Structure-Activity relationship study of sesquiterpene lactones and their semi-synthetic amino derivatives as potential antitrypanosomal products

Article abstract of DOI:10.3390/molecules19033523

Sesquiterpene lactones (STLs) are natural products that have potent antitrypanosomal activity in vitro and, in the case of cynaropicrin, also reduce parasitemia in the murine model of trypanosomiasis. To explore their structure-Antitrypanosomal activity relationships, a set of 34 natural and semi-synthetic STLs and amino-STLs was tested in vitro against T. b. rhodesiense (which causes East African sleeping sickness) and mammalian cancer cells (rat bone myoblast L6 cells). It was found that the a-methylene-?- lactone moiety is necessary for both antitrypanosomal effects and cytotoxicity. Antitrypanosomal selectivity is facilitated by 2-(hydroxymethyl)acrylate or 3,4-dihydroxy-2- methylenebutylate side chains, and by the presence of cyclopentenone rings. Semi-synthetic STL amines with morpholino and dimethylamino groups showed improved in vitro activity over the native STLs. The dimethylamino derivative of cynaropicrin was prepared and tested orally in the T. b. rhodesiense acute mouse model, where it showed reduced toxicity over cynaropicrin, selectivity is facilitated by 2-(hydroxymethyl)acrylate or 3,4-dihydroxy-2-methylenebutylate side chains, and by the presence of cyclopentenone rings. Semi-synthetic STL amines with morpholino and dimethylamino groups showed improved in vitro activity over the native STLs. The dimethylamino derivative of cynaropicrin was prepared and tested orally in the T. b. rhodesiense acute mouse model, where it showed reduced toxicity over cynaropicrin, but also lost antitrypanosomal activity.

Full text of DOI:10.3390/molecules19033523

Molecules 2014, 19, 3523-3538; doi:10.3390/molecules19033523
OPEN ACCESS
molecules
ISSN 1420-3049
www.mdpi.com/journal/molecules
Article
Structure-Activity Relationship Study of Sesquiterpene
Lactones and Their Semi-Synthetic Amino Derivatives as
Potential Antitrypanosomal Products
Stefanie Zimmermann 1,2, Gerda Fouché 3, Maria De Mieri 1, Yukiko Yoshimoto 4, Toyonobu Usuki 4,
Rudzani Nthambeleni 3, Christopher J. Parkinson 5, Christiaan van der Westhuyzen 3,
Marcel Kaiser 2,6, Matthias Hamburger 1 and Michael Adams 1,*
1
Department Pharmaceutical Biology, University of Basel, Klingelbergstrasse 50, 4056 Basel,
Switzerland; E-Mails: stefanie.zimmermann03@gmail.com (S.Z.); maria.demieri@unibas.ch (M.D.M.);
matthias.hamburger@unibas.ch (M.H.)
2
Department Medical Parasitology & Infection Biology, Swiss TPH, Socinstrasse 57, 4000 Basel,
Switzerland; E-Mail: marcel.kaiser@unibas.ch
3
CSIR Biosciences, Meiring Naudé Road, Brummeria, Pretoria 0001, Gauteng, South Africa;
E-Mails: gfouche@csir.co.za (G.F.); rnthambeleni@csir.co.za (R.N.);
cwvdwesthuyzen@csir.co.za (C.W.)
4
Department of Materials and Life Sciences, Faculty of Science and Technology, Sophia University,
7-1 Kioicho, Chiyoda, Tokyo 102-8554, Japan; E-Mails: tkmh-937@sophia.ac.jp (Y.Y.);
t-usuki@sophia.ac.jp (T.U.)
5
School of Biomedical Sciences, Charles Sturt University, Orange, NSW 2800, Australia;
E-Mail: cparkinson@csu.edu.au
6
University of Basel, Petersplatz 1, 4003 Basel, Switzerland
* Author to whom correspondence should be addressed; E-Mail: michael.adams78@gmail.com;
Tel.: +41-58-934-57-94; Fax: +41-58-934-50-01.
Received: 12 November 2013; in revised form: 13 March 2014 / Accepted: 13 March 2014 /
Published: 21 March 2014
Abstract: Sesquiterpene lactones (STLs) are natural products that have potent
antitrypanosomal activity in vitro and, in the case of cynaropicrin, also reduce parasitemia
in the murine model of trypanosomiasis. To explore their structure-antitrypanosomal
activity relationships, a set of 34 natural and semi-synthetic STLs and amino-STLs was
tested in vitro against T. b. rhodesiense (which causes East African sleeping sickness) and
mammalian cancer cells (rat bone myoblast L6 cells). It was found that the α-methylene-γ-
lactone moiety is necessary for both antitrypanosomal effects and cytotoxicity. Antitrypanosomal

Molecules 2014, 19
selectivity is facilitated by 2-(hydroxymethyl)acrylate or 3,4-dihydroxy-2-methylenebutylate
3524
side chains, and by the presence of cyclopentenone rings. Semi-synthetic STL amines with
morpholino and dimethylamino groups showed improved in vitro activity over the native
STLs. The dimethylamino derivative of cynaropicrin was prepared and tested orally in the
T. b. rhodesiense acute mouse model, where it showed reduced toxicity over cynaropicrin,
but also lost antitrypanosomal activity.
Keywords: cynaropicrin; sesquiterpene lactones; antitrypanosomal; cytotoxicity; structure-
activity-relationship; dimethylamino analogues; T. b. rhodesiense acute mouse model
1. Introduction
Sleeping sickness, or human African trypanosomiasis (HAT), is a deadly protozoal disease caused
by Trypanosoma brucei species spread by tsetse flies (Glossina spp.). The two human pathogenic
subspecies, T. b. rhodesiense (95% of cases) and T. b. gambiense (5% of cases), differ in terms of their
geographic distribution, clinical pictures, and the drugs used to treat parasitemia [1]. Currently, there
are about 30,000 new HAT cases annually, and as many as 30 million people live in HAT endemic
areas [2]. Despite some recent successes like nifortimox-eflornithine combination therapy (NECT) [3],
HAT drugs are still inefficient by modern standards and need to be replaced by compounds that are
safer and easier to administer [4].
Natural products from plants have been instrumental in developing drugs to treat protozoal diseases,
such as quinine and artemisinin against malaria [5,6]. Currently, though, no natural product-based
antitrypanosomal drugs are in use or even in late stage clinical development. Recently, we reported the
in vivo activity [7] and mode of action [8] of cynaropicrin (1), a natural sesquiterpene lactone (STL).
Although more than 883 plant-derived small molecules have shown antiprotozoal (antitrypanosomal,
antiplasmodial, and antileishmanial) effects in vitro, of which 87 were STLs [5,6], this was the first
reported plant compound with in vivo anti-T. brucei action specifically. STLs are a chemotaxonomic
feature of the largest plant family, the Asteraceae [9], and to date more than 5,000 STLs are known [5,10].
STLs are a promising compound class for antitrypanosomal drug discovery [11–13], thus a better
understanding of the structural features that contribute to activity is expedient [14,15]. This study
explores the antitrypanosomal structure-activity relationships within this compound class using a
group of 18 molecules comprising natural STLs and 16 semi-synthetic STL-amines and two other
derivatives against T. b. rhodesiense in vitro. Mammalian cancer cells (L6 cell line) were used to
evaluate cytotoxicity. The antitrypanosomal effects of the eight compounds 1, 2, 5–9,and 13 have been
reported before [7,11,12], but were included for comparison. Additionally, based on the in vivo
antitrypanosomal effects of 1 after intraperitoneal application [7,8], 1 and the dimethylamino
derivative 19 were tested in vivo in the acute mouse model with oral application. The rationale behind
derivative 19 was that masking the α,β-unsaturated enoate in the lactone ring would possibly create a
prodrug with increased water solubility, improved pharmacokinetic properties, and reduced unspecific
binding to biological thiols via Michael addition to the α-methylene-γ-lactone. Through subsequent
bioactivation it would be converted to the parent compounds and, hence, display its biological activity

