TWI851441B - 作為a2a/a2b抑制劑之稠合吡嗪衍生物 - Google Patents
作為a2a/a2b抑制劑之稠合吡嗪衍生物 Download PDFInfo
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- TWI851441B TWI851441B TW112138314A TW112138314A TWI851441B TW I851441 B TWI851441 B TW I851441B TW 112138314 A TW112138314 A TW 112138314A TW 112138314 A TW112138314 A TW 112138314A TW I851441 B TWI851441 B TW I851441B
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- alkyl
- membered
- independently selected
- cycloalkyl
- membered heterocycloalkyl
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- 239000003112 inhibitor Substances 0.000 title description 6
- 150000003216 pyrazines Chemical class 0.000 title description 2
- 150000001875 compounds Chemical class 0.000 claims abstract description 171
- 150000003839 salts Chemical class 0.000 claims abstract description 82
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 46
- 201000010099 disease Diseases 0.000 claims abstract description 34
- 125000000217 alkyl group Chemical group 0.000 claims description 1418
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims description 645
- 125000001313 C5-C10 heteroaryl group Chemical group 0.000 claims description 339
- -1 aminoformyl Chemical group 0.000 claims description 328
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 321
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 315
- 125000001424 substituent group Chemical group 0.000 claims description 286
- 125000003118 aryl group Chemical group 0.000 claims description 223
- 125000006376 (C3-C10) cycloalkyl group Chemical group 0.000 claims description 222
- 125000001072 heteroaryl group Chemical group 0.000 claims description 214
- 229910052739 hydrogen Inorganic materials 0.000 claims description 204
- 229910052799 carbon Inorganic materials 0.000 claims description 182
- 229910052736 halogen Inorganic materials 0.000 claims description 175
- 150000002367 halogens Chemical class 0.000 claims description 174
- 125000003545 alkoxy group Chemical group 0.000 claims description 155
- 125000006719 (C6-C10) aryl (C1-C6) alkyl group Chemical group 0.000 claims description 152
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 135
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 103
- 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 claims description 81
- 125000004432 carbon atom Chemical group C* 0.000 claims description 73
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 57
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 54
- 125000004429 atom Chemical group 0.000 claims description 51
- 229910052796 boron Inorganic materials 0.000 claims description 50
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 43
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 claims description 40
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims description 39
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims description 38
- 229910052805 deuterium Inorganic materials 0.000 claims description 38
- 125000000041 C6-C10 aryl group Chemical group 0.000 claims description 36
- 125000006568 (C4-C7) heterocycloalkyl group Chemical group 0.000 claims description 28
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 22
- 125000004076 pyridyl group Chemical group 0.000 claims description 21
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims description 18
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims description 16
- 125000006559 (C1-C3) alkylamino group Chemical group 0.000 claims description 14
- 125000006698 (C1-C3) dialkylamino group Chemical group 0.000 claims description 14
