AR038712A1 - Uso de epotilonas en el tratamiento de enfermedades cerebrales asociados con procesos proliferativos - Google Patents

Uso de epotilonas en el tratamiento de enfermedades cerebrales asociados con procesos proliferativos

Info

Publication number
AR038712A1
AR038712A1 ARP030100696A ARP030100696A AR038712A1 AR 038712 A1 AR038712 A1 AR 038712A1 AR P030100696 A ARP030100696 A AR P030100696A AR P030100696 A ARP030100696 A AR P030100696A AR 038712 A1 AR038712 A1 AR 038712A1
Authority
AR
Argentina
Prior art keywords
alkyl
hydrogen
group
aralkyl
aryl
Prior art date
Application number
ARP030100696A
Other languages
English (en)
Inventor
Rosemarie Lichtner
Andrea Rotgeri
Ulrich Klar
Jens Hoffmann
Bernd Buchmann
Wolfgang Schwede
Dr Skuballa Werner Prof
Original Assignee
Schering Ag
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=27675676&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=AR038712(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Schering Ag filed Critical Schering Ag
Publication of AR038712A1 publication Critical patent/AR038712A1/es

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • 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
    • A61K31/42Oxazoles
    • A61K31/423Oxazoles condensed with carbocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • 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
    • A61K31/425Thiazoles
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • 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
    • A61K31/425Thiazoles
    • A61K31/427Thiazoles not condensed and containing further heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • 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
    • A61K31/425Thiazoles
    • A61K31/428Thiazoles condensed with carbocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/47Quinolines; Isoquinolines
    • A61K31/4709Non-condensed quinolines and containing further heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents

Landscapes

  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Epidemiology (AREA)
  • Organic Chemistry (AREA)
  • Neurology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Biomedical Technology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Neurosurgery (AREA)
  • Psychiatry (AREA)
  • Hospice & Palliative Care (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

) Uso de una epotilona que presenta un coeficiente de distribución promedio entre plasma y cerebro que comprende entre 0,3 y 1,5 en el ensayo de inyección de bolo intravenoso en ratón, en la preparación de un medicamento para el tratamiento de una enfermedad cerebral asociada con procesos proliferativos. Reivindicación 4: El uso de un compuesto, caracterizado porque dicho compuesto responde a la fórmula general (1) donde: R1a, R1b son, independientemente entre sí, hidrógeno, alquilo C1-10, arilo aralquilo; o forman juntos un grupo -(CH2)m-, donde m comprende entre 2 y 5; R2a, R2b son, independientemente entre sí, hidrógeno, alquilo C1-10, arilo, aralquilo; o forman juntos un grupo -(CH2)n, donde n comprende entre 2 y 5; o alquenilo C2-10; R3 es hidrógeno, alquilo C1-0, arilo, aralquilo; R4a, R4b son, independientemente entre sí, hidrógeno, alquilo C1-10, arilo, aralquilo; o forman juntos un grupo -(CH2)p, donde p comprende entre 2 y 5; R5 es hidrógeno, alquilo C1-10, arilo, aralquilo, CO2H, CO2 alquilo, CH2OH, CH2O alquilo, CH2O acilo, CN, CH2NH2, CH2N(alquilo, acilo)1,2 o CH2Hal; R6, R7 son, cada uno, hidrógeno; o forman juntos un enlace adicional o forman juntos una función epoxi; G es O ó CH2; D-E es un grupo H2C-CH2, HC=CH, C?C, CH(OH)-CH(OH); CH(OH)-CH2, CH2-CH(OH), CH2-O, O-CH2; o un resto de fórmula (2); W es un grupo C(=X)R8 o es un radical aromático o heteroaromático bi- o tricíclico; X es O ó dos grupos OR20 o un grupo alquilen(C2-10)-dioxi (que puede ser de cadena lineal o ramificada) o H/OR9 o un grupo CR10R11; R8 es hidrógeno, alquilo C1-10, arilo, aralquilo, halógeno, CN; R9 es hidrógeno o un grupo protector PGx; R10, R11 son, independientemente entre sí, hidrógeno, alquilo C1-20, arilo, aralquilo; o junto con el carbono del metileno forman un anillo carbocíclico de 5 a 7 miembros; Z es O ó H/OR12; R12 es hidrógeno o un grupo protector PGz; A-Y es un grupo O-C(=O), O-CH2, CH2-C(=O), NR21-C(=O), o NR21-SO2; R20 es un grupo alquilo C1-20; R21 es hidrógeno o alquilo C1-10; PGx, PGz es alquilo C1-20, cicloalquilo C4-7, que puede contener un átomo de oxígeno en el anillo, arilo, aralquilo, acilo C1-20, aroílo, alquilsulfonilo C1-20, arilsulfonilo, tri(alquil C1-20)sililo, di(alquil C1-20)arilsililo, (alquil C1-20)diarilsililo o tri(aralquil)sililo; como un estereoisómero único o una mezcla de distintos estereoisómeros y/o como una sal aceptable para uso farmacéutico del mismo, para la preparación de un medicamento destinado al tratamiento de una enfermedad cerebral asociada con procesos proliferativos.
ARP030100696A 2002-03-01 2003-03-03 Uso de epotilonas en el tratamiento de enfermedades cerebrales asociados con procesos proliferativos AR038712A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US36106202P 2002-03-01 2002-03-01
EP02004745A EP1340498A1 (en) 2002-03-01 2002-03-01 Use of epothilones in the treatment of brain diseases associated with proliferative processes

