NZ503044A - Bisethers of 1-oxa, aza and thianaphthalen-2-ones as phospholamban inhibitors - Google Patents

Bisethers of 1-oxa, aza and thianaphthalen-2-ones as phospholamban inhibitors

Info

Publication number: NZ503044A
Authority: NZ; New Zealand
Prior art keywords: alkyl; aryl; hydrogen; compound; aryialkyl
Prior art date: 1997-09-24

Application number

NZ503044A

Other languages

English (en)

Inventor

Jarmo Pystynen

Eija Tiainen

Kari Lonnberg

Pentti Nore

Seppo Parhi

Arto Karjalainen

Heimo Haikala

Jouko Levijoki

Original Assignee

Orion Corp

Priority date (The priority date 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 date listed.)

1997-09-24

Filing date

1998-09-24

Publication date

2001-08-31

1998-09-24 Application filed by Orion Corp filed Critical Orion Corp

2001-08-31 Publication of NZ503044A publication Critical patent/NZ503044A/en

Links

102000005681 phospholamban Human genes 0.000 title abstract description 12
108010059929 phospholamban Proteins 0.000 title abstract description 12
239000003112 inhibitor Substances 0.000 title description 6
150000001875 compounds Chemical class 0.000 claims abstract description 65
125000000217 alkyl group Chemical group 0.000 claims abstract description 44
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 38
239000001257 hydrogen Substances 0.000 claims abstract description 37
125000003118 aryl group Chemical group 0.000 claims abstract description 36
125000003545 alkoxy group Chemical group 0.000 claims abstract description 19
125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 18
125000003342 alkenyl group Chemical group 0.000 claims abstract description 15
125000004104 aryloxy group Chemical group 0.000 claims abstract description 10
125000001188 haloalkyl group Chemical group 0.000 claims abstract description 10
125000002768 hydroxyalkyl group Chemical group 0.000 claims abstract description 9
125000002252 acyl group Chemical group 0.000 claims abstract description 7
125000004181 carboxyalkyl group Chemical group 0.000 claims abstract description 7
150000002367 halogens Chemical class 0.000 claims abstract description 5
206010019280 Heart failures Diseases 0.000 claims abstract description 4
229910052736 halogen Inorganic materials 0.000 claims abstract description 4
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 4
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims abstract description 4
125000000547 substituted alkyl group Chemical group 0.000 claims abstract description 3
150000002431 hydrogen Chemical group 0.000 claims abstract 21
-1 aryialkyl Chemical group 0.000 claims description 20
150000002148 esters Chemical class 0.000 claims description 18
150000003839 salts Chemical class 0.000 claims description 17
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 15
229910052760 oxygen Inorganic materials 0.000 claims description 8
229910052717 sulfur Inorganic materials 0.000 claims description 8
208000002089 myocardial stunning Diseases 0.000 claims description 7
125000002947 alkylene group Chemical group 0.000 claims description 4
239000003814 drug Substances 0.000 claims description 4
125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims description 2
125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 2
239000004480 active ingredient Substances 0.000 claims description 2
