ZA200405249B - Substituted benzoxazoles and analogues as estrogenic agents - Google Patents
Substituted benzoxazoles and analogues as estrogenic agents Download PDFInfo
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- ZA200405249B ZA200405249B ZA200405249A ZA200405249A ZA200405249B ZA 200405249 B ZA200405249 B ZA 200405249B ZA 200405249 A ZA200405249 A ZA 200405249A ZA 200405249 A ZA200405249 A ZA 200405249A ZA 200405249 B ZA200405249 B ZA 200405249B
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- hydroxyphenyl
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- 239000008188 pellet Substances 0.000 description 1
- 238000002823 phage display Methods 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 230000026731 phosphorylation Effects 0.000 description 1
- 238000006366 phosphorylation reaction Methods 0.000 description 1
- 230000035479 physiological effects, processes and functions Effects 0.000 description 1
- 230000004983 pleiotropic effect Effects 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 230000003389 potentiating effect Effects 0.000 description 1
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- PBMFSQRYOILNGV-UHFFFAOYSA-N pyridazine Chemical compound C1=CC=NN=C1 PBMFSQRYOILNGV-UHFFFAOYSA-N 0.000 description 1
- GZUITABIAKMVPG-UHFFFAOYSA-N raloxifene Chemical compound C1=CC(O)=CC=C1C1=C(C(=O)C=2C=CC(OCCN3CCCCC3)=CC=2)C2=CC=C(O)C=C2S1 GZUITABIAKMVPG-UHFFFAOYSA-N 0.000 description 1
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- BCNZYOJHNLTNEZ-UHFFFAOYSA-N tert-butyldimethylsilyl chloride Chemical compound CC(C)(C)[Si](C)(C)Cl BCNZYOJHNLTNEZ-UHFFFAOYSA-N 0.000 description 1
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- FPGGTKZVZWFYPV-UHFFFAOYSA-M tetrabutylammonium fluoride Chemical compound [F-].CCCC[N+](CCCC)(CCCC)CCCC FPGGTKZVZWFYPV-UHFFFAOYSA-M 0.000 description 1
- 150000003536 tetrazoles Chemical class 0.000 description 1
- 230000002103 transcriptional effect Effects 0.000 description 1
- 230000002463 transducing effect Effects 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- SANWDQJIWZEKOD-UHFFFAOYSA-N tributyl(furan-2-yl)stannane Chemical compound CCCC[Sn](CCCC)(CCCC)C1=CC=CO1 SANWDQJIWZEKOD-UHFFFAOYSA-N 0.000 description 1
- YLGRTLMDMVAFNI-UHFFFAOYSA-N tributyl(prop-2-enyl)stannane Chemical compound CCCC[Sn](CCCC)(CCCC)CC=C YLGRTLMDMVAFNI-UHFFFAOYSA-N 0.000 description 1
- 230000001228 trophic effect Effects 0.000 description 1
- 241000701161 unidentified adenovirus Species 0.000 description 1
- JFALSRSLKYAFGM-UHFFFAOYSA-N uranium(0) Chemical compound [U] JFALSRSLKYAFGM-UHFFFAOYSA-N 0.000 description 1
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- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 230000005186 women's health Effects 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
- GTLDTDOJJJZVBW-UHFFFAOYSA-N zinc cyanide Chemical compound [Zn+2].N#[C-].N#[C-] GTLDTDOJJJZVBW-UHFFFAOYSA-N 0.000 description 1
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical class [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 1
Classifications
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- 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
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- 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
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Landscapes
- Health & Medical Sciences (AREA)
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Applications Claiming Priority (1)
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| US33666301P | 2001-12-05 | 2001-12-05 |
Publications (1)
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| ZA200405249B true ZA200405249B (en) | 2007-01-31 |
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| JP (2) | JP4689960B2 (uk) |
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| CN (2) | CN101423500A (uk) |
| AR (1) | AR037745A1 (uk) |
| AU (2) | AU2002353014A1 (uk) |
| BR (1) | BR0214767A (uk) |
| CA (1) | CA2467517C (uk) |
| CO (1) | CO5580830A2 (uk) |
| EC (1) | ECSP045133A (uk) |
| HU (1) | HUP0500010A2 (uk) |
| IL (1) | IL162256A0 (uk) |
| IN (1) | IN2005KO00272A (uk) |
| MX (1) | MXPA04005306A (uk) |
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| UA (1) | UA83620C2 (uk) |
| WO (1) | WO2003050095A1 (uk) |
| ZA (1) | ZA200405249B (uk) |
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| JP4381810B2 (ja) | 2001-11-19 | 2009-12-09 | イーライ リリー アンド カンパニー | 選択的エストロゲン受容体βアゴニストとしての置換ベンゾピラン |
| UA83620C2 (uk) | 2001-12-05 | 2008-08-11 | Уайт | Заміщені бензоксазоли та їх аналоги як естрогенні агенти |
| US20040002524A1 (en) * | 2002-06-24 | 2004-01-01 | Richard Chesworth | Benzimidazole compounds and their use as estrogen agonists/antagonists |
| TW200409759A (en) * | 2002-09-25 | 2004-06-16 | Wyeth Corp | Substituted 4-(indazol-3-yl)phenols |
| CA2510455C (en) | 2002-12-19 | 2013-03-12 | The Scripps Research Institute | Compositions and methods for stabilizing transthyretin and inhibiting transthyretin misfolding |
| DE602004016150D1 (de) * | 2003-04-21 | 2008-10-09 | Lilly Co Eli | Substituierte benzopyrane als selektive antagonisten am östrogenrezeptor-beta |
| TW200500065A (en) * | 2003-05-21 | 2005-01-01 | Wyeth Corp | Antiarthritic combinations |
| EP2314584A1 (en) * | 2004-05-20 | 2011-04-27 | Foldrx Pharmaceuticals, Inc. | 2-(heteroaryl)-benzoxazole compounds and derivatives, compositions and methods for stabilizing transthyretin and inhibiting transthyretin misfolding |
| WO2006007503A1 (en) * | 2004-07-01 | 2006-01-19 | Wyeth | Tetracyclic compounds as estrogen ligands |
| TW200612925A (en) * | 2004-08-26 | 2006-05-01 | Wyeth Corp | Prodrug substituted benzoxazoles as estrogenic agents |
| AR050719A1 (es) * | 2004-09-02 | 2006-11-15 | Wyeth Corp | Carbonilfenoles de fenantridina que actuan como ligandos del receptor de estrogeno |
| JP2008512458A (ja) | 2004-09-07 | 2008-04-24 | ワイス | ６Ｈ−［１］ベンゾピラノ［４，３−ｂ］キノリン及びエストロゲン様物質としてのそれらの使用 |
| AU2005312031A1 (en) * | 2004-12-02 | 2006-06-08 | Wyeth | Formulations of substituted benzoxazoles |
| RU2007120253A (ru) * | 2004-12-02 | 2009-01-10 | Вайет (Us) | Составы, содержащие замещенные бензоксазолы |
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| CN101321524A (zh) * | 2004-12-17 | 2008-12-10 | 惠氏公司 | 雌激素β激动剂的新用途 |
| US8093302B2 (en) * | 2005-02-15 | 2012-01-10 | Eli Lilly And Company | Substituted tetralins as selective estrogen receptor-β agonists |
| BRPI0608154A2 (pt) * | 2005-02-16 | 2016-10-11 | Wyeth Corp | métodos de tratar ou inibir mucosite, cistite por radiação em um indivíduo, e de tratar pelo menos um sintoma de exposição de um indivíduo a um agente citotóxico ou à radiação, e, composição farmacêutica |
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