Tetrahedron 65 (2009) 7730 7740
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Contents lists available at ScienceDirect
Tetrahedron
Tetrahedron
journal homepage: www.elsevier.com/locate/tet
journal homepage: www.elsevier.com/locate/tet
Syntheses, structural and antimicrobial studies of a new N-allylamide
of monensin A and its complexes with monovalent metal cations
a a b a,*
Daniel qowicki , Adam Huczyński , Joanna Stefańska , Bogumil Brzezinski
a
Faculty of Chemistry, Adam Mickiewicz University, Grunwaldzka 6, 60-780 Poznan, Poland
b
Medical University, Department of Pharmaceutical Microbiology, Oczki 3, 02-007 Warsaw, Poland
a r t i c l e i n f o a b s t r a c t
Article history:
AnewN-allylamide of monensin A (M-AM2) was synthesized and its capacity to form complexes with Liþ, Naþ
1 13
Received 25 March 2009
and Kþcations was studied by ESI MS, Hand C NMR, FTIR spectroscopy and PM5 semi-empirical methods.
Received in revised form 28 May 2009
ESI mass spectrometry indicates that M-AM2 forms complexes with Liþ, Naþand Kþof exclusively 1:1 stoi-
Accepted 19 June 2009
chiometry which are stable up to cvź70 V, and the formation of 1:1 complexes between M-AM2 and Naþ
Available online 24 June 2009
cations is strongly favoured. Above cvź90 V we observe fragmentation of the respective complexes involving
several dehydration steps. The spectroscopic studies show that the structures of the M-AM2 and its complexes
Keywords:
with Liþ, Naþand Kþcations are stabilized by intramolecular hydrogen bonds in which the OH groups are
Ionophores
always involved. The data also demonstrate that the C]O amide group is engaged in the complexation process
Antibacterial activity
of each cation. However with the Kþcation we also found a structure in which this C]O amide group does not
Complexes
participate in the complexation to a significant extent. The in vitro biological tests of M-AM2 amide show its
Monovalent cations
Hydrogen bonds good activity towards some strains of Gram-positive bacteria (Giz 13 19 mm; MIC 25 100 mg/ml).
Ó 2009 Elsevier Ltd. All rights reserved.
1. Introduction biological activities.20 34 Antimicrobial studies of monensin A esters
demonstrate that only three of them, including allyl ester, show an-
Monensin A, besides monensin B and other metabolites produced tibacterial activity against human pathogenic bacteria.31 The antimi-
by various strains of Streptomyces cinnamonensis, is a well known crobial activity was shown to depend on the substituted group (allyl
natural polyether antibiotic.1 3 Monensin acid exists in a pseudo-cy- group) and therefore allylamine was also chosen as a substrate in the
clic structure due to the formation of hydrogen bonds between the synthesis of a new N-allylamide of monensin A.
carboxylic group on the one side of the molecule and two hydroxyl In this contribution we describe the synthesis and the spectro-
groups on the opposite side.4 The polyether skeleton of the pseudo- scopic as well as semiempirical characterization of a new N-allyl-
cyclic structure is able to form complexes with metal cations,5 10 amide of monensin A (M-AM2) and its complexes with metal
similar to some artificial analogues, such as crown ethers.11 13 The cations in solution.
lipophilic exterior of the monensin A molecule enables transport of
the metal complexes across biological membranes.14 16 Because of
2. Results and discussion
these properties, monensin A shows various biological activities such
as the growth inhibition of Gram positive micro-organisms and
The structures of monensin A (MONA) and the N-allylamide of
control of chicken coccidiosis, for which it is applied commercially.17,18 monensin A (M-AM2) together with the atom numbering are shown
Despite these interesting and useful effects, the application of mon-
(3)
ensin A as a therapeutic or antimicrobial agent is limited because of
OH
33 29 28 27
a number of serious side-effects. A convenient way to obtain less toxic
Me
Me
(1) (2) Me Me
32
35
compounds based on monensin A is its conversion into esters or other 30-31
7
23
O MeO
Me
8
Et H
derivatives, which show lower median lethal dose (LD50) values than 10 (10)
5 25
21
12 13 16 17 20
26
OH
2 4
parent monensin while maintaining or even enhancing the biological
9
1 3
R O O
O O O
OH
H
H
activities.19 Recently, we described the synthesis of some new esters H H
(4) (5) (8)
(6) (7)
(9)
Me Me
and one amide of monensin A. We reported on their ability to form
36 34
H
complexes with monovalent and divalent metal cations and their
N(1)
2'
N
3'
MONA R=OH M-AM2 R=
1'
* Corresponding author.
Scheme 1. The structures and atom numbering of MONA and M-AM2.
E-mail address: bbrzez@main.amu.edu.pl (B. Brzezinski).
0040-4020/$ see front matter Ó 2009 Elsevier Ltd. All rights reserved.
doi:10.1016/j.tet.2009.06.077
D. Aowicki et al. / Tetrahedron 65 (2009) 7730 7740 7731
Table 1
in Scheme 1. M-AM2 amide was synthesized by condensing mon-
The main peaks in the ESI mass spectra of the complexes of M-AM2 with cations at
ensic acid with allylamine in the presence of 1,3-dicyclohexyl-
various cone voltages
carbodiimide (DCC) with the addition of 1-hydroxybenzotriazole
Cation Cone voltage [V] Main peaks m/z (HOBt) as a catalyst. This one-pot reaction led to M-AM2 with a good
yield (67%). It is interesting to note that in the absence of the HOBt
Liþ 10 717
30 717
catalyst, under the same reaction conditions, no amide was formed.
50 717
70 717
90 717, 699, 681, 485, 467,445, 427, 220
2.1. Electrospray mass spectrometry (ESI) measurements
110 717, 699, 681, 485, 467,445, 427, 220
130 717, 699, 681, 485, 467,445, 427, 220
The main m/z signals in the ESI mass spectra of M-AM2 with the
Naþ 10 733
Liþ, Naþand Kþcations used separately at various cone voltages are
30 733
collected in Table 1 and one exemplary ESI mass spectrum of the
50 733
1:1 complex of M-AM2 with Liþ cation measured at various cone
70 733
90 733, 715
voltages is shown in Figure 1. According to these data, M-AM2
110 733, 715, 697, 507, 501, 489, 483, 479, 461, 443, 236
forms exclusively complexes of 1:1 stoichiometry with metal cat-
130 733, 715, 697, 507, 501, 489, 483, 479, 461, 443, 236
ions and the complexes are very stable up to about cvź70 V. At
Kþ 10 749
cvź90 V, the fragmentation of the respective complexes is ob-
30 749
served. The proposed fragmentation pathways starting from
50 749
structure A are depicted in Scheme 2. The first step of the frag-
70 749
mentation is the loss of one water molecule as a result of loss of
90 749
110 749, 731, 713 O(3)H or O(9)H hydroxyl groups yielding B or H cations, re-
130 749, 731, 713
spectively. The regioselectivity of loss of the first water molecule,
especially in formation of cation B, can be explained by strong
engagement of the electron from O(3) atom in complexation of the
Figure 1. ESI mass spectra of 1:1 mixture of M-AM2 with Liþat various cone voltages (cv).
