Results 181 to 190 of about 23,915 (334)
Efficient Synthesis of Cyclopropane-Fused Heterocycles with Bromoethylsulfonium Salt [PDF]
Aggarwal+66 more
core +2 more sources
Water‐Soluble Peptoids with Two Different Binding Sites for Strong ATP Chelation
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
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
Regiodivergent α- and β-Functionalization of Saturated <i>N</i>-Heterocycles by Photocatalytic Oxidation. [PDF]
Rackl JW+3 more
europepmc +1 more source
N-(N4-Aryl-N1 piperazinylmethyl)-4-(4'-methoxyphenyl)- piperidine-2,6-diones : CNS Depressants [PDF]
S. D. SAMANT, R. A. KULKARNI
openalex +1 more source
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]
O'Connell A+10 more
europepmc +1 more source
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
Syntheses of N-(Chlorobenzoylaminoalkyl)piperidines and N-(Chlorothiobenzoylaminoalkyl)piperidines
去来川 覚三+2 more
openalex +2 more sources