239000008194 pharmaceutical composition Substances 0.000 claims description 2
238000004519 manufacturing process Methods 0.000 claims 2
CHGJHKQZZYYATJ-MGUWIHFFSA-N (7s,9r,10r)-7-[(2r,4s,5s,6s)-4-(dimethylamino)-5-[(2s,4s,5s,6s)-4-hydroxy-6-methyl-5-[(2r,6s)-6-methyl-5-oxooxan-2-yl]oxyoxan-2-yl]oxy-6-methyloxan-2-yl]oxy-9-ethyl-1,4,6,9,10,11-hexahydroxy-8,10-dihydro-7h-tetracene-5,12-dione Chemical compound O([C@H]1[C@@H](O)C[C@@H](O[C@H]1C)O[C@H]1[C@H](C[C@@H](O[C@H]1C)O[C@H]1C[C@]([C@@H](C2=C(O)C=3C(=O)C4=C(O)C=CC(O)=C4C(=O)C=3C(O)=C21)O)(O)CC)N(C)C)[C@H]1CCC(=O)[C@H](C)O1 CHGJHKQZZYYATJ-MGUWIHFFSA-N 0.000 claims 1
125000000172 C5-C10 aryl group Chemical group 0.000 claims 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
239000003937 drug carrier Substances 0.000 claims 1
230000002265 prevention Effects 0.000 claims 1
230000002401 inhibitory effect Effects 0.000 abstract description 5
125000004093 cyano group Chemical group *C#N 0.000 abstract description 4
125000003710 aryl alkyl group Chemical group 0.000 abstract 7
239000000047 product Substances 0.000 description 95
IAZDPXIOMUYVGZ-WFGJKAKNSA-N Dimethyl sulfoxide Chemical compound [2H]C([2H])([2H])S(=O)C([2H])([2H])[2H] IAZDPXIOMUYVGZ-WFGJKAKNSA-N 0.000 description 92
238000005160 1H NMR spectroscopy Methods 0.000 description 72
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 42
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 41
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 41
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-dimethylformamide Substances CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 40
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 33
NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 32
PXIPVTKHYLBLMZ-UHFFFAOYSA-N Sodium azide Chemical compound [Na+].[N-]=[N+]=[N-] PXIPVTKHYLBLMZ-UHFFFAOYSA-N 0.000 description 32
238000002844 melting Methods 0.000 description 32
230000008018 melting Effects 0.000 description 32
239000000243 solution Substances 0.000 description 32
239000000203 mixture Substances 0.000 description 28
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 28
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 27
238000002360 preparation method Methods 0.000 description 26
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 22
229910000027 potassium carbonate Inorganic materials 0.000 description 21
235000011181 potassium carbonates Nutrition 0.000 description 17
235000019270 ammonium chloride Nutrition 0.000 description 16
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 15
238000002474 experimental method Methods 0.000 description 15
239000011541 reaction mixture Substances 0.000 description 15
RENMDAKOXSCIGH-UHFFFAOYSA-N Chloroacetonitrile Chemical compound ClCC#N RENMDAKOXSCIGH-UHFFFAOYSA-N 0.000 description 14
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 14
239000000872 buffer Substances 0.000 description 13
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 12
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 12
230000000694 effects Effects 0.000 description 11
239000005457 ice water Substances 0.000 description 11
230000010412 perfusion Effects 0.000 description 11
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 10
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 10
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 9
239000002244 precipitate Substances 0.000 description 9
