Practical approaches to evaluating and optimizing brain exposure in early drug discovery
Developing drugs for CNS related diseases continues to be one of the most challenging endeavors in drug discovery. This is at least in part related to the existence of the Blood Brain Barrier (BBB), a complex multicellular organization that provides selective access to required nutrients and hormone...
Ausführliche Beschreibung
Autor*in: |
Freeman, Burgess B. [verfasserIn] |
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E-Artikel |
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Sprache: |
Englisch |
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2019transfer abstract |
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Enthalten in: Electrochemical synthesis, photodegradation and antibacterial properties of PEG capped zinc oxide nanoparticles - Jose, Ajay ELSEVIER, 2018, Amsterdam [u.a.] |
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Übergeordnetes Werk: |
volume:182 ; year:2019 ; day:15 ; month:11 ; pages:0 |
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DOI / URN: |
10.1016/j.ejmech.2019.111643 |
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10.1016/j.ejmech.2019.111643 doi /cbs_pica/cbs_olc/import_discovery/elsevier/einzuspielen/GBV00000000000788.pica (DE-627)ELV048263524 (ELSEVIER)S0223-5234(19)30777-9 DE-627 ger DE-627 rakwb eng 570 540 VZ BIODIV DE-30 fid 42.00 bkl Freeman, Burgess B. verfasserin aut Practical approaches to evaluating and optimizing brain exposure in early drug discovery 2019transfer abstract nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Developing drugs for CNS related diseases continues to be one of the most challenging endeavors in drug discovery. This is at least in part related to the existence of the Blood Brain Barrier (BBB), a complex multicellular organization that provides selective access to required nutrients and hormones, while removing waste and restricting exposure to potential harmful toxins, pathogens, and xenobiotics. Consequently, designing and selecting molecules that can overcame this protection system are unique and critical aspects of the CNS drug discovery. Here we review modern CNS pharmacokinetic concepts and methods suitable for early drug discovery, and medicinal chemistry strategies towards molecules with optimal CNS exposure. Developing drugs for CNS related diseases continues to be one of the most challenging endeavors in drug discovery. This is at least in part related to the existence of the Blood Brain Barrier (BBB), a complex multicellular organization that provides selective access to required nutrients and hormones, while removing waste and restricting exposure to potential harmful toxins, pathogens, and xenobiotics. Consequently, designing and selecting molecules that can overcame this protection system are unique and critical aspects of the CNS drug discovery. Here we review modern CNS pharmacokinetic concepts and methods suitable for early drug discovery, and medicinal chemistry strategies towards molecules with optimal CNS exposure. Brain Elsevier Free drug hypothesis Elsevier BBB Elsevier Penetration Elsevier CNS Elsevier Drug design Elsevier Pharmacokinetics Elsevier Yang, Lei oth Rankovic, Zoran oth Enthalten in Elsevier Science Jose, Ajay ELSEVIER Electrochemical synthesis, photodegradation and antibacterial properties of PEG capped zinc oxide nanoparticles 2018 Amsterdam [u.a.] (DE-627)ELV000457477 volume:182 year:2019 day:15 month:11 pages:0 https://doi.org/10.1016/j.ejmech.2019.111643 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U FID-BIODIV SSG-OLC-PHA 42.00 Biologie: Allgemeines VZ AR 182 2019 15 1115 0 |
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Practical approaches to evaluating and optimizing brain exposure in early drug discovery |
abstract |
Developing drugs for CNS related diseases continues to be one of the most challenging endeavors in drug discovery. This is at least in part related to the existence of the Blood Brain Barrier (BBB), a complex multicellular organization that provides selective access to required nutrients and hormones, while removing waste and restricting exposure to potential harmful toxins, pathogens, and xenobiotics. Consequently, designing and selecting molecules that can overcame this protection system are unique and critical aspects of the CNS drug discovery. Here we review modern CNS pharmacokinetic concepts and methods suitable for early drug discovery, and medicinal chemistry strategies towards molecules with optimal CNS exposure. |
abstractGer |
Developing drugs for CNS related diseases continues to be one of the most challenging endeavors in drug discovery. This is at least in part related to the existence of the Blood Brain Barrier (BBB), a complex multicellular organization that provides selective access to required nutrients and hormones, while removing waste and restricting exposure to potential harmful toxins, pathogens, and xenobiotics. Consequently, designing and selecting molecules that can overcame this protection system are unique and critical aspects of the CNS drug discovery. Here we review modern CNS pharmacokinetic concepts and methods suitable for early drug discovery, and medicinal chemistry strategies towards molecules with optimal CNS exposure. |
abstract_unstemmed |
Developing drugs for CNS related diseases continues to be one of the most challenging endeavors in drug discovery. This is at least in part related to the existence of the Blood Brain Barrier (BBB), a complex multicellular organization that provides selective access to required nutrients and hormones, while removing waste and restricting exposure to potential harmful toxins, pathogens, and xenobiotics. Consequently, designing and selecting molecules that can overcame this protection system are unique and critical aspects of the CNS drug discovery. Here we review modern CNS pharmacokinetic concepts and methods suitable for early drug discovery, and medicinal chemistry strategies towards molecules with optimal CNS exposure. |
collection_details |
GBV_USEFLAG_U GBV_ELV SYSFLAG_U FID-BIODIV SSG-OLC-PHA |
title_short |
Practical approaches to evaluating and optimizing brain exposure in early drug discovery |
url |
https://doi.org/10.1016/j.ejmech.2019.111643 |
remote_bool |
true |
author2 |
Yang, Lei Rankovic, Zoran |
author2Str |
Yang, Lei Rankovic, Zoran |
ppnlink |
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isOA_txt |
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hochschulschrift_bool |
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author2_role |
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doi_str |
10.1016/j.ejmech.2019.111643 |
up_date |
2024-07-06T18:22:07.113Z |
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