ES2902409T3 - Compuestos para modular acuaporinas - Google Patents
Compuestos para modular acuaporinas Download PDFInfo
- Publication number
- ES2902409T3 ES2902409T3 ES17720125T ES17720125T ES2902409T3 ES 2902409 T3 ES2902409 T3 ES 2902409T3 ES 17720125 T ES17720125 T ES 17720125T ES 17720125 T ES17720125 T ES 17720125T ES 2902409 T3 ES2902409 T3 ES 2902409T3
- Authority
- ES
- Spain
- Prior art keywords
- triazol
- acetamide
- sulfanyl
- alkylene
- cycloalkyl
- 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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- 150000001875 compounds Chemical class 0.000 title claims abstract description 107
- 102000010637 Aquaporins Human genes 0.000 title description 9
- 108010063290 Aquaporins Proteins 0.000 title description 9
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims abstract description 36
- -1 C1-C6 alkylene-OR12a Chemical group 0.000 claims abstract description 28
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims abstract description 26
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 25
- 125000001072 heteroaryl group Chemical group 0.000 claims abstract description 23
- 125000003118 aryl group Chemical group 0.000 claims abstract description 21
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 21
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 15
- 229910052731 fluorine Inorganic materials 0.000 claims abstract description 15
- 150000003839 salts Chemical class 0.000 claims abstract description 15
- 229910052801 chlorine Inorganic materials 0.000 claims abstract description 14
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 14
- 150000002367 halogens Chemical class 0.000 claims abstract description 14
- 125000000753 cycloalkyl group Chemical group 0.000 claims abstract description 10
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims abstract description 8
- MBIZXFATKUQOOA-UHFFFAOYSA-N 1,3,4-thiadiazole Chemical group C1=NN=CS1 MBIZXFATKUQOOA-UHFFFAOYSA-N 0.000 claims abstract description 6
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims abstract description 6
- 125000006163 5-membered heteroaryl group Chemical group 0.000 claims abstract description 5
- 125000005275 alkylenearyl group Chemical group 0.000 claims abstract 4
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims abstract 3
- 125000000000 cycloalkoxy group Chemical group 0.000 claims abstract 2
- 239000008194 pharmaceutical composition Substances 0.000 claims description 29
- 125000002947 alkylene group Chemical group 0.000 claims description 27
- 125000003161 (C1-C6) alkylene group Chemical group 0.000 claims description 15
- 206010012601 diabetes mellitus Diseases 0.000 claims description 13
- 239000003814 drug Substances 0.000 claims description 11
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 10
- 239000003085 diluting agent Substances 0.000 claims description 9
- 208000027866 inflammatory disease Diseases 0.000 claims description 9
- 206010039073 rheumatoid arthritis Diseases 0.000 claims description 9
- 206010012442 Dermatitis contact Diseases 0.000 claims description 7
- 201000004681 Psoriasis Diseases 0.000 claims description 7
