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公开(公告)号:US4788339A
公开(公告)日:1988-11-29
申请号:US894311
申请日:1986-08-14
申请人: George G. I. Moore , John C. Hansen
发明人: George G. I. Moore , John C. Hansen
IPC分类号: C07D295/06 , C07C67/00 , C07C213/00 , C07C217/08 , C07C217/54 , C07D207/10 , C07D211/38 , C07D265/30 , C09K5/00 , C25B3/08 , C07C87/22
CPC分类号: C07D265/30 , C07D207/10 , C07D211/38 , C09K5/00 , C25B3/08
摘要: Perfluoroaminoethers are provided. The perfluoroaminoethers have two or more tertiary amino nitrogen atoms each of which is connected to the other(s) adjacent thereto by (1) a catenary, ether oxygen-containing, perfluoroalkylene linking group the catenary carbon atoms of which are in the form of segments of vicinal carbon atoms that are 2 to 4 in number, said segments having up to 5 carbon atoms, a catenary ether oxygen-containing perfluorocyclohexylene linking group, or (3) a catenary ether oxygen-containing linking group having perfluoroalkylene and perfluorocyclohexylene moieties, the sum of the catenary ether oxygen atoms being 1 to 6.
摘要翻译: 提供全氟氨基醚。 全氟氨基醚具有两个或更多个叔氨基氮原子,其中每个氨基氮原子通过(1)连接链,含醚氧的全氟亚烷基连接基团与其相邻的另一个连接,其中链状碳原子为链段 2〜4个连续碳原子,所述链段具有至多5个碳原子,链状醚含氧全氟环己基连接基团,或(3)具有全氟亚烷基和全氟环己基部分的链状含氧连接基团, 悬链醚氧原子的总和为1至6。
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公开(公告)号:US4707498A
公开(公告)日:1987-11-17
申请号:US818848
申请日:1986-01-14
申请人: Michael Kolb , David A. Kendrick
发明人: Michael Kolb , David A. Kendrick
IPC分类号: C12N9/99 , A61K20060101 , A61K31/13 , A61P17/00 , A61P35/00 , A61P43/00 , C07C20060101 , C07C67/00 , C07C209/00 , C07C209/14 , C07C209/16 , C07C209/62 , C07C211/23 , C07C211/24 , C07C229/40 , C07F20060101 , C07F13/00 , C07C87/24 , C07C87/22
CPC分类号: C07C211/24
摘要: Novel fluorinated diaminoalkyne derivatives are inhibitors of ornithine decarboxylase enzyme and have the following general Formula I: ##STR1## wherein R represents C.sub.1 -C.sub.4 alkyl, or preferably, hydrogen.
摘要翻译: 新型氟化二氨基炔衍生物是鸟氨酸脱羧酶的抑制剂,并具有以下通式I:其中R表示C1-C4烷基,或优选氢。
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公开(公告)号:US4695654A
公开(公告)日:1987-09-22
申请号:US767928
申请日:1985-08-21
申请人: Fritz Gerhart , Pierre Mamont
发明人: Fritz Gerhart , Pierre Mamont
IPC分类号: A61K31/13 , A61K49/06 , A61P35/00 , C07C67/00 , C07C209/00 , C07C209/50 , C07C209/62 , C07C211/14 , C07C211/15 , C07C309/66 , C07C311/18 , C07C87/22
CPC分类号: A61K49/06
摘要: Gem-dihalo-1,8-diamino-4-aza-octane derivatives useful as antiproliferative or antitumor agents.
