AU743366B2 - Novel nucleosides - Google Patents
Novel nucleosides Download PDFInfo
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- AU743366B2 AU743366B2 AU48659/00A AU4865900A AU743366B2 AU 743366 B2 AU743366 B2 AU 743366B2 AU 48659/00 A AU48659/00 A AU 48659/00A AU 4865900 A AU4865900 A AU 4865900A AU 743366 B2 AU743366 B2 AU 743366B2
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Description
't Regulation 3.2
AUSTRALIA
Patents Act 1990 COMPLETE SPECIFICATION DIVISIONAL APPLICATION
(ORIGINAL)
0 0 0 0000 .00.
00000 0 0 0 0 .:0.0 Name of Applicant: Actual Inventor(s): Address for Service: Invention Title: ICN Pharmaceuticals, Inc.
Robert Tam; Guangyi Wang; Devron Averett; and Kandasamy Ramasamy.
DAVIES COLLISON CAVE, Patent Attorneys, 1 Little Collins Street, Melbourne, Victoria 3000.
"Novel Nucleosides" The following statement is a full description of this invention, including the best method of performing it known to us: P:\OPERUMS\60238-99-div.doc-17A)700 -1- NOVEL NUCLEOSIDES This application is a divisional application of Australian Patent Application No.60238/98, the entire contents of which are incorporated herein by reference.
FIELD OF THE INVENTION The present invention relates to the field of nucleosides.
BACKGROUND OF THE INVENTION Mammalian immune systems contain two major classes of lymphocytes: B lymphocytes (B cells), which originate in the bone marrow; and T lymphocytes (T cells) which originate in the thymus. B cells are largely responsible for cell-mediated immunity.
T cells are generally considered to fall into two subclasses, helper cells and cytotoxic T cells. Helper T cells activate other lymphocytes, including B cells and cytotoxic T cells, and 15 macrophages, by releasing soluble protein mediators called cytokines which are involved in cellmediated immunity. As used herein, lymphokines are a subset of cytokines.
Helper T cells are also generally considered to fall into two subclasses, Thl and Th2. Thl cells (also known as Type 1 cells) produce interleukin 2 tumour necrosis factor (TNFa) and interferon gamma (IFNy), and are responsible primarily for cell-mediated immunity such as delayed type hypersensitivity and antiviral immunity. In contrast, Th2 cells (also known as Type 2 cells) produce interleukins, IL4, IL-5, IL-6, IL-9, IL-10 and IL-13, and are primarily involved in assisting humoral immune responses such as those seen in response to allergens, e.g. IgE and IgG4 antibody isotype switching (Mosmann, 1989, Annu. Rev Immunol., 7:145-173).
As used herein, the terms Thl and Th2 "responses" are meant to include the entire range of effects resulting from induction of Thl and Th2 lymphocytes, respectively. Among other things such responses include variation in production of the corresponding cytokines through transcription, translation, secretion and possibly other mechanisms, increased proliferation of the corresponding lymphocytes, and other effects associated with increased production of cytokines, including motility effects.
The mechanisms by which nucleosides and other compounds selectively modulate Thi and Th2 responses relative to each other are still unclear. One possibility contemplated by the present inventors is that effective nucleosides alter the pool of guanosine triphosphate (GPP), which in turn affects the rate at which cytokines are produced. In this theory, relatively large variations in available GTP are sufficient to affect concentrations of both Th and Th2 cytokines, while relatively smaller variations in available GTP tend to affect concentrations of Thl and Th2 cytokines to different extents.
These discoveries are especially significant because modem treatment strategies for many of the above-listed diseases have either limited effectiveness, significant side effects, or both.
Treatment of autoimmune disease, for example, is frequently limited to palliative measures, removal of toxic antibodies (as in myasthenia gravis), and administration of hazardous drugs including corticosteroids, chloroquine derivatives, and antimetabolic or antitumor drugs, and drugs such as cyclosporines which target immune system cells.
SUMMARY OF THE INVENTION This application relates to novel nucleosides. Nucleosides contemplated are those nucleosides corresponding to Formulas 1 and 2.
DETAILED DESCRIPTION Where the following terms are used in this specification, they are used as defined below.
The terms and indicate the specific stereochemical configuration of a substituent at an asymmetric carbon atom in a chemical structure as drawn.
The term "aryl" refers to a monovalent unsaturated aromatic carbocyclic radical having a single ring phenyl) or two condensed rings naphthyl), which can optionally be substituted with hydroxyl, lower alky, chloro, and/or cyano.
The term "enantiomers" refers to a pair of stereoisomers that are non-superimposable mirror images of each other. A mixture of a pair of enantiomers, in a 1:1 ratio, is a "racemic" mixture.
