http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-105112047-A
Outgoing Links
Predicate | Object |
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assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_d9de52bba13e16028dffa8775e3f3f28 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09K11-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C49-753 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C49-747 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N21-64 |
filingDate | 2015-08-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c473d140f28f3f2baa57e60f979df51b http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3319c016138fd52bafde3de82bbcb901 |
publicationDate | 2015-12-02-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | CN-105112047-A |
titleOfInvention | A kind of curcumin derivative fluorescent molecular probe and its application |
abstract | The invention discloses a novel curcumin derivative fluorescent molecular probe, which has the general formula of the following structure: Wherein, R may be hydrogen, fluorine, chlorine, bromine, iodine, methoxy, ethoxy, nitro or an alkyl chain having 1 to 3 carbon atoms. The invention also discloses the application of the novel fluorescent molecular probe in the field of pH-responsive fluorescence detection. The fluorescent-response region of the probe is acidic-neutral pH, and the pH range is 2-8. Compared with the existing traditional curcumin molecular probes, the fluorescent molecular probes of the present invention eliminate the influence of intramolecular hydrogen bonds and metal chelation effects, and the fluorescence enhancement times are multiplied. |
priorityDate | 2015-08-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 18.