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Chiral Cyclic Aliphatic Linkers as Building Blocks for Sele..:

Francisco O. Battiti (6894923) ; Saheem A. Zaidi (1448953) ; Vsevolod Katritch (213067)..
https://figshare.com/articles/dataset/Chiral_Cyclic_Aliphatic_Linkers_as_Building_Blocks_for_Selective_Dopamine_D_sub_2_sub_or_D_sub_3_sub_Receptor_Agonists/16877162. , 2021

Link: https://doi.org/10.1021/acs.jmedchem.1c01433.s001

RT Journal
T1 <Title>Chiral Cyclic Aliphatic Linkers as Building Blocks for Selective Dopamine D 2 or D 3 Receptor Agonists</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftsmithonian:oai:figshare.com:article_16877162&Exemplar=1&LAN=DE
				
A1 Francisco O. Battiti (6894923)
A1 Saheem A. Zaidi (1448953)
A1 Vsevolod Katritch (213067)
A1 Amy Hauck Newman (1307901)
A1 Alessandro Bonifazi (1322385)
YR 2021
K1 Biophysics
K1 Biochemistry
K1 Medicine
K1 Molecular Biology
K1 Pharmacology
K1 Biotechnology
K1 Cancer
K1 Science Policy
K1 Infectious Diseases
K1 Biological Sciences not elsewhere classified
K1 Chemical Sciences not elsewhere classified
K1 protein coupled receptors
K1 modulating subtype selectivity
K1 introduce several potent
K1 cyclic aliphatic linkers
K1 b >(−)-( 1
K1 b >(+)-( 1
K1 r via inversion
K1 r selectivity toward
K1 dopaminergic ligands described
K1 receptor agonists linkers
K1 3 </ sub
K1 2 </ sub
K1 receptor subtypes
K1 >
K1 2
K1 r </
K1 </ sub
K1 >< sub
K1 trans </
K1 rel </
K1 k </
K1 cis </
K1 stereospecific fashion
K1 pharmacological observations
K1 new class
K1 key component
K1 innovative approach
K1 g
K1 characterized primary
K1 building blocks
K1 also introduced
K1 72 nm
K1 58 nm
JF https://figshare.com/articles/dataset/Chiral_Cyclic_Aliphatic_Linkers_as_Building_Blocks_for_Selective_Dopamine_D_sub_2_sub_or_D_sub_3_sub_Receptor_Agonists/16877162
LK http://dx.doi.org/https://doi.org/10.1021/acs.jmedchem.1c01433.s001
DO https://doi.org/10.1021/acs.jmedchem.1c01433.s001
SF ELIB - SuUB Bremen

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