BRPI1010768A8 - composto, e, composição farmacêutica. - Google Patents

composto, e, composição farmacêutica. Download PDF

Info

Publication number
BRPI1010768A8
BRPI1010768A8 BRPI1010768A BRPI1010768A BRPI1010768A8 BR PI1010768 A8 BRPI1010768 A8 BR PI1010768A8 BR PI1010768 A BRPI1010768 A BR PI1010768A BR PI1010768 A BRPI1010768 A BR PI1010768A BR PI1010768 A8 BRPI1010768 A8 BR PI1010768A8
Authority
BR
Brazil
Prior art keywords
group
compound
alkyl
pharmaceutical composition
hydroxyl
Prior art date
Application number
BRPI1010768A
Other languages
English (en)
Inventor
Brock Carsten
Scherrer Didier
Mahuteau Florence
Gadea Gilles
Tazi Jamal
Cahuzac Nathalie
Roux Pierre
Najman Romain
Original Assignee
Abivax
Centre Nat Rech Scient
Inst Curie
Soc Splicos
Univ Montpellier
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 EP09162630A external-priority patent/EP2261214A1/en
Priority claimed from EP20090305540 external-priority patent/EP2266972A1/en
Application filed by Abivax, Centre Nat Rech Scient, Inst Curie, Soc Splicos, Univ Montpellier filed Critical Abivax
Priority to BR122019013686-6A priority Critical patent/BR122019013686B1/pt
Priority to BR122019013687A priority patent/BR122019013687B1/pt
Publication of BRPI1010768A2 publication Critical patent/BRPI1010768A2/pt
Publication of BRPI1010768A8 publication Critical patent/BRPI1010768A8/pt
Publication of BRPI1010768B1 publication Critical patent/BRPI1010768B1/pt
Publication of BRPI1010768B8 publication Critical patent/BRPI1010768B8/pt
Publication of BRPI1010768C8 publication Critical patent/BRPI1010768C8/pt

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • 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
    • 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
    • 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
    • A61K31/495Heterocyclic 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
    • A61K31/4985Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic 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
    • C07D213/02Heterocyclic 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
    • C07D213/04Heterocyclic 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
    • C07D213/60Heterocyclic 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
    • C07D213/72Nitrogen atoms
    • C07D213/74Amino or imino radicals substituted by hydrocarbon or substituted hydrocarbon radicals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D215/00Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
    • C07D215/02Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
    • C07D215/16Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms 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
    • C07D215/38Nitrogen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D215/00Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
    • C07D215/02Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
    • C07D215/16Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms 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
    • C07D215/38Nitrogen atoms
    • C07D215/42Nitrogen atoms attached in position 4
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D215/00Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
    • C07D215/02Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
    • C07D215/16Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms 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
    • C07D215/38Nitrogen atoms
    • C07D215/42Nitrogen atoms attached in position 4
    • C07D215/46Nitrogen atoms attached in position 4 with hydrocarbon radicals, substituted by nitrogen atoms, attached to said nitrogen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D215/00Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
    • C07D215/58Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems with hetero atoms directly attached to the ring nitrogen atom
    • C07D215/60N-oxides
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D241/00Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
    • C07D241/36Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings condensed with carbocyclic rings or ring systems
    • C07D241/38Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings condensed with carbocyclic rings or ring systems with only hydrogen or carbon atoms directly attached to the ring nitrogen atoms
    • C07D241/40Benzopyrazines
    • C07D241/44Benzopyrazines 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 carbon atoms of the hetero ring
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Epidemiology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Quinoline Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Steroid Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

composto, e, composição farmacêutica a presente invenção diz respeito a composto (i) em que: significa um grupo piridazina, pirimidina ou pirazina, r independentemente representa um átomo de hidrogênio, um átomo de halogênio ou um grupo escolhido entre um grupo -cn, um grupo hidroxila, um grupo -coor1, um grupo fluoralquila (c1-c3), um grupo fluoralcóxi (c1-c3), um grupo -n02, um grupo -nr1r2, um grupo alcóxi (c1-c4), um grupo fenóxi e um grupo alquila (c1-c3), o dito alquila sendo opcionalmente mono-substituído por um grupo hidroxila, n é 1, 2 ou 3, n' é 1 ou 2, r' é um átomo de hidrogênio, um átomo de halogênio ou um grupo escolhido entre um grupo alquila (c1-c3), um grupo hidroxila, um grupo -coor1, um grupo -n02, um grupo -nr1r2, um morfolinila ou um grupo morfolino, um grupo n-metilpiperazinila, um grupo fluoralquila (c1-c3), um grupo alcóxi (c1-c4) e um grupo -cn, z é n ou c, y é n ou c, x é n ou c, w é n ou c, t é n ou c, u é n ou c, para uso como um agente para prevenir, inibir ou tratar câncer. alguns dos ditos compostos são inéditos e também formam parte da invenção.
BRPI1010768A 2009-06-12 2010-06-14 composto de fórmula (i) BRPI1010768C8 (pt)

Priority Applications (2)

Application Number Priority Date Filing Date Title
BR122019013686-6A BR122019013686B1 (pt) 2009-06-12 2010-06-14 Composto de fórmula (i), composto de fórmula (iq) e composição farmacêutica
BR122019013687A BR122019013687B1 (pt) 2009-06-12 2010-06-14 composto de fórmula (i)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US18655209P 2009-06-12 2009-06-12
US18654409P 2009-06-12 2009-06-12
EP09162630A EP2261214A1 (en) 2009-06-12 2009-06-12 Compounds useful to treat premature aging and in particular progeria
EP20090305540 EP2266972A1 (en) 2009-06-12 2009-06-12 New chemical molecules that inhibit the splicing mechanism for treating diseases resulting from splicing anomalies
PCT/IB2010/052650 WO2010143168A2 (en) 2009-06-12 2010-06-14 Compounds useful for treating cancer

