Results 181 to 190 of about 23,915 (334)

Efficient Synthesis of Cyclopropane-Fused Heterocycles with Bromoethylsulfonium Salt [PDF]

open access: yes, 2013
Aggarwal   +66 more
core   +2 more sources

Water‐Soluble Peptoids with Two Different Binding Sites for Strong ATP Chelation

open access: yesChemistry – A European Journal, Volume 31, Issue 51, September 11, 2025.
ATP is key for activating enzymes associated with cancer. A potential therapeutic approach is strong binding of ATP, making it unavailable to enzymes. The water‐soluble peptoid P1‐TB incorporates two synergistic binding sites for ATP: terpyridine‐Zn²⁺ and 4‐CPBA that bind ATP's phosphate and diol groups, respectively, and exhibits an exceptional Kᴅ‐ATP
Nicole Vorobyov, Galia Maayan
wiley   +1 more source

Directing Effects of Silyl and Germyl Groups in Transition‐Metal‐Catalyzed Allylic Substitution

open access: yesChemistry – A European Journal, EarlyView.
Despite the maturity of transition‐metal‐catalyzed allylic substitution, unsymmetrical 1,3‐disubstituted electrophiles remain underexplored due to inherent regioselectivity challenges. This Concept highlights the strategic use of silyl and germyl groups to overcome this limitation, steering bond formation with high regiocontrol and serving as linchpins
Daniel Brösamlen, Martin Oestreich
wiley   +1 more source

4‐Dimethylamino‐1,8‐Naphthalimide as a Fluorescence Signal Amplification for Site Selective and in Situ Probing of the Hydroxyl Radical

open access: yesChemistry – A European Journal, EarlyView.
4‐dimethylamino‐1,8‐naphthalimide (NMI) as new fluorescence‐responsive tool for HO• detection. Proof of concept illustrating that NMI selectively probes HO• produced by Cu‐bound to Aβ16 in presence of scavengers with an amplified response. Abstract Overproduction of reactive oxygen species (ROS) is involved in several diseases.
Yelisetty Venkata Suseela   +4 more
wiley   +1 more source

Transaminase-Triggered Cascades for the Synthesis and Dynamic Kinetic Resolution of Chiral N-Heterocycles. [PDF]

open access: yesAngew Chem Int Ed Engl
O'Connell A   +10 more
europepmc   +1 more source

Potent, Selective, and Drug‐like G Protein‐coupled Receptor Kinase 5 and 6 Inhibitors: Design, Synthesis, and X‐ray Structural Studies

open access: yesChemMedChem, Accepted Article.
We report here the design, synthesis, and evaluation of small molecules, drug‐like G protein‐coupled receptor kinase 5 (GRK5) inhibitors. GRK5 has become an important drug development target against heart failure and cancer. GRK6, a close homolog of GRK5, is considered as a possible therapeutic target for multiple myeloma.
Arun K Ghosh   +5 more
wiley   +1 more source

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