Marinopyrrole derivatives as potential antibiotic agents against methicillin-resistant Staphylococcus aureus (I)

Article abstract of DOI:10.3390/md10040953

Infections caused by drug-resistant pathogens are on the rise. The ongoing spread of methicillin-resistant Staphylococcus aureus (MRSA) strains exemplifies the urgent need for new antibiotics. The marine natural product, marinopyrrole A, was previously sh

Full text of DOI:10.3390/md10040953

Mar. Drugs 2012, 10, 953-962; doi:10.3390/md10040953
OPEN ACCESS
Marine Drugs
ISSN 1660-3397
www.mdpi.com/journal/marinedrugs
Article
Marinopyrrole Derivatives as Potential Antibiotic Agents
against Methicillin-Resistant Staphylococcus aureus (I)
Yan Liu 1,†, Nina M. Haste 2,†, Wdee Thienphrapa 3, Victor Nizet 2,3, Mary Hensler 3 and
Rongshi Li 1,*
1
Department of Drug Discovery, H. Lee Moffitt Cancer Center and Research Institute,
12902 Magnolia Drive, Tampa, FL 33612, USA; E-Mail: Yan.Liu@moffitt.org
2
Skaggs School of Pharmacy and Pharmaceutical Sciences, University of California San Diego,
La Jolla, CA 92093, USA; E-Mails: nhaste@ucsd.edu (N.M.H.); vnizet@ucsd.edu (V.N.)
3
Department of Pediatrics, University of California San Diego, La Jolla, CA 92093, USA;
E-Mails: wthienph@ucsd.edu (W.T.); mhensler@ucsd.edu (M.H.)
†
These authors contributed equally to this work.
* Author to whom correspondence should be addressed; E-Mail: Rongshi.Li@moffitt.org;
Tel.: +1-813-745-6485; Fax: +1-813-745-6875.
Received: 12 March 2012; in revised form: 31 March 2012 / Accepted: 18 April 2012 /
Published: 24 April 2012
Abstract: Infections caused by drug-resistant pathogens are on the rise. The ongoing
spread of methicillin-resistant Staphylococcus aureus (MRSA) strains exemplifies the urgent
need for new antibiotics. The marine natural product, marinopyrrole A, was previously
shown to have potent antibiotic activity against Gram-positive pathogens, including
MRSA. However, its minimum inhibitory concentration (MIC) against MRSA was increased
by >500 fold in the presence of 20% human serum, thus greatly limiting therapeutic
potential. Here we report our discovery of a novel derivative of marinopyrrole A,
designated 1a, featuring a 2–4 fold improved MIC against MRSA and significantly less
susceptibility to serum inhibition. Importantly, compound 1a displayed rapid and
concentration-dependent killing of MRSA. Compared to the natural product counterpart,
compound 1a provides an important natural product based scaffold for further Structure
Activity Relationship (SAR) and optimization.
Keywords: marinopyrrole; asymmetrical marinopyrroles; MRSA; antibiotics; SAR

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1. Introduction
Marinopyrroles were first reported to show antibiotic activity against methicillin-resistant
Staphylococcus aureus (MRSA) several years ago [1]. Structural elucidation of the isolated
marinopyrroles from an obligate marine Streptomyces (strain CNQ-418, collected from the sea floor
near La Jolla, CA) by 2D NMR and X-ray crystallography revealed an unprecedented structure class.
The densely halogenated 1,3-bipyrroles represented by marinopyrrole A (±)-1 exist as enantiopure
M-(−)-atropisomer, (−)-1, at ambient temperature (Chart 1). The enantiomer (+)-1 was obtained after a
chiral separation of synthetic (±)-1 using chiral HPLC [2]. Due to their novel class of molecular
structures and promising biological properties, the marinopyrroles have attracted considerable
attention. In the last few years since the discovery of this uncommon bispyrrole structure of marine
natural products, several synthetic and semi-synthetic efforts have successfully yielded a few series of
novel marinopyrrole derivatives [2–6].
Chart 1. Chemical structures of marinopyrrole A.
