Next Article in Journal
An Unsymmetrical Tetrathiafulvalene with a Fused 1,2,5-Thiadiazole Ring and Methylthio Groups
Previous Article in Journal
Soft Alkyl Ether Prodrugs of a Model Phenolic Drug: The Effect of Incorporation of Ethyleneoxy Groups on Transdermal Delivery
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Molecules
Volume 14
Issue 10
10.3390/molecules14104246
molecules-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Investigating Biological Activity Spectrum for Novel Styrylquinazoline Analogues

by
Josef Jampilek
1,2,*,
Robert Musiol
3,
Jacek Finster
3,
Matus Pesko
4,
James Carroll
5,
Katarina Kralova
6,
Marcela Vejsova
7,
Jim O'Mahony
5,
Aidan Coffey
5,
Jiri Dohnal
1,2 and
Jaroslaw Polanski
3
1
Zentiva k.s., U kabelovny 130, 102 37 Prague 10, Czech Republic
2
Department of Chemical Drugs, Faculty of Pharmacy, University of Veterinary and Pharmaceutical Sciences, Palackeho 1-3, 612 42 Brno, Czech Republic
3
Institute of Chemistry, University of Silesia, Szkolna 9, 40007 Katowice, Poland
4
Department of Ecosozology and Physiotactics, Faculty of Natural Sciences, Comenius University, Mlynska dolina Ch-2, 84215 Bratislava, Slovakia
5
Department of Biological Sciences, Cork Institute of Technology, Bishopstown, Cork, Ireland
6
Institute of Chemistry, Faculty of Natural Sciences, Comenius University, Mlynska dolina Ch-2, 84215 Bratislava, Slovakia
7
Department of Biological and Medical Sciences, Faculty of Pharmacy in Hradec Kralove, Charles University in Prague, Heyrovskeho 1203, 500 05 Hradec Kralove, Czech Republic
*
Author to whom correspondence should be addressed.
Molecules 2009, 14(10), 4246-4265; https://doi.org/10.3390/molecules14104246
Submission received: 21 September 2009 / Revised: 13 October 2009 / Accepted: 21 October 2009 / Published: 23 October 2009
Browse Figures
Versions Notes

Abstract

:
In this study, series of ring-substituted 2-styrylquinazolin-4(3H)-one and 4-chloro-2-styrylquinazoline derivatives were prepared. The syntheses of the discussed compounds are presented. The compounds were analyzed by RP-HPLC to determine lipophilicity. They were tested for their inhibitory activity on photosynthetic electron transport (PET) in spinach (Spinacia oleracea L.) chloroplasts. Primary in vitro screening of the synthesized compounds was also performed against four mycobacterial strains and against eight fungal strains. Several compounds showed biological activity comparable with or higher than that of the standard isoniazid. It was found that the electronic properties of the R substituent, and not the total lipophilicity of the compound, were decisive for the photosynthesis-inhibiting activity of tested compounds.

1. Introduction

A quinoline moiety is present in many classes of biologically-active compounds. A number of them have been clinically used as antifungal, antibacterial and antiprotozoic drugs [1,2], as well as antituberculotic agents [3,4,5]. Some quinoline-based compounds have also shown antineoplastic, antiasthmatic and antiplatelet activity [6,7,8,9,10,11]. A series of compounds derived from 8-hydroxyquinoline and styrylquinoline derivatives were recently synthesized as potential HIV-1 integrase inhibitors [12,13,14,15]. Our previous study dealing with 8-hydroxyquinoline and styrylquinoline derivatives showed that they could also possess strong antifungal activity [16,17]. According to recently reported results, some new hydroxyquinoline derivatives also possess interesting herbicidal activities [16,18,19,20]. In addition, some of the investigated quinoline derivatives also showed antineoplastic activity [18,21].
Over 50% of commercially available herbicides act by reversibly binding to photosystem II (PS II), a membrane-protein complex in the thylakoid membranes which catalyses the oxidation of water and the reduction of plastoquinone [22] and thereby inhibit photosynthesis [23,24,25]. Some organic compounds, e.g. substituted benzanilides [26] or substituted anilides of 2,6-disubstituted pyridine-4-thiocarboxamides [27] or pyrazine-2-carboxylic acids [28,29] were found to interact with tyrosine radicals TyrZ and TyrD which are situated in D1 and D2 proteins on the donor side of PS II. Due to this interaction interruption of the photosynthetic electron transport occurred.
Tuberculosis (TB) is a worldwide pandemic. About 1/3 of the world's population is infected with Mycobacterium tuberculosis, and almost two million people die every year as a result. A large number of infected people are carriers of the latent form, which creates a potentially dangerous future source of the illness. The HIV pandemic has also led to the rapid growth of the TB epidemic, and increased the likelihood of people dying of TB. Another factor contributing to the rise in TB infections, and consequently to the increased number of deaths, is the appearance of multiple drug-resistance (MDR), i.e., rise of multidrug-resistant TB (MDR-TB) [30,31].
The Mycobacterium genus is composed of the M. tuberculosis complex and other species known as nontuberculous mycobacteria (NTM, or MOTT – mycobacteria other than tuberculosis). In recent decades, the decrease in the prevalence of tuberculosis in developed countries has resulted in an increase in the proportion of diseases caused by NTM [32]. Among these species, the M. avium complex (MAC) has emerged as a major human pathogen, being a common cause of disseminated disease and death in patients with HIV/AIDS [33].
Chronic pulmonary disease is the most common clinical manifestation among the diseases caused by NTM, and the most common pathogens are the species belonging to the MAC, followed by M. kansasii. The clinical characteristics of NTM-related pulmonary disease are, in many cases, extremely similar to those of tuberculosis. Other clinical manifestations are caused principally by M. fortuitum, M. smegmatis and M. abscessus due to peritoneal infection as a result of catheterization or postsurgical infections [34]. The above mentioned non-tuberculous strains are sometimes resistant to commonly used drugs (isoniazid, rifampicin, pyrazinamide and ethambutol) and other antituberculous drugs [30]. Therefore, systematic development of new effective compounds is necessary. Similarly, there is also an urgent need for discovery of new drugs with novel modes of action for the treatment of systemic mycoses. This is due to the rapid growth of the immunocompromised patient population and development of resistance to current azole therapies, and the high toxicity of polyenes [35]. It should be stressed that hydroxyquinolines and their derivatives were introduced as antifungal or antimycobacterial agents in clinical practice and novel compounds of this type are still being investigated [3,4,5,36,37].
This is a follow-up paper to our previous articles [12,13,14,15,16,17,18,19,20,21] dealing with synthesis and biological activities of ring-substituted quinazolinone derivatives. In the context of our previously-described azanaphtalenes, new modifications of quinoline moiety that can trigger interesting biological activity were investigated.
Primary in vitro screening of the synthesized compounds was performed against four mycobacterial strains and against eight fungal strains. The compounds were also tested for their photosynthesis-inhibiting activity (the inhibition of photosynthetic electron transport) in spinach chloroplasts (Spinacia oleracea L.). Lipophilicity (log k) of the compounds was determined using RP-HPLC. Relationships among the structure and in vitro antimicrobial activities or/and inhibitory activity related to inhibition of photosynthetic electron transport (PET) in spinach chloroplasts of the new compounds are discussed.

2. Results and Discussion

2.1. Chemistry

All the studied compounds were prepared according to Scheme 1. Microwave-assisted synthesis facilitated the preparation of quinazoline-related structures. 2-Methyl-4H-benzo[d][1,3]oxazin-4-one was synthesized from anthranilic acid and acetic anhydride. A further reaction with ammonia or hydroxylamine afforded 2-methylquinazolin-4(3H)-one (1) or 3-(2-hydroxyethyl)-2-methylquinazolin-4(3H)-one (2). 2-Styrylquinazolin-4(3H)-ones 3a-k were obtained from appropriate aldehydes using neat microwave-assisted synthesis [38]. Further chlorination/dehydratation with POCl3 yielded 4-chloro-2-styrylquinazoline derivatives 4a-e. Styrylquinazolines can exist as E- or Z-isomers according to the orientation of the ethylene linker. This can greatly affect their biological activity i.e., behaviour at the site of action and complexation mechanism(s). Thus we have studied the isomerism of all the obtained compounds with NMR techniques and crystallography, as formerly described for similar structures [39,40]. Fortunately this feature can be easily determined by examination of the coupling constants of both vinyl protons in the spectra. These are much higher in the case of E-isomers (J > 16 Hz) compared to Z-isomers (J < 12 Hz) [39]. All styrylquinazolines were found to be pure E-isomers, which is in good agreement with previous results [13,17,18,39,40].
Molecules 14 04246 g002 550
Scheme 1. Synthetic pathway and general formula of prepared quinazolinone derivatives:
Scheme 1. Synthetic pathway and general formula of prepared quinazolinone derivatives:
Molecules 14 04246 g002

