AU779230C - Curcumin analogues for treating cancer - Google Patents
Curcumin analogues for treating cancerInfo
- Publication number
- AU779230C AU779230C AU19428/01A AU1942801A AU779230C AU 779230 C AU779230 C AU 779230C AU 19428/01 A AU19428/01 A AU 19428/01A AU 1942801 A AU1942801 A AU 1942801A AU 779230 C AU779230 C AU 779230C
- Authority
- AU
- Australia
- Prior art keywords
- substituted
- mmol
- compound
- alkyl
- compounds
- 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.)
- Ceased
Links
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- 125000002252 acyl group Chemical group 0.000 claims description 7
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- 125000000753 cycloalkyl group Chemical group 0.000 claims description 7
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- 229910052757 nitrogen Inorganic materials 0.000 claims description 7
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Classifications
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- C07D295/20—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carbonic acid, or sulfur or nitrogen analogues thereof
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- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/30—Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
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- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen 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
- C07D213/62—Oxygen or sulfur atoms
- C07D213/63—One oxygen atom
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- C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
- C07D317/44—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D317/46—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems condensed with one six-membered ring
- C07D317/48—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring
- C07D317/50—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to atoms of the carbocyclic ring
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- C07D451/00—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof
- C07D451/02—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof
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Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US16891399P | 1999-12-03 | 1999-12-03 | |
| US60/168913 | 1999-12-03 | ||
| PCT/US2000/032870 WO2001040188A1 (en) | 1999-12-03 | 2000-12-04 | Curcumin analogues for treating cancer |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2005203131A Division AU2005203131A1 (en) | 1999-12-03 | 2005-07-19 | Curcumin analogues for treating cancer |
Publications (3)
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| AU1942801A AU1942801A (en) | 2001-06-12 |
| AU779230B2 AU779230B2 (en) | 2005-01-13 |
| AU779230C true AU779230C (en) | 2006-05-25 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU19428/01A Ceased AU779230C (en) | 1999-12-03 | 2000-12-04 | Curcumin analogues for treating cancer |
Country Status (6)
