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Structure–Activity Relationship of 3‑Methylcytidine-5′-α,β-..:

Mirko Scortichini (4007366) ; Riham Mohammed Idris (12004297) ; Susanne Moschütz (8682114)...
https://figshare.com/articles/journal_contribution/Structure_Activity_Relationship_of_3_Methylcytidine-5_-_-methylenediphosphates_as_CD73_Inhibitors/19074061. , 2022

Link: https://doi.org/10.1021/acs.jmedchem.1c01852.s001

RT Journal
T1 <Title>Structure–Activity Relationship of 3‑Methylcytidine-5′-α,β-methylenediphosphates as CD73 Inhibitors</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftsmithonian:oai:figshare.com:article_19074061&Exemplar=1&LAN=DE
				
A1 Mirko Scortichini (4007366)
A1 Riham Mohammed Idris (12004297)
A1 Susanne Moschütz (8682114)
A1 Antje Keim (12004300)
A1 Veronica Salmaso (2609254)
A1 Clemens Dobelmann (6493580)
A1 Paola Oliva (5065214)
A1 Karolina Losenkova (6493583)
A1 Heikki Irjala (456636)
A1 Samuli Vaittinen (4233496)
A1 Jouko Sandholm (620280)
A1 Gennady G. Yegutkin (421106)
A1 Norbert Sträter (1550494)
A1 Anna Junker (1950910)
A1 Christa E. Müller (1550497)
A1 Kenneth A. Jacobson (117993)
YR 2022
K1 Biophysics
K1 Biochemistry
K1 Cell Biology
K1 Molecular Biology
K1 Neuroscience
K1 Pharmacology
K1 Biotechnology
K1 Cancer
K1 Virology
K1 Chemical Sciences not elsewhere classified
K1 predicted conformational diversity
K1 benzyloxyimino group (<
K1 >- amido group
K1 5 ′- α
K1 blocking cd73 activity
K1 two inhibitors indicated
K1 human cd73 inhibitors
K1 3 ‑ methylcytidine
K1 24 </ b
K1 cd73 inhibitors
K1 adenine inhibitors
K1 p </
K1 k </
K1 e </
K1 </ sub
K1 ∼ 20
K1 tumor tissues
K1 subsequent conjugation
K1 reporter moieties
K1 recently reported
K1 ray structures
K1 pyrimidine nucleotides
K1 potentially useful
K1 inhibitory potency
K1 greatly enhanced
K1 functionalized congeners
K1 cancer immunotherapy
K1 anticancer drugs
K1 >< sup
K1 >< sub
K1 673 nm
K1 436 nm
JF https://figshare.com/articles/journal_contribution/Structure_Activity_Relationship_of_3_Methylcytidine-5_-_-methylenediphosphates_as_CD73_Inhibitors/19074061
LK http://dx.doi.org/https://doi.org/10.1021/acs.jmedchem.1c01852.s001
DO https://doi.org/10.1021/acs.jmedchem.1c01852.s001
SF ELIB - SuUB Bremen

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