2.2. Lipophilicity

Many low molecular weight drugs cross biological membranes through passive transport, which strongly depends on their lipophilicity. Lipophilicity is a property that has a major effect on absorption, distribution, metabolism, excretion, and toxicity (ADME/Tox) properties, as well as pharmacological activity. Lipophilicity has been studied and applied as an important drug property for decades [41].
This thermodynamic parameter describes the partitioning of a compound between aqueous and organic phases and is characterized by the partition (log P) coefficient [42,43]. With new computerized methods of log P calculation, the possibility of predicting hydrophobicity in large libraries of compounds came into being. Lipophilicity computing software can usually calculate log P and Clog P. The software calculates log P values as lipophilicity contributions/increments of individual atoms, fragments and the pairs of interacting fragments in the chemical structure, i.e., increments of carbon and hetero atoms, aromatic systems and functional groups. The software calculates lipophilicity contributions according to different internal databases/libraries, so the calculated lipophilicity values are dependent on the software used, and the values for individual compounds may be different. This fact, as well as various ionic/zwitterionic forms and intramolecular interactions, may cause differences between calculated and experimentally determined lipophilicities.
Classical methods for determination of these partition constants are time consuming and not always adequately reliable. It was recognised some time ago that the retention of a compound in reversed-phase liquid chromatography is governed by its lipophilicity, and thus shows correlation with the octanol–water partition coefficient [44]. Reversed phase high performance liquid chromatography (RP-HPLC) provides an excellent platform for computer controlled automated measurements with computerised data acquisition for a large number of investigated compounds. Other advantages in the use of HPLC retention data for lipophilicity determination are the absence of need for concentration determination and method validation, simultaneous separation of small impurities from the main component, sufficiency of small amounts of material for measurements and possibility of their full automation. Therefore the investigation of the true potential of this method is of great importance [45].
The effect of stationary and mobile phase selection has been published by van der Waterbeemd et al. [43] and more recently by Claessens et al. [46]. RP-HPLC methods have become popular and widely used for lipophilicity measurement [47]. A general procedure is the measurement of the directly accessible retention time under isocratic conditions with varying amounts of methanol as an organic modifier in the mobile phase using end-capped non-polar C18 stationary RP columns and calculating the logarithm of capacity factors (log k). Log k is the logarithm of capacity factors in chromatographic approaches, which is related to the partitioning of a compound between a mobile and a (pseudo-)stationary phase. Log k is used as the lipophilicity index converted to log P scale [43,45,46,47,48,49].
Some groups have used a C18 chromatographic column with methanol-water mobile phases to obtain log kw, i.e., the retention factor extrapolated to 0% organic modifier, as an alternative to log P [50]. The log kw is obtained by performing several measurements with various ratios of water/organic solvent. Nevertheless determination of log kw has some disadvantages in that it is time consuming due to the various measurements that need to be undertaken before calculation of log kw [44]. The main reason for the measurement is that it is more convenient to perform a systematic study of log k of various heteroaromatic compounds using mobile phases containing around 50% methanol due to various intramolecular interactions between heteroatoms and substituents [51,52,53]. Therefore this study was performed using methanol/water (55:45) as the mobile phase. The conditions (non-buffered mobile phase) were chosen with respect to conditions of biological evaluations, which are performed mostly under neutral conditions (pH ~ 7). The lipophilicity data can be strongly influenced by intramolecular interactions under the applied chromatographic conditions which were investigated in the paper [54,55].
Lipophilicities (log P/Clog P) of all eighteen compounds 1-4e were calculated using two commercially available programs (ChemDraw Ultra and ACD/LogP) and also measured by means of the RP-HPLC determination of capacity factors k with subsequent calculation of log k. The procedure was performed under isocratic conditions. Neither programme succeeded in resolving the differing lipophilicity values of individual positional isomers inasmuch as the same log P/Clog P values were calculated for 3b-d, 3g-i and 4b-d. The results are shown in Table 1 and illustrated in Figure 1.
The results obtained with respect to all compounds show that the experimentally-determined lipophilicities (log k values) of all compounds are lower than those indicated by the calculated log P/Clog P, as shown in Figure 1, indicating that experimentally-determined log k values correlate relatively poorly with the calculated log P/Clog P. These facts are caused by both the above mentioned limitation of the software programmes used and also possibly to intramolecular interactions between heterocyclic nitrogens and substituents [19,54,55,56,57,58,59]. As expected, compound 3i showed the highest lipophilicity, while compound 1 exhibited the lowest. Series 4a-e showed lower lipophilicity (log k) than series 3a-e, contrary to all calculated log P/Clog P data. The higher lipophilicity of 3a-e compared with 4a-e is caused by intramolecular interactions between N(3) and carbonyl oxygen in the position 4. Similar interactions were described recently [19,55,56,57,58,59]. This hypothesis can be supported by the fact that log k of 1 was lower than 2, although this is contrary to calculated log P/Clog P. When the lipophilicity of both compounds was calculated with intramolecular interactions between N(3)-H···O=C(4), the lipophilicity increased (Clog P (1): 1.343 and Clog P (2): 2.2306). Similar facts may be observed at 3a-e and 4a-e, therefore the experimental log k data of 4a-e were slightly lower than those log k of 3a-e.
Table
Table 1. Comparison of the calculated lipophilicities (log P/Clog P) with the determined log k values, electronic Hammett's parameters (σ) and bulk parameters MR (volume of substituents) [60].
Table 1. Comparison of the calculated lipophilicities (log P/Clog P) with the determined log k values, electronic Hammett's parameters (σ) and bulk parameters MR (volume of substituents) [60].
Comp.Rlog klog P/Clog P ChemOfficelog P ACD/LogPσ [60]MR [60]
1 Molecules 14 04246 i0010.11700.98 / 0.804-0.36 ± 0.59––
2 Molecules 14 04246 i0020.70470.69 / 0.6149-1.23 ± 0.69––
Molecules 14 04246 i003
3aH1.11483.21 / 2.9972.37 ± 0.610.00.0
3b2-OCH31.15093.09 / 2.9162.35 ± 0.62-0.390 [61]6.5
3c3-OCH31.18373.09 / 2.9162.35 ± 0.620.1156.5
3d4-OCH31.13513.09 / 2.9162.32 ± 0.62-0.2686.5
3e2,4-OCH31.19822.96 / 3.0052.20 ± 0.62-0.65813.0
3f3-Cl1.50593.77 / 3.7102.96 ± 0.610.3734.8
3g2-Br1.48304.04 / 3.8603.14 ± 0.64–7.6
3h3-Br1.59044.04 / 3.8603.14 ± 0.640.3917.6
3i4-Br1.59274.04 / 3.8603.14 ± 0.640.2327.6
3j4-CHO0.80052.96 / 2.3501.79 ± 0.631.0305.3
3k2,3,4-OH0.55102.05 / 1.0661.84 ± 0.63–4.5
Molecules 14 04246 i004
4aH1.10885.50 / 4.515224.47 ± 0.560.00.0
4b2-OCH31.14975.38 / 4.434224.47 ± 0.57-0.390 [61]6.5
4c3-OCH31.18275.38 / 4.434224.44 ± 0.570.1156.5
4d4-OCH31.13375.38 / 4.434224.41 ± 0.57-0.2686.5
4e2,4-OCH31.19535.25 / 4.523224.30 ± 0.57-0.65813.0
The presence of phenolic and carbonyl moieties decreased the lipophilicity. Nevertheless, the observation that the lipophilicity of compounds 3k and 3j was close to the lipophilicity of compound 2 was unexpected. Compound 3f showed less lipophilicity compared with 3h. On the basis of comparison of the lipophilicity data log k of both Br-substituted isomers 3g-3i, it can be stated that 4-bromo derivative 3i possessed higher lipophilicity than the 3-bromo isomer 3h and the 2-bromo isomer 3g. A diverse trend can be observed at methoxy moiety substituted compounds 3b-e and 4b-e. Compounds 3e and 4e showed the highest lipophilicity, while compounds 3a and 4a possessed the lowest lipophilicity within individual series of methoxy moiety substituted compounds, according to log k data. Compounds 3a and 4a showed lower lipophilicity in comparison with the results calculated by the software. If the lipophilicity data log k of three position isomers 3b-d, 4b-d are compared, it can be stated that 3-methoxy derivative 3c/4c possessed higher lipophilicity than 2-methoxy derivative 3b/4b and 4-methoxy derivative 3d/4d showed the lowest lipophilicity.
Molecules 14 04246 g001 550
Figure 1. Comparison of the log P/Clog P values computed using the two programs with the calculated log k values. The discussed compounds 1-4e are ordered according to the increase in log k values.
Figure 1. Comparison of the log P/Clog P values computed using the two programs with the calculated log k values. The discussed compounds 1-4e are ordered according to the increase in log k values.
Molecules 14 04246 g001
Generally, based on the facts discussed above, it can be stated that intramolecular interactions, especially within styrylquinazolinone derivatives, play a significant role in the lipophilicity of the discussed compounds. It can be assumed that the determined log k data specify lipophilicity within the individual series of compounds. Lipophilicity increased in the following order: 2,3,4-OH < 4-CHO < H < 4-OCH3 < 2-OCH3 < 3-OCH3 < 2,4-OCH3 < 2-Br < 3-Cl < 3-Br < 4-Br.