Publications (1)

Publication Number Publication Date
AR038712A1 true AR038712A1 (es) 2005-01-26

Family

ID=27675676

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP030100696A AR038712A1 (es) 2002-03-01 2003-03-03 Uso de epotilonas en el tratamiento de enfermedades cerebrales asociados con procesos proliferativos

Country Status (23)

Country Link
US (1) US20040019088A1 (es)
EP (2) EP1340498A1 (es)
JP (1) JP2005525360A (es)
KR (1) KR20040095244A (es)
CN (1) CN100473381C (es)
AR (1) AR038712A1 (es)
AU (1) AU2003215618B2 (es)
BR (1) BR0308154A (es)
CA (1) CA2477403A1 (es)
CR (1) CR7444A (es)
EC (1) ECSP045340A (es)
HK (1) HK1079998A1 (es)
HR (1) HRP20040892A2 (es)
IL (1) IL163752A0 (es)
MX (1) MXPA04008450A (es)
NO (1) NO20044175L (es)
NZ (1) NZ546617A (es)
PL (1) PL370768A1 (es)
RU (1) RU2351330C2 (es)
UA (1) UA83798C2 (es)
WO (1) WO2003074053A1 (es)
YU (1) YU76404A (es)
ZA (1) ZA200407905B (es)

Families Citing this family (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1999001124A1 (en) 1996-12-03 1999-01-14 Sloan-Kettering Institute For Cancer Research Synthesis of epothilones, intermediates thereto, analogues and uses thereof
AU9340998A (en) 1997-08-09 1999-03-01 Schering Aktiengesellschaft New epothilone derivatives, method for producing same and their pharmaceutical use
EA200100833A1 (ru) * 1999-02-11 2002-02-28 Шеринг Акциенгезельшафт Производные эпотилона, способ их получения и их применение в фармацевтике
US7125893B1 (en) 1999-04-30 2006-10-24 Schering Ag 6-alkenyl-, 6-alkinyl- and 6-epoxy-epothilone derivatives, process for their production, and their use in pharmaceutical preparations
PT1767535E (pt) 2002-08-23 2010-02-24 Sloan Kettering Inst Cancer Síntese de epotilonas, respectivos intermediários, análogos e suas utilizações
US7649006B2 (en) 2002-08-23 2010-01-19 Sloan-Kettering Institute For Cancer Research Synthesis of epothilones, intermediates thereto and analogues thereof
DE10331004A1 (de) * 2003-07-03 2005-02-24 Schering Ag Verfahren für die Herstellung von C1-C15-Fragmenten von Epothilonen und deren Derivaten
EP1559447A1 (en) 2004-01-30 2005-08-03 Institut National De La Sante Et De La Recherche Medicale (Inserm) Use of epothilones in the treatment of neuronal connectivity defects such as schizophrenia and autism
US20060069136A1 (en) * 2004-09-24 2006-03-30 Ulrich Klar Use of Epothilones in the treatment of bone metastasis
US20060121511A1 (en) 2004-11-30 2006-06-08 Hyerim Lee Biomarkers and methods for determining sensitivity to microtubule-stabilizing agents
EP1674098A1 (en) * 2004-12-23 2006-06-28 Schering Aktiengesellschaft Stable and tolerable parental formulations of highly reactive organic drug substances with low or no solubility in water
EP1700596A1 (en) * 2005-03-09 2006-09-13 Max-Planck-Gesellschaft Zur Förderung Der Wissenschaften E.V. Use of microtubule stabilizing compounds for the treatment of lesions of CNS axons
DE102007016046A1 (de) 2007-03-30 2008-10-23 Bayer Schering Pharma Aktiengesellschaft Verfahren zur Herstellung von Epothilonderivaten durch selektive katalytische Epoxidierung
WO2009132253A1 (en) * 2008-04-24 2009-10-29 Bristol-Myers Squibb Company Use of epothelone d in treating tau-associated diseases including alzheimer's disease
WO2013092998A1 (en) 2011-12-23 2013-06-27 Innate Pharma Enzymatic conjugation of antibodies
US10132799B2 (en) 2012-07-13 2018-11-20 Innate Pharma Screening of conjugated antibodies
WO2014072482A1 (en) 2012-11-09 2014-05-15 Innate Pharma Recognition tags for tgase-mediated conjugation
US10611824B2 (en) 2013-03-15 2020-04-07 Innate Pharma Solid phase TGase-mediated conjugation of antibodies
EP3010547B1 (en) 2013-06-20 2021-04-21 Innate Pharma Enzymatic conjugation of polypeptides
KR20160042871A (ko) 2013-06-21 2016-04-20 이나뜨 파르마, 에스.아. 폴리펩티드의 효소적 콘쥬게이션
WO2019092148A1 (en) 2017-11-10 2019-05-16 Innate Pharma Antibodies with functionalized glutamine residues

