HK1102367A1 - Methods for treatment of disease-induced peripheral neuropathy and related conditions - Google Patents
Methods for treatment of disease-induced peripheral neuropathy and related conditionsInfo
- Publication number
- HK1102367A1 HK1102367A1 HK07109356.2A HK07109356A HK1102367A1 HK 1102367 A1 HK1102367 A1 HK 1102367A1 HK 07109356 A HK07109356 A HK 07109356A HK 1102367 A1 HK1102367 A1 HK 1102367A1
- Authority
- HK
- Hong Kong
- Prior art keywords
- treatment
- disease
- methods
- peripheral neuropathy
- related conditions
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/02—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6
- C07D473/18—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 one oxygen and one nitrogen atom, e.g. guanine
-
- 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
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
- A61K31/404—Indoles, e.g. pindolol
-
- 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
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
-
- 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
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/513—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim having oxo groups directly attached to the heterocyclic ring, e.g. cytosine
-
- 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
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
- A61K31/52—Purines, e.g. adenine
-
- 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
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
- A61K31/52—Purines, e.g. adenine
- A61K31/522—Purines, e.g. adenine having oxo groups directly attached to the heterocyclic ring, e.g. hypoxanthine, guanine, acyclovir
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/26—Heterocyclic compounds containing purine ring systems with an oxygen, sulphur, or nitrogen atom directly attached in position 2 or 6, but not in both
- C07D473/28—Oxygen atom
- C07D473/30—Oxygen atom attached in position 6, e.g. hypoxanthine
-
- 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)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Medicinal Preparation (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Saccharide Compounds (AREA)
- Magnetic Treatment Devices (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US21684400P | 2000-07-07 | 2000-07-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
HK1102367A1 true HK1102367A1 (en) | 2007-11-16 |
Family
ID=22808722
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HK07109356.2A HK1102367A1 (en) | 2000-07-07 | 2007-08-28 | Methods for treatment of disease-induced peripheral neuropathy and related conditions |
Country Status (9)
Country | Link |
---|---|
US (2) | US6630478B2 (fr) |
EP (3) | EP1790344B1 (fr) |
AT (2) | ATE499103T1 (fr) |
AU (2) | AU2001273212A1 (fr) |
DE (2) | DE60143850D1 (fr) |
DK (2) | DK1790344T3 (fr) |
ES (2) | ES2385931T3 (fr) |
HK (1) | HK1102367A1 (fr) |
WO (2) | WO2002004452A2 (fr) |
Families Citing this family (45)
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CA2195302A1 (fr) * | 1994-07-25 | 1996-02-08 | Alvin J. Glasky | Modificateurs du guanylyle dependants du monoxyde de carbone |
US20020156277A1 (en) * | 2001-04-20 | 2002-10-24 | Fick David B. | Synthesis and methods of use of purine analogues and derivatives |
US6759427B2 (en) * | 2001-04-20 | 2004-07-06 | Spectrum Pharmaceuticals, Inc. | Synthesis and methods of use of tetrahydroindolone analogues and derivatives |
US20030055249A1 (en) * | 2001-07-17 | 2003-03-20 | Fick David B. | Synthesis and methods of use of pyrimidine analogues and derivatives |
WO2003105845A1 (fr) * | 2002-06-14 | 2003-12-24 | Takeda Chemical Industries, Ltd. | Promedicaments de derives d'imidazole servant d'inhibiteurs de pompe a protons dans le traitement de l'ulcere gastro-duodenal |
