Antimicrobial Diterpene Alkaloids from an Agelas citrina Sponge Collected in the Yucatán Peninsula

Abstract

Three new diterpene alkaloids, (+)-8-epiagelasine T (1), (+)-10-epiagelasine B (2), and (+)-12-hydroxyagelasidine C (3), along with three known compounds, (+)-ent-agelasine F (4), (+)-agelasine B (5), and (+)-agelasidine C (6), were isolated from the sponge Agelas citrina, collected on the coasts of the Yucatán Peninsula (Mexico). Their chemical structures were elucidated by 1D and 2D NMR spectroscopy, HRESIMS techniques, and a comparison with literature data. Although the synthesis of (+)-ent-agelasine F (4) has been previously reported, this is the first time that it was isolated as a natural product. The evaluation of the antimicrobial activity against the Gram-positive pathogens Staphylococcus aureus, Streptococcus pneumoniae, Enterococcus faecalis showed that all of them were active, with (+)-10-epiagelasine B (2) being the most active compound with an MIC in the range of 1–8 µg/mL. On the other hand, the Gram-negative pathogenes Acinetobacter baumannii, Pseudomonas aeruginosa, and Klebsiella pneumoniae were also evaluated, and only (+)-agelasine B (5) showed a moderate antibacterial activity with a MIC value of 16 μg/mL.

1. Introduction

One of the most common sponges in tropical and subtropical areas around the world are marine sponges of the genus Agelas (class Demospongiae, order Agelasida, family Agelasidae) [1]. Covering the period from 1971 to November 2021, 355 compounds have been isolated from Agelas sponges with interesting biological activities [2]. Many of these metabolites are of mixed biogenetic origins, as illustrated by alkaloids (especially pyrrole alkaloids and terpenoid alkaloids) [3,4], glycosphingolipids, sterols, and carotenoids that display diverse biological activities and unique structural features [5,6,7].

In particular, the nitrogenated diterpenes that include hypotaurocyamines (agelasidines) and N⁹-adeninium alkaloids (agelasines) represent an important class of compounds isolated from this genus and they show interesting biological activities, including antibacterial, cytotoxic, antifouling, antifungal, and inhibitory effects on Na⁺/K⁺-ATPase [8].

As part of our ongoing efforts to find new bioactive natural compounds from marine organisms collected off the coast of the Yucatán Peninsula (Mexico) [9,10,11,12], specimens of the sponge A. citrina were investigated due to the antibacterial activity displayed by their organic extracts. Former studies of the sponge A. citrina reported the presence of diterpene alkaloids [13] and pyrrole—imidazole alkaloids [14]. Our preliminary chemical investigation of this sponge led to the isolation of the major known component (−)-agelasine B, which showed significant antibacterial activity against two Gram-positive bacteria S. aureus strains [10]. Further bioactivity-guided fractionation of the CH₂Cl₂ and aqueous methanolic fractions led to the isolation of three new compounds (1, 2, and 3), as well as three known compounds (4, 5, and 6). All isolated compounds (1–6) were evaluated for their antibacterial activity. Herein, we describe the isolation, structure elucidation, and antibacterial activity of 1–6.

2. Results and Discussion

2.1. Isolation and Identification of Agelasines

Specimens of the sponge A. citrina collected on Cozumel Island of the Yucatán Penisula (Mexico) were extracted several times with CH₃OH/CH₂Cl₂ to produce an organic extract, which was partitioned following our standard partitioning procedure [15] into several fractions of differing polarities. The CH₂Cl₂ and aqueous methanolic fractions were submitted to Solid Phase Extraction (SPE) with RP-18 cartridges and finally to RP-HPLC to produce pure compounds 1–6 (Figure 1).

Compound 1 was obtained as a yellow oil [α]²⁵_D = +12 (c 0.36, MeOH). The molecular formula of 1 was established based on the [M]⁺ peak at m/z 440.3375, observed in its (+)-HRESIMS (calculated for C₂₆H₄₂N₅O, m/z 440.3384, Δ = 2.04 ppm).

The ¹H and ¹³C NMR spectral data, along with an HSQC spectrum of 1 in DMSO-d₆ (

Table 1. ¹H NMR (500 MHz) and ¹³C NMR (125 MHz) data for 8-epiagelasine T (1), 10-epiagelasine B (2), and agelasine B (5).

