AR108586A1 - Compuestos de 2,3-dihidro-1h-indol - Google Patents

Compuestos de 2,3-dihidro-1h-indol

Info

Publication number
AR108586A1
AR108586A1 ARP170101413A ARP170101413A AR108586A1 AR 108586 A1 AR108586 A1 AR 108586A1 AR P170101413 A ARP170101413 A AR P170101413A AR P170101413 A ARP170101413 A AR P170101413A AR 108586 A1 AR108586 A1 AR 108586A1
Authority
AR
Argentina
Prior art keywords
cancer
hydrogen
compounds
fluoro
methyl
Prior art date
Application number
ARP170101413A
Other languages
English (en)
Original Assignee
Lilly Co Eli
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 Lilly Co Eli filed Critical Lilly Co Eli
Publication of AR108586A1 publication Critical patent/AR108586A1/es

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Classifications

    • 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
    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/403Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/10Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing aromatic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/06Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • 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
    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/403Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
    • A61K31/404Indoles, e.g. pindolol
    • A61K31/4045Indole-alkylamines; Amides thereof, e.g. serotonin, melatonin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C233/00Carboxylic acid amides
    • C07C233/57Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of rings other than six-membered aromatic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/13Crystalline forms, e.g. polymorphs
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C233/00Carboxylic acid amides
    • C07C233/01Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D309/00Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Epidemiology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Hematology (AREA)
  • Oncology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Peptides Or Proteins (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

La presente se refiere a ciertos compuestos de 2,3-dihidro-1H-indol, composiciones farmacéuticas que comprenden los compuestos, y métodos para usar los compuestos para tratar cáncer, más particularmente para el tratamiento de cáncer seleccionado a partir del grupo que consiste de melanoma, leucemia mieloide aguda, leucemia linfocítica crónica, cáncer colorrectal, cáncer de mama, cáncer de pulmón, cáncer de ovario, carcinoma de tubos de falopio, carcinoma peritoneal primario, cáncer cervical, cáncer gástrico, cáncer hepático, cáncer pancreático, cáncer tiroideo, glioma, linfoma no Hodgkin, y linfoma de Hodgkin. Reivindicación 1: Un compuesto de la fórmula (1), caracterizado porque: R¹ᵃ es hidrógeno, metilo, etenilo, ciano, fluoro, cloro, fluorometilo, o difluorometilo; R¹ᵇ es hidrógeno, fluoro, o cloro; R¹ᶜ es hidrógeno, hidroxi, fluoro, benciloxi, o hidroxietilamino; R² es hidrógeno o metilo; R²ᵃ es hidrógeno o metilo; y R³ᵃ es tetrahidropiranilo.
ARP170101413A 2016-06-10 2017-05-24 Compuestos de 2,3-dihidro-1h-indol AR108586A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US201662348457P 2016-06-10 2016-06-10

Publications (1)

Publication Number Publication Date
AR108586A1 true AR108586A1 (es) 2018-09-05

Family

ID=59031409

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP170101413A AR108586A1 (es) 2016-06-10 2017-05-24 Compuestos de 2,3-dihidro-1h-indol

Country Status (40)

Country Link
US (2) US9872853B2 (es)
EP (1) EP3468965B1 (es)
JP (1) JP6632746B2 (es)
KR (1) KR102241258B1 (es)
CN (1) CN109641881B (es)
AR (1) AR108586A1 (es)
AU (1) AU2017277833B2 (es)
BR (1) BR112018072872A2 (es)
CA (1) CA3027035C (es)
CL (1) CL2018003543A1 (es)
CO (1) CO2018013251A2 (es)
CR (1) CR20180579A (es)
CY (1) CY1123660T1 (es)
DK (1) DK3468965T3 (es)
DO (1) DOP2018000278A (es)
EA (1) EA037419B1 (es)
EC (1) ECSP19001734A (es)
ES (1) ES2797981T3 (es)
HR (1) HRP20200769T1 (es)
HU (1) HUE050155T2 (es)
IL (1) IL263497B (es)
JO (1) JOP20170131B1 (es)
LT (1) LT3468965T (es)
MA (1) MA45224B1 (es)
MD (1) MD3468965T2 (es)
ME (1) ME03744B (es)
MX (1) MX2018015275A (es)
MY (1) MY197462A (es)
NZ (1) NZ748500A (es)
PE (1) PE20190378A1 (es)
PH (1) PH12018502572A1 (es)
PL (1) PL3468965T3 (es)
PT (1) PT3468965T (es)
RS (1) RS60322B1 (es)
SG (1) SG11201809625RA (es)
SI (1) SI3468965T1 (es)
TW (1) TWI671294B (es)
UA (1) UA122526C2 (es)
WO (1) WO2017213919A1 (es)
ZA (1) ZA201807688B (es)