Publications (5)

Publication Number Publication Date
BRPI1010768A2 BRPI1010768A2 (pt) 2016-11-01
BRPI1010768A8 true BRPI1010768A8 (pt) 2019-07-30
BRPI1010768B1 BRPI1010768B1 (pt) 2019-10-22
BRPI1010768B8 BRPI1010768B8 (pt) 2020-03-10
BRPI1010768C8 BRPI1010768C8 (pt) 2020-04-07

Family

ID=43309298

Family Applications (5)

Application Number Title Priority Date Filing Date
BRPI1010768A BRPI1010768C8 (pt) 2009-06-12 2010-06-14 composto de fórmula (i)
BR122019013686-6A BR122019013686B1 (pt) 2009-06-12 2010-06-14 Composto de fórmula (i), composto de fórmula (iq) e composição farmacêutica
BRPI1012892A BRPI1012892B8 (pt) 2009-06-12 2010-06-14 compostos de fórmula (i), como tal, composição farmacêutica que os compreende e seu uso no tratamento de hgps, progeria, desordem de charcot-marie-tooth, síndrome de werner, diabetes, osteoporose e envelhecimento da pele
BR122019013687A BR122019013687B1 (pt) 2009-06-12 2010-06-14 composto de fórmula (i)
BRPI1010772A BRPI1010772B8 (pt) 2009-06-12 2010-06-14 compostos de quinolina, suas composições farmacêuticas e seus usos para tratar aids

Family Applications After (4)

Application Number Title Priority Date Filing Date
BR122019013686-6A BR122019013686B1 (pt) 2009-06-12 2010-06-14 Composto de fórmula (i), composto de fórmula (iq) e composição farmacêutica
BRPI1012892A BRPI1012892B8 (pt) 2009-06-12 2010-06-14 compostos de fórmula (i), como tal, composição farmacêutica que os compreende e seu uso no tratamento de hgps, progeria, desordem de charcot-marie-tooth, síndrome de werner, diabetes, osteoporose e envelhecimento da pele
BR122019013687A BR122019013687B1 (pt) 2009-06-12 2010-06-14 composto de fórmula (i)
BRPI1010772A BRPI1010772B8 (pt) 2009-06-12 2010-06-14 compostos de quinolina, suas composições farmacêuticas e seus usos para tratar aids

Country Status (24)

Country Link
US (7) US9145367B2 (pt)
EP (6) EP2440547B1 (pt)
JP (8) JP5905385B2 (pt)
KR (14) KR101982461B1 (pt)
CN (13) CN102596935B (pt)
AU (3) AU2010258294B2 (pt)
BR (5) BRPI1010768C8 (pt)
CA (5) CA2965791C (pt)
CU (4) CU24245B1 (pt)
DK (4) DK2440546T3 (pt)
ES (3) ES2736198T3 (pt)
FI (3) FI2440546T3 (pt)
HK (8) HK1173153A1 (pt)
HR (3) HRP20230143T1 (pt)
HU (2) HUE045548T2 (pt)
LT (1) LT2440547T (pt)
MX (9) MX338823B (pt)
PL (4) PL2440547T3 (pt)
PT (4) PT3517534T (pt)
RU (1) RU2567752C2 (pt)
SI (1) SI2440547T1 (pt)
TR (1) TR201910781T4 (pt)
WO (3) WO2010143168A2 (pt)
ZA (2) ZA201109032B (pt)

