http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2014142253-A1
Outgoing Links
Predicate | Object |
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assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_d7ab7cf39d1e9e75496dec2e09d8bf21 |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H21-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F9-655345 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F9-2408 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F9-6553 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H21-00 |
filingDate | 2013-10-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_754be9987a5377b325d7154fe47d547f http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2510e548007e334b9ba5d66802cac187 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_42ba477cd0a333d0858a47e5335e5ed5 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_03081ae2d808ca0c1daa9e9c284be8ee http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ded88eeed88fffb3fec5294e3149ee20 |
publicationDate | 2014-05-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | US-2014142253-A1 |
titleOfInvention | Dithiolane Based Thiol Modifier For Labeling and Stronger Immobilization of Bio-Molecules On Solid Surfaces |
abstract | The thiol modified oligonucleotides have vast number of applications in the field of nucleic acid chemistry. The conjugates generated by mono thiol groups are unstable at higher temperature, in high salt concentration buffers and in presence other thiols. There is strong need to develop a novel thiol modifier probes that can generate multiple thiol groups. Described herein are efficient processes and compounds, dithiolane phosphoramidites derivative and dithiolane succinyl supports. The advantage of our cyclic disulfide thiol modifier is multifold a) each incorporation introduces two thiol groups; b) it can be introduced at any desired site of oligonucleotides; c) The symmetrical branching nature of the spacer in the linker arm of dithiolane allows for clean oligo synthesis, where cleavage of the linker arm and thereby of loss of oligo chain is prevented. We have successfully made 20-mer oligonucleotide containing single dithiolane derivative at 3′, and 21-mer oligonucleotides containing single dithiolane derivative at 5′ or in the middle of the mixed base sequence. HPLC and ESI MS analysis of these oligonucleotides indicated satisfactory purity and correct composition of these oligos, respectively. |
isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-11447451-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-3674407-A4 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-11236334-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2018181428-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-10786582-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-10406249-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-10781175-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2016210290-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2020109428-A1 |
priorityDate | 2012-10-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
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