Carbocyclic analogues of inosine-5'-monophosphate: synthesis and biological activity.

9-(4’-Phosphonomethoxy-2’-cyclopenten-1’-yl)hypoxanthine and 9-(4’-phosphonomethoxy-2’,3’-dihydroxycyclopenten-1’-yl)hypoxanthine were synthesized as isosteric carbocyclic analogues of inosine-5’-monophosphate. The synthesized compounds were shown to be capable of inhibiting the activity of human type II inosine-5′-monophosphate dehydrogenase (IMPDH II) (IC50 = 500 µM) and to have no significant effects on the growth ofMycobacterium tuberculosis.

Human IMPDH exists in 2 isoforms, types I and II, showing 84% homology. type I enzyme is prevalent in normal lymphocytes and leucocytes; type II is found mostly in actively dividing and cancerous cells. Bacterial IMPDH molecules isolated from different sources significantly differ from the human enzyme, showing 30-41% homology. the affinity of IMPDH isolated from different sources may vary significantly for the same types of inhibitors [2]. thus, human IMPDH type II is more sensitive to mycophenolic acid (K i = 7nM) as compared to human IMPDH type I (K i = 33nM). the sensitivity of bacterial enzymes to mycophenolic acid is considerably lower (K i = 0.2-20 μM). the selectivity of IMPDH with respect to inhibitors makes this enzyme a rather attractive target for potential anticancer, antimicrobial, and antiparasitic compounds [2].
It has been shown recently that the inhibition of IMP-DH isolated from Mycobacterium tuberculosis suppresses the growth of the bacterium [3]. the main objective in efforts to treat tuberculosis today is searching for new drugs that are effective against strains resistant to existing medicinal agents. new compounds should work via different mechanisms compared to those of the existing therapeutic agents. Hence, searching for new anti-tuberculosis agents not only among classes of antibiotics, but also among compounds of another nature seems reasonable. there are no analogues of nucleosides among the therapeutic agents currently used to treat tuberculosis; in combination with their potential to inhibit IMPDH, it makes these analogues primary candidates for investigation as antimycobacterial agents.
the solvent was removed under reduced pressure; the residue was applied onto a silica gel column; system B was used for elution; the target fractions were concentrated under reduced pressure. Product 4 (220 mg, 78%) was isolated as a white foamy substance. 1  6-Ethoxy-9-(4'-ethylphosphonomethoxy-2'-cyclopenten-1'-yl)purine (5). naH (33.5 mg, 1.4 mmol) and cs 2 cO 3 (234 mg, 0.72 mmol) were added to the solution of compound 4 (230 mg, 0.93 mmol) in 5 ml of dimethylformamide (DMF) under stirring in an argon atmosphere. the reaction mixture was stirred for 1.5 h at room temperature, then ethyl ester of p-toluene sulfonyloxymethyl phosphonic acid (334 mg, 1.8 mmol) solution in DMF (2 ml) was added. the mixture was stirred for 12 h at room temperature. the course of the reaction was controlled using tLc (system B). After removing the solvent under reduced pressure, the residue was applied onto the DeAe-toyopearl column and eluted with a linear gradient of nH-4 HcO 3 (0-0.2 M). the target compound 5 was eluted using 0.1 M nH 4 HcO 3 ; the fraction was concentrated, and the target product was isolated on a Lichroprep rP-18 and eluted using a linear gradient of aqueous ethanol (0-10%). the product was eluted using an 8% aqueous ethanol solution.
A total of 240 mg (67%) of compound 5 was obtained in the form of a colorless oil. 1
Antituberculosis activity. the compounds were tested on a laboratory strain of M. tuberculosis H37rv sensitive to antituberculosis drugs. the mycobacteria was transferred into a singlecell suspension of single cells at the same growth phase and standardized with respect to cFu [5]. the enriched liquid growth medium Dubois (Difco, uSA) was used.
Evaluation of compound efficacy. the effect of the compounds on the growth of mycobacterial strains was estimated using a Bactec MGIt 960 automated growth detection system (BD, uSA). the suspension of mycobacterial cells (500 μl) was inoculated in a nutrient medium (7.9 ml). the final concentration of M. tuberculosis in the sample was 10 6 cFu/ml. three replicates for each sample (concentration) were analyzed, including the control samples. the antimicrobial activity of the compounds was evaluated using the proportion method with the tB exist software [6]. the growth of mycobacterial cells cul- Scheme a -Ethanol (pure), K 2 CO 3 , refluxing for 1 hour; b -NaH, TosOCH 2 P(O)OC 2 H 5 OH, Cs 2 CO 3 , DMF; c -OsO 4 , NMMO, dioxane; d -(CH 3 ) 3 SiBr, DMF tured in the presence of the compound and the growth of the control culture diluted 100 times as compared to the test sample is assessed in this analysis. the culture is considered to be sensitive to such a concentration of the compound at which the growth rates in the experiment do not exceed 100 growth units (Gu), when 400 Gu are recorded in the control sample; the compound is regarded as active in this case. Furthermore, the absolute concentration method was used to assess the effect of the compounds at concentrations lower than the minimum inhibitory concentration (MIc) on the viability of mycobacterial cells on the basis of the inhibition of bacterial growth as compared to the control. Bacterial growth was determined automatically at 1 h intervals and recorded using the epicenter software (BD, uSA).

