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Method for diagnosing and for the therapeutic treatment of tumors and/or infectious diseases of different types with alkaloid-compounds
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This application corresponds to my German Patent application No. P 31 28 018.8, filed on July 13, 1981 which is relied upon and incorporated by reference herein.
FIELD OF THE INVENTION
The invention is directed to a method for diagnosing and for therapeutic treatment of tumors and infectious
Compositions having neuroprotective and analgesic activity
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FIELD OF THE INVENTION
This invention involves means for treating neuronal injury and achieving analgesia by administration of compositions containing compounds of the formula: ##STR2## wherein R.sup.1 and R.sup.2 are alkyl having 1-8 carbon atoms.
BACKGROUND OF THE INVENTION
Compounds having an
Compositions having neuroprotective and analgesic activity
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FIELD OF THE INVENTION
This invention involves means for treating neuronal injury and achieving analgesia by administration of compositions containing compounds of the formula: ##STR2##
wherein R.sup.1 and R.sup.2 are alkyl having 1-8 carbon atoms.
BACKGROUND OF THE INVENTION
Compounds having an
Agent and method for prevention and treatment of cancer in animals
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STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH OR DEVELOPMENT
None
BACKGROUND OF THE INVENTION
The invention relates to the prevention and treatment of cancers in animals. More specifically the invention relates to the use of metal chelating materials including, picolinic acid, fusaric acid and
Iontophoresis preparation for treating breast cancer and/or mastitis
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CROSS-REFERENCE TO RELATED APPLICATIONS
This application is a National Stage of PCT/JP09/001770 filed Apr. 17, 2009 and claims the benefit of JP 2008-108754 filed Apr. 18, 2008.
TECHNICAL FIELD
The present invention relates to an iontophoretic preparation for treatment of breast cancer and/or
Interleukin-1 and tumor necrosis factor-.alpha. modulators, synthesis of said modulators and their enantiomers and methods of using said modulators
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FIELD OF THE INVENTION
The invention relates to chemical compounds and pharmaceutical compositions, including novel chemical compounds and pharmaceutical compositions thereof, useful in the treatment of various diseases and disease states. The invention also relates to methods of synthesizing
Interleukin-1 and tumor necrosis factor-.alpha. modulators, synthesis of said modulators and their enantiomers and methods of using said modulators
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FIELD OF THE INVENTION
The invention relates to chemical compounds and pharmaceutical compositions, including novel chemical compounds and pharmaceutical compositions thereof, useful in the treatment of various diseases and disease states. The invention also relates to methods of synthesizing
Coupling compounds of NSAID anti-inflammatory and analgesic drugs and EGFR kinase inhibitors, synthesis methods and applications thereof
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TECHNICAL FIELD
The present invention belongs to the field of chemical pharmaceuticals, particularly relates to coupling compounds of NSAID anti-inflammatory and analgesic drugs and EGFR inhibitors or pharmaceutically acceptable salts or stereoisomers thereof and prodrug molecules thereof, synthesis
Use of a peptide and an analgesic pharmaceutical agent
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This application is a .sctn.371 national stage of PCT International Application No. PCT/PL2008/000020, filed Mar. 7, 2008, and claims priority of Polish Patent Application No. P.381925, filed Mar. 7, 2007, the contents of all of which are hereby incorporated by reference into this application.
BRIEF
Use of cobratoxin as an analgesic
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BACKGROUND OF THE INVENTION
1. Field of the Invention
The present invention relates to a protein composition of matter and a method for the treatment of chronic pain, especially to the treatment of heretofore intractable pain as associated with advanced cancer. The pain associated with neurological
Compositions and methods for the prevention of esophageal cancer
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FIELD OF THE INVENTION
The present invention relates to the field of cancer prevention. Specifically, compositions and methods for slowing and/or inhibiting Barrett's esophagus progression to its associated adenocarcinoma are disclosed.
BACKGROUND OF THE INVENTION
Several publications and patent
Sulfonyl heteroaryl triazoles as anti-inflammatory/analgesic agents
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BACKGROUND OF THE INVENTION
This invention relates to sulfonyl heteroaryl triazoles, methods of treatment and pharmaceutical compositions for the treatment of cyclooxygenase mediated diseases.
Nonsteroidal anti-inflammatory drugs (NSAIDs) are widely used in treating pain and the signs and symptoms
Sulfonyl heteroaryl triazoles as anti-inflammatory/analgesic agents
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BACKGROUND OF THE INVENTION
This invention relates to sulfonyl heteroaryl triazoles, methods of treatment and pharmaceutical compositions for the treatment of cyclooxygenase mediated diseases.
Nonsteroidal anti-inflammatory drugs (NSAIDs) are widely used in treating pain and the signs and symptoms
Analgesics
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This application is a national stage U.S. application filed under 35 U.S.C. 371 of International application PCT/JP03/00350, filed Jan. 17, 2003, which claimed the priority of Japanese Patent 2002-11914 filed Jan. 21, 2002, the disclosures of which are incorporated herein in its entirety by
Anandamide amidase inhibitors as analgesic agents
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BACKGROUND
.DELTA..sup.9 -Tetrahydrocannabinol, the pyschoactive marijuana derived cannabinoid, binds to the CB1 receptor in the brain and to the CB2 receptor in the spleen. Compounds which stimulate the CB1 receptor have been shown to induce analgesia and sedation, to cause mood elevation, to
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