The global crisis of antibiotic resistance has spread rapidly over the last several decades. MRSA
infections have reached epidemic proportions in many countries [7] and represent the most common
cause of skin and soft tissue infections in the United States [8]. Both hospital-associated and
community-associated MRSA can exhibit broader resistance to multiple classes of antibiotics [7,9–11].
Hospital-associated MRSA (HA-MRSA) infections are common among healthcare facilities and are
resistant to many antibiotics. However, community-associated MRSA (CA-MRSA) strains are highly
virulent and infect even healthy individuals; the incidence of these infections has skyrocketed in the
last decade. The relative abandonment of antibiotic discovery and development by the pharmaceutical
industry has created a vacuum in the introduction of new antibiotics to treat these increasingly
problematic infections. Except for the addition of the oxazolidinone linezolid [12] in 2000, the
lipopeptide daptomycin [13] in 2003, and FDA’s most recent approval of ceftaroline (Teflaro) [14] as
an injectable antibiotic to treat adults with community acquired bacterial pneumonia (CABP) and acute
bacterial skin and skin structure infections (ABSSSI) including MRSA, a very limited number of new
antibiotics have been discovered over the last half a century, with only two new classes of anti-MRSA
drugs having been approved in the last 40 years. Clearly, novel agents for the treatment of MRSA
infections are urgently needed [15].
Recently, evaluation of the pharmacological properties has revealed that marinopyrrole A has
potent concentration-dependent antibacterial activity against clinically-relevant hospital- and
community-acquired MRSA strains, a prolonged post-antibiotic effect superior to the first-line current

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agents vancomycin and linezolid, and a favorable resistance profile [16]. Although marinopyrrole A
(±)-1, (−)-1 and (+)-1 showed potent antibiotic activity [2] with limited toxicity to mammalian cell
lines at >20× MIC, their antibiotic activity against MRSA were inhibited by 20% human serum [16].
Previous studies of synthetic or semi-synthetic marinopyrrole derivatives to date have yielded no new
analogs that retained antibacterial activity in the presence of human serum [16], constituting a major
challenge for therapeutic development. Here, we report our design and synthesis of novel
marinopyrrole derivatives with excellent antibiotic activity against MRSA but only limited
serum inactivation.
2. Results and Discussion
2.1. Synthesis and Structure Activity Relationships of Asymmetrical Marinopyrrole Derivatives
Two years ago, we reported the first total synthesis of marinopyrrole A along with “symmetrical”
derivatives, (±)-1 and 12 analogs, which bear the same substituents with the same substitution pattern
on both phenyl ring A and B attached to the carbonyl groups (Chart 1) [6]. In addition to those
symmetrical marinopyrrole derivatives, we envisage that the “asymmetrical” marinopyrrole derivatives
shown in Scheme 1 should have different biological activity than their symmetrical counterparts.
In particular, the molecules with diverse functional groups decorated on this unique 1,3-bipyrrole
system may adopt specific conformations due to the restricted free rotation of the chiral axis. To this
end, a series of novel asymmetrical marinopyrrole derivatives were designed and synthesized.
Scheme 1. Synthesis of Novel Asymmetrical Marinopyrrole Derivatives a.
a
Conditions: (i) PPTS, 1,4-dioxane, reflux, 53%; (ii) 6.0 eq. 5, THF, −78 °C, 85%; (iii) SOCl2,
benzene, reflux; (iv) 1.2 eq. 8, 1.3 eq. AlCl3, DCM, 0–25 °C, 70%; (v) 1.0 eq. 9a, 4.1 eq. SO2Cl2,
DCM, 0 °C, 85%; (vi) 1.0 eq. 10a, 4.0 eq. BBr3, DCM, −78 °C, 96%.
