims description 5
- BMDWOFRPWOGVFM-UHFFFAOYSA-N 6-chloro-1-pentan-3-yl-7-(1h-pyrazol-5-yl)-3h-imidazo[4,5-b]pyridin-2-one Chemical compound ClC1=CN=C2NC(=O)N(C(CC)CC)C2=C1C1=CC=NN1 BMDWOFRPWOGVFM-UHFFFAOYSA-N 0.000 claims description 4
- RXAZLVNEEDRDDS-NSHDSACASA-N 6-chloro-7-(4-chlorophenyl)-1-[(2s)-1-hydroxybutan-2-yl]-3h-imidazo[4,5-b]pyridin-2-one Chemical compound C=12N([C@H](CO)CC)C(O)=NC2=NC=C(Cl)C=1C1=CC=C(Cl)C=C1 RXAZLVNEEDRDDS-NSHDSACASA-N 0.000 claims description 4
- 239000000443 aerosol Substances 0.000 claims description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 4
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 4
- 125000004353 pyrazol-1-yl group Chemical group [H]C1=NN(*)C([H])=C1[H] 0.000 claims description 4
- 230000035945 sensitivity Effects 0.000 claims description 4
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 4
- YNIJFAACHRCCOR-UHFFFAOYSA-N 6-chloro-1-pentan-3-yl-7-phenyl-3h-imidazo[4,5-b]pyridin-2-one Chemical compound C=12N(C(CC)CC)C(O)=NC2=NC=C(Cl)C=1C1=CC=CC=C1 YNIJFAACHRCCOR-UHFFFAOYSA-N 0.000 claims description 3
- 101710167936 Troponin T, skeletal muscle Proteins 0.000 claims description 3
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 3
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 3
- 239000003937 drug carrier Substances 0.000 claims description 3
- 125000001188 haloalkyl group Chemical group 0.000 claims description 3
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 claims description 3
- 239000003826 tablet Substances 0.000 claims description 3
- 125000003831 tetrazolyl group Chemical group 0.000 claims description 3
- ADUPQRNIROZRKO-SSDOTTSWSA-N 1-[(2r)-butan-2-yl]-6-chloro-7-(1h-pyrazol-5-yl)-3h-imidazo[4,5-b]pyridin-2-one Chemical compound C=12N([C@H](C)CC)C(O)=NC2=NC=C(Cl)C=1C=1C=CNN=1 ADUPQRNIROZRKO-SSDOTTSWSA-N 0.000 claims description 2
- FDQQWYUUSDMLTI-MRVPVSSYSA-N 1-[(2r)-butan-2-yl]-7-(1h-pyrazol-5-yl)-3h-imidazo[4,5-b]pyridin-2-one Chemical compound C=12N([C@H](C)CC)C(O)=NC2=NC=CC=1C=1C=CNN=1 FDQQWYUUSDMLTI-MRVPVSSYSA-N 0.000 claims description 2
- BMSYQEMQEWHEJK-NSHDSACASA-N 1-[(2s)-1-aminobutan-2-yl]-6-chloro-7-(4-fluorophenyl)-3h-imidazo[4,5-b]pyridin-2-one Chemical compound C=12N([C@H](CN)CC)C(O)=NC2=NC=C(Cl)C=1C1=CC=C(F)C=C1 BMSYQEMQEWHEJK-NSHDSACASA-N 0.000 claims description 2
- CMHYCJNHMIZLFA-VIFPVBQESA-N 1-[(2s)-1-aminobutan-2-yl]-6-chloro-7-(5-fluoropyridin-2-yl)-3h-imidazo[4,5-b]pyridin-2-one Chemical compound C=12N([C@H](CN)CC)C(O)=NC2=NC=C(Cl)C=1C1=CC=C(F)C=N1 CMHYCJNHMIZLFA-VIFPVBQESA-N 0.000 claims description 2
- JYUYITBVXQHPKD-LURJTMIESA-N 1-[(2s)-butan-2-yl]-6-chloro-3h-imidazo[4,5-b]pyridin-2-one Chemical compound C1=C(Cl)C=C2N([C@@H](C)CC)C(O)=NC2=N1 JYUYITBVXQHPKD-LURJTMIESA-N 0.000 claims description 2