Families Citing this family (81)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FI2440546T3 (fi) * 2009-06-12 2023-03-30 Abivax Ennenaikaisen vanhenemisen ja erityisesti progerian hoitamiseen hyödyllisiä yhdisteitä
MX2019008390A (es) * 2009-06-12 2019-09-09 Abivax Compuestos utiles para tratar cancer.
US10253020B2 (en) 2009-06-12 2019-04-09 Abivax Compounds for preventing, inhibiting, or treating cancer, AIDS and/or premature aging
CA2772714C (en) 2009-09-03 2017-09-26 Bioenergenix Heterocyclic compounds for the inhibition of pask
GB201007286D0 (en) 2010-04-30 2010-06-16 Astex Therapeutics Ltd New compounds
GB201020179D0 (en) 2010-11-29 2011-01-12 Astex Therapeutics Ltd New compounds
EP2465502A1 (en) * 2010-12-15 2012-06-20 Société Splicos Compounds useful for treating AIDS
US9073902B2 (en) 2011-01-05 2015-07-07 Bioenergenix, Llc Substituted quinoxaline carboxylic acid compounds for the inhibition of PASK
US8916561B2 (en) 2011-03-02 2014-12-23 Bioenergenix, Llc Substituted quinoxaline compounds for the inhibition of PASK
US8912188B2 (en) 2011-03-02 2014-12-16 Bioenergenix, Llc Substituted quinoxaline carboxylic acids for the inhibition of PASK
GB201118654D0 (en) 2011-10-28 2011-12-07 Astex Therapeutics Ltd New compounds
GB201118675D0 (en) 2011-10-28 2011-12-14 Astex Therapeutics Ltd New compounds
GB201118652D0 (en) 2011-10-28 2011-12-07 Astex Therapeutics Ltd New compounds
GB201118656D0 (en) 2011-10-28 2011-12-07 Astex Therapeutics Ltd New compounds
FR2987627B1 (fr) * 2012-03-05 2016-03-18 Splicos Utilisation de rbm39 comme biomarqueur
GB201209613D0 (en) 2012-05-30 2012-07-11 Astex Therapeutics Ltd New compounds
GB201209609D0 (en) 2012-05-30 2012-07-11 Astex Therapeutics Ltd New compounds
US20150150869A1 (en) 2012-06-20 2015-06-04 Eutropics Pharmaceuticals, Inc. Methods and compositions useful for treating diseases involving bcl-2 family proteins with quinoline derivatives
TW201410657A (zh) 2012-08-02 2014-03-16 Endo Pharmaceuticals Inc 經取代胺基-嘧啶衍生物
US9487526B2 (en) 2012-08-13 2016-11-08 Takeda Pharmaceutical Company Limited Quinoxaline derivatives as GPR6 modulators
WO2014065209A1 (ja) * 2012-10-23 2014-05-01 日本曹達株式会社 ピリジン化合物またはその塩、有害生物防除剤、殺虫剤または殺ダニ剤、および外部寄生虫防除剤
EP2922544B1 (en) 2012-11-21 2018-08-01 Eutropics Pharmaceuticals, Inc. Methods and compositions useful for treating diseases involving bcl-2 family proteins with quinoline derivatives
GB201301571D0 (en) * 2012-11-27 2013-03-13 Fundanci N Pedro Barri De La Maza Product and use
US20140194465A1 (en) * 2013-01-04 2014-07-10 Novarx Corporation Compositions for treatment of cancer
EP2757161A1 (en) 2013-01-17 2014-07-23 Splicos miRNA-124 as a biomarker of viral infection
GB201307577D0 (en) 2013-04-26 2013-06-12 Astex Therapeutics Ltd New compounds
ES2898385T3 (es) * 2013-07-05 2022-03-07 Abivax Compuestos bicíclicos útiles para el tratamiento de enfermedades causadas por retrovirus
EP3020829B1 (en) * 2013-07-12 2021-11-17 Kyoto University Pharmaceutical composition capable of inhibiting abnormal splicing causative of onset or progress of a genetic disease
WO2015017788A1 (en) 2013-08-01 2015-02-05 Eutropics Pharmaceuticals, Inc. Method for predicting cancer sensitivity
EP3063302B1 (en) 2013-10-30 2019-12-04 Eutropics Pharmaceuticals, Inc. Methods for determining chemosensitivity and chemotoxicity
JO3466B1 (ar) 2013-12-20 2020-07-05 Takeda Pharmaceuticals Co مواد ضابطة لتترا هيدرو بيريدوبيرازينات من gpr6
WO2015123505A1 (en) 2014-02-14 2015-08-20 Takeda Pharmaceutical Company Limited Pyridopyrazines modulators of gpr6
AU2015238301B2 (en) 2014-03-26 2020-06-25 Astex Therapeutics Ltd Combinations
KR102479696B1 (ko) 2014-03-26 2022-12-22 아스텍스 테라퓨틱스 리미티드 Fgfr 억제제 및 igf1r 억제제의 조합물
JO3512B1 (ar) 2014-03-26 2020-07-05 Astex Therapeutics Ltd مشتقات كينوكسالين مفيدة كمعدلات لإنزيم fgfr كيناز
EP2974729A1 (en) * 2014-07-17 2016-01-20 Abivax Quinoline derivatives for use in the treatment of inflammatory diseases
EP2975034A1 (en) 2014-07-17 2016-01-20 Abivax A quinoline derivative for the treatment of inflammatory diseases and AIDS
WO2016120495A1 (en) 2015-01-30 2016-08-04 Centre National De La Recherche Scientifique (Cnrs) Delta133p53beta and delta133p53gamma isoforms are biomarkers of cancer stem cells
JOP20200201A1 (ar) 2015-02-10 2017-06-16 Astex Therapeutics Ltd تركيبات صيدلانية تشتمل على n-(3.5- ثنائي ميثوكسي فينيل)-n'-(1-ميثيل إيثيل)-n-[3-(ميثيل-1h-بيرازول-4-يل) كينوكسالين-6-يل]إيثان-1.2-ثنائي الأمين
EP3058940A1 (en) * 2015-02-23 2016-08-24 Abivax Quinoline derivatives for use in the treatment or prevention of viral infection
EP3059591A1 (en) * 2015-02-23 2016-08-24 Abivax Methods for screening compounds for treating or preventing a viral infection or a virus-related condition
