AR082341A1 - Derivados anticancerosos, su preparacion y agentes de seleccion para su aplicacion terapeutica - Google Patents
Derivados anticancerosos, su preparacion y agentes de seleccion para su aplicacion terapeuticaInfo
- Publication number
- AR082341A1 AR082341A1 ARP110102680A ARP110102680A AR082341A1 AR 082341 A1 AR082341 A1 AR 082341A1 AR P110102680 A ARP110102680 A AR P110102680A AR P110102680 A ARP110102680 A AR P110102680A AR 082341 A1 AR082341 A1 AR 082341A1
- Authority
- AR
- Argentina
- Prior art keywords
- group
- alkyl
- different
- single bond
- hal
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
- C07K16/40—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against enzymes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/551—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
- A61K31/5513—1,4-Benzodiazepines, e.g. diazepam or clozapine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/551—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
- A61K31/5513—1,4-Benzodiazepines, e.g. diazepam or clozapine
- A61K31/5517—1,4-Benzodiazepines, e.g. diazepam or clozapine condensed with five-membered rings having nitrogen as a ring hetero atom, e.g. imidazobenzodiazepines, triazolam
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
- A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
- A61K47/56—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic macromolecular compound, e.g. an oligomeric, polymeric or dendrimeric molecule
- A61K47/59—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic macromolecular compound, e.g. an oligomeric, polymeric or dendrimeric molecule obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyureas or polyurethanes
- A61K47/60—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic macromolecular compound, e.g. an oligomeric, polymeric or dendrimeric molecule obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyureas or polyurethanes the organic macromolecular compound being a polyoxyalkylene oligomer, polymer or dendrimer, e.g. PEG, PPG, PEO or polyglycerol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic 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
- C07D207/18—Heterocyclic 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 one double bond between ring members or between a ring member and a non-ring member
- C07D207/20—Heterocyclic 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 one double bond between ring members or between a ring member and a non-ring member with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D243/00—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms
- C07D243/06—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms having the nitrogen atoms in positions 1 and 4
- C07D243/10—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms having the nitrogen atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems
- C07D243/14—1,4-Benzodiazepines; Hydrogenated 1,4-benzodiazepines
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
- C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
- C07K16/28—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
- C07K16/2866—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against receptors for cytokines, lymphokines, interferons
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Immunology (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Epidemiology (AREA)
- Biochemistry (AREA)
- Biophysics (AREA)
- Genetics & Genomics (AREA)
- Molecular Biology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Abstract
