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公开(公告)号:US07329759B2
公开(公告)日:2008-02-12
申请号:US11312236
申请日:2005-12-20
IPC分类号: C07D233/54 , C07C62/24 , C07C215/02
CPC分类号: C07D317/72 , C07C35/37 , C07C39/17 , C07C49/737 , C07C49/755 , C07C49/757 , C07C59/90 , C07C69/007 , C07C69/96 , C07C205/45 , C07C323/22 , C07C323/52 , C07C323/58 , C07C2601/14 , C07C2603/94 , C07D233/54 , C07D319/08 , C07F7/1804 , C07H15/18
摘要: The present invention provides illudin analogs of the general formula (I): where R1 is (CH2)n—X—Y or H; n is 0 to 4; X is O or S or N or absent; and Y is an optionally substituted (C1-C8)alkyl, (C6-C10)aryl, (C6-C10)aryl(C1-C4)alkyl or cyclo(C3-C6)alkyl optionally comprising one or more heteroatoms; a monosaccharide, an amino acid residue, or H when n is 2-4; R2 is absent; or R1 and R2 together comprise a 5-7 membered cyclic ring; R3 is (C1-C4)alkyl or H; R4 is H, SCH2CO2(C1-C4)alkyl, O—(C5-C12)aryl or —S—(C5-C12)aryl; R5 is H, OH or absent; R6 is (C1-C4)alkyl or absent; R7 is OH or OSi((C1-C4)alkyl)3; or R6 and R7 together are ethylenedioxy; R8 is optionally substituted (C1-C4)alkyl; and the bonds represented by ----- are individually present or absent. The invention further provides dimers comprising analogs of formula (I).
摘要翻译: 本发明提供了通式(I)的illudin类似物:其中R 1是(CH 2)n -X-Y或H; n为0〜4; X为O或S或N或不存在; 和Y是任选取代的(C 1 -C 8 - )烷基,(C 6 -C 10)烷基, 芳基(C 6 -C 10)芳基(C 1 -C 4 -C 4)烷基或环(C(C 1 -C 6) 任选地包含一个或多个杂原子的C 3 -C 6烷基; 当n为2-4时,单糖,氨基酸残基或H; R 2不存在; 或R 1和R 2一起包含5-7元环; R 3是(C 1 -C 4 -C 4)烷基或H; R 4是H,SCH 2 CO 2(C 1 -C 4) )烷基,O-(C 5 -C 12 - )芳基或-S-(C 5 -C 12) )芳基; R 5是H,OH或不存在; R 6是(C 1 -C 4 -C 4)烷基或不存在; R 7是OH或OSi((C 1 -C 4 -C 4烷基)烷基)3。 或R 6和R 7一起是亚乙二氧基; R 8是任选取代的(C 1 -C 4 -C 4)烷基; 而-----表示的债券是单独存在或不存在的。 本发明还提供包含式(I)的类似物的二聚体。
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公开(公告)号:US20050250675A1
公开(公告)日:2005-11-10
申请号:US11151013
申请日:2005-06-13
申请人: Trevor McMorris , Michael Kelner
发明人: Trevor McMorris , Michael Kelner
IPC分类号: A61K31/16 , A61K31/704 , A61K38/16
CPC分类号: C07C49/737 , A61K38/063 , A61K38/08 , C07B2200/07 , C07C49/753 , C07C69/007 , C07C323/58 , C07C323/59 , C07C323/60 , C07C2603/94 , C07D207/16 , C07K5/06078 , C07K5/0812 , C07K5/1016
摘要: The present invention provides compounds of general formula I or II: wherein R1, R2, R3, R4, R5, R6, and R7 have any of the values defined in the specification, and pharmaceutically acceptable salts thereof, as well as pharmaceutical compositions comprising compounds of formula I or II, intermediates and processes useful for preparing compounds of formula I or II, and methods comprising inhibiting tumor growth or treating cancer by administering one or more compounds of formula I or H.
摘要翻译: 本发明提供通式I或II的化合物:其中R 1,R 2,R 3,R 4, R 5,R 6,R 7和R 7具有本说明书中定义的任何值及其药学上可接受的盐,如 以及包含式I或II化合物的药物组合物,用于制备式I或II化合物的中间体和方法,以及通过施用一种或多种式I或H化合物抑制肿瘤生长或治疗癌症的方法。
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公开(公告)号:US06855696B2
公开(公告)日:2005-02-15
申请号:US10013009
申请日:2001-11-05
IPC分类号: A61K31/12 , A61K31/16 , A61K31/195 , A61K31/25 , A61K38/00 , A61P35/00 , C07C49/737 , C07C49/753 , C07C69/013 , C07C69/16 , C07C69/18 , C07C323/58 , C07C323/59 , C07C323/60 , C07D207/16 , C07K5/02 , C07K5/065 , C07K5/083 , C07K5/103 , A61K38/05 , A61K38/06
CPC分类号: C07C69/013 , A61K38/00 , C07C49/737 , C07C49/753 , C07C323/58 , C07C323/59 , C07C323/60 , C07D207/16 , C07K5/0215 , C07K5/081 , C07K5/1013 , Y02A50/395
摘要: The present invention provides illudin analogs of the general formula I: wherein R1, R2, R3, R4, R5, and R6 have any of the values defined in the specification, and pharmaceutically acceptable salts thereof, as well as pharmaceutical compositions comprising compounds of formula I, intermediates and processes useful for preparing compounds of formula I, and methods comprising inhibiting tumor growth or treating cancer by administering one or more compounds of formula I.