- ADUPQRNIROZRKO-ZETCQYMHSA-N 1-[(2s)-butan-2-yl]-6-chloro-7-(1h-pyrazol-5-yl)-3h-imidazo[4,5-b]pyridin-2-one Chemical compound C=12N([C@@H](C)CC)C(O)=NC2=NC=C(Cl)C=1C=1C=CNN=1 ADUPQRNIROZRKO-ZETCQYMHSA-N 0.000 claims description 2
- DVNDHQNSEPGITP-UHFFFAOYSA-N 1-tert-butyl-6-chloro-7-(4-fluorophenyl)-3h-imidazo[4,5-b]pyridin-2-one Chemical compound C=12N(C(C)(C)C)C(O)=NC2=NC=C(Cl)C=1C1=CC=C(F)C=C1 DVNDHQNSEPGITP-UHFFFAOYSA-N 0.000 claims description 2
- VARIKNWGMWEYDL-UHFFFAOYSA-N 2-(6-chloro-2-oxo-1-pentan-3-yl-3h-imidazo[4,5-b]pyridin-7-yl)benzaldehyde Chemical compound ClC1=CN=C2NC(=O)N(C(CC)CC)C2=C1C1=CC=CC=C1C=O VARIKNWGMWEYDL-UHFFFAOYSA-N 0.000 claims description 2
- CAPRZPQXPSVBFI-UHFFFAOYSA-N 2-(6-chloro-2-oxo-1-pentan-3-yl-3h-imidazo[4,5-b]pyridin-7-yl)benzoic acid Chemical compound ClC1=CN=C2NC(=O)N(C(CC)CC)C2=C1C1=CC=CC=C1C(O)=O CAPRZPQXPSVBFI-UHFFFAOYSA-N 0.000 claims description 2
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims description 2
- TZZHUHOXXQAMTC-UHFFFAOYSA-N 3-(6-chloro-2-oxo-1-pentan-3-yl-3h-imidazo[4,5-b]pyridin-7-yl)-n,n-dimethylbenzamide Chemical compound ClC1=CN=C2NC(=O)N(C(CC)CC)C2=C1C1=CC=CC(C(=O)N(C)C)=C1 TZZHUHOXXQAMTC-UHFFFAOYSA-N 0.000 claims description 2
- INEIAIHSNQMWTN-UHFFFAOYSA-N 3-(6-chloro-2-oxo-1-pentan-3-yl-3h-imidazo[4,5-b]pyridin-7-yl)benzaldehyde Chemical compound ClC1=CN=C2NC(=O)N(C(CC)CC)C2=C1C1=CC=CC(C=O)=C1 INEIAIHSNQMWTN-UHFFFAOYSA-N 0.000 claims description 2
- MWQGUGFJIDKFDD-UHFFFAOYSA-N 3-(6-chloro-2-oxo-1-pentan-3-yl-3h-imidazo[4,5-b]pyridin-7-yl)benzonitrile Chemical compound ClC1=CN=C2NC(=O)N(C(CC)CC)C2=C1C1=CC=CC(C#N)=C1 MWQGUGFJIDKFDD-UHFFFAOYSA-N 0.000 claims description 2
- QOXOZONBQWIKDA-UHFFFAOYSA-N 3-hydroxypropyl Chemical group [CH2]CCO QOXOZONBQWIKDA-UHFFFAOYSA-N 0.000 claims description 2
- CGQZMRRXIUYXQO-UHFFFAOYSA-N 4-(6-chloro-2-oxo-1-pentan-3-yl-3h-imidazo[4,5-b]pyridin-7-yl)-2-fluorobenzonitrile Chemical compound C=12N(C(CC)CC)C(O)=NC2=NC=C(Cl)C=1C1=CC=C(C#N)C(F)=C1 CGQZMRRXIUYXQO-UHFFFAOYSA-N 0.000 claims description 2
- WDBLLNRUCIKLJB-UHFFFAOYSA-N 4-(6-chloro-2-oxo-1-pentan-3-yl-3h-imidazo[4,5-b]pyridin-7-yl)benzonitrile Chemical compound ClC1=CN=C2NC(=O)N(C(CC)CC)C2=C1C1=CC=C(C#N)C=C1 WDBLLNRUCIKLJB-UHFFFAOYSA-N 0.000 claims description 2
- DTPGHZLCYAHKFV-UHFFFAOYSA-N 4-(6-chloro-2-oxo-1-pentan-3-yl-3h-imidazo[4,5-b]pyridin-7-yl)pyridine-2-carbonitrile Chemical compound C=12N(C(CC)CC)C(O)=NC2=NC=C(Cl)C=1C1=CC=NC(C#N)=C1 DTPGHZLCYAHKFV-UHFFFAOYSA-N 0.000 claims description 2
- IEOAODVZVIXPKD-LBPRGKRZSA-N 4-[6-chloro-1-[(2s)-1-hydroxybutan-2-yl]-2-oxo-3h-imidazo[4,5-b]pyridin-7-yl]benzonitrile Chemical compound C=12N([C@H](CO)CC)C(O)=NC2=NC=C(Cl)C=1C1=CC=C(C#N)C=C1 IEOAODVZVIXPKD-LBPRGKRZSA-N 0.000 claims description 2