The term "heterocycle" refers to a monovalent saturated or unsaturated carbocyclic adical having at least one hetero atom, such as N, 0 or S, within the ring each available position of which can be optionally substituted, independently, with, hydroxy, oxo, amino, imino, lower alkyl, bromo, chloro and/or cyano. Included within this class of substituents are purines, pyrimidines.
The term "isomers" refers to different compounds that have the same formula.
"Stereoisomers" are isomers that differ only in the way the atoms are arranged in space.
The term "L-configuration" is used throughout the present invention to describe the chemical configuration of the ribofuranosyl moiety of the compounds that is linked to the nucleobases. The L-configuration of the sugar moiety of compounds of the present invention contrasts with the D-configuration of ribose sugar moieties of the naturally occurring nucleosides such as cytidine, adenosine, thymidine, guanosine and uridine.
The term "lower alkyl" refers to methyl, ethyl, n-propyl, isopropyl, n-butyl, t-butyl, Ibutyl or n-hexyl. This term is further exemplified to a cyclic, branched or straight chain from one to six carbon atoms.
The term "monocyclic" refers to a monovalent saturated carbocyclic radical having at least one hetero atom, such as O, N, S, Se or P, within the ring, each available position of which can be optionally substituted, independently, with a sugar moiety or any other groups like bromo, chloro and/or cyano, so that the monocyclic ring system eventually aromatized.
The term "nucleoside" refers to a compound composed of any pentose or modified pentose moiety attached to a specific position of a heterocycle or to the natural position of a purine 9 -position) or pyrimidine (1-position).
The term "C-nucleosides" is used throughout the specification to describe the linkage type that formed between the ribose sugar moiety and the heterocyclic base. In C-nucleosides, the linkage originates from the C-1 position of the ribose sugar moiety and joins the carbon of the heterocyclic base. The linkage that forms in C-nucleosides is carbon-to-carbon type.
The term "D-nucleosides" refers to nucleoside compounds that have a D-ribose sugar moiety Adenosine).
The term "L-nucleosides" refers to nucleoside compounds that have an L-ribose sugar moiety.
S. The term "N-nucleosides" is used throughout the specification to describe the linkage type that formed between the ribose sugar moiety and the heterocyclic base. In N-nucleosides, the linkage originates from the C-l position of the ribose sugar moiety and joins the nitrogen of the S. heterocyclic base. The linkage that forms in N-nucleosides is carbon to nitrogen type.
The term "nucleotide" refers to a phosphate ester substituted on the 5-position of a nucleoside.
The term "Purine" refers to nitrogenous bicyclic heterocycles depicted in Figures 1 and 2 herein.
Examples of compounds contemplated to be effective in the invention are shown in Formula 1 and 2.
ooo00: Formula 1 has the structure: 0 N
N
N: N 'KNH 2 0
OH
HO OH Formula 2 has the structure: 00* 0
H
2 N AN N/ O HO 0 HO OH Administration It is contemplated that compounds according to the present invention will be administered in any appropriate pharmaceutical formulation, and under any appropriate protocol. Preferred monotherapeutic dosages and protocols for such drugs are set forth in the PDR, or are at least o available from the manufacturer or distributor.
Of course, one of ordinary skill in the art will recognize that a therapeutically effective amount will vary with the infection or condition to be treated, its severity, the treatment regimen to be employed, the pharmacokinetics of the agent used, as well as the patient (animal or human) treated. Thus, effective dosages may range from 1 mg/kg of body weight, or less, to 25 mg/kg of body weight or more. This dosage range generally produces effective blood level concentrations of active compound ranging from about 0.04 to about 100 micrograms/cc of blood in the patient. It is contemplated, however, that appropriate patient-specific regimens will be developed by administering a small amount, and then increasing the amount until either the side effects become unduly adverse, or the intended effect is achieved.
Administration of compounds according to the present invention may take place orally, parenterally (including subcutaneous injections, intravenous, intramuscularly, by intrasternal injection or infusion techniques), by inhalation spray, or rectally, topically and so forth, and in dosage unit formulations containing conventional non-toxic pharmaceutically acceptable carriers, adjuvants and vehicles.
It is contemplated that compounds according to the present invention can be formulated in admixture with a pharmaceutically acceptable carrier. For example, the compounds of the present invention can be administered orally as pharmacologically acceptable salts. Because the compounds of the present invention are mostly water soluble, they can be administered intravenously in physiological saline solution buffered to a pH of about 7.2 to Conventional buffers such as phosphates, bicarbonates or citrates can be used for this purpose. Of course, one of ordinary skill in the art may modify the formulations within the teachings of the specification to provide numerous formulations for a particular route of administration without rendering the compositions of the present invention unstable or compromising their therapeutic activity. In particular, the modification of the present compounds to render them more soluble in water or other vehicle, for example, may be easily accomplished by minor modifications (salt formulation, esterification, etc.) which are well within the ordinary skill in the art. It is also well within the ordinary skill of the art to modify the route of administration and dosage regimen of a particular compound in order to manage the pharmacokinetics of the present compounds for maximum beneficial effect in patients.