| Country | Link |
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| US (3) | US6664272B2 (https=) |
| EP (1) | EP1242379A1 (https=) |
| JP (1) | JP2003515590A (https=) |
| AU (1) | AU779230C (https=) |
| CA (1) | CA2393440A1 (https=) |
| WO (1) | WO2001040188A1 (https=) |
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| US20040266883A1 (en) * | 1999-10-27 | 2004-12-30 | Yale University | Conductance of improperly folded proteins through the secretory pathway and related methods for treating disease |
| US20030236300A1 (en) * | 1999-10-27 | 2003-12-25 | Yale University | Conductance of improperly folded proteins through the secretory pathway and related methods for treating disease |
| US20030149113A1 (en) * | 2001-10-12 | 2003-08-07 | Caplan Michael J. | Conductance of improperly folded proteins through the secretory pathway and related methods for treating disease |
| NL1019782C2 (nl) * | 2002-01-18 | 2003-07-21 | Tno | Optische leesinrichting. |
| US20090011991A1 (en) * | 2002-03-08 | 2009-01-08 | Emory University | Novel Curcuminoid-Factor VIIA Constructs as Suppressors of Tumor Growth and Angiogenesis |
| US20050069551A1 (en) * | 2002-03-08 | 2005-03-31 | Emory University | Cytotoxic compound-protein conjugates as suppressors of tumor growth and angiogenesis |
| JP2005529080A (ja) * | 2002-03-08 | 2005-09-29 | エモリー ユニバーシティ | 腫瘍の増殖および脈管形成のサプレッサとしての新規のクルクミノイド−第VIIa因子構築物 |
| US6790979B2 (en) | 2002-04-17 | 2004-09-14 | University Of North Carolina At Chapel Hill | Curcumin analogues and uses thereof |
| US7355081B2 (en) | 2002-04-17 | 2008-04-08 | The University Of North Carolina At Chapel Hill | Curcumin analogues and uses thereof |
| JP2005529123A (ja) * | 2002-04-24 | 2005-09-29 | リサーチ ディベロップメント ファンデーション | 核転写調節因子NF−κB抑制剤と抗腫瘍薬の相乗効果 |
| CA2489947A1 (en) * | 2002-06-24 | 2003-12-31 | Research Development Foundation | Treatment of human multiple myeloma by curcumin |
| BRPI0207141B8 (pt) * | 2002-11-28 | 2021-05-25 | Acad Paulista Anchieta Ltda | processo para preparar compostos, uso de compostos, composição farmacêutica e método para tratamento de câncer |
| DE60226181T2 (de) * | 2002-12-20 | 2009-05-07 | Dabur Research Foundation | Cyclopentenon-derivate für krebs-therapie |
| KR100907479B1 (ko) * | 2002-12-31 | 2009-07-13 | 삼성전자주식회사 | 컬러 필터 기판과 이를 갖는 액정 표시 장치 |
| GB0302512D0 (en) * | 2003-02-03 | 2003-03-05 | Arrow Therapeutics Ltd | Compounds |
| US7968115B2 (en) | 2004-03-05 | 2011-06-28 | Board Of Regents, The University Of Texas System | Liposomal curcumin for treatment of cancer |
| WO2005025623A2 (en) * | 2003-07-28 | 2005-03-24 | Emory University | Ef-24-factor vii conjugates |
| US20050181036A1 (en) * | 2003-08-26 | 2005-08-18 | Research Development Foundation | Aerosol delivery of curcumin |
| US20050049299A1 (en) * | 2003-08-26 | 2005-03-03 | Aggarwal Bharat B. | Selective inhibitors of stat-3 activation and uses thereof |
| US7462646B2 (en) | 2003-08-26 | 2008-12-09 | Research Development Foundation | Osteoclastogenesis inhibitors and uses thereof |