La presente se refiere a compuestos de fórmula (1), en la que: - - - - - representa un enlace sencillo o un enlace doble; U y/o U’, idéntico o diferente, representa(n) independientemente el uno del otro, H; W y/o W’, idéntico o diferente, representa(n) independientemente el uno del otro: H, OH, -OR, -OCOR, -COOR, -OCOOR, -OCONRR’, un carbamato cíclico tal que N10 y C11 estén incluidos en un ciclo, -NRCONRR’, -OCSNHR, un tiocarbamato cíclico tal que N10 y C11 estén incluidos en un ciclo, -SH, -SR, -SOR, -SOOR, -SO3-, -NRSOOR’, -NRR’, una amina cíclica tal que N10 y C11 estén incluidos en un ciclo, -NROR’, -NRCOR’, -N3, -CN, Hal, un grupo trialquilfosfonio o triarilfosfonio; R1, R2, R1’, R2’, idénticos o diferentes, representan independientemente el uno del otro: H, Hal o un grupo alquilo C1-6 sustituido opcionalmente; o bien R1 y R2 y/o R1’ y R2’ forman juntos respectivamente un enlace doble =CH2 o =CH-CH3; Y e Y’, idénticos o diferentes, representan independientemente el uno del otro H u -OR; M representa CH o N; ALK y ALK’ designan un grupo alquileno C1-6; R y R’ representan independientemente el uno del otro, H o un grupo alquilo C1-6 o arilo sustituido opcionalmente; L1 y L2 representan conectores; Q representa un enlace sencillo o el grupo C(=O); G representa un grupo -OR o -NRR’; GCR1 representa el grupo -SZa o -C(=O)-ZbRb; Za representa Ac, Ra o SRa; Ra representa H, o un grupo alquilo C1-6, cicloalquilo C3-8, arilo, heteroarilo o heterocicloalquilo C4-10 sustituido opcionalmente; Zb representa un enlace sencillo, -O- o -NH- y representando Rb H o un grupo alquilo C1-6, cicloalquilo C3-8, arilo, heteroarilo o heterocicloalquilo C4-10 o bien Zb representa un enlace sencillo y Rb representa Hal; con la condición de que si L1 representa un enlace sencillo entonces GCR1 representa -SZa. Los compuestos de la presente son útiles como agentes anticancerosos.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR1056103A FR2963007B1 (fr) | 2010-07-26 | 2010-07-26 | Derives anticancereux, leur preparation et leur application therapeutique |
Publications (1)
Publication Number | Publication Date |
---|---|
AR082341A1 true AR082341A1 (es) | 2012-11-28 |
Family
ID=43027561
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP110102680A AR082341A1 (es) | 2010-07-26 | 2011-07-25 | Derivados anticancerosos, su preparacion y agentes de seleccion para su aplicacion terapeutica |
Country Status (30)
Country | Link |
---|---|
US (1) | US9056914B2 (es) |
EP (1) | EP2598507B1 (es) |
JP (1) | JP5814366B2 (es) |
KR (1) | KR20130094806A (es) |
CN (1) | CN103140491B (es) |
AR (1) | AR082341A1 (es) |
AU (1) | AU2011284339B2 (es) |
BR (1) | BR112013001978B1 (es) |
CA (1) | CA2806665A1 (es) |
CL (1) | CL2013000250A1 (es) |
CO (1) | CO6650375A2 (es) |
CR (1) | CR20130035A (es) |
DO (1) | DOP2013000021A (es) |
EA (1) | EA201390162A1 (es) |
EC (1) | ECSP13012404A (es) |
ES (1) | ES2638520T3 (es) |
FR (1) | FR2963007B1 (es) |
GT (1) | GT201300025A (es) |
MA (1) | MA34469B1 (es) |
MX (1) | MX2013001069A (es) |
MY (1) | MY159197A (es) |
NI (1) | NI201300010A (es) |
NZ (1) | NZ606246A (es) |
PE (1) | PE20130489A1 (es) |
SG (1) | SG187191A1 (es) |
TW (1) | TW201208689A (es) |
UA (1) | UA111164C2 (es) |
UY (1) | UY33531A (es) |
WO (1) | WO2012014147A1 (es) |
ZA (1) | ZA201300685B (es) |
Families Citing this family (24)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2949469A1 (fr) * | 2009-08-25 | 2011-03-04 | Sanofi Aventis | Derives anticancereux, leur preparation et leur application en therapeutique |
CN104837502B (zh) | 2012-10-12 | 2018-08-10 | 麦迪穆有限责任公司 | 吡咯并苯并二氮杂卓及其结合物 |
US9649390B2 (en) * | 2013-03-13 | 2017-05-16 | Medimmune Limited | Pyrrolobenzodiazepines and conjugates thereof |
CA2901941C (en) | 2013-03-13 | 2020-04-07 | Spirogen Sarl | Pyrrolobenzodiazepines and conjugates thereof |