WO2005030148A2 (fr) * | 2003-09-25 | 2005-04-07 | Cenomed, Inc. | Derives de tetrahydroindolone destines au traitement d'etats neurologiques |
WO2005048926A2 (fr) | 2003-11-13 | 2005-06-02 | The General Hospital Corporation | Methodes pour traiter la douleur |
US8012964B2 (en) * | 2004-03-26 | 2011-09-06 | Dainippon Sumitomo Pharma Co., Ltd. | 9-substituted 8-oxoadenine compound |
AU2006244074B2 (en) * | 2005-05-09 | 2012-12-13 | Hydra Biosciences, Inc. | Compounds for modulating TRPV3 function |
US8916550B2 (en) | 2005-05-09 | 2014-12-23 | Hydra Biosciences, Inc. | Compounds for modulating TRPV3 function |
TW200801003A (en) * | 2005-09-16 | 2008-01-01 | Astrazeneca Ab | Novel compounds |
US20100048713A1 (en) * | 2006-01-06 | 2010-02-25 | Aarhus Universitet | Compounds acting on the serotonin transporter |
US8138172B2 (en) * | 2006-07-05 | 2012-03-20 | Astrazeneca Ab | 8-oxoadenine derivatives acting as modulators of TLR7 |
JP2009545619A (ja) * | 2006-08-01 | 2009-12-24 | スペクトラム ファーマシューティカルズ インコーポレイテッド | 化学療法誘発神経障害の治療に寄与するための方法および医薬製剤 |
TW200831105A (en) * | 2006-12-14 | 2008-08-01 | Astrazeneca Ab | Novel compounds |
JP5329444B2 (ja) * | 2007-03-19 | 2013-10-30 | アストラゼネカ・アクチエボラーグ | Toll様受容体(tlr7)モジュレーターとしての9−置換−8−オキソ−アデニン化合物 |
PT2132209E (pt) * | 2007-03-19 | 2014-04-15 | Astrazeneca Ab | Compostos de 8-oxo-adenina substituídos na posição 9, como moduladores do recetor de tipo ¿toll¿ (tlr7) |
EP2138497A4 (fr) * | 2007-03-20 | 2012-01-04 | Dainippon Sumitomo Pharma Co | Nouveau composé d'adénine |
TW200902018A (en) * | 2007-03-20 | 2009-01-16 | Dainippon Sumitomo Pharma Co | Novel adenine compound |
PL2155743T3 (pl) * | 2007-05-08 | 2013-01-31 | Astrazeneca Ab | Imidazochinoliny o właściwościach immunomodulacyjnych |
WO2009031154A2 (fr) * | 2007-09-07 | 2009-03-12 | Beta O2 Technologies Ltd. | Couche d'air pour soutenir des cellules |
EA018414B1 (ru) * | 2007-10-11 | 2013-07-30 | ГЛЭКСОСМИТКЛАЙН ЭлЭлСи | ИНГИБИТОРЫ sEH И ИХ ПРИМЕНЕНИЕ |
EP2219648A4 (fr) * | 2007-11-09 | 2010-11-03 | Cenomed Biosciences Llc | Traitement des troubles du stress post-traumatique avec des composés de tétrahydroindolone et d'arylpipérazine |
PE20091156A1 (es) | 2007-12-17 | 2009-09-03 | Astrazeneca Ab | Sales de (3-{[[3-(6-amino-2-butoxi-8-oxo-7,8-dihidro-9h-purin-9-il)propil](3-morfolin-4-ilpropil)amino]metil}fenil)acetato de metilo |
JPWO2009091031A1 (ja) * | 2008-01-17 | 2011-05-26 | 大日本住友製薬株式会社 | アデニン化合物の製造方法 |
KR20100125245A (ko) | 2008-01-17 | 2010-11-30 | 다이닛본 스미토모 세이야꾸 가부시끼가이샤 | 아데닌 화합물의 제조 방법 |
US9483755B2 (en) * | 2008-03-04 | 2016-11-01 | Apple Inc. | Portable multifunction device, method, and graphical user interface for an email client |
US20090264443A1 (en) * | 2008-04-18 | 2009-10-22 | David Helton | Treatment of organophosphate exposure with tetrahydroindolone arylpiperazine compounds |
JP2010043063A (ja) | 2008-05-09 | 2010-02-25 | Agency For Science Technology & Research | 川崎病の診断及び治療 |
MX340198B (es) | 2008-08-29 | 2016-06-30 | A Schulman Inc * | Composiciones polimericas con sabor optimizado. |
EP2507237A1 (fr) * | 2009-12-03 | 2012-10-10 | Dainippon Sumitomo Pharma Co., Ltd. | Imidazoquinolines agissant par l'intermédiaire des récepteurs de type toll (tlr) |
US9067988B2 (en) | 2010-12-01 | 2015-06-30 | Alderbio Holdings Llc | Methods of preventing or treating pain using anti-NGF antibodies |
US9078878B2 (en) | 2010-12-01 | 2015-07-14 | Alderbio Holdings Llc | Anti-NGF antibodies that selectively inhibit the association of NGF with TrkA, without affecting the association of NGF with p75 |
MX359070B (es) | 2010-12-01 | 2018-09-13 | Alderbio Holdings Llc | Composiciones anti-ngf y uso de las mismas. |
US9539324B2 (en) | 2010-12-01 | 2017-01-10 | Alderbio Holdings, Llc | Methods of preventing inflammation and treating pain using anti-NGF compositions |
US11214610B2 (en) | 2010-12-01 | 2022-01-04 | H. Lundbeck A/S | High-purity production of multi-subunit proteins such as antibodies in transformed microbes such as Pichia pastoris |
