JP2005526812A5 - ステロイドスルファターゼのインヒビターとしてのピペラジニル−またはピペリジニルアミンスルファミン酸アミド - Google Patents
ステロイドスルファターゼのインヒビターとしてのピペラジニル−またはピペリジニルアミンスルファミン酸アミド Download PDFInfo
- Publication number
- JP2005526812A5 JP2005526812A5 JP2003580309A JP2003580309A JP2005526812A5 JP 2005526812 A5 JP2005526812 A5 JP 2005526812A5 JP 2003580309 A JP2003580309 A JP 2003580309A JP 2003580309 A JP2003580309 A JP 2003580309A JP 2005526812 A5 JP2005526812 A5 JP 2005526812A5
- Authority
- JP
- Japan
- Prior art keywords
- piperidinylamine
- piperazinyl
- inhibitors
- acid amides
- sulfamic acid
- 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
- 102000009134 Steryl-Sulfatase Human genes 0.000 title 1
- 108010087999 Steryl-Sulfatase Proteins 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
- 230000002401 inhibitory effect Effects 0.000 title 1
- JUTQLSRBKSVCLI-UHFFFAOYSA-N piperidin-1-amine;sulfamide Chemical class NS(N)(=O)=O.NN1CCCCC1 JUTQLSRBKSVCLI-UHFFFAOYSA-N 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- 229910052731 fluorine Inorganic materials 0.000 description 2
- 239000011737 fluorine Substances 0.000 description 2
- YCKRFDGAMUMZLT-UHFFFAOYSA-N fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 2
- 125000004453 alkoxycarbonyl group Chemical group 0.000 description 1
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 125000000286 phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
Description
（Ｃ１−６）アルコキシカルボニルは、非置換または置換（Ｃ１−６）アルコキシカルボニル、たとえば、当該アルキル基が（Ｃ６−１８）アリール、たとえばフェニルで置換されたアルコキシカルボニル、たとえばベンジルオキシカルボニルを含む。ハロゲンは、フッ素、塩素、臭素、ヨウ素、たとえばフッ素、塩素を含む。
（Ｃ６−１８）アリール（Ｃ１−４）アルキルは、好ましくはフェニル（Ｃ１−４）アルキル、たとえばフェニルエチルであり、ここで、当該フェニルは、置換（Ｃ６−１８）アリールに関して記載したように置換されている。
（Ｃ６−１８）アリール（Ｃ１−４）アルキルは、好ましくはフェニル（Ｃ１−４）アルキル、たとえばフェニルエチルであり、ここで、当該フェニルは、置換（Ｃ６−１８）アリールに関して記載したように置換されている。
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB0207500A GB0207500D0 (en) | 2002-03-28 | 2002-03-28 | Organic compounds |
| GB0225679A GB0225679D0 (en) | 2002-11-04 | 2002-11-04 | Organic compounds |
| PCT/EP2003/003214 WO2003082842A1 (en) | 2002-03-28 | 2003-03-27 | Piperazinyl- or piperidinylamine-sulfamic acid amides as inhibitors of steroid sulfatase |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2005526812A JP2005526812A (ja) | 2005-09-08 |
| JP2005526812A5 true JP2005526812A5 (ja) | 2006-05-18 |
| JP4580652B2 JP4580652B2 (ja) | 2010-11-17 |
Family
ID=28676499
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2003580309A Expired - Fee Related JP4580652B2 (ja) | 2002-03-28 | 2003-03-27 | ステロイドスルファターゼのインヒビターとしてのピペラジニル−またはピペリジニルアミンスルファミン酸アミド |
Country Status (20)
| Country | Link |
|---|---|
| US (2) | US7439362B2 (ja) |
| EP (1) | EP1492782A1 (ja) |
| JP (1) | JP4580652B2 (ja) |
| KR (1) | KR20040094877A (ja) |
| CN (1) | CN1293065C (ja) |
| AR (1) | AR039156A1 (ja) |
| AU (1) | AU2003226732B2 (ja) |
| BR (1) | BR0308795A (ja) |
| CA (1) | CA2480686A1 (ja) |
| CO (1) | CO5640113A2 (ja) |
| IL (1) | IL164267A0 (ja) |
| MX (1) | MXPA04009453A (ja) |
| MY (1) | MY136880A (ja) |
| NO (1) | NO20044321L (ja) |
| NZ (1) | NZ535617A (ja) |
| PE (1) | PE20040167A1 (ja) |
| PL (1) | PL372602A1 (ja) |
| RU (1) | RU2329258C2 (ja) |
| TW (1) | TW200306806A (ja) |
| WO (1) | WO2003082842A1 (ja) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB0505541D0 (en) * | 2005-03-17 | 2005-04-27 | Novartis Ag | Organic compounds |