GB201416112D0 (en) | 2014-09-12 | 2014-10-29 | Medimmune Ltd | Pyrrolobenzodiazepines and conjugates thereof |
US9518118B2 (en) | 2014-09-12 | 2016-12-13 | Genentech, Inc. | Anti-HER2 antibodies and immunoconjugates |
KR20170055521A (ko) * | 2014-09-17 | 2017-05-19 | 제넨테크, 인크. | 항-her2 항체를 포함하는 면역콘주게이트 |
CN107231804B (zh) | 2015-01-14 | 2019-11-26 | 百时美施贵宝公司 | 亚杂芳基桥连苯并二氮杂*二聚体、其缀合物及制备和使用方法 |
CA2973354A1 (en) | 2015-01-14 | 2016-07-21 | Bristol-Myers Squibb Company | Benzodiazepine dimers, conjugates thereof, and methods of making and using |
BR112017027258A2 (pt) | 2015-06-23 | 2018-08-28 | Bristol-Myers Squibb Company | dímeros de benzodiazepina macrocíclicos, conjugados dos mesmos, preparação e usos |
MA43345A (fr) | 2015-10-02 | 2018-08-08 | Hoffmann La Roche | Conjugués anticorps-médicaments de pyrrolobenzodiazépine et méthodes d'utilisation |
GB201601431D0 (en) | 2016-01-26 | 2016-03-09 | Medimmune Ltd | Pyrrolobenzodiazepines |
GB201602356D0 (en) | 2016-02-10 | 2016-03-23 | Medimmune Ltd | Pyrrolobenzodiazepine Conjugates |
GB201602359D0 (en) | 2016-02-10 | 2016-03-23 | Medimmune Ltd | Pyrrolobenzodiazepine Conjugates |
GB201607478D0 (en) | 2016-04-29 | 2016-06-15 | Medimmune Ltd | Pyrrolobenzodiazepine Conjugates |
GB201617466D0 (en) | 2016-10-14 | 2016-11-30 | Medimmune Ltd | Pyrrolobenzodiazepine conjugates |
RS61795B1 (sr) | 2017-02-08 | 2021-06-30 | Adc Therapeutics Sa | Konjugati pirolobenzodiazepin antitela |
GB201702031D0 (en) | 2017-02-08 | 2017-03-22 | Medlmmune Ltd | Pyrrolobenzodiazepine-antibody conjugates |
JP2020517609A (ja) | 2017-04-18 | 2020-06-18 | メディミューン リミテッド | ピロロベンゾジアゼピン複合体 |
WO2019034764A1 (en) | 2017-08-18 | 2019-02-21 | Medimmune Limited | CONJUGATES OF PYRROLOBENZODIAZEPINE |
BR112020004126A2 (pt) | 2017-09-29 | 2020-09-08 | Daiichi Sankyo Company, Limited | conjugado anticorpo-derivado de pirrolbenzodiazepina |
GB201803342D0 (en) | 2018-03-01 | 2018-04-18 | Medimmune Ltd | Methods |
GB201806022D0 (en) | 2018-04-12 | 2018-05-30 | Medimmune Ltd | Pyrrolobenzodiazepines and conjugates thereof |
CN115466231B (zh) * | 2022-10-23 | 2024-03-08 | 浙江大学 | 管道化制备3-[2-(4-吗啉基)乙氧基]丙腈的方法 |
Family Cites Families (29)
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FR1516743A (fr) | 1966-04-01 | 1968-02-05 | Rhone Poulenc Sa | Nouvel antibiotique et son procédé de préparation par culture de streptomyces croceus |
US4981979A (en) | 1987-09-10 | 1991-01-01 | Neorx Corporation | Immunoconjugates joined by thioether bonds having reduced toxicity and improved selectivity |
EP0454726A4 (en) | 1988-12-22 | 1991-11-27 | Xoma Corporation | Hindered linking agents and methods |
US5208020A (en) | 1989-10-25 | 1993-05-04 | Immunogen Inc. | Cytotoxic agents comprising maytansinoids and their therapeutic use |
DE69930328T2 (de) | 1998-08-27 | 2006-12-14 | Spirogen Ltd., Ryde | Dimere Pyrrolobenzodiazepine |
GB9818731D0 (en) | 1998-08-27 | 1998-10-21 | Univ Portsmouth | Compounds |
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GB0404577D0 (en) * | 2004-03-01 | 2004-04-07 | Spirogen Ltd | Pyrrolobenzodiazepines |
JP5166861B2 (ja) | 2004-03-09 | 2013-03-21 | スピロゲン リミティッド | ピロロベンゾジアゼピン |
EP1669358A1 (en) | 2004-12-07 | 2006-06-14 | Aventis Pharma S.A. | Cytotoxic agents comprising new taxanes |
MX2007007590A (es) | 2004-12-22 | 2007-12-10 | Ambrx Inc | Composiciones que contienen, metodos que involucran y usos de aminoacidos no naturales y polipeptidos. |
EP1813614B1 (en) * | 2006-01-25 | 2011-10-05 | Sanofi | Cytotoxic agents comprising new tomaymycin derivatives |
WO2007093873A1 (en) * | 2006-02-13 | 2007-08-23 | Council Of Scientific And Industrial Research | Bis-pyrr0l0[2,l-c] [1, 4] benzodiazepine- anthraquinone conjugates as antitumour agents and a process for the preparation thereof |