Molecules 2014, 19
3525
on the target. A similar approach had been previously successfully applied to several STLs with
anticancer activity like helenalin, costunolide, and parthenolide [16].
2. Results and Discussion
The in vitro antitrypanosomal activity of compounds 1–34 was determined against T. b. rhodesiense
(STIB 900 strain), while their cytotoxicity was evaluated using rat myoblast L6 cells to determine the
selectivity indices (SI; IC50 L6/IC50 T. b.) of each compound (Figure 1, Table 1).
Figure 1. Structures of sesquiterpene lactones (STLs) 1–18 and semi-synthetic STL amino
derivatives 19–34.
Cynaropicrin (1) and onopordopicrin (2), which both have 2-(hydroxymethyl)acrylate side chains,
showed IC50s of 0.3 and 0.4 µM, and SIs of 7.8 and 8.2 [7,8,12], respectively. Extension of the side
chain in 2 to a 3,4-dihydroxy-2-methylenebutylate, as in cnicin (3), had little effect on activity
(0.4 µM) or selectivity (SI 10). Compound 5, which lacked the 2-(hydroxymethyl)acrylate side chain
of 1, had a 16 fold lower antitrypanosomal activity (4.9 µM) and a nine fold lower cytotoxicity
(19 µM) as compared to 1 [8]. Compound 14, a 2-methylbut-2-enoate (tiglate) STL, was less active
and selective than the 2-(hydroxymethyl)acrylate STLs 1, 2, and 3. Compounds 15–18, which lack an
exocyclic methylene group in the lactone ring, showed reduced antitrypanosomal activities (IC50s > 12 μM)
and a total lack of cytotoxicity.

Molecules 2014, 19
3526
Table 1. In vitro activity of compounds against STIB 900 strain and L6 cells. Citations are
shown for previously reported antitrypanosomal compounds.
Compound
T. brucei STIB 900 IC50 (μM) a L6 cells IC50 (μM) a SI b
1 [7,8]
0.3 ± 0.001
0.4 ± 0.01
0.4 ± 0.1
0.2 ± 0.01
4.9 ± 0.34
4.4 ± 1.2
1.3 ± 0.4
0.8 ± 0.5
10.8 c
2.2 ± 0.3
3.1 ± 1.1
4.2 ± 0.9
0.6 ± 0.02
19.2 ± 3.2
8.3 ± 1.9
7.7 ± 1.3
5.2 ± 0.9
15.6
7.8
8.2
10
2 [12]
3
4
3
5 [8]
3.9
1.9
5.9
6.5
1.4
7.6
1.2
2.5
1.3
3.4
6.4
>6.4
>8.8
2.6
10.4
2.5
2.2
10.3
5.6
13.3
3.8
>35.0
4
6 [11]
7 [11]
8 [11]
9 [11]
10
0.6 ± 0.2
5.8 ± 0.7
0.9 ± 0.2
1.2 ± 0.2
3.1 ± 0.3
54.7 ± 8.0
45.7 ± 5.0
41.5 ± 0.8
12.9 ± 2.4
0.5 ± 0.003
3.6 ± 1.0
4.2 ± 0.8
0.7 ± 0.1
11.8 ± 2.7
2.4 ± 0.7
2.6 ± 0.5
6.7 ± 1.3
13.0 ± 1.4
13.4 ± 1.1
6.6 ± 0.7
9.9 ± 1.6
7.0 ± 2.2
10.6 ± 1.5
10.2 ± 3.2
5.4 ± 1.1
0.01 ± 0.01
4.3 ± 0.5
6.9 ±1.8
11
12
2.2 ± 0.1
1.6 ± 0.1
10.5 ± 0.1
353.2 ± 4.0
>292.2
13 [11]
14
15
16
17
>365.9
18
34.0 ± 1.5
5.2 ± 1.3
8.6 ± 1.3
9.4 ± 2.2
7.4 ± 0.8
65.6 ± 9.7
31.3 ± 1.4
9.9 ± 1.6
>236.2
19
20
21
22
23
24
25
26
27
45.6 ± 3.2
87.9 ± 2.2
22.1 ± 4.0
31.8 ± 1.3
21.8 ± 2.7
34.8 ± 1.2
27.6 ± 6.7
22.5 ± 1.6
21.7 ± 8.7
0.02 ± 0.01
28
6.5
3.3
3.2
3.1
3.4
2.7
4.2
2170
29
30
31
32
33
34
Melarsoprol d
Podophyllotoxin e
a
b
Average of three independent assays. Selectivity Index (SI): IC50 against L6 cells divided by IC50 against
STIB 900 strain. c tested once. d positive control for STIB 900 assay. e positive control for cytotoxicity assay.
The antitrypanosomal activity of the semi-synthetic dimethylamino derivative 19 (IC50 0.5 µM) was
moderately higher than that of the parent compound 1 (0.3 µM). Compound 21, a diethylamine
derivative of 16, was markedly more active than its parent compound (IC50 4.2 µM for 21, compared to
46 µM for 16). The morpholino STL derivatives 22–25 exhibited fairly wide variations in activity. The

Molecules 2014, 19
3527
adduct 22 (IC50 0.7 µM) was as potent as starting methylene compound 10 (IC50 0.7 µM), with slightly
increased selectivity (SIs of 10.3 and 7.6, respectively). Compounds 23 and 24 showed low
cytotoxicity (IC50s 65.6 µM and 31.3 µM, respectively), but 24 had much higher antitrypanosomal
activity (IC50 2.4 µM) than 23 (IC50 11.8 μM). Compound 25 had a similar (IC50 2.6 µM) activity
against T. b. rhodesiense as 24.
The STL tyramine adducts 26–30 showed low cytotoxicities (IC50s 22.1 µM to > 236 µM), and 29
had the highest antitrypanosomal activity (IC50 6.6 µM) of the Michael adducts tested. The 1-(2-
chlorophenyl)piperazinyl STL 31 and the 2-(4-chlorophenyl)ethylamino STLs 32-34 all showed low
antitrypanosomal activity (IC50s > 5 µM) and modest cytotoxicity (IC50s > 20 µM).
We recently reported in vivo antitrypanosomal effects of 1 [7,8]. Upon intraperitoneal administration,
the parasitemia was decreased over several days, but the compound was not able to cure the mice when
they were treated with 10 mg/kg/b.i.d. for four consecutive days. In an attempt to improve the
bioavailability, the exocyclic double bond in the lactone ring was masked to obtain water soluble
dimethylamino derivative 19. Compounds 1 and 19 were orally administered in the acute sleeping
sickness mouse model. Four mice, each treated with 50 mg/kg body weight/day of 1, showed reduced
parasitemia on day 7 after infection. However, the animals were euthanized on day 10 post infection
due to obvious signs of cytotoxicity of the compound. Mice treated with compound 19 exhibited less
signs of toxicity. However, the compound showed no in vivo efficacy, since the mean survival time
was the same as for the control (Table 2).
Table 2. Activity of compound 1 and 19 in the STIB 900 mouse model of trypanosomiasis.
Compound RA a dose (mg/kg) survival (days) b
1
po
po
po
4 × 50
4 × 50
4 × 25
9.5
10
19
8.5
a RA, route of administration: per oral (po). b Average days of survival of
all mice; untreated controls euthanized at day 10 post infection.
Discussion
This structure-activity relationship (SAR) study showed the STL 2-(hydroxymethyl)acrylates 1, 2,
and 4 along with the STL 3,4-dihydroxy-2-methylenebutylate 3 are the most active and selective STLs
against T. b. rhodesiense. These compounds have two active α,β-unsaturated enoate moieties in
common, one on the lactone ring and the other on the side chain. Compound 10 has no side chain with
an enoate moiety, but does possess a cyclopentenone group, which can serve as the additional reactive
enone. In fact, vernodalin (4), which has a third reactive α,β-unsaturated enoate group, had slightly
higher potency (along with greater toxicity) than 1. STLs lacking a reactive α,β-enoate function in their
side chains (12, 13, and 14) or with no side chain (5, 6) showed weaker antitrypanosomal and
cytotoxicity effects compared to their analogues (1, 2, and 3). The results are in accordance with
findings by others [16–18]. Schmidt et al. showed in a SAR study using 40 STLs that bifunctionality
as Michael acceptors is very important for a high level of antitrypanosomal activity but that very
similar structural features determine both antiprotozoal and cytotoxic activity [14]. This was recently
confirmed by the same authors with a larger data set of over 70 STLs [17]. Many bioactivities in STLs

