PE20180530A1 - Derivados de amidas policiclicas como inhibidores de cdk9 - Google Patents

Derivados de amidas policiclicas como inhibidores de cdk9

Info

Publication number
PE20180530A1
PE20180530A1 PE2017002874A PE2017002874A PE20180530A1 PE 20180530 A1 PE20180530 A1 PE 20180530A1 PE 2017002874 A PE2017002874 A PE 2017002874A PE 2017002874 A PE2017002874 A PE 2017002874A PE 20180530 A1 PE20180530 A1 PE 20180530A1
Authority
PE
Peru
Prior art keywords
pyridin
lymphoma
tetrahydroimidazo
carboxamide
chloro
Prior art date
Application number
PE2017002874A
Other languages
English (en)
Spanish (es)
Inventor
Kurt Gordon Pike
Bernard Christophe Barlaam
Janet Hawkins
Savi Christopher De
Melissa Marie Vasbinder
Alexander Hird
Michelle Lamb
Original Assignee
Astrazeneca Ab
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
Application filed by Astrazeneca Ab filed Critical Astrazeneca Ab
Publication of PE20180530A1 publication Critical patent/PE20180530A1/es

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D498/04—Ortho-condensed systems
    • 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
    • A61K31/4353—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 ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437—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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
    • 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
    • A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
    • 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
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04—Ortho-condensed systems
    • 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
    • C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00—Indexing scheme relating to specific properties of organic compounds
    • C07B2200/13—Crystalline forms, e.g. polymorphs

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Detergent Compositions (AREA)
  • Polyesters Or Polycarbonates (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
PE2017002874A 2015-06-29 2016-06-27 Derivados de amidas policiclicas como inhibidores de cdk9 PE20180530A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US201562185852P 2015-06-29 2015-06-29

Publications (1)

Publication Number Publication Date
PE20180530A1 true PE20180530A1 (es) 2018-03-19

Family

ID=56292699

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2017002874A PE20180530A1 (es) 2015-06-29 2016-06-27 Derivados de amidas policiclicas como inhibidores de cdk9

Country Status (38)

Country Link
US (4) US9845331B2 (cg-RX-API-DMAC10.html)
EP (2) EP3539961B1 (cg-RX-API-DMAC10.html)
JP (1) JP6997627B2 (cg-RX-API-DMAC10.html)
KR (1) KR102663113B1 (cg-RX-API-DMAC10.html)
CN (1) CN107873028B (cg-RX-API-DMAC10.html)
AR (1) AR105179A1 (cg-RX-API-DMAC10.html)
AU (1) AU2016286200B2 (cg-RX-API-DMAC10.html)
BR (1) BR122019013677B1 (cg-RX-API-DMAC10.html)
CA (1) CA2989499C (cg-RX-API-DMAC10.html)
CL (1) CL2017003306A1 (cg-RX-API-DMAC10.html)
CO (1) CO2017013713A2 (cg-RX-API-DMAC10.html)
CR (2) CR20170596A (cg-RX-API-DMAC10.html)
CY (2) CY1122111T1 (cg-RX-API-DMAC10.html)
DK (2) DK3313838T3 (cg-RX-API-DMAC10.html)
DO (2) DOP2017000295A (cg-RX-API-DMAC10.html)
EA (1) EA035383B1 (cg-RX-API-DMAC10.html)
ES (2) ES2902148T3 (cg-RX-API-DMAC10.html)
HR (2) HRP20211970T1 (cg-RX-API-DMAC10.html)
HU (2) HUE057343T2 (cg-RX-API-DMAC10.html)
IL (1) IL256393B (cg-RX-API-DMAC10.html)
LT (2) LT3313838T (cg-RX-API-DMAC10.html)
ME (1) ME03404B (cg-RX-API-DMAC10.html)
MX (1) MX371034B (cg-RX-API-DMAC10.html)
MY (1) MY201673A (cg-RX-API-DMAC10.html)
NI (1) NI201700174A (cg-RX-API-DMAC10.html)
PE (1) PE20180530A1 (cg-RX-API-DMAC10.html)
PH (1) PH12017502334B1 (cg-RX-API-DMAC10.html)
PL (2) PL3313838T3 (cg-RX-API-DMAC10.html)
PT (2) PT3313838T (cg-RX-API-DMAC10.html)
RS (2) RS58712B1 (cg-RX-API-DMAC10.html)
SI (2) SI3313838T1 (cg-RX-API-DMAC10.html)
SM (2) SMT202200005T1 (cg-RX-API-DMAC10.html)
SV (1) SV2017005598A (cg-RX-API-DMAC10.html)
TN (1) TN2017000486A1 (cg-RX-API-DMAC10.html)
TR (1) TR201909286T4 (cg-RX-API-DMAC10.html)
TW (1) TWI723028B (cg-RX-API-DMAC10.html)
WO (1) WO2017001354A1 (cg-RX-API-DMAC10.html)
ZA (1) ZA201800563B (cg-RX-API-DMAC10.html)

