Monocyclic L-nucleosides, analogs and uses thereof

Details Monocyclic L-nucleosides, analogs and uses thereof Monocyclic L-nucleosides, analogs and uses thereof

2002-04-09

2003-11-04

Wilson, James O. (Department: 1623)

Drug, bio-affecting and body treating compositions

Designated organic active ingredient containing

Carbohydrate doai

C536S028700

Reexamination Certificate

active

06642206

ABSTRACT:

FIELD OF THE INVENTION
The present invention relates to the field of L-nucleosides.
BACKGROUND OF THE INVENTION
The last few decades have seen significant efforts expended in exploring possible uses of D-nucleoside analogs as antiviral agents. Some of this work has borne fruit, and a number of nucleoside analogs are currently being marketed as antiviral drugs, including the HIV reverse transcriptase inhibitors (AZT, ddI, ddC, d4T, and 3TC).
Nucleoside analogs have also been investigated for use as immune system modulators, (Bennet, P. A. et al.,
J. Med. Chem.,
36, 635, 1993), but again with less than completely satisfactory results. For example, guanosine analogs such as 8-bromo-, 8-mercapto-, 7-methyl-8-oxoguanosine (Goodman, M. G.
Immunopharmacology,
21, 51-68, 1991) and 7-thia-8-oxoguanosine (Nagahara, K.
J. Med. Chem.,
33, 407-415, 1990; U.S. Pat. No. 5,041,426) have been studied over the years for their ability to activate the immune system. These guanosine derivatives show excellent antiviral and/or antitumor activity in vivo. But, these C
8
-substituted guanosines were unable to activate T-cells (Sharma, B. S. et al.,
Clin. Exp. Metastasis,
9, 429-439, 1991). The same was found to be true with 6-arylpyrimidinones (Wierenga, W.
Ann. N. Y. Acad. Sci.,
685, 296-300, 1993). In other research, a series of 3-deazapurine nucleosides were synthesized and evaluated as immuno-modulating agents. U.S. Pat. No. 4,309,419 describes the use of 3-deazaadenosine as being an inhibitor of the immune system. The ∃-D-nucleoside, ∃-2′-deoxy-3-deazaguanosine (U.S. Pat. No. 4,950,647) displayed the most potent immunoenhancing potency on activated T-cell response. Antiinflamatory and immunosuppressant activity has also been disclosed for certain 2′-deoxynucleosides (EPO Application 0 038 569). However, these compounds undergo facile in vivo metabolic cleavage of their glycosyl bond, which effectively inactivates their biological potency. Adenosine derivatives disclosed in U.S. Pat. No. 4,148,888 are also catabolized in vivo by deaminase enzymes. In still other research, Levamisole, a thymomimetic immunostimulant (Hadden et al,
Immunol. Today,
14, 275-280, 1993), appears to act on the T-cell lineage in a manner similar to thymic hormones. Tucaresol (Reitz et al, Nature, 377, 71-75,1995), another T-cell stimulant, is now undergoing clinical trials. More recently, 6-substituted purine linker amino acid (Zacharie et al, J. Med. Che., 40, 2883-2894, 1997) has been described as a promising immunostimulant which may be targeted for those disease states which require an increased CTL or Th1 type response.
One possible target of immunomodulation involves stimulation or suppression of Th1 and Th2 lymphokines. Type I (Th1) cells produce interleukin 2 (IL-2), tumor necrosis factor (TNF∀) and interferon gamma (IFN( ) and they are responsible primarily for cell-mediated immunity such as delayed type hypersensitivity and antiviral immunity. Type 2 (Th2) 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 lgG4 antibody isotype switching (Mosmann, 1989,
Annu Rev Immunol,
7:145-173). D-guanosine analogs have been shown to elicit various effects on lymphokines IL-1, IL-6, IFN∀ and TNF∀ (indirectly) in vitro (Goodman, 1988,
Int J Immunopharmacol,
10, 579-88) and in vivo (Smee et al., 1991,
Antiviral Res
15: 229). However, the ability of the D-guanosine analogs such as 7-thio-8-oxoguanosine to modulate Type I or Type 2 cytokines directly in T cells was ineffective or has not been described.
Significantly, most of the small molecule research has focused on the synthesis and evaluation of D-nucleosides. This includes Ribavirin (Witkowski, J. T. et al.,
