1994
DOI: 10.1016/0965-1748(94)90005-1
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Two new allatostatins from the brains of Diploptera punctata

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Cited by 88 publications
(38 citation statements)
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“…Third HPLC Run-The conditions were as follows: column: 150 ϫ 4.6-mm Shiseido CAPCELL PAK C 8 SG 300 with 10 ϫ 4.6-mm guard column (same material; Grom); solvent A: 20 mM NH 4 Ac (pH 6.9); solvent B: 20 mM NH 4 Ac in 80% CH 3 CN; gradient: 0 -40 min of 6.25-62.5% solvent B (corresponding to 5-50% CH 3 CN) (linear gradient, 1.4% solvent B/min ϭ 1.125% CH 3 CN/min) followed by a 12-min wash at 100% solvent B; and flow rate: 1 ml/min. The active fractions (2300 brain equivalents) from the second HPLC run were dried down to ϳ50 l, diluted with 50 l of 20 mM NH 4 Ac in 10% CH 3 CN, and loaded separately onto the column.…”
Section: Chromatographymentioning
confidence: 99%
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“…Third HPLC Run-The conditions were as follows: column: 150 ϫ 4.6-mm Shiseido CAPCELL PAK C 8 SG 300 with 10 ϫ 4.6-mm guard column (same material; Grom); solvent A: 20 mM NH 4 Ac (pH 6.9); solvent B: 20 mM NH 4 Ac in 80% CH 3 CN; gradient: 0 -40 min of 6.25-62.5% solvent B (corresponding to 5-50% CH 3 CN) (linear gradient, 1.4% solvent B/min ϭ 1.125% CH 3 CN/min) followed by a 12-min wash at 100% solvent B; and flow rate: 1 ml/min. The active fractions (2300 brain equivalents) from the second HPLC run were dried down to ϳ50 l, diluted with 50 l of 20 mM NH 4 Ac in 10% CH 3 CN, and loaded separately onto the column.…”
Section: Chromatographymentioning
confidence: 99%
“…The active fractions (2300 brain equivalents) from the second HPLC run were dried down to ϳ50 l, diluted with 50 l of 20 mM NH 4 Ac in 10% CH 3 CN, and loaded separately onto the column. Peaks were collected manually into 1.5-ml reaction tubes, preloaded with 5 l of 0.1% bovine serum albumin solution, and assayed for allatostatic activity (50 brain equivalents/ assay).…”
Section: Chromatographymentioning
confidence: 99%
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“…Chemical shifts are reported in ␦. The reference signal for the proton spectra (1.73 ppm) was caused by residual protons at C 3 and C 4 in the THF-d 8 . The reference signal for the carbon spectra (25.37 ppm) was the result of the signal from C 3 and C 4 (27,28).…”
mentioning
confidence: 99%
“…NMR analysis confirmed that the minor components had been substantially eliminated. As THF-d 8 appeared to be a superior solvent for NMR analyses, the benzene was removed, and the oil was redissolved in THF-d 8 . The spectra were obtained in THF-d 8 solutions on a Bruker (Billerica, MA) WM 500 spectrometer.…”
mentioning
confidence: 99%