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3
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0029911570
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Bromme D., Klaus J.L., Okamoto K., Rasnick D., Palmer J.T. Biochem. J. 315:1996;85.
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Bromme, D.1
Klaus, J.L.2
Okamoto, K.3
Rasnick, D.4
Palmer, J.T.5
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4
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0031010398
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Bogyo M., McMaster J.S., Gaczynska M., Tortorella D., Goldberg A.L., Ploegh H.L. Proc. Natl. Acad. Sci. U.S.A. 94:1997;6629.
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Proc. Natl. Acad. Sci. U.S.A.
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Bogyo, M.1
McMaster, J.S.2
Gaczynska, M.3
Tortorella, D.4
Goldberg, A.L.5
Ploegh, H.L.6
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7
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0032885416
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Teicher B.A., Ara G., Herbst R., Palombella V.J., Adams J. Clin. Cancer Res. 5:1999;2638.
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Teicher, B.A.1
Ara, G.2
Herbst, R.3
Palombella, V.J.4
Adams, J.5
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9
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0013446908
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note
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6) δ 7.85 (d, 2H, J=8.1 Hz), 7.70 (br, 1H), 7.25 (d, 2H, J=8.1 Hz), 4.13 (s, 2H), 3.62 (t, 2H, J=6.4 Hz), 3.21 (t, 2H, J=6.4 Hz).
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-
-
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10
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0013403258
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note
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2=9.2 Hz), 6.27 (d, 1H, J=16.6 Hz), 5.95 (d, 1H, J=9.2 Hz), 4.82 (t, 1H, J=6.1 Hz), 4.32 (d, 2H, J=6.1 Hz), 2.92 (s, 4H). (a) Part of the 2-chloroethanesulfonyl chloride molecules apparently acted as the activation reagent by reacting with 2b to form a 'mixed anhydride' intermediate. Attack of this intermediate by a second molecule of 2b yielded the dimer 5.
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11
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0034829959
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Li M., Tsai S.-F., Rosen S.M., Wu R.S., Reddy K.B., DiCesare J., Salamone S.J. J. Agric. Food Chem. 49:2001;1287.
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J. Agric. Food Chem.
, vol.49
, pp. 1287
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Li, M.1
Tsai, S.-F.2
Rosen, S.M.3
Wu, R.S.4
Reddy, K.B.5
DiCesare, J.6
Salamone, S.J.7
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12
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0004141509
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CRC. Boca Raton, FL
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(a) For a comprehensive review of heterobifunctional cross-linking reagents, see: (a) Wong S.S. Chemistry of Protein Conjugation and Cross-Linking. 1991;CRC, Boca Raton, FL, (b) Hermanson G.T. Bioconjugate Techniques. 1996;Academic Press, San Diego, CA.
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(1991)
Chemistry of Protein Conjugation and Cross-Linking
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Wong, S.S.1
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13
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0003648954
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San Diego, CA: Academic Press
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(a) For a comprehensive review of heterobifunctional cross-linking reagents, see: (a) Wong S.S. Chemistry of Protein Conjugation and Cross-Linking. 1991;CRC, Boca Raton, FL, (b) Hermanson G.T. Bioconjugate Techniques. 1996;Academic Press, San Diego, CA.
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(1996)
Bioconjugate Techniques
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Hermanson, G.T.1
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14
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0028501413
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-1. UV (MeOH) 217 (ε 19,117), 322 nm (ε 13,773). The corresponding fluorescent 4-(aminomethyl)-7-methoxycoumarin was synthesized according to the procedure of Li and White:
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-1. UV (MeOH) 217 (ε 19,117), 322 nm (ε 13,773). The corresponding fluorescent 4-(aminomethyl)-7-methoxycoumarin was synthesized according to the procedure of Li and White: Li M., White E.H. Bioconjugate Chem. 5:1994;454.
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(1994)
Bioconjugate Chem.
, vol.5
, pp. 454
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Li, M.1
White, E.H.2
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15
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0013408394
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note
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2O/DCl) δ 7.41 (d, 2H, J=8.7 Hz), 6.79 (d, 2H, J=8.7 Hz), 3.62 (s, 2H), 3.56 (m, 1H), 2.65 (m, 2H), 2.49-2.27 (m, 2H), 2.15 (m, 2H). (3) The yield for the adduct (7) derived from lysine and 1 was quite low isolation of the product was not attempted.
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18
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0020695584
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The content of the free sulfhydryl groups were assayed using the Ellman's reagent:
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The content of the free sulfhydryl groups were assayed using the Ellman's reagent: Riddles P.W., Blakeley R.L., Zerner B. Methods Enzymol. 91:1983;49.
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(1983)
Methods Enzymol.
, vol.91
, pp. 49
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Riddles, P.W.1
Blakeley, R.L.2
Zerner, B.3
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