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Article

Simplexidine, a 4-Alkylpyridinium Alkaloid from the Caribbean Sponge Plakortis simplex

Dipartimento di Chimica delle Sostanze Naturali, Università di Napoli “Federico II”, Via D. Montesano 49, 80131 Napoli, Italy
*
Author to whom correspondence should be addressed.
Received: 25 June 2008 / Accepted: 16 July 2008 / Published: 17 July 2008
(This article belongs to the Special Issue Alkaloids: Novel Therapeutic Perspectives)

Abstract

Chemical analysis of the secondary metabolites of the Caribbean sponge Plakortis simplex, a source of many bioactive compounds, showed the presence of the new metabolite simplexidine (4), belonging to the extremely rare class of 4-alkyl-pyridinium alkaloids. The structural characterization of this molecule, based on spectroscopic methods, is reported.
Keywords: Simplexidin; alkaloids; pyridinium; Plakortis; NMR. Simplexidin; alkaloids; pyridinium; Plakortis; NMR.

Introduction

As part of an ongoing search for biologically active compounds from marine invertebrates, our research group has been devoting considerable efforts to the chemical investigation of the Caribbean sponge Plakortis simplex. This research project, started about ten years ago, has been strongly fostered by the discovery of a large array of structurally unique and biologically active metabolites. This richness of secondary metabolite production has been discussed in a review paper [1] and has been recently correlated to the wide presence of bacterial and fungal symbionts associated to the sponge host cells [2].
For example, P. simplex provided a series of promising lead compounds for drug development, including the immunosuppressive glycolipids plakosides [3] and simplexides [4] and a series of endoperoxide-containing derivatives related to plakortin (1, Figure 1) [5,6], for which a potent antimalarial activity (in the nM range) has been discovered [7].
Structurally unique metabolites were also disclosed as components of the most polar fractions obtained from the organic extracts of P. simplex. Indeed, these fractions showed to contain the first natural betaine derivatives to be characterized by a iodinated indole ring [8,9], e.g. plakohypaphorine E (2, Figure 1), and the unique 4-alkylpyridinium alkaloid simplakidine (3, Figure 1) [10]. Careful examination of the polar fractions of P. simplex has now yielded to the isolation of a new 4-alkyl-pyridinium alkaloid that we have named simplexidine (4, Figure 1) and for which we report herein details about isolation and structural elucidation.
Figure 1. Representative molecules from Plakortis simplex, including the new simplexidine (4).
Figure 1. Representative molecules from Plakortis simplex, including the new simplexidine (4).
Molecules 13 01465 g001

