HUP0301387A2 - Szintetikus módszerek aplidin és új tumorellenes származékok előállítására - Google Patents

Szintetikus módszerek aplidin és új tumorellenes származékok előállítására

Info

Publication number
HUP0301387A2
HUP0301387A2 HU0301387A HUP0301387A HUP0301387A2 HU P0301387 A2 HUP0301387 A2 HU P0301387A2 HU 0301387 A HU0301387 A HU 0301387A HU P0301387 A HUP0301387 A HU P0301387A HU P0301387 A2 HUP0301387 A2 HU P0301387A2
Authority
HU
Hungary
Prior art keywords
independently
organic group
aplidine
preparation
synthetic methods
Prior art date
Application number
HU0301387A
Other languages
English (en)
Inventor
Carmen Cuevas
Felix Cuevas
Pilar Gallego
Ignacio Manzanares
Simon Munt
Paloma Méndez
Concepción Polanco
Ignacio Rodriguez
Original Assignee
Pharma Mar, S.A.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from GB0016148A external-priority patent/GB0016148D0/en
Priority claimed from GB0103750A external-priority patent/GB0103750D0/en
Application filed by Pharma Mar, S.A. filed Critical Pharma Mar, S.A.
Publication of HUP0301387A2 publication Critical patent/HUP0301387A2/hu
Publication of HUP0301387A3 publication Critical patent/HUP0301387A3/hu
Publication of HU228998B1 publication Critical patent/HU228998B1/hu

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K11/00Depsipeptides having up to 20 amino acids in a fully defined sequence; Derivatives thereof
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/08Tripeptides
    • C07K5/0802Tripeptides with the first amino acid being neutral
    • C07K5/0804Tripeptides with the first amino acid being neutral and aliphatic
    • C07K5/0808Tripeptides with the first amino acid being neutral and aliphatic the side chain containing 2 to 4 carbon atoms, e.g. Val, Ile, Leu
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K7/00Peptides having 5 to 20 amino acids in a fully defined sequence; Derivatives thereof
    • C07K7/02Linear peptides containing at least one abnormal peptide link
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00Medicinal preparations containing peptides

Abstract

A találmány (I) általános képletű vegyületekre és e vegyületekgyógyászatilag elfogadható sóira, valamint előállításukra vonatkozik.A képletben a szubsztituensek főbb jelentései a következők: Xjelentése egymástól függetlenül -C(R)2-, -O-, -S- vagy -NR-, ahol Rjelentése egymástól függetlenül H vagy egy szerves csoport; X2jelentése egymástól függetlenül, CR, O, S vagy N, ahol R jelentéseegymástól függetlenül H vagy egy szerves csoport; Y jelentése -(COR')nC0-, ahol a jelentése 0 vagy 1 és R' jelentése szerves csoport;X1 jelentése O vagy S; R1, R2 és R4 jelentése egymástól függetlenül Hvagy egy szerves csoport; vagy R1 és R2 X2-vel együtt egy adottesetben N-szubsztituált aa8 képletű prolincsoportot jelenthet, ahol R3jelentése egymástól függetlenül H vagy egy szerves csoport; vagy R1 ésR2 jelentése X2-vel együtt egy cikloalkilcsoport, arilcsoport vagyheterociklusos csoport; vagy R1, R2, X2, R4 és a nitrogént hordozó R4egy oxadiaza-spiroalkán-csoportot képez. A találmány szerintivegyületek főleg tumorok kezelésére használhatók. Ó
HU0301387A 2000-06-30 2001-07-02 Synthetic methods for preparation of aplidine and new antitumoral derivatives HU228998B1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GB0016148A GB0016148D0 (en) 2000-06-30 2000-06-30 Synthetic methods for aplidine and new antitiumoral derivatives
GB0103750A GB0103750D0 (en) 2001-02-15 2001-02-15 Synthetic methods for aplidine and new antitumoral derivatives methods of making and using them
PCT/GB2001/002901 WO2002002596A2 (en) 2000-06-30 2001-07-02 Synthetic methods for aplidine and new antitumoral derivatives, methods of making and using them

