Exploiting intracellular oncogenic proteins to release cytotoxins. [PDF]
Schild M, Gillingham D.
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Two-Step Ligand-Directed Covalent Fluorescent Labeling of the Adenosine A<sub>1</sub>-Receptor That Maintains Its Orthosteric Binding Site's Availability to Bind Ligands. [PDF]
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Unveiling the Electrochemical Reversibility of Multielectron Redox in s-Tetrazine Derivatives for Large-Capacity Electrode Materials. [PDF]
Min S, Jo DH, Byon HR, Kwon JE.
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Synthesis of Cyclopropene-Modified Fatty Acids Allows Single-Cell Quantification of Uptake by Immune Cells. [PDF]
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Live-cell 3D-SIM of Rift Valley fever virus NSs filaments reveals a polygon web architecture. [PDF]
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ChemCell: Chemical Tethering of Large Biomolecules to Cell Surfaces through Diels-Alder Ligation
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Related searches:
The unknown unsubstituted tetrazines: 1,2,3,4-tetrazine and 1,2,3,5-tetrazine
The Journal of Organic Chemistry, 1991Ab initio theoretical methods have been used to determine the equilibrium geometry of the unsubstituted 1,2,3,4- and 1,2,3,5-tetrazines. Double zeta (DZ) and double zeta plus polarization (DZP) basis sets have been used at both the self-consistent field (SCF) and single and double excitation configuration interaction (CISD) levels of theory.
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The photodissociation of s-tetrazine and dimethyl-s-tetrazine
Chemical Physics Letters, 1978Abstract The photodissociation of s -tetrazine (ST) and its dimethyl derivative (DMST) has been investigated in hexane solutions at room temperature and in argon matrices and organic molecular crystals at cryogenic temperatures. Contrary to what has generally been assumed, only ST photodissociates upon excitation into its lowest excited singlet ...
D.M. Burland, F. Carmona, J. Pacansky
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