| US8841326B2 (en) | 2004-02-12 | 2014-09-23 | Stc.Unm | Therapeutic curcumin derivatives |
| US8784881B2 (en) * | 2004-03-05 | 2014-07-22 | Board Of Regents, The University Of Texas System | Liposomal curcumin for treatment of diseases |
| US20080103213A1 (en) * | 2004-03-05 | 2008-05-01 | Board Of Regents, The University Of Texas System | Liposomal curcumin for treatment of neurofibromatosis |
| JP2005289817A (ja) * | 2004-03-09 | 2005-10-20 | Daicho Kikaku:Kk | 抗癌剤 |
| WO2005113069A2 (en) * | 2004-05-14 | 2005-12-01 | Research Development Foundation | Use of circumin and analogues as inhibitors of acc2 |
| US8058313B2 (en) | 2004-06-24 | 2011-11-15 | Temple University—Of the Commonwealth System of Higher Education | Alpha, beta-unsaturated sulfones, sulfoxides, sulfonimides, sulfinimides, acylsulfonamides and acylsulfinamides and therapeutic uses thereof |
| US8377918B2 (en) * | 2005-01-31 | 2013-02-19 | ACC Therapeutics Inc | Apigenin for chemoprevention, and chemotherapy combined with therapeutic reagents |
| US20070010488A1 (en) * | 2005-04-13 | 2007-01-11 | Khairia Youssef | Compounds for modulating cell proliferation |
| JP5050206B2 (ja) * | 2005-06-27 | 2012-10-17 | 国立大学法人東北大学 | ビス(アリールメチリデン)アセトン化合物、抗癌剤、発癌予防剤、Ki−Ras、ErbB2、c−Myc及びCyclinD1の発現抑制剤、β−カテニン分解剤並びにp53の発現増強剤 |
| US7582655B2 (en) * | 2005-11-22 | 2009-09-01 | University Of Saskatchewan | Antineoplastic compounds |
| US20070270464A1 (en) * | 2006-02-24 | 2007-11-22 | Emory University | Prodrugs of curcumin analogs |
| CA2670837C (en) * | 2006-12-18 | 2016-03-29 | Jack Arbiser | Novel palladium complexes inhibit n-myristoyltransferase activity in vitro and cancer growth in vivo |
| JP2010524959A (ja) * | 2007-04-17 | 2010-07-22 | コドマン・アンド・シャートレフ・インコーポレイテッド | アルツハイマー病を処置するためのヘリウムガスボーラス中のクルクミンの鼻腔投与 |
| US8383865B2 (en) | 2007-04-17 | 2013-02-26 | Codman & Shurtleff, Inc. | Curcumin derivatives |
| WO2008150899A1 (en) * | 2007-05-29 | 2008-12-11 | Emory University | Combination therapies for treatment of cancer and inflammatory diseases |
| US20100197584A1 (en) * | 2007-07-27 | 2010-08-05 | Research Foundations of the City University of- New York | Use of curcumin to block brain tumor formation in mice |
| US7745670B2 (en) * | 2008-06-27 | 2010-06-29 | Codman & Shurtleff, Inc. | Curcumin-Resveratrol hybrid molecule |
| EP2285989B1 (en) * | 2008-05-15 | 2016-11-16 | The University of North Carolina At Chapel Hill | Novel targets for regulation of angiogenesis |
| CN101434525B (zh) * | 2008-06-05 | 2012-07-04 | 福建医科大学 | 4-(4-羟基-3-甲氧基苯甲基)姜黄素及其用于制备抗肿瘤药物的应用 |
| US7985776B2 (en) | 2008-06-27 | 2011-07-26 | Codman & Shurtleff, Inc. | Iontophoretic delivery of curcumin and curcumin analogs for the treatment of Alzheimer's Disease |
| WO2010017094A2 (en) * | 2008-07-31 | 2010-02-11 | The General Hospital Corporation | CURCUMIN DERIVATIVES FOR AMYLOID-β PLAQUE IMAGING |
| WO2010045395A2 (en) * | 2008-10-14 | 2010-04-22 | Danyang Chen | Curcumin analog compositions and related methods |