- 208000002029 allergic contact dermatitis Diseases 0.000 claims description 7
- 201000001320 Atherosclerosis Diseases 0.000 claims description 6
- 208000009304 Acute Kidney Injury Diseases 0.000 claims description 5
- 208000022559 Inflammatory bowel disease Diseases 0.000 claims description 5
- 208000001132 Osteoporosis Diseases 0.000 claims description 5
- 208000033626 Renal failure acute Diseases 0.000 claims description 5
- 201000011040 acute kidney failure Diseases 0.000 claims description 5
- 229910052757 nitrogen Inorganic materials 0.000 claims description 5
- 206010063897 Renal ischaemia Diseases 0.000 claims description 4
- 206010063837 Reperfusion injury Diseases 0.000 claims description 4
- 125000005842 heteroatom Chemical group 0.000 claims description 4
- 229910052760 oxygen Inorganic materials 0.000 claims description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
- 229910052717 sulfur Inorganic materials 0.000 claims description 4
- 208000008338 non-alcoholic fatty liver disease Diseases 0.000 claims description 3
- 239000003937 drug carrier Substances 0.000 claims description 2
- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 claims 18
- 125000003396 thiol group Chemical group [H]S* 0.000 claims 9
- HBEDSQVIWPRPAY-UHFFFAOYSA-N 2,3-dihydrobenzofuran Chemical group C1=CC=C2OCCC2=C1 HBEDSQVIWPRPAY-UHFFFAOYSA-N 0.000 claims 1
- JYVPAIBUQJTZID-UHFFFAOYSA-N 2-[(4,5-diethyl-1,2,4-triazol-3-yl)sulfanyl]-N-(5-phenyl-1,3,4-thiadiazol-2-yl)acetamide Chemical compound C(C)C=1N(C(=NN=1)SCC(=O)NC=1SC(=NN=1)C1=CC=CC=C1)CC JYVPAIBUQJTZID-UHFFFAOYSA-N 0.000 claims 1
- OODMANOWQGOPLA-UHFFFAOYSA-N 2-[(4,5-diethyl-1,2,4-triazol-3-yl)sulfanyl]-N-(5-pyridin-2-yl-1,3,4-thiadiazol-2-yl)acetamide Chemical compound C(C)N1C(=NN=C1CC)SCC(=O)NC=1SC(=NN=1)C1=NC=CC=C1 OODMANOWQGOPLA-UHFFFAOYSA-N 0.000 claims 1
- HBURMPNBKOAVLW-UHFFFAOYSA-N 2-[(4,5-diethyl-1,2,4-triazol-3-yl)sulfanyl]-N-[5-(2,3-dihydro-1-benzofuran-5-yl)-1,3,4-thiadiazol-2-yl]acetamide Chemical compound CCc1nnc(SCC(=O)Nc2nnc(s2)-c2ccc3OCCc3c2)n1CC HBURMPNBKOAVLW-UHFFFAOYSA-N 0.000 claims 1
- PXVMDWKJRUOEIY-UHFFFAOYSA-N 2-[(4,5-diethyl-1,2,4-triazol-3-yl)sulfanyl]-N-[5-(4-ethoxyphenyl)-1,3,4-thiadiazol-2-yl]acetamide Chemical compound C(C)C=1N(C(=NN=1)SCC(=O)NC=1SC(=NN=1)C1=CC=C(C=C1)OCC)CC PXVMDWKJRUOEIY-UHFFFAOYSA-N 0.000 claims 1
- OJZKDMNXROTKJK-UHFFFAOYSA-N 2-[(4,5-diethyl-1,2,4-triazol-3-yl)sulfanyl]-N-[5-(4-ethylphenyl)-1,3,4-thiadiazol-2-yl]acetamide Chemical compound C(C)C=1N(C(=NN=1)SCC(=O)NC=1SC(=NN=1)C1=CC=C(C=C1)CC)CC OJZKDMNXROTKJK-UHFFFAOYSA-N 0.000 claims 1
- JOSOMNOHNHFDBA-UHFFFAOYSA-N 2-[(4,5-diethyl-1,2,4-triazol-3-yl)sulfanyl]-N-[5-(4-methoxyphenyl)-1,3,4-thiadiazol-2-yl]acetamide Chemical compound C(C)C=1N(C(=NN=1)SCC(=O)NC=1SC(=NN=1)C1=CC=C(C=C1)OC)CC JOSOMNOHNHFDBA-UHFFFAOYSA-N 0.000 claims 1
- ORKWVSPBFJMHJQ-UHFFFAOYSA-N 2-[(4,5-diethyl-1,2,4-triazol-3-yl)sulfanyl]-N-[5-(4-methylsulfonylphenyl)-1,3,4-thiadiazol-2-yl]acetamide Chemical compound C(C)C=1N(C(=NN=1)SCC(=O)NC=1SC(=NN=1)C1=CC=C(C=C1)S(=O)(=O)C)CC ORKWVSPBFJMHJQ-UHFFFAOYSA-N 0.000 claims 1
