KR20200036914A - 디히드로옥사디아지논 - Google Patents
디히드로옥사디아지논 Download PDFInfo
- Publication number
- KR20200036914A KR20200036914A KR1020207005998A KR20207005998A KR20200036914A KR 20200036914 A KR20200036914 A KR 20200036914A KR 1020207005998 A KR1020207005998 A KR 1020207005998A KR 20207005998 A KR20207005998 A KR 20207005998A KR 20200036914 A KR20200036914 A KR 20200036914A
- Authority
- KR
- South Korea
- Prior art keywords
- group
- dihydro
- trifluoromethyl
- phenyl
- oxadiazin
- 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.)
- Withdrawn
Links
- 0 *CC1OC1c1cc(*)c(*)c(*)c1 Chemical compound *CC1OC1c1cc(*)c(*)c(*)c1 0.000 description 14
- FZESPVBONPPRAW-UHFFFAOYSA-N Cc1nc(nccc2)c2[nH]1 Chemical compound Cc1nc(nccc2)c2[nH]1 FZESPVBONPPRAW-UHFFFAOYSA-N 0.000 description 2
- KNMKLBIEFWXRMO-UHFFFAOYSA-N CC(C(c(cc1)ccc1Br)=NN1)OC1=O Chemical compound CC(C(c(cc1)ccc1Br)=NN1)OC1=O KNMKLBIEFWXRMO-UHFFFAOYSA-N 0.000 description 1
- AEHBLEUGQTXZCM-UHFFFAOYSA-N CC(C)(C1)C1/N=C\Nc(cc1)c(C(F)(F)F)cc1C(CO1)=NNC1=O Chemical compound CC(C)(C1)C1/N=C\Nc(cc1)c(C(F)(F)F)cc1C(CO1)=NNC1=O AEHBLEUGQTXZCM-UHFFFAOYSA-N 0.000 description 1
- IJIXSFTWANOINL-UHFFFAOYSA-N CC(c(cc1F)cc(C(F)(F)F)c1Cl)=O Chemical compound CC(c(cc1F)cc(C(F)(F)F)c1Cl)=O IJIXSFTWANOINL-UHFFFAOYSA-N 0.000 description 1
- CAHDPRAPCFFDOO-UHFFFAOYSA-N CCCNc(cc1)c(C(F)(F)F)cc1C(CO1)=NNC1=O Chemical compound CCCNc(cc1)c(C(F)(F)F)cc1C(CO1)=NNC1=O CAHDPRAPCFFDOO-UHFFFAOYSA-N 0.000 description 1
- LMSLRBRLMMNGRO-UHFFFAOYSA-N CN(C(c(cc1)cc(C(F)(F)F)c1Cl)=O)OC Chemical compound CN(C(c(cc1)cc(C(F)(F)F)c1Cl)=O)OC LMSLRBRLMMNGRO-UHFFFAOYSA-N 0.000 description 1
- KEONFINAMASGKS-UHFFFAOYSA-N CN(C)CCNc(cc1)c(C(F)(F)F)cc1C(CO1)=NNC1=O Chemical compound CN(C)CCNc(cc1)c(C(F)(F)F)cc1C(CO1)=NNC1=O KEONFINAMASGKS-UHFFFAOYSA-N 0.000 description 1
- SLFLVMDVUVUVSU-RDDDGLTNSA-N C[C@H]([C@@H](CO)Nc(cc1)c(C(F)(F)F)cc1C(CO1)=NN[IH]1=O)O Chemical compound C[C@H]([C@@H](CO)Nc(cc1)c(C(F)(F)F)cc1C(CO1)=NN[IH]1=O)O SLFLVMDVUVUVSU-RDDDGLTNSA-N 0.000 description 1
- DHFMKSFJSZQVFE-UHFFFAOYSA-N C[n]1c(CNc(cc2)c(C(F)(F)F)cc2C(CO2)=NNC2=O)ncc1 Chemical compound C[n]1c(CNc(cc2)c(C(F)(F)F)cc2C(CO2)=NNC2=O)ncc1 DHFMKSFJSZQVFE-UHFFFAOYSA-N 0.000 description 1
- IBJVKSNORDBFND-UHFFFAOYSA-N Cc([nH]nc1C)c1-c(c(C(F)(F)F)c1)ccc1C(CO1)=NNC1=O Chemical compound Cc([nH]nc1C)c1-c(c(C(F)(F)F)c1)ccc1C(CO1)=NNC1=O IBJVKSNORDBFND-UHFFFAOYSA-N 0.000 description 1
- LWMHRSVMMMBCSM-UHFFFAOYSA-N Cc(cc(cc1)C(CO2)=NNC2=O)c1-c1cnc(C)nc1 Chemical compound Cc(cc(cc1)C(CO2)=NNC2=O)c1-c1cnc(C)nc1 LWMHRSVMMMBCSM-UHFFFAOYSA-N 0.000 description 1