Families Citing this family (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2018335617B2 (en) 2017-09-25 2021-12-09 Astrazeneca Ab Combination of a BTK inhibitor and an inhibitor of CDK9 to treat cancer
US11319295B2 (en) 2017-10-09 2022-05-03 Merck Sharp & Dohme Corp. Substituted phenyloxetane and phenyltetrahydrofuran compounds as indoleamine 2,3-dioxygenase (IDO) inhibitors
CN108129288B (zh) * 2017-12-27 2021-01-22 上海毕得医药科技股份有限公司 一种反式-3-羟基环丁基甲酸的合成方法
TWI810397B (zh) 2018-11-14 2023-08-01 瑞典商阿斯特捷利康公司 治療癌症之方法
CN114008046B (zh) * 2019-06-27 2023-08-18 南京明德新药研发有限公司 作为cdk9抑制剂的氮杂吲哚连吡唑类化合物
AU2020345950A1 (en) 2019-09-11 2022-03-31 Prelude Therapeutics Incorporated CDK inhibitors and their use as pharmaceuticals
AU2020401999B2 (en) * 2019-12-09 2024-01-18 Cspc Zhongqi Pharmaceutical Technology (Shijiazhuang) Co., Ltd. Compound as cyclin-dependent kinase 9 inhibitor and use thereof
JP7451765B2 (ja) * 2020-05-12 2024-03-18 蘇州阿尓脈生物科技有限公司 Cdk阻害剤としてのピリジンアセトアミド系誘導体、その調製方法及び用途
EP4141004A4 (en) * 2020-05-12 2023-08-23 Suzhou Alphama Biotechnology Co., Ltd. POLYCYCLIC AMIDE DERIVATIVE SERVING AS A CDK9 INHIBITOR, METHOD FOR PREPARING IT AND ITS USE
CN116615248A (zh) 2020-06-24 2023-08-18 阿斯利康(英国)有限公司 抗体-药物缀合物和cdk9抑制剂的组合
EP4194450A4 (en) 2020-08-07 2024-10-30 Pharmablock Sciences (Nanjing), Inc. CDK9 INHIBITOR AND USE THEREOF
TWI809330B (zh) * 2020-11-20 2023-07-21 大陸商勁方醫藥科技(上海)有限公司 Cdk9抑制劑的多晶型物及其製法和用途
CN115381824B (zh) * 2021-05-24 2024-11-05 石药集团中奇制药技术(石家庄)有限公司 周期蛋白依赖性激酶9抑制剂的用途
WO2022247785A1 (zh) * 2021-05-24 2022-12-01 石药集团中奇制药技术(石家庄)有限公司 一种周期蛋白依赖性激酶9抑制剂的用途
CN117813289A (zh) * 2021-07-14 2024-04-02 上海海雁医药科技有限公司 吡唑衍生物及其中间体和制备方法
CN115703738B (zh) * 2021-08-16 2024-06-21 中国科学院上海药物研究所 含2-芳杂环取代的脲类化合物、其制备方法和用途
CN118613257A (zh) * 2021-12-23 2024-09-06 鲁汶大学 用于抑制yap/taz-tead的四氢吡唑并嘧啶及相关类似物
CA3251059A1 (en) 2022-05-02 2023-11-09 The Board Of Trustees Of The Leland Stanford Junior University Compositions, systems and methods for modulating a target gene
WO2024039210A1 (ko) 2022-08-17 2024-02-22 한국화학연구원 Cdk2 및/또는 cdk9의 억제 또는 분해용 화합물 및 이들의 의약 용도
CN117659022A (zh) * 2022-09-06 2024-03-08 苏州阿尔脉生物科技有限公司 脲基取代吡啶类化合物、包含其的药物组合物及其医药用途
WO2024220876A1 (en) * 2023-04-19 2024-10-24 Alcon Inc. N-substituted c6 cyclyl carboxamide compounds and uses thereof
WO2025076115A1 (en) * 2023-10-02 2025-04-10 Prelude Therapeutics Incorporated Cdk inhibitors and their use as pharmaceuticals
WO2026024933A1 (en) * 2024-07-24 2026-01-29 Prelude Therapeutics Incorporated Cdk inhibitors and their use as pharmaceuticals

