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Structure Activity Relationships for a Series of Eticloprid..:

Anver Basha Shaik (7500401) ; Comfort A. Boateng (3617120) ; Francisco O. Battiti (10830442)...
https://figshare.com/articles/journal_contribution/Structure_Activity_Relationships_for_a_Series_of_Eticlopride-Based_Dopamine_D_sub_2_sub_D_sub_3_sub_Receptor_Bitopic_Ligands/16797486. , 2021

Link: https://doi.org/10.1021/acs.jmedchem.1c01353.s001

RT Journal
T1 <Title>Structure Activity Relationships for a Series of Eticlopride-Based Dopamine D 2 /D 3 Receptor Bitopic Ligands</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftsmithonian:oai:figshare.com:article_16797486&Exemplar=1&LAN=DE
				
A1 Anver Basha Shaik (7500401)
A1 Comfort A. Boateng (3617120)
A1 Francisco O. Battiti (10830442)
A1 Alessandro Bonifazi (1322385)
A1 Jianjing Cao (1307898)
A1 Li Chen (5749)
A1 Rezvan Chitsazi (4751388)
A1 Saiprasad Ravi (11551926)
A1 Kuo Hao Lee (8436282)
A1 Lei Shi (8144)
A1 Amy Hauck Newman (1307901)
YR 2021
K1 Biophysics
K1 Biochemistry
K1 Molecular Biology
K1 Neuroscience
K1 Pharmacology
K1 Biotechnology
K1 Cancer
K1 Chemical Sciences not elsewhere classified
K1 sterically bulky groups
K1 require long linkers
K1 molecular models confirmed
K1 structure activity relationships
K1 r bioconjugate tools
K1 >- alkyl groups
K1 position modifications would
K1 33 </ b
K1 11 </ b
K1 r binding affinities
K1 pyrrolidine ring system
K1 >- alkylated compounds
K1 3 nm )
K1 3 </ sub
K1 receptor bitopic ligands
K1 2 </ sub
K1 bitopic ligands
K1 pyrrolidine ring
K1 >- alkylated
K1 n </
K1 improved affinities
K1 crystal structure
K1 small pyrrolidine
K1 r antagonists
K1 pyrrolidine nitrogen
K1 97 nm
K1 77 nm
K1 436 nm
K1 >- alkylations
K1 >- alkylation
K1 secondary pharmacophore
K1 lead molecules
K1 g
JF https://figshare.com/articles/journal_contribution/Structure_Activity_Relationships_for_a_Series_of_Eticlopride-Based_Dopamine_D_sub_2_sub_D_sub_3_sub_Receptor_Bitopic_Ligands/16797486
LK http://dx.doi.org/https://doi.org/10.1021/acs.jmedchem.1c01353.s001
DO https://doi.org/10.1021/acs.jmedchem.1c01353.s001
SF ELIB - SuUB Bremen

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