Monoindole Alkaloids from a Marine Sponge Spongosorites sp.

Seven (1–7) monoindole derivatives were isolated from the MeOH extract of a marine sponge Spongosorites sp. by bioactivity-guided fractionation. The planar structures were established on the basis of NMR and MS spectroscopic analyses. Compounds 1–5 are unique indole pyruvic acid derivatives. Compounds 1–2 and 4–6 are isolated for the first time from a natural source although they were previously reported as synthetic intermediates. Compound 3 was defined as a new compound. Co-occurring bisindoles such as hamacanthins and topsentins might be biosynthesized by condensation of two units of these compounds. The compounds were tested for cytotoxicity against a panel of five human solid tumor cell lines, and compound 7 displayed weak activity.

In our previous study on cytotoxic compounds from the marine sponge Spongosorites sp., we isolated a series of bisindole alkaloids [11,12]. In our continuing search for cytotoxic metabolites from the same sponge, seven monoindole alkaloids were isolated. Compounds 1−2 and 4−6 were isolated for the first time from a natural source although they were previously reported as synthetic intermediates (Figure 1). Compound 3 was defined as a new compound. Herein we describe the structure elucidation and the biological evaluation of these compounds.

Result and discussion
Compound 1 was isolated as a yellow, amorphous powder. The molecular formula was established as C 11 H 8 BrNO 3 on the basis of the EIMS and NMR data. In the LREIMS of 1, a (M) + ion cluster was observed at m/z 281/283 in the ratio of 1:1 that is characteristic of a monobrominated compound. The NMR spectrum of 1 were reminiscent of reported indole alkaloids. 11,12 Analysis of the 1 H, 13 C, COSY, HMBC, and HSQC data, along with comparison of chemical shift values with those of known indole alkaloids, allowed us to establish a 6-bromoindol-3-yl residue as a partial structure of 1. The singlet at δ H 8.45 (H-2), and a spin system comprised of signals at δ H 8.07 (1H, d, J=8.0 Hz, H-4), 7.40 (1H, dd, J=8.0, 2.0 Hz, H-5), and 7.73 (1H, d, J=2.0, H-7) indicated the presence of a 6-bromoindol-3-yl moiety (Table 1). Long-range correlations from H-4 (δ H 8.07) to C-3 (δ C 112.5) and C-6 (δ C 116.2), along with the COSY correlation between H-4 and H-5, and the long-range correlations from H-5 (δ H 7.40) to C-3a (δ C 124.8) and C-7 (115.5) strongly suggested the presence of a 6-bromoindol-3-yl moiety.
The NMR signals at δ C 178.2 (C-8), δ C 164.0 (C-9), and δ H 3.89 (-OCH 3 , 3H), along with the HMBC correlations of -OCH 3 /C-9, suggested an oxoacetic acid methyl ester moiety. The EIMS fragments at m/z 194/196, corresponding to C 8 H 5 BrN, corroborated the presence of a bromoindole group. These fragments, along with the fragments at m/z 222/224 revealed the presence of a 3-carbonyl-bromoindole group, and established the connectivity between the 6-bromoindole moiety and the oxoacetic acid methyl ester moiety ( Figure 2). Therefore, compound 1 was defined as (6-bromo-1H-indol-3-yl) oxoacetic acid methyl ester. Compound 1 was known as an intermediate in the synthesis of some marine natural products, such as didemnimides A and B [13], whereas it has not been reported from a natural source. Pyruvic acid derivatives are unusual natural products, and most of indole pyruvic acid derivatives were isolated from marine sponges [14−16] and ascidians [6].  Compound 2 was isolated as a yellow, amorphous powder. The molecular formula was established as C 11 H 9 NO 3 on the basis of the FABMS and NMR data. In the LRFABMS of 2, a (M + H) + ion was observed at m/z 204. The main difference from compound 1 was lack of bromine atom on the indole ring. Therefore, compound 2 was defined as (1H-indol-3-yl) oxoacetic acid methyl ester. Compound 2 was known as an intermediate in the synthesis of natural products, such as didemnimides A and B [13], rebeccamycin, and 11-dechlororebeccamycin [17], whereas it has not been reported as a natural product.
Compound 3 was isolated as a yellow, amorphous powder. The molecular formula was established as C 11 H 9 NO 4 on the basis of the EIMS and NMR data. In the LREIMS of 1, a (M) + ion was observed at m/z 219. The main difference from compound 2 was an additional hydroxyl group on the indole ring. , and H-7 (δ H 6.87) to C-3a (δ C 118.5), from H-2 to C-3 (δ C 112.5) and C-7a (δ C 138.5), and from H-5 (δ H 6.74) to C-6 (δ C 154.4), indicated the presence of a 6-hydroxyindol-3-yl moiety. The EIMS fragments at m/z 132 and 160 corroborated the proposed structure ( Figure 2). Therefore, compound 3 was defined as (6-hydroxy-1H-indol-3-yl) oxoacetic acid methyl ester. To the best of our knowledge, compound 3 has not been reported previously either from a natural source or as a synthetic product.