210000002027 skeletal muscle Anatomy 0.000 description 9
235000019439 ethyl acetate Nutrition 0.000 description 8
AOJFQRQNPXYVLM-UHFFFAOYSA-N pyridin-1-ium;chloride Chemical compound [Cl-].C1=CC=[NH+]C=C1 AOJFQRQNPXYVLM-UHFFFAOYSA-N 0.000 description 8
230000002861 ventricular Effects 0.000 description 8
JPYHHZQJCSQRJY-UHFFFAOYSA-N Phloroglucinol Natural products CCC=CCC=CCC=CCC=CCCCCC(=O)C1=C(O)C=C(O)C=C1O JPYHHZQJCSQRJY-UHFFFAOYSA-N 0.000 description 7
238000000034 method Methods 0.000 description 7
QCDYQQDYXPDABM-UHFFFAOYSA-N phloroglucinol Chemical compound OC1=CC(O)=CC(O)=C1 QCDYQQDYXPDABM-UHFFFAOYSA-N 0.000 description 7
229960001553 phloroglucinol Drugs 0.000 description 7
239000007787 solid Substances 0.000 description 7
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 6
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 6
ILAHWRKJUDSMFH-UHFFFAOYSA-N boron tribromide Chemical compound BrB(Br)Br ILAHWRKJUDSMFH-UHFFFAOYSA-N 0.000 description 6
229910052757 nitrogen Inorganic materials 0.000 description 6
125000004169 (C1-C6) alkyl group Chemical group 0.000 description 5
125000000041 C6-C10 aryl group Chemical group 0.000 description 5
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 5
230000003185 calcium uptake Effects 0.000 description 5
125000004432 carbon atom Chemical group C* 0.000 description 5
230000000747 cardiac effect Effects 0.000 description 5
125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 5
239000004816 latex Substances 0.000 description 5
229920000126 latex Polymers 0.000 description 5
LISFMEBWQUVKPJ-UHFFFAOYSA-N quinolin-2-ol Chemical class C1=CC=C2NC(=O)C=CC2=C1 LISFMEBWQUVKPJ-UHFFFAOYSA-N 0.000 description 5
229930185107 quinolinone Natural products 0.000 description 5
239000002904 solvent Substances 0.000 description 5
239000006228 supernatant Substances 0.000 description 5
AZUYLZMQTIKGSC-UHFFFAOYSA-N 1-[6-[4-(5-chloro-6-methyl-1H-indazol-4-yl)-5-methyl-3-(1-methylindazol-5-yl)pyrazol-1-yl]-2-azaspiro[3.3]heptan-2-yl]prop-2-en-1-one Chemical compound ClC=1C(=C2C=NNC2=CC=1C)C=1C(=NN(C=1C)C1CC2(CN(C2)C(C=C)=O)C1)C=1C=C2C=NN(C2=CC=1)C AZUYLZMQTIKGSC-UHFFFAOYSA-N 0.000 description 4
WNRGWPVJGDABME-UHFFFAOYSA-N 3,5-Dimethoxyaniline Chemical compound COC1=CC(N)=CC(OC)=C1 WNRGWPVJGDABME-UHFFFAOYSA-N 0.000 description 4
241000700199 Cavia porcellus Species 0.000 description 4
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 4
229930006000 Sucrose Natural products 0.000 description 4
CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 4
ZYGHJZDHTFUPRJ-UHFFFAOYSA-N benzo-alpha-pyrone Natural products C1=CC=C2OC(=O)C=CC2=C1 ZYGHJZDHTFUPRJ-UHFFFAOYSA-N 0.000 description 4
AGEZXYOZHKGVCM-UHFFFAOYSA-N benzyl bromide Chemical compound BrCC1=CC=CC=C1 AGEZXYOZHKGVCM-UHFFFAOYSA-N 0.000 description 4
238000006243 chemical reaction Methods 0.000 description 4
239000004615 ingredient Substances 0.000 description 4
235000015320 potassium carbonate Nutrition 0.000 description 4
239000005720 sucrose Substances 0.000 description 4
230000035488 systolic blood pressure Effects 0.000 description 4
POSZUTFLHGNLHX-KSBRXOFISA-N tris maleate Chemical compound OCC(N)(CO)CO.OCC(N)(CO)CO.OC(=O)\C=C/C(O)=O POSZUTFLHGNLHX-KSBRXOFISA-N 0.000 description 4
239000008096 xylene Substances 0.000 description 4
