http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-112724085-B
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09K2211-1029 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09K11-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N21-6428 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D221-16 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N21-64 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09K11-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D221-16 |
| filingDate | 2021-01-11-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2022-05-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2022-05-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-112724085-B |
| titleOfInvention | Fluorescent molecular probes induced by pyrroloisoquinoline aggregation and their preparation and application |
| abstract | The present invention provides a fluorescent molecular probe induced by pyrrole isoquinoline aggregation and its preparation and application. The pyrrole isoquinoline derivatives in the present invention have a simple synthesis method, the synthesized fluorescent probes have various emission wavelengths, have large Stokes shifts, good photostability, and have aggregation-induced fluorescence properties. At the same time, this type of fluorescent probe molecule can specifically bind to lipid droplets in cells to realize labeling and fluorescence imaging of lipid droplets in cells. The structure of described pyrrole isoquinoline derivatives is as follows: |
| priorityDate | 2021-01-11-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 71.