|
PT100905A
(pt)
*
|
1991-09-30 |
1994-02-28 |
Eisai Co Ltd |
Compostos heterociclicos azotados biciclicos contendo aneis de benzeno, ciclo-hexano ou piridina e de pirimidina, piridina ou imidazol substituidos e composicoes farmaceuticas que os contem
|
|
AU661533B2
(en)
*
|
1992-01-20 |
1995-07-27 |
Astrazeneca Ab |
Quinazoline derivatives
|
|
JP2657760B2
(ja)
*
|
1992-07-15 |
1997-09-24 |
小野薬品工業株式会社 |
4−アミノキナゾリン誘導体およびそれを含有する医薬品
|
|
PH31122A
(en)
*
|
1993-03-31 |
1998-02-23 |
Eisai Co Ltd |
Nitrogen-containing fused-heterocycle compounds.
|
|
EP0669324A4
(fr)
*
|
1993-09-10 |
1996-04-03 |
Eisai Co Ltd |
Compose de quinazoline.
|
|
IL112249A
(en)
|
1994-01-25 |
2001-11-25 |
Warner Lambert Co |
Pharmaceutical compositions containing di and tricyclic pyrimidine derivatives for inhibiting tyrosine kinases of the epidermal growth factor receptor family and some new such compounds
|
|
IL112248A0
(en)
|
1994-01-25 |
1995-03-30 |
Warner Lambert Co |
Tricyclic heteroaromatic compounds and pharmaceutical compositions containing them
|
|
US5654307A
(en)
*
|
1994-01-25 |
1997-08-05 |
Warner-Lambert Company |
Bicyclic compounds capable of inhibiting tyrosine kinases of the epidermal growth factor receptor family
|
|
CZ288955B6
(cs)
*
|
1994-02-23 |
2001-10-17 |
Pfizer Inc. |
Substituované chinazolinové deriváty, jejich pouľití a farmaceutické prostředky na jejich bázi
|
|
US5776962A
(en)
*
|
1994-08-03 |
1998-07-07 |
Cell Pathways, Inc. |
Lactone compounds for treating patient with precancerous lesions
|
|
US5696159A
(en)
*
|
1994-08-03 |
1997-12-09 |
Cell Pathways, Inc. |
Lactone compounds for treating patients with precancerous lesions
|
|
US5658902A
(en)
*
|
1994-12-22 |
1997-08-19 |
Warner-Lambert Company |
Quinazolines as inhibitors of endothelin converting enzyme
|
|
US5869486A
(en)
*
|
1995-02-24 |
1999-02-09 |
Ono Pharmaceutical Co., Ltd. |
Fused pyrimidines and pyriazines as pharmaceutical compounds
|
|
US6262059B1
(en)
|
1995-06-07 |
2001-07-17 |
Cell Pathways, Inc. |
Method of treating a patient having precancerous lesions with quinazoline derivatives
|
|
US6232312B1
(en)
|
1995-06-07 |
2001-05-15 |
Cell Pathways, Inc. |
Method for treating patient having precancerous lesions with a combination of pyrimidopyrimidine derivatives and esters and amides of substituted indenyl acetic acides
|
|
US6046206A
(en)
*
|
1995-06-07 |
2000-04-04 |
Cell Pathways, Inc. |
Method of treating a patient having a precancerous lesions with amide quinazoline derivatives
|
|
US5874440A
(en)
*
|
1995-06-07 |
1999-02-23 |
Cell Pathways, Inc. |
Method of treating a patient having precancerous lesions with phenyl pyrimidinone derivatives
|
|
US6060477A
(en)
*
|
1995-06-07 |
2000-05-09 |
Cell Pathways, Inc. |
Method of treating a patient having precancerous lesions with phenyl cycloamino pyrimidinone derivatives
|
|
US6200980B1
(en)
|
1995-06-07 |
2001-03-13 |
Cell Pathways, Inc. |
Method of treating a patient having precancerous lesions with phenyl purinone derivatives
|
|
US6046216A
(en)
*
|
1995-06-07 |
2000-04-04 |
Cell Pathways, Inc. |
Method of treating a patient having precancerous lesions with phenyl pyridinone derivatives
|
|
TW381092B
(en)
*
|
1995-07-07 |
2000-02-01 |
Otsuka Pharma Co Ltd |
Novel benzimidazole derivatives for use in treating arteriosclerotic diseases
|
|
ES2185750T3
(es)
*
|
1995-08-08 |
2003-05-01 |
Ono Pharmaceutical Co |
Derivados de acido hidroxamico utiles para la inhibicion gelatinasa.
