Next Article in Journal
Nutritional Profiling and the Value of Processing By-Products from Gilthead Sea Bream (Sparus aurata)
Next Article in Special Issue
Polyketide Derivatives from Mangrove Derived Endophytic Fungus Pseudopestalotiopsis theae
Previous Article in Journal
Novel Vibrio spp. Strains Producing Omega-3 Fatty Acids Isolated from Coastal Seawater
Previous Article in Special Issue
Four New Insecticidal Xanthene Derivatives from the Mangrove-Derived Fungus Penicillium sp. JY246
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Marine Drugs
Volume 18
Issue 2
10.3390/md18020100
marinedrugs-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Monarubins A–C from the Marine Shellfish-Associated Fungus Monascus ruber BB5

by
Yan-Qin Ran
1,
Wen-Jian Lan
2,
Yi Qiu
3,
Qi Guo
3,
Gong-Kan Feng
4,
Rong Deng
4,
Xiao-Feng Zhu
4,
Hou-Jin Li
3,* and
Jun Dong
1,*
1
School of Traditional Chinese Medicine, Guangdong Pharmaceutical University, Guangzhou 510006, China
2
School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510006, China
3
School of Chemistry, Sun Yat-sen University, Guangzhou 510275, China
4
State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Cancer Center, Sun Yat-sen University, Guangzhou 510060, China
*
Authors to whom correspondence should be addressed.
Mar. Drugs 2020, 18(2), 100; https://doi.org/10.3390/md18020100
Submission received: 14 January 2020 / Revised: 2 February 2020 / Accepted: 3 February 2020 / Published: 3 February 2020
(This article belongs to the Special Issue New Challenges in Structure Elucidation of Marine Natural Products: NMR Analyses and Other Advanced Methods)
Browse Figures
Versions Notes

Abstract

:
Three new compounds, monarubins A–C (1, 6 and 13), together with ten known compounds, including four alkaloids (2–5), two isocoumarins (7 and 8) and four polyketides (9–12), were isolated from marine shellfish-associated fungus Monascus ruber BB5. The structures were determined on the basis of the 1D and 2D NMR, MS, UV and IR data. The absolute configurations of compounds 3, 6 and 13 were determined by ECD calculations. The NMR data of compounds deoxyhydroxyaspergillic acid (3) and 2-hydroxy-6-(1-hydroxy-1-methylpropyl)-3-sec-buthylpyrazine (4) were first reported. All of the isolated compounds were evaluated for their cytotoxic activities against human nasopharyngeal carcinoma cell lines CNE1, CNE2, SUNE1 and HONE1 and hepatocellular carcinoma cell lines QGY7701 and HepG2. Monarubin B (6) displayed potent cytotoxicities against the cancer cell lines HepG2 and QGY7701 with IC50 values of 1.72 and 0.71 μΜ, respectively; lunatinin (7) showed moderate cytotoxic activities against the cancer cell lines HepG2, QGY7701 and SUNE1 with the IC50 values of 9.60, 7.12 and 28.12 μΜ, respectively.

Graphical Abstract

1. Introduction

Since 1990, marine aquatic production in China has ranked first in the world, among them, edible marine shellfishes are exceeding 75% of the total output [1]. From an academic perspective, the current researches on marine shellfishes mainly focus on the cultivation, breeding methods, heavy metal accumulation and shellfish toxins [2,3,4,5]. Molluscan shellfish concentrate microorganisms from surrounding waters during the filter-feeding process. Consequently, filter feeders are recognized as reservoirs for various microorganisms [6]. However, up to now, the marine shellfish-associated fungi are virtually untouched and represent new promising sources of bioactive metabolites.
Recently, a fungal strain Monascus ruber (collection number BB5) was isolated from the inner tissue of marine shellfish Meretrix meretrix collected from Hailing island, Yangjiang, China. The genera Monascus mainly consists of four species: M. ruber, M. purpureus, M. anka and M. pilosus [7]. In Asia, Monascus fermented rice has been used as a traditional medicine for centuries and as a healthy food to improve the color and delicacy of meat, fish and soybean products [7]. Monascus species can produce chemodiverse secondary metabolites including monascus pigments, monacolins, azaphilones, furanoisophthalides, amino acids, γ-lactams, pyranoindole alkaloids, benzenoids, furans, fatty acids and other structural types [8,9,10,11,12]. Some metabolites display various biological activities, such as anticancer, antibacterial, anti-inflammatory, antioxidative, enzyme inhibitor, antihypertensive and reducing plasma cholesterol activities [13,14,15,16,17]. For example, monacolin K, a polyketide first isolated from the Monascus ruber in 1973, is considered as the most efficacious compound for lowering plasma cholesterol and has been approved as a clinical prescription named lovastatin [8,17]. According to the data from IMS Health, over 10 billion tablets of monacolin K were distributed and more than 100 million prescriptions were written worldwide between the years 1988 and 2003 [17]. Considering the fungal biodiversity and huge metabolic potential, it is still worthwhile to investigate the secondary metabolites of Monascus species and their bioactivities.
In recent years, we have continuously conducted research on the metabolites of marine fungi associated with marine invertebrates such as soft corals, starfishes and sponges from the South China Sea. Our primary objective is to search for chemotherapeutic agents for prevalent malignancies with remarkably high incidence in South China, such as nasopharyngeal carcinoma and hepatocellular carcinoma. As a result, we obtained a series of cytotoxic metabolites, for example hirsutanol A [18], incarnal [19], chondrosterins A and J–M [20,21,22], pseudaboydin A [23], xanthocillin X dimethyl ether [24], 7-deacetylpyripyropene A [25], pyripyropene O [25], 13-dehydroxypyripyropene A [25] and 3,3′-cyclohexylidenebis(1H-indole) [26]. As part of our continuous project, culture of the fungus Monascus ruber BB5 with liquid GPY culture medium led to the isolation of three new compounds, monarubins A–C (1, 6 and 13), together with ten known metabolites (2–5 and 7–12) (Figure 1). Here, we reported the isolation, the structure identification and cytotoxic activities of these compounds.