Family Cites Families (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CZ292233B6 (cs) * 1995-06-09 2003-08-13 Novartis Ag Deriváty rapamycinu a jejich použití jako léčiv
US6515016B2 (en) * 1996-12-02 2003-02-04 Angiotech Pharmaceuticals, Inc. Composition and methods of paclitaxel for treating psoriasis
US6495579B1 (en) * 1996-12-02 2002-12-17 Angiotech Pharmaceuticals, Inc. Method for treating multiple sclerosis
SK285969B6 (sk) * 1997-02-18 2007-12-06 Canji, Inc. Prípravky na liečenie cicavčích nádorových alebo hyperproliferatívnych buniek
GB9801231D0 (en) * 1997-06-05 1998-03-18 Merck & Co Inc A method of treating cancer
US6605599B1 (en) * 1997-07-08 2003-08-12 Bristol-Myers Squibb Company Epothilone derivatives
AU9340998A (en) * 1997-08-09 1999-03-01 Schering Aktiengesellschaft New epothilone derivatives, method for producing same and their pharmaceutical use
JP4434484B2 (ja) * 1997-12-04 2010-03-17 ブリストル−マイヤーズ スクイブ カンパニー オキシラニルエポチロン化合物のオレフィン性エポチロン化合物への還元法
US6302838B1 (en) * 1998-02-25 2001-10-16 Novartis Ag Cancer treatment with epothilones
FR2775187B1 (fr) * 1998-02-25 2003-02-21 Novartis Ag Utilisation de l'epothilone b pour la fabrication d'une preparation pharmaceutique antiproliferative et d'une composition comprenant l'epothilone b comme agent antiproliferatif in vivo
AU4775299A (en) * 1998-06-22 2000-01-10 Nicolaou, Kyriacos Costa Desmethyl epothilones
KR100718616B1 (ko) * 1999-02-18 2007-05-16 바이엘 쉐링 파마 악티엔게젤샤프트 16-할로겐-에포틸론 유도체, 그 제조 방법 및 제약학적 용도
PE20010116A1 (es) * 1999-04-30 2001-02-15 Schering Ag Derivados de 6-alquenil-, 6-alquinil- y 6-epoxi-epotilona, procedimientos para su preparacion
EP2266607A3 (en) * 1999-10-01 2011-04-20 Immunogen, Inc. Immunoconjugates for treating cancer
DE10020517A1 (de) * 2000-04-19 2001-10-25 Schering Ag Neue Epothilon-Derivate, Verfahren zu deren Herstellung und ihre pharmazeutische Verwendung
AU2001266583A1 (en) * 2000-05-26 2001-12-11 Kosan Biosciences, Inc. Epothilone derivatives and methods for making and using the same
GB0013643D0 (en) * 2000-05-31 2000-07-26 Unilever Plc Targeted moieties for use in bleach catalysts
WO2002098868A1 (en) * 2001-06-01 2002-12-12 Bristol-Myers Squibb Company Epothilone derivatives

