ATE500263T1 - Neue 2',3'-methylidenacetyladenosine prodrugs zur verwendung als adenosinrezeptoragonisten - Google Patents
Neue 2',3'-methylidenacetyladenosine prodrugs zur verwendung als adenosinrezeptoragonistenInfo
- Publication number
- ATE500263T1 ATE500263T1 AT07765638T AT07765638T ATE500263T1 AT E500263 T1 ATE500263 T1 AT E500263T1 AT 07765638 T AT07765638 T AT 07765638T AT 07765638 T AT07765638 T AT 07765638T AT E500263 T1 ATE500263 T1 AT E500263T1
- Authority
- AT
- Austria
- Prior art keywords
- drugs
- compounds
- receptor agonists
- adenosine receptor
- pro
- Prior art date
Links
Classifications
-
- 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
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/7042—Compounds having saccharide radicals and heterocyclic rings
- A61K31/7052—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
- A61K31/706—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom
- A61K31/7064—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines
- A61K31/7076—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines containing purines, e.g. adenosine, adenylic acid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/02—Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/02—Drugs for disorders of the nervous system for peripheral neuropathies
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/14—Vasoprotectives; Antihaemorrhoidals; Drugs for varicose therapy; Capillary stabilisers
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
- C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
- C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
- C07H19/16—Purine radicals
- C07H19/167—Purine radicals with ribosyl as the saccharide radical
-
- 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
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Molecular Biology (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Genetics & Genomics (AREA)
- Biochemistry (AREA)
- Rheumatology (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Biotechnology (AREA)
- Vascular Medicine (AREA)
- Epidemiology (AREA)
- Physical Education & Sports Medicine (AREA)
- Urology & Nephrology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Immunology (AREA)
- Dermatology (AREA)
- Pain & Pain Management (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Saccharide Compounds (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SE0601396 | 2006-06-27 | ||
US83730806P | 2006-08-11 | 2006-08-11 | |
PCT/EP2007/056375 WO2008000743A2 (en) | 2006-06-27 | 2007-06-26 | Novel 2',3'-methylidene acetyl adenosine prodrugs for use as prodrugs for adenosine receptor agonists |
Publications (1)
Publication Number | Publication Date |
---|---|
ATE500263T1 true ATE500263T1 (de) | 2011-03-15 |
Family
ID=38545430
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AT07765638T ATE500263T1 (de) | 2006-06-27 | 2007-06-26 | Neue 2',3'-methylidenacetyladenosine prodrugs zur verwendung als adenosinrezeptoragonisten |
Country Status (12)
Country | Link |
---|---|
US (1) | US7906518B2 (de) |
EP (1) | EP2066685B1 (de) |
JP (1) | JP2009541436A (de) |
CN (1) | CN101479290A (de) |
AT (1) | ATE500263T1 (de) |
AU (1) | AU2007263726A1 (de) |
BR (1) | BRPI0713901A2 (de) |
CA (1) | CA2657973A1 (de) |
DE (1) | DE602007012904D1 (de) |
ES (1) | ES2361886T3 (de) |
RU (1) | RU2009102512A (de) |
WO (1) | WO2008000743A2 (de) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2274007B1 (de) * | 2008-03-10 | 2016-12-14 | Cornell University | Modulation der durchlässigkeit der blut-hirn-schranke |
US20100160250A1 (en) * | 2008-12-18 | 2010-06-24 | Douglass Iii James G | Method for treating inflammatory conditions |
RU2478392C2 (ru) * | 2011-05-20 | 2013-04-10 | Евгений Петрович Измайлов | Способ консервативного и физиотерапевтического лечения серозно-геморрагического плеврита |
