WO2011009059A3 - Method of treating or preventing cancer - Google Patents
Method of treating or preventing cancer Download PDFInfo
- Publication number
- WO2011009059A3 WO2011009059A3 PCT/US2010/042306 US2010042306W WO2011009059A3 WO 2011009059 A3 WO2011009059 A3 WO 2011009059A3 US 2010042306 W US2010042306 W US 2010042306W WO 2011009059 A3 WO2011009059 A3 WO 2011009059A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- cancer
- treating
- preventing
- inhibiting
- animal
- 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
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Classifications
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- 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
- A61K31/095—Sulfur, selenium, or tellurium compounds, e.g. thiols
- A61K31/10—Sulfides; Sulfoxides; Sulfones
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- 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
- A61K31/16—Amides, e.g. hydroxamic acids
- A61K31/165—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
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- 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
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/34—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide
- A61K31/343—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide condensed with a carbocyclic ring, e.g. coumaran, bufuralol, befunolol, clobenfurol, amiodarone
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- 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
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/35—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom
-
- 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
- A61K31/38—Heterocyclic compounds having sulfur as a ring hetero atom
- A61K31/381—Heterocyclic compounds having sulfur as a ring hetero atom having five-membered 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
- A61K31/40—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
- A61K31/403—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 condensed with carbocyclic rings, e.g. carbazole
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- 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
-
- 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
- A61K31/425—Thiazoles
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- 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
-
- 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
- A61K31/54—Heterocyclic 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
- A61K31/5415—Heterocyclic 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 ortho- or peri-condensed with carbocyclic ring systems, e.g. phenothiazine, chlorpromazine, piroxicam
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Epidemiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Disclosed is a method for inhibiting Akt, activating AMPK, inhibiting mTOR, treating or preventing development of cancer, and/or preventing progression of premalignant lesions to cancer in an animal comprising administering to the animal an effective amount of a compound as described herein, for example, NSC 743411, whose formula is set forth below. The method involves the use of these compounds as single agents or in combination with conventional chemotherapy, biological therapy, or radiation therapy. The invention further provides novel compounds and pharmaceutical compositions for use in treating or preventing development of cancer or preventing the progression of premalignant lesions into cancer. Also disclosed is a method of inhibiting CSF1R.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US22632809P | 2009-07-17 | 2009-07-17 | |
| US61/226,328 | 2009-07-17 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| WO2011009059A2 WO2011009059A2 (en) | 2011-01-20 |
