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L 6000

Manufactured by Hitachi
Sourced in Japan

The L-6000 is a piece of laboratory equipment manufactured by Hitachi. It is a high-performance instrument designed for analytical purposes. The core function of the L-6000 is to perform accurate and precise measurements and analyses. Further details on the intended use or specific applications of this product are not available.

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3 protocols using l 6000

1

ACE Inhibition Assay Protocol

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Inhibition of ACE was determined according to the method described by Cushman and Cheung [22 (link)] with modifications. After incubating 45-μL Hip-His-Leu (3mM in pH 8.3 sodium borate buffer) and 10-μL sample or lisinopril (used as the standard) at 37°C for 10 minutes, 45-μL ACE (33 mU/mL in pH 8.3 sodium borate buffer) was added to react for 30 minutes, and then 150-μL TFA (0.1%) was added to terminate the reaction. While Hip-His-Leu was converted into hippuric acid (HA) and histidylleucine by ACE, HA concentration was determined using a high performance liquid chromatographer (L-6000, Hitachi, Tokyo, Japan) equipped with a Lichrospher 100 RP-18 column (Merck, Darmstadt, Germany). The methanol containing 0.1% TFA as an eluting solvent was at a flow rate of 0.6 mL/min and HA was detected at 228 nm. All of these determinations were repeated three times.
ACE inhibition was calculated according to the following equation:
where AC and AS were the peak areas of buffer (control) or sample, respectively.
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2

Spectroscopic Analysis of Compounds

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Melting points were measured on a Yanagimoto micro apparatus without correction. Measurement of optical rotation was carried out on a JASCO P-2300 in CHCl3 solution at 23 °C. IR spectra were recorded using a Perkin-Elmer Model Spectrum 100. 1H (400 or 600 MHz)- and 13C (100 or 150 MHz)-NMR spectra were recorded on a JEOL AL-400 or ECA-600 spectrometer using tetramethylsilane as an internal standard. The chemical shifts are expressed on the δ scale. EI-MS and HREI-MS were measured at 30–60 eV (direct inlet) with a JEOL Model JMS-700 and the relative intensities of peaks are reported with reference to the most intense peak higher than m/z 100. TLC was carried out on pre-coated silica gel 60 (Merck 5554) with n-hexane-EtOAc or CHCl3-MeOH as the developing phase. Detection was carried out by spraying with concentrated H2SO4 followed by heating. HPLC was performed on a Hitachi L-6000 equipped with a Hitachi L-7490 RI detector. The following column and solvents were used for elution: Mightysil, RP-18 GP 250–10 (25 cm x 10 mm i.d., 5μm) with MeOH-H2O or CH3CN-H2O.
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3

Amperometric Measurement of Hydrogen

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Amperometric measurements of H2 were performed using an electrochemical measurement apparatus in connection with a potentiostat (NPOT-2501, Nikko Keisoku Corp., Japan), and a digital recorder (GR-3500, KEYENCE, Japan). The FIA system consisted of a carrier reservoir, sample injector with 10 μL loop, interconnecting PTFE tubing, HPLC pump (L-6000, Hitachi, Japan) and the electrochemical detector. A working Pt-NGC electrode (6 mm diameter, BAS Inc., Japan), an aqueous Ag/ AgCl (3 M NaCl electrolyte) reference and a platinum counter electrode were integrated on a radial flow cell (BAS Inc., Japan). Phosphate buffer (0.10 M, pH 7.0) was used as the carrier solution. The test solution used was 0.1 M phosphate buffer (pH 7.0) to which the bubbling of the H2 gas was performed.
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