7732 D. Aowicki et al. / Tetrahedron 65 (2009) 7730 7740
+
+ +
O
O O
O
O O
O
O O
O
O O
M M
M
-H2O
O
O O
HO
or
OH
OH
OH
O
O O
(J)
(I)
(H)
O
O O NH
NH
NH
+
O
H
-
H2O
O
HN
(N)
O
M
+
+ +
or
O
O
O
O
O
O
O
O
O
O
O
O O
M
OH M
M OH O
O
O -H2O
-H2O
HO
HO
OH
O
O
O
(C)
(B)
(A)
O NH
O NH
O
NH
+ + +
O
-H2O O
O O
O
O
O
O
O
O
O
O M M
OH M
O
OH
HO
HO
HO
H (K)
(D) (E)
O
- CO
+
+
+
O O
-H2O
O O -H2O O
O
O O
O
O O
M
M
O
M
OH O
OH
HO
HO
(F) (G)
HO
(L)
E
D
A B, H C, I, J
M=Li+ m/z=485 M=Li+ m/z=467
M=Li+ m/z=717 M=Li+ m/z=699 M=Li+ m/z=681
M=Na+ m/z=501 M=Na+ m/z=483
M=Na+ m/z=697
M=Na+ m/z=733 M=Na+ m/z=715
M=K+ m/z=749 M=K+ m/z=731 M=K+ m/z=713
N
G L
F K
M=Li+ m/z=220
M=Na+ m/z=479 M=Na+ m/z=507
M=Li+ m/z=445 M=Li+ m/z=427
M=Na+ m/z=236
M=Na+ m/z=461 M=Na+ m/z=443
Scheme 2. The proposed fragmentation pathways of M-AM2 complexes with monovalent cations.
metal cation. This is in accordance with the previously published also previously observed for monensin sodium salt and was lengthy
data on the three-dimensional structure of monensin A,35 and its discussed in the literature.35 37
derivatives in the solid and gas states,8 10,41 as well as in the so- Cation H yields cations I or J by loss of a second water molecule.
lution.20 31 A similar regioselectivity of the dehydratation steps was Further fragmentation of cation B, of M-AM2 with Liþ and Naþ
D. Aowicki et al. / Tetrahedron 65 (2009) 7730 7740 7733
cations, is realized in two directions with the formation of other OH groups are separate and their chemical shifts depend on the
types of complexes (C, D, E, F and finally G). The epoxide structures kind of the cation, as illustrated in Figure 3. In the spectrum of M-
of cations C, E and G have been previously postulated by Lopes AM2 the OH proton signals observed at 4.00 ppm, 3.89 ppm and
et al.35 Furthermore, cation B can undergo fragmentation to cation 2.86 ppm, are assigned to the O(3)H, O(9)H and O(10)H groups,
N due to complexation of Liþand Naþcations by the part of mole- respectively, whereas in the spectra of the complexes between M-
cule with the amide group. Cation C is formed from cation B by loss AM2 and the Liþ, Naþ and Kþ cations these signals are shifted in
of the second water molecule. The formation of D and E fragmen- different directions depending on the cation. The most significantly
tary complexes is achieved by abstraction of the part of the mole- shifted signal of all the OH groups is found in the spectrum of M-
cule with the amide moiety. The discussed fragmentation pathways AM2 Naþ complex at 6.40 ppm assigned to O(9)H proton. How-
correspond very well with those proposed for the salts of monensin ever, in the spectrum of M-AM2 Liþ complex the most shifted
described in Refs. 35 37. It has been demonstrated that the com- signal is that of the O(3)H proton found at 6.10 ppm. Both these
mon fragmentation ions were produced via a Grob Wharton type signals are involved in the strongest intramolecular hydrogen
mechanism.35 bonds in comparison with other hydroxyl groups. In contrast, in the
Cations F and G can be formed from cations D and E, re- spectra of the M-AM2 complexes with Naþ and Kþ cations, the
spectively, by abstraction of one C3H4 group. Additionally, cation G signals of the O(3)H protons are shifted towards lower ppm values
can be formed by loss of one water molecule from cation F. For the indicating that the hydrogen bonds, in which the O(3)H protons are
complex of M-AM2 with Kþcation no abstraction of the part of the involved, are weaker. This demonstrates that depending on the
molecule which contains the amide group was detected. kind of the cation, the respective hydroxyl groups form different
For the M-AM2 Naþcomplex, an additional pathway (A/B/ intramolecular hydrogen bonds and therefore the complexes ex-
K/L) takes place. The cation K at m/z 507 is form via Grob hibit different structures.
13
Wharthon fragmentation,35 which after the abstraction of one CO A comparison of the C NMR chemical shifts in the spectra of
molecule, forms cation L. Further, cation L undergoes fragmenta- the complexes with those observed in the spectrum of M-AM2
tions typical of other cations with abstraction of further water (Table 3) suggests that the involvement of the oxygen atoms in the
molecules yielding cations F and G, respectively. cations coordination evokes some conformational changes. For
Figure 2 presents the ESI spectrum of the 1:1:1:3 mixture of Liþ, instance the value of D at the C20 atom in the complex of M-AM2
Naþ, Kþcations with M-AM2 measured at cvź30 V. In this figure with Liþ cation is positive, for the complex of M-AM2 with Naþ
only three characteristic signals at m/zź717, m/zź733 and m/zź749 cation it is negative and for the M-AM2 Kþ complex it is almost
assigned to the 1:1 complexes of M-AM2 with Liþ, Naþ and Kþ unchanged. This result indicates that O(7) oxygen atom is involved
cations are shown, respectively. The intensity of the M-AM2 Naþ in the coordination only in the complex of M-AM2 with Naþ
complex signal is the strongest, clearly indicating that M-AM2 cation.