| WO2011009059A3 true WO2011009059A3 (en) | 2011-04-21 |
Family
ID=42668073
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/US2010/042306 Ceased WO2011009059A2 (en) | 2009-07-17 | 2010-07-16 | Method of treating or preventing cancer |
Country Status (1)
| Country | Link |
|---|---|
| WO (1) | WO2011009059A2 (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI849808B (en) | 2022-03-18 | 2024-07-21 | 共信醫藥科技股份有限公司 | Use of pharmaceutical composition and chemotherapy agent in the manufacture of medicament for treating cancer |
| CN115073495B (en) * | 2022-08-09 | 2024-03-19 | 苏州大学 | An indoline compound and its preparation method |
Citations (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4845128A (en) * | 1984-06-27 | 1989-07-04 | Eli Lilly And Company | N([(4-trifluoromethylphenyl)amino]carbonyl)benzene sulfonamides |
| US5116874A (en) * | 1985-09-23 | 1992-05-26 | Eli Lilly And Company | Anti-tumor method and compounds |
| EP0550157A1 (en) * | 1991-12-20 | 1993-07-07 | Eli Lilly And Company | Antitumor compositions and methods of treatment |
| EP0602878A1 (en) * | 1992-12-10 | 1994-06-22 | Eli Lilly And Company | Diarylsulfonylureas and their use as antitumor agents |
| WO2005040101A1 (en) * | 2003-10-27 | 2005-05-06 | S*Bio Pte Ltd | Acylurea connected and sulfonylurea connected hydroxamates |
| EP1859797A1 (en) * | 2005-02-28 | 2007-11-28 | Eisai R&D Management Co., Ltd. | Novel concomitant use of sulfonamide compound with anti-cancer agent |
| WO2010005534A2 (en) * | 2008-06-30 | 2010-01-14 | H. Lee Moffitt Cancer Center And Research Institute, Inc. | Proteasome inhibitors for selectively inducing apoptosis in cancer cells |
| WO2010129596A1 (en) * | 2009-05-04 | 2010-11-11 | Agios Pharmaceuticals, Inc. | Pmk2 modulators for use in the treatment of cancer |
| WO2010130665A1 (en) * | 2009-05-12 | 2010-11-18 | F. Hoffmann-La Roche Ag | Azacyclic spiroderivatives as hsl inhibitors |
-
2010
- 2010-07-16 WO PCT/US2010/042306 patent/WO2011009059A2/en not_active Ceased
Patent Citations (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4845128A (en) * | 1984-06-27 | 1989-07-04 | Eli Lilly And Company | N([(4-trifluoromethylphenyl)amino]carbonyl)benzene sulfonamides |
| US5116874A (en) * | 1985-09-23 | 1992-05-26 | Eli Lilly And Company | Anti-tumor method and compounds |
| EP0550157A1 (en) * | 1991-12-20 | 1993-07-07 | Eli Lilly And Company | Antitumor compositions and methods of treatment |
| EP0602878A1 (en) * | 1992-12-10 | 1994-06-22 | Eli Lilly And Company | Diarylsulfonylureas and their use as antitumor agents |
| WO2005040101A1 (en) * | 2003-10-27 | 2005-05-06 | S*Bio Pte Ltd | Acylurea connected and sulfonylurea connected hydroxamates |
| EP1859797A1 (en) * | 2005-02-28 | 2007-11-28 | Eisai R&D Management Co., Ltd. | Novel concomitant use of sulfonamide compound with anti-cancer agent |
| WO2010005534A2 (en) * | 2008-06-30 | 2010-01-14 | H. Lee Moffitt Cancer Center And Research Institute, Inc. | Proteasome inhibitors for selectively inducing apoptosis in cancer cells |
| WO2010129596A1 (en) * | 2009-05-04 | 2010-11-11 | Agios Pharmaceuticals, Inc. | Pmk2 modulators for use in the treatment of cancer |
| WO2010130665A1 (en) * | 2009-05-12 | 2010-11-18 | F. Hoffmann-La Roche Ag | Azacyclic spiroderivatives as hsl inhibitors |
Non-Patent Citations (15)
| Title |
|---|
| AVDEENKO A P ET AL: "Thiocyanation of N-Arylsulfonyl-, N-Aroyl-, and N-(N-Arylsulfonyl)benzimidoyl)-1,4-benzoquinone Iminies", RUSSIAN JOURNAL OF ORGANIC CHEMISTRY, CONSULTANTS BUREAU, US, vol. 45, no. 3, 29 April 2009 (2009-04-29), pages 408 - 416, XP002586945, ISSN: 1070-4280 * |
| BAXTER I ET AL: "Preparation and some reactions of 6-arylsulphonimidobenzoxazol-2(3H)-one", JOURNAL OF THE CHEMICAL SOCIETY, SECTION C: ORGANIC CHEMISTRY, CHEMICAL SOCIETY. LETCHWORTH, GB, 1 January 1970 (1970-01-01), pages 850 - 853, XP008122990, ISSN: 0022-4952, DOI: DOI:10.1039/J39700000850 * |