- WKLIMMLZGHORGN-UHFFFAOYSA-N 2-[(4,5-diethyl-1,2,4-triazol-3-yl)sulfanyl]-N-[5-(4-propan-2-ylphenyl)-1,3,4-thiadiazol-2-yl]acetamide Chemical compound C(C)C=1N(C(=NN=1)SCC(=O)NC=1SC(=NN=1)C1=CC=C(C=C1)C(C)C)CC WKLIMMLZGHORGN-UHFFFAOYSA-N 0.000 claims 1
- BIZZDYDNZIENET-UHFFFAOYSA-N 2-[(4,5-diethyl-1,2,4-triazol-3-yl)sulfanyl]-N-[5-(4-propylphenyl)-1,3,4-thiadiazol-2-yl]acetamide Chemical compound C(C)C=1N(C(=NN=1)SCC(=O)NC=1SC(=NN=1)C1=CC=C(C=C1)CCC)CC BIZZDYDNZIENET-UHFFFAOYSA-N 0.000 claims 1
- BNANJVIGNMKQMM-UHFFFAOYSA-N 2-[(4,5-diethyl-1,2,4-triazol-3-yl)sulfanyl]-N-[5-[4-(2-fluoroethoxy)phenyl]-1,3,4-thiadiazol-2-yl]acetamide Chemical compound C(C)C=1N(C(=NN=1)SCC(=O)NC=1SC(=NN=1)C1=CC=C(C=C1)OCCF)CC BNANJVIGNMKQMM-UHFFFAOYSA-N 0.000 claims 1
- YZBUONAMYGQWET-UHFFFAOYSA-N 2-[(4,5-diethyl-1,2,4-triazol-3-yl)sulfanyl]-N-[5-[4-(2-methoxyethoxy)phenyl]-1,3,4-thiadiazol-2-yl]acetamide Chemical compound C(C)C=1N(C(=NN=1)SCC(=O)NC=1SC(=NN=1)C1=CC=C(C=C1)OCCOC)CC YZBUONAMYGQWET-UHFFFAOYSA-N 0.000 claims 1
- PAYLDTZGHLDSLZ-UHFFFAOYSA-N 2-[(4,5-diethyl-1,2,4-triazol-3-yl)sulfanyl]-N-[5-[4-(2-methylpropoxy)phenyl]-1,3,4-thiadiazol-2-yl]acetamide Chemical compound C(C)C=1N(C(=NN=1)SCC(=O)NC=1SC(=NN=1)C1=CC=C(C=C1)OCC(C)C)CC PAYLDTZGHLDSLZ-UHFFFAOYSA-N 0.000 claims 1
- DNHHMHHCXGLCMT-UHFFFAOYSA-N 2-[(4,5-diethyl-1,2,4-triazol-3-yl)sulfanyl]-N-[5-[4-(2-methylpropyl)phenyl]-1,3,4-thiadiazol-2-yl]acetamide Chemical compound C(C)C=1N(C(=NN=1)SCC(=O)NC=1SC(=NN=1)C1=CC=C(C=C1)CC(C)C)CC DNHHMHHCXGLCMT-UHFFFAOYSA-N 0.000 claims 1
- WRQGVPWGMBIYOS-UHFFFAOYSA-N 2-[(4,5-diethyl-1,2,4-triazol-3-yl)sulfanyl]-N-[5-[4-(trifluoromethyl)phenyl]-1,3,4-thiadiazol-2-yl]acetamide Chemical compound C(C)N1C(=NN=C1CC)SCC(=O)NC=1SC(=NN=1)C1=CC=C(C=C1)C(F)(F)F WRQGVPWGMBIYOS-UHFFFAOYSA-N 0.000 claims 1
- JUUIDXYNHCZLMO-UHFFFAOYSA-N 2-[(4-ethyl-5-methyl-1,2,4-triazol-3-yl)sulfanyl]-N-[5-(4-methylsulfonylphenyl)-1,3,4-thiadiazol-2-yl]acetamide Chemical compound C(C)N1C(=NN=C1C)SCC(=O)NC=1SC(=NN=1)C1=CC=C(C=C1)S(=O)(=O)C JUUIDXYNHCZLMO-UHFFFAOYSA-N 0.000 claims 1
- MISLNVCPDYRVIZ-UHFFFAOYSA-N 2-[(4-ethyl-5-propan-2-yl-1,2,4-triazol-3-yl)sulfanyl]-N-[5-(4-methylsulfonylphenyl)-1,3,4-thiadiazol-2-yl]acetamide Chemical compound C(C)N1C(=NN=C1C(C)C)SCC(=O)NC=1SC(=NN=1)C1=CC=C(C=C1)S(=O)(=O)C MISLNVCPDYRVIZ-UHFFFAOYSA-N 0.000 claims 1
- XJYLCCBYAFDRNM-UHFFFAOYSA-N 2-[(4-ethyl-5-propan-2-yl-1,2,4-triazol-3-yl)sulfanyl]-N-[5-(4-propan-2-yloxyphenyl)-1,3,4-thiadiazol-2-yl]acetamide Chemical compound C(C)N1C(=NN=C1C(C)C)SCC(=O)NC=1SC(=NN=1)C1=CC=C(C=C1)OC(C)C XJYLCCBYAFDRNM-UHFFFAOYSA-N 0.000 claims 1
- IFLOIXARGBGIMJ-UHFFFAOYSA-N 2-[(4-ethyl-5-propan-2-yl-1,2,4-triazol-3-yl)sulfanyl]-N-[5-[4-(2-fluoroethoxy)phenyl]-1,3,4-thiadiazol-2-yl]acetamide Chemical compound C(C)N1C(=NN=C1C(C)C)SCC(=O)NC=1SC(=NN=1)C1=CC=C(C=C1)OCCF IFLOIXARGBGIMJ-UHFFFAOYSA-N 0.000 claims 1
- ZVACOPHIRUBZKN-UHFFFAOYSA-N 2-[(4-ethyl-5-propan-2-yl-1,2,4-triazol-3-yl)sulfanyl]-N-[5-[4-(2-methoxyethoxy)phenyl]-1,3,4-thiadiazol-2-yl]acetamide Chemical compound C(C)N1C(=NN=C1C(C)C)SCC(=O)NC=1SC(=NN=1)C1=CC=C(C=C1)OCCOC ZVACOPHIRUBZKN-UHFFFAOYSA-N 0.000 claims 1