- REHHNNUDJRUUQE-KRWDZBQOSA-N 6,7-bis(4-fluorophenyl)-1-[(2s)-1-hydroxybutan-2-yl]-3h-imidazo[4,5-b]pyridin-2-one Chemical compound C=1C=C(F)C=CC=1C1=C2N([C@H](CO)CC)C(O)=NC2=NC=C1C1=CC=C(F)C=C1 REHHNNUDJRUUQE-KRWDZBQOSA-N 0.000 claims description 2
- ZUFCFJYQKULJLB-UHFFFAOYSA-N 6-(6-chloro-2-oxo-1-pentan-3-yl-3h-imidazo[4,5-b]pyridin-7-yl)pyridine-3-carbonitrile Chemical compound ClC1=CN=C2NC(=O)N(C(CC)CC)C2=C1C1=CC=C(C#N)C=N1 ZUFCFJYQKULJLB-UHFFFAOYSA-N 0.000 claims description 2
- FCPYQGKOURADIN-UHFFFAOYSA-N 6-chloro-1-(1,3-dimethoxypropan-2-yl)-7-(1h-pyrazol-5-yl)-3h-imidazo[4,5-b]pyridin-2-one Chemical compound C=12N(C(COC)COC)C(O)=NC2=NC=C(Cl)C=1C=1C=CNN=1 FCPYQGKOURADIN-UHFFFAOYSA-N 0.000 claims description 2
- LZCYJOKCZJGJCD-UHFFFAOYSA-N 6-chloro-1-(2-hydroxyethyl)-7-phenyl-3h-imidazo[4,5-b]pyridin-2-one Chemical compound C=12N(CCO)C(O)=NC2=NC=C(Cl)C=1C1=CC=CC=C1 LZCYJOKCZJGJCD-UHFFFAOYSA-N 0.000 claims description 2
- IZYHHJIHNBKLPM-ZETCQYMHSA-N 6-chloro-1-[(2s)-1-hydroxybutan-2-yl]-7-(1h-pyrazol-5-yl)-3h-imidazo[4,5-b]pyridin-2-one Chemical compound C=12N([C@H](CO)CC)C(O)=NC2=NC=C(Cl)C=1C=1C=CNN=1 IZYHHJIHNBKLPM-ZETCQYMHSA-N 0.000 claims description 2
- ODSBHTXNCGPDNG-NSHDSACASA-N 6-chloro-1-[(2s)-1-hydroxybutan-2-yl]-7-(4-methoxyphenyl)-3h-imidazo[4,5-b]pyridin-2-one Chemical compound C=12N([C@H](CO)CC)C(O)=NC2=NC=C(Cl)C=1C1=CC=C(OC)C=C1 ODSBHTXNCGPDNG-NSHDSACASA-N 0.000 claims description 2
- WJHCPNLTDZTXNU-LBPRGKRZSA-N 6-chloro-1-[(2s)-1-hydroxybutan-2-yl]-7-(4-methylphenyl)-3h-imidazo[4,5-b]pyridin-2-one Chemical compound C=12N([C@H](CO)CC)C(O)=NC2=NC=C(Cl)C=1C1=CC=C(C)C=C1 WJHCPNLTDZTXNU-LBPRGKRZSA-N 0.000 claims description 2
- CPAVEBWOKYZZFT-NSHDSACASA-N 6-chloro-1-[(2s)-1-hydroxybutan-2-yl]-7-phenyl-3h-imidazo[4,5-b]pyridin-2-one Chemical compound C=12N([C@H](CO)CC)C(O)=NC2=NC=C(Cl)C=1C1=CC=CC=C1 CPAVEBWOKYZZFT-NSHDSACASA-N 0.000 claims description 2
- IXYFLNDXZLKTBB-QMMMGPOBSA-N 6-chloro-1-[(2s)-1-hydroxybutan-2-yl]-7-pyrazin-2-yl-3h-imidazo[4,5-b]pyridin-2-one Chemical compound C=12N([C@H](CO)CC)C(O)=NC2=NC=C(Cl)C=1C1=CN=CC=N1 IXYFLNDXZLKTBB-QMMMGPOBSA-N 0.000 claims description 2
- ZOIMMIXUBNWRDN-QMMMGPOBSA-N 6-chloro-1-[(2s)-1-hydroxybutan-2-yl]-7-thiophen-2-yl-3h-imidazo[4,5-b]pyridin-2-one Chemical compound C=12N([C@H](CO)CC)C(O)=NC2=NC=C(Cl)C=1C1=CC=CS1 ZOIMMIXUBNWRDN-QMMMGPOBSA-N 0.000 claims description 2
- VQDRPDVJXKHQKI-VIFPVBQESA-N 6-chloro-1-[(2s)-1-hydroxybutan-2-yl]-7-thiophen-3-yl-3h-imidazo[4,5-b]pyridin-2-one Chemical compound C=12N([C@H](CO)CC)C(O)=NC2=NC=C(Cl)C=1C=1C=CSC=1 VQDRPDVJXKHQKI-VIFPVBQESA-N 0.000 claims description 2
