JP2007526285A5 - - Google Patents
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- Publication number
- JP2007526285A5 JP2007526285A5 JP2007501295A JP2007501295A JP2007526285A5 JP 2007526285 A5 JP2007526285 A5 JP 2007526285A5 JP 2007501295 A JP2007501295 A JP 2007501295A JP 2007501295 A JP2007501295 A JP 2007501295A JP 2007526285 A5 JP2007526285 A5 JP 2007526285A5
- Authority
- JP
- Japan
- Prior art keywords
- methyl
- dihydro
- pyrimidin
- triazolo
- phenylbutyl
- 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.)
- Granted
Links
- -1 2- Isopropyl-4,5,6,7-tetrahydropyrazolo [1,5-a] pyridin-3-yl Chemical group 0.000 claims 7
- BNRNXUUZRGQAQC-UHFFFAOYSA-N sildenafil Chemical compound CCCC1=NN(C)C(C(N2)=O)=C1N=C2C(C(=CC=1)OCC)=CC=1S(=O)(=O)N1CCN(C)CC1 BNRNXUUZRGQAQC-UHFFFAOYSA-N 0.000 claims 5
- 239000008194 pharmaceutical composition Substances 0.000 claims 4
- WOXKDUGGOYFFRN-IIBYNOLFSA-N tadalafil Chemical compound C1=C2OCOC2=CC([C@@H]2C3=C(C4=CC=CC=C4N3)C[C@H]3N2C(=O)CN(C3=O)C)=C1 WOXKDUGGOYFFRN-IIBYNOLFSA-N 0.000 claims 4
- 208000014644 Brain disease Diseases 0.000 claims 3
- 208000032274 Encephalopathy Diseases 0.000 claims 3
- SECKRCOLJRRGGV-UHFFFAOYSA-N Vardenafil Chemical compound CCCC1=NC(C)=C(C(N=2)=O)N1NC=2C(C(=CC=1)OCC)=CC=1S(=O)(=O)N1CCN(CC)CC1 SECKRCOLJRRGGV-UHFFFAOYSA-N 0.000 claims 3
- FBCDRHDULQYRTB-UHFFFAOYSA-N 2-[2-ethoxy-5-(4-ethylpiperazin-1-yl)sulfonylphenyl]-5-methyl-7-propyl-1h-imidazo[5,1-f][1,2,4]triazin-4-one;trihydrate;hydrochloride Chemical compound O.O.O.Cl.CCCC1=NC(C)=C(C(N=2)=O)N1NC=2C(C(=CC=1)OCC)=CC=1S(=O)(=O)N1CCN(CC)CC1 FBCDRHDULQYRTB-UHFFFAOYSA-N 0.000 claims 2
- LSBDFXRDZJMBSC-UHFFFAOYSA-N 2-phenylacetamide Chemical compound NC(=O)CC1=CC=CC=C1 LSBDFXRDZJMBSC-UHFFFAOYSA-N 0.000 claims 2
- 208000030836 Hashimoto thyroiditis Diseases 0.000 claims 2
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 claims 2
- 229940123333 Phosphodiesterase 5 inhibitor Drugs 0.000 claims 2
- 229940099471 Phosphodiesterase inhibitor Drugs 0.000 claims 2
- 206010040047 Sepsis Diseases 0.000 claims 2
- ZVNYJIZDIRKMBF-UHFFFAOYSA-N Vesnarinone Chemical compound C1=C(OC)C(OC)=CC=C1C(=O)N1CCN(C=2C=C3CCC(=O)NC3=CC=2)CC1 ZVNYJIZDIRKMBF-UHFFFAOYSA-N 0.000 claims 2
- CCXIVOGMSQZBSB-UHFFFAOYSA-N [5-(1-benzyl-6-fluoroindazol-3-yl)furan-2-yl]methanol Chemical compound O1C(CO)=CC=C1C(C1=CC=C(F)C=C11)=NN1CC1=CC=CC=C1 CCXIVOGMSQZBSB-UHFFFAOYSA-N 0.000 claims 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 2
- 239000002590 phosphodiesterase V inhibitor Substances 0.000 claims 2
- 150000003839 salts Chemical class 0.000 claims 2