|
|
SK284073B6
(sk)
|
1996-04-12 |
2004-09-08 |
Warner-Lambert Company |
Polycyklické zlúčeniny, ich použitie a farmaceutické kompozície na ich báze
|
|
EP2223920A3
(fr)
*
|
1996-06-19 |
2011-09-28 |
Aventis Pharma Limited |
Composes azabicycliques substitues
|
|
DE19644228A1
(de)
*
|
1996-10-24 |
1998-04-30 |
Merck Patent Gmbh |
Thienopyrimidine
|
|
US6331543B1
(en)
|
1996-11-01 |
2001-12-18 |
Nitromed, Inc. |
Nitrosated and nitrosylated phosphodiesterase inhibitors, compositions and methods of use
|
|
US5958926A
(en)
*
|
1996-11-01 |
1999-09-28 |
Nitromed, Inc. |
Nitrosated and nitrosylated phosphodiesterase inhibitor compounds, compositions and their uses
|
|
CA2238283C
(fr)
|
1997-05-30 |
2002-08-20 |
Cell Pathways, Inc. |
Methode d'identification de composes visant a inhiber les lesions neoplasiques, compositions pharmaceutiques a prtir de ces composes et compositions pour traiter les lesions neoplasiques
|
|
US5858694A
(en)
*
|
1997-05-30 |
1999-01-12 |
Cell Pathways, Inc. |
Method for identifying compounds for inhibition of cancerous lesions
|
|
ZA986729B
(en)
*
|
1997-07-29 |
1999-02-02 |
Warner Lambert Co |
Irreversible inhibitors of tyrosine kinases
|
|
ZA986732B
(en)
*
|
1997-07-29 |
1999-02-02 |
Warner Lambert Co |
Irreversible inhibitiors of tyrosine kinases
|
|
US5852035A
(en)
*
|
1997-12-12 |
1998-12-22 |
Cell Pathways, Inc. |
Method for inhibiting neoplastic cells and related conditions by exposure to substituted N- arylmethyl and heterocyclmethyl-1H-pyrazolo (3,4-B) quinolin-4-amines
|
|
US6410584B1
(en)
|
1998-01-14 |
2002-06-25 |
Cell Pathways, Inc. |
Method for inhibiting neoplastic cells with indole derivatives
|
|
US6046199A
(en)
*
|
1998-01-14 |
2000-04-04 |
Cell Pathways, Inc. |
Method of inhibiting neoplastic cells with tetracyclic pyrido[3,4-B]indole derivatives
|
|
JPH11209350A
(ja)
|
1998-01-26 |
1999-08-03 |
Eisai Co Ltd |
含窒素複素環誘導体およびその医薬
|
|
US5942520A
(en)
*
|
1998-01-27 |
1999-08-24 |
Cell Pathways, Inc. |
Method for inhibiting neoplastic cells by exposure to substituted N-cycloalkylmethyl-1-H-pyrazolo (3,4-B) quinolone-4 amines
|
|
US6150533A
(en)
*
|
1998-04-08 |
2000-11-21 |
American Home Products Corp. |
N-aryloxyethyl-indoly-alkylamines for the treatment of depression
|
|
US5990117A
(en)
*
|
1998-04-15 |
1999-11-23 |
Cell Pathways, Inc. |
Method for inhibiting neoplastic cells and related conditions by exposure to quinazoline derivatives
|
|
CA2337422C
(fr)
*
|
1998-08-18 |
2010-11-02 |
The Regents Of The University Of California |
Inhibition de la production de mucus dans les voies respiratoires par l'administration d'antagonistes d'egf-r
|
|
US6184226B1
(en)
|
1998-08-28 |
2001-02-06 |
Scios Inc. |
Quinazoline derivatives as inhibitors of P-38 α
|
|
US6268372B1
(en)
|
1998-09-11 |
2001-07-31 |
Cell Pathways, Inc. |
Method for inhibiting neoplastic cells and related conditions by exposure to 2,9-disubstituted purin-6-ones
|
|
US6124303A
(en)
*
|
1998-09-11 |
2000-09-26 |
Cell Pathways, Inc. |
Method for inhibiting neoplastic cells and related conditions by exposure to 9-substituted 2-(2-N-aloxyphenyl) purin-6-ones
|
|
JP2000178204A
(ja)
*
|
1998-10-05 |
2000-06-27 |
Eisai Co Ltd |
ホスフォジエステラ―ゼ阻害剤を含有する口腔内速崩壊性錠剤
|
|
CA2346350C
(fr)
*
|
1998-10-05 |
2008-01-08 |
Eisai Co., Ltd. |
Comprimes se delitant rapidement dans la cavite buccale
|
|
US6130053A
(en)
*
|
1999-08-03 |
2000-10-10 |
Cell Pathways, Inc. |
Method for selecting compounds for inhibition of neoplastic lesions
|
|
US6200771B1
(en)
|
1998-10-15 |
2001-03-13 |
Cell Pathways, Inc. |
Method of using a novel phosphodiesterase in pharmaceutical screeing to identify compounds for treatment of neoplasia
|
|
JP2000191518A
(ja)
*
|
1998-10-19 |
2000-07-11 |
Eisai Co Ltd |
溶解性の改善された口腔内速崩壊性錠剤
|
|
US6133271A
(en)
*
|
1998-11-19 |
2000-10-17 |
Cell Pathways, Inc. |
Method for inhibiting neoplastic cells and related conditions by exposure thienopyrimidine derivatives
|
|
US6187779B1
(en)
|
1998-11-20 |
2001-02-13 |
Cell Pathways, Inc. |
Method for inhibiting neoplastic cells and related conditions by exposure to 2,8-disubstituted quinazoline derivatives
|
|
US6369092B1
(en)
|
1998-11-23 |
2002-04-09 |
Cell Pathways, Inc. |
Method for treating neoplasia by exposure to substituted benzimidazole derivatives
|
|
US6077842A
(en)
*
|
1998-11-24 |
2000-06-20 |
Cell Pathways, Inc. |
Method of inhibiting neoplastic cells with pyrazolopyridylpyridazinone derivatives
|
|
US6034099A
(en)
*
|
1998-11-24 |
2000-03-07 |
Cell Pathways, Inc. |
Method for inhibiting neoplastic lesions by administering 4-(arylmethylene)- 2, 3- dihydro-pyrazol-3-ones
|
|
US6486155B1
(en)
|
1998-11-24 |
2002-11-26 |
Cell Pathways Inc |
Method of inhibiting neoplastic cells with isoquinoline derivatives
|
|
US6130333A
(en)
*
|
1998-11-27 |
2000-10-10 |
Monsanto Company |
Bicyclic imidazolyl derivatives as phosphodiesterase inhibitors, pharmaceutical compositions and method of use
|
|
US6025394A
(en)
|
1999-01-29 |
2000-02-15 |
Cell Pathways, Inc. |
Method for treating patients with acne by administering substituted sulfonyl indenyl acetic acids, amides and alcohols
|
|
US6020379A
(en)
*
|
1999-02-19 |
2000-02-01 |
Cell Pathways, Inc. |
Position 7 substituted indenyl-3-acetic acid derivatives and amides thereof for the treatment of neoplasia
|
|
US6080747A
(en)
|
1999-03-05 |
2000-06-27 |
Hughes Institute |
JAK-3 inhibitors for treating allergic disorders
|
|
CA2412345A1
(fr)
|
1999-06-16 |
2000-12-21 |
University Of Iowa Research Foundation |
Antagonisme des oligonucleotides cpg immunostimulateurs par des 4-aminoquinolines et autres bases faibles
|
|
US7235625B2
(en)
|
1999-06-29 |
2007-06-26 |
Palatin Technologies, Inc. |
Multiple agent therapy for sexual dysfunction
|
|
AU5636900A
(en)
|
1999-06-30 |
2001-01-31 |
Merck & Co., Inc. |
Src kinase inhibitor compounds
|
|
WO2001000207A1
(fr)
|
1999-06-30 |
2001-01-04 |
Merck & Co., Inc. |
Composes inhibiteurs de la src kinase
|
|
JP2003503354A
(ja)
|
1999-06-30 |
2003-01-28 |
メルク エンド カムパニー インコーポレーテッド |
Srcキナーゼ阻害剤化合物
|
|
WO2001012608A1
(fr)
*
|
1999-08-18 |
2001-02-22 |
Nippon Soda Co., Ltd. |
Composes de quinoline et procede de preparation desdits composes
|
|
IL139073A0
(en)
*
|
1999-10-21 |
2001-11-25 |
Pfizer |
Treatment of neuropathy
|
|
AU1071301A
(en)
*
|
1999-11-01 |
2001-05-14 |
Eli Lilly And Company |
Pharmaceutical compounds
|
|
HN2000000203A
(es)
*
|
1999-11-30 |
2001-06-13 |
Pfizer Prod Inc |
Procedimiento para la obtencion de 1,2,3,4-tetrahidroquinolinas 4-carboxiamino-2- sustituidas.