DVNOTHMAOBZNRF-UHFFFAOYSA-N 1,3-dibenzyl-5,7-dihydroxy-4-methylquinolin-2-one Chemical compound O=C1N(CC=2C=CC=CC=2)C2=CC(O)=CC(O)=C2C(C)=C1CC1=CC=CC=C1 DVNOTHMAOBZNRF-UHFFFAOYSA-N 0.000 description 3
229910015845 BBr3 Inorganic materials 0.000 description 3
102000004612 Calcium-Transporting ATPases Human genes 0.000 description 3
108010017954 Calcium-Transporting ATPases Proteins 0.000 description 3
241000700198 Cavia Species 0.000 description 3
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 3
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
125000003282 alkyl amino group Chemical group 0.000 description 3
FXRDPPFLWGSMQT-UHFFFAOYSA-N benzo[f]chromen-3-one Chemical compound C1=CC=C2C(C=CC(O3)=O)=C3C=CC2=C1 FXRDPPFLWGSMQT-UHFFFAOYSA-N 0.000 description 3
125000000753 cycloalkyl group Chemical group 0.000 description 3
239000000706 filtrate Substances 0.000 description 3
RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 3
229940098779 methanesulfonic acid Drugs 0.000 description 3
239000008188 pellet Substances 0.000 description 3
LPNYRYFBWFDTMA-UHFFFAOYSA-N potassium tert-butoxide Chemical compound [K+].CC(C)(C)[O-] LPNYRYFBWFDTMA-UHFFFAOYSA-N 0.000 description 3
125000006239 protecting group Chemical group 0.000 description 3
230000010410 reperfusion Effects 0.000 description 3
239000011734 sodium Substances 0.000 description 3
229910052708 sodium Inorganic materials 0.000 description 3
125000001412 tetrahydropyranyl group Chemical group 0.000 description 3
125000004178 (C1-C4) alkyl group Chemical group 0.000 description 2
XVCYZZIPWMCYGZ-UHFFFAOYSA-N 1,3-dibenzyl-4-methylquinolin-2-one Chemical compound O=C1N(CC=2C=CC=CC=2)C2=CC=CC=C2C(C)=C1CC1=CC=CC=C1 XVCYZZIPWMCYGZ-UHFFFAOYSA-N 0.000 description 2
DJBYUZAGHDRFHL-UHFFFAOYSA-N 1,3-dihydroxy-2,4-bis(2h-tetrazol-5-ylmethoxy)-7,8,9,10-tetrahydrobenzo[c]chromen-6-one Chemical compound OC1=C2C=3CCCCC=3C(=O)OC2=C(OCC2=NNN=N2)C(O)=C1OCC=1N=NNN=1 DJBYUZAGHDRFHL-UHFFFAOYSA-N 0.000 description 2
QYSAYAUOLUTQSC-UHFFFAOYSA-N 1-benzyl-4-methyl-5,7-bis(2h-tetrazol-5-ylmethoxy)quinolin-2-one Chemical compound C12=CC(OCC=3NN=NN=3)=CC(OCC=3NN=NN=3)=C2C(C)=CC(=O)N1CC1=CC=CC=C1 QYSAYAUOLUTQSC-UHFFFAOYSA-N 0.000 description 2
CIFXXADFFYSRII-UHFFFAOYSA-N 3-benzyl-1-[(4-fluorophenyl)methyl]-4-methyl-5,7-bis(2h-tetrazol-5-ylmethoxy)quinolin-2-one Chemical compound O=C1N(CC=2C=CC(F)=CC=2)C2=CC(OCC=3NN=NN=3)=CC(OCC=3NN=NN=3)=C2C(C)=C1CC1=CC=CC=C1 CIFXXADFFYSRII-UHFFFAOYSA-N 0.000 description 2
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
OZLGRUXZXMRXGP-UHFFFAOYSA-N Fluo-3 Chemical compound CC1=CC=C(N(CC(O)=O)CC(O)=O)C(OCCOC=2C(=CC=C(C=2)C2=C3C=C(Cl)C(=O)C=C3OC3=CC(O)=C(Cl)C=C32)N(CC(O)=O)CC(O)=O)=C1 OZLGRUXZXMRXGP-UHFFFAOYSA-N 0.000 description 2
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 2
WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 2
WTDHULULXKLSOZ-UHFFFAOYSA-N Hydroxylamine hydrochloride Chemical compound Cl.ON WTDHULULXKLSOZ-UHFFFAOYSA-N 0.000 description 2
TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
OHULVMOXKLLMJR-MSOLQXFVSA-N [(2s,6r)-4-benzoyloxy-2-methoxy-5-oxo-2h-pyran-6-yl]methyl benzoate Chemical compound C([C@H]1O[C@@H](C=C(OC(=O)C=2C=CC=CC=2)C1=O)OC)OC(=O)C1=CC=CC=C1 OHULVMOXKLLMJR-MSOLQXFVSA-N 0.000 description 2
WDJHALXBUFZDSR-UHFFFAOYSA-M acetoacetate Chemical compound CC(=O)CC([O-])=O WDJHALXBUFZDSR-UHFFFAOYSA-M 0.000 description 2
239000002253 acid Substances 0.000 description 2
