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Part 1: Nishida H., Miyazaki Y., Kitamura Y., Ohashi M., Matsusue T., Okamoto A., Hosaka Y., Ohnishi S., Mochizuki H., Chem. Pharm. Bull., 49, 1237-1244 (2001).
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Part 1: Nishida H., Miyazaki Y., Kitamura Y., Ohashi M., Matsusue T., Okamoto A., Hosaka Y., Ohnishi S., Mochizuki H., Chem. Pharm. Bull., 49, 1237-1244 (2001).
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Part 2: Nishida H., Miyazaki Y., Mukaihira T., Saitoh F., Fukui M., Harada K., Itoh M., Muraoka A., Matsusue T., Okamoto A., Hosaka Y., Matsumoto M., Ohnishi S., Mochizuki H., Chem. Pharm. Bull., 50, 1187-1194 (2002).
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Part 2: Nishida H., Miyazaki Y., Mukaihira T., Saitoh F., Fukui M., Harada K., Itoh M., Muraoka A., Matsusue T., Okamoto A., Hosaka Y., Matsumoto M., Ohnishi S., Mochizuki H., Chem. Pharm. Bull., 50, 1187-1194 (2002).
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Part 3: Nishida H., Miyazaki Y., Mukaihira T., Shimada H., Suzuki K., Saitoh F., Mizuno M., Matsusue T., Okamoto A., Hosaka Y., Matsumoto M., Ohnishi S., Mochizuki H., Chem. Pharm. Bull., 52, 459-462 (2004).
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Part 3: Nishida H., Miyazaki Y., Mukaihira T., Shimada H., Suzuki K., Saitoh F., Mizuno M., Matsusue T., Okamoto A., Hosaka Y., Matsumoto M., Ohnishi S., Mochizuki H., Chem. Pharm. Bull., 52, 459-462 (2004).
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Part 4: Nishida H., Mukaihira T., Saitoh F., Harada K., Fukui M., Matsusue T., Okamoto A., Hosaka Y., Matsumoto M., Shiromizu I., Ohnishi S., Mochizuki H., Chem. Pharm. Bull., 52, 406-412 (2004).
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Part 4: Nishida H., Mukaihira T., Saitoh F., Harada K., Fukui M., Matsusue T., Okamoto A., Hosaka Y., Matsumoto M., Shiromizu I., Ohnishi S., Mochizuki H., Chem. Pharm. Bull., 52, 406-412 (2004).
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Part 5: Saitoh F., Mukaihira T., Nishida H., Satoh T., Okano A., Yumiya Y., Ohkouchi M., Johka R., Matsusue T., Shiromizu I., Hosaka Y., Matsumoto M., Ohnishi S., Chem. Pharm. Bull., 54, 1535-1544 (2006).
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Part 5: Saitoh F., Mukaihira T., Nishida H., Satoh T., Okano A., Yumiya Y., Ohkouchi M., Johka R., Matsusue T., Shiromizu I., Hosaka Y., Matsumoto M., Ohnishi S., Chem. Pharm. Bull., 54, 1535-1544 (2006).
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33846966497
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MOPAC PM3 calculation was used in SYBYL7.1 (Tripos Inc.).
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MOPAC PM3 calculation was used in SYBYL7.1 (Tripos Inc.).
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43
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33846959651
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It has been unclear that compound 18 reduced FXa inhibitory activity IC50; 18.2 nM, The overall conformation of compound 18 might be changed by both N-mathylation and without a side chain
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50; 18.2 nM). The overall conformation of compound 18 might be changed by both N-mathylation and without a side chain.
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