2.3. Inhibition of photosynthetic electron transport (PET) in spinach chloroplasts

The evaluated quinazoline derivatives showed relatively low activity related to inhibition of photosynthetic electron transport (PET) in spinach chloroplasts (Table 2). Compounds 4a and 4c expressed the highest PET-inhibiting activity (IC50: 285 and 303 µmol/L, respectively). PET inhibition by several compounds (1, 3a-c, 3g, 3j and 4b) could not be determined due to precipitation of the compounds during the experiment and compound 3k interacted with the artificial electron acceptor DCPIP (change of the colour). The PET-inhibiting activity was expressed by negative logarithm of IC50 value (compound concentration in mol/L causing 50% inhibition of PET). Despite the relatively low inhibitory activity of the studied compounds as well as the relative scarcity of compounds for which PET-inhibiting activity could be determined, the correlations between log (1/IC50) and log k or Hammett's parameters (σ) of the R substituent for both tested groups (3d-i, as well as 4a-d) were performed. The σ values [60,61] mentioned in Table 1 were used for calculations; the σ value for R: 2,4-OCH3 was calculated from the sum of corresponding σ values for R: 2-OCH3 and R: 4-OCH3.
Table
Table 2. IC50 values related to PET inhibition in spinach chloroplasts in comparison with 3-(3,4-dichlorophenyl)-1,1-dimethylurea (DCMU) standard and in vitro antimycobacterial activity MIC/IC90 of compounds 1-3i, 4a-4e in comparison with the standard, isoniazid (INH).
Table 2. IC50 values related to PET inhibition in spinach chloroplasts in comparison with 3-(3,4-dichlorophenyl)-1,1-dimethylurea (DCMU) standard and in vitro antimycobacterial activity MIC/IC90 of compounds 1-3i, 4a-4e in comparison with the standard, isoniazid (INH).
Comp.PET inhibition IC50 [μmol/L]MIC/IC90 [µg/mL]
M. smegmatisM. absessusM. kansasiiM. avium complex
1a>300>300>300>300
2362>300>300>300>300
3aa>300>300>300>300
3ba>100>100>100>100
3ca>100>100>100>100
3d693>100>100>100>100
3e391>100802080
3f1034>300>300>300>300
3ga>100>100>100>100
3h561>100>100>100>100
3i665>100>100>100>100
4a285>100>100>100>100
4ba>100806080
4c303>100>10060>100
4d390>100>100>100>100
4e508>100>100>100>100
DCMU1.9––––
INH–39>100<10<10
a precipitation during the experiment or interaction with DCPIP.
The importance of electronic properties of the R substituent was for the inhibitory activity (IC50 in mol/L) of compounds 3a-i unambiguously much more significant than the compound lipophilicity (log k):
Molecules 14 04246 i005
Molecules 14 04246 i006
Similarly, the inhibitory activity (IC50 in mol/L) of compounds 4a-e depended predominantly on the Hammett's constants (σ) of R substituents:
Molecules 14 04246 i007
Molecules 14 04246 i008
From Equations 1-4 it is evident that in both studied groups of compounds (3d-i and 4a-d) the electronic properties of the R substituent were decisive for photosynthesis-inhibiting activity. For estimation of the potential contribution of the compound lipophilicity to its biological activity, a larger data set for both groups of compounds tested would be necessary.

2.4. In vitro antimycobacterial evaluation

Sixteen compounds 1-3i, 4a-4e were evaluated for their in vitro antimycobacterial activity against four mycobacterial strains and the results are shown in Table 2. According to the results, it is evident that the tested compounds were poorly soluble in the testing medium and therefore concentrations of the compounds in the medium were not sufficient for determination of real antimycobacterial activity. Due to this fact, it can be concluded that the majority of compounds evaluated did not show any significant antimycobacterial activity. Only 2-[(E)-2-(2,4-dimethoxyphenyl)vinyl]quinazolin-4(3H)-one (3e) and 4-chloro-2-[(E)-2-(2-methoxyphenyl)vinyl]quinazoline (4b) expressed an interesting MIC especially against M. kansasii, M. avium complex and M. absessus. Both compounds were more active than INH in case of M. absessus.
With the available data it is difficult to attempt to determine any structure-activity relationships, although some observations can be made. The 4-chloroquinazoline nucleus (series 4) seems to be more advantageous for higher antimycobacterial activity than the quinazolin-4(3H)-one scaffold (series 3); e.g., unsubstituted 3a showed lower activity than 4a.
The benzylidene part of the molecule is also important for antimycobacterial activity. Bulk parameters (the volume of substituents) MR [60] are also very important for activity. According to Table 1, Table 2 it can be assumed that compounds with bulky substituents showed higher antimycobacterial activity. Unsubstituted compounds 3a and chloro substituted 3f possessed less activity than methoxy or bromo substituted compounds. The highest effect was shown by disubstituted 2,4-methoxy derivative 3e. The position of substituents on the benzylidene part of the molecule is important especially for compounds within series 4; compare the activity of compounds 4b > 4c > 4d > 4e.

2.5. In vitro antifungal susceptibility testing

All quinazoline derivatives 1-4e were tested for their in vitro antifungal activity against eight fungal strains. The antifungal activity of all the compounds were in the range from >125 to >500 μmol/L and therefore the activities are not presented in detail. According to these results, it can be concluded that all the compounds are almost completely insoluble in aqueous solvents as they precipitated from the testing medium. Generally, compounds 1 and 2 showed lower activity than most compounds 3 and 4. The substitution of benzylidene part of the molecule by 3-OCH3 (3c, 4c) or 2,3,4-OH (3k) seems to contribute to antifungal activity within both series of compounds.

3. Conclusions

Series of ring-substituted 2-styrylquinazolin-4(3H)-one and 4-chloro-2-styrylquinazoline derivatives were prepared and characterized. All eighteen prepared quinazoline derivatives were analyzed using a RP-HPLC method for lipophilicity measurement and their lipophilicity was determined. The prepared compounds were tested for their antifungal and antimycobacterial activity and for their activity related to the inhibition of photosynthetic electron transport (PET) in spinach chloroplasts (Spinacia oleracea L.). 2-[(E)-2-(2,4-Dimethoxyphenyl)vinyl]quinazolin-4(3H)-one (3e) and 4-chloro-2-[(E)-2-(2-methoxyphenyl)vinyl]quinazoline (4b) exhibited the highest in vitro antimycobacterial activity. 4-Chloro-2-[(E)-2-(3-methoxyphenyl)vinyl]quinazoline (4c) showed the highest PET-inhibiting activity.

4. Experimental

4.1. General

All reagents were purchased from Aldrich. Kieselgel 60, 0.040–0.063 mm (Merck, Darmstadt, Germany) was used for column chromatography. TLC experiments were performed on alumina-backed silica gel 40 F254 plates (Merck, Darmstadt, Germany). The plates were illuminated under UV (254 nm) and evaluated in iodine vapour. The melting points were determined on Boetius PHMK 05 (VEB Kombinat Nagema, Radebeul, Germany) and are uncorrected. The purity of the final compounds was checked by the HPLC separation module Waters Alliance 2695 XE (Waters Corp., Milford, MA, U.S.A.). The detection wavelength 210 nm was chosen. The peaks in the chromatogram of the solvent (blank) were deducted from the peaks in the chromatogram of the sample solution. The purity of individual compounds was determined from the area peaks in the chromatogram of the sample solution. UV spectra (λ, nm) were determined on a Waters Photodiode Array Detector 2996 (Waters Corp., Milford, MA, U.S.A.) in ca 6×10-4 mol methanolic solution and log ε (the logarithm of molar absorption coefficient ε) was calculated for the absolute maximum λmax of individual target compounds. Infrared spectra were recorded using KBr pellets on the FT-IR spectrometer Nicolet 6700 (Nicolet - Thermo Scientific, U.S.A.). All 1H-NMR spectra were recorded on a Bruker AM-500 (499.95 MHz for 1H) instrument (Bruker BioSpin Corp., Germany). Chemicals shifts are reported in ppm (δ) to internal Si(CH3)4, when diffused easily exchangeable signals are omitted.

4.2. Synthesis

2-Methylquinazolin-4(3H)-one (1): Yield 77% of a white crystalline compound; mp 245-247 °C (lit. mp 242-244 °C [62]); HPLC purity: 98.64%; UV (nm), λmax/log ε: 305.1/3.53; 1H-NMR [(CD3)2CO] δ: 2.45 (s, 3H, CH3), 7.44 (t, 1H, Ar-H), 7.59 (d, J = 8.15 Hz, 1H, Ar-H), 7.76 (t, 1H, Ar-H), 8.13 (d, J = 7.94 Hz, 1H, Ar-H), 11.00 (s, 1H, NH).
3-(2-Hydroxyethyl)-2-methylquinazolin-4(3H)-one (2). Yield 52% of a white crystalline compound; mp 154-156 °C; HPLC purity: 99.67%; UV (nm), λmax/log ε: 305.8/3.58; 1H-NMR (DMSO-d6) δ: 2.65 (s, 3H, CH3), 3.66 (q, 2H, CH2), 4.12 (t, 2H, CH2), 5.00 (t, 1H, OH), 7.46 (t, 1H, Ar-H), 7.57 (d, J = 8.14 Hz, 1H, Ar-H), 7.77 (t, 1H, Ar-H), 8.08 (d, J = 8.00 Hz, 1H, Ar-H).

