MA52492B1 - Composés inhibiteurs de rip1, procédés de préparation et d'utilisation associés - Google Patents

Composés inhibiteurs de rip1, procédés de préparation et d'utilisation associés

Info

Publication number
MA52492B1
MA52492B1 MA52492A MA52492A MA52492B1 MA 52492 B1 MA52492 B1 MA 52492B1 MA 52492 A MA52492 A MA 52492A MA 52492 A MA52492 A MA 52492A MA 52492 B1 MA52492 B1 MA 52492B1
Authority
MA
Morocco
Prior art keywords
rip1
preparation
methods
kinase
inhibitory compounds
Prior art date
Application number
MA52492A
Other languages
English (en)
Other versions
MA52492A (fr
Inventor
Yan Chen
Jiaxin Yu
Esteban Masuda
Vanessa Taylor
Ihab Darwish
Original Assignee
Rigel Pharmaceuticals Inc
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 Rigel Pharmaceuticals Inc filed Critical Rigel Pharmaceuticals Inc
Publication of MA52492A publication Critical patent/MA52492A/fr
Publication of MA52492B1 publication Critical patent/MA52492B1/fr

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero 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
    • A61K31/55Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • A61K31/553Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having at least one nitrogen and one oxygen as ring hetero atoms, e.g. loxapine, staurosporine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic 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
    • C07D471/02Heterocyclic 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
    • C07D471/08Bridged systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic 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
    • C07D471/02Heterocyclic 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
    • C07D471/10Spiro-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic 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
    • C07D487/08Bridged systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D491/00Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/10Spiro-condensed systems
    • C07D491/107Spiro-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D498/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/02Heterocyclic 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
    • C07D498/08Bridged systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Immunology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Rheumatology (AREA)
  • Engineering & Computer Science (AREA)
  • Pain & Pain Management (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)

Abstract

L'invention concerne des composés inhibiteurs de kinase, tels que des composés inhibiteurs de protéine kinase 1 interagissant avec le récepteur (rip1), ainsi que des compositions pharmaceutiques et des combinaisons comprenant de tels composés inhibiteurs. Les composés selon l'invention, les compositions pharmaceutiques et/ou les combinaisons peuvent être utilisés pour inhiber une kinase rip1 in vivo ou ex vivo, et peuvent également traiter ou prévenir une maladie ou un état pathologique associé à une kinase, en particulier une maladie ou un état pathologique associé à rip1.
MA52492A 2018-05-03 2019-05-02 Composés inhibiteurs de rip1, procédés de préparation et d'utilisation associés MA52492B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201862666452P 2018-05-03 2018-05-03
PCT/US2019/030473 WO2019213445A1 (fr) 2018-05-03 2019-05-02 Composés inhibiteurs de rip1, procédés de préparation et d'utilisation associés

Publications (2)

Publication Number Publication Date
MA52492A MA52492A (fr) 2021-03-10
MA52492B1 true MA52492B1 (fr) 2023-09-27

Family

ID=66554488

Family Applications (1)

Application Number Title Priority Date Filing Date
MA52492A MA52492B1 (fr) 2018-05-03 2019-05-02 Composés inhibiteurs de rip1, procédés de préparation et d'utilisation associés

Country Status (38)