Molecules 2014, 19
3528
have been attributed to a Michael addition of the methylene-γ-lactone moiety to biological thiols [19].
Recent findings on the adduct formation of the two α,β-unsaturated nucleophilic enoate groups at C13
and C3' in 1 with trypanothione and glutathione in trypanosomes corroborated the long presumed
mode of action of STLs, in addition to an inhibition of ornithine decarboxylase [8]. The same mode of
action can be expected for 2, 3, and 4. Regarding the 14 semisynthetic STL amines tested here, it was
observed that the addition of morpholino and dimethylamino groups maintained or even enhanced the
in vitro activity compared to their parent structures, whereas tyramino-, 2-(4-chlorophenyl)ethylamino-
and 1-(2-chlorophenyl)piperazyl derivatives were generally two to four fold more active than their
parent compounds having no enoate moiety, albeit with the disadvantage of higher toxicity (SI in the
range 3–7, generally).
Compared to 1, the toxicity and antitrypanosomal activity of 19 in the T. brucei rhodesiense acute
mouse model after oral application was poorer. Since the amino derivative 19 –in spite of a reasonably
high level of in vitro activity- did not show any in vivo efficacy, it will have to be investigated in
further studies whether other types of derivatives could be useful prodrugs of STLs for the p.o.
treatment of HAT.
3. Experimental
3.1. Test Compounds
Cynaropicrin (1) was isolated from artichoke leaves as previously reported [7]. Compound 5 was
prepared by mild alkaline hydrolysis of 1 as described by Zimmermann et al. [7]. Zaluzanin D (9) and
dehydrocostuslactone (6) were isolated from Saussurea costus as referenced [11]. Compound 10 [20],
the precursors for synthesis of compounds 23‒31, and as well as the synthesis of 16 [20,21] were
performed according to literature methods. Vernodalin (4) was provided from Prof. Hajime Ohigashi,
Kyoto University, Japan. Psilostachyin A (11) was kindly supplied by Dr. Wolfgang Schühly,
University of Graz, Austria. Onopordopicrin (2) was isolated from Arctium nemorosum [12]. Nobilin (14)
was kindly supplied by Prof. Imanidis from the University Applied Sciences and Arts Northwestern
Switzerland. Compound 12 was from Prof. Merfort, University of Freiburg, Germany. Cnicin (3) was
isolated from Cnidus benedictus L [22]. Eupatoriopicrin (13), costunolide (7), and parthenolide (8)
were isolated from Saussurea costus [11]. Santonin (17) was purchased from Fluka Chemie (Buchs,
Switzerland, >98% purity).
3.2. General Experimental Information
NMR spectra were run on a 400 MHz Varian INOVA instrument. Samples were referenced against
13
1
chloroform at 77.00 ppm for C and against tetramethylsilane at 0.00 ppm for H. High resolution
mass spectra were recorded on a Waters SYNAPT G1 HDMS mass spectrometer operated in
electrospray mode. Leucine enkephalin (50 pg/mL) was used as reference calibrant to obtain typical
mass accuracies between 1 and 3 mDa. Melting points were determined using a Mettler FP62 capillary
melting point apparatus and are uncorrected. All reagents were of reagent grade purchased from
Sigma-Aldrich (Schnelldorf, Germany) and were used without any further purification. Solvents used for
chromatography or extractions were distilled prior to use. Thin-layer chromatography was carried out

Molecules 2014, 19
3529
using pre-coated aluminum-backed plates (Merck Silica Gel 60 F254). Column chromatography was
performed on Fluka silica gel 60 (70–230 mesh). Dry solvents were purified as described by Perrin and
Armarego [23]. All starting materials were obtained commercially and used without further purification.
3.3. Syntheses and Spectral Data of Analogues 15, 21–34
3-Hydroxyisophotosantonin (15). A solution of O-acetylisophotosantonin (1.475 g, 4.813 mmol) in
MeOH (49 mL) at 0 °C was treated with sodium borohydride (0.293 g, 7.750 mmol) carefully. The
reaction was left at 0 °C for 3 h, then left to warm to room temperature overnight. The mixture was
extracted from saturated aqueous NH4Cl (50 mL) with ethyl acetate (3 × 50 mL), the extracts pooled
and dried (MgSO4). The dried filtrate was concentrated to a tacky white foam, then dissolved in
absolute ethanol (16 mL). 5% Aqueous KOH (150 mL) was added and the mixture stirred for 18 h at
room temperature. The mixture was acidified to pH < 2 with 18% aqueous HCl, stirred for 30 min,
extracted with ethyl acetate (3 × 50 mL) and washed with saturated aqueous K2CO3. Concentration
yielded a yellow solid, which was recrystallized (EtOAc/hexane) to a white amorphous powder (0.313 g,
36%). NMR showed an approximately 2.2:1 mixture of secondary alcohols had been isolated. Major
isomer: 1H-NMR (400 MHz, CDCl3 + CD3OD): δ 4.73 (1H, d, J = 11.0 Hz, H-6), 4.49 (1H, t, J = 6.8 Hz,
H-3), 2.90 (1H, ~ br td, J = 7.5 and 1.9 Hz, H-1), 2.45 (1H, dt, J = 13.8 and 8.0 Hz, H-2a),
2.34–2.12 (2H, m, H-9a and H-11), 2.03–1.91 (2H, m, H-7 and H-9b), 1.89 (3H, s, C-10 Me), 1.65
(1H, dd, J = 16.0 and 2.3 Hz, H-8a), 1.61 (1H, td, J = 13.7 and 6.7 Hz, H-2b), 1.46–1.30 (1H, m, H-
8b), 1.22 (3H, d, J = 6.9 Hz, C-11 Me), 1.03 (3H, s, C-4 Me); 13C-NMR (101MHz, CDCl3 + CD3OD):
δ 178.82 (C, C-12), 143.96 (C, C-14), 131.28 (C, C-5), 82.04 (CH, C-6), 76.97 (C, C-10), 74.40 (CH,
C-3), 54.31 (CH, C-1), 48.92 (CH, C-7), 44.87 (CH2, C-9), 41.34 (CH, C-11), 34.36 (CH2, C-2), 25.41
(CH2, C-8), 20.88 (CH3, C-4 Me), 13.23 (CH3, C-11 Me), 12.23 (CH3, C-10 Me); minor isomer:
1H-NMR (400MHz, CDCl3 + CD3OD): δ 4.64 (1H, d, J = 11.0 Hz, H-6), 4.54 (1H, d, J = 7.1 Hz, H-3),
1.92 (3H, s, C-10 Me), 1.22 (3H, d, J = 6.9 Hz, C-11 Me), 0.91 (3H, s, C-4 Me); 13C-NMR (101 MHz,
CDCl3 + CD3OD): δ 178.71 (C, C-12), 143.79 (C, C-4), 133.32 (C, C-5), 81.71 (CH, C-6), 79.59 (C,
C-10), 74.23 (CH, C-3), 55.57 (CH, C-1), 48.96 (CH, C-7), 44.27 (CH2, C-9), 41.51 (CH, C-11), 34.81
(CH2, C-2), 25.26 (CH2, C-8), 20.56 (CH3, C-4 Me), 13.23 (CH3, C-11 Me), 12.20 (CH3, C-10 Me);
HRMS (ESI) calculated for C15H21O3 249.1491; found 249.1423 (MH+–H2O); and calculated for
C15H21O4 265.1440; found 265.1392 (MH+–H2).
Cynaropicrin dimethylamine adduct hydrochloride 19. To a cold solution of 1 (0.50 g; 1.44 mmol) in
absolute EtOH (15 mL), dimethylamine, (0.72 mL, 2.0 M solution in MeOH) was added under argon
atmosphere. The solution was stirred at 5 °C for 5 h, then, after concentration of the solvent under
reduced pressure, the crude compound was recrystallized from acetone/Et2O. The amino adduct (0.222 g;
0.566 mmol) was then dissolved in MeOH (5 mL) and a solution of HCl (0.45 mL; 1.25 N solution in
MeOH) was added dropwise. After evaporation of the solvent compound 19 was recovered as a brown
1
solid (0.242 g; 40%). H-NMR (500 MHz, CD3OD): δ 6.28 (1H, br s, H-4'a), 5.97 (1H, br s, H-4'b),
5.35 (1H, br s, H-15a), 5.33 (1H, br s, H-15b), 5.15 (2H, m, H-8, H-14a), 5.00 (1H, br s, H-14b), 4.50
(1H, dddd, J = 9.0, 8.0, 2.2 and 2.2 Hz, H-3), 4.44 (1H, m, H-6), 4.30 (2H, s, H2-3'), 3.62 (1H, m,
H-13a), 3.50–3.42 (2H, m, H-11, H-13b), 3.03–2.91 (8H, m, H-1, H-5, NH(CH3)2), 2.83 (1H, dd,