| CN101434600B (zh) * | 2008-12-25 | 2014-08-06 | 福建医科大学 | 姜黄素哌啶酮结构类似物及其用于制备抗肿瘤药物的应用 |
| KR101011028B1 (ko) * | 2009-01-19 | 2011-01-26 | 주식회사 알앤엘바이오 | 차가버섯 추출물, 영지버섯 추출물 및 상황버섯 추출물을 함유하는 조혈모세포 증식 촉진용 조성물 |
| US7723515B1 (en) * | 2009-01-26 | 2010-05-25 | Codman & Shurtleff, Inc. | Methylene blue—curcumin analog for the treatment of alzheimer's disease |
| US20100286585A1 (en) | 2009-01-26 | 2010-11-11 | Codman & Shurtleff, Inc. | Shunt Delivery of Curcumin |
| US8247435B2 (en) * | 2009-02-19 | 2012-08-21 | Thornthwaite Jerry T | Formulations for treating human and animal diseases |
| BRPI0902039B8 (pt) | 2009-06-09 | 2021-05-25 | Anhanguera Educacional Ltda | composição farmacêutica e uso de composição farmacêutica para o tratamento, profilaxia ou prevenção de doenças neoplásicas em humanos e animais |
| US8722707B1 (en) | 2009-07-06 | 2014-05-13 | The Ohio State University | Compositions and methods for inhibition of smooth muscle cell proliferation and neointimal hyperplasia |
| US20120316203A1 (en) * | 2009-07-06 | 2012-12-13 | The Ohio State University Research Foundation | Compositions and Methods for Inhibition of Cancers |
| US9359196B2 (en) | 2009-09-10 | 2016-06-07 | The Board Of Regents Of The University Of Oklahoma | Antiproliferative compositions comprising curcumin analogs and methods of producing and using same |
| US8410177B2 (en) * | 2009-12-30 | 2013-04-02 | Indian Institute Of Technology Bombay | Curcumin derivatives |
| US20140303109A1 (en) * | 2010-03-25 | 2014-10-09 | Fazlul H. Sarkar | Novel Analogs of Curcumin and Methods of Use |
| WO2012021692A1 (en) * | 2010-08-11 | 2012-02-16 | Rutgers, The State University Of New Jersey | Curcumin analogs and methods of use thereof |
| CA2807776C (en) | 2010-08-20 | 2018-10-09 | Charles C-Y Shih | 1,5-diphenyl-penta-1,4-dien-3-one compounds |
| CA2813510A1 (en) | 2010-10-14 | 2012-04-19 | Abbott Gmbh & Co. Kg | Curcuminoid solid dispersion formulation |
| CN102154004A (zh) * | 2011-02-23 | 2011-08-17 | 广东工业大学 | 基于单羰基姜黄素化合物做为可视化pH荧光探针的应用 |
| CN102180849A (zh) * | 2011-03-24 | 2011-09-14 | 广东工业大学 | 一种二芳基二烯环酮衍生物及其制备方法与应用 |
| CN102240288A (zh) * | 2011-05-06 | 2011-11-16 | 上海师范大学 | N-取代-3,5-双苄叉基哌啶-4-酮化合物的应用 |
| CN102293770A (zh) * | 2011-05-25 | 2011-12-28 | 温州医学院 | 新型成纤维细胞生长因子受体酪氨酸激酶抑制剂 |
| CN102477013B (zh) * | 2011-07-28 | 2014-04-02 | 暨南大学 | 一种可抑制人1型11β-羟基类固醇脱氢酶活性的姜黄素类化合物的制备及其应用 |
| PT2780326T (pt) * | 2011-10-19 | 2019-03-04 | Vivolux Ab | Método para inibição da atividade da desubiquitinação |
| CN103086958A (zh) * | 2011-11-04 | 2013-05-08 | 中国科学院上海药物研究所 | NFκB通路激活抑制剂、其制备方法、药物组合物及用途 |
| CN103373983A (zh) * | 2012-04-16 | 2013-10-30 | 南京大学连云港高新技术研究院 | 一类含噻吩或呋喃结构的姜黄素类似物及其制法 |
| US9884825B2 (en) | 2012-08-03 | 2018-02-06 | Georgia State University Research Foundation, Inc. | Curcumin analogs and methods of making and using thereof |
| CN103044224A (zh) * | 2013-01-29 | 2013-04-17 | 牡丹江医学院 | 一种戊-1,4-二烯-3-酮类似物及其制备方法与应用 |