- YLUKCTBUOSXKSW-UHFFFAOYSA-N Cc1c(-c(cc2)ccc2F)ccc(C(CO2)=NNC2=O)c1 Chemical compound Cc1c(-c(cc2)ccc2F)ccc(C(CO2)=NNC2=O)c1 YLUKCTBUOSXKSW-UHFFFAOYSA-N 0.000 description 1
- QXGXIMVUONSLBZ-UHFFFAOYSA-N Cc1cc(C(CO2)=NNC2=O)ccc1-c1cccnc1 Chemical compound Cc1cc(C(CO2)=NNC2=O)ccc1-c1cccnc1 QXGXIMVUONSLBZ-UHFFFAOYSA-N 0.000 description 1
- HKMIWVOZJIODIY-UHFFFAOYSA-N N#Cc1cc(C(CO2)=NNC2=O)cc(Cl)c1N1CCOCC1 Chemical compound N#Cc1cc(C(CO2)=NNC2=O)cc(Cl)c1N1CCOCC1 HKMIWVOZJIODIY-UHFFFAOYSA-N 0.000 description 1
- MRAKZGZXMJKEHM-UHFFFAOYSA-N NCCNc(cc1)c(C(F)(F)F)cc1C(CO1)=NNC1=O Chemical compound NCCNc(cc1)c(C(F)(F)F)cc1C(CO1)=NNC1=O MRAKZGZXMJKEHM-UHFFFAOYSA-N 0.000 description 1
- APDMMPQGTUFMNL-UHFFFAOYSA-N Nc(nc1)ncc1-c(ccc(C(CO1)=NN[IH]1=O)c1)c1F Chemical compound Nc(nc1)ncc1-c(ccc(C(CO1)=NN[IH]1=O)c1)c1F APDMMPQGTUFMNL-UHFFFAOYSA-N 0.000 description 1
- BUNOSKWLVXNWEH-UHFFFAOYSA-N O=C(CBr)c(cc1)cc(C(F)(F)F)c1F Chemical compound O=C(CBr)c(cc1)cc(C(F)(F)F)c1F BUNOSKWLVXNWEH-UHFFFAOYSA-N 0.000 description 1
- IPFKZFUYGAMYLV-UHFFFAOYSA-N O=C1OCC(c(cc2)cc(C(F)(F)F)c2-c(c(F)c2F)ccc2F)=NN1 Chemical compound O=C1OCC(c(cc2)cc(C(F)(F)F)c2-c(c(F)c2F)ccc2F)=NN1 IPFKZFUYGAMYLV-UHFFFAOYSA-N 0.000 description 1
- YLAALOFZOYCMGZ-UHFFFAOYSA-N O=C1OCC(c(cc2)cc(C(F)(F)F)c2-c2ccc(cc[nH]3)c3c2)=NN1 Chemical compound O=C1OCC(c(cc2)cc(C(F)(F)F)c2-c2ccc(cc[nH]3)c3c2)=NN1 YLAALOFZOYCMGZ-UHFFFAOYSA-N 0.000 description 1
- LKPHAELTCVRPDD-UHFFFAOYSA-N O=C1OCC(c(cc2)cc(C(F)F)c2-c(cc2)ccc2Cl)=NN1 Chemical compound O=C1OCC(c(cc2)cc(C(F)F)c2-c(cc2)ccc2Cl)=NN1 LKPHAELTCVRPDD-UHFFFAOYSA-N 0.000 description 1
- YQNZHHDYPPXVSY-UHFFFAOYSA-N O=C1OCC(c(cc2)cc(C(F)F)c2C2=CCCC2)=NN1 Chemical compound O=C1OCC(c(cc2)cc(C(F)F)c2C2=CCCC2)=NN1 YQNZHHDYPPXVSY-UHFFFAOYSA-N 0.000 description 1
- JQDCNNPSPGGZTR-UHFFFAOYSA-N O=C1OCC(c(cc2)cc(F)c2-c(cc2F)ccc2F)=NN1 Chemical compound O=C1OCC(c(cc2)cc(F)c2-c(cc2F)ccc2F)=NN1 JQDCNNPSPGGZTR-UHFFFAOYSA-N 0.000 description 1
- ONOBXOKMJSCRHY-UHFFFAOYSA-N O=C1OCC(c(cc2C(F)(F)F)ccc2-c(cc(cc2)F)c2F)=NN1 Chemical compound O=C1OCC(c(cc2C(F)(F)F)ccc2-c(cc(cc2)F)c2F)=NN1 ONOBXOKMJSCRHY-UHFFFAOYSA-N 0.000 description 1
- PGBJPGOKOJDZBV-UHFFFAOYSA-N O=[IH]1OCC(c(cc2)cc(C(F)(F)F)c2NC2CCNCC2)=NN1 Chemical compound O=[IH]1OCC(c(cc2)cc(C(F)(F)F)c2NC2CCNCC2)=NN1 PGBJPGOKOJDZBV-UHFFFAOYSA-N 0.000 description 1
- ZYZSXZNSWHTZTD-UHFFFAOYSA-N O=[IH]1OCC(c(cc2)cc(C(F)(F)F)c2NCC2CCOCC2)=NN1 Chemical compound O=[IH]1OCC(c(cc2)cc(C(F)(F)F)c2NCC2CCOCC2)=NN1 ZYZSXZNSWHTZTD-UHFFFAOYSA-N 0.000 description 1