EP3059236A1 (en) 2015-02-23 2016-08-24 Abivax A new quinoline derivative for use in the treatment and prevention of viral infections
US10478494B2 (en) 2015-04-03 2019-11-19 Astex Therapeutics Ltd FGFR/PD-1 combination therapy for the treatment of cancer
US11542247B2 (en) 2015-09-23 2023-01-03 Janssen Pharmaceutica Nv Bi-heteroaryl substitute 1,4-benzodiazepines and uses thereof for the treatment of cancer
BR112018005637B1 (pt) 2015-09-23 2023-11-28 Janssen Pharmaceutica Nv Compostos derivados de quinoxalina, quinolina e quinazolinona,composições farmacêuticas que os compreende, e uso dos referidos compostos
US10646465B2 (en) 2015-12-17 2020-05-12 Biokine Therapeutics Ltd. Small molecules against cancer
MX2020011500A (es) 2015-12-17 2020-12-07 Alonbio Ltd Moléculas pequeñas para inhibir la actividad de quimiocinas, la actividad de una cinasa y/o el crecimiento de células cancerosas.
MA43954A (fr) * 2016-02-03 2018-12-12 Janssen Pharmaceutica Nv Ligands d'imagerie tau-pet
WO2017158201A1 (en) 2016-03-18 2017-09-21 Ratiopharm Gmbh Process for preparing quinolin-2-yl-phenylamine derivatives and their salts
EP3484528B1 (en) 2016-07-18 2020-11-25 Janssen Pharmaceutica NV Tau pet imaging ligands
CN106496061B (zh) * 2016-10-20 2018-06-05 湘潭大学 一种萃取分离酰化反应液中乙酰精胺的方法
AR112027A1 (es) 2017-06-15 2019-09-11 Biocryst Pharm Inc Inhibidores de alk 2 quinasa que contienen imidazol
CN110996983A (zh) * 2017-06-26 2020-04-10 巴斯德研究所 清除hiv储库并降低病毒载量的治疗
US10889566B2 (en) 2017-08-29 2021-01-12 Chulabhorn Foundation Derivatives and composition of quinoline and naphthyridine
US20200039989A1 (en) * 2018-03-01 2020-02-06 Arizona Board Of Regents On Behalf Of The University Of Arizona Small molecule inhibitors of dyrk/clk and uses thereof
WO2019186277A1 (en) 2018-03-28 2019-10-03 Institut Pasteur Ultrasensitive hiv-1 p24 detection assay
EP3594205A1 (en) 2018-07-09 2020-01-15 Abivax Phenyl-n-aryl derivatives for treating a rna virus infection
EP3594206A1 (en) 2018-07-09 2020-01-15 Abivax Phenyl-n-quinoline derivatives for treating a rna virus infection
EP3669874A1 (en) * 2018-12-20 2020-06-24 Abivax Quinoline derivatives for use in the treatment or prevention of cancer
EP3669873A1 (en) 2018-12-20 2020-06-24 Abivax Quinoline derivatives for use ine the traeatment of inflammation diseases
WO2020128033A1 (en) 2018-12-20 2020-06-25 Institut Pasteur Cellular metabolism of hiv-1 reservoir seeding in cd4+ t cells
CA3090315C (en) 2019-05-15 2023-09-19 Biokine Therapeutics Ltd. 8-phenoxy-quinolinone derivatives for treating cancer, inhibiting chemokine activity and/or inducing cell death
EP3858336A1 (en) 2020-01-31 2021-08-04 Abivax Amorphous solid dispersion of 8-chloro-n-(4-(trifluoromethoxy)phenyl)quinolin-2-amine
MX2022009019A (es) * 2020-01-31 2022-08-11 Abivax Dispersion solida amorfa de 8-cloro-n-(4-(trifluorometoxi)fenil)qu inolin-2-amina.
EP3858815A1 (en) 2020-01-31 2021-08-04 Abivax Co-crystals and salts of 8-chloro-n-(4-(trifluoromethoxy)phenyl)quinolin-2-amine
CN115605205A (zh) 2020-03-20 2023-01-13 Abivax公司(Fr) 用于治疗或预防冠状病毒科感染的化合物以及用于评估冠状病毒科感染的发生的方法和用途
US11753413B2 (en) 2020-06-19 2023-09-12 Incyte Corporation Substituted pyrrolo[2,1-f][1,2,4]triazine compounds as JAK2 V617F inhibitors
US11691971B2 (en) 2020-06-19 2023-07-04 Incyte Corporation Naphthyridinone compounds as JAK2 V617F inhibitors
TW202216713A (zh) 2020-07-02 2022-05-01 美商英塞特公司 作為jak2 v617f抑制劑之三環脲化合物
US11767323B2 (en) 2020-07-02 2023-09-26 Incyte Corporation Tricyclic pyridone compounds as JAK2 V617F inhibitors
WO2022046989A1 (en) 2020-08-27 2022-03-03 Incyte Corporation Tricyclic urea compounds as jak2 v617f inhibitors
TW202237119A (zh) 2020-12-10 2022-10-01 美商住友製藥腫瘤公司 Alk﹘5抑制劑和彼之用途
WO2022140231A1 (en) 2020-12-21 2022-06-30 Incyte Corporation Deazaguaine compounds as jak2 v617f inhibitors
US11958861B2 (en) 2021-02-25 2024-04-16 Incyte Corporation Spirocyclic lactams as JAK2 V617F inhibitors
EP4063351A1 (en) 2021-03-26 2022-09-28 Abivax Preparation method of quinoline derivative compounds
TW202313592A (zh) 2021-05-27 2023-04-01 大陸商江蘇恆瑞醫藥股份有限公司 喹啉胺類化合物、其製備方法及其在醫藥上的應用
KR20230072900A (ko) 2021-11-18 2023-05-25 동우 화인켐 주식회사 마이크로 led 구조체 및 이의 제조방법
EP4212156A1 (en) 2022-01-13 2023-07-19 Abivax Combination of 8-chloro-n-(4-(trifluoromethoxy)phenyl)quinolin-2-amine and its derivatives with a s1p receptor modulator
WO2023138657A1 (zh) * 2022-01-24 2023-07-27 江苏恒瑞医药股份有限公司 喹啉胺类化合物、其制备方法及其在医药上的应用
EP4215196A1 (en) 2022-01-24 2023-07-26 Abivax Combination of 8-chloro-n-(4-(trifluoromethoxy)phenyl)quinolin-2-amine and its derivatives with a jak inhibitor
TW202337453A (zh) 2022-03-17 2023-10-01 美商英塞特公司 作為jak2 v617f抑制劑之三環脲化合物