RU2478391C2 (ru) * | 2011-05-20 | 2013-04-10 | Евгений Петрович Измайлов | Способ физиотерапевтического и консервативного лечения плеврита |
MX367879B (es) * | 2012-08-01 | 2019-09-10 | Lewis And Clark Pharmaceuticals Inc | N-alquil 2-(disustituido)alquiladenosin-5-uronamidas como agonistas a2a. |
US9822141B2 (en) | 2012-08-01 | 2017-11-21 | Lewis And Clark Pharmaceuticals, Inc. | N-alkyl 2-(disubstituted)alkynyladenosine-5-uronamides as A2A agonists |
US11541071B1 (en) | 2021-12-16 | 2023-01-03 | Ascletis BioScience Co., Ltd | Nucleoside derivatives and methods of use thereof |
Family Cites Families (41)
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US5968914A (en) | 1987-10-28 | 1999-10-19 | Pro-Neuron, Inc. | Treatment of chemotherapeutic agent and antiviral agent toxicity with acylated pyrimidine nucleosides |
US5691188A (en) * | 1994-02-14 | 1997-11-25 | American Cyanamid Company | Transformed yeast cells expressing heterologous G-protein coupled receptor |
ATE236922T1 (de) | 1997-06-03 | 2003-04-15 | Itochu Techno Chem Inc | Natürliche antitumor- oder antivirale substanzen und ihre anwendung |
US6117878A (en) * | 1998-02-24 | 2000-09-12 | University Of Virginia | 8-phenyl- or 8-cycloalkyl xanthine antagonists of A2B human adenosine receptors |
US6958324B2 (en) * | 1998-12-02 | 2005-10-25 | Inotek Pharmaceuticals Corporation | Inosine compounds and their use for treating or preventing an inflamation or a reperfusion disease |
US6214807B1 (en) * | 1999-06-22 | 2001-04-10 | Cv Therapeutics, Inc. | C-pyrazole 2A A receptor agonists |
US6894021B2 (en) * | 2000-02-17 | 2005-05-17 | Cv Therapeutics, Inc. | Method for identifying and using A2B adenosine receptor antagonists to mediate mammalian cell proliferation |
US6995148B2 (en) * | 2001-04-05 | 2006-02-07 | University Of Pittsburgh | Adenosine cyclic ketals: novel adenosine analogues for pharmacotherapy |
US6713638B2 (en) * | 2001-05-18 | 2004-03-30 | Joel M. Linden | 2-amino-3-aroyl-4,5 alkylthiophenes: agonist allosteric enhancers at human A1 adenosine receptors |
GB0114286D0 (en) * | 2001-06-12 | 2001-08-01 | Hoffmann La Roche | Nucleoside Derivatives |
GB0228723D0 (en) | 2002-12-09 | 2003-01-15 | Cambridge Biotechnology Ltd | Treatment of pain |
GB0305150D0 (en) | 2003-03-07 | 2003-04-09 | Cambridge Biotechnology Ltd | Use of therapeutic compounds |
GB0305149D0 (en) | 2003-03-07 | 2003-04-09 | Cambridge Biotechnology Ltd | Compounds for the treatment of pain |
CA2528367A1 (en) * | 2003-06-09 | 2004-12-23 | Endacea, Inc. | A1 adenosine receptor antagonists |
EP1646390B1 (de) * | 2003-07-22 | 2008-10-08 | Cv Therapeutics, Inc. | A1 adenosin-rezeptor-antagonisten |
EP1663982B1 (de) * | 2003-07-31 | 2007-11-21 | Sanofi-Aventis | Aminochinolinderivate und deren verwendung als adenosin-a3-liganden |
US7504497B2 (en) * | 2003-10-21 | 2009-03-17 | Inspire Pharmaceuticals, Inc. | Orally bioavailable compounds and methods for inhibiting platelet aggregation |
DE602004027409D1 (de) * | 2003-10-21 | 2010-07-08 | Inspire Pharmaceuticals Inc | Tetrahydrofuroä3,4-düdioxolverbindungen und zusammensetzungen und verfahren zur inhibierung der trombozytenaggregation |
JP2007509180A (ja) * | 2003-10-21 | 2007-04-12 | インスパイアー ファーマシューティカルズ,インコーポレイティド | 疼痛を治療するための、非ヌクレオチド組成物および方法 |
WO2006033709A2 (en) * | 2004-07-29 | 2006-03-30 | Metabasis Therapeutics, Inc. | Novel nucleoside derivatives |
BRPI0508488A (pt) * | 2004-03-05 | 2007-07-31 | Cambridge Biotechnology Ltd | compostos terapêuticos |
JP2007531729A (ja) * | 2004-04-02 | 2007-11-08 | アデノシン、セラピューティックス、リミテッド、ライアビリティ、カンパニー | A2aアデノシンレセプターの選択的アンタゴニスト |
JP2007536241A (ja) * | 2004-05-03 | 2007-12-13 | ユニバーシティ オブ バージニア パテント ファウンデーション | 糖尿病性腎症の処置のためのa2aアデノシンレセプターアゴニスト |
JP2008512457A (ja) * | 2004-09-09 | 2008-04-24 | アメリカ合衆国 | A3及びa1アデノシン受容体作用薬としてのプリン誘導体 |