Chemistries to access both symmetrical and asymmetrical marinopyrrole derivatives were
reported previously [2,6]. Briefly, 2-ethoxycarbonyl-3-aminopyrrole 2 was obtained using a
published procedure [17]. A PPTS-promoted Clauson–Kaas reaction [2,18] between 2 and

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2,5-dimethoxy-tetrahydrafuran 3 in dioxane under reflux gave rise to bispyrrole 4 in 53% yields. The
mono-addition of lithiated anisole 5 to bispyrrole ester 4 in THF at −78 °C furnished mono acylated
bispyrrole 6 in 85% yield [2]. Friedel–Crafts arylation of 6 with the acid chlorides 8, generated in situ
from the corresponding carboxylic acids 7 with thionyl chloride, afforded a series of marinopyrrole
precursor 9a–9c. A novel series of asymmetrical marinopyrrole derivatives 10a–10c were obtained by
tetrachlorination of the corresponding 9a–9c using 4.1 equivalents of sulfuryl chloride (SO2Cl2)
in DCM at 0 °C. Demethylation of 10a–10c using BBr3 in DCM furnished 1a–1c in >90% yield
(Scheme 1) [2,6].
The anti-MRSA activity of the novel asymmetrical marinopyrroles shown in Scheme 1 was
evaluated against a USA300 strain of community-associated MRSA. One of the derivatives,
(4-chloro-2-hydroxyphenyl) (4,4′,5,5′-tetrachloro-2′-(2-hydroxybenzoyl)-1′H-1,3′-bipyrrol-2-yl)methanone
(1a), exhibited potent antibacterial activity. The 2–4 fold improvement in antibacterial activity from
the parent compound 1 was observed for this novel marinopyrrole derivative 1a as shown in Table 1.
The corresponding dimethoxy-congener, (4-chloro-2-methoxyphenyl)(4,4′,5,5′-tetrachloro-2′-(2-methoxy
benzoyl)-1′H-1,3′-bipyrrol-2-yl)methanone, 10a, was found to be inactive against MRSA at >200 μM.
This observation is consistent with the result reported previously for compound 1 and its
corresponding methoxy analog [2] as compound 1a showed >1000 fold more potency than 10a. This
observed SAR was also supported by the current results from compounds 1b and 1c. Compound 1b,
with a chloro-substituent ortho to the hydroxyl group, was >128-fold more potent than 10a, whereas
derivative 1c with chloro-substituent para to the hydroxyl group showed >64-fold more anti-MRSA
activity than 10b. Compound 1a has the chloro-substituent meta to the hydroxyl group exhibiting
8–16-fold and 4–8-fold more anti-MRSA activity than 1c and 1b, respectively. The fact that the free
hydroxyl groups are essential for the antibacterial activity suggested that the binding sites may contain
both hydrogen bond donors and hydrogen bond receptors. Although the internal hydrogen bonding
between the phenyl hydroxyl and adjacent carbonyl group was observed in an X-ray structure of
(−)-1 [1] and compounds 1a–1c may behave similarly, this interaction can be weakened or interrupted
if appropriate amino acid residues, such as Arg, His, Asn, Asp, Glu or Gln, are close by for
interactions. Although thorough investigation is required to understand the observed structure activity
relationships generated by compounds 1a–1c, their physicochemical properties on the OR5 group in B
ring due to the difference in pKa values of their hydroxyl groups might, at least in part, play an
essential role in addition to the different substitution pattern.
Table 1. Minimum inhibitory concentration (MIC) of Marinopyrrole Derivatives against
methicillin-resistant Staphylococcus aureus (MRSA).
Compound
THB
0.74
THB + 20% Serum
94–188
1 (parent)
10a
1a
>200
>200
0.19–0.39
1.56
12.5–25
>200
1b
1c
3.13
>200
MIC in μM in Todd-Hewitt broth (THB) in the absence or presence of 20% human serum. All data were
generated from experiments repeated four times.

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Most significantly, not only did compound 1a show increased antibacterial activity compared to the
parent compound, marinopyrrole A (1), but its activity was also less inhibited upon the addition of
20% human serum (MIC 12.5–25 µM vs. 100–200 µM). In comparison to contemporary MRSA
agents, compound 1a is more potent than vancomycin and linezolid against USA300 MRSA strain
TCH1516 [16].
