MA54985A - Pharmacophores d'acide alpha-hydroxy phénylacétique ou antagonistes de la protéine bio-isostère mcl-1 - Google Patents

Pharmacophores d'acide alpha-hydroxy phénylacétique ou antagonistes de la protéine bio-isostère mcl-1

Info

Publication number
MA54985A
MA54985A MA054985A MA54985A MA54985A MA 54985 A MA54985 A MA 54985A MA 054985 A MA054985 A MA 054985A MA 54985 A MA54985 A MA 54985A MA 54985 A MA54985 A MA 54985A
Authority
MA
Morocco
Prior art keywords
bioisostery
pharmacophores
mcl
antagonists
alpha
Prior art date
Application number
MA054985A
Other languages
English (en)
Inventor
Sean P Brown
Buenrostro Ana Gonzalez
Salman Yojiro Jabri
Yihong Li
Mike Lizarzaburu
Julio C Medina
Gwenaella Rescourio
Yosup Rew
Scott Preston Simonovich
Daqing Sun
Xuelei Yan
Original Assignee
Amgen 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 Amgen Inc filed Critical Amgen Inc
Publication of MA54985A publication Critical patent/MA54985A/fr

Links

Classifications

    • 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
    • C07D498/10Spiro-condensed 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
    • C07D498/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/12Heterocyclic 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 three hetero rings
    • C07D498/20Spiro-condensed systems
    • 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
    • C07D498/22Heterocyclic 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 four or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D519/00Heterocyclic 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/63Compounds containing para-N-benzenesulfonyl-N-groups, e.g. sulfanilamide, p-nitrobenzenesulfonyl hydrazide
    • A61K31/635Compounds containing para-N-benzenesulfonyl-N-groups, e.g. sulfanilamide, p-nitrobenzenesulfonyl hydrazide having a heterocyclic ring, e.g. sulfadiazine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/70Carbohydrates; Sugars; Derivatives thereof
    • A61K31/7042Compounds having saccharide radicals and heterocyclic rings
    • A61K31/7052Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
    • A61K31/706Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom
    • A61K31/7064Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines
    • A61K31/7068Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines having oxo groups directly attached to the pyrimidine ring, e.g. cytidine, cytidylic acid
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00Medicinal preparations containing peptides
    • A61K38/04Peptides having up to 20 amino acids in a fully defined sequence; Derivatives thereof
    • A61K38/07Tetrapeptides

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
MA054985A 2018-03-05 2019-03-04 Pharmacophores d'acide alpha-hydroxy phénylacétique ou antagonistes de la protéine bio-isostère mcl-1 MA54985A (fr)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US201862638846P 2018-03-05 2018-03-05

Publications (1)

Publication Number Publication Date
MA54985A true MA54985A (fr) 2021-12-29

Family

ID=65991891

Family Applications (1)

Application Number Title Priority Date Filing Date
MA054985A MA54985A (fr) 2018-03-05 2019-03-04 Pharmacophores d'acide alpha-hydroxy phénylacétique ou antagonistes de la protéine bio-isostère mcl-1

Country Status (4)

Country Link
US (1) US11274105B2 (fr)
EP (1) EP3762393B1 (fr)
MA (1) MA54985A (fr)
WO (1) WO2019173181A1 (fr)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MA49908A (fr) 2017-08-18 2021-04-28 Amgen Inc Composés inhibant la protéine mcl-1
US11279712B2 (en) 2017-08-29 2022-03-22 Amgen Inc. Macrocyclic compounds that inhibit MCL-1 protein
CN112118845B (zh) 2018-05-14 2023-06-13 吉利德科学公司 Mcl-1抑制剂
WO2021047616A1 (fr) * 2019-09-12 2021-03-18 苏州亚盛药业有限公司 Composé spiro à base d'heptane hétérocyclique d'oxynitrure, intermédiaire et procédé de préparation associé
TWI778443B (zh) 2019-11-12 2022-09-21 美商基利科學股份有限公司 Mcl1抑制劑
PT4065567T (pt) 2019-11-26 2024-11-08 Gilead Sciences Inc Processos e intermediários para a preparação de inibidores de mcl1
US20230136910A1 (en) * 2020-05-06 2023-05-04 Amgen Inc. Synthesis of vinylic alcohol intermediates
CN115698023A (zh) 2020-06-10 2023-02-03 詹森药业有限公司 作为mcl-1抑制剂的大环2-氨基-3-氟-丁-3-烯酰胺
JP7659630B2 (ja) * 2020-11-19 2025-04-09 ギリアード サイエンシーズ, インコーポレイテッド 大環状mcl1阻害剤を調製するための方法及び中間体
CN116670141A (zh) 2020-12-17 2023-08-29 詹森药业有限公司 作为mcl-1抑制剂的大环支化3-氟-丁-3-烯酰胺
JP2024516641A (ja) 2021-04-26 2024-04-16 ヤンセン ファーマシューティカ エヌ.ベー. Mcl-1阻害剤としての大環状2-アリルテトラヒドロフラン
JP7673255B2 (ja) 2021-06-11 2025-05-08 ギリアード サイエンシーズ, インコーポレイテッド Mcl-1阻害剤と抗体薬物コンジュゲートとの組み合わせ
TWI910028B (zh) 2021-06-11 2025-12-21 美商基利科學股份有限公司 Mcl-1抑制劑與抗癌劑之組合
JP2024544570A (ja) 2021-11-16 2024-12-03 ヤンセン ファーマシューティカ エヌ.ベー. Mcl-1阻害剤としての大環状2-アミノ-ブト-3-エナミド

