204644-44-0Relevant articles and documents
Structure activity relationship study of benzo[d]thiazol-2(3H)one based σ receptor ligands
Bhat, Rohit,Fishback, James A.,Matsumoto, Rae R.,Poupaert, Jacques H.,McCurdy, Christopher R.
, p. 5011 - 5013 (2013/09/02)
Herein we report the SAR study which involved structural modifications to the linker length, aryl substitution and alkylamine ring size of the benzo[d]thiazol-2(3H)one based sigma receptor (σ) ligands. Many compounds in this series displayed low nanomolar affinity for the σ receptor subtypes. In particular, 8a showed high affinity (σ-1 Ki = 4.5 nM) for σ-1 receptors and moderately high selectivity (483-fold) over σ-2 receptors.
Synthesis and characterization of [3H]-SN56, a novel radioligand for the σ1 receptor
Fishback, James A.,Mesangeau, Christophe,Poupaert, Jacques H.,McCurdy, Christopher R.,Matsumoto, Rae R.
, p. 1 - 7 (2011/12/21)
The study of the binding characteristics of σ ligands in vivo and in vitro requires radiolabeled probes with high affinity and selectivity. The radioligand presently used for in vitro studies of the σ1 receptor, [3H](+)-pentazocine, has significant limitations; it is difficult to synthesize, has limited chemical stability, and can be problematic to obtain. Evaluation of a series of novel 2(3H)-benzothiazolone compounds revealed SN56 to have sub-nanomolar and preferential affinity for the σ1 subtype, relative to σ2 and non-sigma, binding sites. The goal of this study was to characterize the binding of [ 3H]-SN56 to σ1 receptors isolated from rat brain. Standard in vitro binding techniques were utilized to 1) determine the specificity and affinity of binding to σ1 receptors, 2) confirm that [3H]-SN56 labels sites previously identified as σ1 by comparing binding to sites labeled by [ 3H](+)-pentazocine, and 3) characterize the kinetics of binding. The results indicate that [3H]-SN56 exhibits 1) specific, saturable, and reversible binding to the σ1 receptor, with Bmax = 340 ± 10 fmol/mg and Kd = 0.069 ± 0.0074 nM, 2) competitive displacement by classical sigma compounds, yielding σ1 Ki values consistent with those reported in the literature, and 3) binding kinetics compatible with a 90 min incubation, and filtration for separation of free and bound radioligand. The results of these studies suggest that [3H]-SN56 may serve as a viable alternative to [3H](+)-pentazocine in radioligand binding assays.
New substituted benzothiazolinones
-
, (2008/06/13)
Compounds of general formula (I): STR1 in which: R1 represents a hydrogen atom or a lower alkyl group, and R2 represents a substituted or unsubstituted alkyl, a phenyl or a substituted or unsubstituted heteroaryl, their enantiomers,