| US9913834B2 (en) | 2013-05-08 | 2018-03-13 | The Johns Hopkins University | Bis-benzylidine piperidone proteasome inhibitor with anticancer activity |
| US9907786B2 (en) | 2014-10-21 | 2018-03-06 | Ions Pharmaceutical S.À R.L. | Therapeutic compositions containing harmine and isovanillin components, and methods of use thereof |
| US10092550B2 (en) | 2014-10-21 | 2018-10-09 | Ions Pharmaceutical S.À R.L. | Therapeutic compositions containing curcumin, harmine, and isovanillin components, and methods of use thereof |
| US20160106687A1 (en) | 2014-10-21 | 2016-04-21 | Life Plus, LLC | Human therapeutic agents |
| WO2016109470A1 (en) * | 2014-12-30 | 2016-07-07 | Baylor College Of Medicine | Small molecule stimulators of steroid receptor coactivator proteins and their use in the treatment of cancer |
| CN105037252B (zh) * | 2015-05-21 | 2018-05-04 | 温州医科大学 | N-取代-3,5-二(2-(三氟甲基)亚苄基)哌啶-4-酮衍生物及其制备方法与应用 |
| US9486444B1 (en) | 2016-03-21 | 2016-11-08 | King Saud University | Anti-cancer compound |
| CN105924436A (zh) * | 2016-05-19 | 2016-09-07 | 中国科学院昆明植物研究所 | 托品酮衍生物及其药物组合物和其制备方法与应用 |
| CN106187967A (zh) * | 2016-07-14 | 2016-12-07 | 温州医科大学 | 一种对称单羰基姜黄素类似物6b及其制备方法和应用 |
| CN108069906A (zh) * | 2016-11-11 | 2018-05-25 | 武汉科技大学 | (1e,4e)-1-(吡唑-4-基)-5-苯基-1,4戊二烯-3-酮衍生物及其制备方法和医药用途 |
| CN106800547B (zh) * | 2017-01-03 | 2019-07-23 | 中国人民解放军第二军医大学 | 一种双取代芳基类化合物及其应用 |
| CN107737124A (zh) * | 2017-01-04 | 2018-02-27 | 温州医科大学 | 一种姜黄素类似物在制备抗肿瘤药物中的应用 |
| US10421786B2 (en) | 2017-06-19 | 2019-09-24 | Emory University | Peptides that target inflamed or distressed cardiac tissue and uses related thereto |
| CN107501219B (zh) * | 2017-08-18 | 2020-09-25 | 温州医科大学 | 不对称姜黄色素类化合物及其在制备抗胃癌药物中的应用 |
| WO2019152536A1 (en) | 2018-01-30 | 2019-08-08 | The Regents Of The University Of California | Inhibitors of the wnt/beta-catenin pathway |
| BR112020018094A2 (pt) | 2018-03-08 | 2020-12-22 | Incyte Corporation | Compostos de aminopirazina diol como inibidores de pi3k-¿ |
| US11046658B2 (en) | 2018-07-02 | 2021-06-29 | Incyte Corporation | Aminopyrazine derivatives as PI3K-γ inhibitors |
| CN120136844A (zh) | 2018-08-29 | 2025-06-13 | 贝勒医学院 | 类固醇受体共激活剂-3的小分子刺激剂以及它们用作心脏保护剂和/或血管再生剂的方法 |
| WO2020165779A1 (en) | 2019-02-15 | 2020-08-20 | Shashvi Remedies (Opc) Private Limited | Synergistic composition with anti-proliferative activity |
| CN110452163A (zh) * | 2019-08-13 | 2019-11-15 | 温州医科大学附属第二医院、温州医科大学附属育英儿童医院 | 一种姜黄素衍生物的制备方法和其抗前列腺癌的应用 |
| CN110615733B (zh) * | 2019-11-07 | 2021-09-03 | 温州医科大学 | 一种姜黄素衍生物的晶型i及其制备方法和应用 |
| US12129265B2 (en) | 2020-07-21 | 2024-10-29 | Ankh Life Sciences Limited | Therapeutic agents and uses thereof |
| AU2022308041A1 (en) | 2021-07-07 | 2024-01-18 | Immix Biopharma, Inc. | Nanoparticles for cancer treatment |
| CA3232657A1 (en) | 2021-09-27 | 2023-03-30 | Ilya RACHMAN | Nanoparticles for cancer treatment |
| CN114671779B (zh) * | 2022-03-15 | 2023-08-22 | 温州医科大学 | 含环戊酮片段的化合物及其作为抗肿瘤药物的应用 |
| WO2024007011A1 (en) | 2022-06-30 | 2024-01-04 | Immix Biopharma, Inc | Nanoparticles for the treatment of inflammatory diseases |