2.2. In Vitro Time-Kill of Marinopyrrole Derivative 1a
In vitro time-kill studies were performed to characterize killing kinetics of derivative 1a at 20×, 10×
and 1× MIC and to compare them with that of the parent natural product marinopyrrole A
(−)-1 [16]. Derivative 1a displayed strong concentration-dependent MRSA killing that was much more
rapid than vancomycin or linezolid and was similar in profile to the parent compound [16].
The potency of derivative 1a was especially evident at 20× the MIC (3.8 μM), yielding greater than a
4-log kill of MRSA at 4 h. This feature parallels the effects seen with the natural product parent
compound (−)-1.
Compound (−)-1 was also shown to have a favorable therapeutic index at 24 h in treated
mammalian cells [16]. The natural product marinopyrrole A had a low propensity for toxicity at
concentrations below 20× MIC. Upon closer examination, derivative 1a displays more potent MRSA
killing effects. For example, the tested concentration of 1a (MIC 0.39 μM) was half of the concentration
of the parent natural product tested in time-kill analyses (MIC 0.75 μM or 0.375 μg/mL) [16].
Secondly, at 3.9 μM (10× MIC) and 6 h incubation, 1a causes 3-log decrease in bacterial survival
(Figure 1). This improved upon the kinetics of the natural product, (−)-1, which generated only a
two-log decrease in bacterial survival [16]. Furthermore, the actual tested compound concentration of
(−)-1 was 7.5 μM, a fold higher than that of derivative 1a (3.9 μM) (Figure 1). Similar to (−)-1, this
activity is much more rapid than vancomycin or linezolid [16]. In summary, we have discovered a
novel natural product based derivative that retains the favorable and potent concentration-dependent
bacterial killing characteristic of the natural product but at a lower concentration.
Figure 1. In vitro Time-kill Analysis for Marinopyrrole Derivative (1a) against the
USA300 Community-associated MRSA Strain TCH1516. MRSA was subjected to
increasing concentrations of 1× (0.39 μM), 10× (3.9 μM) and 20× (7.8 μM) the MIC
of derivative 1a or vehicle control (none). Derivative 1a showed potent
concentration-dependent in vitro bactericidal kinetics against MRSA at 10× (3.9 μM) and
20× (7.8 μM) MIC, along with bacteriostatic activity at 1× MIC (0.39 μM).

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3. Experimental Section
3.1. Synthesis of Compounds 4–10c
All chemicals and solvents were purchased from commercial suppliers and used without further
purification. Preparative flash column chromatography was performed on silica gel 60, 0.040–0.063 mm
1
(EMD Chemicals). H NMR (400 MHz) spectra were recorded on a Varian AS400 with a 60-place
automated sample changer. High resolution ESI-MS spectra were recorded on an Agilent ESI-TOF
LC-MS 6200 system. Preparative HPLC was performed on a Gilson HPLC system with UV detectors
and Gilson 215 liquid handler for auto injection and fraction collections (customized by HT Labs,
San Diego, CA, USA). Analytical HPLC was performed on an Agilent 1100 series with diode array
detectors and auto samplers. The specifications of HPLC analysis are as follows: flow rate, 1 mL/min;
column, Intertsil, 2.5 μm, 4.6 × 150 mm; wavelength, 254 and 280 nm; mobile phase, A: H2O with
0.1% HCO2H, B: MeOH, gradient of 50–95% B in 25 min. All tested compounds possessed a purity of
not less than 95%.
Ethyl 1′H-1,3′-bipyrrole-2′-carboxylate (4). To a stirred solution of 2,5-dimethoxy-tetrahydrofuran 3
(1.6 mL, 12.4 mmol, 1.3 equiv) and PPTS (3.2 g, 12.4 mmol, 1.3 equiv) in 1,4-dioxane (20 mL) at
50 °C, a solution of aminopyrrole 2 (1.47 g, 9.55 mmol, 1.0 eq.) in 1,4-dioxane (6 mL) was added
slowly. The resulting mixture was brought to reflux and stirred for 1 h. The reaction mixture was then
concentrated, dissolved in EtOAc (50 mL) and dried over anhydrous MgSO4. The crude product was
purified by flash column chromatography (10% EtOAc in hexane) to give 4 as a yellow solid (1.036 g,
1
53% yield). H NMR (400 MHz, CDCl3) δ 8.99 (s, 1H), 7.04–7.01 (m, 2H), 6.89 (t, J = 3.1 Hz, 1H),
6.29 (t, J = 2.9 Hz, 1H), 6.27–6.24 (m, 2H), 4.28 (q, J = 7.1 Hz, 2H), 1.29 (t, J = 7.1 Hz, 3H).