Country Link
US (3) US10975064B2 (fr)
EP (1) EP3788045B1 (fr)
JP (1) JP7379467B2 (fr)
KR (1) KR102823195B1 (fr)
CN (1) CN112384510B (fr)
AU (1) AU2019262142B2 (fr)
BR (1) BR112020022423A2 (fr)
CA (1) CA3099018A1 (fr)
CL (1) CL2020002840A1 (fr)
CO (1) CO2020015153A2 (fr)
CR (1) CR20200582A (fr)
CY (1) CY1126152T1 (fr)
DK (1) DK3788045T3 (fr)
DO (1) DOP2020000197A (fr)
EA (1) EA202092581A1 (fr)
EC (1) ECSP20077518A (fr)
ES (1) ES2947446T3 (fr)
FI (1) FI3788045T3 (fr)
HR (1) HRP20230909T1 (fr)
HU (1) HUE062277T2 (fr)
IL (1) IL278416B2 (fr)
JO (1) JOP20200277B1 (fr)
LT (1) LT3788045T (fr)
MA (1) MA52492B1 (fr)
MD (1) MD3788045T2 (fr)
MX (1) MX2020011622A (fr)
MY (1) MY205388A (fr)
PE (1) PE20210414A1 (fr)
PH (1) PH12020551848A1 (fr)
PL (1) PL3788045T3 (fr)
PT (1) PT3788045T (fr)
RS (1) RS64418B1 (fr)
SG (1) SG11202010913PA (fr)
SI (1) SI3788045T1 (fr)
SM (1) SMT202300203T1 (fr)
UA (1) UA128160C2 (fr)
WO (1) WO2019213445A1 (fr)
ZA (1) ZA202007487B (fr)

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MD3788045T2 (ro) * 2018-05-03 2023-09-30 Rigel Pharmaceuticals Inc Compuși inhibitori ai RIP1 și procedee de obţinere și utilizare a acestora
HRP20231381T1 (hr) * 2018-05-03 2024-03-01 Rigel Pharmaceuticals, Inc. Spojevi inhibitori rip1 i postupci za njihovo dobivanje i upotrebu
CA3149926A1 (fr) 2019-09-06 2021-03-11 Yan Chen Composes inhibiteurs de rip1 et leurs procedes de fabrication et d'utilisation
WO2021046515A1 (fr) 2019-09-06 2021-03-11 Board Of Regents, The University Of Texas System Inhibiteurs de la protéine kinase i interagissant avec le récepteur pour le traitement d'une maladie
JP7493586B2 (ja) 2019-09-06 2024-05-31 ライジェル ファーマシューティカルズ, インコーポレイテッド Rip1阻害化合物ならびにそれを作製および使用するための方法
IL291665B2 (en) 2019-09-27 2025-07-01 Univ Texas Inhibitors of receptor interacting protein kinase i for the treatment of disease
SI4055021T1 (sl) * 2019-11-07 2026-02-27 Rigel Pharmaceuticals, Inc. Heterociklične spojine, ki inhibirajo rip1
BR112022010082A2 (pt) * 2019-11-26 2022-08-30 Univ Texas Composto de fórmula estrutural i ou sal do mesmo, composição farmacêutica, uso do composto e uso da composição farmacêutica
AR121717A1 (es) 2020-04-02 2022-06-29 Rigel Pharmaceuticals Inc Inhibidores de rip1k
TWI840311B (zh) 2020-07-01 2024-04-21 美商雷傑製藥公司 Rip1k抑制劑
JP7775288B2 (ja) * 2020-08-18 2025-11-25 ハチメド リミテッド ピリミジノン化合物およびその使用
AR125587A1 (es) 2021-03-11 2023-08-02 Rigel Pharmaceuticals Inc Inhibidores heterocíclicos de la quinasa de rip1
WO2022237890A1 (fr) * 2021-05-14 2022-11-17 中国医药研究开发中心有限公司 Composé à cycle fusionné du type azépine et son utilisation pharmaceutique
CN115894489A (zh) * 2021-09-22 2023-04-04 中国药科大学 一种受体相互作用蛋白激酶1的抑制剂及其制备方法、应用
EP4422621A4 (fr) * 2021-10-27 2025-08-27 Merck Sharp & Dohme Llc Inhibiteurs de ripk1 spirotricycliques et leurs procédés d'utilisation
KR20230100646A (ko) * 2021-12-24 2023-07-05 제일약품주식회사 Ripk1 저해제로서의 신규한 화합물 및 이를 포함하는 약학적 조성물
TW202400588A (zh) * 2022-02-28 2024-01-01 香港商維泰瑞隆(香港)生物科技有限公司 Rip1調製劑、其製備及用途