| CZ310480B6 (cs) * | 2023-07-21 | 2025-07-30 | Ústav organické chemie a biochemie AV ČR, v. v. i. | Bis(fenylmethylen)cykloalkanony a jejich heterocyklické analogy pro použití jako léčiva |
Family Cites Families (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3114775A (en) * | 1961-10-23 | 1963-12-17 | Monsanto Chemicals | Process for the oxidation of organic sulfides |
| US3515559A (en) * | 1966-09-30 | 1970-06-02 | Minnesota Mining & Mfg | Dry process proof sheet composition |
| US3897420A (en) * | 1973-06-28 | 1975-07-29 | Squibb & Sons Inc | 2-Aminoalkyl-7-substituted-3,3a,4,5,6,7-hexahydro-3-substituted-2H-pyrazolo(4,3-c)pyridines |
| CA1055937A (en) * | 1973-06-28 | 1979-06-05 | Chester F. Turk | 2-aminoalkyl-7-substituted-3,3a,4,5,6,7-hexahydro-3-substituted-2h-pyrazolo (4,3-a) pyridines |
| US3911129A (en) * | 1974-07-01 | 1975-10-07 | Squibb & Sons Inc | Pyrazolo-pyridine biologically active compounds |
| US3979381A (en) * | 1975-08-11 | 1976-09-07 | E. R. Squibb & Sons, Inc. | Thiopyrano[4,3-c] pyrazoles |
| US3994880A (en) * | 1976-04-21 | 1976-11-30 | E. R. Squibb & Sons, Inc. | 2,3,3A,4,6,7-Hexahydro-2-heterocyclicalkyl-3-aryl-7-(arylmethylene)thiopyrano[4,3-c]pyrazoles and analogs thereof |
| US4127667A (en) * | 1978-04-05 | 1978-11-28 | E. R. Squibb & Sons, Inc. | Substituted thiopyrano(4,3-b)pyrans |
| US4415621A (en) * | 1980-02-25 | 1983-11-15 | Eastman Kodak Company | Use of α,α-bis(dialkylaminobenzylidene) ketone dyes in optical recording elements |
| US4755450A (en) * | 1986-04-22 | 1988-07-05 | Minnesota Mining And Manufacturing Company | Spectral sensitizing dyes in photopolymerizable systems |
| JP2536594B2 (ja) * | 1987-06-08 | 1996-09-18 | 日立化成工業株式会社 | 光重合開始剤及びこれを用いた光重合性組成物 |
| EP0359431B1 (en) * | 1988-09-07 | 1993-12-22 | Minnesota Mining And Manufacturing Company | Halomethyl-1,3,5-triazines containing a sensitizer moiety |
| JP2626070B2 (ja) * | 1989-07-12 | 1997-07-02 | 住友化学工業株式会社 | フォトレジスト組成物 |
| GB9217331D0 (en) * | 1992-08-14 | 1992-09-30 | Xenova Ltd | Pharmaceutical compounds |
| JPH06181264A (ja) * | 1992-12-14 | 1994-06-28 | Hitachi Ltd | 配線構造体及びその製造方法 |
| US5811218A (en) * | 1993-07-28 | 1998-09-22 | Hitachi Chemical Company, Ltd. | Photoinitiator compositions including amino acids, coumarin and titanocene and photosensitive materials using the same |
| GB9402809D0 (en) * | 1994-02-14 | 1994-04-06 | Xenova Ltd | Pharmaceutical compounds |
| US6022597A (en) * | 1996-11-08 | 2000-02-08 | Yan; Mingdi | Chemical functionalization of surfaces |
| JPH10198055A (ja) * | 1997-01-09 | 1998-07-31 | Mitsubishi Chem Corp | 電子写真感光体 |
| US6673843B2 (en) | 1999-06-30 | 2004-01-06 | Emory University | Curcumin and curcuminoid inhibition of angiogenesis |
| CA2395191A1 (en) | 1999-12-23 | 2001-06-28 | Tedman Ehlers | Chalcone and its analogs as agents for the inhibition of angiogenesis and related disease states |
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