Molecules 2014, 19
3530
J = 13.4 and 5.0 Hz, H-9a), 2.72 (1H, m, H-7), 2.33 (1H, dd, J = 13.4 and 7.0 Hz, H-9b), 2.24 (1H, m,
13
H-2a), 1.75 (1H, m, H-2b); C-NMR (125 MHz, CD3OD): δ 177.55 (C, C-12), 166.72 (C, C-1'),
154.17 (C, C-4), 143.95 (C, C-10), 141.84 (C, C-2'), 127.82 (CH2, C-4'), 117.58 (CH2, C-14), 111.28
(CH2, C-15), 81.77 (CH, C-6), 77.26 (CH, C-8), 73.82 (CH, C-3), 61.98 (CH2, C-3'), 58.34 (CH2,
C-13), 50.74 (CH, C-5), 49.85 (CH, C-7), 44.98 (CH, C-1), 44.77 (CH3, N(CH3)2), 42.02 (CH, C-11),
40.54 (CH, C-9), 39.51 (CH2, C-2).HRMS (ESI) calculated for C21H30NO6 [M+H]+, 392.2067;
found 392.2062.
Deacylcynaropicrin dimethylamine adduct 20. To a cold solution of 5 (0.050 g; 0.191 mmol) in
absolute EtOH (5 mL), dimethylamine, (0.1 mL, 2.0 M solution in methanol) was added under argon
atmosphere. The solution was stirred at 5 °C for 5 h and then the mixture was concentrated under
reduced pressure. The crude residue was then purified by column chromatography on silica gel
1
(CH2Cl2/MeOH 9:1) to afford compound 20 as a yellow oil (0.052 g; 88%). H-NMR (500 MHz,
CD3OD): δ 5.32 (1H, br s, H-15a), 5.28 (1H, br s, H-15b), 5.05 (1H, br s, H-14a), 5.00 (1H, br s,
H-14b), 4.48 (1H, dddd, J = 9.0, 8.0, 2.2 and 2.2 Hz, H-3), 4.16 (1H, dd, J = 9.8 and 9.7 Hz, H-6),
3.67 (1H, ddd, J = 9.0, 7.3 and 5.0 Hz, H-8), 3.02–2.80 (3H, m, H-1, H-5, H-11), 2.76 (1H, dd,
J = 12.7 and 2.7, H-13a), 2.68 (1H, m, H-9a), 2.60 (1H, m, H-13b), 2.34 (6H, s, N(CH3)2), 2.26–2.14
13
(3H, m, H-2a, H-7, H-9b), 1.70 (1H, ddd, J = 12.8, 9.7 and 8.8 Hz, H-2b); C-NMR (125 MHz,
CD3OD): δ 177.71 (C, C-12), 154.33 (C, C-4), 145.14 (C, C-10), 116.01 (CH2, C-14), 111.70 (CH2,
C-15), 80.53 (CH, C-6), 74.00 (CH, C-3 and C-8), 60.81 (CH2, C-13), 58.34 (CH, C-7), 50.53 (CH,
C-5), 46.44 (CH, C-1), 44.89 (CH3, N(CH3)2), 44.82 (CH, C-11), 43.08 (CH2, C-9), 39.49 (CH2, C-2).
HRMS (ESI) calculated for C17H26NO4 [M+H]+, 308.1856; found 308.1862.
General Procedure for Preparing Lactone Methylamines: A solution of the appropriate enoate (1 eq.)
in ethanol (0.1M) containing the required volatile amine (2.5 eq.) or non-volatile amine (0.6 eq.) and
triethylamine (1.1–2.5 eq., for the appropriate hydrochloride salt) was heated at 85 °C under
microwave irradiation set at 30 W for 30 min to 1 h, depending on the amine. All were prepared on a
sufficiently small scale that the solutions could simply be concentrated and purified by column
chromatography. The following compounds were produced this way:
Deacylated diethylamine adduct 21. A mixture of 15 and its lumisantonin equivalent (~2:1 mixture,
0.128 g, 0.325 mmol) and diethylamine (68 μL, 0.663 mmol) in ethanol (3.3 mL) was stirred at room
temperature for 18 h, and then concentrated to a brown oil. Column chromatography (10%
ethanol/ethyl acetate as eluent) afforded an orange oil (48.9 mg, 45%); Rf 0.11 (10% ethanol/ethyl
1
acetate); H-NMR (400 MHz, CDCl3) δ 4.76 (1H, br d, J = 9.6), 3.31–3.12 (1H, m), 2.82 (1H, dd,
J = 3.9, 13.8), 2.68 (1H, dd, J = 6.0, 13.7), 2.61–2.48 (4H, m), 2.48–2.31 (5H, m), 2.09 (1H, d,
J = 12.1), 1.97 (1H, dt, J = 3.5, 13.6), 1.82 (3H, br t), 1.79 (1H, td, J = 3.9, 13.4), 1.44–1.28 (1H, m),
13
0.91 (6H, t, J = 7.1), 0.91 (3H, s); C-NMR (101 MHz, CDCl3) δ 208.14, 176.47, 162.00, 161.98,
142.69, 81.45, 74.35, 52.04, 50.40, 47.18, 45.76, 45.17, 44.97, 37.15, 26.11, 21.18, 11.63, 9.41;
HRMS (ESI) calculated C19H30NO4 336.2175, found 336.2135 (MH+).
Morpholine adduct 23. α-Methylenesantonin (51.7 mg, 0.213 mmol), morpholine (46.5 μL, 0.534 mmol)
and ethanol (2 mL) afforded, after column chromatography (2%–4% methanol/chloroform as eluent), a

