WO2009065131A1 - Carboxamide, sulfonamide and amine compounds for metabolic disorders - Google Patents

Carboxamide, sulfonamide and amine compounds for metabolic disorders Download PDF

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Publication number
WO2009065131A1
WO2009065131A1 PCT/US2008/083801 US2008083801W WO2009065131A1 WO 2009065131 A1 WO2009065131 A1 WO 2009065131A1 US 2008083801 W US2008083801 W US 2008083801W WO 2009065131 A1 WO2009065131 A1 WO 2009065131A1
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WO
WIPO (PCT)
Prior art keywords
alkyl
piperidin
yloxy
trifluoromethyl
phenyl
Prior art date
Legal status (The legal status 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 status listed.)
Ceased
Application number
PCT/US2008/083801
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English (en)
French (fr)
Inventor
Hui Hong
Xiang Xu
Jiaxin Yu
Rajinder Singh
Ihab S. Darwish
Sambaiah Thota
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Rigel Pharmaceuticals Inc
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Rigel 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
Priority to CN200880124960.1A priority Critical patent/CN101910131B/zh
Priority to MX2014005186A priority patent/MX382569B/es
Priority to EA201070619A priority patent/EA019509B1/ru
Priority to AU2008322426A priority patent/AU2008322426C1/en
Priority to EP08848677.4A priority patent/EP2231600B1/en
Priority to MX2010005298A priority patent/MX2010005298A/es
Priority to JP2010534263A priority patent/JP5544296B2/ja
Priority to NZ585298A priority patent/NZ585298A/xx
Priority to CA2705947A priority patent/CA2705947C/en
Priority to BRPI0820171A priority patent/BRPI0820171B8/pt
Priority to ES08848677.4T priority patent/ES2552733T3/es
Priority to HK11102635.4A priority patent/HK1148525B/en
Application filed by Rigel Pharmaceuticals Inc filed Critical Rigel Pharmaceuticals Inc
Publication of WO2009065131A1 publication Critical patent/WO2009065131A1/en
Priority to IL205624A priority patent/IL205624A/en
Priority to ZA2010/03412A priority patent/ZA201003412B/en
Anticipated expiration legal-status Critical
Priority to AU2014202572A priority patent/AU2014202572B2/en
Priority to AU2017202766A priority patent/AU2017202766B2/en
Ceased legal-status Critical Current

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic 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
    • C07D401/14—Heterocyclic 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 three or more hetero rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic 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
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445—Non condensed piperidines, e.g. piperocaine
    • A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • A61K31/4545—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/06—Antihyperlipidemics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00—Drugs for disorders of the blood or the extracellular fluid
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/10—Drugs 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members 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
    • C07D211/40—Oxygen atoms
    • C07D211/44—Oxygen atoms attached in position 4
    • C07D211/46—Oxygen atoms attached in position 4 having a hydrogen atom as the second substituent in position 4
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members 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
    • C07D211/56—Nitrogen atoms
    • C07D211/58—Nitrogen atoms attached in position 4
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic 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
    • C07D401/02—Heterocyclic 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
    • C07D401/12—Heterocyclic 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic 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
    • C07D405/14—Heterocyclic 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 three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings

Definitions

  • AMPK switches on catabolic pathways (such as fatty acid oxidation and glycolysis) and switches off ATP-consuming pathways (such as lipogenesis).
  • Adiponectin improves insulin sensitivity by directly stimulating glucose uptake in adipocytes and muscle and by increasing fatty acid oxidation in liver and muscle, resulting in reduced circulating fatty acid levels and reduced intracellular triglyceride contents.
  • adiponectin decreases glycogen concentration by reducing the activity of glycogen synthase.
  • Adiponectin also plays a protective role against inflammation and atherosclerosis.
  • each R 20 , R 22 and R 23 is independently Ar or Het
  • each Ar is an optionally substituted aryl
  • each Het is an optionally substituted heteroaryl
  • each Cak is an optionally substituted cycloalkyl
  • each Hca is an optionally substituted heterocycloalkyl
  • each alkyl is optionally substituted.
  • E is -C(O)-, -S(O) 2 - or a single bond, provided that when "B" is phenyl, E is not -C(O)-;
  • Q is -(C 0 -C 3 alkyl)-, in which each carbon of the -(C 0 -Cs alkyl)- is optionally and independently substituted with one or two R 16 , or -S(O) 2 -; the ring system denoted by "A" is heteroaryl, aryl, cycloalkyl or heterocycloalkyl; each R 5 is independently selected from -(Ci-C 6 alkyl), -(Ci-C 6 haloalkyl), -(C 0 -C 6 alkyl)-Ar, -(C 0 -C 6 alkyl)-Het, -(C 0 -C 6 alkyl)-Cak, -(C 0 -C 6 alkyl)-Hca, -(C 0 -C 6 alkyl)-L-R 7 , -(C 0 -C 6 alkyl)-NR 8 R 9 , -(C 0
  • each R 7 , R 8 and R 10 is independently selected from H, -(Ci-C 6 alkyl), -(Ci-C 6 haloalkyl), -(C 0 -C 6 alkyl)-L-(C 0 -C 6 alkyl), -(C 0 -C 6 alkyl)-NR 9 (C 0 -C 6 alkyl), -(C 0 -C 6 alkyl)-O-(C 0 -C 6 alkyl), -(C 0 -C 6 alkyl)-C(O)-(C 0 -C 6 alkyl), and -(C 0 -C 6 alkyl)-S(O) 0 _ 2 -(C 0 -C 6 alkyl), and in which no alkyl or haloalkyl
  • the presently disclosed compounds include S-oxidized forms of the benzothiophene compounds described (e.g., with reference to structural formulae (XVI) and
  • R 2 has the structure , in which b is 0, 1, 2, 3 or 4, and each R 21 is independently selected from -(Ci-C 6 alkyl), -(Ci-C 6 haloalkyl), -(C 0 -C 6 alkyl)-Ar, -(C 0 -C 6 alkyl)-Het, -(C 0 -C 6 alkyl)-Cak, -(C 0 -C 6 alkyl)-Hca, -(C 0 -C 6 alkyl)-L-R 7 , -(C 0 -C 6 alkyl)-NR 8 R 9 , -(C 0 -C 6 alkyl)-OR 10 , -(C 0 -C 6 alkyl)-C(O)R 10 , -(C 0 -C 6 alkyl)-S(O) 0 _ 2 R 10 , -halogen, -NO 2 and -CN, and
  • each R 4 is independently selected from -(C 1 -C 6 alkyl), -(C r C 6 haloalkyl) (e.g., trifluoromethyl), -(C 0 -C 6 alkyl)-L-R 7 , -(C 0 -C 6 alkyl)-NR 8 R 9 , -(C 0 -C 6 alkyl)-OR 10 , -(C 0 -C 6 alkyl)-C(O)R 10 , -(C 0 -C 6 alkyl)-S(O) 0 _ 2 R 10 , -halogen, -NO 2 and -CN, in which each R 7 , R 8 and R 10 is independently selected from H, -(Ci-C 6 alkyl), -(Ci-C 6 haloalkyl), -(C 0
  • the presently disclosed compounds have the structural formula (XXXIX):
  • R 25 can be, for example, -Cl, -F, cyano, -C(O)CH 3 , -C(O)OH, -C(O)NH 2 , trifiuoromethyl, difiuoromethyl, difluoromethoxy or trifluoromethoxy.
  • the presently disclosed compounds have the structural formula (LIII):
  • the presently disclosed compounds have the structural formula (LIX):
  • R 14 is halo (e.g., -Cl or -F), cyano unsubstituted -(C1-C4 alkyl) (e.g., methyl or ethyl), unsubstituted -(Ci-C 4 haloakyl) (e.g., trifluoromethyl).
  • no R 14 is substituted on the furano carbon.
  • R 18 is H, -(Ci-C 6 alkyl), -(Ci-C 6 haloalkyl) (e.g., trifluoromethyl), -(C 0 -C 6 alkyl)-L-(C 0 -C 6 alkyl), -(C 0 -C 6 alkyl)-NR 9 (C 0 -C 6 alkyl), -(C 0 -C 6 alkyl)-O-(C 0 -C 6 alkyl), -(C 0 -C 6 alkyl)-C(O)-(C 0 -C 6 alkyl) and -(C 0 -C 6 alkyl)-S(O) 0 _ 2 -(C 0 -C 6 alkyl), in which no alkyl or haloalkyl is substituted with an aryl-, heteroaryl-,
  • the presently disclosed compounds have the structural formula (LXXV):
  • the presently disclosed compounds have the structural formula (XC):
  • R 11 , R 12 and R 13 are not H.
  • the presently disclosed compounds have the structural formula (XCII): in which Q is -CH 2 - or a single bond; G is CH 2 or C(O); R 3 is as described above with respect to structural formulae (I) and (XXXVIII) (e.g., absent or halo); R 14 is as described above with respect to structural formula (I) (e.g., absent, methyl or halo); and R , 11 , R , 12 and R , 13 are independently selected from H, halo, cyano, -(Ci-C 4 haloalkyl), -0-(Ci-C 4 haloalkyl), -(Ci-C 4 alkyl), -0-(Ci-C 4 alkyl), -C(O)-(C 0 -C 4 alkyl), -C(O)O-(C 0 -
  • Alkyl and alkyl groups may be straight or branched and depending on context, may be a monovalent radical or a divalent radical (i.e., an alkylene group).
  • a divalent radical i.e., an alkylene group.
  • the group is simply a single covalent bond if it is a divalent radical or is a hydrogen atom if it is a monovalent radical.
  • the moiety "-(Co-C 6 alkyl)-Ar" signifies connection of an optionally substituted aryl through a single bond or an alkylene bridge having from 1 to 6 carbons.
  • oxa means a divalent oxygen radical in a chain, sometimes designated as -O-.
  • Substituent groups for hydrogens on nitrogen atoms in "substituted" heteroalkyl and heterocycloalkyl groups are, unless otherwise specified, -R 60 , -0 " M + , -OR 70 , -SR 70 , -S M + , -NR 80 R 80 , trihalomethyl, -CF 3 , -CN, -NO, -NO 2 , -S(O) 2 R 70 , -S(O) 2 O M + , -S(O) 2 OR 70 , -OS(O) 2 R 70 , -OS(O) 2 O M + , -OS(O) 2 OR 70 , -P(O)(O " ) 2 (M + ) 2 , -P(O)(OR 70 )O " M + , -P(O)(OR 70 XOR 70 ), -C(O)R 70 , -C(S)R 70 , -C(C(S
  • adjuvants such as local anesthetics, preservatives and buffering agents can be dissolved in the vehicle.
  • the compounds disclosed herein can be made using procedures familiar to the person of ordinary skill in the art and as described herein.
  • compounds of structural formulae (II)-(VI) can be prepared according to Scheme 1, below, or analogous synthetic schemes:
  • Step 2 tert-but ⁇ l 4-(5-(l-(4-(trifluoromethyl)phenyl)piperidin-4-yloxy)-2,3-dihvdro- lH-inden- 1 -ylamino)piperidine- 1 -carboxylate
  • Step 4 1 -(4-fluorobenzyl)-iV-(5 -( 1 -(4-(trifluoromethyl)phenyl)piperidin-4-yloxy)-2,3 - dihydro- lH-inden- 1 -yl)piperidin-4-amine

