TW200700404A - Anticancer compounds, intermediates and the method for preparation thereof - Google Patents
Anticancer compounds, intermediates and the method for preparation thereofInfo
- Publication number
- TW200700404A TW200700404A TW095108794A TW95108794A TW200700404A TW 200700404 A TW200700404 A TW 200700404A TW 095108794 A TW095108794 A TW 095108794A TW 95108794 A TW95108794 A TW 95108794A TW 200700404 A TW200700404 A TW 200700404A
- Authority
- TW
- Taiwan
- Prior art keywords
- dione
- furan
- hydroxynaphtho
- present
- provides
- Prior art date
Links
- 230000001093 anti-cancer Effects 0.000 title 1
- 150000001875 compounds Chemical class 0.000 title 1
- 239000000543 intermediate Substances 0.000 title 1
- XJGFVZBTNKODFQ-UHFFFAOYSA-N 5-hydroxy-2-(1-hydroxyethyl)benzo[f][1]benzofuran-4,9-dione Chemical compound O=C1C2=CC=CC(O)=C2C(=O)C2=C1OC(C(O)C)=C2 XJGFVZBTNKODFQ-UHFFFAOYSA-N 0.000 abstract 3
- KQPYUDDGWXQXHS-UHFFFAOYSA-N juglone Chemical compound O=C1C=CC(=O)C2=C1C=CC=C2O KQPYUDDGWXQXHS-UHFFFAOYSA-N 0.000 abstract 3
- DWMJEEGBCMSGAH-UHFFFAOYSA-N 2-acetyl-5-hydroxy-2,3-dihydrobenzo[f][1]benzofuran-4,9-dione Chemical compound O=C1C2=CC=CC(O)=C2C(=O)C2=C1OC(C(=O)C)C2 DWMJEEGBCMSGAH-UHFFFAOYSA-N 0.000 abstract 1
- 239000004480 active ingredient Substances 0.000 abstract 1
- 239000002246 antineoplastic agent Substances 0.000 abstract 1
- 229940041181 antineoplastic drug Drugs 0.000 abstract 1
- VYTBDSUNRJYVHL-UHFFFAOYSA-N beta-Hydrojuglone Natural products O=C1CCC(=O)C2=C1C=CC=C2O VYTBDSUNRJYVHL-UHFFFAOYSA-N 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 239000007858 starting material Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D307/92—Naphthofurans; Hydrogenated naphthofurans
-
- 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
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/34—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide
- A61K31/343—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide condensed with a carbocyclic ring, e.g. coumaran, bufuralol, befunolol, clobenfurol, amiodarone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Furan Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2005075291 | 2005-03-16 | ||
| JP2006002482A JP2006290871A (ja) | 2005-03-16 | 2006-01-10 | 抗癌性を示す化合物およびその中間体ならびにそれらの製造方法 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| TW200700404A true TW200700404A (en) | 2007-01-01 |
| TWI363056B TWI363056B (en) | 2012-05-01 |
Family
ID=36991697
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TW095108794A TWI363056B (en) | 2005-03-16 | 2006-03-15 | Anticancer compounds, intermediates and the method for preparation thereof |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US7910752B2 (zh) |
| EP (1) | EP1860103B1 (zh) |
| JP (1) | JP2006290871A (zh) |
| KR (1) | KR20070114287A (zh) |
| TW (1) | TWI363056B (zh) |