|
|
US6555547B1
(en)
|
2000-02-28 |
2003-04-29 |
Cell Pathways, Inc. |
Method for treating a patient with neoplasia by treatment with a vinca alkaloid derivative
|
|
US6569638B1
(en)
|
2000-03-03 |
2003-05-27 |
Cell Pathways, Inc |
Method for screening compounds for the treatment of neoplasia
|
|
ATE449084T1
(de)
|
2000-03-31 |
2009-12-15 |
Nippon Shinyaku Co Ltd |
Derivate von heterocyclen und arzneistoffe
|
|
UA73993C2
(uk)
*
|
2000-06-06 |
2005-10-17 |
Астразенека Аб |
Хіназолінові похідні для лікування пухлин та фармацевтична композиція
|
|
US6448281B1
(en)
|
2000-07-06 |
2002-09-10 |
Boehringer Ingelheim (Canada) Ltd. |
Viral polymerase inhibitors
|
|
US20020165237A1
(en)
*
|
2000-08-11 |
2002-11-07 |
Fryburg David Albert |
Treatment of the insulin resistance syndrome
|
|
KR100821446B1
(ko)
*
|
2000-08-21 |
2008-04-10 |
아스트라제네카 아베 |
퀴나졸린 유도체
|
|
US20020065286A1
(en)
*
|
2000-08-21 |
2002-05-30 |
Davies Michael John |
Treatment of wounds
|
|
US6576644B2
(en)
*
|
2000-09-06 |
2003-06-10 |
Bristol-Myers Squibb Co. |
Quinoline inhibitors of cGMP phosphodiesterase
|
|
US6548508B2
(en)
|
2000-10-20 |
2003-04-15 |
Pfizer, Inc. |
Use of PDE V inhibitors for improved fecundity in mammals
|
|
US6828473B2
(en)
|
2000-11-01 |
2004-12-07 |
Pfizer Inc. |
Modulation of PDE11A activity
|
|
EP1211313A3
(fr)
*
|
2000-11-01 |
2003-04-23 |
Pfizer Limited |
Modulation de l'activité PDE11A activity
|
|
US20020091129A1
(en)
*
|
2000-11-20 |
2002-07-11 |
Mitradev Boolell |
Treatment of premature ejaculation
|
|
MXPA03007623A
(es)
*
|
2001-02-26 |
2003-12-04 |
Tanabe Seiyaku Co |
Derivado de piridopirimidina o naftiridina.
|
|
EP1371376A4
(fr)
*
|
2001-03-19 |
2009-03-25 |
Nippon Shinyaku Co Ltd |
Antiprurigineux
|
|
DE60229046D1
(de)
*
|
2001-04-19 |
2008-11-06 |
Astrazeneca Ab |
Chinazolin derivate
|
|
MXPA03009925A
(es)
*
|
2001-04-30 |
2004-06-30 |
Bayer Pharmaceuticals Corp |
Nuevas tiofeno [2,3-d]pirimidinas 4-amino-5,6-sustituidas.