2. Results and Discussion

2.1. Structural Elucidation

Compound 1 was isolated as white needles. The molecular formula was determined as C12H18N2O by HR-(+) ESI-MS molecular ion peak at m/z 207.14923 [M + H]+ (calcd. for C12H19N2O, 207.14919) (Supplementary Figure S1), implying five degrees of unsaturation. The IR spectrum showed an amide group (3405 and 1639 cm−1). UV maxima at 201, 239 and 329 nm indicated the presence of a conjugated system. The 13C NMR and DEPT spectra showed three methyls, three methylenes, two methines and four quaternary carbons (Supplementary Figures S3 and S4). The 1H NMR and HMQC spectra displayed one amide proton [δH 10.83 (brs)], one aromatic proton [δH 7.41 (s), δC 120.9], one terminal olefinic double bond [δH 5.66 (s), 5.35 (s), δC 115.0], two methylenes [δH 2.69 (d, 7.0 Hz, 2H), δC 41.8; δH 2.46 (q, 7.0 Hz, 2H), δC 26.0] and three methyls [δH 1.17 (t, 7.0 Hz, 3H), δC 12.6; 0.98 (d, 7.0 Hz, 6H), δC 22.7] (Table 1 and Supplementary Figures S2 and S5). The correlations of H2-7/H-8/H3-9 and H3-10, and of H2-12/H3-13 in the 1H–1H COSY spectrum revealed the presence of isobutyl and −CH2CH3 fragments, respectively (Figure 2 and Supplementary Figure S6). The key HMBC correlations of H-5/C-6 (δC 135.1), C-11 (δC 140.8), and H2-12/C-6, C-11 and C-14 (δC 115.0), H3-13/C-11, H-14a (δH 5.35)/C-6, H-14b (δH 5.66)/C-6 and C-11 indicated the connection of the −CH2CH3 fragment with the C-11, which in turn was linked to C-6. The key HMBC correlations of H2-7/C-2 (δC 156.9), C-3 (δC 159.5), H-8/C-3 displayed the connection of the isobutyl to C-3 (Supplementary Figures S7 and S8). The NOESY correlations of H-5/H2-12, H-14a (δH 5.35)/H2-12, and H-14a/H3-13 suggested that the H-5, H2-12 and H3-13 were oriented on the same side of the molecule, H-14a being close to the ethyl and away from the pyrazinone ring (Figure 2). Therefore, the chemical structure of compound 1 was unambiguously established, and it was named monarubin A.
Compound 6 was obtained as a white solid. The HR-(+)ESI-MS spectrum displayed a strong quasi-molecular ion peak at m/z 265.10703 [M + H]+, corresponding to the molecular formula C14H16O5 (Supplementary Figure S19), requiring seven degrees of unsaturation. IR absorptions at 3380, 1678 and 1633 cm−1 indicated the existence of hydroxyl and ester carbonyl groups. The UV absorptions at λmax 241, 280 and 331 nm displayed the conjugated system containing a benzene ring. The 13C NMR and DEPT spectra showed three methyls, one methylene, three methines and seven quaternary carbons (Supplementary Figures S21 and S22). The 1H NMR and HMQC spectra revealed one phenolic hydroxyl group [δH 11.15 (brs)], two double-bond protons [δH 6.32 (s), δC 97.2; δH 6.30 (s), δC 106.3], one oxygen-bearing methine multiplet [δH 4.26 (m), δC 65.5], one methoxy group [δH 3.90 (s), δC 55.8], one methylene group [δH 2.59 (dd, 14.4, 8.0 Hz), 2.66 (dd, 14.4, 4.4 Hz), δC 43.0], a methyl group on the benzene ring [δH 2.12 (s), δC 7.9] and the other methyl group [δH 1.30 (d, 6.0 Hz), δC 23.2] (Table 2 and Supplementary