http://rdf.ncbi.nlm.nih.gov/pubchem/patent/BR-112012012589-A2

Outgoing Links

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_114e4423ec77cbc8dab9d0a98909704e
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D257-02
filingDate 2011-03-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7219a7adb76f5a4a5406b41c6bc2c82d
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publicationDate 2015-09-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber BR-112012012589-A2
titleOfInvention zn (ii) colorimetric sensor and process for the preparation of this
abstract colorimetric sense to base zn (ii) and process for the preparation thereof. The present invention describes a novel chemosensor-colorimetric molecule having an aza-macrocycle zn (ii) (l.zn) complex (scheme 1, formula 1a), which can selectively and effectively recognize atp (adenosine triphosphate), a biologically significant triphosphate in Since the atp is the source of energy in living organisms, l.zn (Scheme 1, Formula 1a) can also be used as a staining agent in living cells by binding to the generated atp. in situ during metabolic processes. l.zn (scheme 1, formula 1a) was considered to be non-toxic to the living cell and microbial cell growth studies could be monitored. thus, l.zn (scheme 1, formula 1a) could be used as a viable coloring agent. furthermore, the solubility of 1.zn (scheme 1, formula 1a) in water was elevated in the presence of Î ± -cd (cyclodextrin) (scheme 2). This helped to achieve faster and more intense staining of living cells. thus, the coloring efficiency could also be further improved by using <244> -cd.
priorityDate 2010-05-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

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Total number of triples: 25.