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hydrocarbon/neoplasms
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Tumor cell growth-inhibiting pharmaceutical compositions containing phosphino-hydrocarbon-gold, silver or copper complexes
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BACKGROUND OF THE INVENTION
This invention relates to novel bis[bis (diphenylphosphino)hydrocarbon]-, bis[bis(diethylphosphino)hydrocarbon]-, bis[diphenylphosphino-diethylphosphino)hydrocarbon]gold(I), silver(I) or copper(I) complexes or tris[bis(diphenylphosphino)ethane]dicopper (I) derivatives
Antitumor pharmaceutical compositions and methods for treating tumors employing .alpha.,.omega.-bis(disubstitutedphosphino)hydrocarbon derivatives or [.alpha., .omega.-bis(disubstitutedphosphino)hydrocarbon] d i
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BACKGROUND OF THE INVENTION
This invention relates to novel .alpha.,.omega.-bis(disubstitutedphosphino)hydrocarbon compounds, digold(I), digold(III), disilver(I) or dicopper(I) complexes thereof, pharmaceutical compositions containing, as an active ingredient,
Aryl hydrocarbon receptor (AhR) modifiers as novel cancer therapeutics
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SEQUENCE LISTING
The instant application contains a Sequence Listing which has been submitted in ASCII format via EFS-Web and is hereby incorporated by reference in its entirety. Said ASCII copy, created on Mar. 2, 2016 is named 701586-067982-US_SL.txt and is 8,192 bytes in size.
FIELD OF THE
Aryl hydrocarbon receptor (AhR) modifiers as novel cancer therapeutics
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SEQUENCE LISTING
The instant application contains a Sequence Listing which has been submitted in ASCII format via EFS-Web and is hereby incorporated by reference in its entirety. Said ASCII copy, created on Feb. 20, 2013 is named 701586-067982-US_SL.txt and is 8,192 bytes in size.
FIELD OF THE
Aryl hydrocarbon receptor (AhR) modifiers as novel cancer therapeutics
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SEQUENCE LISTING
The instant application contains a Sequence Listing which has been submitted in ASCII format via EFS-Web and is hereby incorporated by reference in its entirety. Said ASCII copy, created on Feb. 20, 2013 is named 701586-067982-US_SL.txt and is 8,192 bytes in size.
FIELD OF THE
Compounds for treatment of cancer
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FIELD OF THE INVENTION
The present invention relates to novel compounds having anti-cancer activity, methods of making these compounds, and their use for treating various forms of cancer.
BACKGROUND OF THE INVENTION
Cancer is the second most common cause of death in the United States, exceeded only
Methods for preventing and treating cancer using N-thiolated .beta.-lactam compounds and analogs thereof
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FIELD OF THE INVENTION
The present invention relates to N-thiolated .beta.-lactam compounds, and analogs and derivatives thereof, which potently induce neoplastic cell apoptosis or inhibit neoplastic cell proliferation. Specifically, the invention relates to methods of treating conditions
Methods for preventing and treating cancer using N-thiolated .beta.-lactam compounds and analogs thereof
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FIELD OF THE INVENTION
The present invention relates to N-thiolated .beta.-lactam compounds, and analogs and derivatives thereof, which potently induce neoplastic cell apoptosis or inhibit neoplastic cell proliferation. Specifically, the invention relates to methods of treating conditions
[.alpha.,.omega.-bis(diphenylphosphino)hydrocarbon]bis[(thiosugar)gold] and bis[(selenosugar)gold] derivatives, pharmaceutical compositions and method of use
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BACKGROUND OF THE INVENTION
This invention relates to novel [bis(diphenylphosphino)alkyl]bis-gold[I] derivatives which have tumor cell growth-inhibiting activity, pharmaceutical compositions containing such novel derivatives, and a method for treating tumor cells sensitive to such derivatives by
Synthetic C-glycolipid and its use for treating cancer, infectious diseases, and autoimmune diseases
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FIELD OF THE INVENTION
The invention is directed to novel synthetic C-glycolipids, which are useful in treating cancer, infectious diseases and autoimmune diseases. Specifically, the invention is directed to novel synthetic analogs of .alpha.-C-galactosylceramides, which are potent mediators of
Synthetic C-glycolipid and its use for treating cancer, infectious diseases and autoimmune diseases
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FIELD OF THE INVENTION
The invention is directed to novel synthetic C-glycolipids, which are useful in treating cancer, infectious diseases and autoimmune diseases. Specifically, the invention is directed to novel synthetic analogs of .alpha.-C-galactosylceramides, which are potent mediators of
Antigenic conjugates of polycyclic aromatic hydrocarbons to nucleosides
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FIELD OF THE INVENTION
The present invention relates to novel immunologic reagents and their use in assays for the detection of polycyclic aromatic hydrocarbon (PAH)-DNA adducts as well as heteropolycyclic aromatic hydrocarbon (HAH)-DNA adducts. These adducts are uniquely important biomarkers for
Near-infrared super-continuum lasers for early detection of breast and other cancers
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This application is related to U.S. provisional application Ser. No. 61/747,477 filed Dec. 31, 2012; Ser. No. 61/747,481 filed Dec. 31, 2012; Ser. No. 61/747,485 filed Dec. 31, 2012; Ser. No. 61/747,487 filed Dec. 31, 2012; Ser. No. 61/747,492 filed Dec. 31, 2012; Ser. No. 61/747,472 filed Dec. 31,
5'-deoxy-cytidine derivative administration to treat solid tumors
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FIELD OF THE INVENTION
The present invention is concerned with novel 5'-deoxy-cytidine derivatives, pharmaceutical compositions, a kit thereof for assisting a delivery of 5-fluorouracil selectively to tumor tissues and process for manufacturing the novel 5'-deoxy-cytidine
Pharmaceutical composition for inhibiting the growth of viruses and cancers
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TECHNICAL FIELD
This invention is a method of treating cancer, both carcinomas and sarcomas, and viral infections, in particular HIV through the administration of a pharmaceutical composition containing a benzimidazole derivative. The composition is also claimed.
BACKGROUND OF THE INVENTION
Cancers
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