HK1107948A1 - Composition for proteasome inhibition - Google Patents

Composition for proteasome inhibition

Info

Publication number
HK1107948A1
HK1107948A1 HK08101858.1A HK08101858A HK1107948A1 HK 1107948 A1 HK1107948 A1 HK 1107948A1 HK 08101858 A HK08101858 A HK 08101858A HK 1107948 A1 HK1107948 A1 HK 1107948A1
Authority
HK
Hong Kong
Prior art keywords
composition
compositions
proteasome inhibition
proteasome inhibitors
cyclodextrin
Prior art date
Application number
HK08101858.1A
Other languages
English (en)
Inventor
Evan R Lewis
Mark Nguyen Ho
Fabiana N Fonseca
Original Assignee
Proteolix Inc
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=36143200&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=HK1107948(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Proteolix Inc filed Critical Proteolix Inc
Publication of HK1107948A1 publication Critical patent/HK1107948A1/xx

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    • A61K31/33Heterocyclic compounds
    • A61K31/335Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/336Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having three-membered rings, e.g. oxirane, fumagillin
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    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/396Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having three-membered rings, e.g. aziridine
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    • A61K47/30Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/08Tripeptides
    • C07K5/0802Tripeptides with the first amino acid being neutral
    • C07K5/0812Tripeptides with the first amino acid being neutral and aromatic or cycloaliphatic
    • YGENERAL 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
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    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/30Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

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  • Proteomics, Peptides & Aminoacids (AREA)
  • Diabetes (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Rheumatology (AREA)
  • Virology (AREA)
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  • Inorganic Chemistry (AREA)
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  • Psychology (AREA)
  • Biophysics (AREA)
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HK08101858.1A 2004-12-07 2008-02-21 Composition for proteasome inhibition HK1107948A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US63436604P 2004-12-07 2004-12-07
US65593005P 2005-02-23 2005-02-23
PCT/US2005/044451 WO2006063154A1 (en) 2004-12-07 2005-12-07 Composition for proteasome inhibition

Publications (1)

Publication Number Publication Date
HK1107948A1 true HK1107948A1 (en) 2008-04-25

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Family Applications (3)

Application Number Title Priority Date Filing Date
HK11105868.5A HK1152047A1 (zh) 2004-12-07 2008-02-21 蛋白酶體抑制劑的成份
HK08101858.1A HK1107948A1 (en) 2004-12-07 2008-02-21 Composition for proteasome inhibition
HK11105867.6A HK1151966A1 (en) 2004-12-07 2008-02-21 Composition for proteasome inhibition

Family Applications Before (1)

Application Number Title Priority Date Filing Date
HK11105868.5A HK1152047A1 (zh) 2004-12-07 2008-02-21 蛋白酶體抑制劑的成份

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Application Number Title Priority Date Filing Date
HK11105867.6A HK1151966A1 (en) 2004-12-07 2008-02-21 Composition for proteasome inhibition

Country Status (18)

Country Link
US (1) US7737112B2 (zh)
EP (3) EP1819353B1 (zh)
JP (1) JP4990155B2 (zh)
KR (1) KR101299821B1 (zh)
CN (2) CN101180071A (zh)
AT (1) ATE499109T1 (zh)
AU (1) AU2005313975B2 (zh)
CA (1) CA2589921C (zh)
CY (1) CY1111489T1 (zh)
DE (1) DE602005026556D1 (zh)
DK (1) DK1819353T3 (zh)
ES (2) ES2549763T3 (zh)
HK (3) HK1152047A1 (zh)
HU (1) HUE027850T2 (zh)
IL (1) IL183607A (zh)
PL (3) PL2260835T3 (zh)
PT (3) PT2260835E (zh)
WO (1) WO2006063154A1 (zh)

Families Citing this family (51)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1745064B1 (en) 2004-04-15 2011-01-05 Proteolix, Inc. Compounds for proteasome enzyme inhibition
US8198270B2 (en) * 2004-04-15 2012-06-12 Onyx Therapeutics, Inc. Compounds for proteasome enzyme inhibition
PL2030981T3 (pl) * 2004-05-10 2014-12-31 Onyx Therapeutics Inc Związki do enzymatycznej inhibicji proteasomu
US9034846B2 (en) * 2004-10-10 2015-05-19 Universite De Liege Use of cyclodextrin for treatment and prevention of bronchial inflammatory diseases
PT2623113T (pt) 2005-11-09 2017-07-14 Onyx Therapeutics Inc Compostos para inibição de enzimas
JP5226679B2 (ja) 2006-06-19 2013-07-03 プロテオリックス, インコーポレイテッド 酵素阻害のための化合物
EA024437B1 (ru) * 2007-10-04 2016-09-30 Оникс Терапьютикс, Инк. Синтез кето-эпоксидов аминокислот
US7635773B2 (en) 2008-04-28 2009-12-22 Cydex Pharmaceuticals, Inc. Sulfoalkyl ether cyclodextrin compositions
WO2010039762A2 (en) * 2008-10-01 2010-04-08 Dr. Reddy's Laboratories Ltd. Pharmaceutical compositions comprising boronic acid compounds
BRPI0919668A2 (pt) * 2008-10-21 2018-05-29 Onyx Therapeutics, Inc. terapia de combinação com epóxi-cetonas de peptídeo
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