DE602007009379D1 - Neue, von podophyllotoxin abgeleitete gem-difluorid-c-glycosidverbindungen, ihre herstellung und anwendungen - Google Patents
Neue, von podophyllotoxin abgeleitete gem-difluorid-c-glycosidverbindungen, ihre herstellung und anwendungenInfo
- Publication number
- DE602007009379D1 DE602007009379D1 DE602007009379T DE602007009379T DE602007009379D1 DE 602007009379 D1 DE602007009379 D1 DE 602007009379D1 DE 602007009379 T DE602007009379 T DE 602007009379T DE 602007009379 T DE602007009379 T DE 602007009379T DE 602007009379 D1 DE602007009379 D1 DE 602007009379D1
- Authority
- DE
- Germany
- Prior art keywords
- difluoride
- gra
- benzyl
- alkyl
- acetyl
- 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.)
- Active
Links
- YJGVMLPVUAXIQN-UHFFFAOYSA-N epipodophyllotoxin Natural products COC1=C(OC)C(OC)=CC(C2C3=CC=4OCOC=4C=C3C(O)C3C2C(OC3)=O)=C1 YJGVMLPVUAXIQN-UHFFFAOYSA-N 0.000 title 1
- YJGVMLPVUAXIQN-XVVDYKMHSA-N podophyllotoxin Chemical compound COC1=C(OC)C(OC)=CC([C@@H]2C3=CC=4OCOC=4C=C3[C@H](O)[C@@H]3[C@@H]2C(OC3)=O)=C1 YJGVMLPVUAXIQN-XVVDYKMHSA-N 0.000 title 1
- 229960001237 podophyllotoxin Drugs 0.000 title 1
- YVCVYCSAAZQOJI-UHFFFAOYSA-N podophyllotoxin Natural products COC1=C(O)C(OC)=CC(C2C3=CC=4OCOC=4C=C3C(O)C3C2C(OC3)=O)=C1 YVCVYCSAAZQOJI-UHFFFAOYSA-N 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 abstract 5
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 5
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 abstract 4
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 abstract 3
- 239000002253 acid Substances 0.000 abstract 2
- 150000004677 hydrates Chemical class 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 229910052500 inorganic mineral Inorganic materials 0.000 abstract 2
- 239000011707 mineral Substances 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- 239000012453 solvate Substances 0.000 abstract 2
- YQTCQNIPQMJNTI-UHFFFAOYSA-N 2,2-dimethylpropan-1-one Chemical group CC(C)(C)[C]=O YQTCQNIPQMJNTI-UHFFFAOYSA-N 0.000 abstract 1
- 101100293276 Caenorhabditis elegans cra-1 gene Proteins 0.000 abstract 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 125000001584 benzyloxycarbonyl group Chemical group C(=O)(OCC1=CC=CC=C1)* 0.000 abstract 1
- 239000000824 cytostatic agent Substances 0.000 abstract 1
- 230000001085 cytostatic effect Effects 0.000 abstract 1
- 230000000694 effects Effects 0.000 abstract 1
- 125000001475 halogen functional group Chemical group 0.000 abstract 1
- 230000010534 mechanism of action Effects 0.000 abstract 1
- UYWQUFXKFGHYNT-UHFFFAOYSA-N phenylmethyl ester of formic acid Natural products O=COCC1=CC=CC=C1 UYWQUFXKFGHYNT-UHFFFAOYSA-N 0.000 abstract 1
- XKJCHHZQLQNZHY-UHFFFAOYSA-N phthalimide Chemical compound C1=CC=C2C(=O)NC(=O)C2=C1 XKJCHHZQLQNZHY-UHFFFAOYSA-N 0.000 abstract 1
- 125000006239 protecting group Chemical group 0.000 abstract 1
- 125000000037 tert-butyldiphenylsilyl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1[Si]([H])([*]C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 abstract 1
- 125000001544 thienyl group Chemical group 0.000 abstract 1
- 125000004665 trialkylsilyl group Chemical group 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H7/00—Compounds containing non-saccharide radicals linked to saccharide radicals by a carbon-to-carbon bond
-
- 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
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H3/00—Compounds containing only hydrogen atoms and saccharide radicals having only carbon, hydrogen, and oxygen atoms
- C07H3/02—Monosaccharides
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biotechnology (AREA)
- Engineering & Computer Science (AREA)
- Molecular Biology (AREA)
- Genetics & Genomics (AREA)
- Biochemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Saccharide Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR0603766A FR2900154B1 (fr) | 2006-04-25 | 2006-04-25 | Nouveaux composes c-glycosides gem-difluores derives de la podophyllotoxine, leur preparation et leurs applications. |
| PCT/FR2007/000697 WO2007125194A1 (fr) | 2006-04-25 | 2007-04-24 | Nouveaux composes c-glycosides gem-difluores derives de la podophyllotoxine, leur preparation et leurs applications |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE602007009379D1 true DE602007009379D1 (de) | 2010-11-04 |
Family
ID=37198762
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE602007009379T Active DE602007009379D1 (de) | 2006-04-25 | 2007-04-24 | Neue, von podophyllotoxin abgeleitete gem-difluorid-c-glycosidverbindungen, ihre herstellung und anwendungen |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US8236935B2 (de) |
| EP (1) | EP2024379B1 (de) |
| AT (1) | ATE482225T1 (de) |
| CA (1) | CA2650384C (de) |
| DE (1) | DE602007009379D1 (de) |
| ES (1) | ES2353436T3 (de) |
| FR (1) | FR2900154B1 (de) |
| WO (1) | WO2007125194A1 (de) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102234283B (zh) | 2010-04-23 | 2013-06-12 | 湖北工业大学 | 4′-去甲基表鬼臼毒素衍生物及其合成方法和应用 |
| BR112013015869A2 (pt) | 2010-12-22 | 2017-07-04 | Tfchem | composto, processo para preparar um composto, uso, peptídeo e composição farmacêutica ou cosmética. |
| CA2844402C (en) | 2011-08-08 | 2019-07-02 | Tfchem | Gem-difluorinated c-isopropylgalactoside derivates |
| KR20150108391A (ko) * | 2013-01-14 | 2015-09-25 | 어드바노믹스 코포레이션 | 항암제로서 젬―디플루오리네이트화된 씨―글리코시드 화합물 |
| US10100088B2 (en) | 2014-03-17 | 2018-10-16 | Tfchem | Glycopeptide derivatives for the preservation and protection of biological materials and microorganisms |
| CN112961135B (zh) * | 2021-02-05 | 2021-11-26 | 安庆奇创药业有限公司 | 一种采用微通道反应装置连续合成苄基取代葡萄糖酸内酯的方法 |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH01197486A (ja) * | 1988-02-03 | 1989-08-09 | Nippon Kayaku Co Ltd | 新規ポドフィロトキシン誘導体、抗腫瘍剤及び中間体 |
| US5300500A (en) * | 1989-02-23 | 1994-04-05 | The University Of North Carolina At Chapel Hill | 4 beta-amino podophyllotoxin analog compounds and methods |
| FR2658824B1 (fr) * | 1990-02-27 | 1992-07-03 | Pf Medicament | Tris acetyl-2",3",4' ethylidene-4",6" beta-d-glucopyranosides, leur preparation et leur utilisation pour la preparation d'ethylidene beta-d-glucopyranoside de demethyl-4' epipodophyllotoxine. |
| WO2001049693A1 (en) * | 2000-01-03 | 2001-07-12 | Korea Research Institute Of Chemical Technology | 4-O-[2-(N,N-DIALKYLAMINO)-2-DEOXY-4,6-O,O-beta-D-GLUCOSYL]-4'-O-DEMETHYL-EPI-PODOPHYLLOTOXIN, DERIVATIVES, AND AN ANTICANCER COMPOSITION CONTAINING SAME |
-
2006
- 2006-04-25 FR FR0603766A patent/FR2900154B1/fr not_active Expired - Fee Related
-
2007
- 2007-04-24 EP EP07731356A patent/EP2024379B1/de active Active
- 2007-04-24 DE DE602007009379T patent/DE602007009379D1/de active Active
- 2007-04-24 US US12/298,642 patent/US8236935B2/en active Active - Reinstated
- 2007-04-24 CA CA2650384A patent/CA2650384C/en active Active
- 2007-04-24 ES ES07731356T patent/ES2353436T3/es active Active
- 2007-04-24 AT AT07731356T patent/ATE482225T1/de not_active IP Right Cessation
- 2007-04-24 WO PCT/FR2007/000697 patent/WO2007125194A1/fr active Application Filing
Also Published As
| Publication number | Publication date |
|---|---|
| EP2024379A1 (de) | 2009-02-18 |
| ATE482225T1 (de) | 2010-10-15 |
| US8236935B2 (en) | 2012-08-07 |
| WO2007125194A1 (fr) | 2007-11-08 |
| FR2900154B1 (fr) | 2008-07-04 |
| CA2650384C (en) | 2014-08-05 |
| US20090318675A1 (en) | 2009-12-24 |
| ES2353436T3 (es) | 2011-03-02 |
| FR2900154A1 (fr) | 2007-10-26 |
| EP2024379B1 (de) | 2010-09-22 |
| CA2650384A1 (en) | 2007-11-08 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| R082 | Change of representative |
Ref document number: 2024379 Country of ref document: EP Representative=s name: BECKER, KURIG, STRAUS, DE |