LU91225I2 - Plenaxis - Google Patents
PlenaxisInfo
- Publication number
- LU91225I2 LU91225I2 LU91225C LU91225C LU91225I2 LU 91225 I2 LU91225 I2 LU 91225I2 LU 91225 C LU91225 C LU 91225C LU 91225 C LU91225 C LU 91225C LU 91225 I2 LU91225 I2 LU 91225I2
- Authority
- LU
- Luxembourg
- Prior art keywords
- moiety
- peptide compound
- lhrh
- lhrh antagonist
- hydrophilic
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K7/00—Peptides having 5 to 20 amino acids in a fully defined sequence; Derivatives thereof
- C07K7/04—Linear peptides containing only normal peptide links
- C07K7/23—Luteinising hormone-releasing hormone [LHRH]; Related peptides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/08—Drugs for disorders of the urinary system of the prostate
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
- A61P15/16—Masculine contraceptives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
- A61P15/18—Feminine contraceptives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/04—Immunostimulants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P5/00—Drugs for disorders of the endocrine system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P5/00—Drugs for disorders of the endocrine system
- A61P5/02—Drugs for disorders of the endocrine system of the hypothalamic hormones, e.g. TRH, GnRH, CRH, GRH, somatostatin
- A61P5/04—Drugs for disorders of the endocrine system of the hypothalamic hormones, e.g. TRH, GnRH, CRH, GRH, somatostatin for decreasing, blocking or antagonising the activity of the hypothalamic hormones
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
-
- 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S930/00—Peptide or protein sequence
- Y10S930/01—Peptide or protein sequence
- Y10S930/13—Luteinizing hormone-releasing hormone; related peptides
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Endocrinology (AREA)
- Reproductive Health (AREA)
- Immunology (AREA)
- Genetics & Genomics (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Molecular Biology (AREA)
- Biophysics (AREA)
- Biochemistry (AREA)
- Diabetes (AREA)
- Urology & Nephrology (AREA)
- Gynecology & Obstetrics (AREA)
- Peptides Or Proteins (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Steroid Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US08/480,494 US5843901A (en) | 1995-06-07 | 1995-06-07 | LHRH antagonist peptides |
PCT/US1996/009852 WO1996040757A2 (fr) | 1995-06-07 | 1996-06-07 | Peptides antagonistes de la lh-rh |
Publications (1)
Publication Number | Publication Date |
---|---|
LU91225I2 true LU91225I2 (fr) | 2006-05-03 |
Family
ID=23908180
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
LU91225C LU91225I2 (fr) | 1995-06-07 | 2006-03-03 | Plenaxis |
LU91857C LU91857I2 (fr) | 1995-06-07 | 2011-08-22 | Abarelix, optionnellement sous forme de sel pharmaceutiquement acceptable |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
LU91857C LU91857I2 (fr) | 1995-06-07 | 2011-08-22 | Abarelix, optionnellement sous forme de sel pharmaceutiquement acceptable |
Country Status (13)
Country | Link |
---|---|
US (4) | US5843901A (fr) |
EP (2) | EP1188768B1 (fr) |
JP (3) | JP4164125B2 (fr) |
AT (2) | ATE432941T1 (fr) |
AU (1) | AU715399B2 (fr) |
CA (1) | CA2219460C (fr) |
DE (4) | DE69623254T2 (fr) |
DK (2) | DK0794961T3 (fr) |
ES (2) | ES2326861T3 (fr) |
HK (1) | HK1045161B (fr) |
LU (2) | LU91225I2 (fr) |
PT (2) | PT794961E (fr) |
WO (1) | WO1996040757A2 (fr) |
Families Citing this family (109)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
IL117175A (en) * | 1995-02-20 | 2005-11-20 | Sankyo Co | Osteoclastogenesis inhibitory factor protein |
US5843901A (en) * | 1995-06-07 | 1998-12-01 | Advanced Research & Technology Institute | LHRH antagonist peptides |
US5780435A (en) | 1995-12-15 | 1998-07-14 | Praecis Pharmaceuticals Incorporated | Methods for treating prostate cancer with LHRH-R antagonists |