US9884909B2 (en) | 2010-12-01 | 2018-02-06 | Alderbio Holdings Llc | Anti-NGF compositions and use thereof |
EP2651937B8 (fr) | 2010-12-16 | 2016-07-13 | Sumitomo Dainippon Pharma Co., Ltd. | Dérivé imidazo[4,5-c]quinolin-1-yle utile en thérapie |
WO2012080730A1 (fr) | 2010-12-17 | 2012-06-21 | Astrazeneca Ab | Dérivés de purine |
US20160166618A1 (en) * | 2012-10-19 | 2016-06-16 | Anthrogenesis Corproation | Treatment of pain using amnion derived adherent cells |
WO2015058141A1 (fr) * | 2013-10-18 | 2015-04-23 | Virginia Tech Intellectual Properties, Inc. | Monomères et copolymères contenant des nucléobases |
US9898162B2 (en) | 2014-05-30 | 2018-02-20 | Apple Inc. | Swiping functions for messaging applications |
WO2016036509A1 (fr) | 2014-09-02 | 2016-03-10 | Apple Inc. | Interface utilisateur de courrier électronique |
AU2016356694B2 (en) | 2015-11-20 | 2021-07-29 | Forma Therapeutics, Inc. | Purinones as ubiquitin-specific protease 1 inhibitors |
WO2023055531A1 (fr) * | 2021-09-28 | 2023-04-06 | University Of Pittsburgh - Of The Commonwealth System Of Higher Education | Méthodes de traitement de la neuropathie périphérique |
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US3300380A (en) | 1963-12-26 | 1967-01-24 | Upjohn Co | Diminishing toxicity of antiviral nu6-(hydroxyalkyl) adenines with 4-hydroxypyrazolo(3, 4-d) pyrimidine |
US3321369A (en) | 1965-05-26 | 1967-05-23 | Abbott Lab | Method of enhancing learning rate and retention level in warm blooded animals |
US3438968A (en) | 1966-06-23 | 1969-04-15 | Int Chem & Nuclear Corp | Substituted ammonium basic addition salts of ribonucleic acid |
BE759011A (fr) | 1969-11-17 | 1971-05-17 | Wellcome Found | Aminopurines |
DE2554453A1 (de) | 1974-12-18 | 1976-06-24 | Experimentales Et Cliniques De | Medikament zur glykaemieregulierung |
GB1530912A (en) | 1975-02-13 | 1978-11-01 | Wellcome Found | Compositions containing 9-(2-hydroxy-3-alkyl)-adenines |
US4138562A (en) | 1977-02-09 | 1979-02-06 | The Regents Of The University Of Minnesota | Adenosine deaminase resistant antiviral purine nucleosides and method of preparation |
US4221910A (en) | 1978-09-15 | 1980-09-09 | Newport Pharmaceuticals International, Inc. | 9-(Hydroxy alkyl)purines |
US4221909A (en) | 1978-09-15 | 1980-09-09 | Sloan-Kettering Institute For Cancer Research | P-Acetamidobenzoic acid salts of 9-(hydroxyalkyl) purines |
US4221794A (en) | 1979-06-21 | 1980-09-09 | Newport Pharmaceuticals International, Inc. | Method of imparting immunomodulating and antiviral activity |
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US5495010A (en) | 1987-04-17 | 1996-02-27 | The United States Of America As Represented By The Department Of Health And Human Services | Acid stable purine dideoxynucleosides |
ATE140729T1 (de) | 1988-04-19 | 1996-08-15 | Pasteur Institut | Verfahren zur gewinnung von schutzantigenen gegen bordetella-infektionen und toxische prozesse |
US5256677A (en) | 1989-05-23 | 1993-10-26 | Abbott Laboratories | Retroviral protease inhibiting compounds |
US5187162A (en) | 1989-09-15 | 1993-02-16 | Gensia Pharmaceuticals | Methods of treating neurodegenerative conditions |
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US5091432A (en) * | 1990-03-28 | 1992-02-25 | Glasky Alvin J | 9-substituted hypoxanthine bi-functional compounds and their neuroimmunological methods of use |
US5237051A (en) | 1990-12-06 | 1993-08-17 | Vanderbilt University | Purified enterotoxin receptor protein |
US5646155A (en) * | 1994-05-12 | 1997-07-08 | University Of Massachusetts Medical Center | Drugs to prevent recurrent herpes virus infections |
CA2195302A1 (fr) * | 1994-07-25 | 1996-02-08 | Alvin J. Glasky | Modificateurs du guanylyle dependants du monoxyde de carbone |
