MX2020008447A - Uso de 5-fluoro-4-(4-fluoro-2-metoxifenil)-n-{4-[(s-metilsulfonimi doil)metil]piridin-2-il}piridin-2-amina para el tratamiento del linfoma difuso de celulas grandes b. - Google Patents
Uso de 5-fluoro-4-(4-fluoro-2-metoxifenil)-n-{4-[(s-metilsulfonimi doil)metil]piridin-2-il}piridin-2-amina para el tratamiento del linfoma difuso de celulas grandes b.Info
- Publication number
- MX2020008447A MX2020008447A MX2020008447A MX2020008447A MX2020008447A MX 2020008447 A MX2020008447 A MX 2020008447A MX 2020008447 A MX2020008447 A MX 2020008447A MX 2020008447 A MX2020008447 A MX 2020008447A MX 2020008447 A MX2020008447 A MX 2020008447A
- Authority
- MX
- Mexico
- Prior art keywords
- pyridin
- fluoro
- cell lymphoma
- diffuse large
- methoxyphenyl
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic 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
- C07D213/02—Heterocyclic 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
- C07D213/04—Heterocyclic 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
- C07D213/60—Heterocyclic 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
- C07D213/72—Nitrogen atoms
-
- 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
- A61K31/435—Heterocyclic 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/444—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
-
- 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
- A61K31/53—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with three nitrogens as the only ring hetero atoms, e.g. chlorazanil, melamine
-
- 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
- C07D401/00—Heterocyclic 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
- C07D401/02—Heterocyclic 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
- C07D401/12—Heterocyclic 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyridine Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
La presente invención se refiere al uso de 5-Fluoro-4-(4-fluoro-2- metoxifenil)-N-{4-[(Smetilsulfonimidoil) metil]piridin-2-il}piridi n-2-amina (compuesto A), más específicamente (+)5-Fluoro-4-(4- fluoro-2-metoxifenil)-N-{4-[(S-metilsulfonimidoil)metil]piridin-2 -il}piridin-5 2-amina (compuesto A´), para el tratamiento del linfoma difuso de células grandes B (LDCGB), especialmente en el tipo de células B del centro germinal del linfoma difuso de células grandes B y especialmente en el linfoma difuso de células grandes B cuyas células tienen una amplificación o translocación del gen MYC y/o del gen BCL2 y/o una sobreexpresión de MYC y/o BCL2.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP18156576 | 2018-02-13 | ||
PCT/EP2019/053407 WO2019158517A1 (en) | 2018-02-13 | 2019-02-12 | Use of 5-fluoro-4-(4-fluoro-2-methoxyphenyl)-n-{4-[(s-methylsulfonimidoyl)methyl]pyridin-2-yl}pyridin-2-amine for treating diffuse large b-cell lymphoma |
Publications (1)
Publication Number | Publication Date |
---|---|
MX2020008447A true MX2020008447A (es) | 2020-09-28 |
Family
ID=61223765
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MX2020008447A MX2020008447A (es) | 2018-02-13 | 2019-02-12 | Uso de 5-fluoro-4-(4-fluoro-2-metoxifenil)-n-{4-[(s-metilsulfonimi doil)metil]piridin-2-il}piridin-2-amina para el tratamiento del linfoma difuso de celulas grandes b. |