|
|
US7030150B2
(en)
*
|
2001-05-11 |
2006-04-18 |
Trimeris, Inc. |
Benzimidazole compounds and antiviral uses thereof
|
|
PE20030008A1
(es)
*
|
2001-06-19 |
2003-01-22 |
Bristol Myers Squibb Co |
Inhibidores duales de pde 7 y pde 4
|
|
WO2003000011A2
(fr)
*
|
2001-06-21 |
2003-01-03 |
Ariad Pharmaceuticals, Inc. |
Nouvelles pyridopyrimidines et leur utilisation
|
|
ATE341545T1
(de)
*
|
2001-07-16 |
2006-10-15 |
Astrazeneca Ab |
Quinolin-derivate und ihre verwendung als inhibitoren der tyrosine kinase
|
|
EP2335700A1
(fr)
|
2001-07-25 |
2011-06-22 |
Boehringer Ingelheim (Canada) Ltd. |
Inhibiteurs de la polymerase du virus hepatitis C avec une structure heterobicylic
|
|
EP1312363A1
(fr)
*
|
2001-09-28 |
2003-05-21 |
Pfizer Products Inc. |
Méthode de traitement et kit comprenant un secrétagogue d'hormone de croissance
|
|
GB0128122D0
(en)
*
|
2001-11-23 |
2002-01-16 |
Astrazeneca Ab |
Therapeutic use
|
|
GB0129274D0
(en)
*
|
2001-12-06 |
2002-01-23 |
Pfizer Ltd |
Novel kit
|
|
US7565683B1
(en)
|
2001-12-12 |
2009-07-21 |
Weiqing Huang |
Method and system for implementing changes to security policies in a distributed security system
|
|
US7921284B1
(en)
|
2001-12-12 |
2011-04-05 |
Gary Mark Kinghorn |
Method and system for protecting electronic data in enterprise environment
|
|
US7921288B1
(en)
|
2001-12-12 |
2011-04-05 |
Hildebrand Hal S |
System and method for providing different levels of key security for controlling access to secured items
|
|
US8006280B1
(en)
|
2001-12-12 |
2011-08-23 |
Hildebrand Hal S |
Security system for generating keys from access rules in a decentralized manner and methods therefor
|
|
US10033700B2
(en)
|
2001-12-12 |
2018-07-24 |
Intellectual Ventures I Llc |
Dynamic evaluation of access rights
|
|
US7380120B1
(en)
|
2001-12-12 |
2008-05-27 |
Guardian Data Storage, Llc |
Secured data format for access control
|
|
US7178033B1
(en)
|
2001-12-12 |
2007-02-13 |
Pss Systems, Inc. |
Method and apparatus for securing digital assets
|
|
GB0130219D0
(en)
*
|
2001-12-18 |
2002-02-06 |
Pfizer Ltd |
Compounds for the treatment of sexual dysfunction
|
|
WO2003055866A1
(fr)
*
|
2001-12-21 |
2003-07-10 |
Bayer Pharmaceuticals Corporation |
Composes derives de quinazoline et de quinoline servant d'inhibiteurs de prolylpeptidase, d'inducteurs d'apoptose et d'agents therapeutiques anticancereux
|
|
US8176334B2
(en)
|
2002-09-30 |
2012-05-08 |
Guardian Data Storage, Llc |
Document security system that permits external users to gain access to secured files
|
|
US7342884B2
(en)
*
|
2002-03-13 |
2008-03-11 |
Harmonic, Inc. |
Method and apparatus for one directional communications in bidirectional communications channel
|
|
US7893101B2
(en)
|
2002-03-20 |
2011-02-22 |
Celgene Corporation |
Solid forms comprising (+)-2-[1-(3-ethoxy-4-methoxyphenyl)-2-methylsulfonylethyl]-4-acetylaminoisoindoline-1,3-dione, compositions thereof, and uses thereof
|
|
US7208516B2
(en)
|
2002-03-20 |
2007-04-24 |
Celgene Corporation |
Methods of the treatment of psoriatic arthritis using (+)-2-[1-(3-ethoxy-4-methoxyphenyl)-2-methylsulfonylethyl]-4-acetylaminoisoindoline-1,3-dione
|
|
US6962940B2
(en)
|
2002-03-20 |
2005-11-08 |
Celgene Corporation |
(+)-2-[1-(3-Ethoxy-4-methoxyphenyl)-2-methylsulfonylethyl]-4-acetylaminoisoindoline-1,3-dione: methods of using and compositions thereof
|
|
US7276529B2
(en)
|
2002-03-20 |
2007-10-02 |
Celgene Corporation |
Methods of the treatment or prevention of exercise-induced asthma using (+)-2-[1-(3-ethoxy-4-methoxyphenyl)-2-methylsulfonylethyl]-4-acetylaminoisoindoline-1,3-dione
|
|
TW200813014A
(en)
|
2002-03-28 |
2008-03-16 |
Astrazeneca Ab |
Quinazoline derivatives
|
|
US6924285B2
(en)
|
2002-03-30 |
2005-08-02 |
Boehringer Ingelheim Pharma Gmbh & Co. |
Bicyclic heterocyclic compounds, pharmaceutical compositions containing these compounds, their use and process for preparing them
|
|
US7049333B2
(en)
*
|
2002-06-04 |
2006-05-23 |
Sanofi-Aventis Deutschland Gmbh |
Substituted thiophenes: compositions, processes of making, and uses in disease treatment and diagnosis
|
|
US7504408B2
(en)
|
2002-07-09 |
2009-03-17 |
Astrazeneca Ab |
Quinzoline derivatives for use in the treatment of cancer
|
|
GB0215823D0
(en)
|
2002-07-09 |
2002-08-14 |
Astrazeneca Ab |
Quinazoline derivatives
|
|
GB0219961D0
(en)
|
2002-08-28 |
2002-10-02 |
Pfizer Ltd |
Oxytocin inhibitors
|
|
DE10256405A1
(de)
*
|
2002-12-02 |
2004-06-17 |