Families Citing this family (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2016183266A1 (en) 2015-05-13 2016-11-17 Enanta Pharmaceuticals, Inc. Ehpatitis b antiviral agents
BR112018067964B1 (pt) 2016-03-07 2024-01-16 Enanta Pharmaceuticals, Inc Composto, composição farmacêutica que o compreende e uso do referido composto
IL272941B2 (en) 2017-08-28 2023-03-01 Enanta Pharm Inc Antiviral agents for viral hepatitis b
EP3703692A4 (en) * 2017-11-01 2021-04-28 Merck Sharp & Dohme Corp. NEW SUBSTITUTED TETRAHYDROQUINOLINE COMPOUNDS USED AS INDOLEAMINE 2,3-DIOXYGENASE (IDO) INHIBITORS
US20210002371A1 (en) * 2017-12-21 2021-01-07 Brian A. Sherer Combination of an anti-pd-l1 antibody and ido1 inhibitor for the treatment of cancer
US11058678B2 (en) 2018-01-22 2021-07-13 Enanta Pharmaceuticals, Inc. Substituted heterocycles as antiviral agents
EP3836928B1 (en) * 2018-08-17 2024-02-14 Merck Sharp & Dohme LLC Novel substituted tetrahydroquinoline compounds as indoleamine 2,3-dioxygenase inhibitors
BR112021005091A2 (pt) 2018-09-21 2021-06-08 Enanta Pharmaceuticals, Inc. heterociclos funcionalizados como agentes antivirais
US12065438B2 (en) 2018-11-06 2024-08-20 Merck Sharp & Dohme Llc Substituted tricyclic compounds as indoleamine 2,3-dioxygenase inhibitors
CN113271946A (zh) 2018-11-21 2021-08-17 英安塔制药有限公司 官能化杂环化合物作为抗病毒剂
US11236111B2 (en) 2019-06-03 2022-02-01 Enanta Pharmaceuticals, Inc. Hepatitis B antiviral agents
WO2020247575A1 (en) 2019-06-04 2020-12-10 Enanta Pharmaceuticals, Inc. Hepatitis b antiviral agents
US11760755B2 (en) 2019-06-04 2023-09-19 Enanta Pharmaceuticals, Inc. Hepatitis B antiviral agents
US11738019B2 (en) 2019-07-11 2023-08-29 Enanta Pharmaceuticals, Inc. Substituted heterocycles as antiviral agents
US11236108B2 (en) 2019-09-17 2022-02-01 Enanta Pharmaceuticals, Inc. Functionalized heterocycles as antiviral agents
US11802125B2 (en) 2020-03-16 2023-10-31 Enanta Pharmaceuticals, Inc. Functionalized heterocyclic compounds as antiviral agents
CN114105961B (zh) * 2021-12-10 2023-09-12 海南梵圣生物科技有限公司 一种ido1抑制剂(ly-3381916)制备方法
CN114213310B (zh) * 2021-12-31 2024-02-23 中国药科大学 吲哚啉化合物及其衍生物、制备方法、药物组合物和应用

