A novel thiazole-sulfonamide hybrid molecule as a promising dual tubulin/carbonic anhydrase IX inhibitor with anticancer activity. [PDF]
Khasawneh HEN+7 more
europepmc +1 more source
Development and Breeding of Herbicide‐Resistant Sorghum for Effective Cereal‐Legume Intercropping
This study identified two SbALS mutations (A93T and S624N) conferring robust herbicide resistance in sorghum, facilitating efficient weed control. Structural analysis revealed that imazamox resistance is mediated by disrupted herbicide binding. Furthermore, 126 imazamox resistant soybean varieties are screened for sorghum‐soybean intercropping ...
Sanyuan Tang+20 more
wiley +1 more source
EFFECT OF SULFONAMIDES UPON EXPERIMENTAL GUNSHOT WOUNDS INVOLVING PERIPHERAL NERVES*
Loyal Davis+3 more
openalex +2 more sources
Synthesis, structural studies, and inhibitory potential of selected sulfonamide analogues: insights from in silico and in vitro analyses. [PDF]
Noor T+8 more
europepmc +1 more source
Weakly solvating electrolytes (WSEs) use anion‐dominated solvation to form stable interphase layers, overcoming energy density and lifespan limitations. This review clarifies their design, anion‐mediated interface regulation, and compatibility with lithium/post‐lithium systems, distinguishing them from conventional electrolytes, high concentration ...
Xue Li+6 more
wiley +1 more source
4-Substituted Pyridine-3-Sulfonamides as Carbonic Anhydrase Inhibitors Modified by Click Tailing: Synthesis, Activity, and Docking Studies. [PDF]
Szafrański K+6 more
europepmc +1 more source
Construction of Biaryl Sulfonamides via Pd(II)-Catalyzed Cross-Coupling of C(sp<sup>2</sup>)-H Bonds with Iodobenzenesulfonamides. [PDF]
Bhattacharya D+3 more
europepmc +1 more source
SULFONAMIDE THERAPY IN CLEAN THORACOPLASTY CASES
Eric K. Johnson+2 more
openalex +2 more sources
Integrated computational and experimental identification of <i>N-[(1H-1,2,4-triazol-3-yl)phenyl]-1-(1H-pyrazolo[3,4-b]pyridin-3-yl)methanamide</i> as a potent and selective TIM-3 inhibitor for NSCLC immunotherapy. [PDF]
Ying X, Lou Y, Wu Y, Hu W.
europepmc +1 more source
EGFR inhibitors can be made especially effective through binding small‐molecule inhibitors that target the allosteric pocket. Structural and functional analysis affords new insights into the compositions and their molecular connections that afford effective inhibitors. ABSTRACT The epidermal growth factor receptor (EGFR) tyrosine kinase is an important
Surbhi P. Chitnis+7 more
wiley +1 more source