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4522811A (en) 1982-07-08 1985-06-11 Syntex (U.S.A.) Inc. Serial injection of muramyldipeptides and liposomes enhances the anti-infective activity of muramyldipeptides
US5858784A (en) 1991-12-17 1999-01-12 The Regents Of The University Of California Expression of cloned genes in the lung by aerosol- and liposome-based delivery
US6042820A (en) 1996-12-20 2000-03-28 Connaught Laboratories Limited Biodegradable copolymer containing α-hydroxy acid and α-amino acid units
US6472375B1 (en) 1998-04-16 2002-10-29 John Wayne Cancer Institute DNA vaccine and methods for its use
ES2705599T3 (es) 2007-04-16 2019-03-26 Abbvie Inc Indoles sustituidos en la posición 7 como inhibidores de mcl-1
EP3138838A1 (fr) 2010-01-29 2017-03-08 Dana-Farber Cancer Institute, Inc. Petites molécules pour la modulation de mcl-1 et procédés de modulation de la mort cellulaire, la division cellulaire, la différenciation cellulaire et procédés de traitement de troubles
WO2013052943A2 (fr) 2011-10-06 2013-04-11 The Regents Of The University Of Michgian Inhibiteurs à petite molécule de mcl-1 et leurs utilisations
WO2013149124A1 (fr) 2012-03-29 2013-10-03 The Regents Of The University Of Michigan Inhibiteurs de mcl-1 à petite molécule et utilisations de ceux-ci
JO3474B1 (ar) 2014-08-29 2020-07-05 Amgen Inc مشتقات تيتراهيدرونافثالين التي تثبط بروتين mcl-1
WO2017147410A1 (fr) * 2016-02-25 2017-08-31 Amgen Inc. Composés inhibant la protéine mcl-1
JP6453507B2 (ja) 2017-03-30 2019-01-16 アムジエン・インコーポレーテツド Mcl−1タンパク質を阻害する化合物
MA49908A (fr) 2017-08-18 2021-04-28 Amgen Inc Composés inhibant la protéine mcl-1
US11279712B2 (en) 2017-08-29 2022-03-22 Amgen Inc. Macrocyclic compounds that inhibit MCL-1 protein

Also Published As

Publication number Publication date
US20210047344A1 (en) 2021-02-18
WO2019173181A1 (fr) 2019-09-12
EP3762393B1 (fr) 2023-01-11
EP3762393A1 (fr) 2021-01-13
US11274105B2 (en) 2022-03-15

Similar Documents

Publication Publication Date Title
EP3721409A4 (fr) Détection d'activité par détection et suivi conjoints d'homme et d'objet
MA51747A (fr) Formulation d'anticorps pharmaceutique à ph faible
EP4062373C0 (fr) Analyse spatiale d'analytes
EP3359023A4 (fr) Évaluation d'une affection pulmonaire par analyse de la parole
EP3772036A4 (fr) Détection d'images quasi-dupliquées
EP3430434A4 (fr) Détermination rapide de position précise à l'aide de données d'assistance
MA47425A (fr) Composition pharmaceutique à faible ph comprenant des constructions d'anticorps d'engagement avec les lymphocytes t
EP3938077A4 (fr) Analyseur de concentration de point d'intervention
MA51998A (fr) Nouveaux polymorphes de sel de calcium en tant qu'agents anti-inflammatoires, immunomodulateurs et anti-prolifératifs
EP3906026A4 (fr) Inhibiteurs irréversibles de l'interaction ménine-mll
EP3725780A4 (fr) Dérivé de sulfonamide ou sel d'addition d'acide pharmaceutiquement acceptable
EP3621640A4 (fr) Constructions d'anticorps d'acide nucléique optimisées
EP3481814A4 (fr) Antagonistes de l'intégrine tetrahydronaphthyridinepentanamide
EP3673076A4 (fr) Molécules de détection de bret pour la détection d'hydrolases
EP3996593C0 (fr) Détection d'impulsion neuronale en temps réel
EP3914608A4 (fr) Nouvelles protéines d'inhibition des insectes
MA46863A (fr) Administration intrathécale de virus adéno-associé recombinant codant pour la protéine 2 de liaison méthyl-cpg
EP3488018A4 (fr) Procédés et compositions pour l'identification de protéines
MA54139A (fr) Formulation d'anticorps
EP3833778A4 (fr) Détection multiplexe d'acides nucléiques
EP3508200A4 (fr) Formulation aqueuse contenant de l'acide 5-aminolévulinique ou similaire
EP3867272A4 (fr) Utilisation d'anticorps anti-fam19a5
MA43685A (fr) Solutions aqueuses d'acides aminés n-acylés
EP3414256A4 (fr) Sel d'amine de l'acide obéticholique
EP3859332A4 (fr) Procédé de dosage d'hémoglobine glyquée (%)