AUPR688101A0 - Protein domains and their ligands - Google Patents

Protein domains and their ligands

Info

Publication number
AUPR688101A0
AUPR688101A0 AUPR6881A AUPR688101A AUPR688101A0 AU PR688101 A0 AUPR688101 A0 AU PR688101A0 AU PR6881 A AUPR6881 A AU PR6881A AU PR688101 A AUPR688101 A AU PR688101A AU PR688101 A0 AUPR688101 A0 AU PR688101A0
Authority
AU
Australia
Prior art keywords
ligands
protein domains
domains
protein
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
AUPR6881A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Luminis Pty Ltd
Original Assignee
Luminis Pty Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Luminis Pty Ltd filed Critical Luminis Pty Ltd
Priority to AUPR6881A priority Critical patent/AUPR688101A0/en
Publication of AUPR688101A0 publication Critical patent/AUPR688101A0/en
Priority to PCT/AU2002/001064 priority patent/WO2003013523A1/en
Abandoned legal-status Critical Current

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
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/47—Quinolines; Isoquinolines
    • 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
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • 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
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • A61P31/14—Antivirals for RNA viruses
    • A61P31/18—Antivirals for RNA viruses for HIV
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
AUPR6881A 2001-08-08 2001-08-08 Protein domains and their ligands Abandoned AUPR688101A0 (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
AUPR6881A AUPR688101A0 (en) 2001-08-08 2001-08-08 Protein domains and their ligands
PCT/AU2002/001064 WO2003013523A1 (en) 2001-08-08 2002-08-08 Sh3 protein domains and their ligands

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
AUPR6881A AUPR688101A0 (en) 2001-08-08 2001-08-08 Protein domains and their ligands

Publications (1)

Publication Number Publication Date
AUPR688101A0 true AUPR688101A0 (en) 2001-08-30

Family

ID=3830837

Family Applications (1)

Application Number Title Priority Date Filing Date
AUPR6881A Abandoned AUPR688101A0 (en) 2001-08-08 2001-08-08 Protein domains and their ligands

Country Status (2)

Country Link
AU (1) AUPR688101A0 (en)
WO (1) WO2003013523A1 (en)

