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. Author manuscript; available in PMC: 2016 Nov 1.
Published in final edited form as: Bioorg Med Chem Lett. 2015 Mar 12;25(21):4961–4969. doi: 10.1016/j.bmcl.2015.03.012

Table 1.

Analytical and in vitro activity data for mSH analogs.

Peptide Composition MW Calc/Found RT [min] EC50 [nM] TREX-hFpn-GFP cells
PR73 C86H133N21O15S 1733.19/1734.34 47.11* 4.2±0.3
mHS1 C46H69N15O9S3 1072.32/1072.85 29.47 >600
mHS2 C52H77N17O11S3 1212.47/1212.20 28.06 >600
mHS3 C50H75N15O11S4 1190.47/1190.96 29.24 >600
mHS4 C54H75N15O9S3 1174.46/1174.73 33.42 585.6±71.1
mHS5 C54H75N15O9S3 1174.46/1174.86 34.19 272.2±18.9
mHS6 C54H75N15O9S3 1174.46/1174.60 34.18 598.9±114.2
mHS7 C53H74N16O9S3 1175.45/1175.90 27.65 >600
mHS8 C58H77N15O9S3 1224.52/1225.92 30.95 >600
mHS9 C60H79N15O10S3 1266.56/1266.74 39.58 477.4±76.3
mHS10 C61H81N15O9S3 1264.58/1264.52 41.14 516.9±131.7
mHS11 C96H134N28O16S5 2096.59/2097.25 34.74 >600
mHS12 C138H193N41O23S7 3018.73/3018.75 34.00/34.89 >600 regioisomers
mHS13 C141H199N41O31S7 3188.80/3188.87 34.33 >600
mHS14 C60H85N17O13S3 1348.62/1348.85 30.44 531.7±36.1
mHS15 C60H79N15O9S3 1250.56/1250.82 36.16 54.3±2.7
mHS16 C66H89N17O13S3 1424.71/1425.16 32.47 75.1±0.3
mHS17 C86H128N18O12S3 1702.25/1702.26 58.73 44.2±6.8
mHS18 C53H69N13O7S3 1096.39/1096.45 40.94 103.8±13.0
mHS19 C59H73N13O7S3 1172.49/1172.74 45.16 112.7±10.5
mHS20 C53H69N13O7S3 1096.39/1096.61 41.01 335.3±41.2
mHS21 C52H68N12O6S3 1053.36/1053.87 44.03 268.8±29.2
mHS22 C66H92N16O11S3 1381.73/1381.51 38.32 164.5±14.7
mHS23 C64H89N15O10S3 1324.68/1324.28 40.54 92.3±19.5
mHS24 C74H107N15O9S3 1446.93/1446.57 50.68* >600
mHS25 C73H106N14O8S3 1403.91/1403.63 50.73* 369.0±35.0
mHS26 C75H112N14O10S3 1465.98/1466.43 55.52* 52.3±10.8
mHS27 C68H99N13O7S3 1306.79/1306.43 57.32* >600
mHS28 C68H99N13O7S3 1306.79/1306.90 57.72* 458.3±87.7

Analytical RP-HPLC was performed on a Varian ProStar 210 HPLC system equipped with ProStar 325 Dual Wavelength UV-Vis detector with the wavelengths set at 220 nm and 280 nm (Varian Inc., Palo Alto, CA). Mobile phases consisted of solvent A, 0.1% TFA in water, and solvent B, 0.1% TFA in acetonitrile. Analyses of peptides were performed with an analytical reversed-phase C18 SymmetryShield column, 4.6×250 mm, 5 μm (Waters, Milford, MA) or (*) an analytical reversed-phase C4 XBridge BEH300 column, 4.6×150 mm, 3.5 μm (Waters, Milford, MA), applying linear gradient of solvent B from 0 to 100% over 100 min (flow rate: 1 ml/min).