WO1996040122A1 - Use of benzimidazoles for the manufacture of a medicament for the treatment of leukemia - Google Patents
Use of benzimidazoles for the manufacture of a medicament for the treatment of leukemia Download PDFInfo
- Publication number
- WO1996040122A1 WO1996040122A1 PCT/US1996/007445 US9607445W WO9640122A1 WO 1996040122 A1 WO1996040122 A1 WO 1996040122A1 US 9607445 W US9607445 W US 9607445W WO 9640122 A1 WO9640122 A1 WO 9640122A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- benzimidazole
- group
- carbon atoms
- less
- hydrogen
- Prior art date
Links
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
- A61K31/41—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
- A61K31/415—1,2-Diazoles
-
- 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
- A61K31/4164—1,3-Diazoles
- A61K31/4184—1,3-Diazoles condensed with carbocyclic rings, e.g. benzimidazoles
-
- 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
- A61K31/427—Thiazoles not condensed and containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- 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
- This invention is a pharmaceutical composition that is useful for the treatment of leukemia, particularly in human and warm blooded animals.
- the composition contains a benzimidazole derivative.
- chemotherapeutic agents Many types have been shown to be effective against leukemia, but not all types of leukemia and tumor cells respond to these agents. Unfortunately, many of these agents also destroy normal cells. The exact mechanism for the action of these chemotherapeutic agents are not always known.
- cytocidal or cytostatic agents work best on cancers with large growth factors, i.e., ones whose cells are rapidly dividing.
- hormones in particular estrogen, progesterone and testosterone, and some antibiotics produced by a variety of microbes, alkylating agents, and anti-metabolites form the bulk of therapies available to oncologists.
- cytotoxic agents that have specificity for leukemia, cancer and tumor cells while not affecting normal cells would be extremely desirable. Unfortunately, none have been found and instead agents which target especially rapidly dividing cells (both diseased and normal) have been used.
- a pharmaceutical composition for treatment of mammals, and in particular, warm blooded animals and humans, which are affected by leukemia comprising a pharmaceutical carrier and an effective amount of a compound selected from the group consisting of:
- X is hydrogen, halogen, alkyl of less than 7 carbon atoms or alkoxy of less than 7 carbon atoms; n is a positive integer of less than 4; Y is hydrogen, chlorine, nitro, methyl or ethyl; and R is hydrogen, or an alkyl group of from 1 to 8 carbon atoms and R2 is 4-thiazolyl, NHCOOR j wherein Rj is aliphatic hydrocarbon of less than 7 carbon atoms, and preferably an alkyl group of less than 7 carbon atoms is claimed.
- the compositions are:
- R is an alkyl of 1 through 8 carbon atoms and R2 is selected from the group consisting of 4-thiazolyl, NHCOORi , wherein Rj is methyl, ethyl or isopropyl and the non-toxic, pharmaceutically acceptable acid addition salts with both organic and inorganic acids.
- the most preferred compounds are 2-(4- thiazolyl)benzimidazole, methyl -(butylcarbamoyl)-2-benzimidazolecarbamate and 2-methoxycarbonylamino-benzimidazole and those wherein Y is chloro.
- compositions can be used to inhibit the growth of leukemia cells in humans or animals by administration of an effective amount either orally, rectally, topically or parenterally, or intravenously. These compositions do not significantly affect healthy cells.
- a "pharmaceutically acceptable” component is one that is suitable for use with humans and/or animals without undue adverse side effects (such as toxicity, irritation, and allergic response) commensurate with a reasonable benefit/risk ratio.
- safe and effective amount refers to the quantity of a component which is sufficient to yield a desired therapeutic response without undue adverse side effects (such as toxicity, irritation, or allergic response) commensurate with a reasonable benefit/risk ratio when used in the manner of this invention.
- the specific "safe and effective amount” will, obviously, vary with such factors as the particular condition being treated, the physical condition of the patient, the type of mammal being treated, the duration of the treatment, the nature of concurrent therapy (if any), and the specific formulations employed and the structure of the compounds or its derivatives.
- a “pharmaceutical addition salts” is salt of the anti-leukemia compound with an organic or inorganic acid.
- These preferred acid addition salts are chlorides, bromides, sulfates, nitrates, phosphates, sulfonates, formates, tartrates, maleates, malates, citrates, benzoates, salicylates, ascorbates, and the like.
- a “pharmaceutical carrier” is a pharmaceutically acceptable solvent, suspending agent or vehicle for debvering the anti-leukemia agent to the animal or human.
