AR104274A1 - Compuestos piridinio como inhibidores de pag - Google Patents

Compuestos piridinio como inhibidores de pag

Info

Publication number
AR104274A1
AR104274A1 ARP160100917A ARP160100917A AR104274A1 AR 104274 A1 AR104274 A1 AR 104274A1 AR P160100917 A ARP160100917 A AR P160100917A AR P160100917 A ARP160100917 A AR P160100917A AR 104274 A1 AR104274 A1 AR 104274A1
Authority
AR
Argentina
Prior art keywords
alkyl
aryl
cycloalkyl
heteroaryl
carboxylic acid
Prior art date
Application number
ARP160100917A
Other languages
English (en)
Inventor
Latad Sachin
Kotecha Jignesh
Mathur Anoop
Kumar Zambad Shital
Deshpande Shailesh
Kesarwani Amit
Mishra Vivek
Abraham Jaya
Patel Manish
Chandra Gupta Ramesh
Dutt Chaitanya
Chaudhari Anita
Original Assignee
Torrent Pharmaceuticals Ltd
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 Torrent Pharmaceuticals Ltd filed Critical Torrent Pharmaceuticals Ltd
Publication of AR104274A1 publication Critical patent/AR104274A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/02Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/06Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms 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
    • A61K31/435Heterocyclic 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4436Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a heterocyclic ring having sulfur as a ring hetero atom
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C53/00Saturated compounds having only one carboxyl group bound to an acyclic carbon atom or hydrogen
    • C07C53/126Acids containing more than four carbon atoms

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (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)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Steroid Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

Reivindicación 1: Un compuesto de la fórmula (1) e isómeros, estereoisómeros, atropisómeros, confórmeros, tautómeros, polimorfos, hidratos y solvatos de los mismos; en donde, Y⁻ es anión de Y; Y se selecciona de ácido nítrico, C₂₋₁₂ alquil ácido sulfónico, C₃₋₁₂ cicloalquil ácido sulfónico, ácidos biliares primarios, ácidos biliares secundarios, ácidos biliares conjugados, CH₃-(CH₂)ᶻ-COOH, C₄₋₁₄ alcano ácido carboxílico ramificado, C₄₋₁₄ alqueno ácido carboxílico, C₄₋₁₄ alquino ácido carboxílico y C₃₋₁₂ cicloalcano ácido carboxílico; z se selecciona de 1 a 14; n se selecciona de 0 a 5; R¹ se selecciona independientemente de hidrógeno, C₁₋₈ alquilo, C₁₋₈ perhaloalquilo, C₃₋₈ cicloalquilo, hetero-C₃₋₁₄ cicloalquilo, arilo, aril-C₁₋₈ alquilo, heteroarilo, heteroaril-C₁₋₈ alquilo, C₁₋₈ alcoxi, carboxamido, -NHCO-C₁₋₈ alquilo, -NR⁵R⁶, acilo, aciloxi, C₁₋₈ alcoxicarbonilo, sulfonamido, halo, ciano y nitro; R² se selecciona de R⁴, -C(O)R⁴, -C(O)NHR⁴, -SO₂R⁴, -C(O)NR⁵R⁶ o estructura de fórmula (2); R³ se selecciona independientemente de C₁₋₈ alquilo, C₁₋₈ perhaloalquilo, C₃₋₈ cicloalquilo, hetero-C₃₋₁₄ cicloalquilo, arilo, aril-C₁₋₈ alquilo, heteroarilo, heteroaril-C₁₋₈ alquilo, C₁₋₈ alcoxi, ariloxi, amino,-NR⁵R⁶, -NHR⁴, aciloxi y sulfonamida; R⁴ se selecciona de C₁₋₈ alquilo, C₁₋₈ perhaloalquilo, C₃₋₈ cicloalquilo, hetero-C₃₋₁₄ cicloalquilo, arilo, aril-C₁₋₈ alquilo y heteroarilo; R⁵ y R⁶ se seleccionan independientemente de hidrógeno, C₁₋₈ alquilo, C₃₋₈ cicloalquilo, arilo, aril-C₁₋₈ alquilo y heteroarilo o R⁵ y R⁶ juntos podrán formar un anillo monocíclico o bicíclico de 4 - 8 miembros saturado o no saturado, podrán fusionarse con benceno que opcionalmente podrá contener uno a dos heteroátomos, seleccionados de O, N y S.
ARP160100917A 2015-04-08 2016-04-05 Compuestos piridinio como inhibidores de pag AR104274A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
IN1473MU2015 2015-04-08

Publications (1)