US5968895A (en) | 1996-12-11 | 1999-10-19 | Praecis Pharmaceuticals, Inc. | Pharmaceutical formulations for sustained drug delivery |
EP2371962A3 (fr) | 1996-12-23 | 2011-12-21 | Immunex Corporation | Activateur du récepteur de NF-KAPPA B, récepteur membre de la superfamille des récepteurs de TNF |
US5925730A (en) * | 1997-04-11 | 1999-07-20 | Ferring Bv | GnRH antagonists |
RU2238949C2 (ru) * | 1997-04-15 | 2004-10-27 | Санкио Компани Лимитед | Белок, специфически связывающийся с ингибирующим остеокластогенез фактором (ocif) (варианты), днк его кодирующая (варианты), днк в качестве зонда (варианты), способ получения белка (варианты), способ скрининга вещества (варианты), антитело (варианты), способ получения поликлонального антитела, гибридома (варианты), способ получения моноклонального антитела, способ измерения ocif-связывающего белка, фармацевтическая композиция (варианты) и лекарственное средство (варианты) |
US6316408B1 (en) * | 1997-04-16 | 2001-11-13 | Amgen Inc. | Methods of use for osetoprotegerin binding protein receptors |
RO128635A2 (ro) | 1997-04-16 | 2013-07-30 | Amgen Inc. | Anticorp sau fragment al acestuia care se leagă la opgbp şi utilizarea acestuia, utilizarea unei forme solubile de odar, şi metodă de identificare a unui compus care descreşte activitatea opgbp |
US6217844B1 (en) * | 1998-04-27 | 2001-04-17 | Praecis Pharmaceuticals, Inc. | Methods for detecting lesions in dense breast tissue using LHRH antagonists |
CN1307481A (zh) * | 1998-04-27 | 2001-08-08 | 普雷西斯药品公司 | 用于治疗热潮红和男子女性型乳房的方法 |
US6191115B1 (en) * | 1998-08-12 | 2001-02-20 | Abbott Laboratories | C-terminus modified heptapeptide LHRH analogs |
US6455499B1 (en) * | 1999-02-23 | 2002-09-24 | Indiana University Foundation | Methods for treating disorders associated with LHRH activity |
US6703367B1 (en) * | 1999-04-27 | 2004-03-09 | Praecis Pharmaceuticals Inc. | Methods for treating hot flashes and gynaecomastia |
JP2003506411A (ja) * | 1999-08-09 | 2003-02-18 | トリペップ アクチ ボラゲット | タンパク質重合阻害剤および使用方法 |
CA2349406C (fr) * | 1999-09-03 | 2011-01-11 | Amgen Inc. | Compositions et procedes permettant la prevention ou le traitement du cancer et de la perte osseuse associee au cancer |
US20030103978A1 (en) | 2000-02-23 | 2003-06-05 | Amgen Inc. | Selective binding agents of osteoprotegerin binding protein |
US7109171B2 (en) * | 2000-02-28 | 2006-09-19 | Praecis Pharmaceuticals Inc. | Methods for treating FSH related conditions with GnRH antagonists |
CN100497384C (zh) | 2000-06-30 | 2009-06-10 | 三得利株式会社 | 新颖的促性腺素释放激素、其前体肽及其前体肽的编码基因 |
US6598784B2 (en) * | 2000-12-20 | 2003-07-29 | Meadwestvaco Packaging Syatens, Llc | Beverage carton with strap type carrying handle |
WO2002056903A2 (fr) * | 2001-01-17 | 2002-07-25 | Praecis Pharmaceuticals Inc. | Methodes pour traiter des etats lies aux hormones au moyen d'une combinaison d'antagonistes de la lhrh et de modulateurs selectifs des recepteurs des oestrogenes |
ES2705016T3 (es) | 2001-02-19 | 2019-03-21 | Novartis Int Pharmaceutical Ag | Derivado de rapamicina para el tratamiento de cáncer de pulmón |
BR0209647A (pt) | 2001-05-16 | 2004-07-27 | Novartis Ag | Combinação que compreende n-{5-[4-(4-metil-piperazino-metil)-benzoilamido]-2-metil fenil}-4-(3-piridil)-2-pirimidina-amina e um agente quimioterapêutico |
CA2451187C (fr) | 2001-06-22 | 2012-08-14 | Southern Biosystems, Inc. | Implants coaxiaux a liberation prolongee d'ordre 0 |
ATE464068T1 (de) | 2001-06-26 | 2010-04-15 | Amgen Fremont Inc | Antikörper gegen opgl |
US6593455B2 (en) * | 2001-08-24 | 2003-07-15 | Tripep Ab | Tripeptide amides that block viral infectivity and methods of use thereof |
GB0128510D0 (en) * | 2001-11-28 | 2002-01-23 | Novartis Ag | Organic compounds |
JP4761710B2 (ja) | 2002-04-05 | 2011-08-31 | アムジェン インコーポレイテッド | 選択的opgl経路インヒビターとしてのヒト抗opgl中和抗体 |
