Results 51 to 60 of about 1,308 (200)
Riluzole metabolism guided the design of benzo[d]thiazole inhibitors of casein kinase 1 delta (CK1δ), a kinase linked to amyotrophic lateral sclerosis (ALS). Docking supported ATP site recognition by the hydroxylamine metabolite and hydrazine analogues, leading to compounds showing improved potency and retained predicted blood brain barrier ...
Simone Adorinni +18 more
wiley +1 more source
Synthesis of novel pyrano[2,3-b]quinolines from simple acetanilides via intramolecular 1,3-dipolar cycloaddition [PDF]
Some novel isoxazole and pyrazole fused pyrano[2,3-b]quinolines were synthesized from simple acetanilides via intramolecular 1,3-dipolar cycloaddition reactions involving nitrones, nitrile oxides and nitrile imines as 1,3-dipoles, in a regioselective ...
BARUAH , B, BHUYAN , P J, KALITA , P K
core
The use of thermochemical cycles makes it possible to determine substituent effects on the homolytic bond dissociation free energies, BDFE, of the oxygen-acetyl bonds in substituted phenyl acetates and the nitrogen-acetyl bonds in substituted ...
Andersen, Mogens L. +11 more
core +1 more source
HIV‐1 reverse transcriptase (HIV‐1 RT) is a polymerase enzyme and a key target in HIV‐1 therapy. The discovery of selective HIV‐1 RT inhibitors has highlighted thiazole scaffolds and their derivatives, thiazolidine‐2‐one and thiazolidine‐2,4‐dione, as promising structures for the rational design of novel non‐nucleoside reverse transcriptase inhibitors (
José Arion da Silva Moura +9 more
wiley +1 more source
Buccal absorption as a parameter of analgesic activity of some p-substituted acetanilides
The extent of buccal absorption of 16 p-substituted acetanilides is related parabolically to analgesic activity. The correlation is slightly better than that between log (partition coefficient) and analgesic activity.
J C DEARDEN, ERIC TOMLINSON
core +1 more source
A series of diethylene glycol‐linked cyclic derivatives with diversity in the heterocyclic motif have been synthesized and screened for antitumor activity. Two bis‐thiazolo[3,2‐a]pyrimidinone derivatives displayed moderate cytotoxicity, high selectivity against hepatocellular carcinoma cells, promising VEGFR2, and remarkable FGFR2 inhibitory activities
Sami A. Al‐Hussain +6 more
wiley +1 more source
Chemical Laboratory, Smt. B. C. J. Science College, Cambay Manuscript received 10 October 1971; revised 17 July 1972; accepted 6 February 1973 Benzyl anilines were condensed with chloroacetyl chloride and the resulting chloroacetanilides on heating ...
J. J. TRIVEDI, P. B. PATEL
core +1 more source
The Dangers of Acetanilid. [PDF]
Dodge City, Kan., July 14, 1905. To the Editor: -I was walking along the street some months ago and overtook my venerable friend, the Methodist minister, who said "Doctor, I'm glad to see you. What is antikamnia?" I told him that it is a mixture of uncertain composition, used with greater or less success for the relief of pain; that its principal ...
openaire +2 more sources
KV7.1 antagonists hold potential for the treatment of diarrhea, reflux esophagitis, and hypoinsulinemia. To derive structure–activity relationships, the lead KV7.1 antagonist L768,673 was thoroughly modified in 1‐ and 3‐positions. The 3‐fluoropropyl‐substituted 1,4‐benzodiazepine showed promising KV7.1 inhibitory activity, qualifying it as a potential ...
Florian Roßner +3 more
wiley +1 more source
Abstract Subsurface microbial ecosystems associated with hydrocarbon reservoirs are shaped by temperature, salinity, redox gradients, and fluid flow. However, the drivers of microbial activity and hydrocarbon biodegradation over geologic timescales remain poorly constrained.
Meera P. Shah +8 more
wiley +1 more source