Family Cites Families (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008133192A1 (ja) * 2007-04-19 2008-11-06 Takeda Pharmaceutical Company Limited 縮合イミダゾール化合物およびその用途
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
EP2137166B1 (en) 2007-04-24 2012-05-30 Ingenium Pharmaceuticals GmbH 4, 6-disubstituted aminopyrimidine derivatives as inhibitors of protein kinases
ES2539518T3 (es) 2007-04-24 2015-07-01 Astrazeneca Ab Inhibidores de proteínas quinasas
US8389521B2 (en) 2007-04-24 2013-03-05 Ingenium Pharmaceuticals Gmbh Inhibitors of protein kinases
WO2008132138A1 (en) 2007-04-25 2008-11-06 Ingenium Pharmaceuticals Gmbh Derivatives of 4,6-disubstituted aminopyrimidines
AU2008309517B2 (en) 2007-10-12 2013-03-14 Astrazeneca Ab Inhibitors of protein kinases
KR20120049940A (ko) * 2009-09-04 2012-05-17 노파르티스 아게 키나제 억제제로서의 헤테로아릴 화합물
US20110113038A1 (en) 2009-11-12 2011-05-12 International Business Machines Corporation Search term security
GB201002911D0 (en) * 2010-02-19 2010-04-07 Medical Res Council Compound
EA201201274A1 (ru) 2010-03-10 2013-04-30 Инджениум Фармасьютиклз Гмбх Ингибиторы протеинкиназ
AR081810A1 (es) * 2010-04-07 2012-10-24 Bayer Cropscience Ag Piridinilpirazoles biciclicos
WO2012066065A1 (en) 2010-11-17 2012-05-24 Novartis Ag Phenyl-heteroaryl amine compounds and their uses
WO2012101062A1 (en) * 2011-01-28 2012-08-02 Novartis Ag Substituted bi-heteroaryl compounds as cdk9 inhibitors and their uses
WO2012101063A1 (en) * 2011-01-28 2012-08-02 Novartis Ag N-acyl pyridine biaryl compounds and their uses
WO2012101064A1 (en) * 2011-01-28 2012-08-02 Novartis Ag N-acyl pyrimidine biaryl compounds as protein kinase inhibitors
IN2014CN02475A (cg-RX-API-DMAC10.html) * 2011-10-06 2015-06-19 Bayer Ip Gmbh
TW201444820A (zh) * 2013-03-13 2014-12-01 Abbvie Inc 吡啶cdk9激酶抑制劑
JP2016512559A (ja) 2013-03-13 2016-04-28 アッヴィ・インコーポレイテッド Cdk9キナーゼ阻害薬
TW201446763A (zh) 2013-03-14 2014-12-16 Abbvie Inc 吡咯并[2,3-b]吡啶cdk9激酶抑制劑
CN105189512A (zh) 2013-03-14 2015-12-23 艾伯维公司 吡咯并嘧啶cdk9激酶抑制剂