- 125000006598 aminocarbonylamino group Chemical group 0.000 claims description 14
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 13
- 125000002947 alkylene group Chemical group 0.000 claims description 13
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 13
- 125000006597 (C1-C3) alkylcarbonylamino group Chemical group 0.000 claims description 12
- 125000004802 cyanophenyl group Chemical group 0.000 claims description 12
- 125000005647 linker group Chemical group 0.000 claims description 12
- 125000006596 (C1-C3) alkylcarbonyloxy group Chemical group 0.000 claims description 11
- 125000006595 (C1-C3) alkylsulfinyl group Chemical group 0.000 claims description 11
- 125000006594 (C1-C3) alkylsulfony group Chemical group 0.000 claims description 11
- 125000004466 alkoxycarbonylamino group Chemical group 0.000 claims description 11
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims description 11
- 125000000304 alkynyl group Chemical group 0.000 claims description 11
- 229910052794 bromium Inorganic materials 0.000 claims description 11
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 11
- 125000004455 (C1-C3) alkylthio group Chemical group 0.000 claims description 10
- 125000003342 alkenyl group Chemical group 0.000 claims description 10
- 125000004527 pyrimidin-4-yl group Chemical group N1=CN=C(C=C1)* 0.000 claims description 10
- 206010060862 Prostate cancer Diseases 0.000 claims description 8
- 208000000236 Prostatic Neoplasms Diseases 0.000 claims description 8
- 125000005195 alkyl amino carbonyloxy group Chemical group 0.000 claims description 8
- 206010009944 Colon cancer Diseases 0.000 claims description 7
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 7
- 125000003226 pyrazolyl group Chemical group 0.000 claims description 7
- 125000000446 sulfanediyl group Chemical group *S* 0.000 claims description 7
- 125000006555 (C3-C5) cycloalkyl group Chemical group 0.000 claims description 6
- 208000001333 Colorectal Neoplasms Diseases 0.000 claims description 6
- 125000005494 pyridonyl group Chemical group 0.000 claims description 6
- 125000000714 pyrimidinyl group Chemical group 0.000 claims description 6
- 125000006603 (C1-C3) alkylaminosulfonyl group Chemical group 0.000 claims description 5
- 125000006602 (C1-C3) alkylsulfonylamino group Chemical group 0.000 claims description 5
- 125000004198 2-fluorophenyl group Chemical group [H]C1=C([H])C(F)=C(*)C([H])=C1[H] 0.000 claims description 5
- 206010006187 Breast cancer Diseases 0.000 claims description 5
- 208000026310 Breast neoplasm Diseases 0.000 claims description 5
- 206010058467 Lung neoplasm malignant Diseases 0.000 claims description 5
- 125000004949 alkyl amino carbonyl amino group Chemical group 0.000 claims description 5
- 125000001207 fluorophenyl group Chemical group 0.000 claims description 5
- 201000005202 lung cancer Diseases 0.000 claims description 5
- 208000020816 lung neoplasm Diseases 0.000 claims description 5
- 208000002154 non-small cell lung carcinoma Diseases 0.000 claims description 5
- 208000029729 tumor suppressor gene on chromosome 11 Diseases 0.000 claims description 5
- 125000006599 (C1-C3) alkylaminocarbonylamino group Chemical group 0.000 claims description 4
- 125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 claims description 4
- 206010005003 Bladder cancer Diseases 0.000 claims description 4
- 206010061902 Pancreatic neoplasm Diseases 0.000 claims description 4
- 208000007097 Urinary Bladder Neoplasms Diseases 0.000 claims description 4