Results and Discussion

A specimen of the sponge Plakortis simplex (Demospongiae, order Homosclerophorida, family Plakinidae) was collected during the summer of 2002 along the coasts of The Bahamas and immediately frozen. After homogenization, the organism was exhaustively extracted, in sequence, with methanol and chloroform. The methanolic layer was partitioned between n-BuOH and water, and, subsequently, the organic phase, combined with the CHCl3 extract, was subjected to chromatography over a reversed phase (RP18) silica column eluted with a solvent gradient from H2O/MeOH 9:1 to MeOH and then to MeOH/CHCl3 9:1. The most polar fractions were preliminarily separated over silica gel (gradient from EtOAc to MeOH) and then re-chromatographed by reverse-phase HPLC (eluent MeOH/H2O 4:6) to finally yield 2.0 mg of pure simplexidine (4).
The molecular formula C15H21NO2 was assigned to simplexidine ([α]D = –5.8) based on mass spectrometry evidence [ESI-MS (negative ions): m/z 246 (M-H)-; ESI-MS (positive ions): m/z 248 (M+H)+, 270 (M+Na)+; HR-FABMS: m/z 248.1647 (M+H)+, calcd. for C15H22NO2 m/z 248.1651].
The 1H-NMR spectrum of simplexidine (Table 1) showed three signals (a singlet at δH 8.81 and two doublets at δH 8.63 and 7.91) in the aromatic region, three methine multiplets (δH 5.48, 5.35, and 3.81) and a methyl singlet (δH 4.34) in the midfield region, and a series of well resolved signals confined in the spectral region ranging from δH 2.50 to 0.80, including two methyl triplets at δH 0.93 and 0.89. The presence of an aromatic chromophore in the structure of simplexidine (4) was further suggested by the UV absorption at λmax 268 nm and by the presence of five signals between δC 127 and 164 in the 13C-NMR spectrum (Table 1).
The 15 carbon signals present in the 13C-NMR spectrum were assigned, with the aid of DEPT experiments, to three methyls, three methylenes, six methines and three unprotonated sp2 type carbons. Among these latter resonances, the signal at δC 168.6 could be ascribed to a carboxylate group, as suggested also by the IR absorption at νmax1642 cm-1. Association of the resonances of the 12 proton-bearing carbons with those of the relevant protons was accomplished through the analysis of a 2D NMR gradient-HSQC spectrum.
Table 1. 1H (500 MHz) and 13C (125 MHz) NMR data of simplexidine (4) in CD3OD.
Table 1. 1H (500 MHz) and 13C (125 MHz) NMR data of simplexidine (4) in CD3OD.
Pos.δH, mult., J in HzδC, mult.Pos.δH, mult., J in Hz δC, mult.
10.93, t, 7.314.5, CH3
21.97, q, 7.325.8, CH22’8.81, s143.1, CH
35.48, dt, 15.4, 7.3136.2, CH3’ 141.9, C
45.35, dt, 15.4, 7.0126.2, CH4’ 163.5, C
52.43, q, 7.038.1, CH25’7.91, d, 6.9127.3, CH
63.81, m43.4, CH6’8.63, d, 6.9143.4, CH
7a1.87, m 27.7, CH27’ 168.6, C
7b1.73, m 8’4.34, s46.7, CH3
80.89, t, 7.512.2, CH3
Inspection of the 1H-1H COSY NMR spectrum of simplexidine (4) allowed us to arrange all the proton multiplets within the two spin systems showed in red in Figure 2. The first fragment includes only the two mutually coupled aromatic doublets at δH 8.63 and 7.91, while the second moiety is an eight-carbon fragment connecting the two methyl triplets (from H3-1 to H3-8) and comprising two coupled sp2 methines (H-3 and H-4) and a single branching at the sp3 methine C-6 (δH 3.81).
Figure 2. 1H-1H COSY and key 2,3JC-H HMBC correlations of simplexidine (4).
Figure 2. 1H-1H COSY and key 2,3JC-H HMBC correlations of simplexidine (4).
Molecules 13 01465 g002
With these data in our hands and taking into account the molecular formula, the assembly of the carbon framework of simplexidine (4) required the elucidation of an aromatic C7H6NO2 subunit, probably linked at C-6 and comprising a carboxylate group. Interpretation of diagnostic gradient-HMBC cross-peaks (Figure 2) was of pivotal importance to resolve this issue and suggested the presence of a disubstituted N-methyl pyridinium ring. This assignment was corroborated by perfect agreement of 1H- and 13C-NMR resonances of this subunit with literature values [10,11].
In particular, the N-methyl singlet at δ 4.34 (H3-8’) showed g-HMBC cross-peaks with two almost overlapped protonated carbons at δC 143.1 (C-2’, H-2’ = δH 8.81, s) and 143.4 (C-6’, H-6’ = δH 8.63, d, J = 6.9 Hz). Substitution at C-2’ and C-6’ of the pyridinium ring was consequently excluded, and, since considering the doublet nature of H-6’, C-5’ must be protonated as well, this leaves only a 3,4 disubstitution as possible. The intense g-HMBC cross-peak H-2’/C-7’ suggested the placement of the carboxylate group at C-3’, while the cross peaks H-6/C-3’, H-6/C-4’, H-6/C-5’ and H-5’/C-6 confirmed the linkage of the alkyl chain at C-4’, thus completely defining the planar structure of simplexidine (4). The coupling constant JH-3/H-4 = 15.4 Hz was indicative of the trans geometry of the Δ3,4 double bond, while, also considering the limited amounts of sample available (2.0 mg), strategies aimed at the definition of the absolute configuration at the single stereogenic carbon C-6 were not undertaken.
Pyridinium alkaloids are frequently isolated from the polar extracts of marine invertebrates, mostly sponges; however, in spite of the wide diffusion, the chemical diversity within this class of compounds is somewhat limited and only two structural groups can be identified. The most common group of pyridinium derivatives includes oligomeric structures with alkyl linear chains linked at positions C-3 and N-1 of the pyridinium ring, e.g. the recently reported pachychaline C (5, Figure 3) [12]. These molecules are known to exhibit a range of bioactivities including cytotoxic [13] and anti-cholinesterase [14] properties. The second structural group includes the carboxyl-containing homarine (6, Figure 3) or trigonelline (7, Figure 3). substituted at C-3 or C-2, respectively, with short alkyl chains.
Figure 3. Chemical structures of pachychaline C (5), homarine (6) and trigonelline (7).
Figure 3. Chemical structures of pachychaline C (5), homarine (6) and trigonelline (7).
Molecules 13 01465 g003
The isolation of simplexidine (4) is particularly remarkable since it confirms the existence, within the Plakortis simplex biosynthetic machinery, of enzymes deputed to the attachment of polyketide-derived carbon chains at the 4 position of pyridinium rings. In the case of simplakidine (3), this unique reaction led to the linkage between the trigonelline nucleus and a C17 moiety that clearly shared the plakortin (1) carbon backbone. On the other hand, the biosynthetic origin of the C8 group present in the structure of simplexidine (4) cannot be unambiguously predicted, although similarly to that postulated for plakortin derivatives [15], a polyketide origin can be hypothesized also in this case. Investigation of the role of microbial symbionts in the elaboration of the incredible pool of structurally unique secondary metabolites of Plakortis simplex is in progress in our lab. Simplexidine (4) exhibited very weak cytotoxicity toward murine macrophages (RAW 264-7) with 30% of growth inhibition at 80 μg/mL.