4.2.1. General procedures of synthesis of Compounds 3a-k

A mixture of compound 1 (0.01 mol) and the appropriate aldehyde (0.02 mol) was mixed thoroughly and irradiated in monomode cavity of microwave reactor using pulse sequence (3×5 minutes with 30 sec. intervals) at 250 W. During irradiation, the temperature was controlled between the range 150-180 °C. After the reaction, the mixture was cooled and washed with boiling ether. The product was crystallized from acetic acid.
2-(E)-Styrylquinazolin-4(3H)-one (3a). [63] Yield 50% of a white crystalline compound; mp 253-255 °C (lit. mp 252 °C [64]); HPLC purity: 97.95%; UV (nm), λmax/log ε: 321.3/3.53; 1H-NMR (DMSO-d6) δ: 7.00 (d, J = 16.23 Hz, 1H, C=C-H), 7.41 (t, 1H, Ar-H), 7.42-7.49 (m, 3H, Ar-H), 7.65-7.68 (m, 3H, Ar-H), 7.80 (t, 1H, Ar-H), 7.95 (d, J = 16.16 Hz, 1H, C=C-H), 8.10 (d, 1H, Ar-H), 12.35 (s, 1H, N-H).
2-[(E)-2-(2-Methoxyphenyl)vinyl]quinazolin-4(3H)-one (3b). [63] Yield 76% of a white crystalline compound; mp 234-236 °C (lit. mp 234-236 °C [64]); HPLC purity: 94.04%; UV (nm), λmax/log ε: 343.4/3.62; 1H-NMR (DMSO-d6) δ: 3.90 (s, 3H, OCH3), 7.02 (t, 1H, Ar-H), 7.07 (d, J = 16.24 Hz, 1H, C=C-H), 7.11 (d, 1H, Ar-H), 7.39 (t, 1H, Ar-H), 7.45 (t, 1H, Ar-H), 7.60 (d, 1H, Ar-H), 7.67 (d, 1H, Ar-H), 7.79 (t, 1H, Ar-H), 8.09 (d, 1H, Ar-H), 8.15 (d, J = 16.12 Hz, 1H, C=C-H), 12.36 (s, 1H, N-H).
2-[(E)-2-(3-Methoxyphenyl)vinyl]quinazolin-4(3H)-one (3c). [63] Yield 68% of a white crystalline compound; mp 239-241 °C; HPLC purity: 96.82%; UV (nm), λmax/log ε: 326.4/3.58; 1H-NMR (DMSO-d6) δ: 3.81 (s, 3H, OCH3), 6.98 (d, 1H, Ar-H), 7.01 (d, J = 16.81 Hz, 1H, C=C-H), 7.22 (s, 1H, Ar-H), 7.23 (d, 1H, Ar-H), 7.37 (t, 1H, Ar-H), 7.47 (t, 1H, Ar-H), 7.66 (d, 1H, Ar-H), 7.80 (t, 1H, Ar-H), 7.91 (d, J = 16.14 Hz, 1H, C=C-H), 8.10 (d, 1H, Ar-H), 12.31 (s, 1H, NH).
2-[(E)-2-(4-Methoxyphenyl)vinyl]quinazolin-4(3H)-one (3d). [63] Yield 33% of a white crystalline compound; mp 280-281 °C (lit. mp 284-285 °C [64]); HPLC purity: 94.36%; UV (nm), λmax/log ε: 322.7/3.59; 1H-NMR (DMSO-d6) δ: 3.80 (s, 3H, OCH3), 6.84 (d, J = 16.23 Hz, 1H, C=C-H), 7.01 (d, 2H, Ar-H), 7.45 (t, 1H, Ar-H), 7.60 (d, 2H, Ar-H), 7.64 (d, 1H, Ar-H), 7.78 (t, 1H, Ar-H), 7.90 (d, J = 16.08 Hz, 1H, C=C-H), 8.08 (d, 1H, Ar-H), 12.25 (s, 1H, N-H).
2-[(E)-2-(2,4-Dimethoxyphenyl)vinyl]quinazolin-4(3H)-one (3e). [63] Yield 57% of a white crystalline compound; mp 228-230 °C (lit. mp 228-230 °C [64]); HPLC purity: 96.27%; UV (nm), λmax/log ε: 350.1/3.67; 1H-NMR (DMSO-d6) δ: 3.82 (s, 3H, OCH3), 3.90 (s, 3H, OCH3), 6.63 (d, 1H, Ar-H), 6.64 (s, 1H, Ar-H), 6.94 (d, J = 16.15 Hz, 1H, C=C-H), 7.43 (t, 1H, Ar-H), 7.53 (d, 1H, Ar-H), 7.64 (d, 1H, Ar-H), 7.77 (t, 1H, Ar-H), 8.07 (d, J = 15.21 Hz, 1H, C=C-H), 8.08 (d, 1H, Ar-H), 12.26 (s, 1H, N-H).
2-[(E)-2-(3-Chlorophenyl)vinyl]quinazolin-4(3H)-one (3f). [63] Yield 93% of a white crystalline compound; mp 289 °C; HPLC purity: 96.51%; UV (nm), λmax/log ε: 326.4/3.59; 1H-NMR (CDCl3) δ: 6.93 (d, J = 16.41 Hz, 1H, C=C-H), 7.39 (d, 2H, Ar-H), 7.46-7.53 (m, 2H, Ar-H), 7.64 (s, 1H, Ar-H), 7.79 (d, J = 16 Hz, 1H, C=C-H), 7.77-7.83 (m, 2H, Ar-H), 8.33 (d, 1H, Ar-H), 10.64 (s, 1H, NH).
2-[(E)-2-(2-Bromophenyl)vinyl]quinazolin-4(3H)-one (3g). [63] Yield 71% of a white crystalline compound; mp 279 °C; HPLC purity: 98.84%; UV (nm), λmax/log ε: 326.9/3.59; 1H-NMR (CDCl3) δ: 6.93 (d, J = 16.47 Hz, 1H, C=C-H), 7.40 (t, 1H, Ar-H), 7.50 (t, 1H, Ar-H), 7.67 (d, J = 7.90 Hz, 1H, Ar-H), 7.74-7.82 (m, 4H, Ar-H), 8.12 (d, J = 16.45 Hz, 1H, C=C-H), 8.36 (d, J = 7.88 Hz, 1H, Ar-H), 10.96 (s, 1H, NH).
2-[(E)-2-(3-Bromophenyl)vinyl]quinazolin-4(3H)-one (3h). [63] Yield 43% of a white crystalline compound; mp 277-279 °C; HPLC purity: 97.34%; UV (nm), λmax/log ε: 326.4/3.58; 1H-NMR (CDCl3) δ: 6.91 (d, J = 16.33 Hz, 1H, C=C-H), 7.33 (t, 1H, Ar-H), 7.50-7.56 (m, 2H, Ar-H), 7.55 (s, 1H, Ar-H), 7.73 (d, J = 16.49 Hz, 1H, C=C-H), 7.76-7.82 (m, 3H, Ar-H), 8.33 (d, 1H, Ar-H), 10.31 (s, 1H, NH).
2-[(E)-2-(4-Bromophenyl)vinyl]quinazolin-4(3H)-one (3i). [63] Yield 66% of a white crystalline compound; mp 332 °C; HPLC purity: 97.64%; UV (nm), λmax/log ε: 326.7/3.58; 1H-NMR (DMSO-d6) δ: 7.03 (d, 1H, C=C-H), 7.49 (t, 1H, Ar-H), 7.61 (d, 1H, Ar-H), 7.64 (d, 2H, Ar-H), 7.66 (d, 1H, Ar-H), 7.68 (d, 1H, Ar-H), 7.81 (t, 1H, Ar-H), 7.91 (d, 1H, C=C-H), 8.11 (d, 1H, Ar-H), 12.36 (s, 1H, N-H).
2-[(E)-2-(4-Carbaldehydephenyl)vinyl]quinazolin-4(3H)-one (3j). [63] Yield 35% of a white crystalline compound; mp 218 °C; HPLC purity: 96.93%;. UV (nm), λmax/log ε: 337.9/3.69; 1H-NMR (CDCl3) δ: 7.16 (d, J = 16.13 Hz, 1H, C=C-H), 7.50 (t, 1H, Ar-H), 7.69 (d, 2H, Ar-H), 7.82 (t, 1H, Ar-H), 7.87 (d, 1H, Ar-H), 7.97 (d, 1H, Ar-H), 8.00 (d, J = 16.21 Hz, 1H, C=C-H), 8.11 (d, 2H, Ar-H), 9.95 (s, 1H, CHO), 10.02 (s, 1H, N-H).
2-[(E)-2-(2,3,4-Trihydroxyphenyl)vinyl]quinazolin-4(3H)-one (3k). [63] Yield 60% of a brown crystalline compound; mp 300 °C (decomp.); HPLC purity: 97.67%; UV (nm), λmax/log ε: 365.0/3.65; 1H-NMR (DMSO-d6), δ: 6.39 (d, 1H, Ar-H), 6.83 (d, J = 15.98 Hz, 1H, C=C-H), 6.88 (d, 1H, Ar-H), 7.40 (t, 1H, Ar-H), 7.63 (d, 1H, Ar-H), 7.75 (t, 1H, Ar-H), 8.05 (d, 1H, Ar-H), 8.10 (d, J = 16.05 Hz, 1H, C=C-H), 8.57 (s, 1H, OH), 9.07 (s, 1H, OH), 9.68 (s, 1H, OH), 12.19 (s, 1H, NH).