Molecules 2014, 19
3531
yellow solid (45.7 mg, 65%); Rf 0.24 (4% methanol/chloroform). Recrystallisation yielded orange
needles, mp. 165–167 °C (ethyl acetate/hexane); 1H-NMR (400 MHz, CDCl3) δ 6.71 (1H, d, J = 9.9),
6.26 (1H, d, J = 9.9), 4.82 (1H, dd, J = 1.3, 11.5), 3.89–3.46 (4H, m), 2.95–2.81 (1H, m), 2.71–2.57
(2H, m), 2.57–2.47 (2H, m), 2.47–2.35 (2H, m), 2.34–2.25 (1H, m), 2.12 (3H, d, J = 1.2), 2.05 (1H,
qd, J = 3.5, 11.6), 1.89 (1H, ddd, J = 2.2, 3.6, 13.4), 1.74 (1H, ddd, J = 3.8, 12.9, 25.1), 1.55 (1H, td,
13
J = 4.5, 13.2), 1.33 (3H, s); C-NMR (101 MHz, CDCl3) δ 186.22, 176.14, 154.93, 150.92, 128.52,
125.73, 81.35, 66.73, 57.70, 53.72, 51.82, 43.46, 41.12, 37.89, 25.00, 23.75, 10.80; HRMS (ESI)
calculated C19H26NO4 332.1862, found 332.1835 (MH+). The resultant dienone (0.434 g, 1.334 mmol),
5% Pd-C (0.470 g), 32% hydrochloric acid (0.5 mL) and ethanol (10 mL) afforded, after column
chromatography (30%–50% acetone/hexane as eluent), an orange foam (0.209 g, 48%); Rf 0.68 (20%
1
ethanol/ethyl acetate); H-NMR (400 MHz, CDCl3) δ 3.91 (1H, t, J = 10.6), 3.76–3.60 (4H, m), 2.82
(1H, dd, J = 4.3, 12.7), 2.65–2.44 (6H, m), 2.44–2.32 (3H, m), 2.19–2.08 (2H, m), 1.92–1.53 (5H, m),
1.42–1.28 (1H, m), 1.25 (3H, d, J = 6.6), 1.18 (3H, s); 13C-NMR (101MHz, CDCl3) δ 211.44, 177.55,
83.11, 66.85, 57.72, 53.88, 53.47, 51.11, 44.93, 43.36, 40.65, 40.28, 37.29, 36.32, 23.77, 18.39, 13.91;
HRMS (ESI) calculated C19H29NaNO4 358.1994, found 358.2048 (M++Na+) and calculated C19H30NO4
336.2175, found 336.2152 (MH+).
Morpholine adduct 24. The appropriate enoate [20,21] (53.8 mg, 0.218 mmol), morpholine (17.7 μL,
0.203 mmol) and ethanol (2 mL) were mixed at 0 °C, then left to warm to room temperature for 72 h.
The mixture was concentrated to afforded, after column chromatography (30% acetone/hexane as
1
eluent), a pale yellow oil (66.0 mg, 985%); Rf 0.25 (30% acetone/hexane); H-NMR (400 MHz,
CDCl3) δ 6.65 (1H, d, J = 9.9), 5.83 (1H, d, J = 9.9), 3.94 (1H, t, J = 10.7), 3.73–3.46 (4H, m), 2.76
(1H, dd, J = 3.6, 12.1), 2.62–2.39 (4H, m), 2.39–2.26 (2H, m), 2.14 (1H, dt, J = 5.7, 8.6), 2.13–2.05
(1H, m), 1.97–1.88 (1H, m), 1.80 (1H, td, J = 5.8, 11.5), 1.70–1.46 (3H, m), 1.29 (3H, d, J = 6.9), 1.11
13
(3H, s); C-NMR (101 MHz, CDCl3) δ 200.54, 177.32, 158.13, 126.55, 81.77, 66.70, 57.61, 53.77,
51.62, 51.08, 43.14, 42.09, 38.14, 37.45, 23.38, 19.18, 14.53; HRMS (ESI) calculated C19H28NO4
334.2018, found 334.1974 (MH+).
Tyramine adduct 26. The appropriate enoate [20,21] (49.7 mg, 0.202 mmol), tyramine (27.9 mg,
0.203 mmol) and ethanol (2 mL) were mixed at 0 °C, then left to warm to room temperature for 72 h.
The mixture was concentrated to afforded, after column chromatography (70% acetone/hexane as
1
eluent), a beige foam (65.5 mg, 85%); Rf 0.40 (70% acetone/hexane); H-NMR (400 MHz, CDCl3) δ
6.95 (2H, d, J = 8.4), 6.65 (2H, d, J = 8.4), 6.60 (1H, d, J = 9.9), 5.81 (1H, d, J = 9.9), 4.93 (1H, s),
3.91 (1H, t, J = 10.5), 2.91–2.72 (4H, m), 2.67 (2H, t, J = 7.0), 2.55–2.40 (2H, m), 1.91–1.69 (3H, m),
13
1.67–1.57 (1H, m), 1.57–1.36 (2H, m), 1.24 (3H, d, J = 6.8), 1.06 (3H, s); C-NMR (101 MHz,
CDCl3) δ 200.76, 177.96, 158.26, 155.00, 130.33, 129.72, 126.54, 115.65, 82.15, 51.55, 51.47, 48.88,
47.26, 45.29, 42.07, 38.26, 37.22, 34.73, 29.18, 22.75, 19.16, 14.49; HRMS (ESI) calculated
C23H30NO4 384.2175, found 384.2130 (MH+).
Tyramine adduct 27. Adduct 28 (0.355 g, 0.945 mmol), 5% Pd-C (0.266 g), 32% hydrochloric acid
(0.5 mL) and ethanol (10 mL) afforded, after column chromatography (30%–50% acetone/hexane as
eluent), a pale orange foam (0.144 g, 40%); Rf 0.44 (20% ethanol/ethyl acetate); 1H-NMR (400 MHz,

Molecules 2014, 19
3532
CDCl3) δ 7.03 (2H, d, J = 8.1), 6.72 (2H, d, J = 8.3), 3.97 (2H, br s), 3.91 (1H, t, J = 10.4), 3.66 (1H,
td, J = 0.7, 6.6), 3.03–2.80 (4H, m), 2.74 (2H, t, J = 6.9), 2.58–2.37 (3H, m), 1.86–1.69 (3H, m),
13
1.69–1.46 (3H, m), 1.33–1.23 (2H, m), 1.21 (3H, d, J = 6.5), 1.15 (3H, s); C-NMR (101 MHz,
CDCl3) δ 211.56, 178.11, 154.76, 130.65, 129.75, 115.57, 83.44, 53.37, 51.48, 48.84, 47.26, 45.41,
44.85, 40.62, 39.98, 37.32, 36.39, 34.79, 23.07, 18.34, 13.81; HRMS (ESI) calculated C23H31NaNO4
408.2151, found 408.2169 (M++Na+) and calculated C23H32NO4 386.2331, found 386.2299 (MH+).
Tyramine adduct 28. α-Methylenesantonin (0.220 g, 0.910 mmol), tyramine (77.1 mg, 0.560 mmol)
and ethanol (2 mL) afforded, after column chromatography (10%–20% ethanol/ethyl acetate as eluent),
1
a yellow foam (89.7 mg, 44%); Rf 0.26 (20% ethanol/ethyl acetate); H-NMR (400 MHz, CDCl3) δ
7.00 (2H, d, J = 8.5), 6.74 (2H, d, J = 8.5), 6.69 (1H, d, J = 9.9), 6.24 (1H, d, J = 9.9), 4.78 (1H, dd,
J = 1.1, 11.4), 4.72 (2H, br s), 2.98–2.88 (2H, m), 2.88–2.80 (2H, m), 2.72 (2H, t, J = 7.0), 2.63 (1H,
dt, J = 6.0, 12.2), 2.08 (3H, d, J = 0.9), 1.98 (2H, ddd, J = 7.0, 15.9, 31.8), 1.88–1.76 (1H, m), 1.66
13
(1H, qd, J = 3.4, 12.8), 1.40 (1H, td, J = 4.2, 13.1), 1.27 (3H, s); C-NMR (101 MHz, CDCl3) δ
186.57, 176.76, 155.42, 155.07, 151.32, 130.17, 129.60, 128.39, 125.49, 115.52, 81.52, 58.08, 51.30,
49.55, 47.17, 45.61, 41.22, 37.51, 34.73, 24.86, 22.92, 18.20, 10.81; HRMS (ESI) calculated
C23H28NO4 382.2018, found 382.1970 (MH+).
1-(2-Chlorophenyl)piperazine adduct 31. α-Methylenesantonin (49.0 mg, 0.202 mmol), 1-(2-
chlorophenyl)piperazine (0.120 g, 0.516 mmol) and ethanol (2 mL) afforded, after column
chromatography (2%–4% methanol/chloroform as eluent), a beige solid (65.3 mg, 73%); Rf 0.41 (4%
methanol/chloroform). Recrystallisation yielded a white powder, mp >190 °C (ethyl acetate/hexane);
1H-NMR (400 MHz, CDCl3) δ 7.35 (1H, dd, J = 1.2, 7.9), 7.27–7.15 (1H, m), 7.06–7.01 (1H, m),
7.01–6.92 (1H, m), 6.71 (1H, d, J = 9.9), 6.26 (1H, d, J = 9.9), 4.83 (1H, d, J = 11.4), 2.99 (4H, s),
2.95 (1H, t, J = 8.4), 2.81–2.64 (4H, m), 2.60 (2H, d, J = 5.5), 2.33 (1H, d, J = 12.8), 2.14 (3H, s),
2.05 (1H, ddd, J = 4.2, 7.6, 17.3), 1.89 (1H, d, J = 13.4), 1.76 (1H, ddd, J = 3.7, 12.8, 25.3), 1.56 (1H,
td, J = 4.3, 13.1), 1.34 (3H, s); 13C-NMR (101 MHz, CDCl3) δ 186.24, 176.26, 154.97, 151.03, 148.93,
130.53, 128.58, 128.49, 127.46, 125.72, 123.65, 120.19, 81.36, 57.26, 53.40, 51.87, 51.00, 43.68,
41.14, 37.92, 25.00, 23.77, 10.82; HRMS (ESI) calculated C25H29ClN2O3Na 463.1764, found
463.1759 (M++Na+), and calculated C25H30ClN2O3 441.1945, found 441.1870 (MH+).
4-Chlorobenzylamine adduct 32. α-Methylenesantonin (0.218 g, 0.902 mmol), 4-chlorobenzylamine
(72.0 μL, 0.589 mmol) and ethanol (2 mL) afforded, after column chromatography (10%–20%
ethanol/ethyl acetate as eluent), a yellow oil (0.156 g, 69%); Rf 0.52 (20% ethanol/ethyl acetate);
1H-NMR (400 MHz, CDCl3) δH 7.28 (2H, d, J = 8.7), 7.24 (2H, d, J = 8.7), 6.71 (1H, d, J = 9.9), 6.24
(1H, d, J = 9.9), 4.83 (1H, dd, J = 1.4, 11.5), 3.79 (1H, d, J = 13.6), 3.74 (1H, d, J = 13.6), 2.94 (1H,
dd, J = 4.9, 12.3), 2.82 (1H, dd, J = 6.1, 12.3), 2.60 (1H, ddd, J = 5.0, 6.0, 12.2), 2.17 (1H, dd,
J = 3.5, 12.1), 2.14–2.06 (1H, m), 2.12 (3H, d, J = 1.3), 2.02–1.93 (1H, m), 1.88 (1H, ddd, J = 2.2,
13
3.6, 13.4), 1.70 (1H, ddd, J = 3.8, 12.9, 25.4), 1.48 (1H, td, J = 4.5, 13.2), 1.32 (3H, s); C-NMR
(101 MHz, CDCl3) δ 186.15, 176.47, 154.92, 150.91, 138.22, 132.46, 129.23, 128.39, 128.31, 125.59,
81.41, 53.00, 49.16, 46.32, 46.09, 41.10, 37.58, 24.93, 23.02, 10.79; HRMS (ESI) calculated
C22H25ClNO3 386.1523, found 386.1474 (MH+).