1 13
preferentially forms complexes with Naþcations. The intensities of The Hand C NMR chemical shifts of M-AM2 amide in CD3CN
1
the signals of M-AM2 Liþand M-AM2 Kþcomplexes are compa- and CD2Cl2 are compared in Table 4. In the H NMR spectrum of
rable, but significantly lower than that of M-AM2-Naþ complex, M-AM2 in CD2Cl2, compared with that in CD3CN, significant
demonstrating that M-AM2 shows much lower affinity to Liþand changes in the chemical shifts are detected for the O H protons:
Kþcations. the O(3) H and O(9) H protons become involved in slightly
stronger hydrogen bonds and the O(10) H proton is involved in
1 13
2.2. H and C NMR measurements a slightly weaker hydrogen bond. Also for the compound in
CD2Cl2, the signal of the N H proton shifts towards smaller ppm
1 13
The H and C NMR data of M-AM2 and its 1:1 complexes with values relative to that in the spectrum taken in CD3CN solvent.
Liþ, Naþand Kþcations all in CD3CN are shown in Tables 2 and 3, This indicates that the N H proton is not involved in an intra-
respectively. Unfortunately, in contrast to the Liþ, Naþ and Kþ molecular hydrogen-bond but only slightly stronger hydrogen-
complexes, the respective M-AM2 complexes with the RbClO4 and bonded to the CD3CN molecules. This interpretation is consistent
1 13
CsClO4 salts are almost insoluble in acetonitrile. The H and C with the observations made on the basis of the FTIR spectra dis-
NMR signals were assigned using one- and two-dimensional cussed below.
13
(COSY, HETCOR) spectra as well as by the addition of CD3OD to the Comparison of the C NMR chemical shifts of M-AM2 in both
sample. solvents indicates that the changes in the strength of hydrogen
1
In the H NMR spectra of M-AM2 and its 1:1 complexes with Liþ, bonds within the structures cause also conformational changes and
Naþand Kþcations (Table 2), the signals of the protons of all three probably also charge distributions at some carbon atoms.
Figure 2. ESI mass spectrum of 1:1:1:3 mixture of cation perchlorates LiClO4, NaClO4 and KClO4 with M-AM2 (cvź30 V).
7734 D. Aowicki et al. / Tetrahedron 65 (2009) 7730 7740
Table 2 Table 3
1 13
H NMR chemical shifts (ppm) of M-AM2 and its complexes in CD3CN C NMR chemical shifts (ppm) of M-AM2 and its complexes in CD3CN
No. Atom Chemical shift (ppm) Differences (D) between No. Chemical shift (ppm) Differences (D) between
chemical shifts (ppm) Atom chemical shifts (ppm)
M-AM2 M-AM2 Liþ M-AM2 Naþ M-AM2 Kþ D1 D2 D3 M-AM2 M-AM2 Liþ M-AM2 Naþ M-AM2 Kþ D1 D2 D3
1 d d d d d d d 1 175.48 178.87 179.03 177.20 3.39 3.55 1.72
2 2.43 2.51 2.64 2.51 0.08 0.21 0.08 2 42.96 42.92 42.50 43.58 0.04 0.46 0.62
3 3.35 3.40 3.38 3.33 0.05 0.03 0.02 3 82.67 80.10 80.19 82.33 2.57 2.48 0.34
4 1.96 2.21 2.20 2.06 0.25 0.24 0.10 4 37.93 35.56 35.78 37.39 2.37 2.15 0.54
5 3.98 4.23 4.00 3.90 0.25 0.02 0.08 5 68.37 69.74 69.50 68.09 1.37 1.13 0.28
6 1.78 1.64 1.60 1.62 0.14 0.18 0.16 6 36.63 36.04 36.56 35.97 0.59 0.07 0.66
7 3.65 3.96 3.84 3.83 0.31 0.19 0.18 7 71.94 70.16 70.54 70.76 1.78 1.40 1.18
8A 1.60 1.98 1.64 1.58 0.38 0.04 0.02 8 35.18 34.42 34.58 34.67 0.76 0.60 0.51
8B 1.99 2.06 2.02 2.01 0.07 0.03 0.02 9 108.37 108.23 108.51 108.26 0.14 0.14 0.11
9 d d d d d d d 10 39.91 39.68 39.77 39.88 0.23 0.14 0.03
10A 1.84 1.82 1.82 1.75 0.02 0.02 0.09 11 32.64 33.05 33.27 34.50 0.41 0.63 1.86
10B 1.84 2.04 2.05 1.90 0.20 0.21 0.06 12 87.02 87.27 86.67 86.27 0.25 0.35 0.75
11A 1.71 1.85 1.86 1.92 0.14 0.15 0.21 13 84.40 82.32 82.36 83.25 2.08 2.04 1.15
11B 1.97 2.01 1.98 2.01 0.04 0.01 0.04 14 28.66 27.25 27.18 27.94 1.41 1.48 0.72
12 d d d d d d d 15 32.08 31.42 30.69 31.85 0.66 1.39 0.23
13 3.64 3.67 3.65 3.54 0.03 0.01 0.10 16 88.05 87.61 86.85 86.89 0.44 1.20 1.16
14A 1.56 1.48 1.51 1.50 0.08 0.05 0.06 17 86.45 85.01 85.56 85.11 1.44 0.89 1.34
14B 1.76 1.92 1.92 1.78 0.16 0.16 0.02 18 35.87 34.13 35.05 35.34 1.74 0.82 0.53
15A 1.57 1.51 1.49 1.47 0.06 0.08 0.10 19 34.84 33.78 33.76 33.23 1.06 1.08 1.61
15B 2.10 2.20 2.30 2.20 0.10 0.20 0.10 20 78.16 78.86 76.97 78.13 0.70 1.19 0.03
16 d d d d d d d 21 77.33 74.62 75.96 75.61 2.71 1.37 1.72
17 3.86 4.25 3.90 3.95 0.39 0.04 0.09 22 34.17 32.97 32.29 33.03 1.20 1.88 1.14
18 2.25 2.38 2.33 2.33 0.13 0.08 0.08 23 37.72 36.43 36.03 36.80 1.29 1.69 0.92
19A 1.52 1.60 1.64 1.55 0.08 0.12 0.03 24 34.91 36.28 37.17 34.15 1.37 2.26 0.76