Country Status (16)
Country | Link |
---|---|
US (1) | US11701347B2 (es) |
EP (1) | EP3752487A1 (es) |
JP (1) | JP7280286B2 (es) |
KR (1) | KR20200119800A (es) |
CN (1) | CN111727183B (es) |
AU (1) | AU2019221019B2 (es) |
BR (1) | BR112020016389A2 (es) |
CA (1) | CA3090843A1 (es) |
CL (1) | CL2020002087A1 (es) |
EA (1) | EA202091894A1 (es) |
IL (1) | IL276437B2 (es) |
JO (1) | JOP20200196A1 (es) |
MA (1) | MA51820A (es) |
MX (1) | MX2020008447A (es) |
SG (1) | SG11202006470RA (es) |
WO (1) | WO2019158517A1 (es) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA3047491A1 (en) | 2016-12-21 | 2018-06-28 | Bayer Aktiengesellschaft | Prodrugs of cytotoxic active agents having enzymatically cleavable groups |
MX2020008447A (es) | 2018-02-13 | 2020-09-28 | Bayer Ag | Uso de 5-fluoro-4-(4-fluoro-2-metoxifenil)-n-{4-[(s-metilsulfonimi doil)metil]piridin-2-il}piridin-2-amina para el tratamiento del linfoma difuso de celulas grandes b. |
Family Cites Families (58)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1307271A (en) | 1970-06-25 | 1973-02-14 | Shell Int Research | Sulphoximine derivatives and their use in herbicidal compositions |
DE60039059D1 (de) | 1999-10-07 | 2008-07-10 | Amgen Inc | Triazin-kinase-hemmer |
US7105530B2 (en) | 2000-12-21 | 2006-09-12 | Smithkline Beecham Corporation | Pyrimidineamines as angiogenesis modulators |
GB0103926D0 (en) | 2001-02-17 | 2001-04-04 | Astrazeneca Ab | Chemical compounds |
WO2003037346A1 (en) | 2001-10-31 | 2003-05-08 | Cell Therapeutics, Inc. | 6-phenyl-n-phenyl-(1,3,5) -triazine-2,4-diamine derivatives and related compounds with lysophphosphatidic acid acyltransferase beta (lpaat-beta) inhibitory activity for use in the treatment of cancer |
WO2004009562A1 (en) | 2002-07-18 | 2004-01-29 | Janssen Pharmaceutica, Nv | Substituted triazine kinase inhibitors |
DE10239042A1 (de) | 2002-08-21 | 2004-03-04 | Schering Ag | Makrozyclische Pyrimidine, deren Herstellung und Verwendung als Arzneimittel |
EP1611125A1 (en) | 2003-02-07 | 2006-01-04 | Vertex Pharmaceuticals Incorporated | Heteroaryl substituted pyrolls useful as inhibitors of protein kinases |
EP1678147B1 (en) | 2003-09-15 | 2012-08-08 | Lead Discovery Center GmbH | Pharmaceutically active 4,6-disubstituted aminopyrimidine derivatives as modulators of protein kinases |
DE10349423A1 (de) | 2003-10-16 | 2005-06-16 | Schering Ag | Sulfoximinsubstituierte Parimidine als CDK- und/oder VEGF-Inhibitoren, deren Herstellung und Verwendung als Arzneimittel |
AU2005291117B2 (en) | 2004-10-05 | 2011-06-09 | Syngenta Limited | Isoxazoline derivatives and their use as herbicides |
CA2589793A1 (en) | 2004-12-17 | 2006-06-22 | Astrazeneca Ab | 4-(4-(imidazol-4-yl)pyrimidin-2-ylamino) benzamides as cdk inhibitors |
DE102005062742A1 (de) | 2005-12-22 | 2007-06-28 | Bayer Schering Pharma Ag | Sulfoximin substituierte Pyrimidine, Verfahren zu deren Herstellung und ihre Verwendung als Arzneimittel |
EP1803723A1 (de) | 2006-01-03 | 2007-07-04 | Bayer Schering Pharma Aktiengesellschaft | (2,4,9-triaza-1(2,4)-pyrimidina-3(1,3)-benzenacyclononaphan-3^4-yl)-sulfoximid derivate als selektive inhibitoren der aurora kinase zur behandlung von krebs |