4.2.2. General procedures of synthesis of Compounds 4a-e

A mixture of styrylquinazolinone derivatives 3 (0.01 mol), N,N-dimethylaniline (0.02 mol) and phosphorus oxychloride (0.015 mol) in dry benzene (50 mL) was stirred and heated under reflux for 3 h. The reaction mixture was then cooled and filtered. The filtrate was diluted with benzene (30 mL) and the solution washed with water (50 mL), twice with 20 % aqueous NaOH (50 mL) and finally twice with water. After drying with MgSO4, the organic solvent was evaporated and the product obtained was crystallized from heptane.
4-Chloro-2-(E)-styrylquinazoline (4a). [63] Yield 81% of an orange crystalline compound; mp 104 °C, (lit. mp 100-101 °C [65]); HPLC purity: 99.34%; UV (nm), λmax/log ε: 314.9/3.67; 1H-NMR (DMSO-d6) δ: 7.34 (d, J = 15.91 Hz, 1H, C=C-H), 7.41 (t, 1H, Ar-H), 7.47 (t, 2H, Ar-H), 7.77-7.80 (m, 3H, Ar-H), 8.02 (d, 1H, Ar-H), 8.06 (t, 1H, Ar-H), 8.12 (d, J = 16.01 Hz, 1H, C=C-H), 8.26 (d, 1H, Ar-H).
4-Chloro-2-[(E)-2-(2-methoxyphenyl)vinyl]quinazoline (4b). [63] Yield 86% of a light yellow crystalline compound; mp 153 °C; HPLC purity: 99.95%; UV (nm), λmax/log ε: 345.1/3.67; 1H-NMR (DMSO-d6) δ: 3.98 (s, 3H, OCH3), 7.04 (t, 1H, Ar-H), 7.12 (d, 1H, Ar-H), 7.37 (d, J = 16.15 Hz, 1H, C=C-H), 7.40 (t, 1H, Ar-H), 7.78 (t, 1H, Ar-H), 7.82 (d, 1H, Ar-H), 8.01 (d, 1H, Ar-H), 8.06 (t, 1H, Ar-H), 8.27 (d, 1H, Ar-H), 8.47 (d, J = 16.15 Hz, 1H, C=C-H).
4-Chloro-2-[(E)-2-(3-methoxyphenyl)vinyl]quinazoline (4c). [63] Yield 81% of a light yellow crystalline compound; mp 137 °C; HPLC purity: 98.62%; UV (nm), λmax/log ε: 342.9/3.64; 1H-NMR (DMSO-d6) δ: 3.90 (s, 3H, OCH3), 6.98 (d, 1H, Ar-H), 7.35 (d, J = 15.75 Hz, 1H, C=C-H), 7.35-7.39 (m, 2H, Ar-H), 7.36 (s, 1H, Ar-H), 7.80 (t, 1H, Ar-H), 8.02 (d, 1H, Ar-H), 8.06 (d, 1H, Ar-H), 8.10 (d, J = 15.82 Hz, 1H, C=C-H), 8.28 (d, 1H, Ar-H).
4-Chloro-2-[(E)-2-(4-methoxyphenyl)vinyl]quinazoline (4d). [63] Yield 51% of a yellow crystalline compound; mp 130-131 °C, (lit. mp 130-131 °C [65]); HPLC purity: 97.43%; UV (nm), λmax/log ε: 339.9/3.64; 1H-NMR (DMSO-d6) δ: 3.87 (s, 3H, OCH3), 7.03 (d, 2H, Ar-H), 7.20 (d, J = 15.87 Hz, 1H, C=C-H), 7.75 (d, 2H, Ar-H), 7.76 (t, 1H, Ar-H), 7.99 (d, 1H, Ar-H), 8.04 (t, 1H, Ar-H), 8.08 (d, J = 15.89 Hz, 1H, C=C-H), 8.25 (d, 1H, Ar-H).
4-Chloro-2-[(E)-2-(2,4-dimethoxyphenyl)vinyl]quinazoline (4e). [63] Yield 48% of a yellow crystalline compound; mp 172 °C; HPLC purity: 98.57%; UV (nm), λmax/log ε: 355.0/3.67; IR (KBr, cm-1): 2980, 2938, 1607, 1556, 1504, 1477, 1450, 1384, 1329, 959, 768, 756; 1H-NMR [(CD3)2CO] δ: 3.88 (s, 3H, OCH3), 3.98 (s, 3H, OCH3), 6.64 (d, 1H, Ar-H), 6.66 (s, 1H, Ar-H), 7.27 (d, J=16.13 Hz, 1H, C=C-H), 7.75 (d, 1H, Ar-H), 7.60 (t, 1H, Ar-H), 7.98 (d, 1H, Ar-H), 8.02 (t, 1H, Ar-H), 8.25 (d, 1H, Ar-H), 8.40 (d, J=16.13 Hz, 1H, C=C-H).

4.3. Lipophilicity HPLC determination (capacity factor k / calculated log k)

The HPLC separation module Waters Alliance 2695 XE and Waters Photodiode Array Detector 2996 (Waters Corp., Milford, MA, U.S.A.) were used. The chromatographic column Symmetry® C18 5 μm, 4.6 × 250 mm, Part No. WAT054275, (Waters Corp., Milford, MA, U.S.A.) was used. The HPLC separation process was monitored by Millennium32® Chromatography Manager Software, Waters 2004 (Waters Corp.). The mixture of MeOH p.a. (55.0%) and H2O-HPLC – Mili-Q Grade (45.0%) was used as a mobile phase. The total flow of the column was 0.9 mL/min, injection 30 μL, column temperature 30 °C and sample temperature 10 °C. The detection wavelength 210 nm was chosen. The KI methanolic solution was used for the dead time (tD) determination. Retention times (tR) were measured in minutes. The capacity factors k were calculated using the Millennium32® Chromatography Manager Software according to formula k = (tR - tD)/tD, where tR is the retention time of the solute, whereas tD denotes the dead time obtained via an unretained analyte. The log k values, calculated from the capacity factor k of the individual compounds, are shown in Table 1.

4.4. Lipophilicity calculations

Log P, i.e., the logarithm of the partition coefficient for n-octanol/water, was calculated using the programs CS ChemOffice Ultra ver. 10.0 (CambridgeSoft, Cambridge, MA, U.S.A.) and ACD/LogP ver. 1.0 (Advanced Chemistry Development Inc., Toronto, Canada). Clog P values (the logarithm of n-octanol/water partition coefficient based on established chemical interactions) were generated by means of the CS ChemOffice Ultra ver. 10.0 software. The results are shown in Table 1.

4.5. Study of inhibition photosynthetic electron transport (PET) in spinach chloroplasts

Chloroplasts were prepared from spinach (Spinacia oleracea L.) according to Masarovicova and Kralova [66]. The inhibition of photosynthetic electron transport (PET) in spinach chloroplasts was determined spectrophotometrically (Genesys 6, Thermo Scientific, U.S.A.) using an artificial electron acceptor 2,6-dichlorophenol-indophenol (DCIPP) according to Kralova et al. [67] and the rate of photosynthetic electron transport was monitored as a photoreduction of DCPIP. The measurements were carried out in phosphate buffer (0.02 mol/L, pH 7.2) containing sucrose (0.4 mol/L), MgCl2 (0.005 mol/L) and NaCl (0.015 mol/L). The chlorophyll content was 30 mg/L in these experiments and the samples were irradiated (~100 W/m2) from 10 cm distance with a halogen lamp (250 W) using a 4 cm water filter to prevent warming of the samples (suspension temperature 22 °C). The studied compounds were dissolved in DMSO due to their limited water solubility. The applied DMSO concentration (up to 4%) did not affect the photochemical activity in spinach chloroplasts. The inhibitory efficiency of the studied compounds was expressed by IC50 values, i.e. by molar concentration of the compounds causing 50% decrease in the oxygen evolution rate relative to the untreated control. The comparable IC50 value for a selective herbicide 3-(3,4-dichlorophenyl)-1,1-dimethylurea, DCMU (Diuron®) was about 1.9 μmol/L [68]. The results are summarized in Table 2.