229910052784 alkaline earth metal Inorganic materials 0.000 description 2
210000000709 aorta Anatomy 0.000 description 2
150000001540 azides Chemical class 0.000 description 2
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
229910052794 bromium Inorganic materials 0.000 description 2
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
229910052791 calcium Inorganic materials 0.000 description 2
239000011575 calcium Substances 0.000 description 2
125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 2
125000001589 carboacyl group Chemical group 0.000 description 2
UBAZGMLMVVQSCD-UHFFFAOYSA-N carbon dioxide;molecular oxygen Chemical compound O=O.O=C=O UBAZGMLMVVQSCD-UHFFFAOYSA-N 0.000 description 2
239000000460 chlorine Substances 0.000 description 2
229910052801 chlorine Inorganic materials 0.000 description 2
230000035487 diastolic blood pressure Effects 0.000 description 2
229910000397 disodium phosphate Inorganic materials 0.000 description 2
GPRDAMCHHGGJNX-UHFFFAOYSA-N ethyl 3-oxo-2-(2-phenylethyl)butanoate Chemical compound CCOC(=O)C(C(C)=O)CCC1=CC=CC=C1 GPRDAMCHHGGJNX-UHFFFAOYSA-N 0.000 description 2
OJCSPXHYDFONPU-UHFFFAOYSA-N etoac etoac Chemical compound CCOC(C)=O.CCOC(C)=O OJCSPXHYDFONPU-UHFFFAOYSA-N 0.000 description 2
229910052731 fluorine Inorganic materials 0.000 description 2
239000011737 fluorine Substances 0.000 description 2
239000008103 glucose Substances 0.000 description 2
210000005003 heart tissue Anatomy 0.000 description 2
INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 2
208000028867 ischemia Diseases 0.000 description 2
210000005246 left atrium Anatomy 0.000 description 2
210000005240 left ventricle Anatomy 0.000 description 2
210000004165 myocardium Anatomy 0.000 description 2
QAXZWHGWYSJAEI-UHFFFAOYSA-N n,n-dimethylformamide;ethanol Chemical compound CCO.CN(C)C=O QAXZWHGWYSJAEI-UHFFFAOYSA-N 0.000 description 2
125000001624 naphthyl group Chemical group 0.000 description 2
125000004430 oxygen atom Chemical group O* 0.000 description 2
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
SCVFZCLFOSHCOH-UHFFFAOYSA-M potassium acetate Chemical compound [K+].CC([O-])=O SCVFZCLFOSHCOH-UHFFFAOYSA-M 0.000 description 2
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 2
XTUSEBKMEQERQV-UHFFFAOYSA-N propan-2-ol;hydrate Chemical compound O.CC(C)O XTUSEBKMEQERQV-UHFFFAOYSA-N 0.000 description 2
102000004169 proteins and genes Human genes 0.000 description 2
108090000623 proteins and genes Proteins 0.000 description 2
210000003492 pulmonary vein Anatomy 0.000 description 2
210000003625 skull Anatomy 0.000 description 2
229910000030 sodium bicarbonate Inorganic materials 0.000 description 2
229910052938 sodium sulfate Inorganic materials 0.000 description 2
235000011152 sodium sulphate Nutrition 0.000 description 2
229910001220 stainless steel Inorganic materials 0.000 description 2
239000010935 stainless steel Substances 0.000 description 2
230000000638 stimulation Effects 0.000 description 2
125000001424 substituent group Chemical group 0.000 description 2
239000000725 suspension Substances 0.000 description 2
150000003573 thiols Chemical class 0.000 description 2
238000005303 weighing Methods 0.000 description 2
125000000229 (C1-C4)alkoxy group Chemical group 0.000 description 1
YGTAZGSLCXNBQL-UHFFFAOYSA-N 1,2,4-thiadiazole Chemical class C=1N=CSN=1 YGTAZGSLCXNBQL-UHFFFAOYSA-N 0.000 description 1