- RYEDLYIBTBQTOE-UHFFFAOYSA-N O=[IH]1OCC(c(cc2)cc(C(F)(F)F)c2NCc2cccnn2)=NN1 Chemical compound O=[IH]1OCC(c(cc2)cc(C(F)(F)F)c2NCc2cccnn2)=NN1 RYEDLYIBTBQTOE-UHFFFAOYSA-N 0.000 description 1
- QYEIFDMKGKWJNH-UHFFFAOYSA-N Oc1cc(-c(cc2)c(C(F)(F)F)cc2C(CO2)=NNC2=O)ccc1F Chemical compound Oc1cc(-c(cc2)c(C(F)(F)F)cc2C(CO2)=NNC2=O)ccc1F QYEIFDMKGKWJNH-UHFFFAOYSA-N 0.000 description 1
- JAQMNYDOINQFGV-UHFFFAOYSA-N Oc1cc(-c(ccc(C(CO2)=NNC2=O)c2)c2F)ccc1 Chemical compound Oc1cc(-c(ccc(C(CO2)=NNC2=O)c2)c2F)ccc1 JAQMNYDOINQFGV-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D273/00—Heterocyclic compounds containing rings having nitrogen and oxygen atoms as the only ring hetero atoms, not provided for by groups C07D261/00 - C07D271/00
- C07D273/02—Heterocyclic compounds containing rings having nitrogen and oxygen atoms as the only ring hetero atoms, not provided for by groups C07D261/00 - C07D271/00 having two nitrogen atoms and only one oxygen atom
- C07D273/04—Six-membered rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines having two or more nitrogen atoms in the same ring, e.g. oxadiazines
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- 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
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/10—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing aromatic 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
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms 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
- C07D417/02—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
- C07D417/10—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 carbon chain containing aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/10—Spiro-condensed systems
- C07D491/107—Spiro-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/10—Spiro-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Catalysts (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201762541627P | 2017-08-04 | 2017-08-04 | |
| US62/541,627 | 2017-08-04 | ||
| PCT/EP2018/071039 WO2019025562A1 (en) | 2017-08-04 | 2018-08-02 | DIHYDROOXADIAZINONES |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR20200036914A true KR20200036914A (ko) | 2020-04-07 |
Family
ID=63207725
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020207005998A Withdrawn KR20200036914A (ko) | 2017-08-04 | 2018-08-02 | 디히드로옥사디아지논 |
Country Status (26)
| Country | Link |