- ZHNUHDYFZUAESO-UHFFFAOYSA-N formamide Substances NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 claims description 4
- 201000010536 head and neck cancer Diseases 0.000 claims description 4
- 208000014829 head and neck neoplasm Diseases 0.000 claims description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
- 208000015486 malignant pancreatic neoplasm Diseases 0.000 claims description 4
- 201000002528 pancreatic cancer Diseases 0.000 claims description 4
- 208000008443 pancreatic carcinoma Diseases 0.000 claims description 4
- 201000005112 urinary bladder cancer Diseases 0.000 claims description 4
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 claims description 3
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 claims description 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 3
- 206010033128 Ovarian cancer Diseases 0.000 claims description 3
- 206010061535 Ovarian neoplasm Diseases 0.000 claims description 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 3
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 3
- 125000006001 difluoroethyl group Chemical group 0.000 claims description 3
- 125000002971 oxazolyl group Chemical group 0.000 claims description 3
- 239000008194 pharmaceutical composition Substances 0.000 claims description 3
- 125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 claims description 3
- 125000006514 pyridin-2-ylmethyl group Chemical group [H]C1=C([H])C([H])=C([H])C(=N1)C([H])([H])* 0.000 claims description 3
- 125000001425 triazolyl group Chemical group 0.000 claims description 3
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 claims description 2
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 claims description 2
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 claims description 2
- 125000006619 (C1-C6) dialkylamino group Chemical group 0.000 claims description 2
- 125000004939 6-pyridyl group Chemical group N1=CC=CC=C1* 0.000 claims description 2
- 101100079340 Rattus norvegicus Nalcn gene Proteins 0.000 claims description 2
- 208000000102 Squamous Cell Carcinoma of Head and Neck Diseases 0.000 claims description 2
- 125000004450 alkenylene group Chemical group 0.000 claims description 2
- 125000004414 alkyl thio group Chemical group 0.000 claims description 2
- 125000004419 alkynylene group Chemical group 0.000 claims description 2
- 239000003814 drug Substances 0.000 claims description 2
- 239000003937 drug carrier Substances 0.000 claims description 2
- 201000000459 head and neck squamous cell carcinoma Diseases 0.000 claims description 2
- 150000004677 hydrates Chemical class 0.000 claims description 2
- 230000001394 metastastic effect Effects 0.000 claims description 2
- 206010061289 metastatic neoplasm Diseases 0.000 claims description 2
- 125000004304 oxazol-5-yl group Chemical group O1C=NC=C1* 0.000 claims description 2
- JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Chemical compound N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 claims 3
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 2
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims 2
- 125000004750 (C1-C6) alkylaminosulfonyl group Chemical group 0.000 claims 2
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims 2
- BTMGZLJLARGJHL-UHFFFAOYSA-N 3-[4-amino-2-(pyridin-2-ylmethyl)-7-pyrimidin-4-ylpyrazolo[1,5-a]pyrazin-6-yl]benzonitrile Chemical compound C1=C(CC=2C=C3C(N)=NC(C4=CC(C#N)=CC=C4)=C(N3N=2)C2=CC=NC=N2)N=CC=C1 BTMGZLJLARGJHL-UHFFFAOYSA-N 0.000 claims 2
- ZOJLFWKYHWHRNS-UHFFFAOYSA-N 3-[4-amino-2-(pyridin-2-ylmethyl)pyrazolo[1,5-a]pyrazin-6-yl]benzonitrile Chemical compound NC=1C=2N(C=C(N=1)C=1C=C(C#N)C=CC=1)N=C(C=2)CC1=NC=CC=C1 ZOJLFWKYHWHRNS-UHFFFAOYSA-N 0.000 claims 2