NZ560662A (en) | 2002-05-16 | 2009-09-25 | Novartis Ag | Use of EDG receptor binding agents in cancer |
US6861236B2 (en) | 2002-05-24 | 2005-03-01 | Applied Nanosystems B.V. | Export and modification of (poly)peptides in the lantibiotic way |
EP2662087A1 (fr) | 2003-04-22 | 2013-11-13 | Ipsen Pharma | Vecteurs de somatostatine |
GB0320806D0 (en) | 2003-09-05 | 2003-10-08 | Astrazeneca Ab | Therapeutic treatment |
JP4407322B2 (ja) * | 2004-03-09 | 2010-02-03 | 味の素株式会社 | ペプチドの製造方法 |
KR20080083220A (ko) | 2004-04-07 | 2008-09-16 | 노파르티스 아게 | Iap 억제제 |
GB0512324D0 (en) | 2005-06-16 | 2005-07-27 | Novartis Ag | Organic compounds |
MX2007008781A (es) | 2005-01-21 | 2007-09-11 | Astex Therapeutics Ltd | Compuestos farmaceuticos. |
GB0510390D0 (en) | 2005-05-20 | 2005-06-29 | Novartis Ag | Organic compounds |
AU2006294850A1 (en) | 2005-09-27 | 2007-04-05 | Novartis Ag | Carboxyamine compounds and their use in the treatment of HDAC dependent diseases |
US7942867B2 (en) * | 2005-11-09 | 2011-05-17 | The Invention Science Fund I, Llc | Remotely controlled substance delivery device |
GB0605120D0 (en) | 2006-03-14 | 2006-04-26 | Novartis Ag | Organic Compounds |
JP2009536180A (ja) | 2006-05-09 | 2009-10-08 | ノバルティス アクチエンゲゼルシャフト | 鉄キレート剤と抗新生物剤を含む組合せ剤およびそれらの使用 |
CA2664378A1 (fr) | 2006-09-29 | 2008-04-03 | Novartis Ag | Pyrazolopyrimidines utilisees comme inhibiteurs des lipides kinases pl3k |
JP5528807B2 (ja) | 2006-10-12 | 2014-06-25 | アステックス、セラピューティックス、リミテッド | 複合薬剤 |
JP5528806B2 (ja) | 2006-10-12 | 2014-06-25 | アステックス、セラピューティックス、リミテッド | 複合薬剤 |
RU2009134223A (ru) | 2007-02-15 | 2011-03-20 | Новартис АГ (CH) | Комбинация lbh589 с другими терапевтическими средствами, предназначенная для лечения рака |
EA020114B1 (ru) | 2008-03-24 | 2014-08-29 | Новартис Аг | Производные арилсульфонамида в качестве ингибиторов матриксной металлопротеазы |
EP2628726A1 (fr) | 2008-03-26 | 2013-08-21 | Novartis AG | Inhibiteurs à hydroxamate de désacétylases B |
ES2621141T3 (es) * | 2008-11-28 | 2017-07-03 | Novartis Ag | Combinación farmacéutica que comprende un inhibidor de Hsp 90 y un inhibidor de mTOR |
WO2010083617A1 (fr) | 2009-01-21 | 2010-07-29 | Oncalis Ag | Pyrazolopyrimidines en tant qu'inhibiteurs de protéines kinases |
CA2750582A1 (fr) | 2009-01-22 | 2010-07-29 | Maatschap Interne Geneeskunde Rijnstate | Methode de traitement prophylactique ou therapeutique des bouffees vasomotrices |
TW201031406A (en) | 2009-01-29 | 2010-09-01 | Novartis Ag | Substituted benzimidazoles for the treatment of astrocytomas |
KR101360725B1 (ko) | 2009-06-26 | 2014-02-07 | 노파르티스 아게 | Cyp17의 억제제로서의 1,3-이치환된 이미다졸리딘-2-온 유도체 |
US8389526B2 (en) | 2009-08-07 | 2013-03-05 | Novartis Ag | 3-heteroarylmethyl-imidazo[1,2-b]pyridazin-6-yl derivatives |
CA2770873A1 (fr) | 2009-08-12 | 2011-02-17 | Novartis Ag | Composes hydrazone heterocycliques et leurs utilisations pour traiter le cancer et l'inflammation |
EP2467383A1 (fr) | 2009-08-20 | 2012-06-27 | Novartis AG | Composés d'oximes hétérocycliques |
US20120149661A1 (en) | 2009-08-26 | 2012-06-14 | Novartis Ag | Tetra-substituted heteroaryl compounds and their use as mdm2 and/or mdm4 modulators |
EP2475668A1 (fr) | 2009-09-10 | 2012-07-18 | Novartis AG | Dérivés éthers d'hétéroaryles bicycliques |
MY156209A (en) | 2009-11-04 | 2016-01-29 | Novartis Ag | Heterocyclic sulfonamide derivatives useful mek inhibitors |
US20120289501A1 (en) | 2009-11-25 | 2012-11-15 | Novartis Ag | Benzene-fused 6-membered oxygen-containing heterocyclic derivatives of bicyclic heteroaryls |
EP2509964B1 (fr) | 2009-12-08 | 2014-04-30 | Novartis AG | Dérivés sulfonamides hétérocycliques |
US8440693B2 (en) | 2009-12-22 | 2013-05-14 | Novartis Ag | Substituted isoquinolinones and quinazolinones |
CU24130B1 (es) | 2009-12-22 | 2015-09-29 | Novartis Ag | Isoquinolinonas y quinazolinonas sustituidas |