|---|---|
| US (3) | US11427553B2 (enExample) |
| EP (1) | EP3661517B1 (enExample) |
| JP (2) | JP7676141B2 (enExample) |
| KR (1) | KR20200036914A (enExample) |
| CN (1) | CN111212647B (enExample) |
| AR (1) | AR112402A1 (enExample) |
| AU (1) | AU2018309356B2 (enExample) |
| BR (1) | BR112020002351A2 (enExample) |
| CA (1) | CA3071800A1 (enExample) |
| CL (1) | CL2020000303A1 (enExample) |
| CO (1) | CO2020001242A2 (enExample) |
| CR (1) | CR20200057A (enExample) |
| CU (1) | CU24608B1 (enExample) |
| EA (1) | EA202090448A1 (enExample) |
| EC (1) | ECSP20008441A (enExample) |
| IL (1) | IL272098B2 (enExample) |
| JO (1) | JOP20200024A1 (enExample) |
| MA (1) | MA49750A (enExample) |
| MX (1) | MX2020001404A (enExample) |
| PE (1) | PE20200936A1 (enExample) |
| PH (1) | PH12020500134A1 (enExample) |
| SG (1) | SG11201913775UA (enExample) |
| TW (1) | TWI791581B (enExample) |
| UA (1) | UA125731C2 (enExample) |
| UY (1) | UY37832A (enExample) |
| WO (1) | WO2019025562A1 (enExample) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JOP20200024A1 (ar) | 2017-08-04 | 2020-02-02 | Bayer Ag | مركبات ثنائي هيدروكساديازينون |
| EP3661917B1 (en) | 2017-08-04 | 2022-05-11 | Bayer Aktiengesellschaft | 6-((3-trifluoromethyl)phenyl)-4,5-dihydropyridazin-3(2h)-one derivatives as pde3a and pde3b inhibitors for treating cancer |
| TW202031677A (zh) | 2018-11-01 | 2020-09-01 | 美商博得學院股份有限公司 | Ｐｄｅ３調節劑反應性癌症之鑑定 |
| WO2020157188A1 (en) * | 2019-02-01 | 2020-08-06 | Bayer Aktiengesellschaft | Dihydrooxadiazinones for the treatment of hyperproliferative diseases |
| AU2020215088A1 (en) | 2019-02-01 | 2021-07-22 | Bayer Aktiengesellschaft | 1,2,4-triazin-3(2H)-one compounds for the treatment of hyperproliferative diseases |
| CN117279644A (zh) | 2021-03-03 | 2023-12-22 | 拜耳股份有限公司 | 用于治疗肉瘤的取代的3,6-二氢-2h-1,3,4-噁二嗪-2-酮 |
| EP4289828A1 (en) | 2022-06-10 | 2023-12-13 | Bayer Aktiengesellschaft | Method for the preparation of a 3,6-dihydro-2h-1,3,4-oxadiazin-2-one |
| EP4289829A1 (en) | 2022-06-10 | 2023-12-13 | Bayer Aktiengesellschaft | Crystalline forms of (6s)-5-[4'-fluoro-2-(trifluoromethyl)biphenyl-4-yl]-6-methyl-3,6-dihydro- 2h-1,3,4-oxadiazin-2-one |
| CN120187704A (zh) * | 2022-11-24 | 2025-06-20 | 盛睿泽华医药科技（苏州）有限公司 | 吡啶酮化合物及其制备方法和用途 |
| CN117903077B (zh) * | 2023-01-13 | 2024-09-03 | 上海超阳药业有限公司 | 二氢噁二嗪酮化合物及其应用 |
| CN118420559B (zh) * | 2023-04-27 | 2025-02-14 | 上海超阳药业有限公司 | 氘代噁二嗪酮化合物及其用途 |
| CN118047833B (zh) * | 2024-01-31 | 2025-03-14 | 海南大学 | 含二茂铁的取代氨基乙酰胺类化合物及其制备方法和应用 |
