WO2017123809A1 - Compounds for inhibiting cancer and virus - Google Patents
Compounds for inhibiting cancer and virus Download PDFInfo
- Publication number
- WO2017123809A1 WO2017123809A1 PCT/US2017/013253 US2017013253W WO2017123809A1 WO 2017123809 A1 WO2017123809 A1 WO 2017123809A1 US 2017013253 W US2017013253 W US 2017013253W WO 2017123809 A1 WO2017123809 A1 WO 2017123809A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- cancer
- compound
- pharmaceutically acceptable
- solvate
- enantiomer
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H15/00—Compounds containing hydrocarbon or substituted hydrocarbon radicals directly attached to hetero atoms of saccharide radicals
- C07H15/20—Carbocyclic rings
- C07H15/203—Monocyclic carbocyclic rings other than cyclohexane rings; Bicyclic carbocyclic ring systems
-
- 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
- A61K31/166—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide having the carbon of a carboxamide group directly attached to the aromatic ring, e.g. procainamide, procarbazine, metoclopramide, labetalol
-
- 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
- A61K31/21—Esters, e.g. nitroglycerine, selenocyanates
- A61K31/215—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids
- A61K31/216—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acids having aromatic rings, e.g. benactizyne, clofibrate
-
- 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
- A61K31/21—Esters, e.g. nitroglycerine, selenocyanates
- A61K31/215—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids
- A61K31/22—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acyclic acids, e.g. pravastatin
- A61K31/222—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acyclic acids, e.g. pravastatin with compounds having aromatic groups, e.g. dipivefrine, ibopamine
-
- 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
- A61K31/435—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
- A61K31/4409—Non condensed pyridines; Hydrogenated derivatives thereof only substituted in position 4, e.g. isoniazid, iproniazid
-
- 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
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/7028—Compounds having saccharide radicals attached to non-saccharide compounds by glycosidic linkages
- A61K31/7034—Compounds having saccharide radicals attached to non-saccharide compounds by glycosidic linkages attached to a carbocyclic compound, e.g. phloridzin
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C235/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms
- C07C235/42—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings and singly-bound oxygen atoms bound to the same carbon skeleton
- C07C235/44—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings and singly-bound oxygen atoms bound to the same carbon skeleton with carbon atoms of carboxamide groups and singly-bound oxygen atoms bound to carbon atoms of the same non-condensed six-membered aromatic ring
- C07C235/58—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings and singly-bound oxygen atoms bound to the same carbon skeleton with carbon atoms of carboxamide groups and singly-bound oxygen atoms bound to carbon atoms of the same non-condensed six-membered aromatic ring with carbon atoms of carboxamide groups and singly-bound oxygen atoms, bound in ortho-position to carbon atoms of the same non-condensed six-membered aromatic ring
- C07C235/64—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings and singly-bound oxygen atoms bound to the same carbon skeleton with carbon atoms of carboxamide groups and singly-bound oxygen atoms bound to carbon atoms of the same non-condensed six-membered aromatic ring with carbon atoms of carboxamide groups and singly-bound oxygen atoms, bound in ortho-position to carbon atoms of the same non-condensed six-membered aromatic ring having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a six-membered aromatic ring
-
- 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
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
Definitions
- ZIKV a mosquito-borne flavivirus
- a reference provides in vitro data suggesting the use of niclosamide in the inhibition of Zika virus infection (Nature Medicine, published online 29 August 2016; doi: 10.1038/nm.4184).
- niclosamide in the inhibition of Zika virus infection
- the invention is based on, at least in part, a potential therapeutic target in human cancer.
- the compounds of the invention can be used as anti-Zika viral agent.
- resolution refers to the separation or concentration or depletion of one of the two enantiomeric forms of a molecule.
- n is an integer of 1 to 5;
- R 3 is CF 3 , F, CI, Br or NO2.
- R 3 is CF 3 , CI or N0 2 .
- Scheme 1 describes the synthesis of a series of the compounds of the invention (2- 4).
- the commercially available compound 1 was reacted with 2,3,4,6-tetra-O-acetyl-a-D- glucopyranosyl bromide in the presence of TBAB and DIPEA, and was subject to the deprotection of acetyl groups carried out by Amberlite ® under basic conditions to afford the glycoside 2.
- the reaction of compound 1 with bromomethyl acetate in the presence of K2CO3 provided compound 3.
- compound 1 was reacted with 1-chlorocarbonyl 4-piperidinopiperidine, yielding compound 4.
- compound 1 was reacted with DMF in the presence of CuCl, 70% /-BuOOH to afford compound 4.
- a FZD-binding agent and a second therapeutic agent may be administered in any order or concurrently.