1′H-1,3′-Bipyrrol-2′-yl(2-methoxyphenyl)methanone (6). To a solution of 2-bromoanisole
(1.39 g, 7.43 mmol, 5.63 equiv) in anhydrous THF (5 mL) at −78 °C, a 2.5M solution of BuLi in
hexane (3 mL, 7.50 mmol, 5.68 eq.) was added dropwise, the resulting mixture was stirred for 1 h. at
−78 °C to generate the lithiated anisole. In an oven-dried flask, compound 4 (270 mg, 1.32 mmol, 1 eq.)
was dissolved in THF (5 mL) and cooled to −78 °C, the lithiated anisole 5 was transferred into the
solution containing 4 dropwise via syringe, and the resulting mixture was stirred for 1 h. at −78 °C. To
the reaction mixture, an aqueous solution of NH4Cl (5 mL) was added, the mixture was extracted with
EtOAc, dried over anhydrous Na2SO4. The crude product was purified by flash column chromatography
1
(10% EtOAc in hexane) to give 6 as a light brown solid (0.30 g, 85% yield). H NMR (400 MHz,
CDCl3) δ 9.35 (s, 1H), 7.28–7.22 (m, 1H), 7.20 (dd, J = 7.5, 1.7 Hz, 1H), 7.02 (t, J = 3.0 Hz, 1H),
6.80 (td, J = 7.5, 0.9 Hz, 1H), 6.68 (d, J = 8.4 Hz, 1H), 6.48–6.43 (m, 2H), 6.27 (t, J = 2.8 Hz, 1H),
5.88 (m, 2H), 3.63 (s, 3H).
(2-(4-Chloro-2-methoxybenzoyl)-1′H-1,3′-bipyrrol-2′-yl)(2-methoxyphenyl)methanone (9a). Into a
solution of 4-chloro-2-methoxybenzoic acid (125 mg, 0.67 mmol, 1.2 eq.) in benzene (1.5 mL), SOCl2
(1.5 mL) was added at room temperature and the resulting solution was refluxed for 2 h. The reaction
mixture was concentrated under vacuum to generate 4-chloro-2-methoxybenzoyl chloride 8a which
was used directly in the next step without purification. A solution of 8a in CH2Cl2 (DCM) (2 mL) was
added to a slurry of AlCl3 (96 mg, 1.3 eq.) in DCM (2.5 mL) at 0 °C and then a solution of 6 (150 mg,

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0.56 mmol, 1.0 equiv) in DCM (1.5 mL) was added dropwise. The resulting solution was allowed to
warm to room temperature and stirred overnight. A saturated solution of NaHCO3 (10 mL) and DCM
(10 mL) was then added and the resulting mixture was stirred for 1 h, and then filtered though Celite®.
The mixture was extracted with DCM (2 × 10 mL), the organic layer was dried over anhydrous
Na2SO4, and purified by flash column chromatography (hexanes:EtOAc) to afford 172 mg of 9a as a
white solid, 70% yield. 1H NMR (400 MHz, CDCl3) δ 9.83 (s, 1H), 7.22–7.14 (m, 2H), 7.12 (d, J = 7.8 Hz,
1H), 7.04 (t, J = 3.0 Hz, 1H), 6.95–6.88 (m, 2H), 6.73–6.63 (m, 3H), 6.31 (dd, J = 4.0, 1.7 Hz, 1H),
6.27 (t, J = 2.8 Hz, 1H), 5.83 (dd, J = 4.0, 2.6 Hz, 1H), 3.77 (s, 3H), 3.69 (s, 3H).