- the carrier may be liquid or solid and is selected with the planned manner of administration in mind.
- cancer or “leukemia” refers to all types of cancers or neoplasm or malignant disease which attack normal healthy blood cells or bone marrow which produces blood cells which are found in mammals.
- the "anti-leukemia compounds” are the benzimidazoles, and their salts.
- the exact " benzimidazoles are described in detail below.
- the preferred materials are the products sold under the names “thiabendazole®”, “benomyl®” and “carbendazim®” by BASF and Hoechst, DuPont and MSD-AgVet.
- the anti-leukemia compounds are benzimidazole derivatives which are known for their antifungal activities. They are systemic fungicides used to prevent and eradicate fungi.
- the compounds have the following structure:
- X is hydrogen, halogen, alkyl of less than 7 carbon atoms or alkoxy of less than 7 carbon atoms; n is a positive integer of less than 4; Y is hydrogen, chlorine, nitro, methyl or ethyl; and R is hydrogen or an alkyl group having from 1 to 8 carbons, and R2 is 4-thiazolyl, NHCOORi wherein R is aliphatic hydrocarbon of less than 7 carbon atoms, and preferably and alkyl group of less than 7 carbon atoms.
- the compositions are:
- R is an alkyl of 1 through 8 carbon atoms and R2 is selected from the group consisting of 4-thiazolyl, NHCOORi , wherein R ⁇ is methyl, ethyl or isopropyl and the non-toxic, pharmaceutically acceptable acid addition salts with both organic and inorganic acids.
- any suitable dosage may be given in the method of the invention.
- the type of compound and the carrier and the amount will vary widely depending on the species of the warm blooded animal or human, body weight, and the type of leukemia being treated. Generally a dosage of between about 2 milligrams (mg) per kilogram (kg) of body weight and about 400 mg per kg of body weight is suitable.
- a dosage unit may comprise a single compound or mixtures thereof with other compounds or other cancer inhibiting compounds.
- the dosage unit can also comprise diluents, extenders, carriers and the like.
- the unit may be in solid or gel form such as pills, tablets, capsules and the like or in liquid form suitable for oral, rectal, topical, intravenous injection or parenteral administration or injection into or around the bone marrow.
- liquid dosage forms examples include solutions or suspensions in water, pharmaceutically acceptable fats and oils, alcohols or other organic solvents, including esters, emulsions, syrups or elixirs, suspensions, solutions and/or suspensions reconstituted from non-effervescent granules and effervescent preparations reconstituted from effervescent granules.
- Such liquid dosage forms may contain, for example, suitable solvents, preservatives, emulsifying agents, suspending agents, diluents, sweeteners, thickeners, and melting agents.
- Oral dosage forms optionally contain flavorants and coloring agents.
- Parenteral and intravenous forms would also include minerals and other materials to make them compatible with the type of injection or delivery system chosen.
- the method of treatment can be any suitable method which is effective in the treatment of the particular leukemia type being treated.
- Treatment may be oral, rectal, topical, parenteral or intravenous administration or by injection into the bone marrow.
- the method of applying an effective amount also varies depending on the leukemia being treated. It is believed that parenteral treatment by intravenous, subcutaneous, or intramuscular application of the benzimidazole compounds, formulated with an appropriate carrier, additional cancer inhibiting compound or compounds or diluent to facilitate application will be the preferred method of administering the compounds to warm blooded animals.
- mice are randomly selected and divided into groups for treatment. Five groups are infected with leukemia. The diseased animals are dosed for five days, off two days and then dosed for another five days and then three days off, then dosed for five days and off for two days. This dosing on and off in an irregualr pattern was not an ideal mitien, but the results do show a positive benefit for the CarbendazimTM.
- mice One group of mice was treated with CytoxanTM, 2-[bis(2- chloroethyl)-amino-l-oxo-2-aza-5-oxophosphoridin, a control was dosed with canola oil and three groups were treated with various levels of CarbendazimTM, methyl -(butylcarbamoyl)-2-benzimidazole-carbamate. A control with no treatment was also used. The CarbendazimTM was dosed at three levels 4000 mg/kg, 2500 mg/kg and 1000 mg/kg. The CytoxanTM was dosed at 125 mg/kg. After 8 days, the no treatment group had lost 1 mouse, by day 10, 8 mice were dead and at day 11 all ten mice were dead.
- the lowest dosage group had 2 mice die on day 12, 13, 14, and 15; and 1 died on each of days 16 and 17.