- the FZD-binding agents will be administered to patients that have previously undergone treatment with the second therapeutic agent.
- the FZD-binding agent and the second therapeutic agent will be administered substantially simultaneously or concurrently.
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Molecular Biology (AREA)
- Emergency Medicine (AREA)
- Genetics & Genomics (AREA)
- Engineering & Computer Science (AREA)
- Biochemistry (AREA)
- Biotechnology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Compounds Containing Sulfur Atoms (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Hydrogenated Pyridines (AREA)
- Pyridine Compounds (AREA)
- Saccharide Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Priority Applications (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US16/069,100 US10745433B2 (en) | 2016-01-12 | 2017-01-12 | Compounds for inhibiting cancer and virus |
| EP17738972.3A EP3402800A4 (en) | 2016-01-12 | 2017-01-12 | COMPOUNDS FOR INHIBITING CANCER AND VIRUSES |
| CA3011289A CA3011289A1 (en) | 2016-01-12 | 2017-01-12 | Compounds for inhibiting cancer and virus |
| CN201780006499.9A CN108884123A (zh) | 2016-01-12 | 2017-01-12 | 抑制癌症及病毒的化合物 |
| JP2018536167A JP2019506382A (ja) | 2016-01-12 | 2017-01-12 | 癌及びウイルスを阻害するための化合物 |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201662277653P | 2016-01-12 | 2016-01-12 | |
| US62/277,653 | 2016-01-12 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2017123809A1 true WO2017123809A1 (en) | 2017-07-20 |
Family
ID=59311465
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/US2017/013253 Ceased WO2017123809A1 (en) | 2016-01-12 | 2017-01-12 | Compounds for inhibiting cancer and virus |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US10745433B2 (https=) |
| EP (1) | EP3402800A4 (https=) |
| JP (1) | JP2019506382A (https=) |
| CN (1) | CN108884123A (https=) |
| CA (1) | CA3011289A1 (https=) |
| TW (1) | TWI638825B (https=) |
| WO (1) | WO2017123809A1 (https=) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2017223491A1 (en) * | 2016-06-23 | 2017-12-28 | Health Research, Inc. | Pharmaceutical compositions with antiflaviviral activity |
| US11384114B2 (en) | 2016-12-09 | 2022-07-12 | Warsaw Orthopedic, Inc. | Polymorphic forms of an oxysterol and methods of making them |
| CN111518147A (zh) * | 2020-04-29 | 2020-08-11 | 华东理工大学 | 苯甲酰苯胺类化合物及在制备铜绿假单胞菌抑制剂的增敏剂中的应用 |
| US11767303B2 (en) | 2020-07-24 | 2023-09-26 | Health Research, Inc. | Compounds and methods for inhibiting viral replication and methods of treating and preventing flaviviral infections |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20070123493A1 (en) * | 2003-12-26 | 2007-05-31 | Chugai Seiyaku Kabushiki Kaisha | Benzamide derivative |
| US20080161324A1 (en) * | 2006-09-14 | 2008-07-03 | Johansen Lisa M | Compositions and methods for treatment of viral diseases |
| WO2010101648A1 (en) * | 2009-03-06 | 2010-09-10 | Wood Richard D | Glutamate receptor modulators and therapeutic agents |
| CN103130696A (zh) * | 2013-03-21 | 2013-06-05 | 山东大学 | 邻氨基苯甲酰胺类化合物及其制备方法与应用 |
| US20150361031A1 (en) * | 2013-01-15 | 2015-12-17 | Board Of Regents, The University Of Texas System | Stat3 inhibitor |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE150471C (https=) * | ||||
| DD150471A1 (de) * | 1979-07-02 | 1981-09-02 | Konrad Schwabe | Verfahren zur herstellung von 5-bromsalizyl-4'-chloranilid-0-glykosiden |
| US6555519B2 (en) * | 2000-03-30 | 2003-04-29 | Bristol-Myers Squibb Company | O-glucosylated benzamide SGLT2 inhibitors and method |
| CA2488363C (en) * | 2002-06-06 | 2011-01-04 | Institute Of Medicinal Molecular Design, Inc. | O-substituted hydroxyaryl derivatives |
| AU2003249244A1 (en) * | 2002-07-15 | 2004-02-02 | Combinatorx, Incorporated | Methods for the treatment of neoplasms |
