Matches in SemOpenAlex for { <https://semopenalex.org/work/W2980895614> ?p ?o ?g. }
Showing items 1 to 92 of
92
with 100 items per page.
- W2980895614 abstract "Conventional approaches for the discovery of bioactive small molecules typically follow a cycle of design, synthesis, purification and testing. This workflow usually employs a narrow toolkit of robust chemical reactions, and places equal value on every chemical entity regardless of bioactivity. Consequently, significant effort is invested into designing, making and purifying large numbers of compounds with low levels of bioactivity.Activity-Directed Synthesis (ADS) places the focus exclusively on bioactive molecules during the discovery phase, using activity to guide syntheses through an iterative discovery cycle. ADS exploits chemistry that may yield multiple product outcomes and are not commonly integrated into traditional discovery workflows. The process is structure-blind and function- driven, permitting the discovery of bioactive small molecules and their associated synthetic routes in parallel, mimicking elements of the process in which small molecule natural products are produced via biosynthetic pathways in nature.Integration of new chemistries into the ADS workflow would permit exploration of more diverse areas of chemical space using the approach. Organocatalysis was recognised to have potential to generate a wide range of scaffolds in a combinatorial manner and is robust enough to tolerate the miniaturised high-throughput format required for ADS. The potential for the use of organocatalysis in ADS was explored and successfully translated into a micro-scale format for application in ADS. Additionally, protocols were developed to remove undesirable functional groups from product mixtures prior to screening.The miniaturised organocatalytic chemistry was then applied in ADS to reaction arrays, seeking to use organocatalysis in ADS to discover novel androgen receptor agonists. Different strategies for reaction array design were developed, in addition to protocols for efficient execution of reaction arrays. Both conversion and bioactivity of product mixtures were assessed using a TR-FRET assay and NMR, highlighting issues that significantly decreased the number of reactions that yielded intermolecular products. However, successful identification of bioactive components within product mixtures that were not the result of intermolecular reactions demonstrated the potential for the protocols developed to be successful in identifying bioactive small molecules. Consequently, ADS is now poised to utilise organocatalysis to attempt to generate bioactive molecules for alternative biological targets." @default.
- W2980895614 created "2019-10-25" @default.
- W2980895614 creator A5058351089 @default.
- W2980895614 date "2019-04-01" @default.
- W2980895614 modified "2023-09-23" @default.
- W2980895614 title "Development of organocatalytic methods for activity-directed bioactive molecule discovery" @default.
- W2980895614 cites W2396443942 @default.
- W2980895614 hasPublicationYear "2019" @default.
- W2980895614 type Work @default.
- W2980895614 sameAs 2980895614 @default.
- W2980895614 citedByCount "0" @default.
- W2980895614 crossrefType "dissertation" @default.
- W2980895614 hasAuthorship W2980895614A5058351089 @default.
- W2980895614 hasConcept C111919701 @default.
- W2980895614 hasConcept C127413603 @default.
- W2980895614 hasConcept C146686406 @default.
- W2980895614 hasConcept C161624437 @default.
- W2980895614 hasConcept C161790260 @default.
- W2980895614 hasConcept C174998907 @default.
- W2980895614 hasConcept C177212765 @default.
- W2980895614 hasConcept C178790620 @default.
- W2980895614 hasConcept C183696295 @default.
- W2980895614 hasConcept C185592680 @default.
- W2980895614 hasConcept C207505557 @default.
- W2980895614 hasConcept C21547014 @default.
- W2980895614 hasConcept C21951064 @default.
- W2980895614 hasConcept C2779396153 @default.
- W2980895614 hasConcept C41008148 @default.
- W2980895614 hasConcept C55493867 @default.
- W2980895614 hasConcept C66972969 @default.
- W2980895614 hasConcept C70721500 @default.
- W2980895614 hasConcept C71240020 @default.
- W2980895614 hasConcept C74187038 @default.
- W2980895614 hasConcept C77088390 @default.
- W2980895614 hasConcept C85345410 @default.
- W2980895614 hasConcept C86803240 @default.
- W2980895614 hasConcept C93453677 @default.
- W2980895614 hasConcept C98045186 @default.
- W2980895614 hasConcept C99726746 @default.
- W2980895614 hasConceptScore W2980895614C111919701 @default.
- W2980895614 hasConceptScore W2980895614C127413603 @default.
- W2980895614 hasConceptScore W2980895614C146686406 @default.
- W2980895614 hasConceptScore W2980895614C161624437 @default.
- W2980895614 hasConceptScore W2980895614C161790260 @default.
- W2980895614 hasConceptScore W2980895614C174998907 @default.
- W2980895614 hasConceptScore W2980895614C177212765 @default.
- W2980895614 hasConceptScore W2980895614C178790620 @default.
- W2980895614 hasConceptScore W2980895614C183696295 @default.
- W2980895614 hasConceptScore W2980895614C185592680 @default.
- W2980895614 hasConceptScore W2980895614C207505557 @default.
- W2980895614 hasConceptScore W2980895614C21547014 @default.
- W2980895614 hasConceptScore W2980895614C21951064 @default.
- W2980895614 hasConceptScore W2980895614C2779396153 @default.
- W2980895614 hasConceptScore W2980895614C41008148 @default.
- W2980895614 hasConceptScore W2980895614C55493867 @default.
- W2980895614 hasConceptScore W2980895614C66972969 @default.
- W2980895614 hasConceptScore W2980895614C70721500 @default.
- W2980895614 hasConceptScore W2980895614C71240020 @default.
- W2980895614 hasConceptScore W2980895614C74187038 @default.
- W2980895614 hasConceptScore W2980895614C77088390 @default.
- W2980895614 hasConceptScore W2980895614C85345410 @default.
- W2980895614 hasConceptScore W2980895614C86803240 @default.
- W2980895614 hasConceptScore W2980895614C93453677 @default.
- W2980895614 hasConceptScore W2980895614C98045186 @default.
- W2980895614 hasConceptScore W2980895614C99726746 @default.
- W2980895614 hasLocation W29808956141 @default.
- W2980895614 hasOpenAccess W2980895614 @default.
- W2980895614 hasPrimaryLocation W29808956141 @default.
- W2980895614 hasRelatedWork W183508233 @default.
- W2980895614 hasRelatedWork W1973319249 @default.
- W2980895614 hasRelatedWork W201202673 @default.
- W2980895614 hasRelatedWork W2017281968 @default.
- W2980895614 hasRelatedWork W2039844339 @default.
- W2980895614 hasRelatedWork W2052567022 @default.
- W2980895614 hasRelatedWork W2063596638 @default.
- W2980895614 hasRelatedWork W2106132690 @default.
- W2980895614 hasRelatedWork W2111160165 @default.
- W2980895614 hasRelatedWork W2122748992 @default.
- W2980895614 hasRelatedWork W2159856147 @default.
- W2980895614 hasRelatedWork W243428369 @default.
- W2980895614 hasRelatedWork W2472153835 @default.
- W2980895614 hasRelatedWork W2794459433 @default.
- W2980895614 hasRelatedWork W2799949122 @default.
- W2980895614 hasRelatedWork W2908985664 @default.
- W2980895614 hasRelatedWork W2953157524 @default.
- W2980895614 hasRelatedWork W2982010076 @default.
- W2980895614 hasRelatedWork W562385480 @default.
- W2980895614 hasRelatedWork W81849507 @default.
- W2980895614 isParatext "false" @default.
- W2980895614 isRetracted "false" @default.
- W2980895614 magId "2980895614" @default.
- W2980895614 workType "dissertation" @default.