Family Cites Families (42)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4097671A (en) * | 1975-08-28 | 1978-06-27 | General Electric Company | Dihydrooxadiazinones and method for making |
| US4052395A (en) | 1975-09-11 | 1977-10-04 | Sankyo Company Limited | Agricultural fungicidal compositions containing 6-(substituted phenyl)-pyridazinones and said pyridazinones |
| US4258094A (en) * | 1979-04-26 | 1981-03-24 | Brunswick Corporation | Melt bonded fabrics and a method for their production |
| US4334030A (en) | 1979-11-23 | 1982-06-08 | General Electric Company | Thermoplastic foamable blends |
| DE3172252D1 (en) | 1980-11-14 | 1985-10-17 | Ici Plc | Heterocyclic compounds |
| DE3263497D1 (en) | 1981-03-04 | 1985-06-20 | Ciba Geigy Ag | Pyridazinones, method for their preparation, pharmaceutical compositions containing these compounds and their use |
| ZA827641B (en) | 1981-11-12 | 1983-09-28 | Ici Plc | Thiadiazine, oxadiazine and triazine derivatives which possess cardiotonic and/or antihypertensive activity |
| US4495185A (en) | 1981-11-12 | 1985-01-22 | Imperial Chemical Industries, Plc | 1,2,4-Triazin-3(2H) ones |
| US4581356A (en) | 1983-03-22 | 1986-04-08 | Fujisawa Pharmaceutical Co., Ltd. | Triazine derivatives, and pharmaceutical compositions comprising the same |
| GB8310435D0 (en) | 1983-04-18 | 1983-05-25 | Fujisawa Pharmaceutical Co | Triazine derivatives |
| JPS59196874A (ja) | 1983-04-22 | 1984-11-08 | Fujisawa Pharmaceut Co Ltd | トリアジン誘導体 |
| JPS6153270A (ja) | 1984-08-17 | 1986-03-17 | チバ・ガイギー・アクチエンゲゼルシヤフト | 置換ピリダジノン、その製造方法及び該化合物を含む医薬製剤 |
| US4816454A (en) | 1984-09-21 | 1989-03-28 | Cassella Aktiengesellschaft | 4,5-dihydro-3(2H)-pyridazinones and their pharmacological use |
| GB8426804D0 (en) | 1984-10-23 | 1984-11-28 | Ciba Geigy Ag | Pyridazinones preparations |
| DE3677316D1 (de) | 1985-10-17 | 1991-03-07 | Smith Kline French Lab | 4(4-oxo-1,4-dihydropyridin-1-yl)phenyl-derivate. |
| EP0303418A3 (en) | 1987-08-11 | 1990-11-07 | Smithkline Beecham Laboratoires Pharmaceutiques | Substituted indolones, useful in the treatment of heart or asthmatic diseases |
| ATE180475T1 (de) | 1990-09-21 | 1999-06-15 | Rohm & Haas | Dihydropyridazinone und pyridazinone als fungizide |
| JPH0676325B2 (ja) * | 1992-05-08 | 1994-09-28 | 三井東圧化学株式会社 | オキサジアジン誘導体を有効成分として含有する抗血栓剤 |
| JPH07508987A (ja) | 1992-07-01 | 1995-10-05 | オーソ・フアーマシユーチカル・コーポレーシヨン | １−アリールスルホニル，アリールカルボニルおよび１−アリールホスホニル−３−フェニル−１，４，５，６−テトラヒドロピリダジン |
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