JP4305477B2 (ja) | 2006-07-25 | 2009-07-29 | トヨタ自動車株式会社 | 火花点火式内燃機関 |
DE102006041382A1 (de) | 2006-08-29 | 2008-03-20 | Bayer Schering Pharma Ag | Carbamoyl-Sulfoximide als Proteinkinaseinhibitoren |
DE102006042143A1 (de) | 2006-09-08 | 2008-03-27 | Bayer Healthcare Aktiengesellschaft | Neue substituierte Bipyridin-Derivate und ihre Verwendung |
WO2008060248A1 (en) | 2006-11-15 | 2008-05-22 | S*Bio Pte Ltd. | Indole sustituted pyrimidines and use thereof in the treatment of cancer |
AU2007336933A1 (en) | 2006-12-22 | 2008-07-03 | Novartis Ag | Heteroaryl-heteroaryl compounds as CDK inhibitors for the treatment of cancer, inflammation and viral infections |
JP2010514688A (ja) | 2006-12-22 | 2010-05-06 | ノバルティス アーゲー | インドール−4−イルピリミジニル−2−イル−アミン誘導体およびサイクリン依存性キナーゼ阻害剤としてのその使用 |
EP3023422A1 (en) | 2007-03-12 | 2016-05-25 | YM BioSciences Australia Pty Ltd | Phenyl amino pyrimidine compounds and uses thereof |
WO2008129070A1 (en) | 2007-04-24 | 2008-10-30 | Ingenium Pharmaceuticals Gmbh | Inhibitors of protein kinases |
JP5379787B2 (ja) | 2007-04-24 | 2013-12-25 | インゲニウム ファーマシューティカルズ ジーエムビーエイチ | プロテインキナーゼの阻害剤 |
US8507498B2 (en) | 2007-04-24 | 2013-08-13 | Ingenium Pharmaceuticals Gmbh | 4, 6-disubstituted aminopyrimidine derivatives as inhibitors of protein kinases |
WO2008132138A1 (en) | 2007-04-25 | 2008-11-06 | Ingenium Pharmaceuticals Gmbh | Derivatives of 4,6-disubstituted aminopyrimidines |
PT2200436E (pt) | 2007-09-04 | 2015-04-29 | Scripps Research Inst | Pirimidinilaminas substituídas como inibidoras da proteína quinase |
WO2009029998A1 (en) | 2007-09-06 | 2009-03-12 | Cytopia Research Pty Ltd | Retrometabolic compounds |
GB0805477D0 (en) | 2008-03-26 | 2008-04-30 | Univ Nottingham | Pyrimidines triazines and their use as pharmaceutical agents |
CA2729965A1 (en) | 2008-07-14 | 2010-01-21 | Gilead Sciences, Inc. | Fused heterocyclyc inhibitor compounds |
US8415381B2 (en) | 2009-07-30 | 2013-04-09 | Novartis Ag | Heteroaryl compounds and their uses |
AU2010291212A1 (en) | 2009-09-04 | 2012-02-23 | Novartis Ag | Heteroaryl compounds as kinase inhibitors |
TW201111378A (en) | 2009-09-11 | 2011-04-01 | Bayer Schering Pharma Ag | Substituted (heteroarylmethyl) thiohydantoins |
CN102791697A (zh) | 2009-10-12 | 2012-11-21 | 瑞科西有限公司 | 作为TBKL和/或IKKε抑制剂的氨基-嘧啶化合物 |
JP5921525B2 (ja) | 2010-03-22 | 2016-05-24 | リード ディスカバリー センター ゲゼルシャフト ミット ベシュレンクテル ハフツング | 医薬的に活性のある二置換のトリアジン誘導体 |
DE102010046720A1 (de) | 2010-09-23 | 2012-03-29 | Bayer Schering Pharma Aktiengesellschaft | Verfahren zur Herstellung von pan-CDK-Inhibitoren der Formel (l), sowie Intermediate der Herstellung |
KR20130116287A (ko) | 2010-11-17 | 2013-10-23 | 노파르티스 아게 | 3-(아미노아릴)-피리딘 화합물 |
WO2012066065A1 (en) | 2010-11-17 | 2012-05-24 | Novartis Ag | Phenyl-heteroaryl amine compounds and their uses |
WO2012101065A2 (en) | 2011-01-28 | 2012-08-02 | Novartis Ag | Pyrimidine biaryl amine compounds and their uses |
WO2012101063A1 (en) | 2011-01-28 | 2012-08-02 | Novartis Ag | N-acyl pyridine biaryl compounds and their uses |
WO2012101066A1 (en) | 2011-01-28 | 2012-08-02 | Novartis Ag | Pyridine biaryl amine compounds and their uses |
WO2012101064A1 (en) | 2011-01-28 | 2012-08-02 | Novartis Ag | N-acyl pyrimidine biaryl compounds as protein kinase inhibitors |