QCBXSNFQJIQQLN-UHFFFAOYSA-N 1,3-dibenzyl-4-methyl-5,7-bis(2h-tetrazol-5-ylmethoxy)quinolin-2-one Chemical compound O=C1N(CC=2C=CC=CC=2)C2=CC(OCC=3NN=NN=3)=CC(OCC=3NN=NN=3)=C2C(C)=C1CC1=CC=CC=C1 QCBXSNFQJIQQLN-UHFFFAOYSA-N 0.000 description 1
WHOXXIZKHZBTOB-UHFFFAOYSA-N 1,3-dihydroxy-7,8,9,10-tetrahydrobenzo[c]chromen-6-one Chemical compound C1CCCC2=C1C1=C(O)C=C(O)C=C1OC2=O WHOXXIZKHZBTOB-UHFFFAOYSA-N 0.000 description 1
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WCPAKWJPBJAGKN-UHFFFAOYSA-N oxadiazole Chemical compound C1=CON=N1 WCPAKWJPBJAGKN-UHFFFAOYSA-N 0.000 description 1
125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
239000000546 pharmaceutical excipient Substances 0.000 description 1
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235000011056 potassium acetate Nutrition 0.000 description 1
HHAVHBDPWSUKHZ-UHFFFAOYSA-N propan-2-ol;propan-2-one Chemical compound CC(C)O.CC(C)=O HHAVHBDPWSUKHZ-UHFFFAOYSA-N 0.000 description 1
RZWZRACFZGVKFM-UHFFFAOYSA-N propanoyl chloride Chemical compound CCC(Cl)=O RZWZRACFZGVKFM-UHFFFAOYSA-N 0.000 description 1
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UJMBCXLDXJUMFB-UHFFFAOYSA-K trisodium;5-oxo-1-(4-sulfonatophenyl)-4-[(4-sulfonatophenyl)diazenyl]-4h-pyrazole-3-carboxylate Chemical compound [Na+].[Na+].[Na+].[O-]C(=O)C1=NN(C=2C=CC(=CC=2)S([O-])(=O)=O)C(=O)C1N=NC1=CC=C(S([O-])(=O)=O)C=C1 UJMBCXLDXJUMFB-UHFFFAOYSA-K 0.000 description 1
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Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D215/20—Oxygen atoms
- C07D215/22—Oxygen atoms attached in position 2 or 4
- C07D215/227—Oxygen atoms attached in position 2 or 4 only one oxygen atom which is attached in position 2
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- 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
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
- C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D311/04—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
- C07D311/06—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 2
- C07D311/08—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 2 not hydrogenated in the hetero ring
- C07D311/16—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 2 not hydrogenated in the hetero ring substituted in position 7
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
- C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D311/04—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
- C07D311/58—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring other than with oxygen or sulphur atoms in position 2 or 4
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Bioinformatics & Cheminformatics (AREA)
General Chemical & Material Sciences (AREA)
Cardiology (AREA)
Chemical Kinetics & Catalysis (AREA)
Veterinary Medicine (AREA)
Medicinal Chemistry (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Pharmacology & Pharmacy (AREA)
Life Sciences & Earth Sciences (AREA)
Animal Behavior & Ethology (AREA)
General Health & Medical Sciences (AREA)
Public Health (AREA)
Heart & Thoracic Surgery (AREA)
Urology & Nephrology (AREA)
Vascular Medicine (AREA)
Hospice & Palliative Care (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Quinoline Compounds (AREA)
Plural Heterocyclic Compounds (AREA)
Indole Compounds (AREA)