19B 2.15 2.23 2.18 2.17 0.08 0.03 0.02 25 98.00 99.16 98.69 98.92 1.16 0.69 0.92
20 4.20 4.42 4.40 4.38 0.22 0.20 0.18 26 67.45 66.98 66.99 66.94 0.47 0.46 0.51
21 3.57 3.90 3.82 3.74 0.33 0.25 0.17 27 16.52 16.10 15.95 16.62 0.42 0.57 0.10
22 1.32 1.40 1.45 1.36 0.08 0.13 0.04 28 17.91 17.29 16.78 17.40 0.62 1.13 0.51
23A 1.33 1.38 1.42 1.45 0.05 0.09 0.12 29 16.21 15.56 14.27 15.67 0.65 1.94 0.54
23B 1.43 1.41 1.58 1.73 0.02 0.15 0.30 30 30.24 29.93 30.30 30.40 0.31 0.06 0.16
24 1.62 1.38 1.60 1.79 0.24 0.02 0.17 31 8.34 8.24 8.14 8.46 0.10 0.20 0.12
25 d d d d d d d 32 26.16 28.42 28.35 28.08 2.26 2.19 1.92
26A 3.36 3.43 3.50 3.39 0.07 0.14 0.03 33 11.26 10.35 10.56 10.68 0.91 0.70 0.58
26B 3.36 3.69 3.70 3.67 0.33 0.34 0.31 34 12.58 12.59 12.53 12.38 0.01 0.05 0.20
27 0.84 0.87 0.82 0.82 0.03 0.02 0.02 35 58.65 57.37 57.38 58.43 1.28 1.27 0.22
28 0.86 0.86 0.82 0.83 0.00 0.04 0.03 36 14.71 13.58 13.92 14.77 1.13 0.79 0.06
29 0.96 0.96 0.89 0.95 0.00 0.07 0.01 10 42.17 42.04 41.96 42.01 0.13 0.21 0.16
30A 1.54 1.50 1.51 1.50 0.04 0.03 0.04 20 136.20 135.56 135.59 135.84 0.64 0.61 0.36
30B 1.54 1.71 1.74 1.69 0.17 0.20 0.15 30 115.60 115.67 115.54 115.59 0.07 0.06 0.01
31 0.92 0.94 0.92 0.90 0.02 0.00 0.02
D1źdM-AM2 Liþ dM-AM2, D2źdM-AM2 Naþ dM-AM2, D3źdM-AM2 Kþ dM-AM2.
32 1.31 1.52 1.48 1.44 0.21 0.17 0.13
33 0.85 0.92 0.91 0.88 0.07 0.06 0.03
34 0.98 1.02 1.00 0.99 0.04 0.02 0.01
of the M-AM2 Liþcomplex (Fig. 4b, dashed blue line) the band at
35 3.32 3.35 3.26 3.35 0.03 0.06 0.03
3509 cm 1 vanishes and two bands arise at 3456 cm 1 and
36 1.12 1.20 1.20 1.19 0.08 0.08 0.07
3280 cm 1. The first band is assigned to stretching vibrations of
10 3.73 3.80 3.78 3.78 0.07 0.05 0.05
20 5.90 5.85 5.82 5.85 0.05 0.08 0.05
both O(10)H and O(9)H groups and the second one to the O(3)H
30A 5.08 5.08 5.05 5.10 0.00 0.03 0.02
group. This indicates that in the structure of M-AM2 Liþcomplex
30B 5.18 5.16 5.12 5.20 0.02 0.06 0.02
the hydrogen bonds of all O H groups become slightly stronger
N(1)H 6.68 7.00 6.86 6.96 0.32 0.18 0.28
when compared to those in the uncomplexed M-AM2 molecule.
O(3)H 4.00 6.10 3.89 3.88 2.10 0.11 0.12
1
O(9)H 3.89 4.24 6.40 2.51 0.35 2.51 1.38 This interpretation is consistent with the H NMR data (Table 2
O(10)H 2.86 4.35 4.16 3.84 1.49 1.30 0.98
and Fig. 3).
In the spectrum of M-AM2 Naþ complex (Fig. 4b, dotted red
D1źdM-AM2 Liþ dM-AM2, D2źdM-AM2 Naþ dM-AM2, D3źdM-AM2 Kþ dM-AM2.
line) a broad band with a maximum at ca. 3447 cm 1 is observed,
demonstrating that the hydrogen bonds formed by the O(3)H and
2.3. FTIR studies O(10)H groups become slightly stronger and that the hydrogen
bond of the O(9)H group is the strongest one because the re-
In Figure 4a the FTIR spectrum of water-free M-AM2 (solid spective broad band shows a maximum at about 3261 cm 1. Also
line) is compared with the corresponding spectra of its 1:1 in the spectrum of M-AM2 Kþ complex (Fig. 4b, dashed-dotted
complexes with Liþ, Naþ and Kþ cations, all recorded in aceto- green line) only one band with a maximum at 3484 cm 1 is ob-
nitrile solution. The regions of the n(OH, NH) and n(C]O) vibra- served indicating that the hydrogen bonds, in which the hydroxyl
tions are additionally shown in Figure 4b and c, in an expanded groups are involved are almost unchanged as in the uncomplexed
scale, because according to the NMR data, the most significant M-AM2. The position of the n(NH) vibrations assigned to the N(1)H
changes should be observed in these spectral regions. Most amide group is independent of the cation and is always observed
1
characteristic, in the FTIR spectrum of water-free M-AM2 (Fig. 4b, at 3385 cm 1. This observation is in agreement with the H NMR
solid, black line), are the bands assigned to the n(OH) vibrations of data, because the N(1)H proton signal in the respective spectra of
the O(3)H, O(9)H and O(10)H groups at 3509 cm 1, the n(NH) M-AM2 and in the spectra of its cation complexes is found about
vibrations of the N(1)H group at 3385 cm 1, as well as the band 7 ppm. The amide I and amide II bands in the FTIR spectrum of M-
assigned to the n(C]O) vibrations at 1670 cm 1. In the spectrum AM2 are observed at 1670 cm 1 and 1528 cm 1, respectively
D. Aowicki et al. / Tetrahedron 65 (2009) 7730 7740 7735
1
Figure 3. H NMR in region of OH and NH proton signals of: (a) M-AM2, (b) M-AM2 Liþ, (c) M-AM2 Naþand (d) M-AM2 Kþin CD3CN.