US8461128B2 (en) * | 2005-04-15 | 2013-06-11 | Sloan-Kettering Institute For Cancer Research | Anti-microbial agents and uses thereof |
JP2008540685A (ja) * | 2005-05-19 | 2008-11-20 | シーブイ・セラピューティクス・インコーポレイテッド | A1アデノシンレセプターアゴニスト |
GB0514809D0 (en) * | 2005-07-19 | 2005-08-24 | Glaxo Group Ltd | Compounds |
ATE502640T1 (de) * | 2006-01-26 | 2011-04-15 | Us Gov Health & Human Serv | Allosterische a3-adenosin-rezeptormodulatoren |
US20080027022A1 (en) * | 2006-02-08 | 2008-01-31 | Linden Joel M | Method to treat gastric lesions |
JP2009528389A (ja) * | 2006-03-02 | 2009-08-06 | シーブイ・セラピューティクス・インコーポレイテッド | A2aアデノシン受容体拮抗剤 |
NZ571324A (en) * | 2006-03-17 | 2011-07-29 | Gilead Palo Alto Inc | Method of preventing and treating hepatic disease using A2B adenoise receptor antagonists |
JP2009541354A (ja) * | 2006-06-22 | 2009-11-26 | シーブイ・セラピューティクス・インコーポレイテッド | 虚血の治療におけるa2aアデノシン受容体アゴニストの使用 |
EP1903044A1 (de) * | 2006-09-14 | 2008-03-26 | Novartis AG | Adenosinderivate als Agonisten des A2A-Rezeptors |
US7723343B2 (en) * | 2007-03-30 | 2010-05-25 | King Pharmaceuticals Research And Development, Inc. | Adenosine A2A receptor antagonists |
WO2008124150A1 (en) * | 2007-04-09 | 2008-10-16 | University Of Virginia Patent Foundation | Method of treating enteritis, intestinal damage, and diarrhea from c. difficile with an a2a adenosine receptor agonist |
US20080262001A1 (en) * | 2007-04-23 | 2008-10-23 | Adenosine Therapeutics, Llc | Agonists of a2a adenosine receptors for treating recurrent tumor growth in the liver following resection |
AU2008270735C1 (en) * | 2007-06-29 | 2014-03-06 | Government Of The United States Of America, Represented By The Secretary, Department Of Health And Human Services | Dendrimer conjugates of agonists and antagonists of the GPCR superfamily |
EP2200615A1 (de) * | 2007-10-16 | 2010-06-30 | Gilead Palo Alto, Inc. | A3-adenosinrezeptorantagonisten |
US8183225B2 (en) * | 2007-11-08 | 2012-05-22 | New York University | Inhibition of bone resorption using medical implants containing adenosine receptor antagonists |
EA201001135A1 (ru) * | 2008-01-09 | 2011-02-28 | ПиДжиИксХЭЛС ЭлЭлСи | Интратекальное лечение невропатической боли агонистами ar |
US20090203689A1 (en) * | 2008-02-07 | 2009-08-13 | Arvinder Dhalla | Abca-1 elevating compounds and methods |
-
2007
- 2007-06-26 AT AT07765638T patent/ATE500263T1/de not_active IP Right Cessation
- 2007-06-26 CA CA002657973A patent/CA2657973A1/en not_active Abandoned
- 2007-06-26 US US11/823,335 patent/US7906518B2/en not_active Expired - Fee Related
- 2007-06-26 DE DE602007012904T patent/DE602007012904D1/de active Active
- 2007-06-26 JP JP2009517173A patent/JP2009541436A/ja active Pending
- 2007-06-26 BR BRPI0713901-2A patent/BRPI0713901A2/pt not_active IP Right Cessation
- 2007-06-26 CN CNA2007800246476A patent/CN101479290A/zh active Pending
- 2007-06-26 WO PCT/EP2007/056375 patent/WO2008000743A2/en active Application Filing
- 2007-06-26 ES ES07765638T patent/ES2361886T3/es active Active
- 2007-06-26 AU AU2007263726A patent/AU2007263726A1/en not_active Abandoned
- 2007-06-26 EP EP07765638A patent/EP2066685B1/de active Active
- 2007-06-26 RU RU2009102512/04A patent/RU2009102512A/ru not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
CN101479290A (zh) | 2009-07-08 |
US7906518B2 (en) | 2011-03-15 |
US20080027081A1 (en) | 2008-01-31 |
WO2008000743A2 (en) | 2008-01-03 |
ES2361886T3 (es) | 2011-06-24 |
EP2066685B1 (de) | 2011-03-02 |
WO2008000743A3 (en) | 2008-02-21 |
AU2007263726A1 (en) | 2008-01-03 |
RU2009102512A (ru) | 2010-08-10 |
DE602007012904D1 (de) | 2011-04-14 |
CA2657973A1 (en) | 2008-01-03 |
JP2009541436A (ja) | 2009-11-26 |
EP2066685A2 (de) | 2009-06-10 |
BRPI0713901A2 (pt) | 2013-01-08 |
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Legal Events
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RER | Ceased as to paragraph 5 lit. 3 law introducing patent treaties |