Families Citing this family (36)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004064730A2 (en) 2003-01-14 2004-08-05 Cytokinetics, Inc. Compounds, compositions and methods
WO2005087775A1 (en) * 2004-03-15 2005-09-22 Ono Pharmaceutical Co., Ltd. Tricyclic heterocyclic compound and medicinal composition containing the compound as active ingredient
RU2410384C2 (en) 2004-06-17 2011-01-27 Цитокинетикс, Инк. Compounds, compositions and methods of their application
EP1781637A1 (en) * 2004-06-29 2007-05-09 Rigel Pharmaceuticals, Inc. 2-substituted quinoline compounds and their uses as inhibitors of the ige receptor signaling cascade
US7176222B2 (en) 2004-07-27 2007-02-13 Cytokinetics, Inc. Syntheses of ureas
US7538223B2 (en) 2005-08-04 2009-05-26 Cytokinetics, Inc. Compounds, compositions and methods
US8686002B2 (en) 2005-08-21 2014-04-01 AbbVie Deutschland GmbH & Co. KG Heterocyclic compounds and their use as binding partners for 5-HT5 receptors
US7825120B2 (en) 2005-12-15 2010-11-02 Cytokinetics, Inc. Certain substituted ((piperazin-1-ylmethyl)benzyl)ureas
EP1959960B1 (en) 2005-12-15 2013-04-10 Cytokinetics, Inc. Certain chemical entities, compositions and methods
WO2007078815A2 (en) 2005-12-16 2007-07-12 Cytokinetics, Inc. Certain chemical entities, compositions, and methods
WO2007078839A2 (en) 2005-12-19 2007-07-12 Cytokinetics, Inc. Compounds, compositions and methods
US9689879B2 (en) 2006-08-21 2017-06-27 Eidgenoessische Technische Hochschule Zurich Specific and high affinity binding proteins comprising modified SH3 domains of Fyn kinase
US9513296B2 (en) 2006-08-21 2016-12-06 Eidgenoessische Technische Hochschule Zurich Specific and high affinity binding proteins comprising modified SH3 domains of Fyn kinase
EP1892248A1 (en) * 2006-08-21 2008-02-27 Eidgenössische Technische Hochschule Zürich Specific and high affinity binding proteins comprising modified SH3 domains of FYN kinase
EP2102165A2 (en) * 2006-11-24 2009-09-23 AC Immune S.A. N-(methyl)-1h-pyrazol-3-amine, n-(methyl)-pyridin-2-amine and n-(methyl)-thiazol-2-amine derivatives for the treatment of diseases associated with amyloid or amyloid-like proteins, like e.g. alzheimer's
PE20090717A1 (en) 2007-05-18 2009-07-18 Smithkline Beecham Corp QUINOLINE DERIVATIVES AS PI3 KINASE INHIBITORS
ES2394126T3 (en) * 2007-07-26 2013-01-22 Novartis Ag Pyrimidine derivatives useful for the treatment of inflammatory or allergic conditions
SI2195312T1 (en) 2007-10-09 2013-01-31 Merck Patent Gmbh Pyridine derivatives useful as glucokinase activators
EP2062578A1 (en) 2007-11-12 2009-05-27 Institut National De La Sante Et De La Recherche Medicale (Inserm) Novel use of chemical compounds for the treatment of AIDS
EP2440204B1 (en) 2009-06-12 2013-12-18 Bristol-Myers Squibb Company Nicotinamide compounds useful as kinase modulators
EP2311823A1 (en) 2009-10-15 2011-04-20 AC Immune S.A. 2,6-Diaminopyridine compounds for treating diseases associated with amyloid proteins or for treating ocular diseases
JP6096807B2 (en) 2012-01-13 2017-03-15 ブリストル−マイヤーズ スクイブ カンパニーＢｒｉｓｔｏｌ−Ｍｙｅｒｓ Ｓｑｕｉｂｂ Ｃｏｍｐａｎｙ Triazolyl-substituted pyridyl compounds useful as kinase inhibitors
JP6096219B2 (en) 2012-01-13 2017-03-15 ブリストル−マイヤーズ スクイブ カンパニーＢｒｉｓｔｏｌ−Ｍｙｅｒｓ Ｓｑｕｉｂｂ Ｃｏｍｐａｎｙ Triazolyl or triasiazolyl substituted pyridyl compounds useful as kinase inhibitors
US9242975B2 (en) 2012-01-13 2016-01-26 Bristol-Myers Squibb Company Heterocyclic-substituted pyridyl compounds useful as kinase inhibitors
US9546153B2 (en) 2012-11-08 2017-01-17 Bristol-Myers Squibb Company Bicyclic heterocycle substituted pyridyl compounds useful as kinase modulators
US9657009B2 (en) 2012-11-08 2017-05-23 Bristol-Myers Squibb Company Heteroaryl substituted pyridyl compounds useful as kinase modulators
CA2891412A1 (en) 2012-11-20 2014-05-30 Vertex Pharmaceuticals Incorporated Compounds useful as inhibitors of indoleamine 2,3-dioxygenase
EP2970199A1 (en) 2013-03-11 2016-01-20 Bristol-Myers Squibb Company Isoquinolines as potassium ion channel inhibitors
UY35935A (en) 2014-01-03 2015-06-30 Bristol Myers Squibb Company Una Corporación Del Estado De Delaware NICOTINAMIDE COMPOUNDS REPLACED WITH HETEROARILO AS QUINASE INHIBITORS AND MODULATORS OF IRAK-4
EP3265445B1 (en) * 2015-03-06 2021-05-05 Pharmakea, Inc. Lysyl oxidase-like 2 inhibitors and uses thereof
UY36748A (en) 2015-06-24 2016-12-30 Bristol Myers Squibb Company Una Corporación Del Estado De Delaware AMINOPIRIDINE COMPOUNDS REPLACED WITH HETEROARILO AS QUINASE INHIBITORS AND IRAK-4 MODULATORS, AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM
TW201713663A (en) 2015-06-24 2017-04-16 必治妥美雅史谷比公司 Heteroaryl substituted aminopyridine compounds
US10618903B2 (en) 2015-06-24 2020-04-14 Bristol-Myers Squibb Company Heteroaryl substituted aminopyridine compounds
JP6946412B2 (en) 2016-07-18 2021-10-06 ヤンセン ファーマシューティカ エヌ．ベー． Tau PET Imaging Ligand
EP3621960B1 (en) 2017-05-11 2021-08-04 Bristol-Myers Squibb Company Thienopyridines and benzothiophenes useful as irak4 inhibitors
CN113121658B (en) * 2020-01-15 2022-10-21 中国农业大学 Gene of protein containing SH3 structural domain in rhizobium and related biological material and application thereof

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2312860C2 (en) * 1999-04-15 2007-12-20 Бристол-Маерс Сквибб Компани Cyclic inhibitors of protein-tyrosine kinase

Also Published As

Publication number Publication date
WO2003013523A1 (en) 2003-02-20

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