UA112517C2 (uk) | 2010-07-06 | 2016-09-26 | Новартіс Аг | Тетрагідропіридопіримідинові похідні |
SG177783A1 (en) | 2010-07-09 | 2012-02-28 | Smart Communications Inc | Content provision system and method |
US8946260B2 (en) | 2010-09-16 | 2015-02-03 | Novartis Ag | 17α-hydroxylase/C17,20-lyase inhibitors |
EP2673277A1 (fr) | 2011-02-10 | 2013-12-18 | Novartis AG | Composés de [1, 2, 4]triazolo [4, 3 -b]pyridazine en tant qu'inhibiteurs de la tyrosine kinase c-met |
EP2683722A1 (fr) | 2011-03-08 | 2014-01-15 | Novartis AG | Composés hétéroaryliques bicycliques de type fluorophényle |
MX359399B (es) | 2011-04-28 | 2018-09-27 | Novartis Ag | Inhibidores de 17alfa-hidroxilasa/c17-20-liasa. |
MX2013014398A (es) | 2011-06-09 | 2014-03-21 | Novartis Ag | Derivados de sulfonamida heterociclicos. |
EP2721007B1 (fr) | 2011-06-20 | 2015-04-29 | Novartis AG | Composés de cyclohexyl-isoquinolinone |
EP2721008B1 (fr) | 2011-06-20 | 2015-04-29 | Novartis AG | Dérivés de isoquinolinone substitués par un radical hydroxylé en tant que inhibiteurs de p53 (mdm2 or mdm4) |
WO2013001445A1 (fr) | 2011-06-27 | 2013-01-03 | Novartis Ag | Formes solides et sels de dérivés de tétrahydro-pyrido-pyrimidine |
ES2691650T3 (es) | 2011-09-15 | 2018-11-28 | Novartis Ag | 3-(quinolin-6-il-tio)-[1,2,4]-triazolo-[4,3-a]-piridinas 6-sustituidas como inhibidores de tirosina quinasa c-Met |
WO2013080141A1 (fr) | 2011-11-29 | 2013-06-06 | Novartis Ag | Composés pyrazolopyrrolidine |
EP2794594A1 (fr) | 2011-12-22 | 2014-10-29 | Novartis AG | Dérivés quinoline |
PL2794600T3 (pl) | 2011-12-22 | 2018-06-29 | Novartis Ag | Pochodne 2,3-dihydro-benzo[1,4]oksazyny i powiązane związki jako inhibitory kinazy fosfoinozytydu-3 (PI3K) do leczenia np. reumatoidalnego zapalenia stawów |
MX2014007731A (es) | 2011-12-23 | 2015-01-12 | Novartis Ag | Compuestos para inhibir la interaccion de bcl2 con los componentes de enlace. |
EA201491259A1 (ru) | 2011-12-23 | 2014-11-28 | Новартис Аг | Соединения и композиции для ингибирования взаимодействия bcl2 с партнерами связывания |
CA2859869A1 (fr) | 2011-12-23 | 2013-06-27 | Novartis Ag | Composes inhibiteurs de l'interaction entre bcl2 et des partenaires de liaison |
BR112014015308A2 (pt) | 2011-12-23 | 2017-06-13 | Novartis Ag | compostos para inibição da interação de bcl2 com contrapartes de ligação |
US9126980B2 (en) | 2011-12-23 | 2015-09-08 | Novartis Ag | Compounds for inhibiting the interaction of BCL2 with binding partners |
JO3357B1 (ar) | 2012-01-26 | 2019-03-13 | Novartis Ag | مركبات إيميدازوبيروليدينون |
JP6171003B2 (ja) | 2012-05-24 | 2017-07-26 | ノバルティス アーゲー | ピロロピロリジノン化合物 |
JP6427097B2 (ja) | 2012-06-15 | 2018-11-21 | ザ ブリガム アンド ウィメンズ ホスピタル インコーポレイテッドThe Brigham and Women’s Hospital, Inc. | 癌を処置するための組成物および該組成物を製造するための方法 |
NZ706635A (en) | 2012-10-02 | 2018-08-31 | Gilead Sciences Inc | Inhibitors of histone demethylases |
TW201422625A (zh) | 2012-11-26 | 2014-06-16 | Novartis Ag | 二氫-吡啶并-□衍生物之固體形式 |
US9403827B2 (en) | 2013-01-22 | 2016-08-02 | Novartis Ag | Substituted purinone compounds |
EP2948453B1 (fr) | 2013-01-22 | 2017-08-02 | Novartis AG | Composés pyrazolo[3,4-d]pyrimidinone utilisés en tant qu'inhibiteurs de l'interaction p53/mdm2 |
WO2014128612A1 (fr) | 2013-02-20 | 2014-08-28 | Novartis Ag | Dérivés de quinazolin-4-one |
SG11201506717UA (en) | 2013-02-27 | 2015-09-29 | Epitherapeutics Aps | Inhibitors of histone demethylases |
US20150018376A1 (en) | 2013-05-17 | 2015-01-15 | Novartis Ag | Pyrimidin-4-yl)oxy)-1h-indole-1-carboxamide derivatives and use thereof |
UY35675A (es) | 2013-07-24 | 2015-02-27 | Novartis Ag | Derivados sustituidos de quinazolin-4-ona |
WO2015022663A1 (fr) | 2013-08-14 | 2015-02-19 | Novartis Ag | Composés et compositions utiles comme inhibiteurs de mek |
US9227969B2 (en) | 2013-08-14 | 2016-01-05 | Novartis Ag | Compounds and compositions as inhibitors of MEK |