Publications (3)

Publication Number Publication Date
HUP0301387A2 true HUP0301387A2 (hu) 2003-08-28
HUP0301387A3 HUP0301387A3 (en) 2005-04-28
HU228998B1 HU228998B1 (en) 2013-07-29

Family

ID=26244577

Family Applications (1)

Application Number Title Priority Date Filing Date
HU0301387A HU228998B1 (en) 2000-06-30 2001-07-02 Synthetic methods for preparation of aplidine and new antitumoral derivatives

Country Status (25)

Country Link
US (2) US7348310B2 (hu)
EP (1) EP1294747B1 (hu)
JP (1) JP5289662B2 (hu)
KR (1) KR100866056B1 (hu)
CN (2) CN104650177A (hu)
AT (1) ATE393775T1 (hu)
AU (1) AU6769801A (hu)
BR (1) BRPI0112375B8 (hu)
CA (1) CA2414609C (hu)
CY (1) CY1108549T1 (hu)
CZ (1) CZ304204B6 (hu)
DE (1) DE60133817T2 (hu)
DK (1) DK1294747T3 (hu)
ES (1) ES2305083T3 (hu)
HK (1) HK1052940B (hu)
HU (1) HU228998B1 (hu)
IL (2) IL153680A0 (hu)
MX (1) MXPA03000202A (hu)
NO (1) NO334096B1 (hu)
NZ (1) NZ523367A (hu)
PL (1) PL208651B1 (hu)
PT (1) PT1294747E (hu)
SI (1) SI1294747T1 (hu)
UA (1) UA76718C2 (hu)
WO (1) WO2002002596A2 (hu)

Families Citing this family (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20030148933A1 (en) 1990-10-01 2003-08-07 Pharma Mar S.A. Derivatives of dehydrodidemnin B
GB9803448D0 (en) 1998-02-18 1998-04-15 Pharma Mar Sa Pharmaceutical formulation
SK287762B6 (sk) * 1999-11-15 2011-09-05 Pharma Mar, S. A. Použitie aplidínu na prípravu farmaceutického prostriedku na liečenie rakoviny
US6509315B1 (en) 2000-04-07 2003-01-21 The Trustees Of The University Of Pennsylvania Didemnin analogs and fragments and methods of making and using them
NZ521844A (en) 2000-04-07 2004-07-30 Univ Pennsylvania Tamandarin and didemnin analogs having deoxo-proline residue or dehydro-proline residue and methods of making and use thereof
UA76718C2 (uk) 2000-06-30 2006-09-15 Фарма Мар, С.А. Протипухлинні похідні аплідину
CN1479622A (zh) 2000-10-12 2004-03-03 联合使用阿普里汀和肌肉保护剂来治疗癌症
JP4584245B2 (ja) 2003-03-12 2010-11-17 ダナ−ファーバー キャンサー インスティテュート,インコーポレイテッド 多発性骨髄腫治療用のアプリジン
JP2006519848A (ja) 2003-03-12 2006-08-31 ファルマ・マール・ソシエダード・アノニマ 改良された抗腫瘍治療
CA2519234A1 (en) 2003-03-21 2004-10-07 Madeleine M. Joullie Tamandarin analogs and fragments thereof and methods of making and using
WO2007100385A2 (en) * 2005-10-31 2007-09-07 Genentech, Inc. Macrocyclic depsipeptide antibody-drug conjugates and methods
HUE028055T2 (hu) 2006-02-28 2016-11-28 Pharma Mar Sa Myeloma multiplex feljavított kezelése
US20100240595A1 (en) * 2007-10-19 2010-09-23 Pharma Mar ,S.A. Improved Antitumoral Treatments
JP2011513429A (ja) * 2008-03-07 2011-04-28 ファルマ・マール・ソシエダード・アノニマ 改善された抗癌治療法
WO2011020913A2 (en) 2009-08-21 2011-02-24 Pharma Mar, S.A. Cyclodepsipeptide antiviral compounds
EP2614089A1 (fr) * 2010-09-10 2013-07-17 Sanofi-Aventis Polysaccharides biotinyles a activite antithrombotique et presentant une stabilite metabolique amelioree
JOP20190254A1 (ar) 2017-04-27 2019-10-27 Pharma Mar Sa مركبات مضادة للأورام
AU2021231197A1 (en) 2020-03-02 2022-10-06 Pharma Mar, S.A. Compounds for use in inflammatory conditions
EP4114436A1 (en) 2020-03-02 2023-01-11 Pharma Mar S.A. Compounds for use in the treatment of coronavirus infection
CA3169528A1 (en) 2020-03-02 2021-09-10 Pharma Mar, S.A.U. Pld for use in combination in the treatment of coronavirus
US20230158104A1 (en) 2020-03-02 2023-05-25 Pharma Mar, S.A. Compounds for use in autoimmune conditions
CN115594739A (zh) * 2021-06-28 2023-01-13 浙江珲达生物科技有限公司(Cn) 一种dehydrodidemnin B类化合物的制备方法