(Fig. 4c). The positions of both bands change strongly with the structure A showing that this structure also exists but is unfav-
formation of the complexes with metal cations. In the spectra of ourable. We made similar observations for the M-AM2 Liþcomplex
the M-AM2 complexes with Liþ and Naþ they are observed at although the DHOF value is generally lower than that found for the
1637 cm 1 and 1542 cm 1, respectively. In the spectrum of the M- respective M-AM2 Naþcomplex. The lowest differences between
AM2 Kþ complex both amide I and amide II bands show a more the DHOF values of structures B and A are found for the M-AM2 Kþ
complex character due to the existence of an equilibrium between complex, 172.00 and 161.92 kcal/mol, respectively. These DHOF
two types of complexes in acetonitrile. In the first complex, the values indicate that both, structure A and B exist, whereas the
oxygen atom of the carbonyl group takes part in the complexation structure B is slightly favoured. These results nicely corroborate the
process while in the second one no contribution of this group is ESI data and the FTIR spectroscopic observations.
observed. The amide I bands observed in the spectra of M-AM2 The interatomic distances between the oxygen atoms of M-
complexes with Liþand Naþrecorded under the same conditions AM2 and the cations together with the partial charges at these
show an intense shoulder around 1667 cm 1 indicating that the atoms are given in Table 6. Analysis of these values for structures
equilibrium described above still exists. However in contrast to the B shows that some oxygen atoms such as O(1), O(3), O(5), O(6),
Kþ complex, the Liþ and Naþ complexes predominantly exist in, O(8) and O(10) are always involved in the coordination of differ-
a structure in which the carbonyl group is involved in the co- ent metal cations, whereas only in the M-AM2 Naþcomplex the
ordination process. O(7) atom does also play a role in this coordination process. For
A hypothetical equilibrium between the complexed and the li- the complexes of A type structure in which the C(1)]O group is
gand-free form can be excluded by the NMR data, since none of the not involved in the complexation of the metal cation, the values of
1
H NMR spectra of the complexes (Fig. 3) exhibit the O(10)H signal the calculated coordination distances are comparable with those
at 2.86 ppm, typical of uncomplexed M-AM2. This unambiguously in the B type structure. The results for the M-AM2 Kþ complex
shows that the above described equilibrium only involves the M- given in Table 6 indicate that both types of complexes can be
AM2 cation complexes. formed.
The calculated lengths and angles of the hydrogen bonds in
2.4. PM5 calculations which the OH groups are engaged are summarized in Table 7. The
calculated structure of M-AM2 (Fig. 5) indicates that the O(1) ox-
On the basis of the spectroscopic results, the heats of formation ygen atom of the C]O amide group is engaged in the bifurcated
(HOF) of the structures of M-AM2 and its complexes with Liþ, Naþ intramolecular hydrogen bonds with two O(9)H and O(10)H hy-
and Kþcations were calculated (Table 5). Their values imply that the droxyl groups. With the formation of the respective B type com-
most stable complexes in the gas phase (under the experimental plexes between M-AM2 and Liþ, Naþand Kþcations (Figs. 6, 7 and
conditions similar to those of ESI measurements) are formed with 8a) these hydrogen bonds get broken because the O(1) oxygen
Naþ>>LiþzKþcations. This result is in good agreement with the atom is involved in the coordination process. For this reason the
13
ESI data discussed above. The DHOF values also show that the signal of the C(1) carbon atom in the C NMR spectra of the com-
structures of M-AM2 with cations in which the carbonyl group is plexes is shifted toward higher ppm values relative to its position in
involved (structure B) are energetically more favourable than those the spectrum of M-AM2 (Table 3). In the A structure of the M-AM2
in which the carbonyl group is not involved (structure A). The Kþcomplex the C(1)]O carbonyl group is not involved in the co-
highest DHOF value is found for the M-AM2 Naþ complex of the ordination process and it is hydrogen bonded only to the O(10)H
structure B indicating that this structure is preferentially formed. hydroxyl group (Fig. 8b). The hydrogen and the coordination bonds
Much lower is the DHOF value for the M-AM2 Naþcomplex of the in the visualized structures of M-AM2 and its complexes with the
7736 D. Aowicki et al. / Tetrahedron 65 (2009) 7730 7740
Table 4
1
H 13C NMR chemical shifts (ppm) of M-AM2 in CD2Cl2 and CD3CN
1 13
No. Atom HNMR C NMR
M-AM2 in CD2Cl2 M-AM2 in CD3CN D1 M-AM2 in CD2Cl2 M-AM2 in CD3CN D2
1 ddd 175.53 175.48 0.05
2 2.47 2.43 0.04 42.69 42.96 0.27
3 3.37 3.35 0.02 82.48 82.67 0.19
4 2.00 1.96 0.04 37.43 37.93 0.50
5 4.14 3.98 0.16 67.65 68.37 0.72
6 1.74 1.78 0.04 36.99 36.63 0.36
7 3.75 3.65 0.10 71.52 71.94 0.42
8A 1.63 1.60 0.03 34.65 35.18 0.53
8B 1.98 1.99 0.01 ddd
9 ddd 107.94 108.37 0.43
10A 1.79 1.84 0.05 39.19 39.91 0.72
10B 1.95 1.84 0.11 ddd
11A 1.81 1.71 0.10 33.02 32.64 0.38
11B 1.87 1.97 0.10 ddd
12 ddd 85.86 87.02 1.16
13 3.58 3.64 0.06 83.51 84.40 0.89
14A 1.63 1.56 0.07 28.00 28.66 0.66
14B 1.73 1.76 0.03 ddd
15A 1.52 1.57 0.05 31.27 32.08 0.81
15B 2.16 2.10 0.06 ddd
16 ddd 86.89 88.05 1.16
17 3.84 3.86 0.02 86.22 86.45 0.23
18 2.24 2.25 0.01 35.31 35.87 0.56
19A 1.48 1.52 0.04 33.60 34.84 1.24
19B 2.12 2.15 0.03 ddd
20 4.26 4.20 0.06 76.82 78.16 1.34
21 3.79 3.57 0.22 75.64 77.33 1.69
22 1.37 1.32 0.05 33.08 34.17 1.09
23A 1.40 1.33 0.07 37.06 37.72 0.66
23B 1.40 1.43 0.03 ddd
24 1.60 1.62 0.02 35.19 34.91 0.28
25 ddd 97.48 98.00 0.52
26A 3.45 3.36 0.09 67.79 67.45 0.34
26B 3.45 3.36 0.09 ddd
27 0.84 0.84 0.00 16.45 16.52 0.07
28 0.85 0.86 0.01 17.47 17.91 0.44
29 0.94 0.96 0.02 15.63 16.21 0.58
30A 1.53 1.54 0.01 30.47 30.24 0.23
30B 1.53 1.54 0.01 ddd
31 0.92 0.92 0.00 8.39 8.34 0.05
32 1.43 1.31 0.12 26.59 26.16 0.43
33 0.89 0.85 0.04 11.15 11.26 0.11
34 1.01 0.98 0.03 12.92 12.58 0.34
35 3.39 3.32 0.07 58.70 58.65 0.05
36 1.18 1.12 0.06 14.16 14.71 0.55
10 3.81 3.73 0.08 41.87 42.17 0.30
20 5.85 5.90 0.05 135.28 136.20 0.92
30A 5.07 5.08 0.01 115.27 115.60 0.33
30B 5.14 5.18 0.04 ddd
N(1)H 6.49 6.68 0.19 ddd
O(3)H 4.49 4.00 0.49 ddd
O(9)H 4.61 3.89 0.72 ddd
O(10)H 2.75 2.86 0.11 ddd
(1H NMR) D1źdM-AM2(CD3CN) dM-AM2(CD2Cl2); (13CNMR) D2źdM-AM2(CD3CN) dM-AM2(CD2Cl2).