Morphochem Aktiengesellschaft für kombinatorische Chemie |
Neue Verbindungen, die Topoisomerase IV inhibieren
|
|
US7250514B1
(en)
|
2002-10-21 |
2007-07-31 |
Takeda San Diego, Inc. |
Histone deacetylase inhibitors
|
|
GB0225579D0
(en)
|
2002-11-02 |
2002-12-11 |
Astrazeneca Ab |
Chemical compounds
|
|
CA2503371C
(fr)
|
2002-11-04 |
2011-01-11 |
Astrazeneca Ab |
Derives de quinazoline utilises comme inhibiteurs de src tyrosine kinase
|
|
US7323462B2
(en)
*
|
2002-12-10 |
2008-01-29 |
Pfizer Inc. |
Morpholine dopamine agonists
|
|
JP2006511606A
(ja)
|
2002-12-13 |
2006-04-06 |
ワーナー−ランバート・カンパニー、リミテッド、ライアビリティ、カンパニー |
下部尿路症状を治療するα−2−δリガンド
|
|
US7429597B2
(en)
*
|
2002-12-23 |
2008-09-30 |
Boehringer Ingelheim Pharma Gmbh & Co., Kg |
Substituted nitrogen-containing heterobicycles, the preparation thereof and their use as pharmaceutical compositions
|
|
US7772188B2
(en)
|
2003-01-28 |
2010-08-10 |
Ironwood Pharmaceuticals, Inc. |
Methods and compositions for the treatment of gastrointestinal disorders
|
|
PA8597401A1
(es)
*
|
2003-03-14 |
2005-05-24 |
Pfizer |
Derivados del acido 3-(1-[3-(1,3-benzotiazol-6-il) propilcarbamoil] cicloalquil) propanoico como inhibidores de nep
|
|
US20040186046A1
(en)
*
|
2003-03-17 |
2004-09-23 |
Pfizer Inc |
Treatment of type 1 diabetes with PDE5 inhibitors
|
|
GB0307333D0
(en)
*
|
2003-03-29 |
2003-05-07 |
Astrazeneca Ab |
Therapeutic agent
|
|
AU2004226353A1
(en)
|
2003-04-01 |
2004-10-14 |
Laboratoires Serono Sa |
Inhibitors of phosphodiesterases in infertility
|
|
GB0309850D0
(en)
|
2003-04-30 |
2003-06-04 |
Astrazeneca Ab |
Quinazoline derivatives
|
|
US20050065158A1
(en)
*
|
2003-07-16 |
2005-03-24 |
Pfizer Inc. |
Treatment of sexual dysfunction
|
|
GB0317665D0
(en)
|
2003-07-29 |
2003-09-03 |
Astrazeneca Ab |
Qinazoline derivatives
|
|
US20060276647A1
(en)
|
2003-07-30 |
2006-12-07 |
Ube Industries, Ltd |
Process for producing 6, 7-bis (2-methoxyethoxy)-quinazolin-4-one
|
|
US8318752B2
(en)
|
2003-09-19 |
2012-11-27 |
Astrazeneca Ab |
4-(3-chloro-2-fluoroanilino)-7-methoxy-6-{[1-(N-methylcarbamoyl-methyl)piperidin-4-yl]oxy}quinazoline, its pharmaceutically acceptable salts, and pharmaceutical compositions comprising the same
|
|
US7291640B2
(en)
*
|
2003-09-22 |
2007-11-06 |
Pfizer Inc. |
Substituted triazole derivatives as oxytocin antagonists
|
|
RU2006124843A
(ru)
|
2003-12-12 |
2008-01-20 |
Уайт (Us) |
Хинолины, пригодные для лечения сердечно-сосудистого заболевания
|
|
WO2005079808A1
(fr)
|
2004-01-22 |
2005-09-01 |
Pfizer Limited |
Derives de triazole inhibant l'activite antagoniste de la vasopressine
|
|
US7649002B2
(en)
|
2004-02-04 |
2010-01-19 |
Pfizer Inc |
(3,5-dimethylpiperidin-1yl)(4-phenylpyrrolidin-3-yl)methanone derivatives as MCR4 agonists
|
|
EP1723134A2
(fr)
*
|
2004-02-18 |
2006-11-22 |
Pfizer Products Incorporated |
Derives tetrahydroisoquinolinyliques de quinazoline et d'isoquinoline
|
|
TWI368508B
(en)
|
2004-02-20 |
2012-07-21 |
Boehringer Ingelheim Int |
Viral polymerase inhibitors
|
|
US20070225308A1
(en)
*
|
2004-03-15 |
2007-09-27 |
Kyowa Hakko Kogyo Co.,Ltd. |
2-Amino Quinazoline Derivative
|
|
CA2584507C
(fr)
*
|
2004-10-20 |
2016-04-26 |
Resverlogix Corp. |
Flavanoides et isoflavanoides pour la prevention et le traitement de maladies cardio-vasculaires
|
|
EP1844023A1
(fr)
*
|
2004-12-31 |
2007-10-17 |
Sk Chemicals Co., Ltd. |
Dérivés de quinazoline pour le traitement prophylactique et thérapeutique du diabète et de l'obésité
|
|
CA2592986C
(fr)
*
|
2005-01-07 |
2011-02-15 |
Pfizer Products Inc. |
Composes heteroaromatiques a base de quinoline
|
|
JP5054544B2
(ja)
|
2005-02-26 |
2012-10-24 |
アストラゼネカ アクチボラグ |
チロシンキナーゼ阻害剤としてのキナゾリン誘導体
|
|
US8252806B2
(en)
*
|
2005-03-14 |
2012-08-28 |
Neurosearch A/S |
Potassium channel modulating agents and their medical use
|
|
WO2006100557A1
(fr)
|
2005-03-21 |
2006-09-28 |
Pfizer Limited |
Derives de triazole substitues en tant qu'antagonistes d'oxytocine
|
|
EP1878727A4
(fr)
|
2005-04-28 |
2013-11-13 |
Kyowa Hakko Kirin Co Ltd |
Dérivés de 2-aminoquinazoline
|
|
JP4769866B2
(ja)
*
|
2005-06-27 |
2011-09-07 |
エフ.ホフマン−ラ ロシュ アーゲー |
クロロ置換グアニジン
|
|
US20070010525A1
(en)
*
|
2005-06-27 |
2007-01-11 |
Meyer Jackson |
Method and compositions for modulating neuropeptide hormone secretion
|
|
AU2006263925A1
(en)
*
|
2005-06-27 |
2007-01-04 |
F. Hoffmann-La Roche Ag |
8-alkoxy-4-methyl-3, 4-dihydro-quinazolin-2-yl amines and their use as 5-HT5A receptor ligands
|
|
EP2314295B1
(fr)
|
2005-07-29 |