US5447939A (en) * | 1994-07-25 | 1995-09-05 | Glasky; Alvin J. | Carbon monoxide dependent guanylyl cyclase modifiers and methods of use |
US5801184A (en) | 1994-07-25 | 1998-09-01 | Glasky; Alvin J. | Carbon monoxide dependent guanylyl cyclase modifiers and methods of use |
US5795756A (en) | 1995-12-11 | 1998-08-18 | Johnson; Roger A. | Method and compounds for the inhibition of adenylyl cyclase |
US5948771A (en) | 1996-01-31 | 1999-09-07 | The Trustees Of Columbia University In The City Of New York | Method for treating heart failure using tetrapyrroles and metallotetrapyrroles |
US5801159A (en) | 1996-02-23 | 1998-09-01 | Galileo Laboratories, Inc. | Method and composition for inhibiting cellular irreversible changes due to stress |
AU709323B2 (en) | 1996-03-15 | 1999-08-26 | Somerset Pharmaceuticals, Inc. | Method for preventing and treating peripheral neuropathy by administering selegiline |
WO1999057120A1 (fr) | 1998-05-04 | 1999-11-11 | Neotherapeutics, Inc. | Nouvelle hypoxanthine 9-substituee apparentee a la serotonine |
WO1999056550A1 (fr) | 1998-05-04 | 1999-11-11 | Neotherapeutics, Inc. | Methode de traitement de la migraine chez des mammiferes |
WO1999057119A1 (fr) | 1998-05-04 | 1999-11-11 | Neotherapeutics, Inc. | Nouvelle hypoxanthine 9-substituee de type dopamine et methodes d'utilisation |
TWI246421B (en) * | 1998-12-03 | 2006-01-01 | Alcon Mfg Ltd | Use of neurotrophic factor stimulators for the treatment of ophthalmic neurodegenerative diseases |
US6297226B1 (en) * | 1999-10-15 | 2001-10-02 | Neotherapeutics, Inc. | Synthesis and methods of use of 9-substituted guanine derivatives |
-
2001
- 2001-07-06 AT AT07075011T patent/ATE499103T1/de active
- 2001-07-06 DE DE60143850T patent/DE60143850D1/de not_active Expired - Lifetime
- 2001-07-06 WO PCT/US2001/021526 patent/WO2002004452A2/fr active Application Filing
- 2001-07-06 EP EP07075011A patent/EP1790344B1/fr not_active Expired - Lifetime
- 2001-07-06 EP EP01952464A patent/EP1334104A2/fr not_active Withdrawn
- 2001-07-06 DK DK07075011.2T patent/DK1790344T3/da active
- 2001-07-06 DE DE60144123T patent/DE60144123D1/de not_active Expired - Lifetime
- 2001-07-06 AU AU2001273212A patent/AU2001273212A1/en not_active Abandoned
- 2001-07-06 ES ES01950964T patent/ES2385931T3/es not_active Expired - Lifetime
- 2001-07-06 DK DK01950964.5T patent/DK1334103T3/da active
- 2001-07-06 ES ES07075011T patent/ES2420354T3/es not_active Expired - Lifetime
- 2001-07-06 AU AU2001271908A patent/AU2001271908A1/en not_active Abandoned
- 2001-07-06 AT AT01950964T patent/ATE495177T1/de active
- 2001-07-06 US US09/899,901 patent/US6630478B2/en not_active Expired - Lifetime
- 2001-07-06 EP EP01950964A patent/EP1334103B1/fr not_active Expired - Lifetime
- 2001-07-06 US US09/900,844 patent/US6630490B2/en not_active Expired - Lifetime
- 2001-07-06 WO PCT/US2001/021373 patent/WO2002004448A2/fr not_active Application Discontinuation
-
2007
- 2007-08-28 HK HK07109356.2A patent/HK1102367A1/xx not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
DK1334103T3 (da) | 2011-04-04 |
US6630478B2 (en) | 2003-10-07 |
ATE499103T1 (de) | 2011-03-15 |
DK1790344T3 (da) | 2011-05-02 |
EP1790344B1 (fr) | 2011-02-23 |
ES2420354T3 (es) | 2013-08-23 |
WO2002004452A3 (fr) | 2003-01-03 |
WO2002004448A3 (fr) | 2003-01-23 |
EP1790344A2 (fr) | 2007-05-30 |
EP1790344A3 (fr) | 2007-06-27 |
WO2002004448A2 (fr) | 2002-01-17 |
AU2001273212A1 (en) | 2002-01-21 |
EP1334103B1 (fr) | 2011-01-12 |
ATE495177T1 (de) | 2011-01-15 |
US20020055506A1 (en) | 2002-05-09 |
US6630490B2 (en) | 2003-10-07 |
US20020061899A1 (en) | 2002-05-23 |
EP1334104A2 (fr) | 2003-08-13 |
EP1334103A2 (fr) | 2003-08-13 |
WO2002004452A2 (fr) | 2002-01-17 |
DE60144123D1 (de) | 2011-04-07 |
DE60143850D1 (de) | 2011-02-24 |
AU2001271908A1 (en) | 2002-01-21 |
ES2385931T3 (es) | 2012-08-03 |
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