Family Cites Families (48)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR400973A (fr) 1909-03-19 1909-08-13 Jean Victor Massillon Nouveau sertisseur à main pour la fabrication des cartouches
GB585362A (en) 1944-08-31 1947-02-05 Francis Henry Swinden Curd New heterocyclic compounds
BE486034A (pt) 1947-11-28
DE958647C (de) 1952-12-28 1957-02-21 Hoechst Ag Verfahren zur Herstellung von 7-Amino-2-oxy-4-methyl-chinolinen
FR2387229A1 (fr) 1977-04-13 1978-11-10 Anvar Dipyrido (4,3-b) (3,4-f) indoles, procede d'obtention, application therapeutique et compositions pharmaceutiques les contenant
FR2436786A1 (fr) 1978-09-21 1980-04-18 Anvar Nouveaux derives des pyrido (4,3-b) carbazoles (ellipticines), substitues en position 1 par une chaine polyaminee, leur obtention et leur application a titre de medicaments
FR2627493B1 (fr) * 1988-02-23 1991-10-31 Sanofi Sa Procede de preparation de derives d'isoquinoleine
FR2645861A1 (fr) * 1989-04-17 1990-10-19 Inst Nat Sante Rech Med Utilisation de dipyrido (4,3-b) (3,4-f) indoles pour la preparation de medicaments utiles pour le traitement du sida
US6177401B1 (en) 1992-11-13 2001-01-23 Max-Planck-Gesellschaft Zur Forderung Der Wissenschaften Use of organic compounds for the inhibition of Flk-1 mediated vasculogenesis and angiogenesis
AU763750B2 (en) 1999-04-05 2003-07-31 City Of Hope Novel inhibitors of formation of advanced glycation endproducts (AGE's)
UA75055C2 (uk) 1999-11-30 2006-03-15 Пфайзер Продактс Інк. Похідні бензоімідазолу, що використовуються як антипроліферативний засіб, фармацевтична композиція на їх основі
DE10013318A1 (de) * 2000-03-17 2001-09-20 Merck Patent Gmbh Formulierung enthaltend Chinoxalinderivate
CZ20031986A3 (cs) 2001-01-22 2003-12-17 Memory Pharmaceuticals Corporation N-substituované aniliny a difenylaminy inhibující PDE4 a farmaceutický prostředek, který je obsahuje
ATE493987T1 (de) 2002-05-22 2011-01-15 Amgen Inc Aminopyrimidin-derivate zur verwendung als vanilloid-rezeptor-liganden zur behandlung von schmerzen
AU2002950217A0 (en) 2002-07-16 2002-09-12 Prana Biotechnology Limited 8- Hydroxy Quinoline Derivatives
AU2003256616B2 (en) * 2002-07-19 2009-08-27 Memory Pharmaceuticals Corporation Phosphodiesterase 4 inhibitors, including N-substituted aniline and diphenylamine analogs
WO2006081444A2 (en) 2005-01-28 2006-08-03 The Government Of The Usa As Represented By The Secretary Of The Dept. Of Health And Human Services Farnesyltransferase inhibitors for treatment of laminopathies, cellular aging and atherosclerosis
FR2849474B3 (fr) 2002-12-27 2004-12-03 Olivier Jean Noel Juin Installation de transformation de l'energie cinetique d'un fluide en energie electrique
WO2004078731A1 (fr) 2003-03-06 2004-09-16 'chemical Diversity Research Institute', Ltd. Acides quinoline-carboxyliques et leurs derives et bibliotheque focalisee
JP2006519846A (ja) 2003-03-10 2006-08-31 シェーリング コーポレイション 複素環式キナーゼインヒビター:使用および合成の方法
FR2859475A1 (fr) 2003-09-04 2005-03-11 Centre Nat Rech Scient Utilisation de composes derives d'ellipticine et d'aza-ellipticine pour la preparation d'un medicament utile pour le traitement de maladies genetiques resultant de l'alteration des processus d'epissage
FR2859474B1 (fr) 2003-09-04 2006-01-13 Centre Nat Rech Scient Utilisation de composes derives d'indole pour la preparation d'un medicament utile pour le traitement de maladies genetiques resultant de l'alteration des processus d'epissage
JP2007509059A (ja) * 2003-10-16 2007-04-12 カイロン コーポレイション 癌の処置のためのRafキナーゼのインヒビターとしての、2,6−二置換キナゾリン、キノキサリン、キノリンおよびイソキノリン
US7598383B2 (en) * 2003-11-19 2009-10-06 Array Biopharma Inc. Heterocyclic inhibitors of MEK and methods of use thereof
JP2008519814A (ja) 2004-11-12 2008-06-12 ガラパゴス・ナムローゼ・フェンノートシャップ プロテインキナーゼ酵素の活性部位と結合する窒素複素環式芳香族化合物
US20090088513A1 (en) 2005-06-29 2009-04-02 Adeka Corporation Resin additive composition and resin composition
FR2903312B1 (fr) 2006-07-05 2008-09-26 Univ Aix Marseille Ii Utilisation d'inhibiteurs d'hmg-coa reductase et de farnesyl-pyrophosphate synthase dans la preparation d'un medicament
US8030487B2 (en) * 2006-07-07 2011-10-04 Targegen, Inc. 2-amino—5-substituted pyrimidine inhibitors
WO2008089459A1 (en) * 2007-01-19 2008-07-24 Ardea Biosciences, Inc. Inhibitors of mek
FR2912745A1 (fr) 2007-02-19 2008-08-22 Centre Nat Rech Scient Nouveaux composes derives d'indole et compositions pharmaceutiques les contenant
WO2008115870A2 (en) * 2007-03-16 2008-09-25 Mount Sinai School Of Medicine Induction and/or maintenance of tumor dormancy by disruption of urokinase plasminogen activator receptor-integrin interaction
WO2008143440A1 (en) * 2007-05-17 2008-11-27 Lg Chem, Ltd. New anthracene derivatives and organic electronic device using the same
UY31272A1 (es) * 2007-08-10 2009-01-30 Almirall Lab Nuevos derivados de ácido azabifenilaminobenzoico
CN101801194A (zh) 2007-08-15 2010-08-11 记忆医药公司 具有5-ht6受体亲和力的3’取代的化合物
WO2009029617A1 (en) * 2007-08-27 2009-03-05 Kalypsys, Inc. Diarylamine-substituted quinolones useful as inducible nitric oxide synthase inhibitors
KR100974562B1 (ko) * 2007-12-31 2010-08-06 다우어드밴스드디스플레이머티리얼 유한회사 신규한 유기 발광 화합물 및 이를 발광재료로서 채용하고있는 유기 발광 소자
FR2926297B1 (fr) 2008-01-10 2013-03-08 Centre Nat Rech Scient Molecules chimiques inhibitrices du mecanisme d'epissage pour traiter des maladies resultant d'anomalies d'epissage.
CA2747790A1 (en) * 2009-01-05 2010-07-08 Fraunhofer-Gesellschaft Zur Foerderung Der Angewandten Forschung E.V. Means and method for the treatment of antibody deficiency diseases based on il-21 and il-21 variants
US20110275791A1 (en) * 2009-01-06 2011-11-10 Ziad Mallat A B Cell Depleting Agent for the Treatment of Atherosclerosis
US20120172617A1 (en) * 2009-01-06 2012-07-05 Werner Bonrath resveratrol intermediates dal
FI2440546T3 (fi) * 2009-06-12 2023-03-30 Abivax Ennenaikaisen vanhenemisen ja erityisesti progerian hoitamiseen hyödyllisiä yhdisteitä
EP2266972A1 (en) 2009-06-12 2010-12-29 Splicos New chemical molecules that inhibit the splicing mechanism for treating diseases resulting from splicing anomalies
MX2019008390A (es) 2009-06-12 2019-09-09 Abivax Compuestos utiles para tratar cancer.
US8962583B2 (en) 2009-06-25 2015-02-24 The Brigham And Women's Hospital, Inc. Treatment of inflammatory diseases using miR-124
EP2465502A1 (en) 2010-12-15 2012-06-20 Société Splicos Compounds useful for treating AIDS
EP2903611A4 (en) 2012-10-04 2016-11-16 Oyagen Inc SMALL MOLECULES AS ANTI-HIV AGENTS FOR INTERRUPTING THE VIF SELF-ASSOCIATION AND METHOD FOR USE THEREOF
EP2757161A1 (en) 2013-01-17 2014-07-23 Splicos miRNA-124 as a biomarker of viral infection
JP2015120566A (ja) * 2013-12-20 2015-07-02 ニチユ三菱フォークリフト株式会社 荷役車両