Family Cites Families (43)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4921475A (en) 1983-08-18 1990-05-01 Drug Delivery Systems Inc. Transdermal drug patch with microtubes
US5087240A (en) 1983-08-18 1992-02-11 Drug Delivery Systems Inc. Transdermal drug patch with conductive fibers
US4738851A (en) 1985-09-27 1988-04-19 University Of Iowa Research Foundation, Inc. Controlled release ophthalmic gel formulation
US5163899A (en) 1987-03-20 1992-11-17 Drug Delivery Systems Inc. Transdermal drug delivery system
US5312325A (en) 1987-05-28 1994-05-17 Drug Delivery Systems Inc Pulsating transdermal drug delivery system
GB8804164D0 (en) 1988-02-23 1988-03-23 Tucker J M Bandage for administering physiologically active compound
US4882150A (en) 1988-06-03 1989-11-21 Kaufman Herbert E Drug delivery system
US5008110A (en) 1988-11-10 1991-04-16 The Procter & Gamble Company Storage-stable transdermal patch
US5088977A (en) 1988-12-21 1992-02-18 Drug Delivery Systems Inc. Electrical transdermal drug applicator with counteractor and method of drug delivery
US5521222A (en) 1989-09-28 1996-05-28 Alcon Laboratories, Inc. Topical ophthalmic pharmaceutical vehicles
DK0431519T3 (da) 1989-12-04 1994-07-04 Searle & Co System til transdermal indgivelse af albuterol
US5077033A (en) 1990-08-07 1991-12-31 Mediventures Inc. Ophthalmic drug delivery with thermo-irreversible gels of polxoxyalkylene polymer and ionic polysaccharide
JP2594486B2 (ja) 1991-01-15 1997-03-26 アルコン ラボラトリーズ インコーポレイテッド 局所的眼薬組成物
US5352456A (en) 1991-10-10 1994-10-04 Cygnus Therapeutic Systems Device for administering drug transdermally which provides an initial pulse of drug
DE69228827T2 (de) 1991-12-18 1999-10-21 Minnesota Mining And Mfg. Co., Saint Paul Mehrschichtige sperrstrukturen
ATE132381T1 (de) 1992-01-29 1996-01-15 Voelkl Franz Ski Ballspielschläger, insbesondere tennisschläger
IL114193A (en) 1994-06-20 2000-02-29 Teva Pharma Ophthalmic pharmaceutical compositions based on sodium alginate
ES2094688B1 (es) 1994-08-08 1997-08-01 Cusi Lab Manoemulsion del tipo de aceite en agua, util como vehiculo oftalmico y procedimiento para su preparacion.
IT1283911B1 (it) 1996-02-05 1998-05-07 Farmigea Spa Soluzioni oftalmiche viscosizzate con polisaccaridi della gomma di tamarindo
US5800807A (en) 1997-01-29 1998-09-01 Bausch & Lomb Incorporated Ophthalmic compositions including glycerin and propylene glycol
US6261547B1 (en) 1998-04-07 2001-07-17 Alcon Manufacturing, Ltd. Gelling ophthalmic compositions containing xanthan gum
US6197934B1 (en) 1998-05-22 2001-03-06 Collagenesis, Inc. Compound delivery using rapidly dissolving collagen film