Also Published As

Publication number Publication date
RS62781B1 (sr) 2022-01-31
LT3539961T (lt) 2021-12-27
CL2017003306A1 (es) 2018-06-29
ES2728356T3 (es) 2019-10-23
TW201718573A (zh) 2017-06-01
HUE057343T2 (hu) 2022-05-28
EA035383B1 (ru) 2020-06-04
EP3313838A1 (en) 2018-05-02
IL256393B (en) 2021-12-01
LT3313838T (lt) 2019-06-10
JP2018522869A (ja) 2018-08-16
AU2016286200B2 (en) 2018-10-04
KR20180021830A (ko) 2018-03-05
HRP20211970T1 (hr) 2022-03-18
SI3539961T1 (sl) 2022-02-28
HRP20190748T1 (hr) 2019-06-14
MY201673A (en) 2024-03-12
DK3313838T3 (da) 2019-06-11
DOP2017000295A (es) 2017-12-31
US20210171541A1 (en) 2021-06-10
US10717746B2 (en) 2020-07-21
DOP2018000207A (es) 2018-10-15
EP3539961B1 (en) 2021-10-06
ES2902148T3 (es) 2022-03-25
PH12017502334B1 (en) 2023-05-26
ME03404B (me) 2020-01-20
CR20210297A (es) 2021-09-29
EA201890094A1 (ru) 2018-07-31
EP3313838B1 (en) 2019-04-03
BR112017027394A2 (pt) 2018-11-06
PL3313838T3 (pl) 2019-08-30
WO2017001354A1 (en) 2017-01-05
TWI723028B (zh) 2021-04-01
EP3539961A1 (en) 2019-09-18
CN107873028A (zh) 2018-04-03
HUE043440T2 (hu) 2019-08-28
CY1125066T1 (el) 2023-03-24
US20220340592A1 (en) 2022-10-27
CR20170596A (es) 2018-07-04
CN107873028B (zh) 2021-02-02
MX2017016244A (es) 2018-04-20
SV2017005598A (es) 2018-02-23
US9845331B2 (en) 2017-12-19
SMT202200005T1 (it) 2022-03-21
BR122019013677B1 (pt) 2024-01-02
PT3313838T (pt) 2019-06-24
US20180093998A1 (en) 2018-04-05
AR105179A1 (es) 2017-09-13
SMT201900298T1 (it) 2019-07-11
TR201909286T4 (tr) 2019-07-22
CO2017013713A2 (es) 2018-03-28
ZA201800563B (en) 2022-08-31
IL256393A (en) 2018-02-28
MX371034B (es) 2020-01-13
DK3539961T3 (da) 2022-01-03
US11352369B2 (en) 2022-06-07
CY1122111T1 (el) 2020-11-25
US20160376287A1 (en) 2016-12-29
CA2989499A1 (en) 2017-01-05
AU2016286200A1 (en) 2018-02-08
RS58712B1 (sr) 2019-06-28
CA2989499C (en) 2023-10-31
JP6997627B2 (ja) 2022-01-17
KR102663113B1 (ko) 2024-05-02
SI3313838T1 (sl) 2019-06-28
PH12017502334A1 (en) 2018-06-25
PT3539961T (pt) 2021-12-20
NI201700174A (es) 2018-10-19
TN2017000486A1 (en) 2019-04-12
PL3539961T3 (pl) 2022-02-14

Similar Documents

Publication Publication Date Title
PH12017502334A1 (en) Polycyclic amide derivative as cdk9 inhibitors
PE20161066A1 (es) Derivados de piperidinil-indol como inhibidores del factor de complemento b y usos de los mismos
EA201692095A1 (ru) Имидазо[4,5-c]хинолин-2-оновые соединения и их применение в лечении рака
MD20170016A2 (ro) Compuşi aminopirimidinici ca inhibitori JAK
CU24265B1 (es) Compuestos derivados de benzamida para inhibir la actividad de abl1, abl2 y bcr-abl1, útiles en el tratamiento del cáncer
EA201790595A1 (ru) Пиримидиноны в качестве ингибиторов фактора xia
NZ749437A (en) Processes and intermediates for making a jak inhibitor
CL2017001422A1 (es) Pirazolo [1,5-a] pirazinas 4,6-sustituidas como inhibidores de janus cinasas
PE20160875A1 (es) Compuestos de biaril-amida como inhibidores de cinasa
MX2015012432A (es) Inhibidores piridinicos de la cinasa cdk9.
HK1254469A1 (zh) 稠合双环嘧啶衍生物及其用途
NZ624068A (en) Fused tricyclic compounds as raf kinase inhibitors
PH12015502047A1 (en) Novel pyrimidine and pyridine compounds and their usage
EA201400182A1 (ru) Производные пиридин-2(1н)-она в качестве ингибиторов jak
UA112795C2 (uk) Біциклічні піразинонові похідні
PE20110549A1 (es) EL COMPUESTO 3-(4-CLORO-2-FLUOROBENCIL)-2-METIL-N-(5-METIL-1H-PIRAZOL-3-IL)-8-(MORFOLINOMETIL)IMIDAZO[1,2-b]PIRIDAZIN-6-AMINA, SUS SALES Y LA COMPOSICION QUE LO COMPRENDE
CY1122514T1 (el) Σουλφονικος υδροξυαιθυλεστερας του αναστολεα της εξαρτωμενης απο κυκλινη πρωτεϊνικης κινασης, κρυσταλλικη μορφη αυτου και μεθοδος παρασκευης αυτου
MX2015012386A (es) Inhibidores de la cinasa cdk9.
MX378932B (es) Triazoles sustituidos y métodos relacionados a estos.
AR106830A1 (es) Usos de piridazinonas para tratar el cáncer
EA201791881A1 (ru) Производные 2-аминопиридина в качестве антагонистов рецептора аденозина aи лигандов рецепторов мелатонина mt
MX2019002627A (es) Compuestos de 8-(azetidin-1-il)-[1,2,4]triazolo[1,5-a]piridinilo, composiciones y métodos de uso del mismo.
HK1227872A1 (en) Polycyclic inhibitors of cyclin-dependent kinase 7 (cdk7)
AR103065A1 (es) Compuestos moduladores de fxr (nr1h4) que contiene grupos hidroxi