Landscapes
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Epidemiology (AREA)
- Hematology (AREA)
- Oncology (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)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SK1686-97A SK168697A3 (en) | 1995-06-07 | 1996-05-22 | A medicament for the treatment of leukemia |
JP9500667A JPH11506732A (ja) | 1995-06-07 | 1996-05-22 | 白血病治療薬の製造に関するベンゾイミダゾール類の使用 |
AU58020/96A AU717382B2 (en) | 1995-06-07 | 1996-05-22 | Use of benzimidazoles for the manufacture of a medicament for the treatment of leukemia |
EP96914749A EP0831816A1 (en) | 1995-06-07 | 1996-05-22 | Use of benzimidazoles for the manufacture of a medicament for the treatment of leukemia |
BR9608730A BR9608730A (pt) | 1995-06-07 | 1996-05-22 | Uso de benzimidazóis para a produção de um medicamento para o tratamento de leucemia |
NO975660A NO975660L (no) | 1995-06-07 | 1997-12-05 | Anvendelse av benzimidazoler for fremstilling av et medikament for behandling av leukemi |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US47381795A | 1995-06-07 | 1995-06-07 | |
US08/473,817 | 1995-06-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1996040122A1 true WO1996040122A1 (en) | 1996-12-19 |
Family
ID=23881113
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US1996/007445 WO1996040122A1 (en) | 1995-06-07 | 1996-05-22 | Use of benzimidazoles for the manufacture of a medicament for the treatment of leukemia |
Country Status (17)
Country | Link |
---|---|
EP (1) | EP0831816A1 (es) |
JP (1) | JPH11506732A (es) |
KR (1) | KR19990022617A (es) |
CN (1) | CN1186433A (es) |
AR (1) | AR003137A1 (es) |
AU (1) | AU717382B2 (es) |
BR (1) | BR9608730A (es) |
CA (1) | CA2223435A1 (es) |
CZ (1) | CZ391197A3 (es) |
HU (1) | HUP9802634A3 (es) |
IL (1) | IL118424A0 (es) |
NO (1) | NO975660L (es) |
PL (1) | PL324026A1 (es) |
SK (1) | SK168697A3 (es) |
TR (1) | TR199701536T1 (es) |
WO (1) | WO1996040122A1 (es) |
ZA (1) | ZA964373B (es) |
Cited By (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1999059585A1 (en) * | 1998-05-19 | 1999-11-25 | The Procter & Gamble Company | Compositions for the treatment of hiv and other viral infections |
US6228876B1 (en) | 1995-06-07 | 2001-05-08 | The Procter & Gamble Company | Pharmaceutical composition for inhibiting the growth of cancers |
US6262093B1 (en) | 1995-04-12 | 2001-07-17 | The Proctor & Gamble Company | Methods of treating cancer with benzimidazoles |
US6265427B1 (en) | 1995-06-07 | 2001-07-24 | The Proctor & Gamble Company | Pharmaceutical composition for the method of treating leukemia |
US6271217B1 (en) | 1997-01-28 | 2001-08-07 | The Procter & Gamble Company | Method of treating cancer with a benzimidazole and a chemotherapeutic agent |
US6380232B1 (en) | 2000-09-26 | 2002-04-30 | The Procter & Gamble Company | Benzimidazole urea derivatives, and pharmaceutical compositions and unit dosages thereof |
US6407131B1 (en) | 1997-05-16 | 2002-06-18 | The Procter & Gamble Company | Compounds and method for use thereof in the treatment of cancer or viral infections |
US6407105B1 (en) | 2000-09-26 | 2002-06-18 | The Procter & Gamble Company | Compounds and methods for use thereof in the treatment of cancer or viral infections |
US6423734B1 (en) | 1999-08-13 | 2002-07-23 | The Procter & Gamble Company | Method of preventing cancer |
US6462062B1 (en) | 2000-09-26 | 2002-10-08 | The Procter & Gamble Company | Compounds and methods for use thereof in the treatment of cancer or viral infections |
US6479526B1 (en) | 1995-04-12 | 2002-11-12 | The Procter & Gamble Company | Pharmaceutical composition for inhibiting the growth of viruses and cancers |
US6498188B1 (en) | 1995-04-12 | 2002-12-24 | The Procter & Gamble Company | Methods of treatment for cancer or viral infections |