Family Cites Families (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4950649A (en) 1980-09-12 1990-08-21 University Of Illinois Didemnins and nordidemnins
DE3161556D1 (en) 1980-09-12 1984-01-05 Univ Illinois Novel antibiotics, derivatives thereof, processes for their extraction, and compositions containing them
US4493796A (en) 1980-09-12 1985-01-15 Board Of Trustees, Univ. Of Ill. Didemnins A, B, C, and derivatives thereof, as antiviral agents
IT1153974B (it) 1982-09-23 1987-01-21 Erba Farmitalia Composizioni farmacologiche a base di cisplatino e metodo per il loro ottenimento
US4948791A (en) * 1989-04-10 1990-08-14 The Board Of Trustees Of The University Of Illinois Novel Cytotoxic cyclic depsipeptides from the tunicate trididemnum solidum
GB8922026D0 (en) 1989-09-29 1989-11-15 Pharma Mar Sa Novel anti-viral and cytotoxic agent
DE4120327A1 (de) * 1991-06-20 1992-12-24 Basf Ag Neue peptide, ihre herstellung und verwendung
US5462726A (en) 1993-12-17 1995-10-31 Bristol-Myers Squibb Company Method of inhibiting side effects of solvents containing ricinoleic acid or castor oil or derivatives thereof employing a thromboxane A2 receptor antagonist and pharmaceutical compositions containing such solvents
US5861439A (en) 1994-11-14 1999-01-19 Alza Corporation Method for enhanced electrotransport agent delivery
US6509316B2 (en) * 1995-03-07 2003-01-21 George Washington University Pharmaceutical compositions, methods, and kits for treatment and diagnosis of lung cancer
ES2102322B1 (es) 1995-07-13 1998-03-01 Pharma Mar Sa Procedimiento de preparacion de didemnina a.
ES2151277T3 (es) 1996-05-22 2000-12-16 Protarga Inc Composiciones que comprenden conjugados de acido cis-docosahexaenoico y taxotere.
US6156724A (en) 1996-06-07 2000-12-05 Rinehart; Kenneth L. Uses of didemnins as immunomodulating agents
ES2262175T3 (es) 1996-10-24 2006-11-16 The Board Of Trustees Of The University Of Illinois Estudios semisinteticos para dar analogos de didemnina.
PT956033E (pt) 1996-10-24 2003-10-31 Univ Illinois SíNTESE TOTAL DE ANALOGOS AMINO HIP DE DIDEMNINA A
US6034058A (en) 1997-04-15 2000-03-07 Rinehart; Kenneth L. Semi-synthetic alanyl dilemnin analogs
AU740598B2 (en) 1997-05-07 2001-11-08 William J. Crumb Aplidine as an L-type calcium channel enhancer
GB9803448D0 (en) 1998-02-18 1998-04-15 Pharma Mar Sa Pharmaceutical formulation
ES2235499T3 (es) 1998-07-30 2005-07-01 Sigma-Tau Industrie Farmaceutiche Riunite S.P.A. Uso de derivados de propionil l-carnitina y de acetil l-carnitina en la preparacion de medicamentos con actividad anticancerigena.
CA2373643A1 (en) 1999-05-25 2000-11-30 Point Therapeutics, Inc. Anti-tumor comprising boroproline compounds
US6890904B1 (en) 1999-05-25 2005-05-10 Point Therapeutics, Inc. Anti-tumor agents
SK287762B6 (sk) 1999-11-15 2011-09-05 Pharma Mar, S. A. Použitie aplidínu na prípravu farmaceutického prostriedku na liečenie rakoviny
US6509315B1 (en) * 2000-04-07 2003-01-21 The Trustees Of The University Of Pennsylvania Didemnin analogs and fragments and methods of making and using them
NZ521844A (en) * 2000-04-07 2004-07-30 Univ Pennsylvania Tamandarin and didemnin analogs having deoxo-proline residue or dehydro-proline residue and methods of making and use thereof
UA76718C2 (uk) 2000-06-30 2006-09-15 Фарма Мар, С.А. Протипухлинні похідні аплідину
JP2004510824A (ja) 2000-10-12 2004-04-08 ファルマ・マール・ソシエダード・アノニマ ガンの治療
WO2003033013A1 (en) 2001-10-19 2003-04-24 Pharma Mar, S.A. Use of aplidine for the treatment of pancreatic cancer
JP2006519848A (ja) 2003-03-12 2006-08-31 ファルマ・マール・ソシエダード・アノニマ 改良された抗腫瘍治療