4.6. In vitro antimycobacterial evaluation

Clinical isolates of Mycobacterium avium complex CIT19/06, M. kansasii CIT11/06, M. absessus CIT21/06 and strain M. smegmatis MC2155 were grown in Middlebrook broth (MB), supplemented with OADC supplement (Oleic, Albumin, Dextrose, Catalase, Becton Dickinson, U.K.). Identification of these isolates was performed using biochemical and molecular protocols. At log phase growth, the 10 mL culture was centrifuged at 15,000 RPM for 20 minutes using a bench top centrifuge (Model CR 4-12 Jouan Inc. U.K). Following the removal of the supernatant, the pellet was washed in fresh Middlebrook 7H9GC broth and re-suspended in 10 mL of fresh supplemented MB. The turbidity was adjusted to match McFarland standard No. 1 (3 × 108 CFU) with MB broth. A further 1:20 dilution of the culture was then performed in MB broth.
The antimicrobial susceptibility of all four mycobacteria was investigated in 96 well plate format. Here, sterile deionised water (150 µL) was added to all outer-perimeter wells of the plates to minimize evaporation of the medium in the test wells during incubation. Each dilution (150 µL) was incubated with each of the mycobacterial species (150 µL). Dilutions of each compound were prepared in duplicate. For all synthesized compounds, final concentrations ranged from 300 µg/mL to 10 µg/mL. All compounds were prepared in DMSO and subsequent dilutions were made in supplemented Middlebrook broth. The plates were sealed with parafilm and were incubated at 37 °C overnight in the case of M. smegmatis and M. absessus and for five days in the case of M. kansasii and M. avium complex. Following incubation, a 10% addition of alamarBlue (AbD Serotec) was mixed into each well and readings at 570 nm and 600 nm were taken, initially for background subtraction and subsequently after 24 hour re-incubation. The background subtraction is necessary with strongly coloured compounds which may interfere with the interpretation of any colour change. In non-interfering compounds, a blue colour in the well was interpreted as an absence of growth, and a pink colour was scored as growth. The MIC was initially defined as the lowest concentration which prevented a visual colour change from blue to pink. The results are shown in Table 2.

4.7. In vitro antifungal susceptibility testing

The broth microdilution test [69,70] was used for the assessment of in vitro antifungal activity of the synthesized compounds against Candida albicans ATCC 44859 (CA), Candida tropicalis 156 (CT), Candida krusei ATCC 6258 (CK), Candida glabrata 20/I (CG), Trichosporon asahii 1188 (TA), Aspergillus fumigatus 231 (AF), Absidia corymbifera 272 (AC), and Trichophyton mentagrophytes 445 (TM). Fluconazole (FLU) was used as the standard of a clinically used antimycotic drug. The procedure was performed with twofold dilution of the compounds in RPMI 1640 (Sevapharma a.s., Prague, Czech Republic) buffered to pH 7.0 with 0.165 mol of 3-morpholino-propane-1-sulfonic acid (MOPS, Sigma, Germany). The final concentrations of the compounds ranged from 500 to 0.975 μmol/L. Drug–free controls were included. The MIC was defined as an 80% or greater (IC80) reduction of growth in comparison with the control. The values of MICs were determined after 24 and 48 h of static incubation at 35 °C. For T. mentagrophytes, the final MICs were determined after 72 and 120 h of incubation. The results are summarized in Table 3.

Acknowledgements

This study was supported by the Polish Ministry of Science N405 178735, by the Ministry of Education of the Czech Republic MSM 6215712403 and by the Irish Department of Education and Science TSR Strand1-06/CR08 and by Sanofi-Aventis Pharma Slovakia.
  • Sample Availability: Samples of the compounds are available from the authors.