Also Published As

Publication number Publication date
BRPI1010768A2 (pt) 2016-11-01
PT2440546T (pt) 2023-03-27
EP3521283B1 (en) 2024-02-28
KR20190018570A (ko) 2019-02-22
EP2440545B1 (en) 2019-04-24
JP2015187152A (ja) 2015-10-29
KR101863021B1 (ko) 2018-05-30
MX353776B (es) 2018-01-29
CA2764026C (en) 2019-10-29
CN106928205A (zh) 2017-07-07
MX2011013122A (es) 2012-07-23
HRP20230143T1 (hr) 2023-03-31
TR201910781T4 (tr) 2019-08-21
ZA201109031B (en) 2013-02-27
AU2010258214B2 (en) 2015-08-20
KR20180100737A (ko) 2018-09-11
CN104844570A (zh) 2015-08-19
KR101982461B1 (ko) 2019-05-24
CU20110230A7 (es) 2012-04-15
EP3517534A1 (en) 2019-07-31
KR20190018571A (ko) 2019-02-22
US20150307478A1 (en) 2015-10-29
DK2440545T3 (da) 2019-07-22
CU24461B1 (es) 2020-01-03
JP5826745B2 (ja) 2015-12-02
HK1173726A1 (zh) 2013-05-24
PL3517534T3 (pl) 2024-06-24
CN106905232A (zh) 2017-06-30
JP2012529494A (ja) 2012-11-22
KR20180101727A (ko) 2018-09-13
KR101769616B1 (ko) 2017-08-18
JP7042245B2 (ja) 2022-03-25
BRPI1012892B8 (pt) 2021-05-25
CA2965791C (en) 2020-06-09
EP3517534B1 (en) 2024-02-28
AU2010258214A1 (en) 2012-01-19
MX364282B (es) 2019-04-22
US20120283265A1 (en) 2012-11-08
EP2440546A2 (en) 2012-04-18
KR102016891B1 (ko) 2019-08-30
KR20190018567A (ko) 2019-02-22
DK2440546T3 (da) 2023-03-27
CN106928205B (zh) 2019-09-24
KR102016889B1 (ko) 2019-08-30
KR101982462B1 (ko) 2019-05-24
KR20180100736A (ko) 2018-09-11
HUE045548T2 (hu) 2019-12-30
SI2440547T1 (sl) 2023-05-31
KR20180100735A (ko) 2018-09-11
MX338823B (es) 2016-05-03
ES2736198T3 (es) 2019-12-26
HUE061262T2 (hu) 2023-05-28
KR20120049860A (ko) 2012-05-17
ES2940885T3 (es) 2023-05-12
BRPI1012892A2 (pt) 2018-03-13
MX367601B (es) 2019-08-28
JP6158251B2 (ja) 2017-07-05
BRPI1010768B8 (pt) 2020-03-10
CN102574835A (zh) 2012-07-11
PL2440547T3 (pl) 2023-09-11
EP2440545A2 (en) 2012-04-18
KR102016892B1 (ko) 2019-08-30
AU2010258295B2 (en) 2015-09-03
PT2440545T (pt) 2019-07-19
CN106928194A (zh) 2017-07-07
WO2010143168A3 (en) 2011-06-09
EP4198022A1 (en) 2023-06-21
KR102016890B1 (ko) 2019-08-30
FI2440546T3 (fi) 2023-03-30
CN109776496A (zh) 2019-05-21
CN104945378A (zh) 2015-09-30
PT3517534T (pt) 2024-05-17
WO2010143170A3 (en) 2011-08-11
KR101982463B1 (ko) 2019-05-24
JP2012529493A (ja) 2012-11-22
CN109776496B (zh) 2021-09-28
CA2764024A1 (en) 2010-12-16
US20120277230A1 (en) 2012-11-01
JP2015187150A (ja) 2015-10-29
DK2440547T3 (da) 2023-02-20
CA2764026A1 (en) 2010-12-16
DK3517534T3 (da) 2024-05-27
MX2011013119A (es) 2012-07-04
ZA201109032B (en) 2013-02-27
PT2440547T (pt) 2023-02-17
BRPI1010772A2 (pt) 2016-11-01
MX359575B (es) 2018-10-03
HK1212702A1 (zh) 2016-06-17
ES2938532T3 (es) 2023-04-12
MX2011013120A (es) 2012-07-23
