JP2001524099A5 - - Google Patents

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JP2001524099A5
JP2001524099A5 JP1998546123A JP54612398A JP2001524099A5 JP 2001524099 A5 JP2001524099 A5 JP 2001524099A5 JP 1998546123 A JP1998546123 A JP 1998546123A JP 54612398 A JP54612398 A JP 54612398A JP 2001524099 A5 JP2001524099 A5 JP 2001524099A5
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JP1998546123A
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JP2001524099A (ja
JP4072208B2 (ja
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Figure 2001524099
Figure 2001524099
Figure 2001524099
Figure 2001524099
Figure 2001524099
Figure 2001524099
Figure 2001524099
JP54612398A 1997-04-19 1998-04-13 レチノイド作動剤、拮抗剤または逆作動剤型の生物学的活性を有する三置換フェニル誘導体 Expired - Fee Related JP4072208B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US08/845,019 1997-04-19
US08/845,019 US6037488A (en) 1997-04-19 1997-04-19 Trisubstituted phenyl derivatives having retinoid agonist, antagonist or inverse agonist type biological activity
PCT/US1998/007394 WO1998047854A1 (en) 1997-04-19 1998-04-13 Trisubstituted phenyl derivatives having retinoid agonist, antagonist or inverse agonist type biological activity

Related Child Applications (1)

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JP2007260033A Division JP2008024719A (ja) 1997-04-19 2007-10-03 レチノイド作動剤、拮抗剤または逆作動剤型の生物学的活性を有する三置換フェニル誘導体

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Publication Number Publication Date
JP2001524099A JP2001524099A (ja) 2001-11-27
JP2001524099A5 true JP2001524099A5 (ja) 2006-01-05
JP4072208B2 JP4072208B2 (ja) 2008-04-09

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JP54612398A Expired - Fee Related JP4072208B2 (ja) 1997-04-19 1998-04-13 レチノイド作動剤、拮抗剤または逆作動剤型の生物学的活性を有する三置換フェニル誘導体
JP2007260033A Pending JP2008024719A (ja) 1997-04-19 2007-10-03 レチノイド作動剤、拮抗剤または逆作動剤型の生物学的活性を有する三置換フェニル誘導体

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JP2007260033A Pending JP2008024719A (ja) 1997-04-19 2007-10-03 レチノイド作動剤、拮抗剤または逆作動剤型の生物学的活性を有する三置換フェニル誘導体

Country Status (9)

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US (3) US6037488A (ja)
EP (1) EP0975573B1 (ja)
JP (2) JP4072208B2 (ja)
AT (1) ATE224351T1 (ja)
AU (1) AU734939B2 (ja)
CA (1) CA2286681A1 (ja)
DE (1) DE69808065T2 (ja)
ES (1) ES2184252T3 (ja)
WO (1) WO1998047854A1 (ja)

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CN111148514A (zh) 2017-08-31 2020-05-12 Io治疗公司 与免疫调节剂联合应用于癌症免疫治疗的rar选择性激动剂
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US10966950B2 (en) 2019-06-11 2021-04-06 Io Therapeutics, Inc. Use of an RXR agonist in treating HER2+ cancers
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