ATE327973T1 - Polyamin-analoge als cytotoxische wirkstoffe - Google Patents

Polyamin-analoge als cytotoxische wirkstoffe

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Publication number
ATE327973T1
ATE327973T1 AT01925146T AT01925146T ATE327973T1 AT E327973 T1 ATE327973 T1 AT E327973T1 AT 01925146 T AT01925146 T AT 01925146T AT 01925146 T AT01925146 T AT 01925146T AT E327973 T1 ATE327973 T1 AT E327973T1
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Austria
Prior art keywords
cytotoxic agents
polyamine analogues
analogues
polyamine
proliferation
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Application number
AT01925146T
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English (en)
Inventor
Mark R Burns
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Mediquest Therapeutics Inc
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Publication of ATE327973T1 publication Critical patent/ATE327973T1/de

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    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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    • A61K31/13—Amines
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    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/72—Nitrogen atoms
    • C07D213/73—Unsubstituted amino or imino radicals
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    • A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
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    • C07C211/27—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to acyclic carbon atoms of an unsaturated carbon skeleton containing at least one six-membered aromatic ring having amino groups linked to the six-membered aromatic ring by saturated carbon chains
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    • C07C211/30—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to acyclic carbon atoms of an unsaturated carbon skeleton containing at least one six-membered aromatic ring the six-membered aromatic ring being part of a condensed ring system formed by two rings
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    • C07C217/56—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by carbon chains not further substituted by singly-bound oxygen atoms
    • C07C217/58—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by carbon chains not further substituted by singly-bound oxygen atoms with amino groups and the six-membered aromatic ring, or the condensed ring system containing that ring, bound to the same carbon atom of the carbon chain
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    • C07C233/35—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by amino groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom
    • C07C233/37—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by amino groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom having the carbon atom of the carboxamide group bound to an acyclic carbon atom of a saturated carbon skeleton containing rings
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    • C07D285/04—Thiadiazoles; Hydrogenated thiadiazoles not condensed with other rings
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    • C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
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AT01925146T 2000-03-24 2001-03-23 Polyamin-analoge als cytotoxische wirkstoffe ATE327973T1 (de)

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USRE43327E1 (en) 2001-01-08 2012-04-24 Aminex Therapeutics, Inc. Hydrophobic polyamine analogs and methods for their use
JP4253503B2 (ja) * 2001-01-08 2009-04-15 メディクエスト セラピューティックス インク 疎水性ポリアミン類似体及びそれらの使用方法
IL147812A0 (en) * 2001-03-16 2002-08-14 N S T Neurosurvival Technologi Method for targeting chemical compounds to cells and pharmaceutical compositions used therein
EP1409483B1 (de) 2001-07-23 2008-12-31 Laboratoires Serono SA Arylsulfonamidderivate als hemmer c-jun-terminaler kinasen (jnk)
WO2003013245A1 (en) 2001-08-07 2003-02-20 Wisconsin Alumni Research Foundation Polyamines and analogs for protecting cells during cancer chemotherapy and radiotherapy
US7199267B1 (en) * 2005-10-21 2007-04-03 Mediquest Therapeutics, Inc. Recognition of oligiosaccaride molecular targets by polycationic small molecule inhibitors and treatment of immunological disorders and infectious diseases
EP2149568A1 (de) * 2008-07-22 2010-02-03 Bracco Imaging S.p.A Aryl-sulphonamid-dimere als metallprotease-hemmer
WO2013184202A1 (en) 2012-06-08 2013-12-12 University Of Pittsburgh - Of The Commonwealth System Of Higher Education Fbxo3 inhibitors
WO2015089087A1 (en) * 2013-12-09 2015-06-18 University Of Pittsburgh - Of The Commonwealth System Of Higher Education Compositions and methods for treating respiratory injury or disease
CN104892449B (zh) * 2014-03-06 2017-06-13 天津红日药业股份有限公司 一种精胺类似物及其药用盐的制备方法和用途
SG11201810861PA (en) * 2014-12-10 2019-01-30 Univ Pittsburgh Commonwealth Sys Higher Education Compositions and methods for treating diseases and conditions
LT3432914T (lt) 2016-03-25 2020-12-10 Aminex Therapeutics, Inc. Biologiškai įsisavinami poliaminai
WO2020033944A2 (en) 2018-08-10 2020-02-13 University Of Central Florida Research Foundation, Inc. Non-polyamine based polyamine transport inhibitors and their use in the treatment of human cancers
AU2021354039A1 (en) 2020-09-30 2023-05-25 Aminex Therapeutics, Inc. Combination drug substance of polyamine transport inhibitor and dfmo
US11752118B2 (en) 2020-12-02 2023-09-12 Gongwin Biopharm Co., Ltd Method for treating melanoma
EP4169902A1 (de) * 2021-10-25 2023-04-26 Consejo Superior de Investigaciones Científicas (CSIC) Sperminderivate als heparinantidote
WO2024130693A1 (zh) * 2022-12-23 2024-06-27 中国医学科学院基础医学研究所 精胺衍生物及其在疾病中的治疗用途
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US4851447A (en) * 1983-12-06 1989-07-25 Merrell Dow Pharmaceuticals Inc. N-2,3-butadienyl-1,4-butanediamine derivatives
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AU5173501A (en) 2001-10-08
WO2001072685A3 (en) 2002-07-18
JP2004500406A (ja) 2004-01-08
WO2001072685A2 (en) 2001-10-04
WO2001072685B1 (en) 2002-08-15
EP1296931B1 (de) 2006-05-31
WO2001072685A9 (en) 2002-10-10
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KR20020081433A (ko) 2002-10-26
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AU2001251735B2 (en) 2005-09-01
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