BR112015026410A2 - derivados de dolastatina 10 e auristatinas - Google Patents

derivados de dolastatina 10 e auristatinas

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Publication number
BR112015026410A2
BR112015026410A2 BR112015026410A BR112015026410A BR112015026410A2 BR 112015026410 A2 BR112015026410 A2 BR 112015026410A2 BR 112015026410 A BR112015026410 A BR 112015026410A BR 112015026410 A BR112015026410 A BR 112015026410A BR 112015026410 A2 BR112015026410 A2 BR 112015026410A2
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BR
Brazil
Prior art keywords
auristatins
dolastatin
derivatives
alkyl
alkyl group
Prior art date
Application number
BR112015026410A
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English (en)
Other versions
BR112015026410B1 (pt
Inventor
Rilatt Ian
Lamothe Marie
Perez Michel
Original Assignee
Pf Medicament
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Publication date
Application filed by Pf Medicament filed Critical Pf Medicament
Publication of BR112015026410A2 publication Critical patent/BR112015026410A2/pt
Publication of BR112015026410B1 publication Critical patent/BR112015026410B1/pt

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    • C07D207/02Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/04Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D207/08Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon radicals, substituted by hetero atoms, attached to ring carbon atoms
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    • A61K31/175Amides, e.g. hydroxamic acids having the group >N—C(O)—N< or >N—C(S)—N<, e.g. urea, thiourea, carmustine having the group, >N—C(O)—N=N— or, e.g. carbonohydrazides, carbazones, semicarbazides, semicarbazones; Thioanalogues thereof
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    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
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    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/4025Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil not condensed and containing further heterocyclic rings, e.g. cromakalim
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    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
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    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
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    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/513Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim having oxo groups directly attached to the heterocyclic ring, e.g. cytosine
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    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
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    • A61K31/7028Compounds having saccharide radicals attached to non-saccharide compounds by glycosidic linkages
    • A61K31/7034Compounds having saccharide radicals attached to non-saccharide compounds by glycosidic linkages attached to a carbocyclic compound, e.g. phloridzin
    • A61K31/704Compounds having saccharide radicals attached to non-saccharide compounds by glycosidic linkages attached to a carbocyclic compound, e.g. phloridzin attached to a condensed carbocyclic ring system, e.g. sennosides, thiocolchicosides, escin, daunorubicin
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    • A61K31/7052Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
    • A61K31/706Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom
    • A61K31/7064Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines
    • A61K31/7068Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines having oxo groups directly attached to the pyrimidine ring, e.g. cytidine, cytidylic acid
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    • A61K33/24Heavy metals; Compounds thereof
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    • C07D207/04Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D207/08Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon radicals, substituted by hetero atoms, attached to ring carbon atoms
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    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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    • C07D417/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/02Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing at least one abnormal peptide link
    • C07K5/0205Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing at least one abnormal peptide link containing the structure -NH-(X)3-C(=0)-, e.g. statine or derivatives thereof
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    • C07K5/06017Dipeptides with the first amino acid being neutral and aliphatic
    • C07K5/06034Dipeptides with the first amino acid being neutral and aliphatic the side chain containing 2 to 4 carbon atoms
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Abstract

resumo patente de invenção: "derivados de dolastatina 10 e auristatinas". a presente invenção refere-se a um composto da seguinte fórmula (i): (i) onde: - r1 é h ou oh, - r2 é um grupo (c1-c6)alquila, cooh, coo-((c1-c6)alquila) ou tiazolila, - r3 é h ou um grupo (c1-c6)alquila, e - r4 é um grupo aril-(c1-c8)alquila substituído por um ou mais grupos escolhidos dentre grupos oh e nr9r10, ou um sal, hidrato ou solvato farmaceuticamente aceitável do mesmo, e seus empregos em particular para o tratamento de câncer, composições farmacêuticas contendo o mesmo e os métodos de preparação das mesmas.
BR112015026410-7A 2013-04-25 2014-04-25 Derivados de dolastatina 10 e auristatinas, seu uso, sua composição farmacêutica e seus métodos para preparação BR112015026410B1 (pt)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
FR1353793 2013-04-25
FR1353793A FR3005051A1 (fr) 2013-04-25 2013-04-25 Derives de la dolastatine 10 et d'auristatines
PCT/EP2014/058427 WO2014174064A1 (en) 2013-04-25 2014-04-25 Derivatives of dolastatin 10 and auristatins

Publications (2)

Publication Number Publication Date
BR112015026410A2 true BR112015026410A2 (pt) 2017-07-25
BR112015026410B1 BR112015026410B1 (pt) 2022-06-07

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BR112015026478A BR112015026478A2 (pt) 2013-04-25 2014-04-25 derivados de dolastatina 10 e auristatinas
BR112015026410-7A BR112015026410B1 (pt) 2013-04-25 2014-04-25 Derivados de dolastatina 10 e auristatinas, seu uso, sua composição farmacêutica e seus métodos para preparação
BR112015026565A BR112015026565A2 (pt) 2013-04-25 2014-04-25 derivados de dolastatina 10 e auristatinas

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EP (4) EP3388427B1 (pt)
JP (3) JP6606489B2 (pt)
KR (4) KR102368136B1 (pt)
CN (3) CN105408318A (pt)
AU (3) AU2014259427B2 (pt)
BR (3) BR112015026478A2 (pt)
CA (4) CA2910176C (pt)
CY (2) CY1119677T1 (pt)
DK (3) DK3388427T3 (pt)
ES (3) ES2654364T3 (pt)
FR (1) FR3005051A1 (pt)
HK (2) HK1215580A1 (pt)
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PT3134124T (pt) 2014-04-25 2019-06-03 Pf Medicament Conjugado anticorpo-fármaco igf-1r e a sua utilização para o tratamento de cancro
ES2764110T3 (es) * 2014-04-25 2020-06-02 Pf Medicament Conjugado anticuerpo-fármaco y su utilización para el tratamiento del cáncer
ES2785551T3 (es) 2014-06-30 2020-10-07 Glykos Finland Oy Derivado de sacárido de una carga útil tóxica y sus conjugados con anticuerpos
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HUE062120T2 (hu) * 2016-03-29 2023-09-28 Toray Industries Peptid-származék és alkalmazása
CN105968038A (zh) * 2016-05-09 2016-09-28 湖北华世通生物医药科技有限公司 二肽类化合物的盐酸盐及其制备方法
CN106432318A (zh) * 2016-08-18 2017-02-22 重庆大学 一种芳炔前体的设计,合成,及在合成多取代芳烃的应用
CN107325033A (zh) * 2017-06-23 2017-11-07 华东师范大学 一种高立体选择性合成海兔毒素Dap片段的方法
CN111712511A (zh) * 2017-11-30 2020-09-25 森托瑞恩生物制药公司 澳瑞他汀e衍生物的白蛋白结合产物
AU2019350536A1 (en) 2018-09-27 2021-05-06 Pierre Fabre Medicament Sulfomaleimide-based linkers and corresponding conjugates
CN110724337B (zh) * 2019-10-16 2022-04-05 江苏德威新材料股份有限公司 一种硅烷交联型阻燃半导电聚烯烃护套材料及其制备方法和应用
CA3230737A1 (en) 2021-09-03 2023-03-09 Toray Industries, Inc. Pharmaceutical composition for cancer treatment and/or prevention

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