References

  1. Roth, H.J.; Fenner, H. Arzneistoffe, 3rd ed; Deutscher Apotheker Verlag: Stuttgart, Germany, 2000; pp. 51–114. [Google Scholar]
  2. Harris, C.R.; Thorarensen, A. Advances in the discovery of novel antibacterial agents during the year 2002. Curr. Med. Chem. 2004, 11, 2213–2243. [Google Scholar]
  3. Andries, K.; Verhasselt, P.; Guillemont, J.; Gohlmann, H.W.; Neefs, J.M.; Winkler, H.; Van Gestel, J.; Timmerman, P.; Zhu, M.; Lee, E.; Williams, P.; de Chaffoy, D.; Huitric, E.; Hoffner, S.; Cambau, E.; Truffot-Pernot, C.; Lounis, N.; Jarlier, V. A diarylquinoline drug active on the ATP synthase of Mycobacterium tuberculosis. Science 2005, 307, 223–227. [Google Scholar]
  4. Vangapandu, S.; Jain, M.; Jain, R.; Kaur, S.; Singh, P.P. Ring-substituted quinolines as potential anti-tuberculosis agents. Bioorg. Med. Chem. 2004, 12, 2501–2508. [Google Scholar]
  5. Carta, A.; Piras, S.; Palomba, M.; Jabes, D.; Molicotti, P.; Zanetti, S. Anti-mycobacterial activity of quinolones. Triazoloquinolones a new class of potent anti-mycobacterial agents. Anti-Infective Agents Med. Chem. 2008, 7, 134–147. [Google Scholar]
  6. Sissi, C.; Palumbo, M. The quinolone family: From antibacterial to anticancer agents. Curr. Med. Chem. Anti-Canc. Agents 2003, 3, 439–450. [Google Scholar] [CrossRef]
  7. Bossu, E.; Agliano, A.M.; Desideri, N.; Sestili, I.; Porra, R.; Grandilone, M.; Quaglia, M.G. LTB4 as marker of 5-LO inhibitory activity of two new N-ethoxycarbonyl-4-quinolones. J. Pharm. Biomed. Anal. 1999, 19, 539–549. [Google Scholar]
  8. Ko, T.C.; Hour, M.J.; Lien, J.C.; Teng, C.M.; Lee, K.H.; Kuo, S.C.; Huang, L.J. Synthesis of 4-alkoxy-2-phenylquinoline derivatives as potent antiplatelet agents. Bioorg. Med. Chem. Lett. 2001, 11, 279–282. [Google Scholar]
  9. Jampilek, J.; Dolezal, M.; Kunes, J.; Vichova, P.; Jun, D.; Raich, I.; O´Connor, R.; Clynes, M. Synthesis of (2E)-2-methyl-3-(4-{[4-(quinolin-2-ylmethoxy)phenyl]sulfanyl}phenyl)prop-2-enoic acid (VUFB 20609) and 2-methyl-3-(4-{[4-(quinolin-2-ylmethoxy)phenyl]sulfanyl}phenyl)propionic acid (VUFB 20584) as potential antileukotrienic agents. J. Pharm. Pharmacol. 2004, 56, 783–794. [Google Scholar]
  10. Jampilek, J.; Dolezal, M.; Kunes, J.; Vichova, P.; Jun, D.; Raich, I.; O´Connor, R.; Clynes, M. Preparation of 2-(4-{[4-(quinolin-2-ylmethoxy)phenyl]sulfanyl}phenyl)propionic acid (VUFB 20615) and 2-methyl-2-(4-{[4-(quinolin-2-ylmethoxy)phenyl]sulfanyl}phenyl)propionic acid (VUFB 20623) as potential antileukotrienic agents. Curr. Org. Chem. 2004, 8, 1235–1243. [Google Scholar]
  11. Jampilek, J.; Dolezal, M.; Opletalova, V.; Hartl, J. 5-Lipoxygenase, leukotrienes biosynthesis and potential antileukotrienic agents. Curr. Med. Chem. 2006, 13, 117–129. [Google Scholar] [CrossRef]
  12. Polanski, J.; Zouhiri, F.; Jeanson, L.; Desmaele, D.; d’Angelo, J.; Mouscadet, J.F.; Gieleciak, R.; Gasteiger, J.; Le Bret, M. Use of Kohonen neural network for rapid screening of ex vivo anti-HIV activity of styrylquinolines. J. Med. Chem. 2002, 45, 4647–4654. [Google Scholar]
  13. Polanski, J.; Niedbala, H.; Musiol, R.; Tabak, D.; Podeszwa, B.; Gieleciak, R.; Bak, A.; Palka, A.; Magdziarz, T. Analogues of the styrylquinoline and styrylquinazoline HIV-1 integrase inhibitors: Design and synthetic problems. Acta Poloniae Pharm. Drug Res. 2004, 61, 3–4. [Google Scholar]
  14. Polanski, J.; Niedbala, H.; Musiol, R.; Podeszwa, B.; Tabak, D.; Palka, A.; Mencel, A.; Finster, J.; Mouscadet, J.F.; Le Bret, M. 5-Hydroxy-8-nitro-6-quinaldic acid as a novel molecular scaffold for HIV-1 integrase inhibitors. Lett. Drugs Des. Disc. 2006, 3, 175–178. [Google Scholar]
  15. Polanski, J.; Niedbala, H.; Musiol, R.; Podeszwa, B.; Tabak, D.; Palka, A.; Mencel, A.; Mouscadet, J.F.; Le Bret, M. Fragment based approach for the investigation of HIV-1 integrase inhibition. Lett. Drugs Des. Disc. 2007, 4, 99–105. [Google Scholar]
  16. Jampilek, J.; Dolezal, M.; Kunes, J.; Buchta, V.; Kralova, K. Quinaldine derivatives: Preparation and biological activity. Med. Chem. 2005, 1, 591–599. [Google Scholar]
  17. Musiol, R.; Jampilek, J.; Buchta, V.; Niedbala, H.; Podeszwa, B.; Palka, A.; Majerz-Maniecka, K.; Oleksyn, B.; Polanski, J. Antifungal properties of new series of quinoline derivatives. Bioorg. Med. Chem. 2006, 14, 3592–3598. [Google Scholar]
  18. Musiol, R.; Jampilek, J.; Kralova, K.; Richardson, D.R.; Kalinowski, D.; Podeszwa, B.; Finster, J.; Niedbala, H.; Palka, A.; Polanski, J. Investigating biological activity spectrum fornovel quinoline analogues. Bioorg. Med. Chem. 2007, 15, 1280–1288. [Google Scholar]
  19. Musiol, R.; Tabak, D.; Niedbala, H.; Podeszwa, B.; Jampilek, J.; Kralova, K.; Dohnal, J.; Finster, J.; Mencel, A.; Polanski, J. Investigating biological activity spectrum for novel quinoline analogues 2: Hydroxyquinolinecarboxamides with photosynthesis inhibiting activity. Bioorg. Med. Chem. 2008, 16, 4490–4499. [Google Scholar]
  20. Jampilek, J.; Musiol, R.; Pesko, M.; Kralova, K.; Vejsova, M.; Carroll, J.; Coffey, A.; Finster, J.; Tabak, D.; Niedbala, H.; Kozik, V.; Polanski, J.; Csollei, J.; Dohnal, J. Ring-substituted 4-hydroxy-1H-quinolin-2-ones: Preparation and biological activity. Molecules 2009, 14, 1145–1159. [Google Scholar]
  21. Podeszwa, B.; Niedbala, H.; Polanski, J.; Musiol, R.; Tabak, D.; Finster, J.; Serafin, K.; Wietrzyk, J.; Boryczka, S.; Mol, W.; Jampilek, J.; Dohnal, J.; Kalinowski, D.; Richardson, D.R. Investigating the antiproliferative activity of quinoline-5,8-dione analogues on tumour cell lines. Bioorg. Med. Chem. Lett. 2007, 17, 6138–6141. [Google Scholar]
  22. Draber, W.; Tietjen, K.; Kluth, J.F.; Trebst, A. Herbicides in photosynthesis research. Angew. Chem. 1991, 3, 1621–1633. [Google Scholar]
  23. Tischer, W.; Strotmann, H. Relationship between inhibitor binding by chloroplasts and inhibition of photosynthetic electron transport. Biochim. Biophys. Acta 1977, 460, 113–125. [Google Scholar] [CrossRef]
  24. Trebst, A.; Draber, W. Structure activity correlations of recent herbicides in photosynthetic reactions. In Advances in Pesticide Science; Greissbuehler, H., Ed.; Pergamon Press: Oxford, UK, 1979; pp. 223–234. [Google Scholar]
  25. Bowyer, J.R.; Camilleri, P.; Vermaas, W.F.J. Herbicides, Topics in Photosynthesis; Baker, N.R., Percival, M.P., Eds.; Elsevier: Amsterdam, The Netherlands, 1991; Volume 10, pp. 27–85. [Google Scholar]
  26. Kralova, K.; Sersen, F.; Kubicova, L.; Waisser, K. Inhibition of photosynthetic electron transport in spinach chloroplasts by 3-and 4-halogeno substituted benzanilides and thiobenzanilides. J. Trace Microprobe Techn. 2000, 18, 251–256. [Google Scholar]
  27. Kralova, K.; Sersen, F.; Miletin, M.; Dolezal, M. Inhibitory effects of substituted benzanilides on photosynthetic electron transport in spinach chloroplasts. Chem. Pap. 2002, 56, 214–217. [Google Scholar]
  28. Dolezal, M.; Miletin, M.; Kunes, J.; Kralova, K. Synthesis and biological evaluation of some amides of pyrazine-2-carboxylic acids. Molecules 2002, 7, 363–373. [Google Scholar] [CrossRef]
  29. Dolezal, M.; Palek, L.; Vinsova, J.; Buchta, V.; Jampilek, J.; Kralova, K. Substituted pyrazinecarboxamides: synthesis and biological evaluation. Molecules 2006, 11, 242–256. [Google Scholar] [CrossRef]
  30. Available online: http://www.who.int/tb/publications/global_report/2008/summary/en/index.html/ (21 September 2009).
  31. Espinal, M.A. The global situation of MDR-TB. Tuberculosis 2003, 83, 44–51. [Google Scholar] [CrossRef]
  32. Field, S.K.; Cowie, R.L. Lung disease due to the more common nontuberculous mycobacteria. Chest 2006, 129, 1653–1672. [Google Scholar] [CrossRef]
  33. Wagner, D.; Young, L.S. Nontuberculous mycobacterial infections: A clinical review. Infection 2004, 32, 257–270. [Google Scholar] [CrossRef]
  34. Morrone, N.; Cruvinel, M.C.; Morrone, N., Jr.; Freire, J.A.; Oliveira, L.M.; Gonçalves, C. Pneumopatia causada por Mycobacterium kansasii. J. Pneumol. 2003, 29, 341–349. [Google Scholar] [CrossRef]
  35. Available online: http://www.doctorfungus.org/ (21 September 2009).
  36. Gershon, H.; Gershon, M.; Clarke, D.D. Synergistic mixtures of fungitoxic monochloro- and dichloro-8-quinolinols against five fungi. Mycopathologia 2004, 158, 131–135. [Google Scholar] [CrossRef]
  37. Dardari, Z.; Lemrani, M.; Bahloul, A.; Sebban, A.; Hassar, M.; Kitane, S.; Berrada, M.; Boudouma, M. Antileishmanial activity of a new 8-hydroxyquinoline derivative designed7-[5′-(3′-phenylisoxazolino)methyl]-8-hydroxyquinoline: preliminary study. Farmaco 2004, 59, 195–199. [Google Scholar] [CrossRef]
  38. Musiol, R.; Podeszwa, B.; Finster, J.; Niedbala, H.; Polanski, J. An efficient microwave-assisted synthesis of structurally diverse styrylquinolines. Monatsh. Chem. 2006, 137, 1211–1217. [Google Scholar]
  39. Musiol, R.; Niedbala, H.; Majerz-Maniecka, K.; Oleksyn, B.; Polanski, J. Synthesis and structure of styrylquinolines. Ann. Pol. Chem. Soc. 2005, 1, 118–122. [Google Scholar]
  40. Majerz-Maniecka, K.; Musiol, R.; Nitek, W.; Oleksyn, B.; Mouscadet, J.F.; Le Bret, M.; Polanski, J. Intermolecular interactions in the crystal structures of potential HIV-1 integrase inhibitors. Bioorg. Med. Chem. Lett. 2006, 16, 1005–1009. [Google Scholar]
  41. Kerns, E.H.; Li, D. Drug-like Properties: Concept, Structure Design and Methods; Elsevier: San Diego, CA, USA, 2008. [Google Scholar]
  42. Avdeef, A. Physicochemical profiling (permeability, solubility, charge state). Curr. Topics Med. Chem. 2001, 1, 277–351. [Google Scholar] [CrossRef]
  43. Pliska, V. Lipophilicity in drug action and toxicology. In Methods and Principles in Medicinal Chemistry, 1st; Pliska, V., Testa, B., van der Waterbeemd, H., Eds.; Wiley-VCH: Weinheim, DE, 1996; Volume 4, pp. 1–6. [Google Scholar]
  44. Valko, K. Application of high-performance liquid chromatography based measurements of lipophilicity to model biological distribution. J. Chromatogr. A 2004, 1037, 299–310. [Google Scholar]
  45. Valko, K.; Du, C.M.; Bevan, C.; Reynolds, D.P.; Abraham, M.H. Rapid method for the estimation of octanol/water partition coefficient (log Poct) from gradient RP-HPLC retention and a hydrogen bond acidity term (Σα2H). Curr. Med. Chem. 2001, 8, 1137–1146. [Google Scholar] [CrossRef]
  46. Cimpan, G.; Irimie, F.; Gocan, S.; Claessens, H.A. Role of stationary phase and eluent composition on the determination of log P values of N-hydroxyethylamide of aryloxyalkylen and pyridine carboxylic acids by reversed-phase high-performance liquid chromatography. J. Chromatogr. B 1998, 714, 247–261. [Google Scholar] [CrossRef]
  47. Gocan, S.; Cimpan, G.; Comer, J. Lipophilicity measurements by liquid chromatography. Adv. Chromatogr. 2006, 44, 79–176. [Google Scholar]
  48. Hartmann, T.; Schmitt, J. Lipophilicity – beyond octanol/water: A short comparison of modern technologies. Drug Discov. Today Technol. 2004, 1, 431–439. [Google Scholar] [CrossRef]
  49. Nasal, A.; Siluk, D.; Kaliszan, R. Chromatographic retention parameters in medicinal chemistry and molecular pharmacology. Curr. Med. Chem. 2003, 10, 381–426. [Google Scholar] [CrossRef]
  50. Piraprez, G.; Herent, M.F.; Collin, S. Determination of the lipophilicity of aroma compounds by RP-HPLC. Flavour Fragr. J. 1998, 13, 400–408. [Google Scholar] [CrossRef]
  51. Yamagami, C.; Iwasaki, K.; Ishikawa, A. Hydrophobicity parameters determined by reversed-phase liquid chromatography. XII. Comparison of capacity factors and octane/methanol-water partition coefficients for monosubstituted pyrazines, and effect of octanol added to both partitioning systems. Chem. Pharm. Bull. 1997, 45, 1653–1658. [Google Scholar] [CrossRef]
  52. Yamagami, C.; Araki, K.; Ohnishi, K.; Hanasato, K.; Inaba, H.; Aono, M.; Ohta, A. Measurement and prediction of hydrophobicity parameters for highly lipophilic compounds: Application of the HPLC column-switching technique to measurement of log P of diarylpyrazines. J. Pharm. Sci. 1999, 88, 1299–1304. [Google Scholar]
  53. Yamagami, C.; Kawase, K.; Iwaki, K. Hydrophobicity parameters determined by reversed-phase liquid chromatography. XV: Optimal conditions for prediction of log Poct by using RP-HPLC procedures. Chem. Pharm. Bull. 2002, 50, 1578–1583. [Google Scholar]
  54. Kucerova-Chlupacova, M.; Opletalova, V.; Jampilek, J.; Dolezel, J.; Dohnal, J.; Kunes, J.; Pour, M.; Kunes, J.; Vorisek, V. New hydrophobicity constants of substituents in pyrazine rings derived from RP-HPLC Study. Collect. Czech. Chem. Comm. 2008, 73, 1–18. [Google Scholar]
  55. Musiol, R.; Jampilek, J.; Podeszwa, B.; Finster, J.; Tabak, D.; Dohnal, J.; Polanski, J. RP-HPLC Determination of drug lipophilicity in series of quinoline derivatives. Cent. Eur. J. Chem. 2009, 7, 586–597. [Google Scholar] [CrossRef]
  56. Dolezal, M.; Jampilek, J.; Osicka, Z.; Kunes, J.; Buchta, V.; Vichova, P. Substituted 5-aroylpyrazine-2-carboxylic acid derivatives: Synthesis and biological activity. Farmaco 2003, 58, 1105–1111. [Google Scholar] [CrossRef]
  57. Jampilek, J.; Vinsova, J.; Dohnal, J. Synthesis and hydrophobic properties of benzoxazoles. In Proceedings of the 9th International Electronic Conference on Synthetic Organic Chemistry (ECSOC-9), November 1–30, 2005; Seijas, J.A., Tato, M.P.V., Eds.; MDPI: Basel, Switzerland, 2005; p. a008. [Google Scholar]
  58. Jampilek, J.; Vinsova, J.; Dohnal, J. Synthesis and hydrophobic properties of substituted 2-aryl-5,7-di-tert-butylbenzoxazoles. In Proceedings of the 10th International Electronic Conference on Synthetic Organic Chemistry (ECSOC-10), November 1–30, 2006; Seijas, J.A., Tato, M.P.V., Eds.; MDPI: Basel, Switzerland, 2006; p. a003. [Google Scholar]
  59. Vinsova, J.; Cermakova, K.; Tomeckova, A.; Ceckova, M.; Jampilek, J.; Cermak, P.; Kunes, J.; Dolezal, M.; Staud, F. Synthesis and antimicrobial evaluation of new 2-substituted 5,7-di-tert-butylbenzoxazoles. Bioorg. Med. Chem. 2006, 14, 5850–5865. [Google Scholar]
  60. Norrington, F.E.; Hyde, R.M.; Williams, S.G.; Wotton, R. Physicochemical-activity relations in practice. 1. Rational and self-consistent data bank. J. Med. Chem. 1975, 18, 604–607. [Google Scholar]
  61. Takahata, Y.; Chong, D.P. Estimation of Hammett sigma constants of substituted benzenes through accurate density-functional calculation of core-electron binding energy shifts. Int. J. Quantum Chem. 2005, 103, 509–515. [Google Scholar] [CrossRef]
  62. Nielsen, K.E.; Pedersen, E.B. Phosphoramides. XII. Phosphorus pentaoxide – amine hydrochloride as reagents in the synthesis of 4-(3H)-quinazolinones and 4-quinazolinamines. Acta Chem. Scand. Ser. B 1980, 34, 637–642. [Google Scholar]
  63. Finster, J.; Kalinowski, D.; Musiol, R.; Mrozek, A.; Szurko, A.; Serafin, A.; Kamalapuram, S.K.; Kovacevic, Z.; Jampilek, J.; Ratuszna, A.; Rezeszowska-Wolny, J.; Richardson, D.R.; Polanski, J. Investigating anti-proliferative activity of styrylazanaftalenes and azanaftalenediones. Bioorg. Med. Chem. 2009. submitted. [Google Scholar]
  64. Kovalenko, S.; Belenichev, I.; Nikitin, V.; Karpenko, A. Search for substances with antioxidant and antiamnestic activities among 2-substituted 4-(3H)-quinazolones. Acta Pol. Pharm. Drug Design 2003, 60, 275–279. [Google Scholar]
  65. Botros, S.; Shaban, M. Synthesis of some 2-styrylquinazoline derivatives structurally related to certain chemotherapeutic agents. Pharmazie 1978, 33, 646–647. [Google Scholar]
  66. Masarovicova, E.; Kralova, K. Approaches to measuring plant photosynthesis activity. In Handbook of Photosynthesis, 2nd; Pessarakli, M., Ed.; Taylor & Francis Group: Boca Raton, London-New York-Singapore, 2005; pp. 617–656. [Google Scholar]
  67. Kralova, K.; Sersen, F.; Sidoova, E. Photosynthesis inhibition produced by 2-alkylthio-6-R-benzothiazoles. Chem. Pap. 1992, 46, 348–350. [Google Scholar]
  68. Fedke, C. Biochemistry and Physiology of Herbicide Action; Springer Verlag: Berlin-Heidelberg/New York, Germany/US, 1982. [Google Scholar]
  69. Sheehan, D.J.; Espinel-Ingroff, A.; Steele, M.; Webb, C.D. Antifungal susceptibility testing of yeasts: A brief overview. Clin. Infect. Dis. 1993, 17, 494–500. [Google Scholar]
  70. National Committee for Clinical Laboratory standards. Reference Method for Broth Dilution Antifungal Susceptibility Testing of Yeast. Approved Standard, NCCLS document M27-A; NCCLS: Villanova, PA, USA, 1997.