- 229960000835 tadalafil Drugs 0.000 claims 2
- 229960002381 vardenafil Drugs 0.000 claims 2
- GODZWYONGRENHA-UHFFFAOYSA-N 1-cyclopentyl-3-methyl-6-pyridin-4-yl-5H-pyrazolo[3,4-d]pyrimidin-4-one Chemical compound C1=2N=C(C=3C=CN=CC=3)NC(=O)C=2C(C)=NN1C1CCCC1 GODZWYONGRENHA-UHFFFAOYSA-N 0.000 claims 1
- MFKZGAAAKCDLHM-UHFFFAOYSA-N 1-cyclopentyl-6-(3-ethoxypyridin-4-yl)-3-ethyl-5H-pyrazolo[3,4-d]pyrimidin-4-one Chemical compound CCOC1=CN=CC=C1C(N1)=NC(=O)C2=C1N(C1CCCC1)N=C2CC MFKZGAAAKCDLHM-UHFFFAOYSA-N 0.000 claims 1
- 125000004066 1-hydroxyethyl group Chemical group [H]OC([H])([*])C([H])([H])[H] 0.000 claims 1
- ZCBNNBZAPHAFLM-UHFFFAOYSA-N 2-(2-propoxyphenyl)-1,2,5,9-tetrahydropurin-6-one Chemical compound CCCOC1=CC=CC=C1C1N=C2N=CNC2C(=O)N1 ZCBNNBZAPHAFLM-UHFFFAOYSA-N 0.000 claims 1
- PQTJTRTXCNZDFT-UHFFFAOYSA-N 2-(2-propoxyphenyl)-3,7-dihydropurin-6-one Chemical compound CCCOC1=CC=CC=C1C(N1)=NC(=O)C2=C1N=CN2 PQTJTRTXCNZDFT-UHFFFAOYSA-N 0.000 claims 1
- NFWIUUMQOPCHNV-UHFFFAOYSA-N 2-(4-ethoxy-2-phenylcycloheptyl)-1h-imidazole Chemical compound C1C(OCC)CCCC(C=2NC=CN=2)C1C1=CC=CC=C1 NFWIUUMQOPCHNV-UHFFFAOYSA-N 0.000 claims 1
- JEMJAABFSYOLAP-UHFFFAOYSA-N 2-[(2-methyl-4-pyridinyl)methyl]-1-oxo-8-(2-pyrimidinylmethoxy)-4-(3,4,5-trimethoxyphenyl)-2,7-naphthyridine-3-carboxylic acid methyl ester Chemical compound C12=CC=NC(OCC=3N=CC=CN=3)=C2C(=O)N(CC=2C=C(C)N=CC=2)C(C(=O)OC)=C1C1=CC(OC)=C(OC)C(OC)=C1 JEMJAABFSYOLAP-UHFFFAOYSA-N 0.000 claims 1
- NOIHTGOGFDFCBN-UHFFFAOYSA-N 2-[2-ethoxy-5-(4-ethylpiperazin-1-yl)sulfonylphenyl]-5-methyl-7-propyl-1h-imidazo[5,1-f][1,2,4]triazin-4-one;dihydrochloride Chemical compound Cl.Cl.CCCC1=NC(C)=C(C(N=2)=O)N1NC=2C(C(=CC=1)OCC)=CC=1S(=O)(=O)N1CCN(CC)CC1 NOIHTGOGFDFCBN-UHFFFAOYSA-N 0.000 claims 1
- 125000006282 2-chlorobenzyl group Chemical group [H]C1=C([H])C(Cl)=C(C([H])=C1[H])C([H])([H])* 0.000 claims 1
- 125000003006 2-dimethylaminoethyl group Chemical group [H]C([H])([H])N(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 claims 1
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims 1
- LNSWDTFYXQGHQZ-UHFFFAOYSA-N 2-imidazol-1-yl-6-methoxy-n-(2-methoxyethyl)quinazolin-4-amine Chemical compound N=1C2=CC=C(OC)C=C2C(NCCOC)=NC=1N1C=CN=C1 LNSWDTFYXQGHQZ-UHFFFAOYSA-N 0.000 claims 1
- 125000005809 3,4,5-trimethoxyphenyl group Chemical group [H]C1=C(OC([H])([H])[H])C(OC([H])([H])[H])=C(OC([H])([H])[H])C([H])=C1* 0.000 claims 1
- 125000002774 3,4-dimethoxybenzyl group Chemical group [H]C1=C([H])C(=C([H])C(OC([H])([H])[H])=C1OC([H])([H])[H])C([H])([H])* 0.000 claims 1