- XUOCAROVDCEWOB-UHFFFAOYSA-N 6-chloro-1-cyclopentyl-7-(4-fluorophenyl)-3h-imidazo[4,5-b]pyridin-2-one Chemical compound C=12N(C3CCCC3)C(O)=NC2=NC=C(Cl)C=1C1=CC=C(F)C=C1 XUOCAROVDCEWOB-UHFFFAOYSA-N 0.000 claims description 2
- FPQHXKMKKCAKLA-UHFFFAOYSA-N 6-chloro-1-pentan-3-yl-7-(1h-pyrazol-4-yl)-3h-imidazo[4,5-b]pyridin-2-one Chemical compound ClC1=CN=C2NC(=O)N(C(CC)CC)C2=C1C=1C=NNC=1 FPQHXKMKKCAKLA-UHFFFAOYSA-N 0.000 claims description 2
- UXGPTZGDPLJBRU-UHFFFAOYSA-N 6-chloro-1-pentan-3-yl-7-[2-(trifluoromethyl)pyridin-4-yl]-3h-imidazo[4,5-b]pyridin-2-one Chemical compound ClC1=CN=C2NC(=O)N(C(CC)CC)C2=C1C1=CC=NC(C(F)(F)F)=C1 UXGPTZGDPLJBRU-UHFFFAOYSA-N 0.000 claims description 2
- LTMJHOSSNGBOLG-UHFFFAOYSA-N 6-chloro-1-pentan-3-yl-7-[3-(trifluoromethoxy)phenyl]-3h-imidazo[4,5-b]pyridin-2-one Chemical compound ClC1=CN=C2NC(=O)N(C(CC)CC)C2=C1C1=CC=CC(OC(F)(F)F)=C1 LTMJHOSSNGBOLG-UHFFFAOYSA-N 0.000 claims description 2
- BWCJXKMPCVIASL-UHFFFAOYSA-N 6-chloro-1-pentan-3-yl-7-[4-(trifluoromethoxy)phenyl]-3h-imidazo[4,5-b]pyridin-2-one Chemical compound ClC1=CN=C2NC(=O)N(C(CC)CC)C2=C1C1=CC=C(OC(F)(F)F)C=C1 BWCJXKMPCVIASL-UHFFFAOYSA-N 0.000 claims description 2
- MOOSGJVEFLEETK-UHFFFAOYSA-N 6-chloro-1-pentan-3-yl-7-[4-(trifluoromethyl)phenyl]-3h-imidazo[4,5-b]pyridin-2-one Chemical compound ClC1=CN=C2NC(=O)N(C(CC)CC)C2=C1C1=CC=C(C(F)(F)F)C=C1 MOOSGJVEFLEETK-UHFFFAOYSA-N 0.000 claims description 2
- DXAZOKMFWXNGDP-UHFFFAOYSA-N 6-chloro-1-pentan-3-yl-7-pyridin-3-yl-3h-imidazo[4,5-b]pyridin-2-one Chemical compound ClC1=CN=C2NC(=O)N(C(CC)CC)C2=C1C1=CC=CN=C1 DXAZOKMFWXNGDP-UHFFFAOYSA-N 0.000 claims description 2
- FHALJWCXXHGPHH-UHFFFAOYSA-N 6-chloro-1-pentan-3-yl-7-pyridin-4-yl-3h-imidazo[4,5-b]pyridin-2-one Chemical compound ClC1=CN=C2NC(=O)N(C(CC)CC)C2=C1C1=CC=NC=C1 FHALJWCXXHGPHH-UHFFFAOYSA-N 0.000 claims description 2
- ONFDDIHJRNPVMI-UHFFFAOYSA-N 6-chloro-1-pentan-3-yl-7-thiophen-2-yl-3h-imidazo[4,5-b]pyridin-2-one Chemical compound ClC1=CN=C2NC(=O)N(C(CC)CC)C2=C1C1=CC=CS1 ONFDDIHJRNPVMI-UHFFFAOYSA-N 0.000 claims description 2
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- NHXLMOGPVYXJNR-ATOGVRKGSA-N somatostatin Chemical compound C([C@H]1C(=O)N[C@H](C(N[C@@H](CO)C(=O)N[C@@H](CSSC[C@@H](C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CC=2C=CC=CC=2)C(=O)N[C@@H](CC=2C=CC=CC=2)C(=O)N[C@@H](CC=2C3=CC=CC=C3NC=2)C(=O)N[C@@H](CCCCN)C(=O)N[C@H](C(=O)N1)[C@@H](C)O)NC(=O)CNC(=O)[C@H](C)N)C(O)=O)=O)[C@H](O)C)C1=CC=CC=C1 NHXLMOGPVYXJNR-ATOGVRKGSA-N 0.000 description 1
- 229960000553 somatostatin Drugs 0.000 description 1
- 229940035044 sorbitan monolaurate Drugs 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 210000000278 spinal cord Anatomy 0.000 description 1
- 230000002269 spontaneous effect Effects 0.000 description 1
- 108010087686 src-Family Kinases Proteins 0.000 description 1