(2-(5-Chloro-2-methoxybenzoyl)-1′H-1,3′-bipyrrol-2′-yl)(2-methoxyphenyl)methanone
(9b).
5-Chloro-2-methoxybenzoyl chloride (8b) was generated in situ from the corresponding acid using the
same method as 8a. Compound 9b (88 mg, 67% yield) was obtained using the same method as 9a
described above. 1H NMR (400 MHz, CDCL3) δ 9.78 (s, 1H), 7.31 (dd, J = 8.8, 2.7 Hz, 1H), 7.25–7.15
(m, 2H), 7.06 (dd, J = 4.3, 1.7 Hz, 2H), 6.85 (d, J = 8.9 Hz, 1H), 6.77–6.66 (m, 3H), 6.32 (dd, J = 4.0,
1.7 Hz, 1H), 6.30 (t, J = 2.8 Hz, 1H), 5.87 (dd, J = 4.0, 2.6 Hz, 1H), 3.75 (s, 3H), 3.69 (s, 3H).
(2-(3-Chloro-2-methoxybenzoyl)-1′H-1,3′-bipyrrol-2′-yl)(2-methoxyphenyl)methanone
(9c).
3-Chloro-2-methoxybenzoyl chloride (8c) was generated in situ from the corresponding acid using the
same method as 8a. Compound 9c (90 mg, 68% yield) was obtained using the same method as 9a
described above. 1H NMR (400 MHz, CDCL3) δ 9.81 (s, 1H), 7.52 (dd, J = 7.8, 1.6 Hz, 1H), 7.39 (dd,
J = 8.0, 1.6 Hz, 1H), 7.24–7.19 (m, 1H), 7.10 (dt, J = 5.7, 2.2 Hz, 2H), 6.87 (dd, J = 2.6, 1.6 Hz, 1H),
6.79 (d, J = 7.9 Hz, 1H), 6.66–6.59 (m, 3H), 6.31 (t, J = 2.8 Hz, 1H), 6.05 (dd, J = 4.1, 2.6 Hz, 1H),
3.57 (s, 3H), 3.52 (s, 3H).
(4-Chloro-2-methoxyphenyl)(4,4′,5,5′-tetrachloro-2′-(2-methoxybenzoyl)-1′H-[1,3′-bipyrrole]-2-yl)
methanone (10a). To a solution of compound 9a (82 mg, 0.19 mmol, 1 eq.) in DCM (5 mL) at 0 °C,
SO2Cl2 (64 μL, 0.78 mmol, 4.1 equiv) was added dropwise, and the solution was allowed to stir at 0 °C
for 1 h. Saturated aqueous NaHCO3 solution (2 mL) was added and the resulting mixture was extracted
with DCM (3 × 4 mL). The combined organic layers were dried with anhydrous MgSO4, filtered, and
concentrated. The residue was purified by flash column chromatography (silica gel, hexane:EtOAc
1
4:1) to afford 10a (92 mg, 85% yield) as an off-white solid. H NMR (400 MHz, CDCl3) δ 10.38
(s, 1H), 7.25–7.21 (m, 2H), 7.13 (d, J = 7.9 Hz, 1H), 6.96–6.94 (m, 2H), 6.76 (d, J = 8.3 Hz, 1H),
6.68 (t, J = 7.8 Hz, 1H), 6.31 (s, 1H), 3.80 (s, 3H), 3.72 (s, 3H); HRMS (ESI-TOF) [M + H]+ calcd for
C24H16Cl5N2O4 570.9547, found 570.9537; HPLC purity, 95.2%.
(5-Chloro-2-methoxyphenyl)(4,4′,5,5′-tetrachloro-2′-(2-methoxybenzoyl)-1′H-1,3′-bipyrrol-2-yl)
methanone (10b). The same procedure described for 10a was used to synthesize 10b (87 mg, 80%
1
yield). H NMR (400 MHz, CDCL3) δ 10.28 (s, 1H), 7.36 (dd, J = 8.9, 2.7 Hz, 1H), 7.31–7.27
(m, 1H), 7.19 (dd, J = 7.5, 1.7 Hz, 1H), 7.07 (d, J = 2.6 Hz, 1H), 6.88 (d, J = 8.9 Hz, 1H), 6.79
(d, J = 8.4 Hz, 1H), 6.73 (td, J = 7.5, 0.8 Hz, 1H), 6.33 (s, 1H), 3.78 (s, 3H), 3.73 (s, 3H).