Post.	1 a		2 b		5 b
	δH, Mult, (J in Hz)	δC, Type	δH, Mult, (J in Hz)	δC, Type	δH, Mult, (J in Hz)	δC, Type
1	1.58, m 0.89, m	39.2, CH2	1.64 m 1.33, m	19.7, CH2	1.38, m 1.15, m	18.2, CH2
2	1.53, m	19.8, CH2	1.98, m	22.9, CH2	1.49, m	26.8, CH2
	1.19, m		1.91, m		1.29, m
3	1.33, m	41.3, CH2	5.30, brs	120.7, CH	5.16, brs	120.5, CH
	1.10, m
4		32.9, C		136.2, C		144.3, C
5	0.81, m	55.3, CH		40.5, C		38.3, C
6	1.34, m	17.7, CH2	1.80, m 1.71, m	33.7, CH2	1.70, d, (12.6) 1.14 m	36.7, CH2
7	1.70, dt, (11.8, 3.0) 1.30, m	43.7, CH2	1.64, m 1.42, m	29.2, CH2	1.43 m	27.4, CH2
8		72.1, C	1.31, m	33.5, CH	1.41, m	36.3, CH
9	0.98, m	59.9, CH		39.1, C		38.9, C
10		38.5, C	2.28, brd, (12.9)	42.0, CH	1.29 m	46.4, CH
11	1.55, m	22.7, CH2	1.35, m	30.0, CH2	1.60 m	32.5, CH2
	1.27, m		1.25, m		1.45 m
12	2.22, td, (12.2, 6.1)	42.2, CH2	2.03, dt, (11.8, 5.6)	35.1, CH2	2.00 m	33.0, CH2
	2.09, td, (12.2, 4.9)		1.97, m		1.92 m
13		147.0, C		149.2, C		148.8, C
14	5.44, t, (7.0)	114.6, CH	5.45, t, (6.4)	115.0, CH	5.43, t, (5.6)	115.0, CH
15	5.13, d, (7.3)	46.6, CH2	5.25, d, (6.5)	48.6, CH2	5.34, d, (6.0)	48.9, CH2
16	1.79, s	16.5, CH3	1.86, s	17.2, CH3	1.85, s	17.2, CH3
17	1.00, s	23.6, CH3	1.07, d, (7.4)	18.7, CH3	0.78, d, (5.9)	15.9, CH3
18	0.84, s	33.0, CH3	1.62, s	21.7, CH3	1.56, s	18.0, CH3
19	0.75, s	21.1, CH3	0.86, s	17.2, CH3	0.98, s	20.0, CH3
20	0.74, s	15.0, CH3	0.94, s	15.6, CH3	0.70, s	18.3, CH3
2′	8.46, s	155.4, CH	8.54, s	155.8, CH	8.52, s	155.2, CH
4′		149.0, C		149.7, C		149.6, C
5′		109.2, C		110.0, C		110.5, C
6′		152.4, C		151.8, C		151.7, C
8′	9.51, s	140.8, CH	9.87, s	142.2, C	10.06, s	142.3, CH
9′-N-Me	3.88, s	31.1, CH3	4.06, s	31.9, CH3	4.07, s	32.2, CH3
NH2	7.92, s

^a In DMSO-d₆. ^b In CDCl₃.

), were indicative of an agelasine-type diterpene alkaloid compound. The adenine moiety was identified by the characteristic signals of two methines at δ_H/δ_C 8.46 (1H, s, H-2′)/155.4 (C-2′) and 9.51 (1H, s, H-8′)/140.8 (C-8′); a N-methyl group at δ_H/δ_C 3.88 (3H, s)/31.1; and three non-protonated sp² carbons at δ_C 152.4 (C-6′), 149.0 (C-4′), and 109.2 (C-5′). The diterpene portion of 1 was assigned from the ¹H and ¹³C NMR signals of the bicyclic ring corresponding to four diasterotopic methylenes observed at δ_H/δ_C 1.58 (1H, m, H-1a)-0.89 (1H, m, H-1b)/39.2 (C-1), 1.53 (1H, m, H-2a)-1.19 (1H, m, H-2b)/19.8 (C-2), 1.33 (1H, m, H-3a)-1.10 (1H, m, H-3b)/41.3 (C-3), and 1.70 (1H, dt, J = 11.8, 3.0 Hz, H-7a)-1.30 (1H, m, C-7b)/43.7 (C-7); one homotopic methylene at δ_H/δ_C 1.34 (2H, m, H-6)/17.7 C-6; two methines at δ_H/δ_C 0.81 (1H, m, H-5)/55.3 (C-5) and 0.98 (1H, m, H-9)/59.9 (C-9); four methyl groups at δ_H/δ_C 1.00 (3H, s, H₃-17)/23.6 (C-17), 0.84 (3H, s, H₃-18)/33.0 (C-18), 0.75 (3H, s, H₃-19)/21.1 (C-19), and 0.74 (3H, s, H₃-20)/15.0 (C-20); two quaternary carbons at δ_C 32.9 (C-4) and 38.5 (C-10); and one non-protonated carbon linked to oxygen at δ_C 72.1 (C-8). Moreover, the ¹H and ¹³C NMR signals corresponding to three methylenes at δ_H/δ_C 1.55 (1H, m, H-11a)-1.27 (1H, m, H-11b)/22.7 (C-11), 2.22 (1H, td, J = 12.2, 6.1 Hz, H-12a)-2.09 (1H, td, J = 12.2, 4.9 Hz, H-12b)/42.2 (C-12), and 5.13 (2H, d, J = 7.3 Hz, H-15)/46.6 (C-15); a vinyl methyl at δ_H/δ_C 1.79 (3H, s, H₃-16)/16.5 (C-16); an olefinic methine at δ_H/δ_C 5.44 (1H, t, J = 7.0 Hz, H-14)/114.6 (CH); and a quaternary sp² carbon at δ_C 147.0 (C-13) confirmed the presence of the 3-methylpentenyl chain.