- IXECHRCYHWEQKW-UHFFFAOYSA-N 3-[4-amino-2-[(2-fluorophenyl)-hydroxymethyl]-7-pyrimidin-4-ylpyrazolo[1,5-a]pyrazin-6-yl]benzonitrile Chemical compound NC=1C=2N(C(=C(N=1)C=1C=C(C#N)C=CC=1)C1=NC=NC=C1)N=C(C=2)C(O)C1=C(C=CC=C1)F IXECHRCYHWEQKW-UHFFFAOYSA-N 0.000 claims 2
- XARDVPMTLNQWJT-UHFFFAOYSA-N 4-amino-6-(3-cyanophenyl)-2-[(2-fluorophenyl)methyl]pyrazolo[1,5-a]pyrazine-7-carbonitrile Chemical compound NC=1C=2N(C(=C(N=1)C1=CC(=CC=C1)C#N)C#N)N=C(C=2)CC1=C(C=CC=C1)F XARDVPMTLNQWJT-UHFFFAOYSA-N 0.000 claims 2
- 125000006164 6-membered heteroaryl group Chemical group 0.000 claims 2
- 125000004845 (C1-C6) alkylsulfonylamino group Chemical group 0.000 claims 1
- JHMULIBFFDZWLO-UHFFFAOYSA-N 3-(4-amino-2-anilino-7-pyridin-4-ylpyrazolo[1,5-a]pyrazin-6-yl)benzonitrile Chemical compound C1=C(NC2=NN3C(C(=NC(C4=CC(C#N)=CC=C4)=C3C3=CC=NC=C3)N)=C2)C=CC=C1 JHMULIBFFDZWLO-UHFFFAOYSA-N 0.000 claims 1
- YHLBTMSONDAJED-UHFFFAOYSA-N 3-[4-amino-2-(3,6-dihydro-2H-pyran-4-yl)-7-pyrimidin-4-ylpyrazolo[1,5-a]pyrazin-6-yl]benzonitrile Chemical compound NC=1C=2N(C(=C(N=1)C=1C=C(C#N)C=CC=1)C1=NC=NC=C1)N=C(C=2)C=1CCOCC=1 YHLBTMSONDAJED-UHFFFAOYSA-N 0.000 claims 1
- CMIFPGGNVQZWNW-UHFFFAOYSA-N 3-[4-amino-2-(azetidine-1-carbonyl)-7-pyrimidin-4-ylpyrazolo[1,5-a]pyrazin-6-yl]benzonitrile Chemical compound N1(CCC1)C(=O)C1=NN2C(C(=NC(C3=CC(C#N)=CC=C3)=C2C2=CC=NC=N2)N)=C1 CMIFPGGNVQZWNW-UHFFFAOYSA-N 0.000 claims 1
- YABLOYKDPWCWKX-UHFFFAOYSA-N 3-[4-amino-2-(piperidine-1-carbonyl)-7-pyrimidin-4-ylpyrazolo[1,5-a]pyrazin-6-yl]benzonitrile Chemical compound C1N(CCCC1)C(=O)C=1C=C2C(=NC(C3=CC(C#N)=CC=C3)=C(N2N=1)C1=CC=NC=N1)N YABLOYKDPWCWKX-UHFFFAOYSA-N 0.000 claims 1
- LTEFHMLRKJGEAV-UHFFFAOYSA-N 3-[4-amino-2-[2-(4-methylpiperazin-1-yl)pyridin-4-yl]-7-pyridin-4-ylpyrazolo[1,5-a]pyrazin-6-yl]benzonitrile Chemical compound N1=C(C=2N(N=C(C=2)C2=CC(N3CCN(CC3)C)=NC=C2)C(C1=C1C=C(C#N)C=C[CH]1)=C1C=CN=C[CH]1)N LTEFHMLRKJGEAV-UHFFFAOYSA-N 0.000 claims 1
- NFWMNPSCIPZPII-UHFFFAOYSA-N 3-[4-amino-7-(3-ethyltriazol-4-yl)-2-(pyridin-2-ylmethyl)pyrazolo[1,5-a]pyrazin-6-yl]benzonitrile Chemical compound C1=C(CC=2C=C3C(N)=NC(C4=CC(C#N)=CC=C4)=C(N3N=2)C2=CN=NN2CC)N=CC=C1 NFWMNPSCIPZPII-UHFFFAOYSA-N 0.000 claims 1
- QYTKFHAWBVTYFM-UHFFFAOYSA-N 3-[4-amino-7-(3-methyltriazol-4-yl)-2-(pyridin-2-ylmethyl)pyrazolo[1,5-a]pyrazin-6-yl]benzonitrile Chemical compound C=1(CC2=NC=CC=C2)C=C2C(N)=NC(C3=CC(C#N)=CC=C3)=C(N2N=1)C1=CN=NN1C QYTKFHAWBVTYFM-UHFFFAOYSA-N 0.000 claims 1
- NITNBOHSZJRAGF-UHFFFAOYSA-N 3-[4-amino-7-[4-(1-hydroxyethyl)-2-methyl-1,3-oxazol-5-yl]-2-(pyridin-2-ylmethyl)pyrazolo[1,5-a]pyrazin-6-yl]benzonitrile Chemical compound NC=1C=2N(C(=C(N=1)C=1C=C(C#N)C=CC=1)C1=C(N=C(O1)C)C(C)O)N=C(C=2)CC1=NC=CC=C1 NITNBOHSZJRAGF-UHFFFAOYSA-N 0.000 claims 1
- LKCAAPOVEFEYOW-UHFFFAOYSA-N 3-[4-amino-7-[4-(2,2-difluoro-1-hydroxyethyl)-2-methyl-1,3-oxazol-5-yl]-2-(pyridin-2-ylmethyl)pyrazolo[1,5-a]pyrazin-6-yl]benzonitrile Chemical compound NC=1C=2N(C(=C(N=1)C=1C=C(C#N)C=CC=1)C1=C(N=C(O1)C)C(C(F)F)O)N=C(C=2)CC1=NC=CC=C1 LKCAAPOVEFEYOW-UHFFFAOYSA-N 0.000 claims 1
- UNPZMEKPIMYZQV-UHFFFAOYSA-N 3-[4-amino-7-bromo-2-[(2-fluorophenyl)-hydroxymethyl]pyrazolo[1,5-a]pyrazin-6-yl]benzonitrile Chemical compound NC=1C=2N(C(=C(N=1)C=1C=C(C#N)C=CC=1)Br)N=C(C=2)C(O)C1=C(C=CC=C1)F UNPZMEKPIMYZQV-UHFFFAOYSA-N 0.000 claims 1
- PRMJUHAJCHICAM-UHFFFAOYSA-N 3-[4-amino-7-pyrimidin-4-yl-2-(1H-pyrrolo[3,2-b]pyridin-3-ylmethyl)pyrazolo[1,5-a]pyrazin-6-yl]benzonitrile Chemical compound N1C=C(CC=2C=C3C(N)=NC(C4=CC(C#N)=CC=C4)=C(N3N=2)C2=CC=NC=N2)C2=NC=CC=C12 PRMJUHAJCHICAM-UHFFFAOYSA-N 0.000 claims 1