Molecules 2014, 19
3533
General Procedure Used for the Conjugate Addition of Amines to Unsaturated Isophotosantonin
Derivatives: Solutions of the enoate in absolute ethanol were dosed into 8 mL ChemSpeed reaction
vessels, warmed to 30 °C and then treated with the appropriate amine in ethanol. The mixtures were
agitated at 600 rpm for 18 h, concentrated to gums and purified by column chromatography. In this
fashion the following were prepared:
Morpholine adducts 22 and 25. A mixture of 15 and its lumisantonin equivalent (~2:1 mixture,
0.100 g, 0.331 mmol), morpholine (57.3 μL, 0.657 mmol) and ethanol (5 mL) were treated as per the
general procedure. The resultant orange gum afforded, after column chromatography (50% ethyl
1
acetate/hexane – ethyl acetate as eluent), 22 (50.8mg, 39%); Rf 0.45 (ethyl acetate); H-NMR
(400 MHz, CDCl3) δ 4.77 (1H, d, J = 10.5), 4.12 (1H, dq, J = 2.2, 6.3), 3.72–3.51 (5H, m), 2.79 (1H,
dd, J = 4.1, 13.3), 2.68–2.59 (1H, m), 2.56 (1H, dd, J = 4.5, 13.6), 2.52–2.29 (10H, m), 2.09 (1H, dt,
J = 3.6, 13.6), 1.94 (3H, s), 1.83 (3H, dd, J = 1.6, 2.2), 1.41 (1H, tdd, J = 3.4, 10.8, 14.0), 1.01 (3H, s);
13C-NMR (101 MHz, CDCl3) δ 206.91, 175.75, 170.33, 160.68, 143.13, 85.51, 81.19, 66.61, 57.11,
53.97, 47.13, 45.81, 43.80, 37.89, 36.70, 25.41, 22.23, 19.97, 9.45; HRMS (ESI) calculated C21H30NO6
392.2073, found 392.2047 (MH+). Also isolated was 25 slightly contaminated with the former product,
as an orange gum (34.4mg, 32%); Rf 0.33 (ethyl acetate). An analytical sample was purified by
1
preparative TLC (ethyl acetate): H-NMR (400MHz, CDCl3) δ 6.70 (1H, d, J = 9.9), 6.27 (1H, d,
J = 9.9), 4.80 (1H, dq, J = 1.3, 11.5), 3.80–3.50 (4H, m), 2.98–2.75 (1H, m), 2.70–2.57 (2H, m),
2.57–2.48 (2H, m), 2.48–2.36 (2H, m), 2.36–2.25 (1H, m), 2.13 (3H, d, J = 1.4), 2.05 (1H, qd,
J = 3.5, 11.7), 1.88 (1H, ddd, J = 2.2, 3.6, 13.4), 1.72 (1H, ddd, J = 3.8, 12.9, 25.0), 1.55 (1H, td,
13
J = 4.5, 13.2), 1.33 (3H, s); C-NMR (101 MHz, CDCl3) δ 186.29, 186.28, 176.15, 154.88, 150.82,
128.75, 125.89, 81.45, 66.82, 57.79, 53.82, 51.90, 43.60, 41.17, 37.99, 25.10, 23.88, 10.88; HRMS
(ESI) calculated C19H26NO4 332.1862, found 332.1836 (MH+).
Tyramine adducts 29 and 30. A mixture of 15 and its lumisantonin equivalent (~2:1 mixture, 0.101 g,
0.331 mmol), tyramine (90.2 mg, 0.657 mmol) and ethanol (5 mL) were treated as per the general
procedure. The resultant brown gum afforded, after column chromatography (50% ethyl
1
acetate:hexane – ethyl acetate as eluent), 29 (60.3 mg, 41.3%); Rf 0.25 (ethyl acetate); H-NMR
(400 MHz, CDCl3) δ 7.13–6.98 (2H, m), 6.84–6.68 (2H, m), 4.98 (1H, d, J = 10.7), 4.16 (1H, br m),
3.00–2.80 (4H, m), 2.76 (2H, d, J = 6.7), 2.65–2.46 (4H, m), 2.46–2.37 (1H, m), 2.18 (1H, dd, J = 3.4,
13.5), 2.09 (1H, s), 2.03 (3H, s), 1.89 (3H, d, J = 1.5), 1.53 (1H, ddd, J = 3.2, 10.5, 14.3), 1.37–1.19
(1H, m), 1.11 (3H, s); 13C-NMR (101 MHz, CD3OD) δ 208.56, 177.44, 171.36, 162.40, 155.73,
143.28, 130.61, 130.15, 130.03, 116.02, 115.80, 86.24, 82.10, 51.93, 47.90, 47.30, 46.40, 44.54, 38.21,
37.29, 35.31, 25.52, 22.54, 20.16, 9.64; HRMS (ESI) calculated C25H32NO6 442.2230, found 442.2229
(MH+). Also isolated was 30 slightly contaminated with the former product, as an orange gum
(21.9 mg, 17.4%); Rf 0.14 (ethyl acetate). An analytical sample was purified by preparative TLC (ethyl
1
acetate): H-NMR (400 MHz, CD3OD) δH 7.04 (2H, d, J = 8.5), 6.73 (2H, d, J = 8.5), 6.69 (1H, d,
J = 9.9), 6.26 (1H, d, J = 9.9), 4.79 (1H, dd, J = 1.4, 11.4), 2.99 (1H, dd, J = 5.0, 12.4), 2.84 (4H, m),
2.72 (2H, t, J = 6.8), 2.63–2.54 (1H, m), 2.11 (3H, d, J = 1.3), 2.10–2.03 (1H, m), 2.03–1.94 (2H, m),
1.88 (1H, ddd, J = 2.1, 3.7, 13.4), 1.74 (1H, ddd, J = 3.9, 13.1, 25.8), 1.50 (1H, td, J = 4.1, 13.1), 1.33
13
(3H, s); C-NMR (101 MHz, CD3OD) δ 186.43, 176.61, 154.93, 154.15, 150.86, 131.40, 129.73,

