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TiDEC

总结
a DNA-encoded substance library for drug screening with a novel encoding approach that allows previously unfeasible chemical reactions that massively broadens the diversity of producible molecules.
技术优势
Handling of large encoded compound screening libraries: tiDELs
Access to biologically relevant chemical space that is inaccessible by conventional DNA-encoded libraries: encoded natural product- and drug-derived compound classes
Efficient and rapid screening on target proteins by selection
Extremely reduced costs in comparison to conventional high-throughput screening
Accelerated identification of starting points for drug development programs
技术应用
The TIDEC platform technology and the tiDEL screening library are offered to pharma-companies, biotech companies, and non-profit organizations for drug identification and development programs.
详细技术说明
TiDEC addresses this severe
limitation. TiDEC exploits the stability
of oligopyrimidine adapter sequences
to a large variety of reaction
conditions, and reagents such as
transition metal catalysts and acidic
organocatalysts. Thus, TiDEC
enables efficient access to diverse
heterocyclic structures conjugated to
oligopyrimidine sequences from
simple and readily available starting
materials by a large variety of
catalysts. These oligonucleotideheterocycle
conjugates are readily
ligated to coding DNA sequences.
合作类型
Licensing
申请日期
20.12.2016
申请号码
EP20160823263 20161220
分类
- international:
C07H21/00; C40B40/06
- cooperative:
C07H21/00
其他
Patent application
ID号码
4452
国家/地区
德国

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