Compound 4 was isolated as a white, amorphous powder. The molecular formula was established as C 10 H 8 N 2 O 2 on the basis of the EIMS and NMR data. In the LREIMS of 3, a (M) + ion was observed at m/z 188. The main difference from compound 2 was the presence of an oxoacetamide moiety instead of the oxoacetic acid methyl ester moiety. The 13 C signals at δ C 182.9 (C-8) and δ C 165.9 (C-9), the 1 H singlets at δ H 8.06 and δ H 7.69 (each 1H, -NH 2 ) (Tables 1 and 2), along with the long-range correlation between -NH 2 (δ H 7.69) and C-8 (δ C 182.9), established an oxoacetamide moiety. The EIMS fragments at m/z 116 and 144 revealed the presence of a 3-carbonylindole group, and established the connectivity between the oxoacetamide moiety and the indole moiety ( Figure 2). Thus, compound 4 was defined as (1H-indol-3-yl) oxoacetamide, which was also known as an intermediate in the synthesis of some marine natural products, such as arborescidines [18] and dihydrohamacanthins [19], but has not been isolated previously from a natural source.
Compound 5 was isolated as a yellow, amorphous powder. The molecular formula was established as C 10 H 7 BrN 2 O 2 on the basis of the EIMS and NMR data. In the EIMS data of 5, a (M) + ion cluster was observed at m/z 266/268. The main difference from compound 4 was an additional bromine atom on the indole ring. The fragments at m/z 194/196 and 222/224 revealed the presence of 3-carbonylbromoindole group (Figure 2). Therefore, compound 5 was defined as (6-bromo-1H-indol-3-yl) oxoacetamide, which was also reported as an intermediate in the synthesis of some natural products, such as arborescidines [18], dihydrohamacanthins [19], but has not been isolated from a natural source.
Compound 6 was isolated as colorless oil. The molecular formula was established as C 10 H 9 NO 3 on the basis of the EIMS and NMR data. In the LREIMS of 6, a [M] + ion was observed at m/z 191. Analysis of the 1 H, 13 C, COSY, HMBC, and HSQC data, allowed us to establish a 6-hydroxyindol residue as a partial structure of 6. The long-range correlation from H-2 (δ H 7.86, 1H, s) and -OCH 3 (δ H 3.76, 3H, s) to C-8 (δ C 164.8) established the presence of a formic acid methyl ester and the connectivity between the 6-hydroxyindol moiety and the carboxylic acid methyl ester. The EIMS fragments at m/z 132 and 160 corroborated the proposed structure ( Figure 1). Therefore, compound 6 was defined as (6-hydroxy-1H-indol-3-yl) carboxylic acid methyl ester, which was known as an intermediate in the organic synthesis of a 5-HT 4 receptor antagonist [20], but has not been reported from a natural source.
Compound 7 was also isolated as a yellow, amorphous powder. According to the MS and NMR data of 7, the main difference from 6 was lack of a hydroxyl group in the indole moiety. The MS and NMR data of 7 matched well with reported data [8], and was identified as (1H-indol-3-yl) carboxylic acid methyl ester which was previously reported from marine-derived bacteria [8] and fungi [21], and red alga [22], with cytotoxicity against K562 human chronic leukemia (MIC s 14.0 μg/mL) [21]. It is expected that (1H-indol-3-yl) oxoacetamide derivatives serve as intermediate for the biogenesis of co-occurring bisindole alkaloids, topsentins and hamacanthins [11,12] (Scheme 1). Schiff base formation between amino and carbonyl groups may (either via a or b) leads to the genesis of hamacanthin A (Ⅰ) and topsentin (Ⅱ) skeletons. Cleavage of the C−N bond (c) in the topsentin skeleton, and successive Schiff base formation between newly generated amino group and the intact carbonyl group may lead to a genesis of hamacanthin B skeleton (Ⅲ).

Animal Material
The sponges were collected by hand using SCUBA (20 m depth) in October 2002, off the coast of Jeju Island, Korea. The collected sample was a loose association of two sponges Spongosorites sp. and Halichondria sp. The two sponges were separated and only Spongosorites sp. was subjected to chemical analysis. The morphology of the sponge was described elsewhere [11]. A voucher specimen (registry No. Spo. 44) is deposited at the Natural History Museum, Hannam University. Korea.

Evaluation of Cytotoxicity
A panel of five human solid tumor cell lines, human lung cancer, human ovarian cancer, human skin cancer, human CNS cancer, and human colon cancer, were used to screen cytotoxicity of the compounds based on an established protocol [11,12].