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(a) Berridge, M.J. Nature (London) 1993, 361, 315.
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Berridge, M.J.1
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3
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0028971813
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(a) Noh, D.-Y.; Shin, S.H.; Rhee, S.G. Biochim. Biophys. Acta 1995, 1242, 99.
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Noh, D.-Y.1
Shin, S.H.2
Rhee, S.G.3
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4
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0028815438
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(b) Shimohama, S.; Perry, G.; Richey, P.; Praprotnik, D.; Takenawa, T.; Fukami K.; Whitehouse, P.J.; Kimura, J. Brain Res. 1995, 669, 217.
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Shimohama, S.1
Perry, G.2
Richey, P.3
Praprotnik, D.4
Takenawa, T.5
Fukami, K.6
Whitehouse, P.J.7
Kimura, J.8
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5
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0029924329
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Essen L.-O., Perisic O., Cheung R., Katan M., Williams R.L. Nature. 380:1996;595.
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Essen, L.-O.1
Perisic, O.2
Cheung, R.3
Katan, M.4
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6
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0025744604
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(a) Rhee, S.G.; Ryu, S.H.; Lee, K.Y.; Cho, K.S. Meth. Enzymol. 1991, 197, 502.
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Rhee, S.G.1
Ryu, S.H.2
Lee, K.Y.3
Cho, K.S.4
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9
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0011176855
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note
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1 2 = 8.0 Hz); 4.27 (q, 1H, J = 9.3 Hz); 7.34 (d, 2H, J = 9.0 Hz); 8.21 (d, 2H, J = 9.0 Hz).
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10
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0011176724
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Satisfactory analytical data (±0.4% of calcd values) were obtained for 2 (C H), mp 114-115 °C (hexane); 3 (C H), mp 111-113 °C (hexane); 5 (C H), mp 138-139 °C (ether-chloroform); 6 (C H), mp 98 °C (ethyl acetate); 13 (C H N), white powder, dec > 120 °C
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Satisfactory analytical data (±0.4% of calcd values) were obtained for 2 (C H), mp 114-115 °C (hexane); 3 (C H), mp 111-113 °C (hexane); 5 (C H), mp 138-139 °C (ether-chloroform); 6 (C H), mp 98 °C (ethyl acetate); 13 (C H N), white powder, dec > 120 °C.
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12
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0024967478
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Nagai H., Fujiwara T., Fujii M., Sekine M., Hata T. Nucl. Ac. Res. 17:1989;8581.
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Nagai, H.1
Fujiwara, T.2
Fujii, M.3
Sekine, M.4
Hata, T.5
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13
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0011185927
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399, background)
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399, background).
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14
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0011253669
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1 was a generous gift from Dr. Mario J. Rebecchi, Health Sciences Center, State University of New York, Stony Brook, NY
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1 was a generous gift from Dr. Mario J. Rebecchi, Health Sciences Center, State University of New York, Stony Brook, NY.
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15
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0026338597
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Earlier, we described the synthesis of myo-inositol 1-(4-nitrophenyl ammonium phosphate), a chromogenic substrate for Bacillus cereus PI-PLC and found that the bacterial enzyme showed activity only towards the D-isomer while the L-isomer was neither a substrate nor an inhibitor
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2 represents the true substrate concentration.
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(1991)
Chem. Phys. Lipids
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, pp. 101
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Shashidhar, M.S.1
Volwerk, J.J.2
Griffith, O.H.3
Keana, J.F.W.4
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19
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0027050183
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2, 0.5 mM dithiothreitol, 0.03% gelatin
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2+, 0.1 mM dithiothreitol (Rebecchi, M.J.; Rosen, O.M. J. Biol. Chem. 1987, 262, 12526).
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(1992)
Biochemistry
, vol.31
, pp. 12742
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Rebecchi, M.1
Peterson, A.2
McLaughlin, S.3
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20
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0027310309
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2+, 5 mM dithiothreitol, 0.1% gelatin
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2+, 0.1 mM dithiothreitol (Rebecchi, M.J.; Rosen, O.M. J. Biol. Chem. 1987, 262, 12526).
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(1993)
J. Biol. Chem.
, vol.268
, pp. 11586
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Cifuentes, M.E.1
Honkanen, L.2
Rebecchi, M.J.3
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21
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0023656224
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2+, 0.1 mM dithiothreitol
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2+, 0.1 mM dithiothreitol (Rebecchi, M.J.; Rosen, O.M. J. Biol. Chem. 1987, 262, 12526).
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(1987)
J. Biol. Chem.
, vol.262
, pp. 12526
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Rebecchi, M.J.1
Rosen, O.M.2
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22
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0027167915
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1 is ≥10μM
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1 is ≥10μM: Hepler, J.R.; Kozasa, T.; Smrcka, A.V.; Simon, M.I.; Rhee, S.G.; Sternweis, P.C.; Gilman, A.G. J. Biol. Chem. 1993, 268, 14367 and Cifuentes, M.E.; Honkanen, L.; Rebecchi, M.J. J. Biol. Chem. 1993, 268, 11586.
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(1993)
J. Biol. Chem.
, vol.268
, pp. 14367
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Hepler, J.R.1
Kozasa, T.2
Smrcka, A.V.3
Simon, M.I.4
Rhee, S.G.5
Sternweis, P.C.6
Gilman, A.G.7
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23
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0027310309
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and
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1 is ≥10μM: Hepler, J.R.; Kozasa, T.; Smrcka, A.V.; Simon, M.I.; Rhee, S.G.; Sternweis, P.C.; Gilman, A.G. J. Biol. Chem. 1993, 268, 14367 and Cifuentes, M.E.; Honkanen, L.; Rebecchi, M.J. J. Biol. Chem. 1993, 268, 11586.
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(1993)
J. Biol. Chem.
, vol.268
, pp. 11586
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Cifuentes, M.E.1
Honkanen, L.2
Rebecchi, M.J.3
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