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Isemura, M.7
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5
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0346117568
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Oku N., Matsukawa M., Yamakawa S., Asai T., Yahara S., Hashimoto F., and Akizawa T. Biol. Pharm. Bull. 26 (2003) 1235
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Oku, N.1
Matsukawa, M.2
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Yahara, S.5
Hashimoto, F.6
Akizawa, T.7
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7
-
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1642281177
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Maeda-Yamamoto M., Inagaki N., Kitaura J., Chikumoto T., Kawahara H., Kawakami Y., Sano M., Miyase T., Tachibana H., Nagai H., and Kawakami T. J. Immunol. 172 (2004) 4486
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Kawakami, Y.6
Sano, M.7
Miyase, T.8
Tachibana, H.9
Nagai, H.10
Kawakami, T.11
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8
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0037174393
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Fujimura Y., Tachibana H., Maeda-Yamamoto M., Miyase T., Sano M., and Yamada K. J. Agric. Food. Chem. 50 (2002) 5729
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Fujimura, Y.1
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Sano, M.5
Yamada, K.6
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9
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0033667625
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Suzuki M., Yoshino K., Maeda-Yamamoto M., Miyase T., and Sano M. J. Agric. Food. Chem. 48 (2000) 5649
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Suzuki, M.1
Yoshino, K.2
Maeda-Yamamoto, M.3
Miyase, T.4
Sano, M.5
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10
-
-
0034133254
-
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Tachibana H., Sunada Y., Miyase T., Sano M., Maeda-Yamamoto M., and Yamada K. Biosci., Biotechnol., Biochem. 64 (2000) 452
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Tachibana, H.1
Sunada, Y.2
Miyase, T.3
Sano, M.4
Maeda-Yamamoto, M.5
Yamada, K.6
-
11
-
-
33746089101
-
-
For synthesis of 4′′-MeEGCG from EGCG, see:
-
For synthesis of 4′′-MeEGCG from EGCG, see:. Miyase T., and Sano M. Jpn. Kokai Tokkyo Koho (2001) 253879
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(2001)
Jpn. Kokai Tokkyo Koho
, pp. 253879
-
-
Miyase, T.1
Sano, M.2
-
12
-
-
34547809453
-
-
For solid phase synthesis of a benzyl protected methylated catechin library, see:
-
For solid phase synthesis of a benzyl protected methylated catechin library, see:. Tanaka H., Miyoshi H., Chuang Y.-C., Ando Y., and Takahashi T. Angew. Chem., Int. Ed. 46 (2007) 5934
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(2007)
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-
Tanaka, H.1
Miyoshi, H.2
Chuang, Y.-C.3
Ando, Y.4
Takahashi, T.5
-
13
-
-
34248160377
-
-
Furuta T., Hirooka Y., Abe A., Sugata Y., Ueda M., Murakami K., Suzuki T., Tanaka K., and Kan T. Bioorg. Med. Chem. Lett. 17 (2007) 3095
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(2007)
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Furuta, T.1
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Abe, A.3
Sugata, Y.4
Ueda, M.5
Murakami, K.6
Suzuki, T.7
Tanaka, K.8
Kan, T.9
-
15
-
-
37549025470
-
-
EGC has been readily obtained from EGCG by enzymatic hydrolysis mediated by tannase, see:
-
EGC has been readily obtained from EGCG by enzymatic hydrolysis mediated by tannase, see:. Battestin V., Macedo G.A., and De Freitas V.A.P. Food Chem. 108 (2008) 228
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(2008)
Food Chem.
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Battestin, V.1
Macedo, G.A.2
De Freitas, V.A.P.3
-
19
-
-
38849093277
-
-
During the course of this investigation, employment of Ns ester as a protecting group for phenol has been independently reported, see:
-
During the course of this investigation, employment of Ns ester as a protecting group for phenol has been independently reported, see:. Koyama Y., Yamaguchi R., and Suzuki K. Angew. Chem., Int. Ed. 47 (2008) 1084
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(2008)
Angew. Chem., Int. Ed.
, vol.47
, pp. 1084
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-
Koyama, Y.1
Yamaguchi, R.2
Suzuki, K.3
-
20
-
-
0041804044
-
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Chang J., Chen R., Guo R., Dong C., and Zhao K. Helv. Chem. Acta. 86 (2003) 2239
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(2003)
Helv. Chem. Acta.
, vol.86
, pp. 2239
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-
Chang, J.1
Chen, R.2
Guo, R.3
Dong, C.4
Zhao, K.5
-
21
-
-
0001358368
-
-
Because utilizing pyrrolidine and/or piperidine causes hydrolysis of Ns-ester a soft nucleophile is required, see:
-
Because utilizing pyrrolidine and/or piperidine causes hydrolysis of Ns-ester a soft nucleophile is required, see:. Honda M., Morita H., and Nagakura I. J. Org. Chem. 62 (1997) 8932
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(1997)
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-
Honda, M.1
Morita, H.2
Nagakura, I.3
-
22
-
-
67649919518
-
-
Detailed synthetic procedures are described in the Supplementary data
-
Detailed synthetic procedures are described in the Supplementary data.
-
-
-
-
24
-
-
67649926515
-
-
note
-
Synthesis of 27 was conducted by protection of 14 with the Ns group and deprotection of the allyl ester. Detailed synthetic procedures are described in the Supplementary data.
-
-
-
-
25
-
-
41449085514
-
-
Similar deprotection of the Ns group using a similar odorless thiol 4-carboxy phenylthiol has been reported, see:
-
Similar deprotection of the Ns group using a similar odorless thiol 4-carboxy phenylthiol has been reported, see:. Matoba M., Kajimoto T., and Node M. Synth. Commun. 38 (2008) 1194
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(2008)
Synth. Commun.
, vol.38
, pp. 1194
-
-
Matoba, M.1
Kajimoto, T.2
Node, M.3
-
26
-
-
0029875424
-
-
Purification and refolding of recombinant human proMMP-7 and expression in Escherichia coli, and its characterization has been reported, see:
-
Purification and refolding of recombinant human proMMP-7 and expression in Escherichia coli, and its characterization has been reported, see:. Itoh M., Masuda K., Ito Y., Akizawa T., Yoshioka M., Imai K., Okada Y., Sato H., and Seiki M. J. Biochem. 119 (1996) 667
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(1996)
J. Biochem.
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Itoh, M.1
Masuda, K.2
Ito, Y.3
Akizawa, T.4
Yoshioka, M.5
Imai, K.6
Okada, Y.7
Sato, H.8
Seiki, M.9
-
27
-
-
67649894621
-
-
note
-
Inhibitory effect of green tea polyphenols on membrane-type 1 matrix metalloproteinase has been reported, see: Ref. 2b.
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