Ford BM - Search Results

1

CB1 and CB2 receptors are novel molecular targets for Tamoxifen and 4OH-Tamoxifen.

Prather PL, FrancisDevaraj F, Dates CR, Greer AK, Bratton SM, Ford BM, Franks LN, Radominska-Pandya A. Prather PL, et al. Among authors: ford bm. Biochem Biophys Res Commun. 2013 Nov 15;441(2):339-43. doi: 10.1016/j.bbrc.2013.10.057. Epub 2013 Oct 19. Biochem Biophys Res Commun. 2013. PMID: 24148245 Free PMC article.

2

Evaluation of (Z)-2-((1-benzyl-1H-indol-3-yl)methylene)-quinuclidin-3-one analogues as novel, high affinity ligands for CB1 and CB2 cannabinoid receptors.

Madadi NR, Penthala NR, Brents LK, Ford BM, Prather PL, Crooks PA. Madadi NR, et al. Among authors: ford bm. Bioorg Med Chem Lett. 2013 Apr 1;23(7):2019-21. doi: 10.1016/j.bmcl.2013.02.025. Epub 2013 Feb 14. Bioorg Med Chem Lett. 2013. PMID: 23466226 Free PMC article.

3

Design, synthesis, and biological evaluation of aminoalkylindole derivatives as cannabinoid receptor ligands with potential for treatment of alcohol abuse.

Vasiljevik T, Franks LN, Ford BM, Douglas JT, Prather PL, Fantegrossi WE, Prisinzano TE. Vasiljevik T, et al. Among authors: ford bm. J Med Chem. 2013 Jun 13;56(11):4537-50. doi: 10.1021/jm400268b. Epub 2013 May 22. J Med Chem. 2013. PMID: 23631463 Free PMC article.

4

Characterization of the intrinsic activity for a novel class of cannabinoid receptor ligands: Indole quinuclidine analogs.

Franks LN, Ford BM, Madadi NR, Penthala NR, Crooks PA, Prather PL. Franks LN, et al. Among authors: ford bm. Eur J Pharmacol. 2014 Aug 15;737:140-8. doi: 10.1016/j.ejphar.2014.05.007. Epub 2014 May 20. Eur J Pharmacol. 2014. PMID: 24858620 Free PMC article.

5

Antinociceptive effects of the 6-O-sulfate ester of morphine in normal and diabetic rats: Comparative role of mu- and delta-opioid receptors.

Yadlapalli JSK, Ford BM, Ketkar A, Wan A, Penthala NR, Eoff RL, Prather PL, Dobretsov M, Crooks PA. Yadlapalli JSK, et al. Among authors: ford bm. Pharmacol Res. 2016 Nov;113(Pt A):335-347. doi: 10.1016/j.phrs.2016.09.012. Epub 2016 Sep 13. Pharmacol Res. 2016. PMID: 27637375 Free PMC article.

6

Tamoxifen Isomers and Metabolites Exhibit Distinct Affinity and Activity at Cannabinoid Receptors: Potential Scaffold for Drug Development.

Ford BM, Franks LN, Radominska-Pandya A, Prather PL. Ford BM, et al. PLoS One. 2016 Dec 9;11(12):e0167240. doi: 10.1371/journal.pone.0167240. eCollection 2016. PLoS One. 2016. PMID: 27936172 Free PMC article.

7

Selective Estrogen Receptor Modulators: Cannabinoid Receptor Inverse Agonists with Differential CB1 and CB2 Selectivity.

Franks LN, Ford BM, Prather PL. Franks LN, et al. Among authors: ford bm. Front Pharmacol. 2016 Dec 22;7:503. doi: 10.3389/fphar.2016.00503. eCollection 2016. Front Pharmacol. 2016. PMID: 28066250 Free PMC article.

8

Synthetic Pot: Not Your Grandfather's Marijuana.

Ford BM, Tai S, Fantegrossi WE, Prather PL. Ford BM, et al. Trends Pharmacol Sci. 2017 Mar;38(3):257-276. doi: 10.1016/j.tips.2016.12.003. Epub 2017 Feb 2. Trends Pharmacol Sci. 2017. PMID: 28162792 Free PMC article. Review.

9

Characterization of structurally novel G protein biased CB₁ agonists: Implications for drug development.

Ford BM, Franks LN, Tai S, Fantegrossi WE, Stahl EL, Berquist MD, Cabanlong CV, Wilson CD, Penthala NR, Crooks PA, Prather PL. Ford BM, et al. Pharmacol Res. 2017 Nov;125(Pt B):161-177. doi: 10.1016/j.phrs.2017.08.008. Epub 2017 Aug 23. Pharmacol Res. 2017. PMID: 28838808 Free PMC article.

10

The tamoxifen derivative ridaifen-B is a high affinity selective CB₂ receptor inverse agonist exhibiting anti-inflammatory and anti-osteoclastogenic effects.

Franks LN, Ford BM, Fujiwara T, Zhao H, Prather PL. Franks LN, et al. Among authors: ford bm. Toxicol Appl Pharmacol. 2018 Aug 15;353:31-42. doi: 10.1016/j.taap.2018.06.009. Epub 2018 Jun 12. Toxicol Appl Pharmacol. 2018. PMID: 29906493 Free PMC article.

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