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85030807677
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-
note
-
2+ concentration is increased
-
-
-
-
30
-
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0030607168
-
-
For a review, see: P. Wipf, and H. Jahn Tetrahedron 52 1996 12853 12909
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Wipf, P.1
Jahn, H.2
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36
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85030805683
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-
note
-
+ 274.0774, found 274.0790
-
-
-
-
37
-
-
85030815900
-
-
note
-
2+) and 380 nm (for unreacted Fura-2) at intervals of 0.5 ms, and fluorescence intensity at 510 nm was measured
-
-
-
-
38
-
-
85030805961
-
-
note
-
50 (50% inhibition concentration) value was determined from at least two independent experiments
-
-
-
-
39
-
-
85030810911
-
-
note
-
5P: C, 43.73; H, 5.71; N, 5.67. Found: C, 43.64; H, 5.67; N, 5.48
-
-
-
-
40
-
-
85030814533
-
-
note
-
2: C, 33.63; H, 4.23; N, 3.92; S, 8.98; Br, 44.75. Found: C, 34.29; H, 4.09; N, 3.91; S, 8.91; Br, 44.62
-
-
-
-
42
-
-
85030809985
-
-
note
-
2 for use in experiments
-
-
-
-
44
-
-
0022207564
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L. Allison, D.J. Arndt-Jovin, H. Gratzner, T. Ternynck, and M. Robert-Nicoud Cytometry 6 1985 584
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45
-
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85030813856
-
-
note
-
A pseudo-blood vessel in vitro inflammation model was constructed as follows: Transwells consisting of two compartments separated by porous membrane were used. A single layer of bovine endothelial cells was cultured on the membrane at the bottom surface of the transwell upper compartment. A suspension of fluorescence-labeled neutrophils was added to the upper compartment, and natural S-1P was suspended in the lower compartment to an end concentration of 10 μM. That is, the upper compartment corresponds to the interior of the blood vessel, while the lower one corresponds to the site of inflammation outside the blood vessel. Fluorescence intensities at 530 nm were measured to determine the number of the neutrophils passing through the endothelial layer and that adhering to it
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-
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46
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0034462185
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0035947050
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