The analysis of COSY and HMBC spectra was able to confirm the planar structure of 1 (Figure 2). The 1D NMR spectral data of 1 were similar to those for agelasine T, a previously reported agelasine isolated from an unidentified Agelas collected in Okinawa [16]. However, the difference of the carbon chemical shift of the C-17 methyl group at δ_C 23.6 in 1 instead of the reported value of that group at δ_C 30.7 in agelasine T, suggested that they differed in the spatial disposition of the C-17 methyl group, and consequently in the stereochemistry at C-8 position.

The relative configuration was assigned by 2D and selective 1D-NOESY experiments of 1. The E-geometry of the Δ¹³ double bond was established by the observed NOESY correlation between the signals assigned to the methylene CH₂-15 at δ_H 5.13 and vinyl methyl CH₃-16 at δ_H 1.79. On the other hand, the irradiation of methyl protons (Figure S6) at the position CH₃-17 (δ_H 1.00) showed a 2.0% NOE response to the methyl protons at the position CH₃-20 (δ_H 0.74); the irradiation of methyl protons (Figure S7) at the position CH₃-18 (δ_H 0.84) also displayed NOE to the methyl protons at the position CH₃-20 (δ_H 0.74) (3.0%) (see Figure 3A). Thus, these NOE correlations suggest that these three methyl groups are located on the same face of the molecule, assigned as the β face. Furthermore, the carbon chemical shift of CH₃-17 (δ_C 23.6) resonates similarly to that of a synthetic terpene having a bicyclic ring bearing the same spatial disposition of the hydroxy group (δ_C 24.2) [17].

This analysis makes it possible to propose the structure of compound 1 as (+)-8-epiagelasine T (Figure 1).

Compound 2 was obtained as a yellow oil [α]²⁵_D = +16 (c 0.13, MeOH) and its molecular formula was established on the basis of the [M]⁺ peak at m/z 422.3280, observed in its HRESIMS spectrum (calculated for C₂₆H₄₀N₅, m/z 422.3279, Δ = 0.23 ppm).

The similarity of ¹H and ¹³C NMR spectral in CDCl₃ of 2 to those of 1 suggested that 2 was also an agelasine-type alkaloid with an N⁹-methyladenine unit.

The adenine moiety was identified by the characteristic signals of two methines at δ_H/δ_C 8.54 (1H, s, H-2′)/155.8 (C-2′) and 9.87 (1H, s, H-8′)/142.2 (C-8′), an N-methyl group at δ_H/δ_C 4.06 (3H, s)/31.9, and three non-protonated sp² carbons at δ_C 151.8 (C-6′), 149.7 (C-4′) and 110.0 (C-5′). The bicyclic ring for the diterpene portion of 2 was assigned from the ¹H and ¹³C NMR signals corresponding to four diasterotopic methylenes observed at δ_H/δ_C 1.64 (1H, m, H-1a)-1.33 (1H, m, H-1b)/19.7 (C-1), 1.98 (1H, m, H-2a)-1.91 (1H, m, H-2b)/22.9 (C-2), 1.80 (1H, m, H-6a)-1.71 (1H, m, H-6b)/33.7 (C-6), and 1.64 (1H, m, H-7a)-1.42 (1H, m, H-7b)/29.2 (C-7); an olefinic methine at δ_H/δ_C 5.30 (1H, brs, H-3)/120.7 (C-3); two aliphatic methines at δ_H/δ_C 1.31 (1H, m, H-8)/33.5 (C-8) and 2.28 (1H, brd, J = 12.9 Hz, H-10)/42.0 (C-10); a vinyl methyl at δ_H/δ_C 1.62 (3H, s, H₃-18)/21.7 (C-18); three methyl groups at δ_H/δ_C 1.07 (3H, d, J = 7.4 Hz, H₃-17)/18.7 (C-17), 0.86 (3H, s, H₃-19)/17.2 (C-19), and 0.94 (3H, s, H₃-20)/15.6 (C-20); two quaternary carbons at δ_C 40.5 (C-5) and 39.1 (C-9); and a quaternary sp² carbon at δ_C 136.2 (C-4). Additionally, the ¹H and ¹³C NMR signals corresponding to three methylenes at δ_H/δ_C 1.35 (1H, m, H-11a)-1.25 (1H, m, H-11b)/30.0 (C-11), 2.03 (1H, dt, J = 11.8, 5.6 Hz, H-12a)-1.97 (1H, m, H-12b)/35.1 (C-12), and 5.25 (2H, d, J = 6.5 Hz, H-15)/48.6 (C-15); a vinyl methyl at δ_H/δ_C 1.86 (3H, s, H₃-16)/17.2 (C-16); an olefinic methine at δ_H/δ_C 5.45 (1H, t, J = 6.4 Hz, H-14)/115.0 (C-14); and a quaternary sp² carbon at δ_C 149.2 (C-13) confirmed the presence of the 3-methylpentenyl chain.

