AR086852A1 - Compuestos de 1,1-dioxido de [1,2,4]tiadiazina para reducir el acido urico serico - Google Patents

Compuestos de 1,1-dioxido de [1,2,4]tiadiazina para reducir el acido urico serico

Info

Publication number
AR086852A1
AR086852A1 ARP120102014A ARP120102014A AR086852A1 AR 086852 A1 AR086852 A1 AR 086852A1 AR P120102014 A ARP120102014 A AR P120102014A AR P120102014 A ARP120102014 A AR P120102014A AR 086852 A1 AR086852 A1 AR 086852A1
Authority
AR
Argentina
Prior art keywords
alkyl
uric acid
patient
formula
tiadiazine
Prior art date
Application number
ARP120102014A
Other languages
English (en)
Inventor
James L Freddo
Original Assignee
Anadys 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 Anadys Pharmaceuticals Inc filed Critical Anadys Pharmaceuticals Inc
Publication of AR086852A1 publication Critical patent/AR086852A1/es

Links

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
    • A61K31/54Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame
    • A61K31/549Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame having two or more nitrogen atoms in the same ring, e.g. hydrochlorothiazide
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/04Drugs for disorders of the urinary system for urolithiasis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/12Drugs for disorders of the urinary system of the kidneys
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/06Antigout agents, e.g. antihyperuricemic or uricosuric agents
    • 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
    • A61P3/00Drugs for disorders of the metabolism
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/12Antihypertensives
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic 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
    • 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
    • C07D417/04Heterocyclic 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 directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D513/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
    • C07D513/02Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
    • C07D513/04Ortho-condensed systems

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Chemical & Material Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Engineering & Computer Science (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Urology & Nephrology (AREA)
  • Epidemiology (AREA)
  • Hematology (AREA)
  • Diabetes (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Obesity (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Vascular Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

La presente describe compuestos de 1,1-dióxido de [1,2,4]tiadiazina y sus sales farmacéuticamente aceptables, que son de utilidad para la reducción de ácido úrico sérico en un paciente que lo necesita que comprende la administración al paciente de una cantidad terapéutica o preventivamente efectiva de un compuesto de 1,1-dióxido de [1,2,4]tiadiazina.Reivindicación 1: Un método para reducir ácido úrico sérico en un paciente que comprende la administración al paciente de una cantidad terapéuticamente efectiva de un compuesto de la fórmula (1) en donde el anillo B es un resto de fórmula (2) ó (3); A es el resto de fórmula (4) ó (5); Z es -(CR11R12)n-; Y es -(CR13R14)m-; n es 1 ó 2; m es 2 ó 3; R1 es H, -NH2 o -(CH2)q-NH-S(O)2CH3, en donde q es 0 ó 1; R2 es alquilo C1-6, cicloalquilo C3-6, arilo o -(CH2)-R15, en donde R15 es un resto de fórmula (6), en donde R16, R17, R18, R19 y R20 son, de modo independiente, H, alquilo C1-6, hidroxi o halo; R3, R4, R5, R6, R7, R8, R9, R10, R11, R12, R13 y R14 son, de modo independiente, H o alquilo C1-6; en donde cada alquilo, cicloalquilo o arilo están opcionalmente sustituidos con uno o varios alquilo, hidroxilo o sustituyentes de halo; o una de sus sales, hidratos, solvatos, tautómeros o estereoisómeros terapéuticamente aceptables.
ARP120102014A 2011-06-07 2012-06-07 Compuestos de 1,1-dioxido de [1,2,4]tiadiazina para reducir el acido urico serico AR086852A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US201161494288P 2011-06-07 2011-06-07

Publications (1)

Publication Number Publication Date
AR086852A1 true AR086852A1 (es) 2014-01-29

Family

ID=47293671

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP120102014A AR086852A1 (es) 2011-06-07 2012-06-07 Compuestos de 1,1-dioxido de [1,2,4]tiadiazina para reducir el acido urico serico

Country Status (17)

Country Link
US (1) US8815847B2 (es)
EP (1) EP2718273A4 (es)
JP (1) JP6010614B2 (es)
KR (1) KR20140037193A (es)
CN (1) CN103827100B (es)
AR (1) AR086852A1 (es)
AU (1) AU2012268119B2 (es)
BR (1) BR112013031484A2 (es)
CA (1) CA2838257A1 (es)
EA (1) EA023336B1 (es)
HK (1) HK1197245A1 (es)
IL (1) IL229701A0 (es)
MX (1) MX2013014240A (es)
MY (1) MY183704A (es)
SG (1) SG195288A1 (es)
WO (1) WO2012170536A1 (es)
ZA (1) ZA201309706B (es)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2908244C (en) * 2013-03-25 2021-04-20 United Therapeutics Corporation Process of making prostacyclin compounds with linker thiol and pegylated forms
CN111233768B (zh) * 2020-03-18 2021-08-03 徐州圣元化工有限公司 一种3-(二氟甲基)-1-甲基-1h-吡唑-4-羧酸乙酯的制备方法

