WO1996013263A3 - Methods of treatment of viral disease with inhibitors of sphingolipid biosynthesis - Google Patents
Methods of treatment of viral disease with inhibitors of sphingolipid biosynthesis Download PDFInfo
- Publication number
- WO1996013263A3 WO1996013263A3 PCT/US1995/014070 US9514070W WO9613263A3 WO 1996013263 A3 WO1996013263 A3 WO 1996013263A3 US 9514070 W US9514070 W US 9514070W WO 9613263 A3 WO9613263 A3 WO 9613263A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- sphingolipid biosynthesis
- inhibitors
- treatment
- methods
- viral disease
- 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
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
The present invention provides a novel method of inhibition of virus replication. In particular, the present invention is directed to the use of an inhibitor of sphingolipid biosynthesis for the treatment or prevention of infection caused by enveloped viruses, including HIV. L-cycloserine is the preferred inhibitor of sphingolipid biosynthesis. Pharmaceutical compositions comprising inhibitors of sphingolipid biosynthesis, including L-cycloserines, are also provided.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US33296994A | 1994-11-01 | 1994-11-01 | |
US08/332,969 | 1994-11-01 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO1996013263A2 WO1996013263A2 (en) | 1996-05-09 |
WO1996013263A3 true WO1996013263A3 (en) | 1996-06-13 |
Family
ID=23300674
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US1995/014070 WO1996013263A2 (en) | 1994-11-01 | 1995-10-30 | Methods of treatment of viral disease with inhibitors of sphingolipid biosynthesis |
Country Status (1)
Country | Link |
---|---|
WO (1) | WO1996013263A2 (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BR0007491A (en) * | 1999-01-13 | 2001-11-20 | Jomaa Pharmaka Gmbh | Use of 3-isoxazolidinones and hydroxylamic acids to treat infections |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5302609A (en) * | 1992-12-16 | 1994-04-12 | The Regents Of The University Of Michigan | Treatment of diabetic nephropathy |
-
1995
- 1995-10-30 WO PCT/US1995/014070 patent/WO1996013263A2/en active Application Filing
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5302609A (en) * | 1992-12-16 | 1994-04-12 | The Regents Of The University Of Michigan | Treatment of diabetic nephropathy |
Non-Patent Citations (3)
Title |
---|
C.M.BATES: "HIV medicine: drug side effects and interactions", POSTGRADUATE MEDICAL JOURNAL, vol. 72, no. 843, pages 30 - 36 * |
N.G. KASPARYAN: "GLYCOSPHINGOLIPID METABOLISM AND SHEDDING IN NON-TRANSFORMED AND MURINE SARCOMA VIRUS TRANSFORMED METASTATIC VARIANT CELLS", DIALOG(R)FILE 35: DISSERTATION ABSTRACTS ONLINE, ABSTRACT 0978983 * |
Y.MIZRACHI ET AL.: "L-Cycloserine, an Inhibitor of Sphingolipid Biosynthesis, Inhibits HIV-1 Cytopathic Effects, Replication, and Infectivity", JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES AND HUMAN RETROVIROLOGY, vol. 11, no. 2, 1 February 1996 (1996-02-01), pages 137 - 141 * |
Also Published As
Publication number | Publication date |
---|---|
WO1996013263A2 (en) | 1996-05-09 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
WO2001090121A3 (en) | Methods and compositions for treating hepatitis c virus | |
EP1340744A3 (en) | Hiv protease inhibitors | |
WO2003026589A3 (en) | Methods and compositions for treating hepatitis c virus using 4'-modified nucleosides | |
UA66767C2 (en) | Serine proteases inhibitors, pharmaceutical composition, a method for inhibitining activity and a method for treatment or prevention of viral infection of hepatitis c | |
WO1996006620A3 (en) | Lipid analogs for treating viral infections | |
WO2001060315A3 (en) | Method for the treatment or prevention of flavivirus infections using nucleoside analogues | |
CA2163456A1 (en) | New procedure to block the replication of reverse transcriptase dependent viruses by the use of inhibitors of deoxynucleotides synthesis | |
NZ515392A (en) | Respiratory syncytial virus replication inhibitors | |
CA2075173A1 (en) | Compounds and methods for inhibition of hiv and related viruses | |
MX9603909A (en) | Sulphonamide derivatives as aspartyl protease inhibitors. | |
MXPA03002022A (en) | Multivalent neuraminidase inhibitor conjugates. | |
WO1997020554B1 (en) | Treatment of the cns effects of hiv with vx-478, alone or in combination with azt or 3tc | |
BR9711095A (en) | Substituted cyclopentane compound, composition and method for inhibiting influenza virus neuraminidase and method for treating influenza virus infection | |
MX9207449A (en) | INHIBITORS OF THE PROTEOLYTIC ENZYME DERIVED FROM SACARINE. | |
DE69518840D1 (en) | N-(3-amino-2-hydroxybutyl)sulfonamid-derivate as hiv-protease-inhibitoren | |
BG102106A (en) | Phermaceutical composition containing proteinase inhibitor and monoglyceride | |
NZ505894A (en) | Methylenebisbenzaldehyde derivatives, methylidynetrisphenol derivative and pharmaceuticals thereof; useful for treating or preventing pneumovirus infection and associated diseases | |
ZA991029B (en) | Composition and methods for treatment of hiv infections. | |
WO1996013263A3 (en) | Methods of treatment of viral disease with inhibitors of sphingolipid biosynthesis | |
WO2001010454A3 (en) | Pharmaceutical composition comprising peg-asparaginase for the treatment of hiv infection | |
WO1996000068A3 (en) | Combination therapy for hiv infection | |
GEP20022764B (en) | HIV Protease Inhibitors, Pharmaceutical Compositions and Methods for Inhibiting HIV Protease | |
WO1998009951A3 (en) | Intermediates for making hiv-protease inhibitors and methods of making hiv-protease inhibitors | |
AU630249B2 (en) | Prevention of glycoprotein enveloped virus infectivity by quinolyloxazole-2-ones | |
WO2003093415A3 (en) | Methods useful in treatment and prevention of hiv infection |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AK | Designated states |
Kind code of ref document: A2 Designated state(s): CA JP |
|
AL | Designated countries for regional patents |
Kind code of ref document: A2 Designated state(s): AT BE CH DE DK ES FR GB GR IE IT LU MC NL PT SE |
|
AK | Designated states |
Kind code of ref document: A3 Designated state(s): CA JP |
|
AL | Designated countries for regional patents |
Kind code of ref document: A3 Designated state(s): AT BE CH DE DK ES FR GB GR IE IT LU MC NL PT SE |
|
DFPE | Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101) | ||
121 | Ep: the epo has been informed by wipo that ep was designated in this application | ||
122 | Ep: pct application non-entry in european phase |