US6608096B1 (en) | 2000-09-26 | 2003-08-19 | University Of Arizona Foundation | Compounds and methods for use thereof in the treatment of cancer or viral infections |
US6686391B2 (en) | 1995-08-04 | 2004-02-03 | University Of Arizona Foundation | N-chlorophenylcarbamate and N-chlorophenylthiocarbamate compositions |
EP2251010A1 (en) | 2009-05-08 | 2010-11-17 | Sygnis Bioscience GmbH & Co. KG | Use of thiabendazole and derivatives thereof for the therapy of neurological conditions |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3370957A (en) * | 1963-05-23 | 1968-02-27 | Merck & Co Inc | Antifungal compositions and methods for their use |
FR2155888A1 (en) * | 1971-10-13 | 1973-05-25 | Agot Aime | Solid anthelmintic composn - for more economical treatment of ruminants |
-
1996
- 1996-05-22 CZ CZ973911A patent/CZ391197A3/cs unknown
- 1996-05-22 BR BR9608730A patent/BR9608730A/pt not_active Application Discontinuation
- 1996-05-22 CN CN96194465A patent/CN1186433A/zh active Pending
- 1996-05-22 EP EP96914749A patent/EP0831816A1/en not_active Withdrawn
- 1996-05-22 PL PL96324026A patent/PL324026A1/xx unknown
- 1996-05-22 JP JP9500667A patent/JPH11506732A/ja active Pending
- 1996-05-22 WO PCT/US1996/007445 patent/WO1996040122A1/en not_active Application Discontinuation
- 1996-05-22 HU HU9802634A patent/HUP9802634A3/hu unknown
- 1996-05-22 KR KR1019970709098A patent/KR19990022617A/ko not_active Application Discontinuation
- 1996-05-22 SK SK1686-97A patent/SK168697A3/sk unknown
- 1996-05-22 AU AU58020/96A patent/AU717382B2/en not_active Ceased
- 1996-05-22 CA CA002223435A patent/CA2223435A1/en not_active Abandoned
- 1996-05-22 TR TR97/01536T patent/TR199701536T1/xx unknown
- 1996-05-27 IL IL11842496A patent/IL118424A0/xx unknown
- 1996-05-29 ZA ZA964373A patent/ZA964373B/xx unknown
- 1996-06-07 AR ARP960103043A patent/AR003137A1/es not_active Application Discontinuation
-
1997
- 1997-12-05 NO NO975660A patent/NO975660L/no not_active Application Discontinuation
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3370957A (en) * | 1963-05-23 | 1968-02-27 | Merck & Co Inc | Antifungal compositions and methods for their use |
FR2155888A1 (en) * | 1971-10-13 | 1973-05-25 | Agot Aime | Solid anthelmintic composn - for more economical treatment of ruminants |
Non-Patent Citations (3)
Title |
---|
P.DELATOUR ET AL.: "Propriétées embryotoxiques et antimitotiques en série benzimidazole", THERAPIE, vol. 31, no. 4, 1976, pages 505 - 515, XP002009247 * |
R.J.A.AUR: "Treatment of parasitic infestation in children with malignant neoplasms", J.PEDIATR., vol. 78, no. 1, 1971, pages 129 - 131, XP002009249 * |
SALWA A. EIGEBALY ET AL.: "Reversal of gamma-radiation induced leukemogenesis in mice by immunomodulation with thiabendazole and dinitrofluorobenzene", J.NATL.CANCER INST., vol. 74, no. 4, 1985, pages 811 - 815, XP002009248 * |
Cited By (27)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6479526B1 (en) | 1995-04-12 | 2002-11-12 | The Procter & Gamble Company | Pharmaceutical composition for inhibiting the growth of viruses and cancers |
US6262093B1 (en) | 1995-04-12 | 2001-07-17 | The Proctor & Gamble Company | Methods of treating cancer with benzimidazoles |
US6362207B1 (en) | 1995-04-12 | 2002-03-26 | The Procter & Gamble Company | Methods of treating viral infections with benzimidazoles |
US6498188B1 (en) | 1995-04-12 | 2002-12-24 | The Procter & Gamble Company | Methods of treatment for cancer or viral infections |
US6228876B1 (en) | 1995-06-07 | 2001-05-08 | The Procter & Gamble Company | Pharmaceutical composition for inhibiting the growth of cancers |
US6265427B1 (en) | 1995-06-07 | 2001-07-24 | The Proctor & Gamble Company | Pharmaceutical composition for the method of treating leukemia |
US6552059B2 (en) | 1995-06-07 | 2003-04-22 | University Of Arizona Foundation | Pharmaceutical composition for and method of treating leukemia |