Also Published As

Publication number Publication date
ATE393775T1 (de) 2008-05-15
US7348310B2 (en) 2008-03-25
SI1294747T1 (sl) 2008-12-31
NO20026242D0 (no) 2002-12-27
DK1294747T3 (da) 2008-10-27
UA76718C2 (uk) 2006-09-15
CZ20024233A3 (cs) 2003-06-18
HK1052940A1 (en) 2003-10-03
ES2305083T3 (es) 2008-11-01
IL153680A (en) 2012-05-31
WO2002002596A2 (en) 2002-01-10
PT1294747E (pt) 2008-08-08
DE60133817T2 (de) 2009-05-20
AU6769801A (en) 2002-01-14
NO20026242L (no) 2003-02-27
BR0112375A (pt) 2003-06-24
HU228998B1 (en) 2013-07-29
KR100866056B1 (ko) 2008-10-30
CA2414609C (en) 2012-04-24
JP5289662B2 (ja) 2013-09-11
DE60133817D1 (de) 2008-06-12
EP1294747B1 (en) 2008-04-30
JP2004502702A (ja) 2004-01-29
CY1108549T1 (el) 2014-04-09
HK1052940B (zh) 2008-10-24
CN104650177A (zh) 2015-05-27
CA2414609A1 (en) 2002-01-10
KR20030013477A (ko) 2003-02-14
PL360531A1 (en) 2004-09-06
BRPI0112375B8 (pt) 2021-05-25
BRPI0112375B1 (pt) 2020-12-01
EP1294747A2 (en) 2003-03-26
PL208651B1 (pl) 2011-05-31
CN1449408A (zh) 2003-10-15
MXPA03000202A (es) 2003-10-15
WO2002002596A3 (en) 2002-05-23
US20040097413A1 (en) 2004-05-20
US7678765B2 (en) 2010-03-16
CZ304204B6 (cs) 2014-01-02
NO334096B1 (no) 2013-12-09
HUP0301387A3 (en) 2005-04-28
NZ523367A (en) 2004-12-24
US20080009435A1 (en) 2008-01-10
IL153680A0 (en) 2003-07-06

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