2015-01-28 |
Resverlogix, Inc |
Compositions pharmaceutiques pour la prevention et le traitement de maladies complexes et leur administration par des dispositifs medicaux inserables
|
|
US20100222365A1
(en)
*
|
2005-08-10 |
2010-09-02 |
Pfizer Inc |
Substituted triazole deriviatives as oxytocin antagonists
|
|
WO2007025177A2
(fr)
|
2005-08-26 |
2007-03-01 |
Braincells, Inc. |
Neurogenese par modulation du recepteur muscarinique
|
|
EP2258359A3
(fr)
|
2005-08-26 |
2011-04-06 |
Braincells, Inc. |
Neurogenèse par modulation des récepteurs muscariniques avec sabcomeline
|
|
EP2377530A3
(fr)
|
2005-10-21 |
2012-06-20 |
Braincells, Inc. |
Modulation de neurogénèse par inhibition PDE
|
|
EP1942879A1
(fr)
|
2005-10-31 |
2008-07-16 |
Braincells, Inc. |
Modulation de la neurogenese dont la mediation est assuree par recepteur gaba
|
|
GB0601951D0
(en)
|
2006-01-31 |
2006-03-15 |
Novartis Ag |
Organic compounds
|
|
EP1996587A1
(fr)
*
|
2006-02-23 |
2008-12-03 |
Pfizer Products Incorporated |
Quinazolines substituées en tant qu'inhibiteurs de pde10
|
|
US20090099175A1
(en)
*
|
2006-03-01 |
2009-04-16 |
Arrington Mark P |
Phosphodiesterase 10 inhibitors
|
|
US20100216734A1
(en)
|
2006-03-08 |
2010-08-26 |
Braincells, Inc. |
Modulation of neurogenesis by nootropic agents
|
|
JP2009535394A
(ja)
*
|
2006-05-02 |
2009-10-01 |
ファイザー・プロダクツ・インク |
Pde10阻害剤としての二環式ヘテロアリール化合物
|
|
EP2021000A2
(fr)
|
2006-05-09 |
2009-02-11 |
Braincells, Inc. |
Neurogenèse par modulation de l'angiotensine
|
|
KR20080015594A
(ko)
*
|
2006-08-16 |
2008-02-20 |
주식회사종근당 |
포스포디에스테라제 저해제로서 유용한 퀴나졸린 유도체 및그 제조방법
|
|
US20100184806A1
(en)
|
2006-09-19 |
2010-07-22 |
Braincells, Inc. |
Modulation of neurogenesis by ppar agents
|
|
US7786139B2
(en)
|
2006-11-21 |
2010-08-31 |
Omeros Corporation |
PDE10 inhibitors and related compositions and methods
|
|
CA2676984C
(fr)
|
2007-02-01 |
2015-03-17 |
Resverlogix Corp. |
Composes destines a la prevention et au traitement de maladies cardiovasculaires
|
|
CN101687818B
(zh)
*
|
2007-02-19 |
2012-08-22 |
卫材R&D管理有限公司 |
甲基n-[3-(6,7-二甲氧基-2-甲氨基喹唑啉-4-基)苯基]对氨羰基苯甲酸的结晶、无定形物或盐
|
|
AU2008261102B2
(en)
|
2007-06-04 |
2013-11-28 |
Bausch Health Ireland Limited |
Agonists of guanylate cyclase useful for the treatment of gastrointestinal disorders, inflammation, cancer and other disorders
|
|
US20100120694A1
(en)
|
2008-06-04 |
2010-05-13 |
Synergy Pharmaceuticals, Inc. |
Agonists of Guanylate Cyclase Useful for the Treatment of Gastrointestinal Disorders, Inflammation, Cancer and Other Disorders
|
|
US8969514B2
(en)
|
2007-06-04 |
2015-03-03 |
Synergy Pharmaceuticals, Inc. |
Agonists of guanylate cyclase useful for the treatment of hypercholesterolemia, atherosclerosis, coronary heart disease, gallstone, obesity and other cardiovascular diseases
|
|
US7928111B2
(en)
|
2007-06-08 |
2011-04-19 |
Senomyx, Inc. |
Compounds including substituted thienopyrimidinone derivatives as ligands for modulating chemosensory receptors
|
|
US9603848B2
(en)
|
2007-06-08 |
2017-03-28 |
Senomyx, Inc. |
Modulation of chemosensory receptors and ligands associated therewith
|
|
CN101878203A
(zh)
*
|
2007-10-29 |
2010-11-03 |
纳科法尔马有限公司 |
作为抗癌剂的新的4-(四唑-5-基)喹唑啉衍生物
|
|
WO2009100438A2
(fr)
|
2008-02-07 |
2009-08-13 |
Massachusetts Eye & Ear Infirmary |
Composés stimulant l’expression du gène atoh-1
|
|
US20110039845A1
(en)
|
2008-04-23 |
2011-02-17 |
Kyowa Hakko Kirin Co., Ltd. |
2-aminoquinazoline derivative
|
|
MY183041A
(en)
|
2008-05-13 |
2021-02-08 |
Astrazeneca Ab |
Fumarate salt of 4- (3-chloro-2-fluoroanilino) -7-methoxy-6- {[1- (n-methylcarbamoylmethyl) piperidin- 4-yl] oxy}quinazoline
|
|
CA2711103C
(fr)
|
2008-06-26 |
2016-08-09 |
Resverlogix Corp. |
Procedes de preparation de derives de quinazolinone
|
|
ES2624828T3
(es)
|
2008-07-16 |
2017-07-17 |
Synergy Pharmaceuticals Inc. |
Agonistas de la guanilato ciclasa útiles para el tratamiento de trastornos gastrointestinales, inflamación, cáncer y otros
|
|
CA2993967A1
(fr)
|
2008-07-31 |
2010-02-04 |
Senomyx, Inc. |
Procedes et intermediaires pour la realisation d'exhausteurs de gout sucre
|
|
EP2310016B1
(fr)
*
|
2008-08-05 |
2017-10-04 |
Omeros Corporation |
Inhibiteurs de pde10 et compositions et procédés associés
|
|
CN102361857B
(zh)
|
2008-09-26 |
2015-09-16 |
默沙东公司 |
可用作抗糖尿病剂的环状苯并咪唑衍生物
|
|
MX2011004258A
(es)
|
2008-10-22 |
2011-06-01 |
Merck Sharp & Dohme |
Derivados de bencimidazol ciclicos novedosos utiles como agentes anti-diabeticos.
