http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-9641174-A1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_c39b670713226dbdaa17ded6cd96a21b |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-533 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-533 |
| filingDate | 1996-06-03-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3add745e8471debe60cc735ecd8ade03 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_557cbfc0c0b6aeeb7eb996dc35aa4648 |
| publicationDate | 1996-12-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | WO-9641174-A1 |
| titleOfInvention | Fluorescent labeling reagents |
| abstract | A class of sulforhodamine labeling reagents capable of binding with a biomolecular species to produce a conjugate with fluorescent properties. The sulforhodamine labeling reagents have the structure (I). The group X is selected from an alkyl, an olefin, a monocyclic aliphatic saturated hydrocarbon, an aryl, or nothing at all. Alkyl denotes an acyclic saturated aliphatic straight or branched chain hydrocarbon. An olefin denotes an unsaturated aliphatic hydrocarbon. An aryl is used to denote an aromatic ring, a substituted aromatic ring, and fused aromatic rings. The group Y is selected from an amide, a substituted amide, or nothing at all. The group Z is selected from a monocyclic aliphatic hydrocarbon, an aryl, or an alkyl, as defined with respect to group X, a polyethylene glycol chain of the general form (CH2CH2O)n, or nothing at all. The alkyl or polyethylene glycol chain may further have inert intermediate amide, ether, or disulfide functionalities. The group X, group Y, and group Z cannot all be nothing at all or non-existent. The group R is an electrophilic moiety suitable for conjugation of the fluorescent labeling reagent with a biomolecular species. Also disclosed is a method of making the reagents. |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-9845705-A3 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-9845705-A2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-2752465-A4 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-6165800-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-9854574-A3 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7588908-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-9854574-A2 |
| priorityDate | 1995-06-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 140.