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2
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14644412355
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4
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27144465524
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The producer of natural product rhizoxins isolated from R. Microsporus was also revised, see:
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The producer of natural product rhizoxins isolated from R. Microsporus was also revised, see:. Partida-Martinez L.P., and Hertweck C. Nature 437 (2005) 884
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Partida-Martinez, L.P.1
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6
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0021282303
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Wilson T., Rabie C.J., Fincham J.E., Steyn P.S., and Schipper M.A.A. Food Chem. Toxicol. 22 (1984) 275
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Wilson, T.1
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Schipper, M.A.A.5
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7
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23744471054
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Rabie C.J., Lübben A., Schipper M.A.A., van Heerden F.R., and Fincham J.E. Int. J. Food Microbiol. 1 (1985) 263
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Rabie, C.J.1
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11
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14
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0001286903
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We attempted the Negishi cross-coupling reaction of organozinc reagent 19 derived from serine and 3-bromo- or 3-iodofuran. However, the desired product 20 was not observed. {A figure is presented} For the references, see:
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We attempted the Negishi cross-coupling reaction of organozinc reagent 19 derived from serine and 3-bromo- or 3-iodofuran. However, the desired product 20 was not observed. {A figure is presented} For the references, see:. Jackson R.F.W., Wythes M.J., and Wood A. Tetrahedron Lett. 30 (1989) 5941
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Jackson, R.F.W.1
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15
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0026708781
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16
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0004789384
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The example of Negishi coupling with 3-halofuran, see:
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The example of Negishi coupling with 3-halofuran, see:. Liu F., and Negishi E. J. Org. Chem. 62 (1997) 8591
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Liu, F.1
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20
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56949096644
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note
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+ 256.1185, found 256.1204.
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-
-
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21
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34547764254
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Hernández D., Riego E., Francesch A., Cuevas C., Albericio F., and Álvarez M. Tetrahedron 63 (2007) 9862
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Hernández, D.1
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Francesch, A.3
Cuevas, C.4
Albericio, F.5
Álvarez, M.6
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22
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56949089576
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note
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+ 834.4742, found 834.4756.
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-
-
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23
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0024542233
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Potgieter M., Steyn P.S., van Heerden F.R., van Rooyen P.H., and Wessels P.L. Tetrahedron 45 (1989) 2337
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Potgieter, M.1
Steyn, P.S.2
van Heerden, F.R.3
van Rooyen, P.H.4
Wessels, P.L.5
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24
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56949083483
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-
note
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2 for 4-7 days. After the cells reached 100% confluence, the culture buffer was changed to a differentiation buffer (150 μL per well) and samples that were dissolved in MeOH or water (7.5 μL) were added. Differentiation buffer was composed of DMEM containing 10% FCS, 1 μM dexamethasone, 0.5 mM 3-isobutyl-1-methylxanthine (IBMX), 90 U/mL penicillin, 90 μg/mL streptomycin, and 10 μg/mL insulin. As a control, MeOH or water (7.5 μL) was added in place of samples. After 7 days, the differentiated 3T3-L1 adipocytes in a 96-well plate were treated with 2% Triton-X 100 (10 μL/well) for 30 min at room temperature followed by sonication for 1 min. Fat accumulation was determined by measuring liberated triglyceride using a Triglyceride E-test Kit (Wako), and the absorbance at 630/690 nm (Microplate Reader EL-800, BIO-TEK Instruments, Inc) was measured according to manufacture's instructions. Fat-accumulation rate was calculated as percentage of the control. To determine the cell viability of differentiated 3T3-L1 adipocytes, another 96-well plate was treated with a Cell Counting Kit-8 Test (Wako), and the absorbance at 450 nm was measured according to manufacture's instructions. The viability was calculated as percentage of the control.
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25
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33646786111
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We have focused on the isolation of potential fat-accumulation inhibitors from natural sources guided by this bioassay, see:
-
We have focused on the isolation of potential fat-accumulation inhibitors from natural sources guided by this bioassay, see:. Shimokawa K., Mashima I., Asai A., Yamada K., Kita M., and Uemura D. Tetrahedron Lett. 47 (2006) 4445
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(2006)
Tetrahedron Lett.
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Shimokawa, K.1
Mashima, I.2
Asai, A.3
Yamada, K.4
Kita, M.5
Uemura, D.6
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26
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40149099636
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Shimokawa K., Mashima I., Asai A., Ohno T., Yamada K., Kita M., and Uemura D. Chem. Asian J. 3 (2008) 438
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Shimokawa, K.1
Mashima, I.2
Asai, A.3
Ohno, T.4
Yamada, K.5
Kita, M.6
Uemura, D.7
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