- 229960001203 stavudine Drugs 0.000 description 1
- 230000004936 stimulating effect Effects 0.000 description 1
- 239000011232 storage material Substances 0.000 description 1
- 238000007920 subcutaneous administration Methods 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 1
- 229950007447 sulbenox Drugs 0.000 description 1
- 230000002459 sustained effect Effects 0.000 description 1
- 238000013268 sustained release Methods 0.000 description 1
- 210000000225 synapse Anatomy 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 229960001603 tamoxifen Drugs 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- OGBMKVWORPGQRR-UMXFMPSGSA-N teriparatide Chemical compound C([C@H](NC(=O)[C@H](CCSC)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H](N)CO)C(C)C)[C@@H](C)CC)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CC(C)C)C(=O)NCC(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC=1N=CNC=1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC=1N=CNC=1)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CC=1C=CC=CC=1)C(O)=O)C1=CNC=N1 OGBMKVWORPGQRR-UMXFMPSGSA-N 0.000 description 1
- 229960000278 theophylline Drugs 0.000 description 1
- 231100001274 therapeutic index Toxicity 0.000 description 1
- 125000005305 thiadiazolinyl group Chemical group 0.000 description 1
- 125000002769 thiazolinyl group Chemical group 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- 238000004809 thin layer chromatography Methods 0.000 description 1
- 210000001685 thyroid gland Anatomy 0.000 description 1
- 208000021510 thyroid gland disease Diseases 0.000 description 1
- 102000004217 thyroid hormone receptors Human genes 0.000 description 1
- 108090000721 thyroid hormone receptors Proteins 0.000 description 1
- 230000000699 topical effect Effects 0.000 description 1
- 229960004394 topiramate Drugs 0.000 description 1
- 125000005424 tosyloxy group Chemical group S(=O)(=O)(C1=CC=C(C)C=C1)O* 0.000 description 1
- 150000003626 triacylglycerols Chemical class 0.000 description 1
- 125000001425 triazolyl group Chemical group 0.000 description 1
- 229940117013 triethanolamine oleate Drugs 0.000 description 1
- YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical compound CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 0.000 description 1
- UPCXAARSWVHVLY-UHFFFAOYSA-N tris(2-hydroxyethyl)azanium;acetate Chemical compound CC(O)=O.OCCN(CCO)CCO UPCXAARSWVHVLY-UHFFFAOYSA-N 0.000 description 1
- 229940070710 valerate Drugs 0.000 description 1
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 1
- 230000002792 vascular Effects 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 230000002861 ventricular Effects 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 235000019166 vitamin D Nutrition 0.000 description 1