WO2012101062A1 (en) | 2011-01-28 | 2012-08-02 | Novartis Ag | Substituted bi-heteroaryl compounds as cdk9 inhibitors and their uses |
CN103562184B (zh) | 2011-03-02 | 2016-04-27 | 利德探索中心有限公司 | 药学活性的二取代的吡啶衍生物 |
EP2680852A1 (en) | 2011-03-02 | 2014-01-08 | Lead Discovery Center GmbH | Pharmaceutically active disubstituted triazine derivatives |
JP2014510794A (ja) | 2011-04-12 | 2014-05-01 | アルツハイマーズ・インスティテュート・オブ・アメリカ・インコーポレイテッド | IKK関連キナーゼεおよびTANK結合キナーゼ1の阻害剤の組成物および治療的使用 |
CN102731413A (zh) | 2011-04-15 | 2012-10-17 | 上海医药工业研究院 | 一种脲类化合物、其制备方法、其中间体及其应用 |
US8916557B2 (en) | 2011-04-19 | 2014-12-23 | Bayer Intellectual Property Gmbh | Substituted 4-Aryl-N-phenyl-1,3,5-triazin-2-amines |
TWI555737B (zh) | 2011-05-24 | 2016-11-01 | 拜耳知識產權公司 | 含有硫醯亞胺基團之4-芳基-n-苯基-1,3,5-三氮雜苯-2-胺 |
EP2527332A1 (en) | 2011-05-24 | 2012-11-28 | Bayer Intellectual Property GmbH | 4-Aryl-N-phenyl-1,3,5-triazin-2-amines containing a sulfoximine group as CDK9 inhibitors |
US9133171B2 (en) | 2011-09-16 | 2015-09-15 | Bayer Intellectual Property Gmbh | Disubstituted 5-fluoro pyrimidine derivatives containing a sulfoximine group |
WO2013037896A1 (en) | 2011-09-16 | 2013-03-21 | Bayer Intellectual Property Gmbh | Disubstituted 5-fluoro-pyrimidines |
US20150259300A1 (en) | 2012-10-18 | 2015-09-17 | Bayer Pharma Aktiengesellschaft | 4-(ortho)-fluorophenyl-5-fluoropyrimidin-2-yl amines containing a sulfone group |
EP2920153B1 (en) | 2012-11-15 | 2017-02-01 | Bayer Pharma Aktiengesellschaft | 4-(ortho)-fluorophenyl-5-fluoropyrimidin-2-yl amines containing a sulfoximine group |
JP6263193B2 (ja) * | 2012-11-15 | 2018-01-17 | バイエル ファーマ アクチエンゲゼルシャフト | スルホキシイミン基を含んでいる5−フルオロ−n−(ピリジン−2−イル)ピリジン−2−アミン誘導体 |
ES2630115T3 (es) | 2013-07-04 | 2017-08-18 | Bayer Pharma Aktiengesellschaft | Derivados de 5-fluoro-n-(piridin-2-il)piridin-2-amina con sulfoximina sustituida y su uso como inhibidores de quinasa cdk9 |
WO2015136028A1 (en) | 2014-03-13 | 2015-09-17 | Bayer Pharma Aktiengesellschaft | 5-fluoro-n-(pyridin-2-yl)pyridin-2-amine derivatives containing a sulfone group |
US20180050040A1 (en) * | 2015-03-24 | 2018-02-22 | Bayer Pharma Aktiengesellschaft | Use of 4-(4-fluoro-2-methoxyphenyl)-n--1,3,5-triazin-2-amine for treating lymphomas |
MX2020008447A (es) | 2018-02-13 | 2020-09-28 | Bayer Ag | Uso de 5-fluoro-4-(4-fluoro-2-metoxifenil)-n-{4-[(s-metilsulfonimi doil)metil]piridin-2-il}piridin-2-amina para el tratamiento del linfoma difuso de celulas grandes b. |
-
2019
- 2019-02-12 MX MX2020008447A patent/MX2020008447A/es unknown
- 2019-02-12 BR BR112020016389-9A patent/BR112020016389A2/pt unknown
- 2019-02-12 EA EA202091894A patent/EA202091894A1/ru unknown
- 2019-02-12 MA MA051820A patent/MA51820A/fr unknown
- 2019-02-12 US US16/969,460 patent/US11701347B2/en active Active
- 2019-02-12 SG SG11202006470RA patent/SG11202006470RA/en unknown
- 2019-02-12 KR KR1020207022928A patent/KR20200119800A/ko not_active Application Discontinuation
- 2019-02-12 JP JP2020565543A patent/JP7280286B2/ja active Active
- 2019-02-12 IL IL276437A patent/IL276437B2/en unknown
- 2019-02-12 CA CA3090843A patent/CA3090843A1/en active Pending
- 2019-02-12 EP EP19704618.8A patent/EP3752487A1/en active Pending
- 2019-02-12 JO JOP/2020/0196A patent/JOP20200196A1/ar unknown