|
|
JP2012507530A
(ja)
|
2008-10-29 |
2012-03-29 |
メルク・シャープ・エンド・ドーム・コーポレイション |
有用な抗糖尿病剤である新規な環状ベンズイミダゾール誘導体
|
|
JP5557845B2
(ja)
|
2008-10-31 |
2014-07-23 |
メルク・シャープ・アンド・ドーム・コーポレーション |
糖尿病用剤として有用な新規環状ベンゾイミダゾール誘導体
|
|
EP2379076B1
(fr)
|
2008-12-23 |
2014-11-12 |
The Trustees of Columbia University in the City of New York |
Inhibiteurs de la phosphodiestérase et utilisations de ces derniers
|
|
AU2010204106B2
(en)
|
2009-01-08 |
2014-05-08 |
Resverlogix Corp. |
Compounds for the prevention and treatment of cardiovascular disease
|
|
WO2010099217A1
(fr)
|
2009-02-25 |
2010-09-02 |
Braincells, Inc. |
Modulation de neurogenèse à l'aide de combinaisons de d-cyclosérine
|
|
GB0903493D0
(en)
|
2009-02-27 |
2009-04-08 |
Vantia Ltd |
New compounds
|
|
WO2010106436A2
(fr)
|
2009-03-18 |
2010-09-23 |
Resverlogix Corp. |
Nouveaux agents anti-inflammatoires
|
|
AU2010239266B2
(en)
|
2009-04-22 |
2015-01-22 |
Resverlogix Corp. |
Novel anti-inflammatory agents
|
|
PH12012500097A1
(en)
*
|
2009-07-21 |
2011-01-27 |
Shanghai Inst Organic Chem |
Potent small molecule inhibitors of autophagy, and methods of use thereof
|
|
AU2010314891A1
(en)
|
2009-11-06 |
2012-06-07 |
Vanderbilt University |
Aryl and heteroaryl sulfones as MGLUR4 allosteric potentiators, compositions, and methods of treating neurological dysfunction
|
|
WO2011081915A2
(fr)
*
|
2009-12-15 |
2011-07-07 |
Cebix Inc. |
Procédés pour traiter un dysfonctionnement érectile chez des patients souffrant de diabète insulino-dépendant
|
|
CA2786314A1
(fr)
|
2010-02-25 |
2011-09-01 |
Merck Sharp & Dohme Corp. |
Nouveaux derives benzimidazole cycliques utiles comme agents antidiabetiques
|
|
DK2544679T3
(da)
|
2010-03-12 |
2019-07-22 |
Omeros Corp |
Pde10-inhibitorer og relaterede sammensætninger og fremgangsmåder
|
|
US9616097B2
(en)
|
2010-09-15 |
2017-04-11 |
Synergy Pharmaceuticals, Inc. |
Formulations of guanylate cyclase C agonists and methods of use
|
|
CN103249732B
(zh)
*
|
2010-10-08 |
2016-08-10 |
生物区欧洲有限公司 |
抑制2-乙基氨甲酰氨基-1,3-苯并噻唑-5-基的细菌拓扑异构酶ii
|
|
EP2677869B1
(fr)
|
2011-02-25 |
2017-11-08 |
Merck Sharp & Dohme Corp. |
Nouveaux dérivés d'azabenzimidazole cyclique utiles en tant qu'agents antidiabétiques
|
|
KR102034748B1
(ko)
|
2011-03-01 |
2019-10-21 |
시너지 파마슈티컬즈 인코포레이티드 |
구아닐레이트 사이클라제 c 작용제의 제조 방법
|
|
EA023998B1
(ru)
|
2011-03-04 |
2016-08-31 |
Глэксосмитклайн Интеллекчуал Проперти Дивелопмент Лимитед |
Аминохинолины в качестве ингибиторов киназ
|
|
US8592423B2
(en)
|
2011-06-21 |
2013-11-26 |
Bristol-Myers Squibb Company |
Inhibitors of PDE10
|
|
US8975276B2
(en)
|
2011-06-29 |
2015-03-10 |
Bristol-Myers Squibb Company |
Inhibitors of PDE10
|
|
TWI547494B
(zh)
|
2011-08-18 |
2016-09-01 |
葛蘭素史克智慧財產發展有限公司 |
作為激酶抑制劑之胺基喹唑啉類
|
|
CA2851996C
(fr)
|
2011-11-01 |
2020-01-07 |
Resverlogix Corp. |
Compositions pharmaceutiques pour des quinazolinones substituees
|
|
US9402877B2
(en)
|
2011-11-04 |
2016-08-02 |
Xion Pharmaceuticals Corporation |
Methods and compositions for oral administration of melanocortin receptor agonist compounds
|
|
US20150119399A1
(en)
|
2012-01-10 |
2015-04-30 |
President And Fellows Of Harvard College |
Beta-cell replication promoting compounds and methods of their use
|
|
WO2013109738A1
(fr)
|
2012-01-17 |
2013-07-25 |
The Trustees Of Columbia University In The City Of New York |
Nouveaux inhibiteurs de la phosphodiestérase et utilisations de ceux-ci
|
|
WO2013143057A1
(fr)
*
|
2012-03-26 |
2013-10-03 |
中国科学院福建物质结构研究所 |
Dérivé de quinazoline et son application
|
|
CA2880901A1
(fr)
|
2012-08-02 |
2014-02-06 |
Merck Sharp & Dohme Corp. |
Composes tricycliques antidiabetiques
|
|
KR20200028050A
(ko)
|
2012-08-06 |
2020-03-13 |
피르메니히 인코포레이티드 |
단맛 향미 개질제
|
|
CN104718004A
(zh)
|
2012-08-22 |
2015-06-17 |
默沙东公司 |
新的氮杂苯并咪唑六氢呋喃并[3,2-b]呋喃衍生物
|
|
WO2014031465A1
(fr)
|
2012-08-22 |
2014-02-27 |
Merck Sharp & Dohme Corp. |
Nouveaux dérivés d'azabenzimidazole tétrahydropyrane
|
|
EP2888008B1
(fr)
|
2012-08-22 |
2018-12-26 |
Merck Sharp & Dohme Corp. |
Nouveaux dérivés d'azabenzimidazole tétrahydrofurane
|
|
WO2014031441A1
(fr)
|
2012-08-22 |
2014-02-27 |
Merck Sharp & Dohme Corp. |
Nouveaux dérivés de benzimidazole tétrahydrofurane utiles en tant qu'activateurs de la protéine kinase activée par l'amp
|
|
EP2906040B1
(fr)
|
2012-08-22 |
2021-02-17 |
Merck Sharp & Dohme Corp. |
Nouveaux dérivés de benzimidazole tétrahydropyrane
|
|
US9556193B2
(en)
|
2012-08-22 |
2017-01-31 |
Merck Shapr & Dohme Corp. |
Benzimidazole hexahydrofuro[3,2-b]furan derivatives
|
|
US20150246888A1
(en)
*
|
2012-09-11 |
2015-09-03 |
Michael Johnson |
Enoyl reductase inhibitors with antibacterial activity
|
|
AR092529A1
(es)
|
2012-09-13 |
2015-04-22 |
Glaxosmithkline Llc |
Compuesto de aminoquinazolina, composicion farmaceutica que lo comprende y uso de dicho compuesto para la preparacion de un medicamento
|
|
WO2014080290A2
(fr)
|
2012-11-21 |
2014-05-30 |
Rvx Therapeutics Inc. |
Amines cycliques servant d'inhibiteurs de bromodomaines
|
|
WO2014080291A2
(fr)
|
2012-11-21 |
2014-05-30 |
Rvx Therapeutics Inc. |