NZ503044A 1997-09-24 1998-09-24 Bisethers of 1-oxa, aza and thianaphthalen-2-ones as phospholamban inhibitors NZ503044A (en)

Applications Claiming Priority (4)

Application Number	Priority Date	Filing Date	Title
US93711997A	1997-09-24	1997-09-24
US99015097A	1997-12-12	1997-12-12
US10411498A	1998-06-25	1998-06-25
PCT/FI1998/000755 WO1999015523A1 (fr)	1997-09-24	1998-09-24	Bisethers de 1-oxa, aza et thianaphtalene-2-one inhibiteurs du phospholambane

Publications (1)

Publication Number	Publication Date
NZ503044A true NZ503044A (en)	2001-08-31

Family

ID=27379660

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NZ503044A NZ503044A (en)	1997-09-24	1998-09-24	Bisethers of 1-oxa, aza and thianaphthalen-2-ones as phospholamban inhibitors

Country Status (18)

Country	Link
EP (1)	EP1017691A1 (fr)
JP (1)	JP2003525838A (fr)
KR (1)	KR20010015607A (fr)
CN (1)	CN1143857C (fr)
AU (1)	AU735729B2 (fr)
BR (1)	BR9813216A (fr)
CA (1)	CA2304849A1 (fr)
EA (1)	EA003084B1 (fr)
EE (1)	EE04494B1 (fr)
HU (1)	HUP0003647A3 (fr)
ID (1)	ID24373A (fr)
IL (1)	IL134662A0 (fr)
NO (1)	NO20001569L (fr)
NZ (1)	NZ503044A (fr)
PL (1)	PL339493A1 (fr)
SK (1)	SK3902000A3 (fr)
TR (1)	TR200000764T2 (fr)
WO (1)	WO1999015523A1 (fr)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
AU2001278980A1 (en) *	2000-07-21	2002-02-05	Chugai Seiyaku Kabushiki Kaisha	Coumarin derivatives useful as tnfalpha inhibitors
EP1491541B1 (fr) *	2001-03-30	2007-01-24	Pfizer Products Inc.	Pyridazinones, inhibiteurs d'aldose reductase.
US7572910B2 (en)	2003-02-20	2009-08-11	Pfizer, Inc.	Pyridazinone aldose reductase inhibitors
FR2970964B1 (fr) *	2011-01-28	2013-12-13	Univ Claude Bernard Lyon	Nouveaux derives d'azacoumarines presentant une activite inhibitrice des pompes mdr

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2543945A1 (de) *	1975-10-02	1977-04-21	Troponwerke Gmbh & Co Kg	2-benzopyranonderivate, verfahren zu ihrer herstellung sowie ihre verwendung als arzneimittel
GB8529362D0 (en) *	1985-11-28	1986-01-02	Pfizer Ltd	Quinolone cardiac stimulants
GB8630702D0 (en) *	1986-12-23	1987-02-04	Wellcome Found	Quinoline compound
US5053514A (en) *	1988-08-10	1991-10-01	Otsuka Pharmaceutical Company, Limited	Cardiotonics
CA2022236A1 (fr) *	1989-07-31	1991-02-01	Hiroaki Yanagisawa	Derives de coumarin, leur preparation et leur utilisation pour le traitement des troubles cerebrovasculaires
DE4337906A1 (de) *	1993-11-08	1995-05-11	Cassella Ag	Verwendung von Cumarinderivaten