- 239000011710 vitamin D Substances 0.000 description 1
- 150000003710 vitamin D derivatives Chemical class 0.000 description 1
- 229940046008 vitamin d Drugs 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 230000003313 weakening effect Effects 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 229960000523 zalcitabine Drugs 0.000 description 1
- 229960002555 zidovudine Drugs 0.000 description 1
- HBOMLICNUCNMMY-XLPZGREQSA-N zidovudine Chemical compound O=C1NC(=O)C(C)=CN1[C@@H]1O[C@H](CO)[C@@H](N=[N+]=[N-])C1 HBOMLICNUCNMMY-XLPZGREQSA-N 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical class [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P21/00—Drugs for disorders of the muscular or neuromuscular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/04—Anorexiants; Antiobesity agents
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Diabetes (AREA)
- Neurology (AREA)
- Obesity (AREA)
- Hematology (AREA)
- Child & Adolescent Psychology (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Medicinal Preparation (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US2606708P | 2008-02-04 | 2008-02-04 | |
| US61/026,067 | 2008-02-04 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR20100119773A true KR20100119773A (ko) | 2010-11-10 |
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| Application Number | Title | Priority Date | Filing Date |
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|---|---|
| US (2) | US7989469B2 (enExample) |
| EP (1) | EP2244711A4 (enExample) |
| JP (1) | JP2011510985A (enExample) |
| KR (1) | KR20100119773A (enExample) |
| CN (1) | CN101983061A (enExample) |
| AR (1) | AR072242A1 (enExample) |
| AU (1) | AU2009210787A1 (enExample) |
| BR (1) | BRPI0907502A2 (enExample) |
| CA (1) | CA2713864A1 (enExample) |
| CL (1) | CL2009000246A1 (enExample) |
| CO (1) | CO6290673A2 (enExample) |
| EA (1) | EA201001224A1 (enExample) |
| EC (2) | ECSP10010430A (enExample) |
| IL (1) | IL207367A0 (enExample) |
| MX (1) | MX2010008518A (enExample) |
| TW (1) | TW200946524A (enExample) |
| WO (1) | WO2009099594A1 (enExample) |
| ZA (1) | ZA201005780B (enExample) |
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| US8299248B2 (en) | 2006-08-02 | 2012-10-30 | Cytokinetics, Incorporated | Certain 1H-imidazo[4,5-b]pyrazin-2(3H)-ones and 1H-imidazo[4,5-b]pyrazin-2-ols and methods for their use |
| MX2010008518A (es) * | 2008-02-04 | 2010-11-10 | Cytokinetics Inc | Ciertas entidades quimicas, composiciones y metodos. |
| CN102127070A (zh) * | 2010-01-15 | 2011-07-20 | 山东轩竹医药科技有限公司 | 吡啶并环衍生物 |
| US8927572B2 (en) | 2011-07-09 | 2015-01-06 | Xuanzhu Pharma Co., Ltd. | Crystal form I of salt of a dipeptidyl peptidase-IV inhibitor and preparation method and use thereof |