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Diabetes (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Cardiology (AREA)
  • Emergency Medicine (AREA)
  • Endocrinology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Epidemiology (AREA)
  • Vascular Medicine (AREA)
  • Urology & Nephrology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Hydrogenated Pyridines (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
PCT/US2008/083801 2007-11-16 2008-11-17 Carboxamide, sulfonamide and amine compounds for metabolic disorders Ceased WO2009065131A1 (en)

Priority Applications (16)

Application Number Priority Date Filing Date Title
MX2014005186A MX382569B (es) 2007-11-16 2008-11-17 Compuesto de carboxamida, sulfonamida y amina para trastornos metabolicos.
EA201070619A EA019509B1 (ru) 2007-11-16 2008-11-17 Карбоксамидные, сульфонамидные и аминовые соединения от метаболических нарушений
AU2008322426A AU2008322426C1 (en) 2007-11-16 2008-11-17 Carboxamide, sulfonamide and amine compounds for metabolic disorders
EP08848677.4A EP2231600B1 (en) 2007-11-16 2008-11-17 Carboxamide, sulfonamide and amine compounds for metabolic disorders
MX2010005298A MX2010005298A (es) 2007-11-16 2008-11-17 Compuestos de carboxamida, sulfonamida y amina para trastornos metabolicos.
JP2010534263A JP5544296B2 (ja) 2007-11-16 2008-11-17 代謝障害のためのカルボキサミド、スルホンアミド、およびアミン化合物
NZ585298A NZ585298A (en) 2007-11-16 2008-11-17 Carboxamide, sulfonamide and amine compounds for metabolic disorders
BRPI0820171A BRPI0820171B8 (pt) 2007-11-16 2008-11-17 compostos de carboxamida, sulfonamida e amina para distúrbios metabólicos, composição farmacêutica, e, uso dos mesmos
CA2705947A CA2705947C (en) 2007-11-16 2008-11-17 Carboxamide, sulfonamide and amine compounds for metabolic disorders
CN200880124960.1A CN101910131B (zh) 2007-11-16 2008-11-17 甲酰胺、磺酰胺和胺化合物及其使用方法
HK11102635.4A HK1148525B (en) 2007-11-16 2008-11-17 Carboxamide, sulfonamide and amine compounds for metabolic disorders
ES08848677.4T ES2552733T3 (es) 2007-11-16 2008-11-17 Compuestos de carboxamida, sulfonamida y amina para trastornos metabólicos
IL205624A IL205624A (en) 2007-11-16 2010-05-09 Carboxamide, Sulfonamide and Amine Compounds, Their Pharmaceutical Preparations
ZA2010/03412A ZA201003412B (en) 2007-11-16 2010-05-14 Carboxamide, sulfonamide and amine compounds for metabolic disorders
AU2014202572A AU2014202572B2 (en) 2007-11-16 2014-05-13 Carboxamide, sulfonamide and amine compounds for metabolic disorders
AU2017202766A AU2017202766B2 (en) 2007-11-16 2017-04-27 Carboxamide, sulfonamide and amine compounds for metabolic disorders