摘要翻译: 本发明提供通式I的illudin类似物:其中R1,R2,R3,R4,R5和R6具有说明书中定义的任何值及其药学上可接受的盐,以及包含式 I,可用于制备式I化合物的中间体和方法,以及通过施用一种或多种式I化合物来抑制肿瘤生长或治疗癌症的方法。
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公开(公告)号:US06469184B2
公开(公告)日:2002-10-22
申请号:US09874839
申请日:2001-06-05
申请人: Trevor C. McMorris
发明人: Trevor C. McMorris
IPC分类号: C07D31772
CPC分类号: C07D493/08 , C07C35/37 , C07C49/737 , C07C2603/94 , Y02P20/55 , Y02P20/582
摘要: The present invention provides a method of synthesizing compounds of formula (I): wherein R and R′ are independently (C1-C4)alkyl.
摘要翻译: 本发明提供合成式(I)化合物的方法:其中R和R'独立地为(C 1 -C 4)烷基。
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公开(公告)号:US5929124A
公开(公告)日:1999-07-27
申请号:US917648
申请日:1997-08-22
IPC分类号: C07C49/737 , C07D307/77 , A01N35/04 , C07C45/00
CPC分类号: C07D307/77 , C07C49/737
摘要: Antimicrobial diterpenes and methods of using them.
摘要翻译: 抗菌二萜类及其使用方法。
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公开(公告)号:US5723632A
公开(公告)日:1998-03-03
申请号:US689461
申请日:1996-08-08
申请人: Trevor C. McMorris
发明人: Trevor C. McMorris
IPC分类号: A61K31/335 , A61P35/00 , C07C35/37 , C07C45/29 , C07C49/633 , C07C49/733 , C07C49/737 , C07D493/08 , C07D307/94
CPC分类号: C07D493/08 , C07C35/37 , C07C49/737 , C07C2103/94 , Y02P20/55 , Y02P20/582
摘要: The present invention provides a method of synthesizing compounds of formula (I): ##STR1## wherein R and R' are independently (C.sub.1 -C.sub.4)alkyl.
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公开(公告)号:US5563176A
公开(公告)日:1996-10-08
申请号:US276169
申请日:1994-07-15
IPC分类号: A61K39/395 , A61K31/12 , A61K31/122 , A61K31/215 , A61K31/22 , A61K31/27 , A61P35/00 , A61P35/02 , C07C45/45 , C07C45/46 , C07C45/65 , C07C45/67 , C07C49/67 , C07C49/683 , C07C49/737 , C07C49/747 , C07C49/753 , C07C49/755 , C07C69/007 , C07C69/16 , C07C69/63 , C07C69/732 , C07C69/76 , C07C271/10 , C07C271/12 , C07C49/403
CPC分类号: A61K31/12 , A61K31/215 , A61K31/22 , A61K31/27 , C07C271/12 , C07C45/455 , C07C45/46 , C07C45/65 , C07C45/673 , C07C49/67 , C07C49/683 , C07C49/737 , C07C49/747 , C07C49/753 , C07C49/755 , C07C69/007 , C07C2103/94
摘要: Antineoplastic illudin analogs are provided of the formula: wherein R.sub.4, R.sub.5 and R.sub.6 are (C.sub.1 -C.sub.4)alkyl, Y is H, (C.sub.1 -C.sub.3)alkyl, (R.sub.4)R.sub.5)(R.sub.6)Si or alkanoyl ((C.sub.1 -C.sub.4)alkylC(O)) and R is CH.sub.2 OH, halo, benzyl optionally substituted with OY, or alkanoylmethyl (CH.sub.2 OC(O)R.sub.7), wherein R.sub.7 is (C.sub.1 -C.sub.4)alkyl, (C.sub.6 -C.sub.2)aryl or N(X).sub.2, wherein each X is H or (C.sub.1 -C.sub.4)alkyl, and the pharmaceutically-acceptable salts thereof.