(3-Chloro-2-methoxyphenyl)(4,4′,5,5′-tetrachloro-2′-(2-methoxybenzoyl)-1′H-1,3′-bipyrrol-2-yl)
methanone (10c). The same procedure described for 10a was used to synthesize 10c (80 mg, 74%).
1H NMR (400 MHz, CDCL3) δ 10.30 (s, 1H), 7.57 (dd, J = 7.9, 1.5 Hz, 1H), 7.37–7.27 (m, 2H), 7.11

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(dd, J = 7.5, 1.7 Hz, 1H), 6.85 (t, J = 7.9 Hz, 1H), 6.76 (d, J = 8.4 Hz, 1H), 6.67 (t, J = 7.5 Hz, 1H),
6.57 (s, 1H), 3.83 (s, 3H), 3.73 (s, 3H).
3.2. Synthesis of Compounds 1a–1c
(4-Chloro-2-hydroxyphenyl)(4,4′,5,5′-tetrachloro-2′-(2-hydroxybenzoyl)-1′H-1,3′-bipyrrol-2-yl)
methanone (1a). To a solution of 10a (33 mg, 0.058 mmol) in anhydrous DCM (1 mL) was slowly
added 1.0 M solution of BBr3 in DCM (23 μL, 0.23 mmol, 4 eq.) via a syringe under N2 at −78 °C.
After being stirred for 0.5 h, the mixture was quenched by addition of MeOH (0.5 mL) and extracted
with DCM (3 × 10 mL). The combined organic layers were dried over anhydrous MgSO4, filtered and
concentrated in vacuum. The residue was purified by column chromatography (silica gel, hexanes:12%
EtOAc) to give 1a (30 mg, 96% yield) as a yellow solid. 1H NMR (400 MHz, CDCl3) δ 11.34 (s, 1H),
10.39 (s, 1H), 9.77 (s, 1H), 7.47 (d, J = 8.6 Hz, 1H), 7.43 (dd, J = 8.0, 1.7 Hz, 1H), 7.36 (ddd, J = 8.8,
7.4, 1.6 Hz, 1H), 7.04 (d, J = 2.0 Hz, 1H), 6.95–6.90 (m, 1H), 6.87 (dd, J = 8.6, 2.0 Hz, 1H), 6.68
(s, 1H), 6.53 (ddd, J = 8.0, 7.3, 1.1 Hz, 1H); HRMS (ESI-TOF) [M + H]+ calcd for C22H12Cl5N2O4
542.9234, found 542.9237; HPLC purity 96.6%.
(5-Chloro-2-hydroxyphenyl)(4,4′,5,5′-tetrachloro-2′-(2-hydroxybenzoyl)-1′H-1,3′-bipyrrol-2-yl)
methanone (1b). The same procedure as 1a was followed to obtain 1b (28 mg, 90%) from 10b
(31 mg, 0.055 mmol). 1H NMR (400 MHz, CDCL3) δ 11.10 (s, 1H), 10.33 (s, 1H), 9.89 (s, 1H), 8.06
(dd, J = 7.9, 1.8 Hz, 1H), 7.95 (d, J = 2.4 Hz, 1H), 7.83 (d, J = 8.3 Hz, 1H), 7.71–7.64 (m, 1H),
7.49–7.41 (m, 2H), 6.97 (dd, J = 8.9, 2.1 Hz, 1H), 6.87 (s, 1H); HRMS (ESI-TOF) [M + Na]+ calcd for
C22H11Cl5N2O4Na 564.9054, found 564.9055; HPLC purity, 95.0%.