Share and Cite

MDPI and ACS Style

Jampilek, J.; Musiol, R.; Finster, J.; Pesko, M.; Carroll, J.; Kralova, K.; Vejsova, M.; O'Mahony, J.; Coffey, A.; Dohnal, J.; et al. Investigating Biological Activity Spectrum for Novel Styrylquinazoline Analogues. Molecules 2009, 14, 4246-4265. https://doi.org/10.3390/molecules14104246

AMA Style

Jampilek J, Musiol R, Finster J, Pesko M, Carroll J, Kralova K, Vejsova M, O'Mahony J, Coffey A, Dohnal J, et al. Investigating Biological Activity Spectrum for Novel Styrylquinazoline Analogues. Molecules. 2009; 14(10):4246-4265. https://doi.org/10.3390/molecules14104246

Chicago/Turabian Style

Jampilek, Josef, Robert Musiol, Jacek Finster, Matus Pesko, James Carroll, Katarina Kralova, Marcela Vejsova, Jim O'Mahony, Aidan Coffey, Jiri Dohnal, and et al. 2009. "Investigating Biological Activity Spectrum for Novel Styrylquinazoline Analogues" Molecules 14, no. 10: 4246-4265. https://doi.org/10.3390/molecules14104246

APA Style

Jampilek, J., Musiol, R., Finster, J., Pesko, M., Carroll, J., Kralova, K., Vejsova, M., O'Mahony, J., Coffey, A., Dohnal, J., & Polanski, J. (2009). Investigating Biological Activity Spectrum for Novel Styrylquinazoline Analogues. Molecules, 14(10), 4246-4265. https://doi.org/10.3390/molecules14104246

Article Metrics

Back to TopTop