Also Published As

Publication number Publication date
ZA200407905B (en) 2006-04-26
BR0308154A (pt) 2005-01-04
ECSP045340A (es) 2004-11-26
HRP20040892A2 (en) 2004-12-31
EP1340498A1 (en) 2003-09-03
US20040019088A1 (en) 2004-01-29
CA2477403A1 (en) 2003-09-12
JP2005525360A (ja) 2005-08-25
MXPA04008450A (es) 2005-07-13
YU76404A (sh) 2006-08-17
RU2004129325A (ru) 2005-07-10
KR20040095244A (ko) 2004-11-12
CN100473381C (zh) 2009-04-01
PL370768A1 (en) 2005-05-30
HK1079998A1 (zh) 2006-04-21
AU2003215618B2 (en) 2009-06-04
IL163752A0 (en) 2005-12-18
CN1649587A (zh) 2005-08-03
WO2003074053A1 (en) 2003-09-12
UA83798C2 (ru) 2008-08-26
NZ546617A (en) 2007-12-21
NO20044175L (no) 2004-12-01
EP1480643A1 (en) 2004-12-01
AU2003215618A1 (en) 2003-09-16
CR7444A (es) 2005-10-05
RU2351330C2 (ru) 2009-04-10

Similar Documents

Publication Publication Date Title
AR038712A1 (es) Uso de epotilonas en el tratamiento de enfermedades cerebrales asociados con procesos proliferativos
AR074822A1 (es) Compuestos heterociclicos de pirazina utiles como inhibidores de proteinquinasas atr, composiciones farmaceuticas que los comprenden y uso de los mismos en el tratamiento del cancer
ES2702128T3 (es) Antagonista o agonista inverso de RAR para uso en el tratamiento de efectos secundarios de quimioterapia y/o terapia de radiación
AR038202A1 (es) Compuestos de indazol utiles como inhibidores de la proteina quinasa
AR057131A1 (es) Derivados de purina como inmunomodulador
UY29938A1 (es) Derivados de pirido-, pirazo- y pirimido-pirimidina y su uso como inhibidores de mtor
AR012588A1 (es) UN INHIBIDOR DE SERINA PROTEASA, UNA COMPOSICIoN FARMACEUTICA QUE LO COMPRENDE Y UN PROCEDIMIENTO PARA PREPARAR UNA COMPOSICIoN FARMACEUTICA
PE20140411A1 (es) Derivados de 2,3-dihidroimidazo[1,2-c]quinazolina sustituidos con aminoalcoholes que son de utilidad para tratar trastornos hiperproliferativos y enfermedades asociadas a la angiogenesis
CO5700741A2 (es) Nuevos conjugados de efectores, procedimientos para su prepa racion y su uso farmaceutico
CY1112178T1 (el) Παραγωγα πιπεραζινης και χρηση αυτων ως θεραπευτικων παραγοντων
AR071300A1 (es) Compuestos; composiciones farmaceuticas en base al compuesto y uso del mismo para la manufactura de un medicamento
AR039222A1 (es) Derivados de quinolina e isoquinolina, un metodo para su preparacion y su uso como inhibidores de la inflamacion
AR068014A1 (es) Derivados de pirimidin-2-il-amina, composiciones farmaceuticas que los comprenden y su uso en la preparacion de medicamentos para el tratamiento de enfermedades mediadas por la inhibicion de la cinasa.
BRPI0413059A (pt) derivados de piridila e seu uso como agentes terapêuticos
GT200000002A (es) Ureas difenilicias x - carboxyaril sustituidas como inhibidores raf kinase.
AR042583A1 (es) Macrolidos
PE20080704A1 (es) Inhibidores ns5b del virus hepatitis c de indolobenzazepina fusionados a ciclopropilo
AR074876A1 (es) Derivados de indol-pirimidina para tratar cancer
ECSP066504A (es) Derivados biciclicos [3.1.0] como inhibidores del transportador de glicina
AR063165A1 (es) Derivados de acido boronico como inhibidores de amidihidrolasa de acidos grasos. composiciones farmaceuticas.
CO6241100A2 (es) Nuevos péptidos inhibidores de la replicación del virus de la hepatitis c
GT200500253A (es) Ligandos de difenil eter terapeuticos
AR053364A1 (es) Compuesto de 1h-imidazo 84,5-c) piridin -2- ilo, composicion farmaceutica que lo comprende, proceso para prepararla y su uso para preparar un medicamento para tratamiento de cancer o artritis
AR074148A1 (es) Derivados de corticoesteroides beta agonistas fosforilados, composiciones farmaceuticas que los contienen y uso de los mismos en el tratamiento de enfermedades del aparato respiratorio
AR041024A1 (es) Derivados de benzimidazol como inhibidores del factor de coagulacion xa

Legal Events

Date Code Title Description
FB Suspension of granting procedure