摘要翻译: 可用作抗增殖剂或抗肿瘤剂的双 - 二卤代-1,8-二氨基-4-氮杂 - 辛烷衍生物。
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公开(公告)号:US4134918A
公开(公告)日:1979-01-16
申请号:US830998
申请日:1977-09-06
申请人: Philippe Bey , Michel Jung
发明人: Philippe Bey , Michel Jung
IPC分类号: A61K31/16 , A61K31/13 , A61K31/165 , A61K31/325 , A61K31/52 , A61P43/00 , C07C67/00 , C07C209/00 , C07C209/62 , C07C211/15 , C07C231/00 , C07C233/36 , C07C239/00 , C07C279/04 , C07C313/00 , C07C323/41 , C07C323/44 , C07D209/48 , C07H19/16 , C07C87/22 , C01B25/26 , C07C69/02 , C07C103/10
CPC分类号: C07D209/48 , C07H19/16
摘要: Novel halomethyl derivatives of amines of the following general structure: ##STR1## WHEREIN Y is FCH.sub.2 --, F.sub.2 CH-- or F.sub.3 C--; Z is .beta.-methylthioethyl, .beta.-benzylthioethyl, S-(5'-desoxyadenosin-5'-yl)-S-methylthioethyl, .gamma.-guanidinopropyl, or ##STR2## WHEREIN N IS 2 OR 3 AND R.sub.1 is hydrogen or lower alkyl of from 1 to 4 carbon atoms with the proviso that when R.sub.1 is other than hydrogen, n is 2; and each of R.sub.a and R.sub.b is hydrogen, alkylcarbonyl wherein the alkyl moiety has from 1 to 4 carbon atoms and is straight or branched, alkoxycarbonyl wherein the alkoxy moiety has from 1 to 4 carbon atoms and is straight or branched, or ##STR3## wherein R.sub.2 is hydrogen, a straight or branched lower alkyl group of from 1 to 4 carbon atoms, benzyl or p-hydroxybenzyl; with the provisos that when Z is .beta.-benzylthioethyl or S-(5'-desoxyadenosin-5'-yl)-S-methylthioethyl, R.sub.b is hydrogen, when Z is .beta.-methylthioethyl, Y is other than F.sub.3 C--, and when Z is ##STR4## EACH OF R.sub.a and R.sub.b can be the same or different; and pharmaceutically acceptable salts and individual optical isomers thereof.
摘要翻译: 胺的新型卤代甲基衍生物具有以下通用结构:其中Y是FCH 2 - ,F 2 CH-或F 3 C-; Z是β-甲硫基乙基,β-苄硫基乙基,S-(5'-脱氧腺苷-5'-基)-S-甲硫基乙基,γ-胍基丙基或其中R是氢或低级烷基 1至4个碳原子,条件是当R1不是氢时,n是2; 并且R a和R b中的每一个是氢,其中烷基部分具有1至4个碳原子并且是直链或支链的烷氧基羰基,其中烷氧基部分具有1至4个碳原子并且是直链或支链的,或其中 R2是氢,1至4个碳原子的直链或支链低级烷基,苄基或对羟基苄基; 条件是当Z是β-苄硫基乙基或S-(5'-脱氧腺苷-5'-基)-S-甲硫基乙基时,R b是氢,当Z是β-甲硫基乙基时,Y不是F3C-,当Z Ra和Rb可以相同或不同; 及其药学上可接受的盐和单独的光学异构体。
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公开(公告)号:US4089977A
公开(公告)日:1978-05-16
申请号:US744617
申请日:1976-11-24
CPC分类号: A01N33/12 , C08G73/0226
摘要: A polymeric quaternary ammonium compound, or a mixture of polymeric quaternary ammonium compounds, having the formula Z[CH.sub.2 CHOHCH.sub.2 -N.sup..sym. (CH.sub.3).sub.2 ].sub.n CH.sub.2 CHOHCH.sub.2 --Z + nX.sup.-, wherein Z is either X or the radical --N(CH.sub.3).sub.2 ; where X is halogen of atomic weight greater than 34; and n is an integer of from 2 to 20.
摘要翻译: 具有式Z [CH2CHOHCH2-N(+)(CH3)2] nCH2CHOHCH2-Z + nX-的聚合季铵化合物或聚合季铵化合物的混合物,其中Z为X或基团-N(CH3 )2; 其中X是原子量大于34的卤素; n为2〜20的整数。
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公开(公告)号:US3687954A
公开(公告)日:1972-08-29
申请号:US3687954D
申请日:1963-05-27
发明人: TYLER WILLIAM E , LOVETT JOHN R
IPC分类号: C07D241/04 , C07D51/72 , C07C87/22
CPC分类号: C07D241/04
摘要: 1. A compound having the composition of the general formula:
摘要翻译: 1.具有以下通式的化合物:(NF2)CH2-N(R') - (CH2)nD“'其中R'是由硝基,磺酰基,醛基,酰基, 羟基和卤素; D“是由-NF 2,酰氧基,烷氧基和卤素官能团组成的组的部分,烷基和-N(R')CH 2 NF 2基团,下标n表示二 - N(R') - 基团,否则为1。 在具有一个至两个-N(R') - 基团的环状模式中的每个连接到环中的两个碳的化合物的化合物,环中的碳在-CH(NF 2) - 基团中而不是(-CH 2 - ) - 除了与所述可取代官能团之一连接的环中的任何其它碳原子和氢原子之外的基团; 并且当D“'是基团-N(R')CH 2 NF 2时,该化合物也得到形式(NF2)CH2-N(R') - (CHNF2)2-D”。