Dérivés biaryle servant d'inhibiteurs de bromodomaines
|
|
US9271978B2
(en)
|
2012-12-21 |
2016-03-01 |
Zenith Epigenetics Corp. |
Heterocyclic compounds as bromodomain inhibitors
|
|
CA2896731A1
(fr)
*
|
2012-12-28 |
2014-07-03 |
The United States Of America, As Represented By The Secretary, Department Of Health And Human Services |
Inhibiteurs du complexe usp1/uaf1 desubiquitinase et leurs utilisations
|
|
JO3155B1
(ar)
|
2013-02-19 |
2017-09-20 |
Senomyx Inc |
معدِّل نكهة حلوة
|
|
WO2014128622A1
(fr)
|
2013-02-21 |
2014-08-28 |
Glaxosmithkline Intellectual Property Development Limited |
Quinazolines en tant qu'inhibiteurs de kinase
|
|
US9545446B2
(en)
|
2013-02-25 |
2017-01-17 |
Synergy Pharmaceuticals, Inc. |
Agonists of guanylate cyclase and their uses
|
|
EP2970119B1
(fr)
|
2013-03-14 |
2021-11-03 |
Merck Sharp & Dohme Corp. |
Nouveaux dérivés d'indole utiles en tant qu'agents antidiabétiques
|
|
HK1220611A1
(zh)
|
2013-03-15 |
2017-05-12 |
Bausch Health Ireland Limited |
用於治疗胃肠道病症的组成物
|
|
US9708367B2
(en)
|
2013-03-15 |
2017-07-18 |
Synergy Pharmaceuticals, Inc. |
Agonists of guanylate cyclase and their uses
|
|
EP3004138B1
(fr)
|
2013-06-05 |
2024-03-13 |
Bausch Health Ireland Limited |
Agonistes ultra-purs de guanylate cyclase c, leur procédé de production et d'utilisation
|
|
EP3022205B1
(fr)
|
2013-07-17 |
2020-02-05 |
The Trustees of Columbia University in the City of New York |
Nouveaux inhibiteurs de la phosphodiestérase et utilisations de ceux-ci
|
|
JP6694385B2
(ja)
|
2013-08-09 |
2020-05-13 |
アーデリクス,インコーポレーテッド |
リン酸塩輸送阻害のための化合物及び方法
|
|
WO2015051496A1
(fr)
|
2013-10-08 |
2015-04-16 |
Merck Sharp & Dohme Corp. |
Composés tricycliques antidiabétiques
|
|
ES2747973T3
(es)
|
2013-11-15 |
2020-03-12 |
Merck Sharp & Dohme |
Compuestos tricíclicos antidiabéticos
|
|
WO2015089809A1
(fr)
|
2013-12-19 |
2015-06-25 |
Merck Sharp & Dohme Corp. |
Composés hétéroaryles substitués antidiabétiques
|
|
NZ630810A
(en)
|
2014-04-28 |
2016-03-31 |
Omeros Corp |
Processes and intermediates for the preparation of a pde10 inhibitor
|
|
NZ716462A
(en)
|
2014-04-28 |
2017-11-24 |
Omeros Corp |
Optically active pde10 inhibitor
|
|
WO2015200177A1
(fr)
|
2014-06-23 |
2015-12-30 |
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|
|
CU20180011A7
(es)
|
2015-03-04 |
2018-06-05 |
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|
|
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(fr)
|
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2016-09-22 |
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|
|
US9879002B2
(en)
|
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|
|
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(es)
|
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|
|
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(fr)
|
2015-11-04 |
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|
|
JP6969800B2
(ja)
*
|
2016-05-04 |
2021-11-24 |
ジェノシアンス ファルマ |
増殖性疾患の治療に使用される置換2,4−ジアミノ−キノリン誘導体
|
|
US10640499B2
(en)
|
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2020-05-05 |
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Toll like receptor modulator compounds
|
|
PL3507276T3
(pl)
|
2016-09-02 |
2022-02-21 |
Gilead Sciences, Inc. |
Związki modulatory receptorów toll-podobnych
|
|
WO2018172250A1
(fr)
|
2017-03-21 |
2018-09-27 |
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2-méthyl-quinazolines
|
|
AR112027A1
(es)
|
2017-06-15 |
2019-09-11 |
Biocryst Pharm Inc |
Inhibidores de alk 2 quinasa que contienen imidazol
|
|
CN107445899A
(zh)
*
|
2017-07-19 |
2017-12-08 |
枣庄学院 |
一种苯并咪唑类化合物及其制备方法
|
|
WO2019201848A1
(fr)
|
2018-04-18 |
2019-10-24 |
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2-méthyl-aza-quinazolines
|
|
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(ja)
|
2018-08-07 |
2024-03-19 |
フィルメニッヒ インコーポレイテッド |
5-置換4-アミノ-1H-ベンゾ[c][1,2,6]チアジアジン2,2-ジオキシド並びにその配合物及び使用
|
|
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(zh)
|
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2022-01-01 |
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類鐸受體調節劑之固體形式
|
|
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(zh)
|
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2022-03-16 |
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|
|
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(zh)
|
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|
|
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(zh)
|
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|
|
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(en)
|
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|
|
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(zh)
|
2020-09-18 |
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|
|
WO2022148879A1
(fr)
*
|
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2022-07-14 |
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|
|
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(fr)
|
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|