EP2192838A4 (fr) 2007-08-15 2011-07-27 Harvard College Inhibiteurs hétérocycliques de la nécroptose
TWI637951B (zh) * 2013-02-15 2018-10-11 英商葛蘭素史克智慧財產發展有限公司 作為激酶抑制劑之雜環醯胺類
US20160024098A1 (en) 2013-03-15 2016-01-28 President And Fellows Of Harvard College Hybrid necroptosis inhibitors
CN106573006A (zh) * 2014-08-21 2017-04-19 葛兰素史密斯克莱知识产权发展有限公司 作为药物的rip1激酶抑制剂杂环酰胺
BR112017017411A2 (pt) 2015-02-13 2018-04-03 Glaxosmithkline Ip Dev Ltd Formas cristalinas de (s)-5-benzil-n-(5-metil-4-oxo- 2,3,4,5-tetraidrobenzo[b][1,4]oxazepin-3-il)-4h-1,2,4- triazol-3-carboxamida
EP3317269B1 (fr) 2015-07-02 2022-09-21 F. Hoffmann-La Roche AG Lactames bicycliques en tant qu'inhibiteurs de la protéine kinase 1 interagissant avec des récepteurs pour le traitment par ex. de maladies inflammatoires
ES2885474T3 (es) 2015-10-13 2021-12-13 Inst Nat Sante Rech Med Derivados de sibirilina para la utilización en la prevención y/o tratamiento de trastornos asociados a la necroptosis celular
AU2016340527B2 (en) 2015-10-23 2020-09-17 Takeda Pharmaceutical Company Limited Heterocyclic compound
US10961258B2 (en) 2015-12-21 2021-03-30 Glaxosmithkline Intellectual Property Development Limited Heterocyclic amides as kinase inhibitors
IL287136B2 (en) 2016-02-05 2023-09-01 Denali Therapeutics Inc Receptor inhibitors - interacting with protein kinase 1
WO2018073193A1 (fr) 2016-10-17 2018-04-26 F. Hoffmann-La Roche Ag Lactames de pyridone bicycliques et leurs méthodes d'utilisation
US11072607B2 (en) 2016-12-16 2021-07-27 Genentech, Inc. Inhibitors of RIP1 kinase and methods of use thereof
US20200062735A1 (en) 2017-02-27 2020-02-27 Glaxosmithkline Intellectual Property Development Limited Heterocyclic amides as kinase inhibitors
HRP20231381T1 (hr) 2018-05-03 2024-03-01 Rigel Pharmaceuticals, Inc. Spojevi inhibitori rip1 i postupci za njihovo dobivanje i upotrebu
MD3788045T2 (ro) 2018-05-03 2023-09-30 Rigel Pharmaceuticals Inc Compuși inhibitori ai RIP1 și procedee de obţinere și utilizare a acestora
TW202019913A (zh) 2018-06-26 2020-06-01 中國科學院上海有機化學研究所 細胞壞死抑制劑及其製備方法和用途
WO2020088194A1 (fr) 2018-11-02 2020-05-07 中国科学院上海药物研究所 Amide hétérocyclique inhibant la kinase rip1 et ses applications
CA3149926A1 (fr) 2019-09-06 2021-03-11 Yan Chen Composes inhibiteurs de rip1 et leurs procedes de fabrication et d'utilisation
JP7493586B2 (ja) 2019-09-06 2024-05-31 ライジェル ファーマシューティカルズ, インコーポレイテッド Rip1阻害化合物ならびにそれを作製および使用するための方法
SI4055021T1 (sl) * 2019-11-07 2026-02-27 Rigel Pharmaceuticals, Inc. Heterociklične spojine, ki inhibirajo rip1
AR121717A1 (es) 2020-04-02 2022-06-29 Rigel Pharmaceuticals Inc Inhibidores de rip1k