- WYFCDXPLQWBYLV-UHFFFAOYSA-N 3-(5-phenylpentan-2-yl)-5-(pyridin-4-ylmethyl)-6H-triazolo[4,5-d]pyrimidin-7-one Chemical compound N1=NC(C(NC(CC=2C=CN=CC=2)=N2)=O)=C2N1C(C)CCCC1=CC=CC=C1 WYFCDXPLQWBYLV-UHFFFAOYSA-N 0.000 claims 1
- JHBGAOYCONJKBW-UHFFFAOYSA-N 3-(5-phenylpentan-2-yl)-5-[(4-phenylphenyl)methyl]-6H-triazolo[4,5-d]pyrimidin-7-one Chemical compound N1=NC(C(NC(CC=2C=CC(=CC=2)C=2C=CC=CC=2)=N2)=O)=C2N1C(C)CCCC1=CC=CC=C1 JHBGAOYCONJKBW-UHFFFAOYSA-N 0.000 claims 1
- YLEPRCOBSGOCCW-UHFFFAOYSA-N 3-ethyl-8-[[2-(morpholin-4-ylmethyl)phenyl]methylamino]-1h-imidazo[4,5-g]quinazoline-2-thione Chemical group C=12C=C3NC(=S)N(CC)C3=CC2=NC=NC=1NCC1=CC=CC=C1CN1CCOCC1 YLEPRCOBSGOCCW-UHFFFAOYSA-N 0.000 claims 1
- VDXZLVXFVYDBNH-UHFFFAOYSA-N 4-[(3-chloro-4-methoxyphenyl)methylamino]-1-(4-hydroxypiperidin-1-yl)phthalazine-6-carbonitrile Chemical compound C1=C(Cl)C(OC)=CC=C1CNC(C1=CC(=CC=C11)C#N)=NN=C1N1CCC(O)CC1 VDXZLVXFVYDBNH-UHFFFAOYSA-N 0.000 claims 1
- LNMMZMTWCOIELH-UHFFFAOYSA-N 4-methyl-5-pyridin-4-yl-1,3-thiazole-2-carboxamide Chemical compound N1=C(C(N)=O)SC(C=2C=CN=CC=2)=C1C LNMMZMTWCOIELH-UHFFFAOYSA-N 0.000 claims 1
- UYBVXOPUCHLFBB-UHFFFAOYSA-N 5-(1,3-benzodioxol-5-ylmethyl)-3-(5-phenylpentan-2-yl)-6H-triazolo[4,5-d]pyrimidin-7-one Chemical compound N1=NC(C(NC(CC=2C=C3OCOC3=CC=2)=N2)=O)=C2N1C(C)CCCC1=CC=CC=C1 UYBVXOPUCHLFBB-UHFFFAOYSA-N 0.000 claims 1
- MTWHVOZRKLKMPK-UHFFFAOYSA-N 5-(1,3-benzodioxol-5-ylmethyl)-3-nonan-3-yl-6H-triazolo[4,5-d]pyrimidin-7-one Chemical compound C1=C2OCOC2=CC(CC2=NC3=C(C(N2)=O)N=NN3C(CC)CCCCCC)=C1 MTWHVOZRKLKMPK-UHFFFAOYSA-N 0.000 claims 1
- YRVSSAHNWIKBOO-UHFFFAOYSA-N 5-[(3,4-dichlorophenyl)methyl]-3-(5-phenylpentan-2-yl)-6H-triazolo[4,5-d]pyrimidin-7-one Chemical compound N1=NC(C(NC(CC=2C=C(Cl)C(Cl)=CC=2)=N2)=O)=C2N1C(C)CCCC1=CC=CC=C1 YRVSSAHNWIKBOO-UHFFFAOYSA-N 0.000 claims 1
- MAFKHHASELEAOY-UHFFFAOYSA-N 5-[(4-aminophenyl)methyl]-3-(5-phenylpentan-2-yl)-6H-triazolo[4,5-d]pyrimidin-7-one Chemical compound N1=NC(C(NC(CC=2C=CC(N)=CC=2)=N2)=O)=C2N1C(C)CCCC1=CC=CC=C1 MAFKHHASELEAOY-UHFFFAOYSA-N 0.000 claims 1
- BLWMVGBZGHLKMW-UHFFFAOYSA-N 5-[(4-bromophenyl)methyl]-3-(5-phenylpentan-2-yl)-6H-triazolo[4,5-d]pyrimidin-7-one Chemical compound N1=NC(C(NC(CC=2C=CC(Br)=CC=2)=N2)=O)=C2N1C(C)CCCC1=CC=CC=C1 BLWMVGBZGHLKMW-UHFFFAOYSA-N 0.000 claims 1
- OUXVHTSANLRICR-UHFFFAOYSA-N 5-[(4-morpholin-4-ylsulfinylphenyl)methyl]-3-(5-phenylpentan-2-yl)-6H-triazolo[4,5-d]pyrimidin-7-one Chemical compound N1=NC(C(NC(CC=2C=CC(=CC=2)S(=O)N2CCOCC2)=N2)=O)=C2N1C(C)CCCC1=CC=CC=C1 OUXVHTSANLRICR-UHFFFAOYSA-N 0.000 claims 1