J. Med. Chem.,
15, 1150, 1972), AZT (De Clercq, E.
Adv. Drug Res.,
17, 1, 1988), DDI (Yarchoan, R. et al.,
Science
(Washington, D.C.), 245, 412, 1989), DDC (Mitsuya, H. et al.,
Proc. Natl. Acad. Sci. U. S. A.,
83, 1911, 1986), d4T (Mansuri, M. M. et al.,
J. Med. Chem.,
32, 461, 1989) and 3TC (Doong, S. L. et al.,
Proc. Natl. Acad. Sci. U.S.A.,
88, 8495-8599, 1991). In this handful of therapeutic agents, only 3TC which contains an unnatural modified L-ribose moiety, the enantiomer of natural D-ribose.
After the approval of 3TC by the FDA, a number of nucleosides with the unnatural L-configuration were reported as having potent chemotherapeutic agents against immunodeficiency virus (HIV), hepatitis B virus (HBV), and certain forms of cancer. These include (−)-∃-L-1-[2-(hydroxymethyl)-1,3-oxathiolan-4-yl]-5-fluorocytosine (FTC; Furman, P. A., et al,
Antimicrob. Agents Chemother.,
36, 2686-2692, 1992), (−)-∃-L-2′,3′-dideoxypentofuranosyl-5-flurocytosine (L-FddC; Gosselin, G., et al,
Antimicrob. Agents Chemother.,
38, 1292-1297, 1994), (−)-∃-L-1-[2-(hydroxymethyl)-1,3-oxathiolan-4-yl]cytosine [(−)-OddC; Grove, K. L., et al,
Cancer Res.,
55, 3008-3011, 1995], 2′,3′-dideoxy-∃-L-cystidine (∃-L-ddC; Lin, T. S., et al,
J. Med. Chem.,
37, 798-803, 1994), 2′fluoro-5-methyl-∃-L-arabinofuranosyluracil (L-FMAU; U.S. Pat. No. 5,567,688), 2′,3′-dideoxy-2′,3′-didehydro-∃-L-cystidine (∃-L-d4C; Lin, T. S., et al,
J. Med. Chem.,
39, 1757-1759, 1996), 2′,3′-dideoxy-2′,3′-didehydro-∃-L-5-fluorocystidine (∃-L-Fd4C; Lin, T. S., et al,
J. Med. Chem.,
39, 1757-1759, 1996), L-cyclopentyl carbocyclic nucleosides (Wang, P., et al,
Tetrahedron Letts.,
38, 4207-4210, 1997) and variety of 9-(2′-deoxy-2′-fluoro-∃-L-arabinofuranosyl)purine nucleosides (Ma, T.' et al,
J. Med. Chem.,
40, 2750-2754, 1997).
Other research on L-nucleosides has also been reported. U.S. Pat. No. 5,009,698, for example, describes the synthesis and use of L-adenosine to stimulate the growth of a plant. WO 92/08727 describes certain L-2′-deoxyuridines and their use for treating viruses. Spadari, S., et al,
J. Med. Chem.,
35, 4214-4220, 1992, describes the synthesis of certain L-∃-nucleosides useful for treating viral infections including Herpes Simplex Virus Type I. U.S. Pat. No. 5,559,101 describes the synthesis of ∀- and ∃-L-ribofuranosyl nucleosides, processes for their preparation, pharmaceutical composition containing them, and method of using them to treat various diseases in mammals. A German patent (De 195 18 216) describes the synthesis of 2′-fluoro-2′-deoxy-L-∃-arabinofuranosyl pyrimidine nucleosides. U.S. Pat. Nos. 5,565,438 and 5,567,688 describe the synthesis and utility of L-FMAU. WO Patent 95/20595 describes the synthesis of 2′-deoxy-2′-fluoro-L-∃-arbinofuranosyl purine and pyrimidine nucleosides and method of treating HBV or EBV. U.S. Pat. No. 5,567,689 describes methods for increasing uridine levels with L-nucleosides. WO patent 96/28170 describes a method of reducing the toxicity of D-nucleosides by co-administering an effective amount of L-nucleoside compounds.
Significantly, while some of the known L-nucleosides have shown potent antiviral activity with lower toxicity profiles than their D-counterparts, none of these L-nucleoside compounds have been shown to posses immunomodulatory properties. Moreover, at present there is no effective treatment for the modulation of the immune system where lymphokine profiles (Th1 and Th2 subsets) have been implicated. Thus, there remains a need for novel L-nucleoside analogs, especially a need for L-nucleoside analogs which modulate the immune system, and most especially L-nucleoside analogs which specifically modulate Th1 and Th2.
BRIEF DESCRIPTION OF THE INVENTION
The present invention is directed to novel L-nucleoside compounds, their therapeutic uses and synthesis.
In one aspect of the invention, novel L-nucleoside compounds are provided according to the following formula:

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