Molecular Characterization of Pharmacological Properties and Selectivity of SWR-0315NA for .BETA.3-Adrenoceptors

Ahmed, Maruf; Hanaoka, Yoko; Kiso, Tatsuya; Kakita, Takao; Ohtsubo, Yoshikazu; Nagatomo, Takafumi

doi:10.1248/bpb.27.718

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(2 citation statements)

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“…Relative to (À)-isoproterenol, SWR-0338SA and SWR-0345HA have respective %E max values of 76.95% and 83.47% for cAMP accumulation in 3 -adrenoceptor CHO cells. Although SWR-0342SA and SWR-0315NA did not show any binding selectivity towards -adrenoceptor subtypes, they showed functional selectivity for 3 -adrenoceptors (Kiso et al 1999;Ahmed et al 2004). SWR-0098NA had a comparatively low binding profile for -adrenoceptor subtypes, whereas SWR-0065HA had high binding affinity for 2 -adrenoceptors only, having a 3-fold and 6-fold higher binding affinity than for 1 -and 3 -adrenoceptor subtypes, respectively.…”

Section: Resultsmentioning

confidence: 99%

“…Affinities of these SWR-compounds for 3 -adrenoceptor subtype have been discussed in our previous article (Ahmed et al 2003). SWR-0315NA has also been proved to be a 3adrenoceptor subtype selective drug in a second messenger accumulation assay (Ahmed et al 2004). The anti-obesity and anti-diabetic activity of SWR-0342SA in mice has also been reported, which reveals it to be a functionally 3 -adrenoceptor selective compound (Kiso et al 1999).…”

Section: Introductionmentioning

confidence: 96%

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Comparison of the binding affinity of some newly synthesized phenylethanolamine and phenoxypropanolamine compounds at recombinant human β- and α1-adrenoceptor subtypes

Ahmed

Hanaoka

Kiso³

et al. 2005

Journal of Pharmacy and Pharmacology

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We evaluated six new compounds, SWR-0065HA ([4-[2-[3-[[(3,4-dihydro-4-oxo-[1,2,4]-triazino(4,5-a)indol)-lyl]oxy]-2-hydroxypropylamino]ethoxy]phenyl]acetic acid methyl ester hydrochloride), SWR-0098NA ((R*R*-UE)-(E)-[4-[3-[(2-phenyl-2-hydroxyethyl)amino]-1-butenyl]phenoxy]acetic acid sodium salt), SWR-0315NA ((E, Z)-[4[[1-[2-[(3-phenoxy-2-hydroxy propyl)]amino]ethyl]-1-propenyl]phenoxy]acetic acid sodium), SWR-0338SA ((E)-[4-[5-[(2-phenyl-2-hydroxyethyl)amino]-2-pentene-3-yl]phenoxy] acetic acid ethanedioic acid), SWR-0342SA ((S)-(Z)-[4-[[1-[2-[(2-hydroxy-3-phenoxypropyl)]amino] ethyl]-1-propenyl]phenoxy]acetic acid ethanedioic acid) and SWR-0345HA ((E)-2-methyl-3-[4-[2-(2-phenyl-2-hydroxyethylamino)ethoxy]phenyl]-2-propenoic acid ethyl ester hydrochloride) for their potencies as selective ligands at human beta-adrenoceptors expressed in COS-7 cells and compared the binding affinities for human alpha(1)-adrenoceptors expressed in Chinese hamster ovary (CHO) cells using a radioligand-binding assay. Phenoxypropanolamine derivatives SWR-0315NA and SWR-0342SA showed higher binding affinities for beta-adrenoceptor subtypes; SWR-0065HA, however, showed a higher affinity for only beta-adrenoceptors, accounting for 3-fold and 6-fold selectivity against beta(1)- and beta(3)-adrenoceptors. Compounds SWR-0315NA and SWR-0342SA did not show any binding selectivity for any of the subtypes. However, functionally these two compounds are selective for beta(3)-adrenoceptors. Among the phenylethanolamine derivatives, SWR-0338SA and SWR-0345HA showed 9-fold and 16-fold higher binding selectivity for beta(3)-adrenoceptors against beta(1)-adrenoceptors, respectively, whereas they both showed a 7-fold higher binding selectivity for beta(3)-adrenoceptors against beta(2)-adrenoceptors. SWR-0098NA did not show any significant binding affinity for any of the beta-adrenoceptor subtypes. These compounds, except for SWR-0098NA, were not found to possess any significant binding affinity for alpha(1)-adrenoceptor subtypes over that for beta-adrenoceptor subtypes. However, SWR-0098NA has about a 3-fold to 22-fold higher binding selectivity for alpha(1)-adrenoceptor subtypes against beta-adrenoceptor subtypes, making it difficult for use in a beta-adrenoceptor receptor study. Compounds SWR-0315NA and SWR-0342SA have similar binding potency for alpha(1)-adrenoceptors as adrenaline (epinephrine), proving the finding of this manuscript that this phenoxypropanolamine group of beta-adrenoceptor ligands could also be used as alpha(1)-adrenoceptor ligands. Functional assays have to be performed to confirm their agonistic activity.

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Section: Resultsmentioning

confidence: 99%

Section: Introductionmentioning

confidence: 96%