| ES2647072T3 (es) | 2011-04-18 | 2017-12-19 | Max-Delbrück-Centrum Für Molekulare Medizin In Der Helmholtz-Gemeinschaft | Niclosamida para el tratamiento de la metástasis en el cáncer |
| WO2014023329A1 (en) | 2012-08-06 | 2014-02-13 | Life And Brain Gmbh | Niclosamide and its derivatives for use in the treatment of solid tumors |
| CN104771386A (zh) | 2014-01-10 | 2015-07-15 | 中国科学院广州生物医药与健康研究院 | 苯甲酰胺类化合物及其应用 |
-
2017
- 2017-01-12 CN CN201780006499.9A patent/CN108884123A/zh active Pending
- 2017-01-12 CA CA3011289A patent/CA3011289A1/en not_active Abandoned
- 2017-01-12 TW TW106101068A patent/TWI638825B/zh not_active IP Right Cessation
- 2017-01-12 JP JP2018536167A patent/JP2019506382A/ja active Pending
- 2017-01-12 WO PCT/US2017/013253 patent/WO2017123809A1/en not_active Ceased
- 2017-01-12 EP EP17738972.3A patent/EP3402800A4/en not_active Withdrawn
- 2017-01-12 US US16/069,100 patent/US10745433B2/en active Active
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20070123493A1 (en) * | 2003-12-26 | 2007-05-31 | Chugai Seiyaku Kabushiki Kaisha | Benzamide derivative |
| US20080161324A1 (en) * | 2006-09-14 | 2008-07-03 | Johansen Lisa M | Compositions and methods for treatment of viral diseases |
| WO2010101648A1 (en) * | 2009-03-06 | 2010-09-10 | Wood Richard D | Glutamate receptor modulators and therapeutic agents |
| US20150361031A1 (en) * | 2013-01-15 | 2015-12-17 | Board Of Regents, The University Of Texas System | Stat3 inhibitor |
| CN103130696A (zh) * | 2013-03-21 | 2013-06-05 | 山东大学 | 邻氨基苯甲酰胺类化合物及其制备方法与应用 |
Non-Patent Citations (1)
| Title |
|---|
| See also references of EP3402800A4 * |
Also Published As
| Publication number | Publication date |
|---|---|
| EP3402800A4 (en) | 2019-11-13 |
| TW201734028A (zh) | 2017-10-01 |
| EP3402800A1 (en) | 2018-11-21 |
| CA3011289A1 (en) | 2017-07-20 |
| TWI638825B (zh) | 2018-10-21 |
| JP2019506382A (ja) | 2019-03-07 |
| CN108884123A (zh) | 2018-11-23 |
| US10745433B2 (en) | 2020-08-18 |
| US20190016743A1 (en) | 2019-01-17 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| ES2504690T3 (es) | Compuestos inhibidores de PARP, composiciones y métodos de uso | |
| US11084786B2 (en) | Compounds and pharmaceutical composition associated with ubiquitination-proteasome system | |
| EP2411010B1 (en) | Novel aminopyridine derivatives having aurora a selective inhibitory action | |
| US10745433B2 (en) | Compounds for inhibiting cancer and virus | |
| JPWO2018117177A1 (ja) | Brk阻害化合物 | |
| US8263632B2 (en) | Aminopyridine derivatives having Aurora A selective inhibitory action | |
| KR20070072562A (ko) | 오로라 a 선택적 억제 활성을 갖는 신규한 아미노피리딘유도체 | |
| CN105837586A (zh) | 二噁烷并喹唑啉胺类化合物及其制备方法和作为表皮生长因子受体抑制剂的应用 | |
| CN103965175A (zh) | 4-(取代苯氨基)喹唑啉类化合物、其制备方法及应用 | |
| CN115707704B (zh) | 氘代稠合三环类化合物及其组合物和用途 | |
| US11795179B2 (en) | Discovery of imidazothiazole- and imidazooxazole-based selective HER4 kinase inhibitors as potential anticancer agents | |
| WO2018167187A1 (en) | 5-carboxamide-2-thiobarbituric acids and use thereof as medicaments | |
| ES2702698T3 (es) | Polimorfo del derivado de dihidropirazolopirimidinona como inhibidor de la cinasa Wee1 | |
| WO2021121276A1 (zh) | 稠合四环类衍生物、其制备方法及其在医药上的应用 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 17738972 Country of ref document: EP Kind code of ref document: A1 |
|
| ENP | Entry into the national phase |
Ref document number: 2018536167 Country of ref document: JP Kind code of ref document: A |
|
| WWE | Wipo information: entry into national phase |
Ref document number: 3011289 Country of ref document: CA |
|
| NENP | Non-entry into the national phase |
Ref country code: DE |
|
| WWE | Wipo information: entry into national phase |
Ref document number: 2017738972 Country of ref document: EP |
|
| ENP | Entry into the national phase |
Ref document number: 2017738972 Country of ref document: EP Effective date: 20180813 |