Liþ, Naþand Kþcations (Figs. 5 8) are marked by dots. A compar- of both MONA and M-AM2 are expressed by the minimum in-
ison of all the calculated structures indicates that only for the M- hibitory concentration (MIC) as well as by the growth inhibition
AM2 complex with Naþcation is the M-AM2 molecule able to form zone (Giz) (Table 8). Monensin A and M-AM2 show comparable
a pseudo-crown ether structure. This type of structure provides the activities against the human pathogenic bacteria (Giz 13 19 mm;
most efficient interactions and therefore M-AM2 has the highest MIC 25 100 mg/ml). However, both compounds are inactive against
affinity to Naþ. strains of Candida (Candida albicans and Candida parapsilosis.). The
cell walls of Gram-negative bacteria do not permit the penetration
2.5. Antimicrobial activity of hydrophobic molecules with high molecular weights and thus
these micro-organisms are not susceptible to the action of mon-
Monensin A (MONA) and its amide (M-AM2) were tested in vitro ensin and its allyl amide.
for their antibacterial and antifungal activity. The micro-organisms
used in this study were as follows: Gram-positive bacteria, Gram- 3. Conclusions
negative rods as well as yeasts. Monensin A and M-AM2 were
efficient against Gram-positive bacteria but no activity against A new N-allylamide of monensin A (M-AM2) is a very good
Gram-negative bacteria was detected. The antimicrobial properties complexation agent especially for Naþ cations, although it forms
D. Aowicki et al. / Tetrahedron 65 (2009) 7730 7740 7737
Table 6
(a) 100
The interatomic distances (Å) and partial charges for O atoms of M-AM2 co-
ordinating metal cations in complexes structures calculated by PM5 method
(WinMopac 2003)
Complex with Monovalent Coordinating Coordinating Distance (Å)
50
monovalent cation atom atom coordinating
cation partial partial charge atom/cation
charge
M-AM2 Liþ(B þ0.439 O(1) 0.371 2.17
0 type) O(3) 0.359 2.11
4000 3500 3000 2500 2000 1500 1000 500
O(5) 0.428 2.11
O(6) 0.419 2.09
(b) 100 O(8) 0.411 2.19
O(10) 0.401 2.12
3456 M-AM2 Naþ(B þ0.308 O(1) 0.435 2.37
type) O(3) 0.423 2.38
O(5) 0.383 2.37
50
O(6) 0.351 2.35
3261
O(7) 0.370 2.32
3280
3484 O(8) 0.381 2.39
3385
3447 O(10) 0.394 2.39
3509
0
M-AM2 Kþ(B þ0.481 O(1) 0.403 2.86
3700 3600 3500 3400 3300 3200
type) O(3) 0.355 2.97
O(5) 0.258 2.85
(c) 100
O(6) 0.351 2.85
O(8) 0.244 2.91
O(10) 0.288 2.81
1645
M-AM2 Kþ(A þ0.501 O(3) 0.359 2.98
50
type) O(5) 0.279 2.94
O(6) 0.351 2.85
O(8) 0.233 2.87
1667
O(10) 0.292 2.83
1542 1528
1670 1637
0
1800 1750 1700 1650 1600 1550 1500 Table 7
The lengths (Å) and angles ( ) of the hydrogen bond for M-AM2 and its complexes
Wavenumber [cm-1]
calculated by PM5 method (WinMopac 2003)
···
Figure 4. FTIR spectra of: (d) M-AM2, (---) M-AM2 Liþ, ( ) M-AM2 Naþ, ( ·· ) M-
Compound Type of structure* Atoms engaged Length (Å) Angle ( )
AM2 Kþ in the ranges of: (a) 4000 400 cm 1, (b) n(OH)3800 3200 cm 1, (c) n(C]O)
in hydrogen bonds
1800 1500 cm 1 stretching vibrations recorded in CH3CN.
AM2 O(3) H/O(8) 2.83 123.0
O(9) H/O(1) 2.72 125.7
Table 5
O(10) H/O(1) 2.87 154.5
Heat of formation (kcal/mol) of M-AM2 and its complexes with the cations without
N(1) H/O(2) 2.93 128.6
(A) and with (B) the engagement of carbonyl group in coordination process calcu-
M-AM2 Liþ B O(3) H/O(8) 2.67 139.0
lated by PM5 method (WinMopac 2003)
O(9) H/O(2) 2.75 138.3
Complex HOF (kcal/mol) DHOF (kcal/mol)
O(10) H/O(2) 2.74 118.8
M-AM2 565.00
M-AM2 Naþ B O(3) H/O(8) 2.82 117.1
M-AM2þLiþ (A) 442.26 131.13
uncomplexed
O(9) H/O(3) 2.69 140.0
M-AM2þLiþ (A) 573.39
complexed
O(10) H/O(2) 2.92 135.3
M-AM2þLiþ (B) 442.26 180.33
uncomplexed
M-AM2þLiþ (B) 622.59
complexed M-AM2 Kþ B O(3) H/O(7) 2.82 124.1
M-AM2þNaþ (A) 423.44 144.17
uncomplexed O(9) H/O(2) 2.95 160.6
M-AM2þNaþ (A) 576.61
complexed O(10) H/O(2) 2.74 116.1
M-AM2þNaþ (B) 423.44 200.71
uncomplexed
M-AM2 Kþ A O(3) H/O(7) 2.89 128.1
M-AM2þNaþ (B) 624.15
complexed
O(9) H/O(2) 2.93 144.3
M-AM2þKþ (A) 448.56 161.92
uncomplexed
O(10) H/O(2) 2.75 116.2
M-AM2þKþ (A) 610.48
complexed
O(10) H/O(1) 2.92 158.6
M-AM2þKþ (B) 448.56 172.00
uncomplexed
M-AM2þKþ (B) 621.16
complexed * A-structure of M-AM2 complex in which the C1]O group is not involved in
coordination of metal cation. B-structure of M-AM2 complex in which the C1]O
DHOFźHOFM-AM2þM complexed HOFM-AM2þM uncomplexed, Mdmetal cation.
group is involved in coordination of metal cation.
