WO2005097103A3 - Diabetes and metabolic syndrome therapy utilizing cathepsin b inhibitors - Google Patents

Diabetes and metabolic syndrome therapy utilizing cathepsin b inhibitors Download PDF

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Publication number
WO2005097103A3
WO2005097103A3 PCT/US2005/011065 US2005011065W WO2005097103A3 WO 2005097103 A3 WO2005097103 A3 WO 2005097103A3 US 2005011065 W US2005011065 W US 2005011065W WO 2005097103 A3 WO2005097103 A3 WO 2005097103A3
Authority
WO
WIPO (PCT)
Prior art keywords
cathepsin
diabetes
inhibitors
metabolic syndrome
therapy utilizing
Prior art date
Application number
PCT/US2005/011065
Other languages
French (fr)
Other versions
WO2005097103A2 (en
Inventor
Samuel E Broder
Robert M Rydzewski
Original Assignee
Axys Pharm Inc
Samuel E Broder
Robert M Rydzewski
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 Axys Pharm Inc, Samuel E Broder, Robert M Rydzewski filed Critical Axys Pharm Inc
Publication of WO2005097103A2 publication Critical patent/WO2005097103A2/en
Publication of WO2005097103A3 publication Critical patent/WO2005097103A3/en

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Classifications

    • 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
    • A61K31/495—Heterocyclic 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
    • A61K31/4965—Non-condensed pyrazines
    • 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
    • A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
    • A61K31/19—Carboxylic acids, e.g. valproic acid
    • A61K31/195—Carboxylic acids, e.g. valproic acid having an amino group
    • A61K31/197—Carboxylic acids, e.g. valproic acid having an amino group the amino and the carboxyl groups being attached to the same acyclic carbon chain, e.g. gamma-aminobutyric acid [GABA], beta-alanine, epsilon-aminocaproic acid, pantothenic acid
    • A61K31/198—Alpha-aminoacids, e.g. alanine, edetic acids [EDTA]
    • 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
    • A61K31/275—Nitriles; Isonitriles
    • 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
    • A61K31/325—Carbamic acids; Thiocarbamic acids; Anhydrides or salts thereof
    • 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
    • A61K31/40—Heterocyclic 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
    • A61K31/401—Proline; Derivatives thereof, e.g. captopril
    • 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
    • A61K31/41—Heterocyclic 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
    • A61K31/4196—1,2,4-Triazoles
    • 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
    • A61K31/41—Heterocyclic 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
    • A61K31/42—Oxazoles
    • A61K31/423—Oxazoles condensed with carbocyclic rings
    • 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

Abstract

The present invention is directed to the treatment of Type II diabetes by administering a cathepsin B inhibitor(s).
PCT/US2005/011065 2004-04-01 2005-04-01 Diabetes and metabolic syndrome therapy utilizing cathepsin b inhibitors WO2005097103A2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US55893304P 2004-04-01 2004-04-01
US60/558,933 2004-04-01

Publications (2)

Publication Number Publication Date
WO2005097103A2 WO2005097103A2 (en) 2005-10-20
WO2005097103A3 true WO2005097103A3 (en) 2006-08-10

Family

ID=34979661

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2005/011065 WO2005097103A2 (en) 2004-04-01 2005-04-01 Diabetes and metabolic syndrome therapy utilizing cathepsin b inhibitors

Country Status (1)

Country Link
WO (1) WO2005097103A2 (en)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8344029B2 (en) * 2005-07-19 2013-01-01 Daiichi Sankyo Company, Limited Substituted propanamide derivative and pharmaceutical composition containing the same
EP2089383B1 (en) 2006-11-09 2015-09-16 Probiodrug AG 3-hydr0xy-1,5-dihydr0-pyrr0l-2-one derivatives as inhibitors of glutaminyl cyclase for the treatment of ulcer, cancer and other diseases
EP2091948B1 (en) 2006-11-30 2012-04-18 Probiodrug AG Novel inhibitors of glutaminyl cyclase
EP2117540A1 (en) 2007-03-01 2009-11-18 Probiodrug AG New use of glutaminyl cyclase inhibitors
ES2533484T3 (en) 2007-04-18 2015-04-10 Probiodrug Ag Thiourea derivatives as glutaminyl cyclase inhibitors
WO2010069069A1 (en) * 2008-12-17 2010-06-24 Merck Frosst Canada Ltd. Cathepsin b inhibitors
EP2408455B1 (en) 2009-03-20 2014-06-04 INSERM (Institut National de la Santé et de la Recherche Médicale) Inhibitors of cathepsin S for prevention or treatment of obesity-associated disorders
ES2548913T3 (en) 2009-09-11 2015-10-21 Probiodrug Ag Heterocyclic derivatives such as glutaminyl cyclase inhibitors
US9181233B2 (en) 2010-03-03 2015-11-10 Probiodrug Ag Inhibitors of glutaminyl cyclase
EA022420B1 (en) 2010-03-10 2015-12-30 Пробиодруг Аг Heterocyclic inhibitors of glutaminyl cyclase (qc, ec 2.3.2.5)
WO2011131748A2 (en) 2010-04-21 2011-10-27 Probiodrug Ag Novel inhibitors
DK2686313T3 (en) 2011-03-16 2016-05-02 Probiodrug Ag Benzimidazole derivatives as inhibitors of glutaminyl cyclase
JP2018515597A (en) * 2015-04-07 2018-06-14 イーエルエイ ファーマ リミテッドＥｌａ Ｐｈａｒｍａ Ｌｔｄ Composition for the treatment and / or prevention of cell and / or tissue necrosis specifically targeting cathepsin C and / or CELA1 and / or CELA3A and / or enzymes structurally related thereto
ES2812698T3 (en) 2017-09-29 2021-03-18 Probiodrug Ag Glutaminyl cyclase inhibitors

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004026851A1 (en) * 2002-09-20 2004-04-01 Axys Pharmaceuticals, Inc. 3-(3,5-disubstituted-4-hydroxyphenyl)propionamide derivatives as cathepsin b inhibitors

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004026851A1 (en) * 2002-09-20 2004-04-01 Axys Pharmaceuticals, Inc. 3-(3,5-disubstituted-4-hydroxyphenyl)propionamide derivatives as cathepsin b inhibitors

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
CUMMINS, CAROLYN L. ET AL: "Unmasking the dynamic interplay between intestinal P-glycoprotein and CYP3A4", JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS , 300(3), 1036-1045 CODEN: JPETAB; ISSN: 0022-3565, 2002, XP002379538 *
SWEENEY DEACON ET AL: "Antidiabetic and antimalarial biguanide drugs are metal-interactive antiproteolytic agents.", BIOCHEMICAL PHARMACOLOGY, vol. 66, no. 4, 15 August 2003 (2003-08-15), pages 663 - 677, XP008063830, ISSN: 0006-2952 *

Also Published As

Publication number Publication date
WO2005097103A2 (en) 2005-10-20

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