- 2019-02-12 WO PCT/EP2019/053407 patent/WO2019158517A1/en unknown
- 2019-02-12 AU AU2019221019A patent/AU2019221019B2/en active Active
- 2019-02-12 CN CN201980013294.2A patent/CN111727183B/zh active Active
-
2020
- 2020-08-12 CL CL2020002087A patent/CL2020002087A1/es unknown
Also Published As
Publication number | Publication date |
---|---|
AU2019221019B2 (en) | 2024-05-02 |
JP2021514386A (ja) | 2021-06-10 |
EP3752487A1 (en) | 2020-12-23 |
MA51820A (fr) | 2021-05-19 |
KR20200119800A (ko) | 2020-10-20 |
CN111727183A (zh) | 2020-09-29 |
US20210015806A1 (en) | 2021-01-21 |
BR112020016389A2 (pt) | 2020-12-15 |
JP7280286B2 (ja) | 2023-05-23 |
CN111727183B (zh) | 2023-12-29 |
IL276437B2 (en) | 2024-03-01 |
IL276437B1 (en) | 2023-11-01 |
CA3090843A1 (en) | 2019-08-22 |
EA202091894A1 (ru) | 2020-12-28 |
SG11202006470RA (en) | 2020-08-28 |
AU2019221019A1 (en) | 2020-07-23 |
CL2020002087A1 (es) | 2020-12-11 |
US11701347B2 (en) | 2023-07-18 |
JOP20200196A1 (ar) | 2020-08-13 |
WO2019158517A1 (en) | 2019-08-22 |
IL276437A (en) | 2020-09-30 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
MX2022014548A (es) | Inhibidores de molecula de muerte programada 1 (pd-1)/ligando de molecula de muerte programada 1 (pd-l1). | |
CR20220351A (es) | Inhibidores de proteínas kras mutantes | |
WO2020102503A8 (en) | Fusosome compositions for t cell delivery | |
MX2021000308A (es) | Composiciones de fusosoma y usos de estas. | |
PH12021500004A1 (en) | Pd-1/pd-l1 inhibitors | |
MX2022002465A (es) | Inhibidores de kras g12d. | |
MX2020005701A (es) | Células efectoras inmunitarias potenciadas y usos de las mismas. | |
MX2021007790A (es) | Inhibidores de idh2 para el tratamiento de neoplasias malignas hematologicas y tumores solidos. | |
EP3852769A4 (en) | ARNI AGENTS FOR INHIBITING EXPRESSION OF 17BETA-HSD TYPE 13- (HSD17B13), THEIR COMPOSITIONS AND METHODS OF USE | |
EA200801301A1 (ru) | ИНГИБИТОРЫ АКТИВНОСТИ Akt | |
MX2020008447A (es) | Uso de 5-fluoro-4-(4-fluoro-2-metoxifenil)-n-{4-[(s-metilsulfonimi doil)metil]piridin-2-il}piridin-2-amina para el tratamiento del linfoma difuso de celulas grandes b. | |
TW200801008A (en) | Protein kinase inhibitors | |
MX361278B (es) | Inhibición o reducción del crecimiento de hongos. | |
AU2016304856A8 (en) | Mechanism of resistance to BET bromodomain inhibitors | |
MX2022001004A (es) | Inhibidores de enzimas. | |
MX2022002461A (es) | Composiciones y métodos para la modificación de cd123. | |
MX2020009922A (es) | Metodos de tratamiento del cancer residual minimo. | |
CO2021018034A2 (es) | Oligonucleótidos gapmer modificados y métodos de uso | |
CR20210311A (es) | Moduladores de la expresión de irf5 | |
MX2022004443A (es) | Metodos para usar inmunoconjugados anti-cd79b para tratar linfoma difuso de linfocitos b grandes. | |
GEP20227437B (en) | 1h-indazole-3-carboxamide compounds as glycogen synthase kinase 3 beta inhibitors | |
MX2021014615A (es) | Control probiotico y quimico de las biopeliculas. | |
MX2022003077A (es) | Terapias de combinacion de antibioticos. | |
MX2021013101A (es) | Terapia anti-cd19 en pacientes que tienen una cantidad limitada de células nk. | |
WO2018183219A3 (en) | Nucleic acid-based compositions and methods for treating small vessel diseases |