US10017498B2 (en) 2018-07-10
PL2440545T3 (pl) 2019-11-29
EP3521283A1 (en) 2019-08-07
JP2015187151A (ja) 2015-10-29
CU24093B1 (es) 2015-04-29
WO2010143168A2 (en) 2010-12-16
CU20110229A7 (es) 2012-06-21
EP2440546B1 (en) 2022-12-28
BRPI1010768B1 (pt) 2019-10-22
CN106905232B (zh) 2019-09-27
HK1212990A1 (zh) 2016-06-24
CA2764027C (en) 2020-11-03
JP6158250B2 (ja) 2017-07-05
JP6041671B2 (ja) 2016-12-14
KR20190018569A (ko) 2019-02-22
RU2567752C2 (ru) 2015-11-10
MX340095B (es) 2016-06-27
KR20120054585A (ko) 2012-05-30
CN102596935B (zh) 2015-02-18
JP2020045342A (ja) 2020-03-26
MX364280B (es) 2019-04-22
AU2010258294B2 (en) 2015-07-30
BRPI1010768C8 (pt) 2020-04-07
CA2965791A1 (en) 2010-12-16
CN102625804B (zh) 2015-04-08
US20140288120A1 (en) 2014-09-25
CU20110228A7 (es) 2012-04-15
CU24124B1 (es) 2015-08-27
BRPI1012892B1 (pt) 2020-10-27
CN103948594B (zh) 2016-10-26
CN102574835B (zh) 2014-04-16
JP5905385B2 (ja) 2016-04-20
KR20190018568A (ko) 2019-02-22
CN102596935A (zh) 2012-07-18
US9145367B2 (en) 2015-09-29
EP2440547A2 (en) 2012-04-18
KR101973348B1 (ko) 2019-04-26
CA2764024C (en) 2017-12-05
BR122019013686B1 (pt) 2020-03-17
BRPI1010772B8 (pt) 2021-05-25
AU2010258295A1 (en) 2012-01-19
FI2440547T3 (fi) 2023-03-14
CU20150024A7 (es) 2015-09-29
CU24245B1 (es) 2017-02-02
KR102016893B1 (ko) 2019-08-30
CN106928194B (zh) 2019-11-12
CN104844510B (zh) 2019-04-23
US9108919B2 (en) 2015-08-18
KR101897221B1 (ko) 2018-09-10
WO2010143169A3 (en) 2011-11-10
CA2764027A1 (en) 2010-12-16
WO2010143170A2 (en) 2010-12-16
CN104945379B (zh) 2018-11-30
JP2015155453A (ja) 2015-08-27
JP2012529495A (ja) 2012-11-22
US9637475B2 (en) 2017-05-02
HK1213246A1 (zh) 2016-06-30
RU2011149572A (ru) 2013-07-20
WO2010143169A2 (en) 2010-12-16
US20120329796A1 (en) 2012-12-27
CN103948594A (zh) 2014-07-30
HRP20240582T1 (hr) 2024-07-19
FI3517534T3 (fi) 2024-05-16
KR20170124646A (ko) 2017-11-10
HK1200363A1 (en) 2015-08-07
EP2440547B1 (en) 2022-11-30
KR20120051643A (ko) 2012-05-22
HRP20230248T1 (hr) 2023-04-14
HK1213247A1 (zh) 2016-06-30
KR20170092720A (ko) 2017-08-11
CN113004249A (zh) 2021-06-22
KR101789275B1 (ko) 2017-11-20
CA3070823C (en) 2021-09-21
RU2011149571A (ru) 2013-07-20
BRPI1010772B1 (pt) 2020-10-27
LT2440547T (lt) 2023-03-10
PL2440546T3 (pl) 2023-07-10
CN102625804A (zh) 2012-08-01
HK1173153A1 (en) 2013-05-10
AU2010258294A1 (en) 2012-01-19
CN104945379A (zh) 2015-09-30
US9908869B2 (en) 2018-03-06
CA3070823A1 (en) 2010-12-16
MX364279B (es) 2019-04-22
HK1173447A1 (zh) 2013-05-16
MX364989B (es) 2019-05-17
BR122019013687B1 (pt) 2020-04-14
CN104844510A (zh) 2015-08-19
US20150299129A1 (en) 2015-10-22
CN104945378B (zh) 2018-11-20
CN104844570B (zh) 2018-11-02
US20140080831A1 (en) 2014-03-20