| WO2013010015A2 (en) | 2011-07-13 | 2013-01-17 | Cytokinetics, Inc. | Combination als therapy |
| CN104395458A (zh) * | 2012-04-11 | 2015-03-04 | 赛特凯恩蒂克公司 | 改善对骨骼肌疲劳的抵抗力 |
| EP3137622B1 (en) | 2014-04-29 | 2021-11-24 | Cytokinetics, Inc. | Methods of reducing decline in vital capacity |
| TW201927738A (zh) * | 2017-12-14 | 2019-07-16 | 丹麥商Ｎｍｄ藥品公司 | 用於治療神經肌肉病症的化合物 |
| TWI794369B (zh) * | 2017-12-14 | 2023-03-01 | 丹麥商Ｎｍｄ藥品公司 | 用於治療神經肌肉病症的化合物 |
| JP7592029B2 (ja) | 2019-05-28 | 2024-11-29 | マンカインド ファーマ リミテッド | ヤヌスキナーゼ１の阻害のための新規化合物 |
| KR20240024062A (ko) * | 2021-05-06 | 2024-02-23 | 엑스사이언티아 에이아이 리미티드 | Pkc-세타 조정제 |
| CN118702622A (zh) * | 2024-08-30 | 2024-09-27 | 阜新达得利化工股份有限公司 | 一种3-溴-2-氰基吡啶的制备方法 |
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| GB0206860D0 (en) * | 2002-03-22 | 2002-05-01 | Glaxo Group Ltd | Compounds |
| GB0212048D0 (en) * | 2002-05-24 | 2002-07-03 | Merck Sharp & Dohme | Therapeutic agents |
| AU2003294249A1 (en) | 2002-11-08 | 2004-06-03 | Trimeris, Inc. | Hetero-substituted benzimidazole compounds and antiviral uses thereof |
| US20060148805A1 (en) | 2003-07-01 | 2006-07-06 | Meng Hsin Chen | Opthalmic compositions for treating ocular hypertension |
| CA2550091A1 (en) | 2003-12-19 | 2005-07-07 | Elixir Pharmaceuticals, Inc. | Methods of treating a disorder |
| EP1715855A4 (en) | 2004-01-29 | 2010-06-16 | Elixir Pharmaceuticals Inc | ANTIVIRAL DRUGS |
| WO2005108374A1 (en) | 2004-04-29 | 2005-11-17 | Fmc Corporation | Insecticidal diazole and triazole derivatives |
| GB0420719D0 (en) | 2004-09-17 | 2004-10-20 | Addex Pharmaceuticals Sa | Novel allosteric modulators |
| EP1959962A2 (en) * | 2005-12-16 | 2008-08-27 | Cytokinetics, Inc. | Certain chemical entities, compositions, and methods |
| US8227603B2 (en) | 2006-08-01 | 2012-07-24 | Cytokinetics, Inc. | Modulating skeletal muscle |
| EP2666777A1 (en) | 2006-08-02 | 2013-11-27 | Cytokinetics, Inc. | Certain chemical entities having an imidazo<4,5-b>pyrazin-2(3H)-one core, compositions and methods |
| NZ576278A (en) | 2006-10-19 | 2011-12-22 | Signal Pharm Llc | Heteroaryl compounds, compositions thereof, and their use as protein kinase inhibitors |
| CL2007002994A1 (es) | 2006-10-19 | 2008-02-08 | Wyeth Corp | Compuestos derivados heterociclicos que contienen sulfamoilo, inhibidores de hsp90; composicion farmaceutica; y uso para el tratamiento del cancer, tal como cancer de mama, de colon y prostata, entre otros. |
| WO2008075007A1 (en) * | 2006-12-21 | 2008-06-26 | Cancer Research Technology Limited | Morpholino-substituted bicycloheteroaryl compounds and their use as anti cancer agents |