WO2015022664A1 (fr) | 2013-08-14 | 2015-02-19 | Novartis Ag | Composés et compositions utiles comme inhibiteurs de mek |
BR112016003229A8 (pt) | 2013-09-22 | 2020-02-04 | Calitor Sciences Llc | composto, composição farmacêutica, e, uso de um composto ou de uma composição farmacêutica |
KR20160101027A (ko) | 2014-01-15 | 2016-08-24 | 노파르티스 아게 | 제약 조합물 |
WO2015148867A1 (fr) | 2014-03-28 | 2015-10-01 | Calitor Sciences, Llc | Composés hétéroaryle substitués et procédés d'utilisation |
EP3126345A1 (fr) | 2014-03-31 | 2017-02-08 | Gilead Sciences, Inc. | Inhibiteurs d'histones déméthylases |
WO2015153345A1 (fr) | 2014-04-03 | 2015-10-08 | Invictus Oncology Pvt. Ltd. | Agents thérapeutiques combinatoires supramoléculaires |
WO2016033169A1 (fr) | 2014-08-27 | 2016-03-03 | Epitherapeutics Aps | Composés et procédés d'inhibition des histones déméthylases |
US10351591B2 (en) | 2015-03-20 | 2019-07-16 | The Regents Of The University Of California | Polypeptides, peptides, and proteins functionalized by alkylation of thioether groups via ring-opening reactions |
EP3124495A1 (fr) | 2015-07-31 | 2017-02-01 | Centre National de la Recherche Scientifique (C.N.R.S.) | Dérivés de polypeptides de type élastine et leurs utilisations |
WO2017044434A1 (fr) | 2015-09-11 | 2017-03-16 | Sunshine Lake Pharma Co., Ltd. | Composés hétéroaryle substitués et leurs méthodes d'utilisation |
WO2017189860A1 (fr) | 2016-04-27 | 2017-11-02 | The Regents Of The University Of California | Préparation de résidus fonctionnels d'homocystéine dans des polypeptides et des peptides |
JP7254076B2 (ja) | 2017-11-19 | 2023-04-07 | サンシャイン・レイク・ファーマ・カンパニー・リミテッド | 置換ヘテロアリール化合物及び使用方法 |
JP7021356B2 (ja) | 2017-12-21 | 2022-02-16 | ヘフェイ インスティテューツ オブ フィジカル サイエンス, チャイニーズ アカデミー オブ サイエンシーズ | ピリミジン誘導体系キナーゼ阻害剤類 |
WO2019143874A1 (fr) | 2018-01-20 | 2019-07-25 | Sunshine Lake Pharma Co., Ltd. | Composés d'aminopyrimidine substitués et procédés d'utilisation |
CN109926430A (zh) * | 2018-11-19 | 2019-06-25 | 云南省环境科学研究院(中国昆明高原湖泊国际研究中心) | 一种重金属废渣还原造锍熔炼处置的方法 |
Family Cites Families (76)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3787385A (en) * | 1971-05-17 | 1974-01-22 | K Folkers | Synthetically produced tetrapeptide having the activity of the luteinizing hormone releasing hormone |
US3974135A (en) * | 1971-06-24 | 1976-08-10 | Karl Folkers | Synthetic decapeptide having the activity of the luteinizing hormone releasing hormone and method for producing the same |
US3953416A (en) * | 1971-12-20 | 1976-04-27 | Karl Folkers | Synthetic decapeptide having the activity of the luteinizing hormone releasing hormone and method for manufacturing the same |
GB1541733A (en) * | 1975-10-29 | 1979-03-07 | Parke Davis & Co | Octapeptides and methods for their production |
JPS5257177A (en) * | 1975-10-29 | 1977-05-11 | Parke Davis & Co | Production of novel nonapeptide |
DE2617646C2 (de) * | 1976-04-22 | 1986-07-31 | Hoechst Ag, 6230 Frankfurt | Nonapeptid-amide und Decapeptid-amide mit Gonadoliberin-Wirkung, Verfahren zu ihrer Herstellung und diese Verbindungen enthaltende pharmazeutische Präparate |
US4215038A (en) * | 1978-10-16 | 1980-07-29 | The Salk Institute For Biological Studies | Peptides which inhibit gonadal function |
US4307083A (en) * | 1978-10-16 | 1981-12-22 | The Salk Institute For Biological Studies | LRF Antagonists |
US4244946A (en) * | 1979-06-11 | 1981-01-13 | The Salk Institute For Biological Studies | Water-soluble peptides affecting gonadal function |
US4292313A (en) * | 1980-04-15 | 1981-09-29 | The Salk Institute For Biological Studies | LRF Antagonists |
US4409208A (en) * | 1980-04-15 | 1983-10-11 | The Salk Institute For Biological Studies | GnRH antagonists |
US4377574A (en) * | 1980-06-26 | 1983-03-22 | The Salk Institute For Biological Studies | Contraceptive treatment of male mammals |
