http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-2646505-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_165f5145d6645a07a1520167fed24600
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N2800-04
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-6893
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-34
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N27-62
filingDate 2007-03-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2db053b5393bf7be7b43493180f12668
publicationDate 2007-09-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2646505-A1
titleOfInvention Substrates and internal standards for mass spectroscopy detection
abstract An inventive substrate is provided which includes a substrate compound of formula A - B1 - B2 - B3: wherein A is a sugar moiety; B1 is a linker moiety allowing the conjugation of moiety A and the remaining structure of the substrate; B2 contains a permanently charged element such as a quaternary ammonium group so as to increase proton affinities and ionization efficiencies for mass spectrometry analysis; and B3 of various carbon length conferring specificities to targeted enzymes. Also provided is a process to detect lysosomal diseases by contacting a sample with the inventive substrate along with an internal standard which is isotope-labeled analog of the product cleaved by a targeted enzyme upon the substrate.
priorityDate 2006-03-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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