- ZWXLRFCLVBVPPN-UHFFFAOYSA-N 5-[[4-(4-methylpiperazin-1-yl)sulfonylphenyl]methyl]-3-(5-phenylpentan-2-yl)-6H-triazolo[4,5-d]pyrimidin-7-one Chemical compound N1=NC(C(NC(CC=2C=CC(=CC=2)S(=O)(=O)N2CCN(C)CC2)=N2)=O)=C2N1C(C)CCCC1=CC=CC=C1 ZWXLRFCLVBVPPN-UHFFFAOYSA-N 0.000 claims 1
- GSGHEAPRWZPGKU-UHFFFAOYSA-N 5-[hydroxy(phenyl)methyl]-3-(5-phenylpentan-2-yl)-6H-triazolo[4,5-d]pyrimidin-7-one Chemical compound N1=NC(C(NC(=N2)C(O)C=3C=CC=CC=3)=O)=C2N1C(C)CCCC1=CC=CC=C1 GSGHEAPRWZPGKU-UHFFFAOYSA-N 0.000 claims 1
- AFEPFRFHBOPKGA-UHFFFAOYSA-N 5-benzoyl-3-(5-phenylpentan-2-yl)-6H-triazolo[4,5-d]pyrimidin-7-one Chemical compound N1=NC(C(NC(=N2)C(=O)C=3C=CC=CC=3)=O)=C2N1C(C)CCCC1=CC=CC=C1 AFEPFRFHBOPKGA-UHFFFAOYSA-N 0.000 claims 1
- JVXOVCCTKADOOP-UHFFFAOYSA-N 9-bromo-2-(3-hydroxypropyloxy)-5-(3-pyridylmethyl)-4h-pyrido [3,2,1-jk]carbazole-4-one Chemical compound O=C1C(C=23)=CC(OCCCO)=CC=2C2=CC=C(Br)C=C2N3C=C1CC1=CC=CN=C1 JVXOVCCTKADOOP-UHFFFAOYSA-N 0.000 claims 1
- KHBQMWCZKVMBLN-UHFFFAOYSA-N Benzenesulfonamide Chemical compound NS(=O)(=O)C1=CC=CC=C1 KHBQMWCZKVMBLN-UHFFFAOYSA-N 0.000 claims 1
- 208000029812 Cerebral Small Vessel disease Diseases 0.000 claims 1
- 206010067466 Cerebral microangiopathy Diseases 0.000 claims 1
- 208000035150 Hypercholesterolemia Diseases 0.000 claims 1
- ZJWGRSIAKWRRCG-UHFFFAOYSA-N N-methyl-4-[[7-oxo-3-(5-phenylpentan-2-yl)-6H-triazolo[4,5-d]pyrimidin-5-yl]methyl]benzenesulfonamide Chemical compound C1=CC(S(=O)(=O)NC)=CC=C1CC(NC1=O)=NC2=C1N=NN2C(C)CCCC1=CC=CC=C1 ZJWGRSIAKWRRCG-UHFFFAOYSA-N 0.000 claims 1
- 208000007125 Neurotoxicity Syndromes Diseases 0.000 claims 1
- 201000001880 Sexual dysfunction Diseases 0.000 claims 1
- 206010044221 Toxic encephalopathy Diseases 0.000 claims 1
- 231100000076 Toxic encephalopathy Toxicity 0.000 claims 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 230000002490 cerebral effect Effects 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 claims 1
- UKJLNMAFNRKWGR-UHFFFAOYSA-N cyclohexatrienamine Chemical group NC1=CC=C=C[CH]1 UKJLNMAFNRKWGR-UHFFFAOYSA-N 0.000 claims 1
- 201000010099 disease Diseases 0.000 claims 1
- 230000006806 disease prevention Effects 0.000 claims 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 1
- 230000004064 dysfunction Effects 0.000 claims 1
- 208000006575 hypertriglyceridemia Diseases 0.000 claims 1
- UVNXNSUKKOLFBM-UHFFFAOYSA-N imidazo[2,1-b][1,3,4]thiadiazole Chemical compound N1=CSC2=NC=CN21 UVNXNSUKKOLFBM-UHFFFAOYSA-N 0.000 claims 1