| GB0505539D0 (en) * | 2005-03-17 | 2005-04-27 | Novartis Ag | Organic compounds |
| GB0511190D0 (en) * | 2005-06-01 | 2005-07-06 | Sterix Ltd | Use |
| JP5543920B2 (ja) | 2007-09-17 | 2014-07-09 | プレグレム エスアー | 閉経前の女性におけるエストロゲン依存症状の治療 |
| US10874746B2 (en) | 2016-02-08 | 2020-12-29 | Synaffix B.V. | Sulfamide linkers for use in bioconjugates |
| US11590239B2 (en) | 2016-02-08 | 2023-02-28 | Synaffix B.V. | Antibody-conjugates with improved therapeutic index for targeting CD30 tumours and method for improving therapeutic index of antibody-conjugates |
| WO2017137456A1 (en) * | 2016-02-08 | 2017-08-17 | Synaffix B.V. | Bioconjugates containing sulfamide linkers for use in treatment |
| AU2017367086A1 (en) * | 2016-11-29 | 2019-07-18 | Epizyme, Inc. | Compounds containing a sulfonic group as KAT inhibitors |
| US20220267300A1 (en) * | 2019-06-12 | 2022-08-25 | NodThera Limited | Sulfonamide derivatives and uses thereof |
| CN110590896B (zh) * | 2019-11-04 | 2022-08-30 | 上海高准医药有限公司 | 雌酚酮硫酸酯哌嗪的制备方法 |
Family Cites Families (33)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US89089A (en) * | 1869-04-20 | Improved car-coupling | ||
| US51547A (en) * | 1865-12-19 | Improvement in guide and tuck-marker for sewing-machines | ||
| US71516A (en) * | 1867-11-26 | William b | ||
| US183459A (en) * | 1876-10-17 | Improvement in hinges | ||
| US478328A (en) * | 1892-07-05 | Glass-heating oven | ||
| US876846A (en) * | 1907-05-28 | 1908-01-14 | Stephen W Smith | Road-machine. |
| US1122242A (en) * | 1912-05-13 | 1914-12-29 | Sanitary Can Company | Can-body-feeding device. |
| US2103610A (en) * | 1935-04-30 | 1937-12-28 | Sofal Ltd | Alloy steels |
| DE876846C (de) * | 1943-06-01 | 1953-05-18 | Bayer Ag | Verfahren zur Herstellung von Abkoemmlingen des Sulfondiamids |
| US3004487A (en) * | 1959-12-07 | 1961-10-17 | Bank Of America Nat Trust & Savings Ass | Imprinters |
| GB1593609A (en) * | 1978-01-31 | 1981-07-22 | Christiaens Sa A | Pyridine sulfonamides |
| FR2510106A1 (fr) | 1981-07-27 | 1983-01-28 | Rhone Poulenc Agrochimie | Composes herbicides derives d'acides phenoxybenzoiques, et leurs procedes de preparation et d'utilisation |
| DK101683A (da) | 1982-03-12 | 1983-09-13 | Duphar Int Res | Phenylpiperazinderivater og fremgangsmaade til fremstilling heraf |
| US5238923A (en) * | 1989-05-26 | 1993-08-24 | Warner-Lambert Company | Amino-substituted heterocycles as renin inhibitors |
| US5256632A (en) * | 1990-05-30 | 1993-10-26 | Bayer Aktiengesellschaft | Herbicidal sulphonylated carboxamides |
| IL99537A (en) | 1990-09-27 | 1995-11-27 | Merck & Co Inc | Fibrinogen receptor antagonists and pharmaceutical preparations containing them |
| FR2716883B1 (fr) * | 1994-03-04 | 1996-04-26 | Roussel Uclaf | Nouveaux dérivés tétrasubstitués de l'imidazole, leur préparation, nouveaux intermédiaires obtenus, leur application à titre de médicaments, compositions pharmaceutiques les renfermant. |
| FR2716882B1 (fr) * | 1994-03-04 | 1996-04-05 | Roussel Uclaf | Utilisation de dérivés de l'imidazole au traitement d'affections impliquant les récepteurs AT1 et AT2 de l'Angiotensine, certains de ces produits, leur préparation, compositions pharmaceutiques. |
| US5464788A (en) | 1994-03-24 | 1995-11-07 | Merck & Co., Inc. | Tocolytic oxytocin receptor antagonists |