Molecules 2014, 19
3534
128.72, 125.84, 115.34, 81.57, 51.51, 49.41, 47.11, 46.15, 41.20, 37.76, 35.09, 25.04, 23.23, 10.90;
HRMS (ESI) calculated C23H28NO4 382.2018, found 382.1986 (MH+).
2-(4-Chlorophenyl)ethylamine adducts 33 and 34. A mixture of 15 and its lumisantonin equivalent
(~2:1 mixture, 0.114 g, 0.376 mmol), 2-(4-chlorophenyl)ethylamine (91.4 μL, 0.657 mmol) and
ethanol (5 mL) were treated as per the general procedure. The resultant orange gum afforded, after
column chromatography (50% ethyl acetate/hexane – ethyl acetate as eluent), 33 (60.8 mg, 35%); Rf
0.27 (ethyl acetate); 1H-NMR (400 MHz, CDCl3) δ H 7.19 (2H, d, J = 8.4), 7.07 (2H, d, J = 8.5), 4.76
(1H, d, J = 10.5), 4.10–4.04 (1H, m), 2.93 (1H, dd, J = 3.9, 12.4), 2.87–2.72 (3H, m), 2.69 (2H, t,
J = 6.9), 2.55–2.36 (4H, m), 2.36–2.27 (1H, m), 2.11–1.98 (2H, m), 1.94 (3H, s), 1.81 (3H, dd,
J = 1.6, 2.1), 1.37 (1H, tdd, J = 3.4, 10.7, 14.1), 1.00 (3H, s); 13C-NMR (101 MHz, CDCl3) δ 206.90,
176.18, 170.23, 160.70, 143.02, 138.14, 131.82, 129.98, 128.44, 85.40, 81.46, 51.29, 47.15, 46.62,
46.50, 43.48, 37.71, 36.71, 35.48, 25.29, 22.21, 19.89, 9.41; HRMS (ESI) calculated C25H31ClNO5
460.1891, found 460.1866 (MH+). Also isolated was 34 slightly contaminated with the former product,
as an orange gum (28.6mg, 19.0%); Rf 0.15 (ethyl acetate). An analytical sample was purified by
1
preparative TLC (ethyl acetate): H-NMR (400 MHz, CDCl3) δ 7.25 (2H, d, J = 8.5), 7.13 (2H, d,
J = 8.5), 6.70 (1H, d, J = 9.9), 6.27 (1H, d, J = 9.9), 4.80 (1H, dd, J = 1.4, 11.4), 2.96 (1H, dd,
J = 5.3, 12.3), 2.90 (1H, dd, J = 5.8, 11.9), 2.89–2.80 (3H, m), 2.80–2.72 (2H, m), 2.62–2.52 (1H, m),
2.13 (3H, d, J = 1.3), 2.02 (1H, ddd, J = 3.7, 12.1, 23.8), 2.02–1.94 (1H, m), 1.86 (1H, ddd, J = 2.2,
13
3.7, 13.5), 1.68 (1H, ddd, J = 3.8, 12.9, 25.3), 1.47 (1H, td, J = 4.5, 13.3), 1.32 (3H, s); C-NMR
(101 MHz, CDCl3) δ 186.28, 176.57, 154.83, 150.72, 138.21, 131.91, 130.01, 128.74, 128.50, 125.88,
81.56, 51.28, 49.51, 47.30, 46.35, 41.18, 37.72, 35.63, 25.12, 23.30, 10.93; HRMS (ESI) calculated
C23H27ClNO3 400.1679, found 400.1645 (MH+).
3.4. Sample Preparation for Biological Testing
Compounds were dissolved in DMSO (10 mg/mL) and stored at −20 °C until testing. Fresh
dilutions in medium were prepared for each bioassay. DMSO concentration in the assay did not exceed
1%. All assays were performed in at least three independent experiments. The purity of all compounds
was >95% if not stated otherwise.
3.5. Trypanosoma Brucei Rhodesiense (STIB 900 strain) Bioassay
Evaluation of in vitro antiprotozoal activity against T. b. rhodesiense was done using the Alamar
Blue assay to determine IC50s as previously described [24]. Serial threefold dilution were prepared in
96-well micro titre plates, and 4000 T. b. rhodesiense STIB 900 bloodstream forms in 50 μL
were added to each well except for the negative controls. Melarsoprol (Arsobal®, purity > 95%,
Sanofi-Aventis, Meyrin, Switzerland) was used as reference drugs. After 70 h of incubation 10 μL of
Alamar blue marker (12.5 mg resazurin (Sigma-Aldrich, Buchs, Switzerland) dissolved in 100 mL of
distilled water) was added, and colour change was developed for 2 to 6 h. A Spectramax Gemini XS
micro plate fluorescence reader (Molecular Devices Cooperation, Sunnyvale, CA, USA) with an
excitation wavelength of 536 nm and an emission wavelength of 588 nm was used to read the plates.

Molecules 2014, 19
3535
The IC50 values were calculated from the sigmoidal growth inhibition curves using Softmax Pro
software (Molecular Devices).
3.6. Rat Myoblast Cell L6-Cytotoxicity Assay
The cytotoxicity assay was performed with rat skeletal myoblasts (L6-cells) seeded in 100 μL
RPMI 1640 in 96-well micro titre plates, using the Alamar Blue assay described above. After 24 h the
medium was removed and replaced by 100 μL of fresh RPMI 1640 with serial threefold drug dilution.
Podophyllotoxin (purity > 95%, Sigma-Aldrich) was used as a reference drug. After 70 h of incubation
under a humidified 5% CO2 atmosphere, 10 μL of the Alamar blue marker (see above) was added to all
wells. The plates were incubated for an additional 2 h. A Spectramax Gemini XS micro plate
fluorescence reader (Molecular Devices) was used to read the plates using an excitation wavelength of
536 nm and an emission wavelength of 588 nm. The IC50s were calculated from the sigmoidal growth
inhibition curves using Softmax Pro software (Molecular Devices).
3.7. Acute Mouse Sleeping Sickness Model
This model mimics the first stage of the human African trypanosomiasis. Adult female NMRI mice
were purchased from Janvier (St. Berthevin, France). They weighed between 20 and 25 g at the
beginning of the study and were kept under standard conditions at 22 °C and 60%–70% humidity in
macrolon type III cages with food pellets and water ad libitum. All protocols and procedures used in
this study were reviewed and approved by the local veterinary authorities of the Canton Basel-Stadt,
Switzerland (authorization N 739; 11.12.2009). The samples were first dissolved in 100% DMSO,
followed by addition of distilled H2O to a final DMSO concentration of 10%. For determination of the
in vivo antitrypanosomal activity, mice were infected intraperitoneally with 1 × 104 STIB900 bloodstream
forms. Experimental groups of four mice were treated orally once a day on four consecutive days from
day 3 to day 6 post infection. A control group of four mice was infected, but remained untreated. The
determination of the parasitaemia was done on day 7 post infection. 6 μL of tail blood were diluted in
24 μL sodium citrate (3.2%), whereby the first μL was discarded to obtain circulating blood. Five μL of
this mixture were transferred to a glass slide and covered with an 18 × 18 mm cover slide. The sample
was examined under a light microscope (200-fold magnification) and parasites were counted in 3 of
the 16 squares of the grid.
4. Conclusions
The conclusions are that the α-methylene-γ-lactone is necessary for both antitrypanosomal
effects and cytotoxicity of these sesquiterpenes. Antitrypanosomal selectivity is facilitated by
2-(hydroxyl-methyl)acrylate or 3,4-dihydroxy-2-methylenebutylate side chains, and by the presence of
cyclopentenone rings. Semi-synthetic STL amines with improved activity over the native STLs were
those with morpholino and dimethylamino groups. The dimethylamino analogue of cynaropicrin was
prepared and tested orally in the T. b. rhodesiense acute mouse model, where it showed reduced
toxicity over cynaropicrin, but also reduced antitrypanosomal effects.