Applications Claiming Priority (10)

Application Number Priority Date Filing Date Title
US98872107P 2007-11-16 2007-11-16
US60/988,721 2007-11-16
US99055807P 2007-11-27 2007-11-27
US99055407P 2007-11-27 2007-11-27
US60/990,558 2007-11-27
US60/990,554 2007-11-27
US99118907P 2007-11-29 2007-11-29
US60/991,189 2007-11-29
US1392407P 2007-12-14 2007-12-14
US61/013,924 2007-12-14

Publications (1)

Publication Number Publication Date
WO2009065131A1 true WO2009065131A1 (en) 2009-05-22

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PCT/US2008/083801 Ceased WO2009065131A1 (en) 2007-11-16 2008-11-17 Carboxamide, sulfonamide and amine compounds for metabolic disorders

Country Status (15)

Country Link
US (3) US8119809B2 (https=)
EP (1) EP2231600B1 (https=)
JP (1) JP5544296B2 (https=)
KR (1) KR101573091B1 (https=)
CN (1) CN101910131B (https=)
AU (3) AU2008322426C1 (https=)
BR (1) BRPI0820171B8 (https=)
CA (1) CA2705947C (https=)
EA (1) EA019509B1 (https=)
ES (1) ES2552733T3 (https=)
IL (1) IL205624A (https=)
MX (2) MX382569B (https=)
NZ (1) NZ585298A (https=)
WO (1) WO2009065131A1 (https=)
ZA (1) ZA201003412B (https=)

Cited By (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2011107494A1 (de) 2010-03-03 2011-09-09 Sanofi Neue aromatische glykosidderivate, diese verbindungen enthaltende arzneimittel und deren verwendung
WO2011115106A1 (ja) * 2010-03-16 2011-09-22 国立大学法人 東京大学 擬似運動療法のための医薬
WO2011123681A1 (en) * 2010-03-31 2011-10-06 Rigel Pharmaceuticals, Inc. Methods for using carboxamide, sulfonamide and amine compounds
WO2011142359A1 (ja) * 2010-05-10 2011-11-17 日産化学工業株式会社 スピロ化合物及びアディポネクチン受容体活性化薬
WO2011161030A1 (de) 2010-06-21 2011-12-29 Sanofi Heterocyclisch substituierte methoxyphenylderivate mit oxogruppe, verfahren zu ihrer herstellung und ihre verwendung als gpr40 rezeptor modulatoren
WO2012004270A1 (de) 2010-07-05 2012-01-12 Sanofi Spirocyclisch substituierte 1,3-propandioxidderivate, verfahren zu ihrer herstellung und ihre verwendung als arzneimittel
WO2012004269A1 (de) 2010-07-05 2012-01-12 Sanofi ( 2 -aryloxy -acetylamino) - phenyl - propionsäurederivate, verfahren zu ihrer herstellung und ihre verwendung als arzneimittel
WO2012010413A1 (de) 2010-07-05 2012-01-26 Sanofi Aryloxy-alkylen-substituierte hydroxy-phenyl-hexinsäuren, verfahren zu ihrer herstellung und ihre verwendung als arzneimittel
US8153814B2 (en) 2009-01-12 2012-04-10 Pfizer Limited Sulfonamide derivatives
WO2012094173A1 (en) 2011-01-06 2012-07-12 Rigel Pharmaceuticals, Inc. Whole blood assay for measuring ampk activation
US8252829B2 (en) 2009-06-05 2012-08-28 Link Medicine Corporation Aminopyrrolidinone derivatives and uses thereof
CN102666485A (zh) * 2009-09-21 2012-09-12 霍夫曼-拉罗奇有限公司 烯烃羟吲哚衍生物及其用于治疗肥胖症，糖尿病和高脂血症的应用
WO2013037390A1 (en) 2011-09-12 2013-03-21 Sanofi 6-(4-hydroxy-phenyl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors
WO2013045413A1 (en) 2011-09-27 2013-04-04 Sanofi 6-(4-hydroxy-phenyl)-3-alkyl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors
CN103201267A (zh) * 2010-07-29 2013-07-10 里格尔药品股份有限公司 Ampk-激活性杂环化合物以及其使用方法
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