In addition, compounds included in combinations according to the present invention may be administered separately or together, and when administered separately this may occur in any order.
The amounts of the active ingredient(s) and pharmaceutically active agent(s) and the relative timings of administration will be selected in order to achieve the desired combined therapeutic effect.
Administration routes of compounds according to the present invention may range from continuous (intravenous drip) to several oral administrations per day (for example, and may include oral, topical, parenteral, intramuscular, intravenous, sub-cutaneous, transdermal (which may include a penetration enhancement agent), buccal and suppository administration, among other routes of administration.
To prepare therapies according to the present invention, a therapeutically effective amount of a compound is preferably intimately admixed with a pharmaceutically acceptable carrier according to conventional pharmaceutical compounding techniques to produce a dose. A carrier may take a wide variety of forms depending on the form of preparation desired for administration, oral or parenteral. In preparing pharmaceutical compositions in oral dosage form, any of the usual •o i pharmaceutical media may be used. Thus, for liquid oral preparations such as suspensions, elixirs and solutions, suitable carriers and additives including water, glycols, oils, alcohols, flavoring agents, preservatives, coloring agents and the like may be used. For solid oral preparations such as powders, tablets, capsules, and for solid preparations such as suppositories, suitable carriers and additives including starches, sugar carrier, such as dextrose, mannitol, lactose and related carriers, diluents, granulating agents, lubricants, binders, disintegrating agents and the like may be used. If desired, the tablets or capsules may be enteric-coated or sustained release by standard techniques.
For parenteral formulations, the carrier will usually comprise sterile water or aqueous sodium chloride solution, though other ingredients including those which aid dispersion may be included. Of course, where sterile water is to be used and maintained as sterile, the compositions and carriers must also be sterilized. Injectable suspensions may also be prepared, in which case appropriate liquid carriers, suspending agents and the like may be employed.
It will also be appreciated that in general, the most preferred uses according to the present invention are those in which the active compounds are relatively less cytotoxic to the non-target host cells and relatively more active against the target.
While specific embodiments have been disclosed herein, the scope of the invention is not be limited except through interpretation of the appended claims.
*eeooe eo *o ee
Claims (2)
1. A nucleoside having the structure of Formula 1. Dated this 2 7 t1h day of November
2001. ICN Pharmaceuticals, Inc. By its Patent Attorneys Davies Colison Cave
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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AU48659/00A AU743366B2 (en) | 1997-01-17 | 2000-07-17 | Novel nucleosides |
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
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US60/028586 | 1996-10-16 | ||
US60/036094 | 1997-01-14 | ||
US60/043974 | 1997-04-23 | ||
US60/055487 | 1997-08-12 | ||
AU48659/00A AU743366B2 (en) | 1997-01-17 | 2000-07-17 | Novel nucleosides |
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AU60238/98A Division AU736075B2 (en) | 1997-01-17 | 1998-01-13 | Cytokine related treatments of disease |
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AU4865900A AU4865900A (en) | 2000-09-14 |
AU743366B2 true AU743366B2 (en) | 2002-01-24 |
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AU48659/00A Ceased AU743366B2 (en) | 1997-01-17 | 2000-07-17 | Novel nucleosides |
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Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU2486088A (en) * | 1987-12-21 | 1989-07-19 | Brigham Young University | Antiviral antitumor antimetastatic immune system enhancing nucleosides and nucleotides |
EP0341065A2 (en) * | 1988-05-05 | 1989-11-08 | Scripps Clinic And Research Foundation | Immunostimulating guanine dervatives, compositions and methods |
AU4899997A (en) * | 1996-10-16 | 1998-05-11 | Icn Pharmaceuticals, Inc. | Purine l-nucleosides, analogs and uses thereof |
-
2000
- 2000-07-17 AU AU48659/00A patent/AU743366B2/en not_active Ceased
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU2486088A (en) * | 1987-12-21 | 1989-07-19 | Brigham Young University | Antiviral antitumor antimetastatic immune system enhancing nucleosides and nucleotides |
EP0341065A2 (en) * | 1988-05-05 | 1989-11-08 | Scripps Clinic And Research Foundation | Immunostimulating guanine dervatives, compositions and methods |
AU4899997A (en) * | 1996-10-16 | 1998-05-11 | Icn Pharmaceuticals, Inc. | Purine l-nucleosides, analogs and uses thereof |
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MK14 | Patent ceased section 143(a) (annual fees not paid) or expired |