The constitution of 2 was established from the analysis of the 2D NMR spectral data (Figure 2). Two spin systems corresponding to the bicyclic system were deduced from the COSY experiment of 2: the first spin system was assigned to the H-1, H-2, H-3, and H-10 protons, and the second spin system to the H-6, H-7, H-8, and H₃-17 protons (Figure 2). Key HMBC correlations from H₃-19 (δ_H 0.86) to C-4 (δ_C 136.2), C-5 (δ_C 40.5)/C-6 (δ_C 33.7) and C-10 (δ_C 42.0); from H₃-17 (δ_H 1.07) to C-8 (δ_C 33.5), C-9 (δ_C 39.1) and C-7 (δ_C 29.2); and from H₃-20 (δ_H 0.94) to C-8 (δ_C 33.5), C-9 (δ_C 39.1) and C-10 (δ_C 42.0) allowed us to connect the two spin systems. Finally, the HMBC correlation from H₃-20 (δ_H 0.94) to C-11 (δ_C 30.0) showed the link between the bicyclic ring and the 3-methylpentenyl chain (Figure 2). All these data indicate the presence of a clerodane skeleton in 2 as in agelasine B (5), also isolated from this sponge.

The relative configuration of 2 was deduced from NOESY data and confirmed by a IPAP-HSQMBC experiment. The E-configuration of the Δ¹³ double bond of 2, as in agelasine B (5), was deduced from NOE correlations observed in the NOESY experiment between the signals assigned to the methylene CH₂-15 at δ_H 5.25 and vinyl methyl CH₃-16 at δ_H 1.86, and between the methylene CH₂-12 at δ_H 2.03 and ofefinic proton CH-14 at δ_H 5.45.

On the other hand, the strong NOE correlations from H₃-17 (δ_H 1.07) to H₃-19 (δ_H 0.86) and H₃-20 (δ_H 0.94) in the NOESY experiment of 2 indicate that these methyl groups (H₃-17, H₃-19, and H₃-20) are oriented on the same face of the molecule, assigned as β-face.

The drastic change in the chemical shift of H-10 in 2 at δ_H 2.28 (1H, brd, J = 12.9 Hz) in relation to that in agelasine B (5) at δ_H 1.29 (1H, m) (Table 1), and considering that agelasine B (5) has the same spatial disposition for the three methyl groups H₃-17, H₃-19, and H₃-20, suggested they must differ in the remaining stereogenic center at C-10. Similar chemical shifts and the same HMBC and NOESY correlations were observed in 2 when the NMR spectra were run in C₆D₆ (Table S1). Therefore, these results suggest a cis-clerodane disposition for compound 2, instead of the trans-clerodane disposition for agelasine B (5).

Curiously, when the NMR spectra of 2 was repeated this time in CDCl₃, an important displacement of the carbon and proton chemical shifts was observed in the NMR spectra after 24 h, probably due to the acidic character of the deuterated solvent. Thus, the carbon and proton chemical were assigned again by 2D-NMR experiments (see Table S1 and Figures S23–S31). The low value of the ³J_CH between H-10 and C-19 of 3.42 Hz measured in an IPAP-HSQMBC experiment of this sample (Figure S31) agrees with the proposed cis-clerodane disposition for 2. Unfortunately, the ³J_CH between H-10 and C-19 in agelasine B (5) could not be determined due to the insufficient amount. In order to obtain a direct proof for the cis- vs. trans-ring connections in decaline-like systems using the IPAP-HSQMBC experiment, we measured the corresponding values in the available synthetic model compounds 7 and 8 (Figure 4) [18]. In this way, the corresponding value of the cis-decalin-like system in 7 (³J_C7H5 = 2.9 Hz) resulted to be similar to that of 2 (Figure S32). As expected, the corresponding value of the trans-decalin-like system (³J_C7H5 = 8.42 Hz) was much larger (Figure S33).

On the other hand, the selective 1D-NOESY correlations from H₃-17 (δ_H 1.10) to H₃-20 (δ_H 0.87) (0.30%), H₃-18 (δ_H 1.62) (0.36%) and H-10 (δ_H 1.25) (0.23%) (Figure S28); from H₃-19 (δ_H 1.15) to H₃-20 (δ_H 0.87) (0.5%) (Figure S29); and from H₃-20 (δ_H 0.87) to H₃-17 (δ_H 1.10) (0.25%), H₃-19 (δ_H 1.15) (0.32%), and H-10 (δ_H 1.25) (0.30% (Figure S30), indicating that H-10, H₃-17, H₃-19, and H₃-20 protons are in the same face of the molecule, confirmed the cis-clerodane disposition for compound 2 (Figure 3B). Thus, we named this new agelasine as 10-epiagelasine B (2).