Also Published As

Publication number Publication date
WO2019213445A1 (fr) 2019-11-07
IL278416A (fr) 2020-12-31
EA202092581A1 (ru) 2021-04-08
IL278416B1 (en) 2023-08-01
PH12020551848A1 (en) 2021-06-28
JP2021523225A (ja) 2021-09-02
PT3788045T (pt) 2023-06-26
KR20210006407A (ko) 2021-01-18
EP3788045B1 (fr) 2023-05-31
HUE062277T2 (hu) 2023-10-28
CN112384510A (zh) 2021-02-19
MD3788045T2 (ro) 2023-09-30
HRP20230909T1 (hr) 2023-12-08
JP7379467B2 (ja) 2023-11-14
FI3788045T3 (fi) 2023-06-28
ES2947446T3 (es) 2023-08-09
JOP20200277B1 (ar) 2024-04-18
DOP2020000197A (es) 2021-04-30
CN112384510B (zh) 2025-06-13
US20210214347A1 (en) 2021-07-15
RS64418B1 (sr) 2023-09-29
CY1126152T1 (el) 2023-11-15
DK3788045T3 (da) 2023-06-26
US20190337934A1 (en) 2019-11-07
CL2020002840A1 (es) 2021-04-16
SG11202010913PA (en) 2020-12-30
CA3099018A1 (fr) 2019-11-07
SI3788045T1 (sl) 2023-07-31
BR112020022423A2 (pt) 2021-02-02
SMT202300203T1 (it) 2023-09-06
AU2019262142A1 (en) 2020-11-26
MX2020011622A (es) 2021-02-17
AU2019262142B2 (en) 2024-11-21
MA52492A (fr) 2021-03-10
ECSP20077518A (es) 2021-03-31
PE20210414A1 (es) 2021-03-04
KR102823195B1 (ko) 2025-06-20
CO2020015153A2 (es) 2021-03-08
US10975064B2 (en) 2021-04-13
MY205388A (en) 2024-10-19
ZA202007487B (en) 2023-01-25
IL278416B2 (en) 2023-12-01
PL3788045T3 (pl) 2023-10-09
CR20200582A (es) 2021-04-14
LT3788045T (lt) 2023-06-26
US20240217958A1 (en) 2024-07-04
UA128160C2 (uk) 2024-04-24
EP3788045A1 (fr) 2021-03-10
US11919890B2 (en) 2024-03-05
JOP20200277A1 (ar) 2020-11-03

Similar Documents

Publication Publication Date Title
MA52492B1 (fr) Composés inhibiteurs de rip1, procédés de préparation et d'utilisation associés
MA52488B1 (fr) Composés inhibiteurs de rip1 et leurs procédés de fabrication et d'utilisation
MA34516B1 (fr) Imidizopyridazines substituees
MA41072A1 (fr) Nouvelles protéines spécifiques de la pyoverdine et de la pyochéline
MA29378B1 (fr) Composition pharmaceutique comprenant une diphenyluree substituee par un omega-carboxyaryle pour le traitement du cancer
MA33419B1 (fr) Composés et compositions pour le traitement de maladies parasitaires
MA40814A1 (fr) Compositions pharmaceutiques pour thérapie combinée
MA42439B1 (fr) Agents, utilisations et procédés pour le traitement d'une synucléinopathie
MA47447B1 (fr) 2-hétéroaryl-3-oxo-2,3-dihydropyridazine-4-carboxamides pour le traitement du cancer
MA46990B1 (fr) Compositions glp-1 et ses utilisations
MA40111A1 (fr) Dérivés du tétrahydronaphtalène inhibant la protéine mcl-1
MA29723B1 (fr) Composes
MA32684B1 (fr) Dérivés de picolinamide en tant qu'inhibiteurs de kinase
MA53668B1 (fr) Traitement de la drépanocytose avec un composé activant la pyruvate kinase r
TNSN07161A1 (en) Compounds and compositions as inhibitors of cannabinoid receptor 1 activity
MY145074A (en) Thiazolidin-4-one derivatives
MA34308B1 (fr) Triazolopyridines substituées
MA66057A1 (fr) Analogues de rifamycine et conjugués anticorps-médicament de ceux-ci
MA40768A (fr) Dérivés d'indole mono ou di-substitué en tant qu'inhibiteurs de réplication du virus de la dengue
CA3156303A1 (fr) Derives de 5-fluoronicotinamide et leurs utilisations
MA30720B1 (fr) Analogues de 2-phenoxypyrimidinone
EP4008718A4 (fr) Dérivé d'hétéroarylamidopyridinol et composition pharmaceutique le comprenant en tant que principe actif pour prévenir ou traiter une maladie auto-immune
MA32688B1 (fr) Composes n-sulfonamido pyrazolyles polycycliques
FR3063645B1 (fr) Acefapc pour le traitement des maladies acetylcholine dependantes
CA3156671A1 (fr) Compositions nutritionnelles pour la gestion de l'hyponatremie