US4386074A (en) * | 1980-08-29 | 1983-05-31 | The Salk Institute For Biological Studies | LRF Antagonists |
US4341767A (en) * | 1980-10-06 | 1982-07-27 | Syntex Inc. | Nonapeptide and decapeptide analogs of LHRH, useful as LHRH antagonists |
US4419347A (en) * | 1980-10-06 | 1983-12-06 | Syntex (U.S.A.) Inc. | Nonapeptide and decapeptide analogs of LHRH, useful as LHRH antagonists |
US4489061A (en) * | 1981-06-12 | 1984-12-18 | The Salk Institute For Biological Studies | Treatment of male mammals |
US4481190A (en) * | 1982-12-21 | 1984-11-06 | Syntex (U.S.A.) Inc. | Nonapeptide and decapeptide analogs of LHRH useful as LHRH antagonists |
US4581169A (en) * | 1982-12-21 | 1986-04-08 | Syntex (U.S.A.) Inc. | Nona-peptide and deca-peptide analogs of LHRH, useful as LHRH antagonists |
US4667014A (en) * | 1983-03-07 | 1987-05-19 | Syntex (U.S.A.) Inc. | Nonapeptide and decapeptide analogs of LHRH, useful as LHRH antagonists |
US4444759A (en) * | 1982-07-26 | 1984-04-24 | The Salk Institute For Biological Studies | GnRH Antagonists II |
US4619914A (en) * | 1983-03-10 | 1986-10-28 | The Salk Institute For Biological Studies | GNRH antagonists IIIB |
US4504414A (en) * | 1983-03-28 | 1985-03-12 | Board Of Regents, The University Of Texas System | Synthetic pyridyl-alanyl decapeptides having antiovulatory activity |
DE3467173D1 (en) * | 1983-08-16 | 1987-12-10 | Akzo Nv | Lh- rh antagonists |
US4547370A (en) * | 1983-11-29 | 1985-10-15 | The Salk Institute For Biological Studies | GnRH Antagonists |
US4569927A (en) * | 1984-02-23 | 1986-02-11 | The Salk Institute For Biological Studies | GnRH Antagonists IV |
US4652550A (en) * | 1984-05-21 | 1987-03-24 | The Salk Institute For Biological Studies | GnRH antagonists VII |
US4647653A (en) * | 1984-08-23 | 1987-03-03 | Tulane Educational Fund | Therapeutic peptides |
US4565804A (en) * | 1984-09-07 | 1986-01-21 | The Salk Institute For Biological Studies | GnRH Antagonists VI |
US4690916A (en) * | 1984-11-13 | 1987-09-01 | Syntex (U.S.A.) Inc. | Nona and decapeptide analogs of LHRH useful as LHRH antagonists |
US4740500A (en) * | 1985-01-31 | 1988-04-26 | The Salk Institute For Biological Studies | GnRH antagonists VIII |
US4659691A (en) * | 1985-02-08 | 1987-04-21 | Merck & Co., Inc. | Novel cyclic Hexapeptide LHRH antagonists |
US4677193A (en) * | 1985-02-22 | 1987-06-30 | The Salk Institute For Biological Studies | Peptides containing an aliphatic-aromatic ketone side chain |
US5003011A (en) * | 1985-04-09 | 1991-03-26 | The Administrators Of The Tulane Educational Fund | Therapeutic decapeptides |
US5073624A (en) * | 1985-04-09 | 1991-12-17 | Administrators Of The Tulane Educational Fund | Therapeutic decapeptides |
US4866160A (en) * | 1985-04-09 | 1989-09-12 | The Administrators Of The Tulane Educational Fund | Therapeutic decapeptides |
US4642332A (en) * | 1985-04-26 | 1987-02-10 | The Board Of Regents, The University Of Texas System | Effective hormonal peptides: D-3-Pal6 -LHRH |
US4656247A (en) * | 1985-04-26 | 1987-04-07 | Board Of Regents, The University Of Texas System | Effective hormonal peptides: D-3-QA1 6-LHRH |
US4661472A (en) * | 1985-05-09 | 1987-04-28 | The Salk Institute For Biological Studies | GnRH antagonists IX |
US4721775A (en) * | 1985-08-26 | 1988-01-26 | Board Of Regents, The University Of Texas System | Effective peptides related to the luteinizing hormone releasing hormone from L-amino acids |
US4705778A (en) * | 1985-10-22 | 1987-11-10 | Sri International | Orally active LHRH analogs |
US5182205A (en) * | 1986-11-27 | 1993-01-26 | Hoffmann-La Roche Inc. | Nucleotide sequences which are selectively expressed in pre-B cells and probes therefor |
US4801577A (en) * | 1987-02-05 | 1989-01-31 | Syntex (U.S.A.) Inc. | Nonapeptide and decapeptide analogs of LHRH useful as LHRH antagonists |