The molecular formula of 3, also obtained as a yellow oil [α]²⁵_D = + 2 (c 0.2, MeOH), was established from its (+)-HRESIMS, which displayed a [M + H]⁺ adduct at m/z 440.2950 (calculated for C₂₃H₄₂N₃SO₃, m/z 440.2942, Δ = 2.04 ppm) and from its ¹³C NMR spectrum.

The ¹H-NMR and ¹³C NMR spectral data of 3 in CDCl₃ (

Table 2. ¹H NMR (500 MHz) and ¹³C (125 MHz) NMR data for 12-hydroxyagelasidine C (3) in CDCl₃.

Position	3
	δH, Mult (J in Hz)	δC, Type
1	1.44, m	27.2, CH2
2	1.95, m	25.7, CH2
3	5.40, brs	124.4, CH
4		139.7, C
5		40.5, C
6	1.71, m	33.3, CH
7	1.43, m	35.3, CH2
8	1.95, m; 1.48, m	34.6, CH2
9		140.1, C
10	5.06, t, (6.5)	118.6, CH
11	2.27, t, (6.5)	34.0, CH2
12	4.09, t, (6.5)	76.3, CH
13		149.2, C
14	5.52, t, (8.0)	110.0, CH
15	3.84, dd, (14.5, 8.0); 3.80, dd, (14.5, 8.0)	53.8, CH2
16	1.71, brs	13.1, CH3
17	1.61, brs	16.6, CH3
18	1.60, brs	19.3, CH3
19	0.84, s	16.0, CH3
20	0.85, d, (6.7)	21.2, CH3
1′	3.28, brs	50.3, CH2
2′	3.70, brs	34.5, CH2
3′		157.5, C

) were indicative of an agelasidine-type diterpene alkaloid compound. The hypotauro-cyamine moiety (-SO₂-CH₂CH₂NHC(NH)NH₃⁺) was identified by the characteristic guanidine carbon signal at δ_C 157.5 (C-3′) and two methylenes at δ_H/δ_C 3.28 (2H, brs, H-1′)/0.3 (C-1′) and 3.70 (2H, brs, H-2′)/34.5 (C-2′). The diterpene portion of 3 was assigned by the ¹H and ¹³C NMR signals of the monocyclic ring corresponding to two homotopic methylenes observed at δ_H/δ_C 1.44 (2H, m, H-1)/27.2 (C-1) and 1.95 (2H, m, H-2)/25.7 (C-2); an olefinic methine at δ_H/δ_C 5.40 (1H, brs, H-3)/124.4 (C-3); an aliphatic methine at δ_H/δ_C 1.71 (1H, m, H-6)/33.3 (C-6); a vinyl methyl at δ_H/δ_C 1.60 (3H, brs, H₃-18)/19.3 (C-18); two methyl groups at δ_H/δ_C 0.84 (3H, s, H-19)/16.0 (C-19) and 0.85 (3H, d, J = 6.7 Hz, H-20)/21.2 (C-20); a quaternary carbon at δ_C 40.5 (C-5); and a quaternary sp² carbon at δ_C 139.7 (C-4). Furthermore, the ¹H and ¹³C NMR signals corresponding to four methylenes at δ_H/δ_C 1.43 (2H, m, H-7)/35.3 (C-7), 1.95 (1H, m, H-8a)-1.48 (1H, m, H-8b)/34.6 (C-8), 2.27 (2H, t, J = 6.5 Hz, H-11)/34.0 (C-11), and 3.84 (1H, dd, J = 14.5, 8.0 Hz, H-15a)-3.80 (1H, dd, J = 14.5, 8.0 Hz, H-15b)/53.8 (C-15); two vinyl methyls at δ_H/δ_C 1.71 (3H, brs, H-16)/13.1 (C-16) and 1.61 (1H, brs, H-17)/16.6 (C-17); two olefinic methines at δ_H/δ_C 5.06 (1H, t, J = 6.5 Hz, H-10)/118.6 (C-10) and 5.52 (1H, t, J = 8.0 Hz, H-14)/110.0 (C-14); and two quaternary sp² carbons at δ_C 140.1 (C-9) and 149.2 (C-13) confirmed the presence of the 3,7-dimethyl-nona-3,7-dienyl chain.

The 1D NMR spectral data of 3 were similar to those of (+)-agelasidine C, isolated from Agelas nakamurai collected in Okinawa [19]. The presence of an additional hydroxyl group in 3 in relation to (+)-agelasidine C was suggested by the difference of an oxygen (16 Da) between their molecular formula. This was confirmed by the presence of an additional oxymethine at δ_H/δ_C 4.09 (1H, t, J = 6.5 Hz, H-12)/76.3 (C-12) in the ¹H and ¹³C NMR spectra of 3, instead of the corresponding methylene group present in (+)-agelasidine C. The HMBC correlations between the vinyl methyl protons at δ_H 1.71 (3H, s, H₃-16) and the oxymethine carbon at δ_C 76.3 (C-12), the quaternary sp² carbon at δ_C 149.2 (C-13) and the olefinic methine carbon at δ_C 110.0 (C-14), located the hydroxyl group at C-12 position (Figure 2). The analysis of COSY and HMBC spectra was able to confirm the constitution of 3 (Figure 2). These data indicate that 3 is a new agelasidine, which was named 12-hydroxyagelasidine C.