Molecules 2014, 19
3536
Acknowledgments
The Swiss National Science Foundation (grant 205320-126888/1) is gratefully acknowledged.
We thank the Freiwillige Akademische Gesellschaft Basel and the Senglet Trust, Switzerland for
additional financial support, and the Basler Naturstofffreunde for their help.
Author Contributions
S.Z. and M.A. were responsible for the conceptualisation of the study, and writing the manuscript.
S.Z. performed the in vitro assays, and isolated compounds. M.K. was responsible for the in vivo tests.
M.D.M performed NMR measurements. M.H. supervised the work and proofread the manuscript. T.U.
and Y.Y. were responsible for conceptualisation and synthesis of materials 9 and 14. G.F. and R.N.
were responsible for the isolation of the natural congener for α-methylenesantonin from plant material,
as well as conceptualising the study leading to the synthesis of materials 10, 15–18, 21–34. C.v.d.W.
was responsible for conceptualisation and synthesis of materials 10, 15–18, 21–34, as well as writing
portions of the experimental section and proofreading. C.J.P. was responsible for conceptualisation and
synthesis of materials 10, 15–18, 21–34.
Conflicts of Interest
The authors declare no conflict of interest.
References
1. Simarro, P.P.; Cecchi, G.; Paone, M.; Franco, J.R.; Diarra, A.; Ruiz, J.A.; Fèvre, E.M.; Courtin, F.;
Mattioli, R.C.; Jannin, J. The atlas of human African trypanosomiasis: A contribution to global
mapping of neglected tropical diseases. Int. J. Health Geogr. 2010, 9, 57–75.
2. WHO. Available online: http://www.who.int/mediacentre/factsheets/fs259/en/ (accessed on 3
April 2013).
3. Torreele, E.; Bourdin, T.B.; Tweats, D.; Kaiser, M.; Brun, R.; Mazué, G.; Bray, M.A.; Pécoul, B.
Fexinidazole—A new oral nitroimidazole drug candidate entering clinical development for the
treatment of sleeping sickness. PLoS. Negl. Trop. Dis. 2010, 4, e923.
4. Brun, R.; Blum, J.; Chappuis, F.; Burri, C. Human African Trypanosomiasis. Lancet 2010, 375,
148–159.
5. Schmidt, T.J.; Khalid, S.A.; Romanha, A.J.; Alves, T.M.A.; Biavatti, M.W.; Brun, R.; da Costa, F.B.;
de Castro, S.L.; Ferreira, V.F.; de Lacerda, M.V.G.; et al. The potential of secondary metabolites
from plants as drugs or leads against protozoan neglected diseases – Part I. Curr. Med. Chem.
2012, 19, 2128–2175.
6. Schmidt, T.J.; Khalid, S.A.; Romanha, A.J.; Alves, T.M.A.; Biavatti, M.W.; Brun, R.; da Costa, F.B.;
de Castro, S.L.; Ferreira, V.F.; de Lacerda, M.V.G.; et al. The potential of secondary metabolites
from plants as drugs or leads against protozoan neglected diseases – Part II. Curr. Med. Chem.
2012, 19, 2176–2228.

Molecules 2014, 19
3537
7. Zimmermann, S.; Kaiser, M.; Brun, R.; Hamburger, M.; Adams, M. Cynaropicrin: The first plant
natural product with in vivo activity against Trypanosoma. brucei. Planta Med. 2012, 78,
553–556.
8. Zimmermann, S.; Oufir, M.; Lerouz, A.; Krauth-Siegel, R.L.; Becker, K.; Kaiser, M.; Brun, R.;
Hamburger, M.; Adams, M. Cynaropicrin targets the trypanothione redox system in Trypanosoma
brucei. Bioorg. Med. Chem. 2013, 15, 7202–7209.
9. The plant list. Available online: http://www.theplantlist.org (accessed on 15 February 2013).
10. Buckingham, J.; Hodgons, A.M.; Walford, S.P. The Dictionary of Natural Products 10.2, [CD-
ROM]; Chapman & Hall/CRC: Boca Raton, FA, USA, 2002.
11. Julianti, T.; Hata, Y.; Zimmermann, S.; Kaiser, M.; Hamburger, M.; Adams, M. Antitrypanosomal
sesquiterpene lactones from Saussurea costus. Fitoterapia 2011, 82, 955–959.
12. Zimmermann, S.; Thomi, S.; Kaiser, M.; Hamburger, M.; Adams, M. Screening and HPLC-based
activity profiling for new antiprotozoal leads from European plants. Sci. Pharm. 2012, 80, 205–213.
13. Schmidt, T.J.; Brun, R.; Willuhn, G.; Khalid, S.A. Anti-trypanosomal activity of helenalin and
some structurally related sesquiterpene lactones. Planta Med. 2002, 68, 750–751.
14. Schmidt, T.J.; Nour, A.M.M.; Khalid, S.A.; Kaiser, M.; Brun, R. Quantitative structure-antiprotozoal
activity relationships of sesquiterpene lactones. Molecules 2009, 1, 2062–2076.
15. Schmidt, T.J. Toxic activities of sesquiterpene latones: Structural and biochemical aspects.
Curr. Org. Chem. 1999, 3, 577–608.
16. Woods, J.R; Mo, H.; Bieberich, A.A.; Alavania, T.; Coly, D.A. Amino-derivatives of the
sesquiterpene lacton class of natural products as prodrugs. Med. Chem. Commun. 2013, 4, 27–33.
17. Schmidt, T.J.; da Costa, F.B.; Lopes, N.P.; Kaiser, M.; Brun, R. In silico prediction and
experimental evaluation of furanoheliangolide sesquiterpene lactones as potent agents against
Trypanosoma brucei rhodesiense. Antimicrob. Agents Chemother. 2014, 58, 325–332.
18. Lee, K.H.; Furukawa, H.; Huan, E.S. Antitumor Agents. 11. Synthesis and cytotoxic activity of
epoxides of helenalin related derivatives. J. Med. Chem. 1972, 15, 607–611.
19. Schmidt, T. Helenanolide-type sesquiterpene lactones III. Rates and stereochemistry in the
reaction of helenalin and related helenanolides with sulfhydryl containing biomolecules.
Bioorg. Med. Chem. 1997, 5, 654–653.
20. Arantes, F.F.P.; Barbosa, L.C.A.; Alvarenga, E.S.; Demuner, A.J.; Bezerra, D.P.; Ferreira, J.R.O.;
Costa-Lotufo, L.V.; Pessoa, C.; Moraes, M.O. Synthesis and cytotoxic activity of α-santonin
derivatives. Eur. J. Med. Chem. 2009, 44, 3739–3745.
21. Becker, J.V.W.; van der Merwe, M.M.; van Brummelen, A.C.; Pillay, P.; Crampton, B.G.;
Mmutlane, E.M.; Parkinson, C.; van Heerden, F.R.; Crouch, N.R.; Smith, P.J.; et al. In vitro
anti-plasmodial activity of Dicoma anomala subsp. gerrardii (Asteraceae): Identification of its
main active constituent, structure-activity relationship studies and gene expression profiling.
Malaria J. 2011, 10, 295.
22. Berger, S.; Sicker, D. Classics in Spectroscopy: Isolation and Structure Elucidation of Natural
Products, 1st ed.; Wiley-VCH Verlag GmbH & Co: Weinheim, Germany, 2009; pp. 444–457.
23. Perrin, D.D.; Armarego, W.L.F. Purification of Laboratory Chemicals (3/e); Pergamon Press:
Oxford, UK, 1994.

Molecules 2014, 19
3538
24. Räz, B.; Iten, M.; Grether-Bühler, Y.; Kaminsky, R.; Brun, R. The alamar blue assay to determine
drug sensivity of African trypanosomes (T.b. rhodesiense and T.b. gambiense) in vitro. Acta Trop.
1997, 68, 139–147.
Sample Availability: Samples of the compounds 1–9, 11, 13, 14, 16–18, 21–24, 26–29, 31, 32 and 34
are available from the authors.
© 2014 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article
distributed under the terms and conditions of the Creative Commons Attribution license
(http://creativecommons.org/licenses/by/3.0/).