| COLLINS I ET AL: "Structure-based design of isoquinoline-5-sulfonamide inhibitors of protein kinase B", BIOORGANIC & MEDICINAL CHEMISTRY, PERGAMON, GB, vol. 14, no. 4, 15 February 2006 (2006-02-15), pages 1255 - 1273, XP025133010, ISSN: 0968-0896, [retrieved on 20060215], DOI: DOI:10.1016/J.BMC.2005.09.055 * |
| D. A. GUERTIN, D. M. SABATINI: "Defining the role of mTOR in cancer", CANCER CELL, vol. 12, July 2007 (2007-07-01), pages 9 - 22, XP002599504 * |
| DATABASE REGISTRY [online] CHEMICAL ABSTRACTS SERVICE, COLUMBUS, OHIO, US; 15 April 2005 (2005-04-15), "Benzoic acid, 4-(1-piperidinylsulfonyl)-, 2-[[4-[(dimethylamino)sulfonyl]phenyl]amino]-2-oxoethyl ester", XP002599503, retrieved from STN accession no. RN 848580-83-6 * |
| DATABASE REGISTRY [Online] CHEMICAL ABSTRACTS SERVICE, COLUMBUS, OHIO, US; 30 December 2004 (2004-12-30), "Benzoic acid, 3-[(2,3-dihydro-1H-indol-1-yl)sulfonyl], 2-[(3-cyano-2-thienyl)amino]-2-oxoethyl ester", XP002599502, retrieved from STN accession no. RN 805306-56-3 * |
| DATABASE ZREGISTRY [online] CHEMICAL ABSTRACTS SERVICE, COLUMBUS, OHIO, US; 28 July 2005 (2005-07-28), ""Acetic acid, 2-[[4-[[(4-ethoxyphenyl)sulfonyl]imino]-1,4-dihydro-1-oxo-2-naphthalenyl]thio]-"", XP002615085, retrieved from STN accession no. RN 857494-31-6 * |
| FAIVRE S ET AL: "Current development of mTOR inhibitors as anticancer agents", NATURE REVIEWS. DRUG DISCOVERY, NATURE PUBLISHING GROUP, GB LNKD- DOI:10.1038/NRD2062, vol. 5, no. 8, 1 August 2006 (2006-08-01), pages 671 - 688, XP002587702, ISSN: 1474-1784 * |
| FUJITA, S. AND SANO K.: "reduction of quinones and quinonemonosulfonimides with N,N-diethylhydroxylamine", JOURNAL OF ORGANIC CHEMISTRY, vol. 44, no. 5, 1979, pages 2647 - 2649, XP007916530 * |
| HAYAKAWA ET AL: "Synthesis and biological evaluation of sulfonylhydrazone-substituted imidazo[1,2-a]pyridines as novel PI3 kinase p110alpha inhibitors", BIOORGANIC & MEDICINAL CHEMISTRY, PERGAMON, GB, vol. 15, no. 17, 19 July 2007 (2007-07-19), pages 5837 - 5844, XP022152373, ISSN: 0968-0896, DOI: DOI:10.1016/J.BMC.2007.05.070 * |
| LIU Q ET AL: "MTOR mediated anti-cancer drug discovery", DRUG DISCOVERY TODAY: THERAPEUTIC STRATEGIES 2009 ELSEVIER LTD GBR LNKD- DOI:10.1016/J.DDSTR.2009.12.001, vol. 6, no. 2, December 2009 (2009-12-01), pages 47 - 55, XP027103036, ISSN: 1740-6773 * |
| MORGENSZTERN D ET AL: "PI3K/Akt/mTOR pathway as a target for cancer therapy", ANTI-CANCER DRUGS, LIPPINCOTT WILLIAMS & WILKINS, US; NL LNKD- DOI:10.1097/01.CAD.0000173476.67239.3B, vol. 16, no. 8, 1 January 2005 (2005-01-01), pages 797 - 803, XP008092039, ISSN: 0959-4973 * |
| PIAO WENHUA ET AL: "Induction of G2/M phase arrest and apoptosis by a new synthetic anti-cancer agent, DW2282, in promyelocytic leukemia (HL-60) cells", BIOCHEMICAL PHARMACOLOGY, vol. 62, no. 11, 1 December 2001 (2001-12-01), pages 1439 - 1447, XP007916529, ISSN: 0006-2952 * |
| SHERMAN E S ET AL: "Pyrrolidine and piperidine formation via copper(II) carboxylate-promoted intramolecular carboamination of unactivated olefins: Diastereoselectivity and mechanism", JOURNAL OF ORGANIC CHEMISTRY 20070511 AMERICAN CHEMICAL SOCIETY US, vol. 72, no. 10, 11 May 2007 (2007-05-11), pages 3896 - 3905, XP002615086, DOI: DOI:10.1021/JO070321U * |
| SUN E ET AL: "Proton release from HeLa cells and alkalization of cytoplasm induced by diferric transferrin or ferricyanide and its inhibition by the diarylsulfonylurea antitumor drug N-(4-methylphenylsulfonyl)-N'-(4-chlorophenyl) urea (LY181984)", BIOCHEMICAL PHARMACOLOGY 1995 US LNKD- DOI:10.1016/0006-2952(95)02050-0, vol. 50, no. 9, 1995, pages 1461 - 1468, XP007916528, ISSN: 0006-2952 * |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2011009059A2 (en) | 2011-01-20 |
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