The relative configuration of the monocyclic ring system in 3 was confirmed by a comparison of its ¹³C NMR spectral data with that of (+)-agelasidine C [19] and other agelasidines [20] having the same relative configuration. The E-configuration of the Δ⁹ and Δ¹³ double bonds was established from the NOESY correlation between the signals assigned to the methylene CH₂-11 at δ_H 2.27 and the vinyl methyl CH₃-17 at δ_H 1.61, and between the methylene CH₂-15 at δ_H 3.84–3.80 and the vinyl methyl CH₃-16 at δ_H 1.71, respectively. Absolute configuration at C-12 in 3 was determined by the Mosher’s method using the MTPA esters [21]. The 12-hydroxyagelasidine C (3) was treated with R-(−)- and S-(+)-α-methoxy-α-(trifluoromethyl) phenyl acetic acid (MTPA-OH) to afford the S- and R-MTPA esters. The analysis of the ¹H NMR and ¹H−¹H COSY led to the assignment of both esters’ chemical shifts in proximity of C-12. The Δδ^SR values between R- and S-MTPA esters of 3 at 12-OH were negative for H-11/10/17 and positive for H-14/15/18 (Figure 5), which suggested the absolute configuration of C-12 as R.

Compounds 4–6 (Figure 1) were identified as the known (+)-ent-agelasine F (4) [22], (+)-agelasine B (5) [8] and (+)-agelasidine C (6) [19], by comparing their NMR data with that reported in the literature. Although (+)-ent-agelasine F (4) have been previously synthetized, this is the first time that is reported as a natural product.

2.2. Antibacterial Activity of Agelasines

The antibacterial evaluation of 1–6 against the Gram-negative pathogens A. baumannii ATCC 17978, K. pneumoniae ATCC 700603, and P. aeruginosa ATCC 27823 displayed that only (+)-agelasine B (5) showed a moderate antibacterial activity with an MIC value of 16 μg/mL. In contrast, all of them exhibited antibacterial activity against Gram-positive pathogens (

Table 3. Antibacterial activity (MIC, μg/mL) of 1–6 against Gram-positive pathogens.

Compound	S. aureus ATCC 29213	S. aureus USA300LAC	S. pneumoniae ATCC 49619	S. pneumoniae 549 CHUAC	E. faecalis ATCC 29212	E. faecalis 256 CHUAC	E. faecium 214 CHUAC
(+)-8-epiagelasine T (1)	16	16	16	32	32	≥64	32
(+)-10-epiagelasine B (2)	1	2	4	8	4	4	4
(+)-12-hydroxyagelasidine C (3)	8	8	16	-	16	32	8
(+)-ent-agelasine F (4)	4	4	4	-	8	8	8
(+)-agelasine B (5)	2	2	4	16	8	8	4
(+)-agelasidine C (6)	8	8	4	-	8	8	8

). These results are in accordance with previous reports, where (+)-ent-agelasine F (4), (+)-agelasine B (5) [8], and (+)-agelasidine C (6) [19] showed antimicrobial activity against Gram-positive bacteria.

Interestingly, the higher activity shown by (+)-10-epiagelasine B (2), having a cis-clerodane, than its isomer (+)-agelasine B (5), bearing a trans-clerodane, in Gram-positive pathogens, was indicative of the impact of decalin stereochemistry in the detected activity.

3. Materials and Methods

3.1. General Experimental Chemical Procedures

Optical rotations were measured on a JASCO DIP-1000 polarimeter, with an Na (589 nm) lamp and filter. ¹H, ¹³C, and 2D NMR spectra were recorded on a Bruker spectrometer of 950 MHz, equipped with a 5 mm Cryo Probe (NEO console); a Bruker spectrometer (800 MHz for ¹H and 200 MHz for ¹³C) equipped with a 5 mm cryo probe and an NEO console; a Bruker (800 MHz for ¹H and 200 MHz for ¹³C) spectrometer equipped with a 3 mm cryo probe and a NEO console; a Bruker spectrometer (700 MHz for ¹H and 175 MHz for ¹³C) equipped with a 5 mm cryo probe and an Avance III console; and a Bruker Avance 500 spectrometer (500 MHz for ¹H and 125 MHz for ¹³C) equipped with a 5 mm cryo probe, using DMSO-d₆ and CDCl₃ as solvents. Chemical shifts are reported in δ scale relative to DMSO-d₆ (δ 2.50 ppm for ¹H NMR, δ 39.51 ppm for ¹³C NMR) and CDCl₃ (δ 7.26 ppm for ¹H NMR, δ 77.0 ppm for ¹³C NMR).