RESULTS AND DISCUSSION
Over the past decades, carbocyclic nucleosides have been intensively studied. these compounds have been found to be biologically active; in particular, they turn out to have antiviral and anticancer properties [7]. these nucleosides are recognized by many enzymes and receptors, since their structure is similar to that of natural nucleosides. Meanwhile, they are highly resistant to c-n bond cleavage by phosphorylases and hydrolases.
Hydroxycyclopentene is used as a carbocyclic moiety in compounds 1 and 2. the analogues with such moiety are known as 5'-norcarbocyclic nucleosides. the substitution of the primary 5'-hydroxyl residue for the secondary 4'-hydroxyl results in toxicity decrease due to the loss of substrate properties with respect to cellular kinases. taking into account the fact that intracellular phosphorylation of 5'-norcarbocyclic nucleosides is infeasible, we synthesized the methylene phosphonates of 9-(4'-hydroxy-2'-cyclopenten-1'-yl)hypoxanthine and 9-(4',2',3'-trihydroxycyclopent-1'-yl)hypoxanthine (scheme). It was previously shown that such isosteric phosphonates imitate the corresponding monophosphates but are more stable to the action of hydrolyzing and dephosphorylizing enzymes [8].
ester 5 was hydrolyzed to 9-(4'-phosphonylmethyloxy-2'-cyclopenten-1'-yl)hypoxanthine 1 using excess amounts of trimethylbromosilane. In order to obtain monophosphonate 2, the double bond of compound 5 was oxidized with osmium tetroxide in the presence of n-methylmorpholine-n-oxide, and the ethyl groups were subsequently removed from compound 6 in the presence of trimethylbromosilane (scheme). the target compounds 1 and 2 were purified on a DeAe-toyopearl column eluted with a linear concentration gradient of nH 4 HcO 3 . the subsequent purification and removal of salts was performed on a Lichroprep rP-18 column. the final yields were 84 and 81%, respectively.
It is clear from Fig. 2 that the carbocylic analogue 1 at a concentration of 500 μM inhibited enzymatic activity by 50% (K i 474 μМ), whereas compound 2 did so by 35-39% (K i 975 μМ). ribavirin monophosphate was used as the control and at a concentration of 2 μМ inhibited the enzymatic activity by 50%; the K m value of the IMP (natural substrate) in this system was 124.4 μМ.
the ability of the monophosphonates 1 and 2 to inhibit the growth of a M. tuberculosis was also tested. the growth of M. tuberculosis culture H37rv under the action of compounds 1 and 2 at concentrations of 2-100 μg/ml (5-320 μМ) was identical to that observed in the control group: the initial phases of culture growth were detected on day 7; entry into stationary phase was detected on day 17. the duration of active bacterial growth is 10 days. compound 2, at concentrations of 200 μg/ml (578 μМ), caused an insignificant delay (2 days) in bacterial growth as compared to the control group.