- IZDAJCQJSVQJDW-UHFFFAOYSA-N 2-[(5-benzyl-4-ethyl-1,2,4-triazol-3-yl)sulfanyl]-N-[5-(4-methoxyphenyl)-1,3,4-thiadiazol-2-yl]acetamide Chemical compound C(C1=CC=CC=C1)C=1N(C(=NN=1)SCC(=O)NC=1SC(=NN=1)C1=CC=C(C=C1)OC)CC IZDAJCQJSVQJDW-UHFFFAOYSA-N 0.000 claims 1
- GQOKEIUIFFWJFO-UHFFFAOYSA-N 2-[(5-cyclopentyl-4-ethyl-1,2,4-triazol-3-yl)sulfanyl]-N-[5-(4-methylsulfonylphenyl)-1,3,4-thiadiazol-2-yl]acetamide Chemical compound C1(CCCC1)C=1N(C(=NN=1)SCC(=O)NC=1SC(=NN=1)C1=CC=C(C=C1)S(=O)(=O)C)CC GQOKEIUIFFWJFO-UHFFFAOYSA-N 0.000 claims 1
- ZBXJLFZZHGUAMQ-UHFFFAOYSA-N 2-[(5-cyclopropyl-4-ethyl-1,2,4-triazol-3-yl)sulfanyl]-N-[5-(4-methylsulfonylphenyl)-1,3,4-thiadiazol-2-yl]acetamide Chemical compound C1(CC1)C=1N(C(=NN=1)SCC(=O)NC=1SC(=NN=1)C1=CC=C(C=C1)S(=O)(=O)C)CC ZBXJLFZZHGUAMQ-UHFFFAOYSA-N 0.000 claims 1
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- WCFJCYJJPZIUGX-UHFFFAOYSA-N 2-[[4-ethyl-5-(2-methoxyethyl)-1,2,4-triazol-3-yl]sulfanyl]-N-[5-(4-propylphenyl)-1,3,4-thiadiazol-2-yl]acetamide Chemical compound C(C)N1C(=NN=C1CCOC)SCC(=O)NC=1SC(=NN=1)C1=CC=C(C=C1)CCC WCFJCYJJPZIUGX-UHFFFAOYSA-N 0.000 claims 1
- FSYPNRQXHILODJ-UHFFFAOYSA-N 2-[[4-ethyl-5-(4-fluorophenyl)-1,2,4-triazol-3-yl]oxy]-N-[5-(4-methoxyphenyl)-1,3,4-thiadiazol-2-yl]acetamide Chemical compound C(C)N1C(=NN=C1C1=CC=C(C=C1)F)OCC(=O)NC=1SC(=NN=1)C1=CC=C(C=C1)OC FSYPNRQXHILODJ-UHFFFAOYSA-N 0.000 claims 1
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- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical class OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 1
- 229920000656 polylysine Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 235000013809 polyvinylpolypyrrolidone Nutrition 0.000 description 1
- 229920000523 polyvinylpolypyrrolidone Polymers 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- 229920001592 potato starch Polymers 0.000 description 1
- 229940116317 potato starch Drugs 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 125000004309 pyranyl group Chemical group O1C(C=CC=C1)* 0.000 description 1
- 150000003217 pyrazoles Chemical class 0.000 description 1
- PBMFSQRYOILNGV-UHFFFAOYSA-N pyridazine Chemical compound C1=CC=NN=C1 PBMFSQRYOILNGV-UHFFFAOYSA-N 0.000 description 1
- 125000000719 pyrrolidinyl group Chemical group 0.000 description 1
- 239000013557 residual solvent Substances 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 229940100486 rice starch Drugs 0.000 description 1
- 125000006413 ring segment Chemical group 0.000 description 1
- 150000003873 salicylate salts Chemical class 0.000 description 1
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical class OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000008159 sesame oil Substances 0.000 description 1
- 235000011803 sesame oil Nutrition 0.000 description 1
- 235000015170 shellfish Nutrition 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 229960001866 silicon dioxide Drugs 0.000 description 1
- 210000003491 skin Anatomy 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 235000010413 sodium alginate Nutrition 0.000 description 1
- 239000000661 sodium alginate Substances 0.000 description 1
- 229940005550 sodium alginate Drugs 0.000 description 1
- WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 1