HRESIMS experiments were performed on the Applied Biosystems QSTAR Elite system or a Thermo MAT95XP spectrometer. HPLC separations were performed on the Agilent 1100 liquid chromatography system equipped with a solvent degasser, quaternary pump, and diode array detector (Agilent Technologies, Waldbronn, Germany) using a semipreparative reversed phase column Luna C18 (5 μ, 100 Å, 250 × 10 mm).

3.2. Animal Material

The sponge A. citrina was collected by hand and traditional SCUBA-diving off Cozumel Island, Quintana Roo (20°41′00.00″ N/87°01′32.66″ W) at depths ranging from 10 to 15 m in March 2017, and frozen immediately after collection. A voucher specimen CZE56 was deposited in the Phylum Porifera Gerardo Green National Collection of the Institute of Marine Sciences and Limnology (ICMyL) at the National Autonomous University of Mexico (UNAM), Mexico City.

3.3. Extraction and Isolation

Sliced bodies of A. citrina (wet weight, 729.6 g; dry weight, 375.3 g) were exhaustively extracted with CH₃OH-CH₂Cl₂ (1:1, 3 × 1.5 L) at 25 °C for 24 h each maceration. The combined extracts were concentrated under reduced pressure to produce 6.1 g of a crude residue. A total of 6.0 g was first partitioned between CH₂Cl₂/H₂O (1:1 v/v) to produce aqueous and organic phases. The organic phase was concentrated under reduced pressure and partitioned between 10% aqueous CH₃OH (400 mL) and hexane (2 × 400 mL). The hexane portion produced, after removing the solvent under reduced pressure, 672.2 mg of the hexane fraction (FH). The H₂O content (% v/v) of the methanolic fraction was adjusted to 50% aqueous CH₃OH, and the mixture was extracted with CH₂Cl₂ (100 mL) to afford, after removing the solvent under reduced pressure, 3.6 g of the CH₂Cl₂ fraction (FD) and 755.8 mg of the remaining aqueous methanolic fraction (FM) (Scheme S1).

The CH₂Cl₂ fraction (3.6 g) was subjected to a Solid Phase Extraction (SPE) with RP-18 (Merck KGaA) using a discontinuous gradient from H₂O to CH₃OH and then CH₂Cl₂.

The fraction eluted with H₂O/CH₃OH (2:1, 181.3 mg) was separated by RP-HPLC eluting, with a mobile phase consisting of 30 min of a gradient from 30% to 100% of CH₃OH in H₂O (v/v, each containing 0.04% trifluoroacetic acid) followed by a 10 min isocratic at 100% of CH₃OH at a flow rate of 2.0 mL/min, afforded (+)-8-epilagelasine T (1) (30.0 mg; R_t = 34.9 min) and (+)-10-epiagelasine B (2) (45.0 mg; R_t = 37.0 min).

The separation of the fraction eluted with H₂O/CH₃OH (1:2, 391.1 mg) was performed by RP-HPLC with a mobile phase consisting of 30 min of a gradient from 40% to 100% of CH₃OH in H₂O (v/v, each containing 0.04% trifluoroacetic acid), followed by a 10 min isocratic at 100% of CH₃OH at a flow rate of 2.0 mL/min, yielded (+)-ent-agelasine F (4) (21.3 mg; R_t = 30.1 min) and (+)-agelasine B (5) (1.5 mg; R_t = 32.5 min).

The aqueous methanolic fraction (755.8 mg) was submitted to a Solid Phase Extraction (SPE) with RP-18 (Merck KGaA) using a discontinuous gradient from H₂O to CH₃OH and then CH₂Cl₂. The separation of the fraction eluted with H₂O/CH₃OH (1:1, 181.5 mg) by RP-HPLC using a mobile phase consisting of 30 min of a gradient from 35% to 100% of CH₃OH in H₂O (v/v, each containing 0.04% trifluoroacetic acid), followed by a 10 min isocratic at 100% of CH₃OH at a flow rate of 2.0 mL/min, afforded (+)-12-hidroxy agelasidine C (3) (7.0 mg; R_t = 29.8 min) and (+)-agelasidine C (6) (27.0 mg; R_t = 34.0 min).

3.4. Structural Characterization

(+)-8-epiagelasine T (1). [α]²⁵_D +12 (c 0.2, MeOH); ¹H and ¹³C NMR see Table 1; (+)-HRESIMS m/z 440.3375 [M]⁺ (calcd. for C₂₆H₄₂N₅O, 440.3384).

(+)-10-epiagelasine B (2). [α]²⁵_D +16 (c 0.2, MeOH); ¹H and ¹³C NMR see Table 1; (+)-HRESIMS m/z 422.3280 [M]⁺ (calcd. for C₂₆H₄₀N₅, 422.3279).

(+)-12-hidroxyagelasidine C (3). [α]²⁵_D +2 (c 0.2, MeOH); ¹H and ¹³C NMR see Table 2; (+)-HRESIMS m/z 440.2950 [M + H]⁺ (calcd. for C₂₃H₄₂N₃SO₃, 440.2942).

(+)-ent-agelasine F (4). [α]²⁵_D +1 (c 0.2, MeOH); ¹H and ¹³C NMR see SI; (+)-HRESIMS m/z 422.3280 [M + H]⁺ (calcd. for C₂₆H₄₀N₅, 422.3279).

