Zobrazeno 1 - 10
of 76
pro vyhledávání: '"Mcnally, James J."'
Autor:
MCNALLY, JAMES J.
Publikováno v:
Family Advocate, 2005 Jan 01. 27(3), 8-11.
Externí odkaz:
https://www.jstor.org/stable/25806406
Autor:
Peter J. Connolly, Cuifen Hou, Mark J. Macielag, Shawn Black, Mcnally James J, Mingde Xia, Matthews Jay M, Yuting Tang, Bin Zhu, Yin Liang, Cailin Chen
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 26:5346-5349
A series of potent and receptor-selective cannabinoid-1 (CB1) receptor inverse agonists has been discovered. Peripheral selectivity of the compounds was assessed by a mouse tissue distribution study, in which the concentrations of a test compound in
Autor:
Matthews, Jay M., McNally, James J., Connolly, Peter J., Xia, Mingde, Zhu, Bin, Black, Shawn, Chen, Cailin, Hou, Cuifen, Liang, Yin, Tang, Yuting, Macielag, Mark J.
Publikováno v:
In Bioorganic & Medicinal Chemistry Letters 1 November 2016 26(21):5346-5349
Publikováno v:
Family Advocate, 1993 Jan 01. 16(2), 30-34.
Externí odkaz:
https://www.jstor.org/stable/25805603
Autor:
Jones, G. Daniel, McNally, James J.
Publikováno v:
Family Advocate, 1989 Oct 01. 12(2), 44-44.
Externí odkaz:
https://www.jstor.org/stable/25804736
Autor:
Maryanoff, Bruce E., Nortey, Samuel O., McNally, James J., Sanfilippo, Pauline J., McComsey, David F., Dubinsky, Barry, Shank, Richard P., Reitz, Allen B.
Publikováno v:
In Bioorganic & Medicinal Chemistry Letters 1999 9(11):1547-1552
Autor:
Sandy J. Wilson, Scott L. Dax, Mcnally James J, Brian C. Zanoni, Allen B. Reitz, Cheryl P. Kordik, Chi Luo, Timothy W. Lovenberg
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 11:2283-2286
1,3-Disubstituted-5-aminopyrazoles were prepared based on a lead compound found through high-throughput screening of our corporate compound library in an assay measuring affinity for the human neuropeptide Y5 receptor. The target compounds were prepa
Autor:
Sandy J. Wilson, Diane Nepomuceno, Mcnally James J, Mark A. Youngman, Timothy W. Lovenberg, Scott L. Dax
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 10:213-216
[3a,4,5,9b-Tetrahydro-1H-benzo[e]indol-2-yl]amines were prepared via reductive amination and concomitant cyclization of alpha-cyanomethyl-beta-aminotetralins. N-acylation with omega-sulfonamido-carboxylic acids and subsequent reduction afforded a ser
Autor:
Matthews, Jay M., Qin, Ning, Colburn, Raymond W., Dax, Scott L., Hawkins, Mike, McNally, James J., Reany, Laura, Youngman, Mark A., Baker, Judith, Hutchinson, Tasha, Liu, Yi, Lubin, Mary Lou, Neeper, Michael, Brandt, Michael R., Stone, Dennis J., Flores, Christopher M.
Publikováno v:
In Bioorganic & Medicinal Chemistry Letters 15 April 2012 22(8):2922-2926
Autor:
Judith Baker, Dennis J. Stone, Mary Lou Lubin, Raymond W. Colburn, Mark A. Youngman, Matthews Jay M, Mike Hawkins, Christopher M. Flores, Tasha Hutchinson, Laura Reany, Mcnally James J, Michael P. Neeper, Yi Liu, Ning Qin, Michael R. Brandt, Scott L. Dax
Publikováno v:
Bioorganicmedicinal chemistry letters. 22(8)
A series of benzothiophene-based phosphonates was synthesized and many analogs within the series were shown to be potent antagonists of the TRPM8 channel. The compounds were obtained as a racemic mixture in 5 synthetic steps, and were tested for TRPM