| EP2139478A4 (en) * | 2007-03-30 | 2010-05-05 | Cytokinetics Inc | CHEMICAL ENTITIES, COMPOSITIONS AND METHODS |
| MX2010008518A (es) * | 2008-02-04 | 2010-11-10 | Cytokinetics Inc | Ciertas entidades quimicas, composiciones y metodos. |
| US7998976B2 (en) | 2008-02-04 | 2011-08-16 | Cytokinetics, Inc. | Certain chemical entities, compositions and methods |
| CN102264743B (zh) | 2008-11-25 | 2015-02-11 | 罗彻斯特大学 | Mlk抑制剂及其使用方法 |
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2009
- 2009-02-02 MX MX2010008518A patent/MX2010008518A/es not_active Application Discontinuation
- 2009-02-02 KR KR1020107018611A patent/KR20100119773A/ko not_active Withdrawn
- 2009-02-02 EP EP09708594A patent/EP2244711A4/en not_active Withdrawn
- 2009-02-02 AU AU2009210787A patent/AU2009210787A1/en not_active Abandoned
- 2009-02-02 US US12/364,394 patent/US7989469B2/en not_active Expired - Fee Related
- 2009-02-02 CA CA2713864A patent/CA2713864A1/en not_active Abandoned
- 2009-02-02 JP JP2010545031A patent/JP2011510985A/ja not_active Withdrawn
- 2009-02-02 WO PCT/US2009/000686 patent/WO2009099594A1/en not_active Ceased
- 2009-02-02 BR BRPI0907502A patent/BRPI0907502A2/pt not_active Application Discontinuation
- 2009-02-02 CN CN2009801121602A patent/CN101983061A/zh active Pending
- 2009-02-02 EA EA201001224A patent/EA201001224A1/ru unknown
- 2009-02-03 TW TW098103382A patent/TW200946524A/zh unknown
- 2009-02-04 CL CL2009000246A patent/CL2009000246A1/es unknown
- 2009-02-04 AR ARP090100372A patent/AR072242A1/es unknown
-
2010
- 2010-08-02 IL IL207367A patent/IL207367A0/en unknown
- 2010-08-13 ZA ZA2010/05780A patent/ZA201005780B/en unknown
- 2010-08-27 EC EC2010010430A patent/ECSP10010430A/es unknown
- 2010-08-30 EC EC2010010432A patent/ECSP10010432A/es unknown
- 2010-08-30 CO CO10106625A patent/CO6290673A2/es not_active Application Discontinuation
-
2011
- 2011-06-21 US US13/165,281 patent/US20110312975A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| AU2009210787A1 (en) | 2009-08-13 |
| ECSP10010432A (es) | 2011-01-31 |
| EP2244711A4 (en) | 2011-08-24 |
| CN101983061A (zh) | 2011-03-02 |
| CO6290673A2 (es) | 2011-06-20 |
| CL2009000246A1 (es) | 2009-06-26 |
| AR072242A1 (es) | 2010-08-18 |
| EA201001224A1 (ru) | 2011-08-30 |
| US7989469B2 (en) | 2011-08-02 |
| BRPI0907502A2 (pt) | 2019-01-15 |
| MX2010008518A (es) | 2010-11-10 |
| TW200946524A (en) | 2009-11-16 |
| WO2009099594A1 (en) | 2009-08-13 |
| US20090253737A1 (en) | 2009-10-08 |
| JP2011510985A (ja) | 2011-04-07 |
| CA2713864A1 (en) | 2009-08-13 |
| EP2244711A1 (en) | 2010-11-03 |
| US20110312975A1 (en) | 2011-12-22 |
| ECSP10010430A (es) | 2011-02-28 |
| IL207367A0 (en) | 2010-12-30 |
| ZA201005780B (en) | 2011-04-28 |
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