(+)-agelasine B (5). [α]²⁵_D +13 (c 0.2, MeOH); ¹H and ¹³C NMR see SI; (+)-HRESIMS m/z 422.3281 [M + H]⁺ (calcd. for C₂₆H₄₀N₅, 422.3284).

(+)-agelasidine C (6). [α]²⁵_D +9 (c 0.2, MeOH); ¹H and ¹³C NMR see SI; (+)-HRESIMS m/z 424.2991 [M + H]⁺ (calcd. for C₂₃H₄₂N₃SO₂, 424.2993).

3.5. Preparation of the MTPA Esters

The (R)- and (S)-MTPA esters were obtained by treatment of 3 (1.5 mg, for each acid) with (R)- and (S)-MTPA (1.60 mg), DCC (1.40 mg), and DMAP (1.0 mg), in dry CH₂Cl₂ (1.0 mL). The reactions were stirred at room temperature for 24 h and the resulting products were purified with SPE cartridges (Hypersep C18 200 mg, MeOH/H₂O 50/50, v/v) to afford the S-(−)- and R-(+)-MTPA esters 3a and 3b. The products were monitored by recording ¹H NMR spectra at 500 MHz:

¹H NMR data of 3a (500 MHz in CDCl₃): δ_H 5.04 (t, 6.5, H-10), 2.22 (m, H-11), 4.94 (t, 6.5, H-12), 5.48 (t, 8.0, H-14), 3.73 (m, H-15a), 3.77 (m, H-15b), 1.58 (brs, CH3-17), 1.69 (brs, CH₃-18).

¹H NMR data of 3b (500 MHz in CDCl₃): δ_H 5.08 (t, 6.5, H-10), 2.30 (m, H-11), 4.77 (t, 6.5, H-12), 5.47 (t, 8.0, H-14), 3.69 (m, H-15a), 3.65 (m, H-15b), 1.60 (brs, CH3-17), 1.67 (brs, CH₃-18).

3.6. Antibacterial Activity Assays

3.6.1. Bacterial Strains and Culture Preparation

The bacterial strains used to study the antibacterial activity of the isolated compounds were the Gram-negative pathogens Acinetobacter baumannii (ATCC 17978), Pseudomonas aeruginosa (ATCC 27823), and Klebsiella pneumoniae (ATCC 700603), and the Gram-positive pathogens, including type-strains and clinical strains isolated from infections in our hospital: Staphylococcus aureus (ATCC 29213 and USA300LAC strains), Streptococcus pneumoniae (ATCC 49619 and 549 CHUAC strains), Enterococcus faecalis (ATCC 29212 and 256 CHUAC strains), and Enterococcus faecium (214 CHUAC strain).

Gram-negative and Gram-positive strains were routinely grown or maintained in Luria–Bertani (LB), and in Trypticase soya broth (TSB) media, respectively, supplemented with 2% agar or the antibiotic ampicillin (30 mg/L), when needed. All strains were grown at 37 °C and stored in 10% glycerol at −80 °C.

3.6.2. Microdilution Method: Minimum Inhibitory Concentration

The minimum inhibitory concentrations (MICs) were determined by the broth microdilution method (Clinical Laboratory Standards Institute (CLSI), 2022). Briefly, the bacterial strains suspensions were cultured overnight at 37 °C in Mueller Hinton II agar plates (Becton Dickinson) and the turbidity of the bacterial suspensions was standarized at 0.5 on the McFarland scale to establish the inocula. The crude extracts of the test samples were dissolved in methanol. Two-fold serial dilutions of the extracts in Mueller Hinton II broth medium (Sigma) were carried out in 96-wells microplates, to produce a range of extract concentrations of 0.5–256 mg/L. Methanol was present at maximum concentration of 0.25% v/v in the well containing the highest concentration of compound. One well in each row contained growth media and bacterial suspension and was used as a positive growth control. Another well, containing medium only, was used as the negative control. Solvent controls of methanol and growth medium were included to determine whether the concentrations used interfered with bacterial growth. The MIC was evaluated after incubation 20–24 h to 37 °C and established as the lowest concentration of the compound at which the bacterial strains did not grow. All compounds were tested in triplicate.

As controls, MIC assays were also performed with imipenem against Gram-negative strains, and with vancomycin against Gram-positive strains (MIC values known).

4. Conclusions

In summary, three new diterpene alkaloids, (+)-8-epiagelasine T (1), (+)-10-epiagelasine B (2), and (+)-12-hydroxy agelasidine C (3), together with three known compounds, (+)-ent-agelasine F (4), (+)-agelasine B (5), and (+)-agelasidine C (6), were isolated from sponge Agelas citrina collected on Cozumel Island in the Mexican Caribbean. This is the first time that (+)-ent-agelasine F (4) is reported as a natural product. All of them display antibacterial activity against Gram-positive bacteria, (+)-10-epiagelasine B (2) being the most active one.