- 239000004299 sodium benzoate Substances 0.000 description 1
- 235000010234 sodium benzoate Nutrition 0.000 description 1
- 229960003885 sodium benzoate Drugs 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 1
- 229920001027 sodium carboxymethylcellulose Polymers 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
- 239000007901 soft capsule Substances 0.000 description 1
- 239000012453 solvate Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000005556 structure-activity relationship Methods 0.000 description 1
- 150000003890 succinate salts Chemical class 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 125000001273 sulfonato group Chemical class [O-]S(*)(=O)=O 0.000 description 1
- 125000004963 sulfonylalkyl group Chemical group 0.000 description 1
- 125000005555 sulfoximide group Chemical group 0.000 description 1
- 125000004962 sulfoxyl group Chemical group 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 238000013268 sustained release Methods 0.000 description 1
- 239000012730 sustained-release form Substances 0.000 description 1
- 239000003765 sweetening agent Substances 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- 150000003892 tartrate salts Chemical class 0.000 description 1
- 239000006068 taste-masking agent Substances 0.000 description 1
- 125000004213 tert-butoxy group Chemical group [H]C([H])([H])C(O*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- BCNZYOJHNLTNEZ-UHFFFAOYSA-N tert-butyldimethylsilyl chloride Chemical compound CC(C)(C)[Si](C)(C)Cl BCNZYOJHNLTNEZ-UHFFFAOYSA-N 0.000 description 1
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 description 1
- 125000001412 tetrahydropyranyl group Chemical group 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- WROMPOXWARCANT-UHFFFAOYSA-N tfa trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F.OC(=O)C(F)(F)F WROMPOXWARCANT-UHFFFAOYSA-N 0.000 description 1
- 229940124597 therapeutic agent Drugs 0.000 description 1
- VLLMWSRANPNYQX-UHFFFAOYSA-N thiadiazole Chemical compound C1=CSN=N1.C1=CSN=N1 VLLMWSRANPNYQX-UHFFFAOYSA-N 0.000 description 1
- 125000005505 thiomorpholino group Chemical group 0.000 description 1
- 229930192474 thiophene Natural products 0.000 description 1
- 210000001519 tissue Anatomy 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical class CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- 125000005490 tosylate group Chemical group 0.000 description 1
- 231100000041 toxicology testing Toxicity 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000003643 water by type Substances 0.000 description 1
- 229940100445 wheat starch Drugs 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- 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
- A61P3/08—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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Diabetes (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Obesity (AREA)
- Hematology (AREA)
- Endocrinology (AREA)
- Emergency Medicine (AREA)
- Immunology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Rheumatology (AREA)
- Physical Education & Sports Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicinal Preparation (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP16167378 | 2016-04-28 | ||