EP1832577A1 (en) | 2006-03-07 | 2007-09-12 | Sanofi-Aventis | Improved prodrugs of CC-1065 analogs |
EP1864682A1 (en) | 2006-06-09 | 2007-12-12 | Sanofi-Aventis | Leptomycin derivatives |
USRE47123E1 (en) | 2006-07-18 | 2018-11-13 | Sanofi | EPHA2 receptor antagonist antibodies |
EP1914242A1 (en) | 2006-10-19 | 2008-04-23 | Sanofi-Aventis | Novel anti-CD38 antibodies for the treatment of cancer |
PL2019104T3 (pl) * | 2007-07-19 | 2014-03-31 | Sanofi Sa | Środki cytotoksyczne obejmujące nowe pochodne tomaymycyny i ich zastosowanie terapeutyczne |
US8865875B2 (en) | 2007-08-22 | 2014-10-21 | Medarex, L.L.C. | Site-specific attachment of drugs or other agents to engineered antibodies with C-terminal extensions |
KR20210100223A (ko) | 2008-04-30 | 2021-08-13 | 이뮤노젠 아이엔씨 | 가교제 및 그 용도 |
BRPI0911442A2 (pt) | 2008-04-30 | 2019-03-12 | Immunogen, Inc. | conjugados potentes e ligantes hidrofílicos |
FR2939795B1 (fr) | 2008-12-17 | 2010-12-17 | Sanofi Aventis | Procede de preparation d'esters actives |
BRPI1008749B8 (pt) * | 2009-02-05 | 2021-05-25 | Immunogen Inc | compostos derivados de benzodiazepina, seus conjugados, composição farmacêutica, seu uso e seus processos de preparação |
AR078471A1 (es) | 2009-10-02 | 2011-11-09 | Sanofi Aventis | COMPUESTOS MAITANSINOIDES Y EL USO DE ESTOS PARA PREPARAR CONJUGADOS CON UN ANTICUERPO LOS CUALES SE UTILIZAN COMO AGENTES ANTICANCERIGENOS Y EL PROCEDIMIENTO DE PREPARACIoN DE ESTOS CONJUGADOS |
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2010
- 2010-07-26 FR FR1056103A patent/FR2963007B1/fr not_active Expired - Fee Related
-
2011
- 2011-07-25 EP EP11749535.8A patent/EP2598507B1/en active Active
- 2011-07-25 AR ARP110102680A patent/AR082341A1/es unknown
- 2011-07-25 EA EA201390162A patent/EA201390162A1/ru unknown
- 2011-07-25 MY MYPI2013000240A patent/MY159197A/en unknown
- 2011-07-25 CN CN201180046298.4A patent/CN103140491B/zh active Active
- 2011-07-25 MX MX2013001069A patent/MX2013001069A/es not_active Application Discontinuation
- 2011-07-25 NZ NZ60624611A patent/NZ606246A/en not_active IP Right Cessation
- 2011-07-25 BR BR112013001978-6A patent/BR112013001978B1/pt not_active IP Right Cessation
- 2011-07-25 JP JP2013521272A patent/JP5814366B2/ja active Active
- 2011-07-25 SG SG2013005855A patent/SG187191A1/en unknown
- 2011-07-25 UA UAA201302391A patent/UA111164C2/uk unknown
- 2011-07-25 MA MA35664A patent/MA34469B1/fr unknown
- 2011-07-25 AU AU2011284339A patent/AU2011284339B2/en not_active Ceased
- 2011-07-25 CA CA2806665A patent/CA2806665A1/en not_active Abandoned
- 2011-07-25 ES ES11749535.8T patent/ES2638520T3/es active Active
- 2011-07-25 WO PCT/IB2011/053310 patent/WO2012014147A1/en active Application Filing
- 2011-07-25 PE PE2013000135A patent/PE20130489A1/es not_active Application Discontinuation
- 2011-07-25 KR KR1020137004626A patent/KR20130094806A/ko not_active Application Discontinuation
- 2011-07-26 TW TW100126452A patent/TW201208689A/zh unknown
- 2011-07-26 UY UY0001033531A patent/UY33531A/es not_active Application Discontinuation
-
2013
- 2013-01-22 NI NI201300010A patent/NI201300010A/es unknown
- 2013-01-23 GT GT201300025A patent/GT201300025A/es unknown
- 2013-01-24 EC ECSP13012404 patent/ECSP13012404A/es unknown
- 2013-01-24 CO CO13013434A patent/CO6650375A2/es not_active Application Discontinuation
- 2013-01-24 DO DO2013000021A patent/DOP2013000021A/es unknown
- 2013-01-25 CL CL2013000250A patent/CL2013000250A1/es unknown
- 2013-01-25 ZA ZA2013/00685A patent/ZA201300685B/en unknown
- 2013-01-25 US US13/750,691 patent/US9056914B2/en active Active
- 2013-01-29 CR CR20130035A patent/CR20130035A/es unknown
Also Published As
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