- KBTVCHCNRWTYRL-UHFFFAOYSA-N 3-[4-amino-7-pyrimidin-4-yl-2-(pyrrolidine-1-carbonyl)pyrazolo[1,5-a]pyrazin-6-yl]benzonitrile Chemical compound NC=1C=2N(C(=C(N=1)C=1C=C(C#N)C=CC=1)C1=NC=NC=C1)N=C(C=2)C(=O)N1CCCC1 KBTVCHCNRWTYRL-UHFFFAOYSA-N 0.000 claims 1
- IXSPUODLNWBCBW-UHFFFAOYSA-N 4-[4-amino-6-(3-cyanophenyl)-2-[(2-fluorophenyl)methyl]pyrazolo[1,5-a]pyrazin-7-yl]-3,6-dihydro-2H-pyridine-1-carboxamide Chemical compound C1=C(CC=2C=C3C(N)=NC(C4=CC(C#N)=CC=C4)=C(N3N=2)C2=CCN(CC2)C(=O)N)C(F)=CC=C1 IXSPUODLNWBCBW-UHFFFAOYSA-N 0.000 claims 1
- LWWMMGGSNTYCOV-UHFFFAOYSA-N 4-amino-6-(3-cyanophenyl)-7-(1,1-difluoroethyl)-N-ethylpyrazolo[1,5-a]pyrazine-2-carboxamide Chemical compound N12C(=CC(=N1)C(=O)NCC)C(N)=NC(C1=CC(C#N)=CC=C1)=C2C(F)(F)C LWWMMGGSNTYCOV-UHFFFAOYSA-N 0.000 claims 1
- FCGSXWDJYLZZIQ-UHFFFAOYSA-N 4-amino-6-(3-cyanophenyl)-N,N-diethyl-7-pyrimidin-4-ylpyrazolo[1,5-a]pyrazine-2-carboxamide Chemical compound C(N(C(=O)C=1C=C2C(=NC(C3=CC(C#N)=CC=C3)=C(N2N=1)C1=CC=NC=N1)N)CC)C FCGSXWDJYLZZIQ-UHFFFAOYSA-N 0.000 claims 1
- CLDMPCJOUVTDBV-UHFFFAOYSA-N 4-amino-6-(3-cyanophenyl)-N-ethyl-7-(1-methyl-6-oxopyridin-3-yl)pyrazolo[1,5-a]pyrazine-2-carboxamide Chemical compound N1=C(C=2N(N=C(C=2)C(=O)NCC)C(=C1C1=CC(C#N)=CC=C1)C=1C=CC(=O)N(C=1)C)N CLDMPCJOUVTDBV-UHFFFAOYSA-N 0.000 claims 1
- YPDIDJKXMPWHJB-UHFFFAOYSA-N 4-amino-6-(3-cyanophenyl)-N-ethyl-7-(2-ethylpyrazol-3-yl)pyrazolo[1,5-a]pyrazine-2-carboxamide Chemical compound NC=1C=2N(C(=C(N=1)C1=CC(=CC=C1)C#N)C1=CC=NN1CC)N=C(C=2)C(=O)NCC YPDIDJKXMPWHJB-UHFFFAOYSA-N 0.000 claims 1
- QADUMPJBBIVCQY-UHFFFAOYSA-N 4-amino-6-(3-cyanophenyl)-N-ethyl-7-(2-propylpyrazol-3-yl)pyrazolo[1,5-a]pyrazine-2-carboxamide Chemical compound N1=C(C=2N(N=C(C=2)C(=O)NCC)C(=C1C1=CC(C#N)=CC=C1)C1=CC=NN1CCC)N QADUMPJBBIVCQY-UHFFFAOYSA-N 0.000 claims 1
- VEWGEGNHOACSJX-UHFFFAOYSA-N 4-amino-6-(3-cyanophenyl)-N-ethyl-7-[1-(trifluoromethyl)cyclopropyl]pyrazolo[1,5-a]pyrazine-2-carboxamide Chemical compound N1=C(C=2N(N=C(C=2)C(=O)NCC)C(=C1C1=CC(C#N)=CC=C1)C1(CC1)C(F)(F)F)N VEWGEGNHOACSJX-UHFFFAOYSA-N 0.000 claims 1
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- 125000003396 thiol group Chemical class [H]S* 0.000 claims 1
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Classifications
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- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
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- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
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- A—HUMAN NECESSITIES
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- A61P35/00—Antineoplastic agents
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- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
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- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
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| WO2021156439A1 (en) | 2020-02-06 | 2021-08-12 | Astrazeneca Ab | Triazole compounds as adenosine receptor antagonists |
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| GB202011996D0 (en) * | 2020-07-31 | 2020-09-16 | Adorx Therapeutics Ltd | Antagonist compounds |
| CN117396490A (zh) * | 2021-05-14 | 2024-01-12 | Bm医药咨询有限公司 | 用于预防和治疗病毒感染的双环杂环化合物 |
| GB2615307A (en) * | 2022-01-28 | 2023-08-09 | Adorx Therapeutics Ltd | Antagonist compounds |
| KR102621694B1 (ko) * | 2022-09-15 | 2024-01-08 | 주식회사 스탠다임 | 아데노신 a2a 수용체 길항제 및 이의 용도 |
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