Experimental

General

Optical rotations were measured in MeOH on a Perkin-Elmer 192 polarimeter equipped with a sodium lamp (λ = 589 nm) and a 10-cm microcell. IR (KBr) spectra were recorded on a Bruker model IFS-48 spectrophotometer. UV spectra were obtained in MeOH using a Beckman DU70 spectrophotometer. ESI-MS spectra were performed on a LCQ Finnigan MAT spectrometer. HR-FABMS were performed on a FISONS Prospec mass spectrometer using a glycerol matrix. 1H (500 MHz) and 13C (125 MHz) NMR spectra were measured on a Varian INOVA 500 spectrometer; chemical shifts are referenced to the residual solvent signal (CD3OD: δH = 3.34, δC = 49.0). The multiplicities of 13C resonances were determined by DEPT experiments. Homonuclear 1H connectivities were determined by using COSY experiments. One bond heteronuclear 1H-13C connectivities were determined with gradient-HSQC pulse sequence. Two- and three-bond 1H-13C connectivities were determined by gradient-selected HMBC experiments optimized for a 2,3J of 7.0 Hz. Medium-pressure liquid chromatographies (MPLC) were performed using a Büchi 861 apparatus with RP18 and SiO2 (230-400 mesh) stationary phases. High performance liquid chromatography (HPLC) separations were achieved in isocratic mode on a Beckmann apparatus equipped with RI detector and LUNA (Phenomenex) columns (SI60, 250 × 4 mm).

Extraction and Isolation Procedure

A specimen of Plakortis simplex was collected in July 2002 along the coasts of The Bahamas. A voucher specimen is deposited at the Dipartimento di Chimica delle Sostanze Naturali, Italy with the ref. n° 02-10. The organism was immediately frozen after collection and kept frozen until extraction, when the sponge (43 g, dry weight after extraction) was homogenized and extracted with methanol (4 × 500 mL) and with chloroform (4 × 500 mL). The methanol extract was initially partitioned between H2O and n-BuOH and then the organic phase was combined with the CHCl3 extract and concentrated in vacuo to afford a brown oil (22.1 g). This was subjected to chromatography on a column packed with RP18 silica gel and eluted with 9:1 H2O/MeOH (A1), 7:3 H2O/MeOH (A2), 4:6 H2O/MeOH (A3), 2:8 H2O/MeOH (A4), MeOH (A5), and 9:1 MeOH/CHCl3 (A6). Fraction A3 (442 mg) was further chromatographed by MPLC (SiO2 230-400 mesh; solvent gradient system of increasing polarity from EtOAc to MeOH). Fractions eluted with EtOAc/MeOH 2:8 were re-chromatographed by reverse-phase HPLC (eluent MeOH/H2O 4:6) affording pure simplexidine (4, 2.0 mg).

Simplexidine (4) Characterization Data

Colorless amorphous solid. [α]D25 –5.8 (c = 2.0 mg/mL in MeOH); IR (KBr): νmax 1642, 1078, 922 cm-1; UV (MeOH): λmax 268 (logε 3.41); ESI-MS (negative ions): m/z 246 (M-H)-. ESI-MS (positive ions): m/z 248 (M+H)+, 270 (M+Na)+. HR-FABMS analysis: m/z 248.1647 (M+H)+, calcd. for C15H22NO2 m/z 248.1651. 1H- and 13C-NMR: Table 1.

Acknowledgements

NMR and MS facilities were provided by “Centro Interdipartimentale di Servizio di Analisi Strumentale”. The assistance of the staff is acknowledged.

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