(A)dstructure of M-AM2 complex in which the C1]O group is not involved in
coordination of metal cation.
(B)dstructure of M-AM2 complex in which the C1]O group is involved in
coordination of metal cation.
complexes the C]O amide groups are engaged in the complexation
process. For the M-AM2 Kþ complex, an alternative structure in
also complexes with other monovalent cations. ESI mass spec- which this carbonyl group is not involved in the coordination pro-
trometry indicates that M-AM2 forms complexes with Liþ, Naþand cess, was also observed. In contrast to the amide molecule in the
Kþof exclusively 1:1 stoichiometry which are stable up to cvź70 V. structures of the ester complexes of monensin A the C]O ester
Above cvź90 V the fragmentation of the respective complexes in- group was generally not involved in the complexation process of the
volving some dehydration steps is observed. The structures of M- metal cations.20 26 In vitro biological tests of M-AM2 amide show
AM2 and its complexes with Liþ, Naþand Kþcations are stabilized that this compound is active against some strains of Gram-positive
by relatively weak intramolecular hydrogen bonds in which the OH bacteria (Giz 13 19 mm; MIC 25 100 mg/ml) and it is slightly more
groups are always involved. In the structures of respective active than monensin A allyl ester.23
Transmittance [%]
Transmittance [%]
Transmittance [%]
7738 D. Aowicki et al. / Tetrahedron 65 (2009) 7730 7740
Figure 5. The structure of M-AM2 calculated by PM5 method (WinMopac2003).
Figure 8. The structures of two types of M-AM2-Kþ complexes: (a) without the en-
gagement of the C1]O carbonyl group in coordination of the cationdtype A, (b) with
the engagement of the C1]O carbonyl group in coordination of the cationdtype B
calculated by PM5 method (WinMopac 2003).
Table 8
Antimicrobial activity of MONA and M-AM2: diameter of the growth inhibition zone
[Giz, mm] and minimal inhibitory concentration (MIC, mg/ml)
Tested strain MONA M-AM2
Figure 6. The structure of M-AM2 Liþ complex calculated by PM5 method
(WinMopac2003). Giz (mm) MIC (mg/ml) Giz (mm) MIC (mg/ml)
S. aureus NCTC 4163 22 2 17 50
S. aureus ATCC 25923 22 1 18 50
S. aureus ATCC 6538 20 2 17 50
S. aureus ATCC 29213 18 1 17 50
S. epidermidis ATCC 12228 15 2 19 100
B. subtilis ATCC 6633 22 1 19 50
B. cereus ATCC 11778 18 2 19 25
E. hirae ATCC 10541 d 12.5 d >400
M. luteus ATCC 9341 12 4 16 50
M. luteus ATCC 10240 12 2 13 50
d denotes lack of the growth inhibition zone.
4. Experimental
4.1. General
Monensin A sodium salt was purchased from Sigma (90 95%).
The perchlorates LiClO4, NaClO4 and KClO4 were commercial
products of Sigma and used without any further purification. Be-
cause the salts were hydrates, it was necessary to dehydrate them
in several (6 10 times) evaporation steps from a 1:5 mixture of
acetonitrile and absolute ethanol. The dehydration of the perchlo-
Figure 7. The structure of M-AM2-Naþ complex calculated by PM5 method
(WinMopac2003). rates was monitored by recording their FTIR spectra in acetonitrile.
D. Aowicki et al. / Tetrahedron 65 (2009) 7730 7740 7739
CH3CN, CD3CN as well as CH2Cl2 and CD2Cl2 spectral-grade The FTIR analysis of M-AM2 amide was also carried out in CH2Cl2
solvents were stored over 3 Å molecular sieves for several days. All solution.
manipulations with the substances were performed in a carefully A cell with Si windows and wedge-shaped layers was used to
dried and CO2-free glove box. avoid interferences (mean layer thickness 170 mm). The spectra
were taken with an IFS 113v FT-IR spectrophotometer (Bruker,
Karlsruhe) equipped with a DTGS detector; resolution 2 cm 1,
4.2. Preparation of N-allylamide of monensin A (M-AM2) and
NSSź125. The Happ-Genzel apodization function was used. All
its complexes with alkali metal cations
manipulations with the compounds were performed in a carefully
dried and CO2-free glove box.
Monensin A sodium salt was dissolved in dichloromethane and
The NMR spectra of M-AM2 and its 1:1 complexes
stirred vigorously with a layer of aqueous sulfuric acid (pHź1.5).
(0.07 mol dm 3) with LiClO4, NaClO4 and KClO4 were recorded in
The organic layer containing MONA was washed with distilled
CD3CN solutions using a Varian Gemini 300 MHz spectrometer. The
water, and dichloromethane evaporated under reduced pressure to
NMR analysis of M-AM2 amide was also carried out in CD2Cl2 so-
dryness to produce the acid.
lution. All spectra were locked to the deuterium resonance of
A solution of MONA (1000 mg, 1.49 mmol), 1,3-dicyclohexyl-
CD3CN and CD2Cl2, respectively.
carbodiimide (140 mg, 2.03 mmol), and allylamine (256 mg,
1
The H NMR measurements in CD3CN and CD2Cl2 were carried
4.49 mmol) in dichloromethane and 1-hydroxybenzotriazole
out at the operating frequency 300.075 MHz; flip angle, pwź45 ;
(330 mg, 2.16 mmol) dissolved in tetrahydrofuran were mixed to-
spectral width, swź4500 Hz; acquisition time, atź2.0 s; relaxation
gether and stirred at a temperature between 4 C to 5 C for
delay, d1ź1.0 s; Tź293.0 K and using TMS as the internal standard.
24 h. After this time, the reaction mixture was stirred at room
No window function or zero filling was used. Digital resolution was
temperature for a further 24 h, diluted with H2O and extracted with
0.2 Hz per point. The error of chemical shift value was 0.01 ppm.
CH2Cl2. The extract was distilled under reduced pressure to dry-
13
C NMR spectra were recorded at the operating frequency
ness. The residue was suspended in hexane and filtered off to
75.454 MHz; pwź60 ; swź19,000 Hz; atź1.8 s; d1ź1.0 s; Tź293.0 K
remove the 1,3-dicyclohexylurea by-product. The filtrate was
and TMS as the internal standard. Line broadening parameters were
evaporated under reduced pressure and purified by chromatogra-
0.5 or 1 Hz. The error of chemical shift value was 0.01 ppm.
phy on silica gel (Fluka type 60) to give M-AM2 as a colourless solid
1 13
The H and C NMR signals were assigned independently for
(710 mg, 67% yield).
each species using one or two-dimensional (COSY, HETCOR) spectra.