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公开(公告)号:US3446847A
公开(公告)日:1969-05-27
申请号:US3446847D
申请日:1963-09-24
申请人: ROHM & HAAS
发明人: FREEMAN JEREMIAH P
CPC分类号: C07F9/113 , C07F9/091 , Y10S149/121
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公开(公告)号:US3423463A
公开(公告)日:1969-01-21
申请号:US3423463D
申请日:1964-09-08
申请人: AEROJET GENERAL CO
发明人: BAUM KURT
CPC分类号: H01J49/42 , Y10S149/122
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公开(公告)号:US4719312A
公开(公告)日:1988-01-12
申请号:US902136
申请日:1986-09-02
申请人: Raymond A. Firestone
发明人: Raymond A. Firestone
IPC分类号: A61K31/13 , A61K31/15 , A61K31/155 , A61K31/27 , A61K31/275 , A61K31/415 , A61K31/425 , A61K31/44 , A61K31/495 , A61K31/535 , A61K31/575 , A61K31/675 , A61K38/00 , A61K47/48 , C07D521/00 , C07J43/00 , C07K5/06 , C07K5/072 , C07C87/22
CPC分类号: C07D231/12 , A61K31/13 , A61K31/15 , A61K31/155 , A61K31/27 , A61K31/275 , A61K31/415 , A61K31/425 , A61K31/44 , A61K31/495 , A61K31/535 , A61K31/575 , A61K31/675 , A61K47/48023 , A61K47/48061 , A61K47/48246 , C07D233/56 , C07D249/08 , C07J43/003 , C07J43/006 , C07K5/06026 , C07K5/06095 , A61K38/00
摘要: The present invention is concerned with the preparation of lysosomotropic detergent agents and pharmaceutical composition useful in the treatment of cancer. These compounds are amine derivatives having a pK of 3.5 of the general structure ##STR1## in which R.sub.1 is C.sub.8-30 alkyl, C.sub.8-30 -alkenyl, substituted C.sub.4-30 alkyl or substituted C.sub.4-30 -alkenyl; R.sub.2 is hydrogen or C.sub.1-4 alkyl and Y is an electron withdrawing group, to control the pK, selected from trifluoroethyl, and difluoroethyl.
摘要翻译: 本发明涉及用于治疗癌症的溶酶体洗涤剂和药物组合物的制备。 这些化合物是具有通式结构“IMAGE”的3.5的pK的胺衍生物,其中R1是C8-30烷基,C8-30-烯基,取代的C4-30烷基或取代的C4-30-烯基; R2是氢或C1-4烷基,Y是吸电子基团,以控制选自三氟乙基和二氟乙基的pK。
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公开(公告)号:US3755404A
公开(公告)日:1973-08-28
申请号:US3755404D
申请日:1963-05-09
申请人: AMERICAN CYANAMID CO
IPC分类号: C07C263/02 , C07C69/00 , C07C87/22 , C07C123/00
CPC分类号: C07C263/00 , C07C263/16 , C07C265/04 , Y10S149/119
摘要: THE PROCESS WHICH COMPRISES REACTING A REAGENT SELECTED FROM THE GROUP CONSISTING OF
Z-N(-F)-C(=N-F)-X, AND Y-N(-F)-CN
WHEREIN-X IS SELECTED FROM THE GROUP CONSISTING OF -F, -NF2,
-NF-C(=NF)-NF2, -NF-C(-NF2)2-F, -NF-CN, AND -NF-CO-NF2
WHEN Z-IS F- AND WHEREIN -X IS -NF-C$N WHEN Z- IS N$C- AND WHEREIN -Y IS SELECTED FROM THE GROUP CONSISTING OF -F,
-C(=NF)-NF2, AND -C(=NF)-NF-CN
WITH AN ADDITIVE SELECTED FROM THE GROUP CONSISTING OF HNCO, HNCS, AND H2NC$N TO PRODUCE AN ADDUCT. 13. A COMPOUND HAVING THE STRUCTURAL FORMULA
NF2-C(-Q)(-NF2)-NF-G
WHEREIN Q IS SELECTED FROM THE GROUP CONSISTING OF -NCO, -NCS, -NFC$N, -NF2 -NHCF=NF, -NFCF=NF, NFCF2NF2, AND -NFCF3, AND WHEREIN G IS SELECTED FROM THE GROUP CONSISTING OF
-C(=NF)-NF2, -CF(-NF2)2, -CN, -CF=NF, -CF2-NF2,
-CO-NF2, -CF3, -C(-N=C=O)=NF, -C(-N=C=S)=NF,
-C(=NF)-NF-CN, -C(-N=C=O)2-NF2, -C(-N=C=S)2-NF2,
-C(-NF-CN)2-NF2, -C(-NF2)3, AND -C(NF-CF2-NF2)2-NF2
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