- SRJOCJYGOFTFLH-UHFFFAOYSA-N isonipecotic acid Chemical compound OC(=O)C1CCNCC1 SRJOCJYGOFTFLH-UHFFFAOYSA-N 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- SANFLTPRLLETKD-UHFFFAOYSA-N n-(1,3-benzodioxol-5-ylmethyl)-2-imidazol-1-yl-6-methylthieno[2,3-d]pyrimidin-4-amine Chemical compound N1=C2SC(C)=CC2=C(NCC=2C=C3OCOC3=CC=2)N=C1N1C=CN=C1 SANFLTPRLLETKD-UHFFFAOYSA-N 0.000 claims 1
- 125000004260 quinazolin-2-yl group Chemical group [H]C1=NC(*)=NC2=C1C([H])=C([H])C([H])=C2[H] 0.000 claims 1
- 125000004547 quinazolin-6-yl group Chemical group N1=CN=CC2=CC(=CC=C12)* 0.000 claims 1
- 208000012201 sexual and gender identity disease Diseases 0.000 claims 1
- 208000015891 sexual disease Diseases 0.000 claims 1
- 229960003310 sildenafil Drugs 0.000 claims 1
- 229960002639 sildenafil citrate Drugs 0.000 claims 1
- DEIYFTQMQPDXOT-UHFFFAOYSA-N sildenafil citrate Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O.CCCC1=NN(C)C(C(N2)=O)=C1N=C2C(C(=CC=1)OCC)=CC=1S(=O)(=O)N1CCN(C)CC1 DEIYFTQMQPDXOT-UHFFFAOYSA-N 0.000 claims 1
- 239000012453 solvate Substances 0.000 claims 1
- 125000000446 sulfanediyl group Chemical group *S* 0.000 claims 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims 1
- WTVSOESDARPVQO-UHFFFAOYSA-N triazolo[4,5-d]pyrimidin-7-one Chemical compound O=C1N=CN=C2N=NN=C12 WTVSOESDARPVQO-UHFFFAOYSA-N 0.000 claims 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 1
- 229960001540 vardenafil hydrochloride Drugs 0.000 claims 1
- 229960004573 vardenafil hydrochloride trihydrate Drugs 0.000 claims 1
- 230000004865 vascular response Effects 0.000 claims 1
- 229950005577 vesnarinone Drugs 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP04100909 | 2004-03-05 | ||
| EP04100909.3 | 2004-03-05 | ||
| PCT/EP2005/050958 WO2005089766A1 (en) | 2004-03-05 | 2005-03-03 | Novel use for pde5 inhibitors |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2007526285A JP2007526285A (ja) | 2007-09-13 |
| JP2007526285A5 true JP2007526285A5 (enExample) | 2008-03-13 |
| JP4838792B2 JP4838792B2 (ja) | 2011-12-14 |
Family
ID=34928893
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2007501295A Expired - Fee Related JP4838792B2 (ja) | 2004-03-05 | 2005-03-03 | Ｐｄｅ５阻害剤のための新規の使用 |
Country Status (9)
| Country | Link |
|---|---|
| US (2) | US7666872B2 (enExample) |
| EP (1) | EP1740183B8 (enExample) |
| JP (1) | JP4838792B2 (enExample) |
| AT (1) | ATE445402T1 (enExample) |
| AU (1) | AU2005224043B2 (enExample) |
| CA (1) | CA2557792C (enExample) |
| DE (1) | DE602005017135D1 (enExample) |
| ES (1) | ES2334682T3 (enExample) |
| WO (1) | WO2005089766A1 (enExample) |