Family Cites Families (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3536809A (en) 1969-02-17 1970-10-27 Alza Corp Medication method
US3598123A (en) 1969-04-01 1971-08-10 Alza Corp Bandage for administering drugs
US3969518A (en) * 1972-05-24 1976-07-13 Merck & Co., Inc. Inhibiting xanthine oxidase with 3-haloalkyl substituted benzothiadiazine-1,1-dioxides
US3845770A (en) 1972-06-05 1974-11-05 Alza Corp Osmatic dispensing device for releasing beneficial agent
US3916899A (en) 1973-04-25 1975-11-04 Alza Corp Osmotic dispensing device with maximum and minimum sizes for the passageway
US4008719A (en) 1976-02-02 1977-02-22 Alza Corporation Osmotic system having laminar arrangement for programming delivery of active agent
IE58110B1 (en) 1984-10-30 1993-07-14 Elan Corp Plc Controlled release powder and process for its preparation
US5073543A (en) 1988-07-21 1991-12-17 G. D. Searle & Co. Controlled release formulations of trophic factors in ganglioside-lipsome vehicle
IT1229203B (it) 1989-03-22 1991-07-25 Bioresearch Spa Impiego di acido 5 metiltetraidrofolico, di acido 5 formiltetraidrofolico e dei loro sali farmaceuticamente accettabili per la preparazione di composizioni farmaceutiche in forma a rilascio controllato attive nella terapia dei disturbi mentali organici e composizioni farmaceutiche relative.
US5120548A (en) 1989-11-07 1992-06-09 Merck & Co., Inc. Swelling modulated polymeric drug delivery device
US5733566A (en) 1990-05-15 1998-03-31 Alkermes Controlled Therapeutics Inc. Ii Controlled release of antiparasitic agents in animals
US5580578A (en) 1992-01-27 1996-12-03 Euro-Celtique, S.A. Controlled release formulations coated with aqueous dispersions of acrylic polymers
US5591767A (en) 1993-01-25 1997-01-07 Pharmetrix Corporation Liquid reservoir transdermal patch for the administration of ketorolac
IT1270594B (it) 1994-07-07 1997-05-07 Recordati Chem Pharm Composizione farmaceutica a rilascio controllato di moguisteina in sospensione liquida
DE60335564D1 (de) * 2002-11-01 2011-02-10 Abbott Lab Antiinfektiöse mittel
BRPI0713684A2 (pt) 2006-06-22 2012-10-30 Anadys Pharmaceuticals Inc compostos, composição farmaceuticamente aceitável e métodos de inibição da replicação de vìrus da hepatite c, de tratamento de célula e de tratamento ou prevenção da infecção do vìrus da hepatite c em maìfero carecido do mesmo
US7662958B2 (en) 2006-07-19 2010-02-16 Rolf Wagner Anti-infective agents
UA100120C2 (en) 2007-04-03 2012-11-26 Анадис Фармасьютикалз, Инк. 5,6-dihydro-1h-pyridin-2-one compounds
WO2008147601A1 (en) * 2007-04-17 2008-12-04 University Of Florida Research Foundation, Inc. Methods and compositions for ameliorating thiazide induced hyperlipidemia
CN102316871B (zh) * 2008-06-10 2014-06-04 安那迪斯药品股份有限公司 [1,2,4]噻二嗪1,1-二氧化合物

Also Published As

Publication number Publication date
EP2718273A1 (en) 2014-04-16
KR20140037193A (ko) 2014-03-26
WO2012170536A1 (en) 2012-12-13
JP2014516077A (ja) 2014-07-07
ZA201309706B (en) 2017-04-26
US8815847B2 (en) 2014-08-26
AU2012268119A1 (en) 2014-01-23
MX2013014240A (es) 2014-01-24
IL229701A0 (en) 2014-01-30
SG195288A1 (en) 2013-12-30
US20120316156A1 (en) 2012-12-13
CN103827100A (zh) 2014-05-28
MY183704A (en) 2021-03-09
BR112013031484A2 (pt) 2018-04-24
JP6010614B2 (ja) 2016-10-19
EA023336B1 (ru) 2016-05-31
HK1197245A1 (zh) 2015-01-09
NZ619685A (en) 2016-01-29
CA2838257A1 (en) 2012-12-13
AU2012268119B2 (en) 2017-03-02
EA201391827A1 (ru) 2014-06-30
CN103827100B (zh) 2015-08-12
EP2718273A4 (en) 2014-12-10

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