Publication Number Publication Date
AR104274A1 true AR104274A1 (es) 2017-07-12

Family

ID=55808799

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP160100917A AR104274A1 (es) 2015-04-08 2016-04-05 Compuestos piridinio como inhibidores de pag

Country Status (19)

Country Link
US (2) US10233175B2 (es)
EP (1) EP3280711A1 (es)
JP (1) JP6782763B2 (es)
KR (1) KR20170134661A (es)
CN (1) CN107438604B (es)
AR (1) AR104274A1 (es)
AU (1) AU2016245418B2 (es)
BR (1) BR112017021631A2 (es)
CA (1) CA2997364A1 (es)
EA (1) EA035406B1 (es)
IL (1) IL254792B (es)
MX (1) MX2017012943A (es)
MY (1) MY182914A (es)
PH (1) PH12017501830A1 (es)
SG (1) SG11201708140RA (es)
TW (1) TWI710559B (es)
UA (1) UA120389C2 (es)
WO (1) WO2016162785A1 (es)
ZA (1) ZA201707090B (es)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2997364A1 (en) * 2015-04-08 2016-10-13 Torrent Pharmaceuticals Limited Novel pyridinium compounds
LT3762368T (lt) 2018-03-08 2022-06-10 Incyte Corporation Aminopirazindiolio junginiai, kaip pi3k-γ inhibitoriai
WO2020010003A1 (en) 2018-07-02 2020-01-09 Incyte Corporation AMINOPYRAZINE DERIVATIVES AS PI3K-γ INHIBITORS
US20200338058A1 (en) * 2019-04-28 2020-10-29 King Faisal University Therapeutic agents for treating and preventing autoimmune diseases and cancer and a screening method
WO2022238921A1 (en) * 2021-05-14 2022-11-17 Torrent Pharmaceuticals Limited In-situ synthesis of 3-substituted pyridinium compounds

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2215000C2 (ru) * 1999-10-06 2003-10-27 Торрент Фармасьютикалз Лтд. Производные солей пиридиния, способ их получения, фармацевтические композиции на их основе и способы лечения
PL348049A1 (en) * 1999-10-06 2002-05-06 Torrent Pharmaceuticals Ltd Pyridinium derivatives for the treatment of diabetic and aging−related vascular complications
US6608094B2 (en) * 1999-10-06 2003-08-19 Torrent Pharmaceuticals Ltd. Compounds for the management of aging-related and diabetic vascular complications, process for their preparation and therapeutic uses thereof
DK1243581T3 (da) 2001-03-21 2005-10-31 Torrent Pharmaceuticals Ltd Pyridiniumforbindelser til behandling af AGE-relaterede sygdomme
PT1373263E (pt) 2001-04-05 2005-03-31 Torrent Pharmaceuticals Ltd Compostos heterociclicos para complicacoes relacionadas com a idade e complicacoes vasculares diabeticas
EP1996588A4 (en) 2006-03-03 2011-10-05 Torrent Pharmaceuticals Ltd NEW DUAL ACTION RECEPTOR (DARA) ANTAGONISTS OF ATI AND ETA RECEPTORS
CA2997364A1 (en) * 2015-04-08 2016-10-13 Torrent Pharmaceuticals Limited Novel pyridinium compounds

Also Published As

Publication number Publication date
IL254792A0 (en) 2017-12-31
KR20170134661A (ko) 2017-12-06
CA2997364A1 (en) 2016-10-13
TW201639834A (zh) 2016-11-16
CN107438604B (zh) 2021-12-03
US10717727B2 (en) 2020-07-21
EA035406B1 (ru) 2020-06-09
US20190169175A1 (en) 2019-06-06
AU2016245418B2 (en) 2020-03-26
UA120389C2 (uk) 2019-11-25
WO2016162785A1 (en) 2016-10-13
JP2018511658A (ja) 2018-04-26
EP3280711A1 (en) 2018-02-14
MX2017012943A (es) 2018-01-30
MY182914A (en) 2021-02-05
JP6782763B2 (ja) 2020-11-11
US20180118728A1 (en) 2018-05-03
EA201792234A1 (ru) 2018-02-28
AU2016245418A1 (en) 2017-11-02
TWI710559B (zh) 2020-11-21
SG11201708140RA (en) 2017-11-29
PH12017501830A1 (en) 2018-04-23
US10233175B2 (en) 2019-03-19
BR112017021631A2 (pt) 2018-07-03
CN107438604A (zh) 2017-12-05
ZA201707090B (en) 2021-03-31
IL254792B (en) 2021-01-31

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