摘要翻译: 抗肿瘤性illudin类似物由下式提供:其中R4,R5和R6是(C1-C4)烷基,Y是H,(C1-C3)烷基,(R4)R5)(R6)Si或烷酰基(( C1-C4)烷基C(O)),R是CH2OH,卤素,任选被OY取代的苄基或烷酰基甲基(CH2OC(O)R7),其中R7是(C1-C4)烷基,(C6-C2) (X)2,其中每个X是H或(C 1 -C 4)烷基,及其药学上可接受的盐。
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公开(公告)号:US5439936A
公开(公告)日:1995-08-08
申请号:US15179
申请日:1993-02-09
IPC分类号: A61K39/395 , A61K31/12 , A61K31/122 , A61K31/215 , A61K31/22 , A61K31/27 , A61P35/00 , A61P35/02 , C07C45/45 , C07C45/46 , C07C45/65 , C07C45/67 , C07C49/67 , C07C49/683 , C07C49/737 , C07C49/747 , C07C49/753 , C07C49/755 , C07C69/007 , C07C69/16 , C07C69/63 , C07C69/732 , C07C69/76 , C07C271/10 , C07C271/12
CPC分类号: C07C271/12 , A61K31/12 , A61K31/215 , A61K31/22 , A61K31/27 , C07C45/455 , C07C45/46 , C07C45/65 , C07C45/673 , C07C49/67 , C07C49/683 , C07C49/737 , C07C49/747 , C07C49/753 , C07C49/755 , C07C69/007 , C07C2103/94
摘要: A therapeutic method is provided to inhibit tumor cell growth in a subject in need of said therapy is provided, comprising parenterally administering a therapeutic amount of a compound in a pharmaceutically acceptable carrier, wherein said compound has the structure: ##STR1## wherein R is selected from the group consisting of: ##STR2## and wherein said tumor cell is sensitive to inhibition by said compound and is selected from the group consisting of a myeloid leukemia cell, a T-cell leukemia cell, a lung carcinoma cell, an ovarian carcinoma cell, and a breast carcinoma cell.
摘要翻译: 提供了一种用于抑制需要所述治疗的受试者的肿瘤细胞生长的治疗方法,其包括在药学上可接受的载体中肠胃外施用治疗量的化合物,其中所述化合物具有以下结构:其中R被选择 来自由以下组成的组:
,其中所述肿瘤细胞对所述化合物的抑制敏感,并且选自骨髓性白血病细胞,T细胞白血病细胞,肺癌细胞, 卵巢癌细胞和乳腺癌细胞。 -
公开(公告)号:US09809615B2
公开(公告)日:2017-11-07
申请号:US14770780
申请日:2014-02-17
发明人: Shiyou Li , Ping Wang , Guangrui Deng , Wei Yuan , Zushang Su
IPC分类号: A61K31/05 , A61K45/06 , C07H17/08 , C07C49/747 , C07C39/17 , C07C49/755 , C07C49/737 , A61K31/11 , A61K31/122 , A61K31/7048 , C07C47/57
CPC分类号: C07H17/08 , A61K31/05 , A61K31/11 , A61K31/122 , A61K31/7048 , A61K45/06 , C07C39/17 , C07C47/57 , C07C49/737 , C07C49/747 , C07C49/755 , A61K2300/00
摘要: Compositions and methods related to anti-cancer terpenoid compounds isolated from plants in the Salviniaceae family, pharmaceutical compositions comprising the same, and methods of treating cancer.
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公开(公告)号:US20060178356A1
公开(公告)日:2006-08-10
申请号:US11387507
申请日:2006-03-22
申请人: Bing Wang , Yong-Kang Zhang , Jian Chen , Wei Zhang , Jiangao Song , Ughetta Balzo , Lesley Brown , Sekhar Boddupalli , Steven Bobzin , Sylvain Gilat , Guy Miller
发明人: Bing Wang , Yong-Kang Zhang , Jian Chen , Wei Zhang , Jiangao Song , Ughetta Balzo , Lesley Brown , Sekhar Boddupalli , Steven Bobzin , Sylvain Gilat , Guy Miller
IPC分类号: C07F1/08 , A61K31/555 , A61K31/426 , A61K31/4152 , A61K31/444
CPC分类号: C07D213/30 , C07C43/23 , C07C45/30 , C07C45/71 , C07C49/737 , C07C69/94 , C07C205/17 , C07C205/20 , C07C205/22 , C07C205/35 , C07C205/57 , C07C235/42 , C07C255/36 , C07C311/29 , C07C2603/24 , C07D213/53 , C07D231/26 , C07D277/20 , C07D277/24 , C07D295/26 , C07D311/72 , C07F9/4021 , C07C47/575
摘要: Cytoprotective compounds, many of which are phenolic derivatives characterized by a substituted phenol having certain conjugated bonds, are useful in the treatment of certain ischemic or inflammatory conditions, including but not limited to stroke, myocardial infarction, congestive heart failure, and skin disorders characterized by inflammation or oxidative damage. They are also useful in the manufacture of pharmaceutical and cosmetic formulations for the treatment of such conditions.
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