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4629657B2 (ja) * 2003-04-11 2011-02-09 ハイ・ポイント・ファーマスーティカルズ、エルエルシー 11β−ヒドロキシステロイドデヒドロゲナーゼ1型化活性化合物
ME02461B (me) * 2005-05-10 2017-02-20 Incyte Holdings Corp Modulatori indoleamina 2,3-dioksigenaze i metode za upotrebu istih
US7622495B2 (en) * 2006-10-03 2009-11-24 Neurim Pharmaceuticals (1991) Ltd. Substituted aryl-indole compounds and their kynurenine/kynuramine-like metabolites as therapeutic agents
KR20100124272A (ko) * 2008-02-07 2010-11-26 아보트 러보러터리즈 양성 알로스테릭 조절제로서의 아미드 유도체 및 이의 사용방법
MY171866A (en) * 2008-07-08 2019-11-05 Incyte Holdings Corp 1,2,5-oxadiazoles as inhibitors of indoleamine 2,3-dioxygenase
NO2694640T3 (es) * 2011-04-15 2018-03-17
ES2733546T3 (es) * 2013-03-15 2019-11-29 Bristol Myers Squibb Co Inhibidores de IDO
WO2015150097A1 (en) * 2014-04-04 2015-10-08 Iomet Pharma Ltd Indole derivatives for use in medicine
UY36391A (es) * 2014-11-05 2016-06-01 Flexus Biosciences Inc Compuestos moduladores de la enzima indolamina 2,3-dioxigenasa (ido1), sus métodos de síntesis y composiciones farmacèuticas que las contienen
US11135221B2 (en) * 2015-12-23 2021-10-05 Moonshot Pharma Llc Methods for inducing an immune response

Also Published As

Publication number Publication date
DOP2018000278A (es) 2018-12-31
EP3468965A1 (en) 2019-04-17
PL3468965T3 (pl) 2020-09-21
EA037419B1 (ru) 2021-03-25
LT3468965T (lt) 2020-06-10
MD3468965T2 (ro) 2020-08-31
UA122526C2 (uk) 2020-11-25
RS60322B1 (sr) 2020-07-31
KR102241258B1 (ko) 2021-04-16
MA45224B1 (fr) 2020-06-30
JP2019518027A (ja) 2019-06-27
HRP20200769T1 (hr) 2020-07-24
CN109641881A (zh) 2019-04-16
JOP20170131B1 (ar) 2021-08-17
DK3468965T3 (da) 2020-06-15
US20170354641A1 (en) 2017-12-14
PE20190378A1 (es) 2019-03-08
CA3027035C (en) 2021-05-04
CL2018003543A1 (es) 2019-03-22
JP6632746B2 (ja) 2020-01-22
EP3468965B1 (en) 2020-04-29
ME03744B (me) 2021-04-20
WO2017213919A1 (en) 2017-12-14
PT3468965T (pt) 2020-07-16
ES2797981T3 (es) 2020-12-04
HUE050155T2 (hu) 2020-12-28
TW201806948A (zh) 2018-03-01
CN109641881B (zh) 2022-01-07
MX2018015275A (es) 2019-04-11
TWI671294B (zh) 2019-09-11
MY197462A (en) 2023-06-19
SG11201809625RA (en) 2018-11-29
ECSP19001734A (es) 2019-01-31
CA3027035A1 (en) 2017-12-14
NZ748500A (en) 2020-04-24
US9872853B2 (en) 2018-01-23
US20190161477A1 (en) 2019-05-30
PH12018502572A1 (en) 2019-10-28
IL263497A (en) 2019-01-31
KR20190003750A (ko) 2019-01-09
US10759786B2 (en) 2020-09-01
ZA201807688B (en) 2020-08-26
AU2017277833A1 (en) 2018-11-15
CR20180579A (es) 2019-02-08
EA201892479A1 (ru) 2019-07-31
BR112018072872A2 (pt) 2019-03-06
SI3468965T1 (sl) 2020-07-31
CO2018013251A2 (es) 2019-01-18
IL263497B (en) 2020-11-30
AU2017277833B2 (en) 2020-07-02
CY1123660T1 (el) 2022-03-24

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