JP2008538178A5 - - Google Patents

Download PDF

Info

Publication number
JP2008538178A5
JP2008538178A5 JP2008503516A JP2008503516A JP2008538178A5 JP 2008538178 A5 JP2008538178 A5 JP 2008538178A5 JP 2008503516 A JP2008503516 A JP 2008503516A JP 2008503516 A JP2008503516 A JP 2008503516A JP 2008538178 A5 JP2008538178 A5 JP 2008538178A5
Authority
JP
Japan
Prior art keywords
fragment
agrin
protein
variant
peptide
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.)
Granted
Application number
JP2008503516A
Other languages
English (en)
Japanese (ja)
Other versions
JP4920675B2 (ja
JP2008538178A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/EP2006/061152 external-priority patent/WO2006103261A2/en
Publication of JP2008538178A publication Critical patent/JP2008538178A/ja
Publication of JP2008538178A5 publication Critical patent/JP2008538178A5/ja
Application granted granted Critical
Publication of JP4920675B2 publication Critical patent/JP4920675B2/ja
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

JP2008503516A 2005-03-30 2006-03-29 ニューロトリプシン阻害剤とその判定 Expired - Fee Related JP4920675B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP05102481 2005-03-30
EP05102481.8 2005-03-30
PCT/EP2006/061152 WO2006103261A2 (en) 2005-03-30 2006-03-29 Inhibitors of neurotrypsin and determination thereof

Publications (3)

Publication Number Publication Date
JP2008538178A JP2008538178A (ja) 2008-10-16
JP2008538178A5 true JP2008538178A5 (https=) 2009-05-14
JP4920675B2 JP4920675B2 (ja) 2012-04-18

Family

ID=34939082

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2008503516A Expired - Fee Related JP4920675B2 (ja) 2005-03-30 2006-03-29 ニューロトリプシン阻害剤とその判定

Country Status (15)

Country Link
US (1) US7897364B2 (https=)
EP (1) EP1868989A2 (https=)
JP (1) JP4920675B2 (https=)
KR (1) KR20070116932A (https=)
CN (1) CN101193858B (https=)
AU (1) AU2006228150B2 (https=)
BR (1) BRPI0609654A2 (https=)
CA (1) CA2600791A1 (https=)
IL (1) IL186120A (https=)
MX (1) MX2007011961A (https=)
NO (1) NO20075461L (https=)
NZ (1) NZ562796A (https=)
RU (1) RU2424228C2 (https=)
WO (1) WO2006103261A2 (https=)
ZA (1) ZA200707359B (https=)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008074813A2 (en) * 2006-12-21 2008-06-26 Neurotune Ag Optiogenin for the treatment of neural diseases
PL1990420T3 (pl) * 2007-05-10 2011-01-31 Neurotune Ag Sposób wykrywania aktywności neurotrypsyny in vivo, zastosowanie tego sposobu i zastosowanie C-końcowego fragmentu agryny 22 kDa jako biomarkera w diagnozowaniu i monitorowaniu zaburzeń związanych z neurotrypsyną
EP2295068A1 (en) * 2009-09-04 2011-03-16 Neurotune AG Modified agrin-fragment capable of restoring muscle strength for use as a medicament
EP2635559A2 (en) 2010-11-01 2013-09-11 Neurotune AG Neurotrypsin inhibitors
WO2012059443A2 (en) 2010-11-01 2012-05-10 Neurotune Ag Novel neurotrypsin inhibitors
EP2631657A1 (en) * 2012-02-25 2013-08-28 Neurotune AG Immunoassay for the detection of the 22kDa C-terminal fragment (CAF) of agrin

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CH692507A5 (de) * 1997-04-26 2002-07-15 Peter Prof Dr Sonderegger Neurotrypsin als aktive Verbindung in einem Medikament.
DE19919634C2 (de) * 1999-04-30 2001-06-07 Aventis Pharma Gmbh Test zur Bestimmung der Integrität komplexer Phospholipid/Lipid-Strukturen mit Hilfe synthetischer fluoreszenz-markierter Acylglyceride und dessen Anwendung zur Bestimmung der Aktivität von Lipasen
DE10247478A1 (de) * 2002-10-11 2004-06-24 Bioagency Ag Verfahren zur Bestimmung der enzymatischen Aktivität von Proteinen

Similar Documents

Publication Publication Date Title
Li et al. Receptor and viral determinants of SARS-coronavirus adaptation to human ACE2
Osman et al. Why all the fury over furin?
JP5008398B2 (ja) クラスi膜融合誘発性エンベロープタンパク質をもつrnaウイルスの融合開始領域の機能を阻害することによってウイルス:細胞融合を妨げる方法
EP1910837B1 (en) Methods and compositions for diagnosis and treatment of influenza
Sainz Jr et al. Identification and characterization of the putative fusion peptide of the severe acute respiratory syndrome-associated coronavirus spike protein
Petit et al. Palmitoylation of the cysteine-rich endodomain of the SARS–coronavirus spike glycoprotein is important for spike-mediated cell fusion
Ghosh et al. Structure-based design, synthesis, and biological evaluation of peptidomimetic SARS-CoV 3CLpro inhibitors
Ghildyal et al. Nuclear import of the respiratory syncytial virus matrix protein is mediated by importin β1 independent of importin α
Guay et al. Therapeutic utility and medicinal chemistry of cathepsin C inhibitors
Prusis et al. Design and evaluation of substrate-based octapeptide and non substrate-based tetrapeptide inhibitors of dengue virus NS2B–NS3 proteases
Ho et al. Design and biological activities of novel inhibitory peptides for SARS-CoV spike protein and angiotensin-converting enzyme 2 interaction
JP2008538178A5 (https=)
Brady et al. Rational design and synthesis of selective BACE-1 inhibitors
Liu et al. Screening of drugs by FRET analysis identifies inhibitors of SARS-CoV 3CL protease
El Najjar et al. Analysis of cathepsin and furin proteolytic enzymes involved in viral fusion protein activation in cells of the bat reservoir host
Cascio et al. Structural determinants driving the binding process between PDZ domain of wild type human PALS1 protein and SLiM sequences of SARS-CoV E proteins
Lange et al. Fragment‐Based Design, Synthesis, and Characterization of Aminoisoindole‐Derived Furin Inhibitors
Shuai et al. An orally available Mpro/TMPRSS2 bispecific inhibitor with potent anti-coronavirus efficacy in vivo
RU2007139754A (ru) Ингибиторы нейротрипсина
CN101287988A (zh) 用于流感诊断和治疗的方法和组合物
Meanwell et al. Respiratory syncytial virus–the discovery and optimization of orally bioavailable fusion inhibitors
Liu et al. Simple nano-luciferase-based assay for the rapid and high-throughput detection of SARS-CoV-2 3C-like protease
Galanopoulos et al. Molecular analysis of hot-spot regions of ACE2 and TMPRSS2 in SARS-CoV-2 “invulnerable” individuals
JP2008522632A5 (https=)
US10502741B2 (en) Means and methods for detecting activated MALT1