MX2022007317A - Inhibidores novedosos. - Google Patents

Inhibidores novedosos.

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Publication number
MX2022007317A
MX2022007317A MX2022007317A MX2022007317A MX2022007317A MX 2022007317 A MX2022007317 A MX 2022007317A MX 2022007317 A MX2022007317 A MX 2022007317A MX 2022007317 A MX2022007317 A MX 2022007317A MX 2022007317 A MX2022007317 A MX 2022007317A
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MX
Mexico
Prior art keywords
amino
heteroaryl
heterocyclyl
cycloalkyl
aryl
Prior art date
Application number
MX2022007317A
Other languages
English (en)
Inventor
Ulrich Heiser
Antje Meyer
Torsten Hoffmann
Ingeborg Lues
Original Assignee
Vivoryon Therapeutics N V
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 Vivoryon Therapeutics N V filed Critical Vivoryon Therapeutics N V
Publication of MX2022007317A publication Critical patent/MX2022007317A/es

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    • C07D417/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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    • C07D285/01Five-membered rings
    • C07D285/02Thiadiazoles; Hydrogenated thiadiazoles
    • C07D285/04Thiadiazoles; Hydrogenated thiadiazoles not condensed with other rings
    • C07D285/121,3,4-Thiadiazoles; Hydrogenated 1,3,4-thiadiazoles
    • C07D285/1251,3,4-Thiadiazoles; Hydrogenated 1,3,4-thiadiazoles with oxygen, sulfur or nitrogen atoms, directly attached to ring carbon atoms, the nitrogen atoms not forming part of a nitro radical
    • C07D285/135Nitrogen atoms
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    • C07D401/02Heterocyclic 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
    • C07D401/12Heterocyclic 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
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    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/41961,2,4-Triazoles
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    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/425Thiazoles
    • A61K31/428Thiazoles condensed with carbocyclic rings
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    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/433Thidiazoles
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    • A61K31/435Heterocyclic 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
    • A61K31/4353Heterocyclic 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
    • A61K31/437Heterocyclic 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
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    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/4965Non-condensed pyrazines
    • A61K31/497Non-condensed pyrazines containing further heterocyclic rings
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    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
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    • C07D235/04Benzimidazoles; Hydrogenated benzimidazoles
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    • C07D249/081,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
    • C07D249/101,2,4-Triazoles; Hydrogenated 1,2,4-triazoles 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
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  • Chemical & Material Sciences (AREA)
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  • Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
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  • Bioinformatics & Cheminformatics (AREA)
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  • Epidemiology (AREA)
  • Neurosurgery (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Immunology (AREA)
  • Rheumatology (AREA)
  • Psychiatry (AREA)
  • Cardiology (AREA)
  • Oncology (AREA)
  • Hospice & Palliative Care (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Pain & Pain Management (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Peptides Or Proteins (AREA)
  • Enzymes And Modification Thereof (AREA)
  • Thiazole And Isothizaole Compounds (AREA)
  • Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

La invención se refiere a un compuesto de la fórmula (I): A-B-D-E (I) o una sal farmacéuticamente aceptable, solvato o polimorfo del mismo, incluyendo todos los tautómeros y estereoisómeros del mismo en donde: A se selecciona de heteroarilo monocíclico y bicíclico, que se puede sustituir independientemente por alquilo o amino; B se selecciona de alquilo, heteroarilo, alquilamino, arilo, heteroarilo, cicloalquilo, heterociclilo y alquileno, en donde los grupos se pueden sustituir independientemente por alquilo; D se selecciona de arilo-amino, heteroaril-amino, cicloalquil-amino, heterociclilo, heterociclilo-amino, urea, tioamida, tiourea, sulfonamida, sulfoximina y sulfamoilo, en donde los grupos arilo, heteroarilo, cicloalquilo y heterociclilo se pueden sustituir independientemente; y E se selecciona de arilo, heteroarilo, cicloalquilo, heterociclilo, en donde los grupos arilo, heteroarilo, cicloalquilo y heterociclilo se pueden sustituir independientemente. Los compuestos de la fórmula (I) son inhibidores de glutaminil ciclasa (QC, EC 2.3.2.5). QC cataliza la ciclización intramolecular de los residuos de glutamina N-terminal en ácido piroglutámico (5-oxo-prolilo, pGlu*) bajo la liberación de amoníaco y la ciclización intramolecular de los residuos de glutamato N-terminales en ácido piroglutámico bajo la liberación de agua.
MX2022007317A 2017-03-31 2019-09-26 Inhibidores novedosos. MX2022007317A (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GBGB1705263.0A GB201705263D0 (en) 2017-03-31 2017-03-31 Novel inhibitors

Publications (1)

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MX2022007317A true MX2022007317A (es) 2022-07-13

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MX2019011544A MX2019011544A (es) 2017-03-31 2018-04-03 Inhibidores novedosos.
MX2022007317A MX2022007317A (es) 2017-03-31 2019-09-26 Inhibidores novedosos.

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US (2) US11339152B2 (es)
EP (1) EP3601269A1 (es)
JP (2) JP2020512373A (es)
KR (1) KR20190136005A (es)
CN (2) CN110719910B (es)
AU (2) AU2018246382B2 (es)
BR (1) BR112019019553A2 (es)
CA (2) CA3057783A1 (es)
EA (1) EA201992120A1 (es)
GB (1) GB201705263D0 (es)
IL (3) IL269196B2 (es)
MX (2) MX2019011544A (es)
NZ (1) NZ757601A (es)
WO (1) WO2018178384A1 (es)
ZA (1) ZA201905811B (es)

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BR112022012758A2 (pt) * 2020-01-17 2022-09-06 Daegu Gyeongbuk Medical Innovation Found Composto, isômero do mesmo ou sal farmaceuticamente aceitável do mesmo, método de preparação e uso do dito composto, composição farmacêutica e alimento funcional saudável
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EP3601269A1 (en) 2020-02-05
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