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8841300B2 (en) * | 2006-10-02 | 2014-09-23 | Jerry M. Held | Treatment for Parkinson's disease—combination high dose serotonergic synaptic reuptake inhibitor with phosphodiesterase inhibitor |
| CA2663436A1 (en) | 2006-10-04 | 2008-04-10 | Pfizer Products Inc. | Pyrido[4,3-d]pyrimidin-4(3h)-one derivatives as calcium receptor antagonists |
| CN101754756A (zh) * | 2007-05-18 | 2010-06-23 | 维瓦斯公司 | 包含磷酸二酯酶-5抑制剂的新组合和它们的用途 |
| KR101002490B1 (ko) * | 2007-06-09 | 2010-12-17 | 동아제약주식회사 | 유데나필을 유효성분으로 함유하는 만성 심부전증 치료용약학적 조성물 |
| US8071557B2 (en) * | 2007-06-13 | 2011-12-06 | Vivus, Inc. | Treatment of pulmonary hypertension with carbonic anhydrase inhibitors |
| AU2012201640B2 (en) * | 2007-06-13 | 2014-09-04 | Vivus, Inc. | Treatment of pulmonary hypertension with carbonic anhydrase inhibitors in combination with a sympathomimetic amine |
| AU2014213552B2 (en) * | 2007-06-13 | 2016-11-24 | Vivus, Inc. | Treatment of pulmonary hypertension with carbonic anhydrase inhibitors in combination with a sympathomimetic amine |
| MX2010011880A (es) * | 2008-04-29 | 2011-05-25 | Pharnext | Nuevos enfoques terapeuticos para tratar la enfermedad del alzheimer y trastornos relacionados mediante una modulacion de la respuesta de estres celular. |
| CN102203067B (zh) * | 2008-08-25 | 2014-01-15 | Irm责任有限公司 | Hedgehog通路调节剂 |
| US8962770B2 (en) * | 2009-12-30 | 2015-02-24 | Sabic Global Technologies B.V. | Blends of isosorbide-based copolycarbonate, method of making, and articles formed therefrom |
| US8888802B2 (en) * | 2010-12-21 | 2014-11-18 | Alcon Research, Ltd. | Vitrectomy probe with adjustable cutter port size |
| EP2535049A1 (en) | 2011-06-17 | 2012-12-19 | Proyecto de Biomedicina Cima, S.L. | Tadalafil for the treatment of dementia |
| AT512084A1 (de) | 2011-10-20 | 2013-05-15 | Univ Wien Tech | Diazabicyclo- und diazaspiro-alkanderivate als phosphodiesterase-5 inhibitoren |
| RU2497203C2 (ru) * | 2012-02-13 | 2013-10-27 | Государственное бюджетное образовательное учреждение высшего профессионального образования "Курский государственный медицинский университет" Министерства здравоохранения и социального развития Российской Федерации | Способ фармакологической коррекции ишемии скелетной мышцы силденафилом, в том числе при l-name-индуцированном дефиците оксида азота |
| ES2635016T3 (es) * | 2013-03-01 | 2017-10-02 | Fundación Para La Investigación Médica Aplicada | Nuevos compuestos como inhibidores duales de fosfodiesterasas e histonas deacetilasas |