US6686391B2 (en) | 1995-08-04 | 2004-02-03 | University Of Arizona Foundation | N-chlorophenylcarbamate and N-chlorophenylthiocarbamate compositions |
US6271217B1 (en) | 1997-01-28 | 2001-08-07 | The Procter & Gamble Company | Method of treating cancer with a benzimidazole and a chemotherapeutic agent |
US6329355B1 (en) | 1997-01-28 | 2001-12-11 | The Procter & Gamble Company | Method for inhibiting the growth of cancers |
US6506783B1 (en) | 1997-05-16 | 2003-01-14 | The Procter & Gamble Company | Cancer treatments and pharmaceutical compositions therefor |
US6423736B1 (en) | 1997-05-16 | 2002-07-23 | The Proctor & Gamble Company | Compounds and methods for use thereof in the treatment of cancer or viral infections |
US6900235B1 (en) | 1997-05-16 | 2005-05-31 | Uaf Technologies And Research, Llc | Benzimidazole compounds, and pharmaceutical compositions and unit dosages thereof |
US6864275B1 (en) | 1997-05-16 | 2005-03-08 | Uaf Technologies And Research, Llc | Compounds and methods for use thereof in the treatment of cancer |
US6482843B1 (en) | 1997-05-16 | 2002-11-19 | The Procter & Gamble Company | Compounds and methods for use thereof in the treatment of cancer or viral infections |
US6407131B1 (en) | 1997-05-16 | 2002-06-18 | The Procter & Gamble Company | Compounds and method for use thereof in the treatment of cancer or viral infections |
US6420411B1 (en) | 1997-05-16 | 2002-07-16 | The Procter & Gamble Company | Compounds and methods for use thereof in the treatment of cancer or viral infections |
US6710065B1 (en) | 1997-05-16 | 2004-03-23 | Uaf Technologies And Research, Llc | Compounds and methods for use thereof in the treatment of cancer |
US6245789B1 (en) | 1998-05-19 | 2001-06-12 | The Procter & Gamble Company | HIV and viral treatment |
WO1999059585A1 (en) * | 1998-05-19 | 1999-11-25 | The Procter & Gamble Company | Compositions for the treatment of hiv and other viral infections |
US6423734B1 (en) | 1999-08-13 | 2002-07-23 | The Procter & Gamble Company | Method of preventing cancer |
US6380232B1 (en) | 2000-09-26 | 2002-04-30 | The Procter & Gamble Company | Benzimidazole urea derivatives, and pharmaceutical compositions and unit dosages thereof |
US6608096B1 (en) | 2000-09-26 | 2003-08-19 | University Of Arizona Foundation | Compounds and methods for use thereof in the treatment of cancer or viral infections |
US6720349B2 (en) | 2000-09-26 | 2004-04-13 | Uaf Technologies And Research, Llc | Compounds for use in the treatment of cancer or viral infections |
US6407105B1 (en) | 2000-09-26 | 2002-06-18 | The Procter & Gamble Company | Compounds and methods for use thereof in the treatment of cancer or viral infections |
US6462062B1 (en) | 2000-09-26 | 2002-10-08 | The Procter & Gamble Company | Compounds and methods for use thereof in the treatment of cancer or viral infections |
EP2251010A1 (en) | 2009-05-08 | 2010-11-17 | Sygnis Bioscience GmbH & Co. KG | Use of thiabendazole and derivatives thereof for the therapy of neurological conditions |
Also Published As
Publication number | Publication date |
---|---|
NO975660D0 (no) | 1997-12-05 |
JPH11506732A (ja) | 1999-06-15 |
AR003137A1 (es) | 1998-07-08 |
AU5802096A (en) | 1996-12-30 |
PL324026A1 (en) | 1998-05-11 |
IL118424A0 (en) | 1996-09-12 |
EP0831816A1 (en) | 1998-04-01 |
TR199701536T1 (xx) | 1998-02-21 |
NO975660L (no) | 1998-02-09 |
AU717382B2 (en) | 2000-03-23 |
KR19990022617A (ko) | 1999-03-25 |
SK168697A3 (en) | 1998-12-02 |
CA2223435A1 (en) | 1996-12-19 |
CZ391197A3 (cs) | 1998-05-13 |
HUP9802634A2 (hu) | 1999-03-29 |
ZA964373B (en) | 1996-09-02 |
HUP9802634A3 (en) | 1999-05-28 |
CN1186433A (zh) | 1998-07-01 |
BR9608730A (pt) | 1999-06-29 |
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