US4851385A (en) * | 1987-07-15 | 1989-07-25 | Indiana University Foundation | LHRH antagonist analogs having low histamine-release activity |
US4800191A (en) * | 1987-07-17 | 1989-01-24 | Schally Andrew Victor | LHRH antagonists |
US4935491A (en) * | 1987-08-24 | 1990-06-19 | Board Of Regents, The University Of Texas System | Effective antagonists of the luteinizing hormone releasing hormone which release negligible histamine |
US5140009A (en) * | 1988-02-10 | 1992-08-18 | Tap Pharmaceuticals, Inc. | Octapeptide LHRH antagonists |
US5300492A (en) * | 1988-02-10 | 1994-04-05 | Tap Pharmaceuticals | LHRH analogs |
US5110904A (en) * | 1989-08-07 | 1992-05-05 | Abbott Laboratories | Lhrh analogs |
EP0328090A3 (fr) * | 1988-02-10 | 1990-08-16 | Abbott Laboratories | Analogues du LHRH |
DK163689A (da) * | 1988-04-08 | 1989-10-30 | Sandoz Ag | Peptidderivater |
US4992421A (en) * | 1988-04-19 | 1991-02-12 | Abbott Laboratories | Luteinizing hormone releasing hormone antagonist |
US5258492A (en) * | 1988-10-21 | 1993-11-02 | The Administrators Of The Tulane Educational Fund | LHRH analogues with cytotoxic moieties at the sixth position |
US5171835A (en) * | 1988-10-21 | 1992-12-15 | The Administrators Of The Tulane Educational Fund | LHRH antagonists |
US5352796A (en) * | 1989-10-30 | 1994-10-04 | The Salk Institute For Biological Studies | Amino acids useful in making GnRH analogs |
US5169932A (en) * | 1989-10-30 | 1992-12-08 | The Salk Institute For Biological Studies | Gnrh analogs |
US5296468A (en) * | 1989-10-30 | 1994-03-22 | The Salk Institute For Biological Studies | GnRH analogs |
US5064939A (en) * | 1990-02-06 | 1991-11-12 | The Salk Institute For Biological Studies | Cyclic gnrh antagonists |
US5180711A (en) * | 1990-06-14 | 1993-01-19 | Applied Research Systems Ars Holding N.V. | Combined treatment with gnrh antagonist and gnrh to control gonadotropin levels in mammals |
CN1036343C (zh) * | 1990-11-10 | 1997-11-05 | 天津市计划生育研究所 | 新促黄体生成素释放激素拮抗类似物的制备方法 |
IL101074A (en) * | 1991-03-14 | 1997-09-30 | Salk Inst For Biological Studi | GnRH ANALOGS AND THEIR PREPARATION |
US5340585A (en) * | 1991-04-12 | 1994-08-23 | University Of Southern California | Method and formulations for use in treating benign gynecological disorders |
DE593491T1 (de) * | 1991-04-25 | 1994-11-17 | Romano S.-Cergue Deghenghi | LHRH-Antagonisten. |
DE4117507A1 (de) * | 1991-05-24 | 1992-11-26 | Schering Ag | Verfahren zur herstellung von n(pfeil hoch)6(pfeil hoch)-substituierten lysin-derivaten |
US5480969A (en) * | 1992-09-15 | 1996-01-02 | The Administrators Of The Tulane Educational Fund | Antagonists of LHRH |
US5371070A (en) * | 1992-11-09 | 1994-12-06 | The Salk Institute For Biological Studies | Bicyclic GnRH antagonists and a method for regulating the secretion of gonadotropins |
JPH08504209A (ja) * | 1992-12-04 | 1996-05-07 | アボツト・ラボラトリーズ | 6位修飾デカペプチドlhrh拮抗薬 |
CA2136079A1 (fr) * | 1992-12-18 | 1994-07-07 | Fortuna Haviv | Antagonistes de lhrh presentant des residus aminoacyle modifies en position 5 et 6 |
WO1994028015A1 (fr) * | 1993-05-20 | 1994-12-08 | Biotech Australia Pty. Limited | Antagonistes de la lhrh |
DE4320201A1 (de) * | 1993-06-18 | 1995-01-12 | Asta Medica Ag | Verwendung von Cetrorelix und weiteren Nona- und Dekapeptiden zur Herstellung eines Arzneimittels zur Bekämpfung von Aids und zur Wachstumsstimulation |
US5502035A (en) * | 1993-08-06 | 1996-03-26 | Tap Holdings Inc. | N-terminus modified analogs of LHRH |
US5413990A (en) * | 1993-08-06 | 1995-05-09 | Tap Pharmaceuticals Inc. | N-terminus modified analogs of LHRH |
US5508383A (en) * | 1994-03-09 | 1996-04-16 | Tap Holdings Inc. | Cyclic peptide LHRH antagonists |
US5506207A (en) * | 1994-03-18 | 1996-04-09 | The Salk Institute For Biological Studies | GNRH antagonists XIII |