| WO (1) | WO2006098355A1 (zh) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4077863B1 (ja) | 2007-05-31 | 2008-04-23 | タヒボジャパン株式会社 | 抗癌活性を有する光学活性２−（１−ヒドロキシエチル）−５−ヒドロキシナフト［２，３−ｂ］フラン−４，９−ジオンの製法 |
| CN105963289B (zh) * | 2007-09-10 | 2021-02-26 | 北京强新生物科技有限公司 | 一类stat3通路抑制剂和癌干细胞通路抑制剂 |
| JP4563493B2 (ja) * | 2009-02-25 | 2010-10-13 | タヒボジャパン株式会社 | ナフトキノン系抗がん活性成分の効率的製造 |
| ES2987670T3 (es) | 2010-03-19 | 2024-11-15 | 1Globe Biomedical Co Ltd | Métodos novedosos para actuar sobre células madre cancerosas |
| HUE066482T2 (hu) * | 2010-03-19 | 2024-08-28 | 1Globe Biomedical Co Ltd | Új eljárások rákõssejtek megcélzására |
| JP5208239B2 (ja) | 2010-09-29 | 2013-06-12 | タヒボジャパン株式会社 | アルキンカップリングによる抗がん活性三環式化合物の新規製法 |
| CN106211758B (zh) | 2013-04-09 | 2021-03-23 | 北京强新生物科技有限公司 | 2-乙酰基萘并[2,3-b]呋喃-4,9-二酮用于治疗癌症的用途 |
| CN106163284A (zh) | 2014-02-07 | 2016-11-23 | 北京强新生物科技有限公司 | 3‑取代的羰基萘并[2,3‑b]呋喃衍生物或其药学上可接受的盐 |
| WO2018096401A1 (en) | 2016-11-22 | 2018-05-31 | Hitoshi Ban | New naphtho[2,3-b]furan derivatives |
| US11299469B2 (en) | 2016-11-29 | 2022-04-12 | Sumitomo Dainippon Pharma Oncology, Inc. | Naphthofuran derivatives, preparation, and methods of use thereof |
| JP2020520923A (ja) | 2017-05-17 | 2020-07-16 | ボストン バイオメディカル， インコーポレイテッド | がんを処置するための方法 |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IT1215287B (it) | 1985-07-09 | 1990-01-31 | Consiglio Nazionale Ricerche | Processo per la produzione di para-chinoni. |
| JPS63196576A (ja) | 1987-02-10 | 1988-08-15 | Tetsuo Ikegawa | フラルナフトキノン誘導体と制癌剤及びその製造方法 |
| JPH04139177A (ja) | 1989-12-28 | 1992-05-13 | Dainippon Ink & Chem Inc | フラルベンゾキノン誘導体及びその製造方法並びに制癌剤 |
| JP2669762B2 (ja) | 1992-09-18 | 1997-10-29 | タヒボジャパン 株式会社 | ２―（１―ヒドロキシエチル）―５―ヒドロキシナフト〔２，３―ｂ〕フラン―４，９―ジオンを含有する発癌プロモーション阻害剤 |
| JPH09235280A (ja) | 1996-02-29 | 1997-09-09 | Kagaku Gijutsu Shinko Jigyodan | フラノナフトキノン誘導体と抗腫瘍剤 |
| JP3598168B2 (ja) | 1996-03-18 | 2004-12-08 | 独立行政法人 科学技術振興機構 | 抗ウイルス剤 |
| JPH1121284A (ja) | 1997-06-30 | 1999-01-26 | Kotobuki:Kk | フラノナフトキノン誘導体及びこれを含有する医薬 |
| JP2001097860A (ja) | 1999-09-29 | 2001-04-10 | Japan Science & Technology Corp | 抗薬剤耐性菌剤と抗クラミジア剤 |
| JP4139177B2 (ja) | 2002-09-24 | 2008-08-27 | 日本ウェーブロック株式会社 | 新規な質感を有する成形用加飾シート |
| JP2004224802A (ja) | 2004-04-21 | 2004-08-12 | Japan Science & Technology Agency | 抗菌剤 |
| JP4077863B1 (ja) | 2007-05-31 | 2008-04-23 | タヒボジャパン株式会社 | 抗癌活性を有する光学活性２−（１−ヒドロキシエチル）−５−ヒドロキシナフト［２，３−ｂ］フラン−４，９−ジオンの製法 |
-
2006
- 2006-01-10 JP JP2006002482A patent/JP2006290871A/ja active Pending
- 2006-03-15 US US11/885,216 patent/US7910752B2/en not_active Expired - Fee Related
- 2006-03-15 WO PCT/JP2006/305111 patent/WO2006098355A1/ja not_active Ceased
- 2006-03-15 TW TW095108794A patent/TWI363056B/zh not_active IP Right Cessation
- 2006-03-15 KR KR1020077021139A patent/KR20070114287A/ko not_active Ceased