| US5783582A (en) | 1994-07-20 | 1998-07-21 | Merck & Co., Inc. | Piperidines and hexahydro-1H-azepines spiro substituted at the 4-position promote release of growth hormone |
| JPH10510512A (ja) | 1994-10-04 | 1998-10-13 | 藤沢薬品工業株式会社 | 尿素誘導体とａｃａｔ阻害剤としての用途 |
| WO1997020820A1 (en) | 1995-12-01 | 1997-06-12 | Novartis Ag | Heteroaryl compounds |
| DE19621482A1 (de) * | 1996-05-29 | 1997-12-04 | Hoechst Ag | Substituierte 1-Naphthoylguanidine, Verfahren zu ihrer Herstellung, ihre Verwendung als Medikament oder Diagnostikum sowie sie enthaltendes Medikament |
| DE19621483A1 (de) * | 1996-05-29 | 1997-12-04 | Hoechst Ag | Substituierte 2-Naphthoylguanidine, Verfahren zur ihrer Herstellung, ihre Verwendung als Medikament oder Diagnostikum sowie sie enthaltendes Medikament |
| NZ500353A (en) | 1997-04-14 | 2002-02-01 | Cor Therapeutics Inc | Cyclic diaza compounds that are selective inhibitors of factor Xa |
| CN1129581C (zh) | 1998-09-22 | 2003-12-03 | 山之内制药株式会社 | 氰基苯基衍生物 |
| EP1165013A4 (en) | 1999-03-03 | 2002-08-07 | Merck & Co Inc | PRENYL PROTEIN TRANSFERASE INHIBITORS |
| WO2000071515A2 (en) | 1999-05-24 | 2000-11-30 | Cor Therapeutics, Inc | INHIBITORS OF FACTOR Xa |
| JP4320089B2 (ja) * | 1999-07-06 | 2009-08-26 | あすか製薬株式会社 | フェニルスルファメート誘導体 |
| US6632815B2 (en) * | 1999-09-17 | 2003-10-14 | Millennium Pharmaceuticals, Inc. | Inhibitors of factor Xa |
| EP1226127B1 (en) | 2000-05-04 | 2009-07-01 | Basf Se | Substituted phenyl sulfamoyl carboxamides |
| US7067507B2 (en) * | 2001-06-12 | 2006-06-27 | Pharmacia & Upjohn Company | Macrocycles useful in the treatment of Alzheimer's disease |
| ES2258642T3 (es) | 2001-07-02 | 2006-09-01 | Astrazeneca Ab | Derivados de piperidina utiles como moduladores de la actividad del receptor de quimiocina. |
-
2003
- 2003-03-26 PE PE2003000308A patent/PE20040167A1/es not_active Application Discontinuation
- 2003-03-26 AR ARP030101062A patent/AR039156A1/es unknown
- 2003-03-27 CA CA002480686A patent/CA2480686A1/en not_active Abandoned
- 2003-03-27 US US10/509,259 patent/US7439362B2/en not_active Expired - Fee Related
- 2003-03-27 JP JP2003580309A patent/JP4580652B2/ja not_active Expired - Fee Related
- 2003-03-27 PL PL03372602A patent/PL372602A1/xx unknown
- 2003-03-27 TW TW092106942A patent/TW200306806A/zh unknown
- 2003-03-27 IL IL16426703A patent/IL164267A0/xx unknown
- 2003-03-27 EP EP03745281A patent/EP1492782A1/en not_active Withdrawn
- 2003-03-27 WO PCT/EP2003/003214 patent/WO2003082842A1/en active Application Filing
- 2003-03-27 BR BR0308795-6A patent/BR0308795A/pt not_active IP Right Cessation
- 2003-03-27 MX MXPA04009453A patent/MXPA04009453A/es active IP Right Grant
- 2003-03-27 AU AU2003226732A patent/AU2003226732B2/en not_active Ceased
- 2003-03-27 CN CNB038083361A patent/CN1293065C/zh not_active Expired - Fee Related
- 2003-03-27 NZ NZ535617A patent/NZ535617A/en unknown
- 2003-03-27 KR KR10-2004-7015312A patent/KR20040094877A/ko not_active Application Discontinuation
- 2003-03-27 RU RU2004131822/04A patent/RU2329258C2/ru not_active IP Right Cessation
- 2003-03-28 MY MYPI20031151A patent/MY136880A/en unknown
-
2004
- 2004-09-28 CO CO04096497A patent/CO5640113A2/es unknown
- 2004-10-12 NO NO20044321A patent/NO20044321L/no not_active Application Discontinuation
-
2008
- 2008-09-16 US US12/211,525 patent/US20090042899A1/en not_active Abandoned
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