Elemental analysis: Calculated: C 65.98%, H 9.51%, N 1.97%.
Found: C 66.03%, H 9.48%, N 1.91%.
4.6. PM5 calculations
4.3. Synthesis of M-AM2 complexes with monovalent cations
PM5 semi-empirical calculations were performed using the
WinMopac 2003 program. In all cases, full geometry optimisation
0.07 mol dm 3 solutions of the 1:1 complexes of M-AM2 with
of M-AM2 and its complexes was carried out without any sym-
monovalent cations (Liþ, Naþ and Kþ) were obtained by adding
metry constraints.38 41
equimolar amounts of MClO4 salts (MźLi, Na, K) dissolved in aceto-
nitrile to an acetonitrile solution of M-AM2. The solvent was
4.7. Elemental analysis
evaporated under reduced pressure to dryness and the residue was
dissolved in an appropriate volume of dry CH3CN and CD3CN to
The elemental analysis of M-AM2 was carried out on Vario ELIII
obtain the complex of the 0.07 mol dm 3 concentration.
(Elementar, Germany).
4.4. ESI MS studies
4.8. Microbiological analysis
The ESI (Electrospray Ionisation) mass spectra were recorded
Micro-organisms used in this study were as follows: Gram-
on a Waters/Micromass (Manchester, UK) ZQ mass spectrometer
positive cocci: Staphylococcus aureus NCTC 4163, S. aureus ATCC
equipped with a Harvard Apparatus syringe pump. All samples
25923, S. aureus ATCC 6538, S. aureus ATCC 29213, Staphylococcus
were prepared in acetonitrile. The measurements were performed
epidermidis ATCC 12228, Bacillus subtilis ATCC 6633, Bacillus cereus
for solutions of M-AM2 (5 10 5 mol dm 3) with: (a) each of the
ATCC 11778, Enterococcus hirae ATCC 10541, Micrococcus luteus
cations Liþ, Naþand Kþ(2.5 10 4 mol dm 3) taken separately and
ATCC 9341, M. luteus ATCC 10240; Gram-negative rods: Escherichia
(b) the cations Liþ, Naþ and Kþ (5 10 5/3 mol dm 3) taken to-
coli ATCC 10538, E. coli ATCC 25922, E. coli NCTC 8196, Proteus
gether. The samples were infused into the ESI source using
vulgaris NCTC 4635, Pseudomonas aeruginosa ATCC 15442, P. aeru-
a Harvard pump at a flow rate of 20 ml min 1. The ESI source po-
ginosa NCTC 6749, P. aeruginosa ATCC 27863, Bordetella bronchi-
tentials were: capillary 3 kV, lens 0.5 kV, extractor 4 V. The stan-
septica ATCC 4617 and yeasts: C. albicans ATCC 10231, C. albicans
dard ESI mass spectra were recorded at the cone voltages: 10, 30,
ATCC 90028, C. parapsilosis ATCC 22019. The micro-organisms used
50, 70, 90, 110 and 130 V. The source temperature was 120 Cand
were obtained from the collection of the Department of Pharma-
the desolvation temperature was 300 C. Nitrogen was used as the
ceutical Microbiology, Medical University of Warsaw, Poland.
nebulizing and desolvation gas at flow-rates of 100 and
Antimicrobial activity was examined by the disc-diffusion
300 dm3 h 1, respectively. Mass spectra were acquired in the
method under standard conditions using Mueller-Hinton II agar
positive ion detection mode with unit mass resolution at a step of
medium (Becton Dickinson) for bacteria and RPMI agar with 2%
1 m/z unit. The mass range for ESI experiments was from m/zź200
glucose (Sigma) according to CLSI (previously NCCLS) guidelines.42
to m/zź1000.
Sterile filter paper discs (9 mm diameter, Whatman No 3 chro-
matography paper) were dripped with tested compound solutions
4.5. Spectroscopic measurements (in MeOH or MeOH/DMSO 1:1) to load 400 mg of a given compound
per disc. Dry discs were placed on the surface of appropriate agar
The FTIR spectra of M-AM2 and its 1:1 complexes (0.07 mol dm 3) medium. The results (diameter of the growth inhibition zone) were
with LiClO4, NaClO4, and KClO4 were recorded in the mid infrared read after 18 h of incubation at 35 C. Compounds which showed
region in acetonitrile solutions using a Bruker IFS 113v spectrometer. activity in disc-diffusion tests were examined by the agar dilution
7740 D. Aowicki et al. / Tetrahedron 65 (2009) 7730 7740
20. Huczyński, A.; Przybylski, P.; Brzezinski, B.; Bartl, F. Biopolymers 2006, 81, 282 294.
method to determine their MICdMinimal Inhibitory Concentration
21. Huczyński, A.; Przybylski, P.; Brzezinski, B.; Bartl, F. Biopolymers 2006, 82, 491 503.
(CLSI).43 Concentrations of the agents tested in solid medium ranged
22. Huczyński, A.; Michalak, D.; Przybylski, P.; Brzezinski, B.; Bartl, F. J. Mol. Struct.
from 3.125 to 400 mg/ml. The final inoculum of all studied organisms
2006, 797, 99 110.
23. Huczyński, A.; Michalak, D.; Przybylski, P.; Brzezinski, B.; Bartl, F. J. Mol. Struct.
was 104 CFU ml 1 (colony forming units per ml), except the final
2007, 828, 130 141.
inoculum for E. hirae ATCC 10541, which was 105 CFU ml 1. Minimal
24. Huczyński, A.;qowicki, D.; Brzezinski, B.; Bartl, F. J. Mol. Struct. 2008, 874, 89 100.
inhibitory concentrations were read after 18 h of incubation at 35 C.
25. Huczyński, A.; Przybylski, P.; Brzezinski, B. Tetrahedron 2007, 63, 8831 8839.
26. Huczyński, A.; qowicki, D.; Brzezinski, B.; Bartl, F. J. Mol. Struct. 2008, 879, 14 24.
27. Huczyński, A.; Przybylski, P.; Brzezinski, B. J. Mol. Struct. 2006, 788, 176 183.
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