- 2006-03-15 EP EP06729132A patent/EP1860103B1/en not_active Not-in-force
Also Published As
| Publication number | Publication date |
|---|---|
| US20090042977A1 (en) | 2009-02-12 |
| EP1860103B1 (en) | 2012-05-16 |
| JP2006290871A (ja) | 2006-10-26 |
| WO2006098355A1 (ja) | 2006-09-21 |
| TWI363056B (en) | 2012-05-01 |
| KR20070114287A (ko) | 2007-11-30 |
| US7910752B2 (en) | 2011-03-22 |
| EP1860103A4 (en) | 2009-12-16 |
| EP1860103A1 (en) | 2007-11-28 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| ATE545639T1 (de) | Alkylsubstituierte tetrahydropyrane als aromastoffe | |
| WO2005002515A3 (en) | Delivery of therapeutic compounds to the brain and other tissues | |
| TW200700404A (en) | Anticancer compounds, intermediates and the method for preparation thereof | |
| WO2006050161A3 (en) | Therapeutic furopyrimidines and thienopyrimidines | |
| WO2006099169A3 (en) | Novel liposome compositions | |
| WO2007099553A3 (en) | 1,3-dioxane carboxylic acids | |
| WO2004096285A3 (en) | Anti-infective phosphonate conjugates | |
| EP2269657A3 (en) | Prodrugs containing novel bio-cleavable linkers | |
| WO2002064083A3 (en) | Synthesis of 3-amino-thalidomide and its enantiomers | |
| UA92349C2 (ru) | Полиморфы этилового эфира 3-[(2-{[4-(гексилоксикарбониламиноиминометил)фениламино]метил}-1-метил-1н-бензимидазол-5-карбонил)пиридин-2-иламино]пропионовой кислоты | |
| IL190905A0 (en) | 4-alkoxy cyclohexane-1-amino carboxylic acids and processes for their prepatation | |
| WO2001096307A3 (en) | Cycloalkyl alkanoic acids as integrin receptor antagonists | |
| WO2005080352A3 (en) | Quinazoline derivatives and therapeutic use thereof | |
| WO2006047288A3 (en) | Asymmetric synthesis of dihydrobenzofuran derivatives | |
| WO2007044796A3 (en) | Pyridazinone compounds as calcilytics | |
| WO2005080345A3 (en) | Imidazoline derivatives having cb1-antagonistic activity | |
| HK1046271A1 (zh) | 2，2-二甲基-1，3-二氧雜環乙烷半成品的鹽及有關製劑加工 | |
| MX2007006387A (es) | Derivados de piridina 3-substituidos como antagonistas h3. | |
| TW200609221A (en) | 4-substituted quinoline derivatives, method and intermediates for their preparation and pharmaceutical compositions containing them | |
| WO2007041076A3 (en) | 1,2,3,5-tetrahydro-cyclopental[c]quinolin-4-one derivatives as rxr agonists for the treatment of dyslipidemia, hypercholesterolemia and diabetes | |
| MX2007007027A (es) | Derivados piperazinilpiridina como agentes anti-obesidad. | |
| BR0109176A (pt) | Método para preparação de citalopram e composto da fórmula | |
| WO2008039894A3 (en) | Atorvastatin pharmaceutical compositions | |
| WO2005033279A3 (en) | Discovery of novel soluble crystalline anesthetics | |
| WO2003076426A3 (en) | Pyridinyloxy derivatives as 5-ht receptor ligands |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MM4A | Annulment or lapse of patent due to non-payment of fees |