1998
- 1998-09-24 EP EP98946482A patent/EP1017691A1/fr not_active Withdrawn
- 1998-09-24 TR TR2000/00764T patent/TR200000764T2/xx unknown
- 1998-09-24 EE EEP200000179A patent/EE04494B1/xx not_active IP Right Cessation
- 1998-09-24 HU HU0003647A patent/HUP0003647A3/hu unknown
- 1998-09-24 IL IL13466298A patent/IL134662A0/xx unknown
- 1998-09-24 SK SK390-2000A patent/SK3902000A3/sk unknown
- 1998-09-24 JP JP2000512828A patent/JP2003525838A/ja active Pending
- 1998-09-24 BR BR9813216-4A patent/BR9813216A/pt not_active IP Right Cessation
- 1998-09-24 WO PCT/FI1998/000755 patent/WO1999015523A1/fr not_active Ceased
- 1998-09-24 ID IDW20000564A patent/ID24373A/id unknown
- 1998-09-24 CA CA002304849A patent/CA2304849A1/fr not_active Abandoned
- 1998-09-24 KR KR1020007003094A patent/KR20010015607A/ko not_active Ceased
- 1998-09-24 AU AU93508/98A patent/AU735729B2/en not_active Ceased
- 1998-09-24 EA EA200000352A patent/EA003084B1/ru not_active IP Right Cessation
- 1998-09-24 NZ NZ503044A patent/NZ503044A/en unknown
- 1998-09-24 PL PL98339493A patent/PL339493A1/xx unknown
- 1998-09-24 CN CNB98809438XA patent/CN1143857C/zh not_active Expired - Fee Related
2000
- 2000-03-24 NO NO20001569A patent/NO20001569L/no not_active Application Discontinuation

Also Published As

Publication number	Publication date
EP1017691A1 (fr)	2000-07-12
IL134662A0 (en)	2001-04-30
NO20001569D0 (no)	2000-03-24
BR9813216A (pt)	2000-08-29
CN1271357A (zh)	2000-10-25
AU735729B2 (en)	2001-07-12
HUP0003647A2 (hu)	2001-08-28
PL339493A1 (en)	2000-12-18
SK3902000A3 (en)	2000-12-11
EA200000352A1 (ru)	2000-10-30
EE200000179A (et)	2001-04-16
CA2304849A1 (fr)	1999-04-01
EA003084B1 (ru)	2002-12-26
WO1999015523A1 (fr)	1999-04-01
JP2003525838A (ja)	2003-09-02
EE04494B1 (et)	2005-06-15
CN1143857C (zh)	2004-03-31
HUP0003647A3 (en)	2002-12-28
KR20010015607A (ko)	2001-02-26
NO20001569L (no)	2000-03-24
ID24373A (id)	2000-07-13
AU9350898A (en)	1999-04-12
TR200000764T2 (tr)	2001-03-21

Legal Events

Date	Code	Title
2002-02-01	PSEA	Patent sealed
2002-09-27	RENW	Renewal (renewal fees accepted)
2005-09-30	RENW	Renewal (renewal fees accepted)

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WO2004050082A1 (fr)	2004-06-17	Nouveaux derives coumarine-amide et leur preparation, composition medicamenteuse associee et son utilisation
JPS6360936A (ja)	1988-03-17	複合薬剤
US4707479A (en)	1987-11-17	Circulation active dihydropyridine-3-carboxamides
US6265421B1 (en)	2001-07-24	Phospholamban inhibitors and a method for increasing coronary flow
US4910206A (en)	1990-03-20	5-hetero-or aryl-substituted-imidazo(2,1-a)isoquinolines and their use as PAF receptor antagonists
HU211149A9 (en)	1995-10-30	Pyridazinedione compounds
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CZ2000937A3 (cs)	2000-08-16	Bisethery 1-oxa, aza a thianaftalen-2-onu jako inhibitory fosfolambanu a farmaceutické prostředky
WO2003028652A2 (fr)	2003-04-10	Utilisation de benzopyranones pour le traitement ou la prevention d'un cancer primitif du cerveau ou d'une metastase cerebrale
JP2000509726A (ja)	2000-08-02	糖尿病処置用のオキシランカルボン酸
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US20030216324A1 (en)	2003-11-20	Airway mucus secretion inhibitors
ZA200402765B (en)	2005-04-08	Use of benzopyranones for treating or preventing a primary brain cancer or a brain metastasis.