| PCT/EP2017/060148 WO2017186893A1 (en) | 2016-04-28 | 2017-04-28 | Compounds for modulating aquaporins |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2902409T3 true ES2902409T3 (es) | 2022-03-28 |
Family
ID=55854711
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES17720125T Active ES2902409T3 (es) | 2016-04-28 | 2017-04-28 | Compuestos para modular acuaporinas |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US10730865B2 (enExample) |
| EP (1) | EP3448853B1 (enExample) |
| JP (1) | JP6921118B2 (enExample) |
| CA (1) | CA3022195C (enExample) |
| DK (1) | DK3448853T3 (enExample) |
| ES (1) | ES2902409T3 (enExample) |
| HR (1) | HRP20212031T1 (enExample) |
| HU (1) | HUE057193T2 (enExample) |
| LT (1) | LT3448853T (enExample) |
| PL (1) | PL3448853T3 (enExample) |
| PT (1) | PT3448853T (enExample) |
| WO (1) | WO2017186893A1 (enExample) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN111393444B (zh) * | 2019-01-02 | 2022-10-28 | 上海迪赛诺化学制药有限公司 | 一种阿巴卡韦羟基醋酸酯的制备方法 |
| WO2025137265A1 (en) | 2023-12-20 | 2025-06-26 | Saint Michael's College, Inc. | Methods and compositions for reducing gliaptosis: macroglia-induced neuronal cell death |
| CN118001408B (zh) * | 2024-04-08 | 2024-06-25 | 北京大学 | 一种水通道蛋白9磷酸化抑制剂的用途 |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US333792A (en) * | 1886-01-05 | Stop watch | ||
| EP1615637A1 (en) * | 2003-04-11 | 2006-01-18 | Novo Nordisk A/S | Pharmaceutical use of substituted 1,2,4-triazoles |
| GB0704394D0 (en) * | 2007-03-07 | 2007-04-11 | Senexis Ltd | Compounds |
| JP6671382B2 (ja) | 2014-10-29 | 2020-03-25 | アポグリクス アクツィエブーラーグＡｐｏＧｌｙｘ ＡＢ | 特に糖尿病の治療に有用である２−（１，２，４−トリアゾール−３−イルスルファニル）−ｎ−１，３，４−チアジアゾール−２−イルアセトアミドの誘導体 |
-
2017
- 2017-04-28 CA CA3022195A patent/CA3022195C/en active Active
- 2017-04-28 PL PL17720125T patent/PL3448853T3/pl unknown
- 2017-04-28 US US16/096,521 patent/US10730865B2/en active Active
- 2017-04-28 DK DK17720125.8T patent/DK3448853T3/da active
- 2017-04-28 WO PCT/EP2017/060148 patent/WO2017186893A1/en not_active Ceased
- 2017-04-28 HU HUE17720125A patent/HUE057193T2/hu unknown
- 2017-04-28 LT LTEPPCT/EP2017/060148T patent/LT3448853T/lt unknown
- 2017-04-28 HR HRP20212031TT patent/HRP20212031T1/hr unknown
- 2017-04-28 EP EP17720125.8A patent/EP3448853B1/en active Active
- 2017-04-28 ES ES17720125T patent/ES2902409T3/es active Active
- 2017-04-28 JP JP2018556376A patent/JP6921118B2/ja active Active
- 2017-04-28 PT PT177201258T patent/PT3448853T/pt unknown
Also Published As
| Publication number | Publication date |
|---|---|
| PT3448853T (pt) | 2021-12-30 |
| PL3448853T3 (pl) | 2022-02-28 |
| LT3448853T (lt) | 2022-01-10 |
| HUE057193T2 (hu) | 2022-04-28 |
| WO2017186893A1 (en) | 2017-11-02 |
| EP3448853B1 (en) | 2021-11-17 |
| US20190127360A1 (en) | 2019-05-02 |
| JP2019516677A (ja) | 2019-06-20 |
| JP6921118B2 (ja) | 2021-08-18 |
| US10730865B2 (en) | 2020-08-04 |
| HRP20212031T1 (hr) | 2022-04-01 |
| EP3448853A1 (en) | 2019-03-06 |
| CA3022195C (en) | 2024-02-13 |
| DK3448853T3 (da) | 2021-12-06 |
| CA3022195A1 (en) | 2017-11-02 |
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