(3-Chloro-2-hydroxyphenyl)(4,4′,5,5′-tetrachloro-2′-(2-hydroxybenzoyl)-1′H-1,3′-bipyrrol-2-yl)
methanone (1c). The same procedure as 1a was followed to obtain 1c (26 mg, 91%) from 10c
1
(29 mg, 0.05mmol). H NMR (400 MHz, CDCL3) δ 11.74 (s, 1H), 10.48 (s, 1H), 9.93 (s, 1H), 8.06
(d, J = 7.9 Hz, 1H), 7.94 (d, J = 8.0 Hz, 1H), 7.82 (d, J = 8.2 Hz, 1H), 7.67 (t, J = 7.8 Hz, 1H), 7.61
(d, J = 7.9 Hz, 1H), 7.45 (t, J = 7.6 Hz, 1H), 6.96 (t, J = 7.9 Hz, 1H), 6.83 (s, 1H); HRMS (ESI-TOF)
[M + Na]+ calcd for C22H11Cl5N2O4Na 564.9054, found 564.9058; HPLC purity, 97.4%.
3.3. In Vitro Antibacterial Assays
TCH1516, a USA300 strain of community-associated MRSA, was obtained from the American
Type Culture Collection and used for biological assays. MICs were determined by broth microdilution
according to Clinical and Laboratory Standards Institute guidelines except that Todd-Hewitt broth
(THB) was used in place of Mueller-Hinton broth. Assays were done in 96-well tissue-culture treated
plates. Vancomycin served as a control antibiotic. MIC assays in 20% human serum were assessed by
bacterial metabolic activity in resazurin as described [16].
3.4. In Vitro Time-Kill Analysis
The bactericidal activity of derivative 1a against the CA-MRSA isolate TCH1516 were assessed by
time-kill analysis essentially as described previously [16,19–21]. Briefly, MRSA was grown overnight
in Todd-Hewitt Broth (THB) at 37 °C with shaking. Following overnight growth, MRSA was

Mar. Drugs 2012, 10
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inoculated in fresh media for growth to mid-logarithmic phase. At the start of the time-kill assay,
bacteria (starting inoculum ~5 × 105 cfu/mL) were added to duplicate 5 mL polystyrene round-bottom
tubes (Falcon, Bedford, MA, USA) containing 20×, 10×, 1×, none of the MIC of derivative 1a
(0.39 μM) or an equivalent amount of DMSO vehicle control (Figure 1, none). These cultures were
incubated in a shaking 37 °C incubator for 24 h. To determine the rate of antibiotic killing, small
aliquots were removed from tubes at 0, 3, 6 and 24 h and serially diluted for cfu enumeration on THA
plates. The limit of detection for the time-kill assay was 1.6 (log10 cfu/mL).
4. Conclusions
In summary, we designed and synthesized a novel series of asymmetrical derivatives of marine
natural product, marinopyrrole A, and discovered that a novel derivative, 1a (MIC = 0.19–0.39 μM),
exhibits significantly greater activity than linezolid and vancomycin against MRSA. Moreover, in vitro
time-kill kinetics of 1a demonstrated potent concentration-dependent killing. These qualities were
similar to those displayed by the parent natural product in time-kill studies, but 1a was
2–4-fold more potent at lower compound concentrations. One of the main drawbacks of the natural
product has been its significant inhibition in the presence of human serum. For example, the antibiotic
activity of (−)-1 was inactivated (MIC increased 256–522×) in the presence of serum [16]. Here, 1a
again exhibits an advantage, with only 32–64 fold increase in MIC in 20% human serum (Table 1).
Further derivatization and SAR optimization will aim to engineer out the propensity for serum
inhibition. Design and synthesis of both symmetrical and asymmetrical marinopyrrole derivatives are
actively ongoing. The optimization of their structure and activity for use as potential antibiotic agents
against MRSA will be reported in due course.
Acknowledgments
This work was partially supported by Moffitt Cancer Center (R.L.) and National Institutes of Health
(NIH) grant GM08555 (V.N.). Work by N.M.H. was supported by the Ruth L. Kirschstein National
Research Service Award (NRSA) from the NIH (5 F31 GM090658-02).
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