Similar Documents

Publication Publication Date Title
BRPI1010768A8 (pt) composto, e, composição farmacêutica.
BR112016000127A8 (pt) compostos bicíclicos úteis para tratar doenças causadas por retrovírus
BR112015024530A8 (pt) compostos derivados de naftiridina úteis como antagonistas de integrina alfa-v-beta-6, composição farmacêutica, e, uso de um composto
BRPI0506760A (pt) derivados de fenil-[4-(3-fenil-1h-pirazol-4-il)-pirimidin-2-il]-amina como inibidores de igf-ir
BR112015020650A2 (pt) inibidores de histona demetilases
BR112012032087A2 (pt) composto, medicamento, e, uso de um composto
CL2011000134A1 (es) Compuestos derivados de aminofenoxiindazoles, inhibidores de c-met; composicion farmaceutica que comprende a estos compuestos; y su uso para tratar el cancer.
BR112012010186B8 (pt) derivados de heteroarila contendo n como inibidores de quinase jak3 e composição farmacêutica compreendendo os mesmos
BR112013014943A8 (pt) Compostos da fórmula (i) e composição farmacêutica
BR112014014909A2 (pt) agonistas de tgr5 não sistêmicos
BR112022012222A2 (pt) Derivados de piperazina substituídos úteis como ativadores de células t
BR112012014858A2 (pt) agente antiplaqueta
BR112012021659A2 (pt) composto, composição farmacêutica, método para tratar e/ou prevenir distúrbios e doenças.
BR112013001632A2 (pt) composto, composição farmacêutica, método de inibir uma atividade uma jak quinase in vitro, uso de um composto, ou da composição farmacêutica, e, método de fabricar um composto
ECSP099330A (es) Compuesto de indol
CR11295A (es) 2-anilinopurin-8-onas como inhibidores de ttk/mps1 para el tratamiento de trastornos proliferativos
UY33539A (es) Compuestos químicos alk
BR112017002214A2 (pt) composto de fórmula (i), composição farmacêutica e usos de um composto
BR112012024822B8 (pt) Composto, uso de um composto e composição farmacêutica
TN2015000261A1 (fr) Dérivés d'imidazopyridazine servant de modulateurs des recepteurs gabaa
ECSP078062A (es) Heterociclos de 1,4-dihidropiridina-condensados, procesos para preparar los mismos, uso y composiciones que los contienen
BRPI0408353A (pt) composto, composição farmacêutica, métodos para o tratamento de neoplasias suscetìveis e para o tratamento de infecções virais, e, uso de um composto
ECSP10010602A (es) Compuestos de anillo fusionados y uso de los mismos
BR112012027387A2 (pt) composição para controle de doenças de plantas e uso da mesma
BR112012024422A2 (pt) uso de novos inibidores pan-cdk para tratamento de tumores

Legal Events

Date Code Title Description
B07D Technical examination (opinion) related to article 229 of industrial property law [chapter 7.4 patent gazette]
B25A Requested transfer of rights approved

Owner name: CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (FR) , INSTITUT CURIE (FR) , UNIVERSITE MONTPELLIER 2 (FR) , ABIVAX (FR)

Owner name: CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (FR)

B06F Objections, documents and/or translations needed after an examination request according [chapter 6.6 patent gazette]
B25A Requested transfer of rights approved

Owner name: CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (FR)

B07E Notification of approval relating to section 229 industrial property law [chapter 7.5 patent gazette]

Free format text: NOTIFICACAO DE ANUENCIA RELACIONADA COM O ART 229 DA LPI

B06T Formal requirements before examination [chapter 6.20 patent gazette]
B09A Decision: intention to grant [chapter 9.1 patent gazette]
B16A Patent or certificate of addition of invention granted [chapter 16.1 patent gazette]

Free format text: PRAZO DE VALIDADE: 20 (VINTE) ANOS CONTADOS A PARTIR DE 14/06/2010, OBSERVADAS AS CONDICOES LEGAIS.

B16C Correction of notification of the grant [chapter 16.3 patent gazette]

Free format text: REFERENTE A RPI 2546 DE 22/10/2019,QUANTO AO ITEM (30) PRIORDADE UNIONISTA.

B16C Correction of notification of the grant [chapter 16.3 patent gazette]

Free format text: REF. RPI 2566 DE 10/03/2020 QUANTO A PRIORIDADE UNIONISTA.