US5516759A (en) * | 1994-12-08 | 1996-05-14 | Tap Holdings Inc. | LHRH antagonists having lactam groups at the N-terminus |
US5843901A (en) * | 1995-06-07 | 1998-12-01 | Advanced Research & Technology Institute | LHRH antagonist peptides |
US5780435A (en) * | 1995-12-15 | 1998-07-14 | Praecis Pharmaceuticals Incorporated | Methods for treating prostate cancer with LHRH-R antagonists |
-
1995
- 1995-06-07 US US08/480,494 patent/US5843901A/en not_active Expired - Lifetime
-
1996
- 1996-06-07 DE DE69623254T patent/DE69623254T2/de not_active Expired - Lifetime
- 1996-06-07 US US08/973,378 patent/US6423686B1/en not_active Expired - Lifetime
- 1996-06-07 AT AT01204149T patent/ATE432941T1/de active
- 1996-06-07 ES ES01204149T patent/ES2326861T3/es not_active Expired - Lifetime
- 1996-06-07 PT PT96919311T patent/PT794961E/pt unknown
- 1996-06-07 ES ES96919311T patent/ES2177789T3/es not_active Expired - Lifetime
- 1996-06-07 AT AT96919311T patent/ATE222924T1/de active
- 1996-06-07 DE DE1996623254 patent/DE122006000012I1/de active Pending
- 1996-06-07 DE DE122006000012C patent/DE122006000012I2/de active Active
- 1996-06-07 DK DK96919311T patent/DK0794961T3/da active
- 1996-06-07 JP JP50205097A patent/JP4164125B2/ja not_active Expired - Fee Related
- 1996-06-07 PT PT01204149T patent/PT1188768E/pt unknown
- 1996-06-07 EP EP01204149A patent/EP1188768B1/fr not_active Expired - Lifetime
- 1996-06-07 AU AU61680/96A patent/AU715399B2/en not_active Ceased
- 1996-06-07 DK DK01204149T patent/DK1188768T3/da active
- 1996-06-07 EP EP96919311A patent/EP0794961B1/fr not_active Expired - Lifetime
- 1996-06-07 WO PCT/US1996/009852 patent/WO1996040757A2/fr active Search and Examination
- 1996-06-07 DE DE69535963T patent/DE69535963D1/de not_active Expired - Lifetime
- 1996-06-07 CA CA002219460A patent/CA2219460C/fr not_active Expired - Fee Related
-
2002
- 2002-04-02 US US10/115,553 patent/US20030040482A1/en not_active Abandoned
- 2002-04-05 US US10/117,364 patent/US7071165B2/en not_active Expired - Fee Related
- 2002-09-11 HK HK02106667.7A patent/HK1045161B/zh not_active IP Right Cessation
-
2006
- 2006-03-03 LU LU91225C patent/LU91225I2/fr unknown
-
2007
- 2007-08-13 JP JP2007211155A patent/JP2007302695A/ja not_active Withdrawn
-
2008
- 2008-10-09 JP JP2008263288A patent/JP2009040793A/ja not_active Withdrawn
-
2011
- 2011-08-22 LU LU91857C patent/LU91857I2/fr unknown
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
LU91225I2 (fr) | Plenaxis | |
DK0528312T3 (da) | Cykliske peptider og anvendelse deraf | |
DK0966297T4 (da) | Regulering af gastrointestinal motilitet | |
AU3943189A (en) | Peptides having bradykinin antagonist action | |
ATE108662T1 (de) | Antimikrobielle peptide, zusammensetzungen, die diese enthalten, und verwendungen daraus. | |
FI102759B (fi) | Menetelmä terapeuttisesti aktiivisten nona- ja dekapeptidien valmistam iseksi | |
ATE331037T1 (de) | Isoliertes frpb nukleinsäuremolekül und entsprechende impfstoff | |
BG97123A (bg) | Производни на човешка, стимулирана от жлъчните соли, липаза и фармацевтични състави на тяхна основа | |
ATE480558T1 (de) | Auf scf peptid basiertes basolaterales sortiersignal und inhibitoren dafür | |
NZ231636A (en) | Anticoagulant peptides analogus to hirudins' active site | |
DE69002881D1 (de) | Peptide und deren Benutzung. | |
DK1612555T3 (da) | Kryptiske peptider til anvendelse til at inducere immunologisk tolerance | |
ATE46347T1 (de) | Immunostimulierende peptide. | |
IT8720701A0 (it) | Composizioni farmaceutiche adattivita' immunomodulante. | |
IT8719949A0 (it) | Composizioni farmaceutiche adattivita' immunomodulante. | |
IT8847610A0 (it) | Composizioni farmaceutiche adattivita' antiprolattinica | |
TH17650EX (th) | "อนุพันธ์เปปไทด์ที่ใช้รักษาโรค"(therapeutic peptide derivatives) | |
TH35998A (th) | Lh-rh เป็ปไทด์ อะนาล็อก ประโยชน์ของสิ่งเหล่านั้นและองค์ประกอบทางเภสัชกรรมซึ่งประกอบด้วยสิ่งเหล่านั้น |