| IT201700085714A1 (it) * | 2017-07-26 | 2019-01-26 | Luigi Maiuri | Approccio terapeutico per il trattamento e/o prevenzione di condizioni di sensibilità al glutine. |
| US10647791B2 (en) | 2018-03-30 | 2020-05-12 | Sekisui Chemical Co., Ltd. | Polyvinyl alcohol used as dispersing agents for polyvinyl chloride suspension polymerization, dispersing agents comprising the polyvinyl alcohol, and method for producing polyvinyl chloride using the polyvinyl alcohol |
| WO2023109513A1 (zh) * | 2021-12-14 | 2023-06-22 | 真奥金银花药业有限公司 | 爱地那非或其盐在制备预防或治疗缺血性脑损伤的药物中的应用 |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2189355A1 (en) | 1995-03-01 | 1996-09-06 | Yasuo Onoda | Imidazoquinazoline derivatives |
| KR20000010919A (ko) | 1996-05-31 | 2000-02-25 | 모치다 에이 | Cgmppde 저해작용이 있는 피리도카르바졸 유도체 |
| JPH10298164A (ja) * | 1997-02-27 | 1998-11-10 | Tanabe Seiyaku Co Ltd | イソキノリノン誘導体、その製法及びその合成中間体 |
| AU6230098A (en) * | 1997-02-27 | 1998-09-18 | Tanabe Seiyaku Co., Ltd. | Isoquinolinone derivatives, process for preparing the same, and their use as phosphodiesterase inhibitors |
| HK1049834A1 (zh) | 1999-10-11 | 2003-05-30 | 辉瑞大药厂 | 用作磷酸二酯酶抑制剂的5-(2-取代的-5-杂环基磺酰基吡啶-3-基)-二氢吡唑并[4，3-d]嘧啶-7-酮类化合物 |
| IL152925A (en) * | 1999-10-21 | 2010-04-15 | Pfizer | Pharmaceutical preparations for the treatment of neurological disease containing an inhibitor of ring guanizine '3', 5 '- monophosphate phosphodiesterase 5 and one of gabapentin or pregabalin |
| AU2002314044B2 (en) * | 2001-05-09 | 2006-09-21 | Bayer Healthcare Ag | Novel use of 2-phenyl-substituted imidazotriazinones |
| GB0129274D0 (en) * | 2001-12-06 | 2002-01-23 | Pfizer Ltd | Novel kit |
| US20050107394A1 (en) | 2001-12-17 | 2005-05-19 | Ardeschir Ghofrani | Novel use of selective pde5 inhibitors |
-
2005
- 2005-03-03 ES ES05716901T patent/ES2334682T3/es not_active Expired - Lifetime
- 2005-03-03 DE DE602005017135T patent/DE602005017135D1/de not_active Expired - Lifetime
- 2005-03-03 JP JP2007501295A patent/JP4838792B2/ja not_active Expired - Fee Related
- 2005-03-03 CA CA2557792A patent/CA2557792C/en not_active Expired - Fee Related
- 2005-03-03 WO PCT/EP2005/050958 patent/WO2005089766A1/en not_active Ceased
- 2005-03-03 EP EP05716901A patent/EP1740183B8/en not_active Expired - Lifetime
- 2005-03-03 US US10/590,992 patent/US7666872B2/en not_active Expired - Fee Related
- 2005-03-03 AU AU2005224043A patent/AU2005224043B2/en not_active Ceased
- 2005-03-03 AT AT05716901T patent/ATE445402T1/de not_active IP Right Cessation
-
2010
- 2010-01-04 US US12/654,787 patent/US8278300B2/en not_active Expired - Fee Related
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