Figures S20 and S23). The presence of the –CH2CH(CH3)– moiety was based on the 1H–1H COSY correlations of H3-11/H-10/H2-9 (Supplementary Figure S24). The HMBC correlations from the phenolic hydroxyl at δH 11.15 (OH-8) to C-7 (δC 112.6), C-8 (δC 159.9) and C-8a (δC 99.9), from the methyl group at δH 2.12 to C-6 (δC 164.6), C-7 and C-8, from the methoxy group H3-13 (δH 3.90) to C-5 (δC 97.2) and C-6, from H-5 to C-4 (δC 106.3), C-6, C-7 and C-8a, from H-4 to C-3 (δC 153.8), C-5 and C-8a revealed the presence of 6-methyoxy-7-methy-8-hydroxy isochromone skeleton (Figure 2 and Supplementary Figure S25). Methoxy linked to C-6 was further supported by the NOESY correlations between proton H-5 and methyl protons H3-13 (Figure 2 and Supplementary Figure S26). The connection of C-3 with carbons C-9 (δC 43.0) and C-4 was established by HMBC correlations from the methylenic protons H2-9 (δH 2.59 and 2.66) to carbons C-3 and C-4, and from the olefinic proton H-4 (δH 6.30) to carbons C-3 and C-9.
The absolute configuration of 6 was elucidated by a comparison of the experimental and calculated electronic circular dichroism (ECD) curves (Figure 3). The calculated ECD curves were obtained by the time-dependent density functional theory (TD-DFT) at the B3LYP/6-311+G (d, p) level. The ECD curve of 10S-6 was in line with the experimental curve. Based on the analysis above, the structure of compound 6 was assigned as (S)-8-hydroxy-3-(2-hydroxypropyl)-6-methoxy-7-methyl-1H-isochromen-1-one, and it was trivially named as monarubin B.
Compound 13 was isolated as a colorless oil. The molecular formula was established as C21H30O5 by HR-(+) ESI-MS at m/z 363.21664 [M + H]+ (calcd. for C21H31O5, 363.21664) (Supplementary Figure S39), which has seven degrees of unsaturation. The IR absorptions at 3422, 1781, 1695 and 1631 cm−1 and UV maxima at 243 nm indicated the presence of hydroxyl group, ketone carbonyl, ester carbonyl and a conjugated system. The 13C NMR, DEPT and HMQC spectra displayed three methyls, seven methylenes, six methines and five quaternary carbons. Among them, the quaternary carbons at δC 192.4 and 174.7 indicated the presence of one ketone carbonyl and one ester carbonyl, respectively and the four carbons at δC 82.9, 73.4, 69.4 and 63.6, their connection to oxygen atoms (Supplementary Figures S41–S43). The 1H NMR and HMQC spectra showed two trans olefinic protons [δH 5.78 (dqd, 15.6, 6.6, 1.2 Hz) and 5.52 (ddq, 15.6, 6.6, 1.2 Hz)], three methylenes [δH 4.44 (brd, 16.2 Hz), 4.37 (brd, 16.2 Hz), δC 63.6; 2.58 (m, 2H), δC 34.0; 2.35 (dd, 18.0, 9.0 Hz), 2.22 (ddd, 18.0, 3.0, 3.0 Hz), δC 36.2] and two oxygen-bearing methine multiplets [δH 4.22 (m), δC 69.4; 4.00 (m), δC 73.4] (Table 2 and Supplementary Figure S40). The 1H−1H COSY correlations of H2-4/H-3/H-13/H-14/H3-15 showed a partial structure –CH2CHCH=CHCH3 (Figure 2 and Supplementary Figure S44). The 1-hydroxyhexyl side chain was deduced from the 1H−1H COSY cross peaks of H3-22/H2-21/H2-20/H2-19/H2-18/H-17 and the HMBC correlations from H3-22 to C-21 (δC 22.5) and C-20 (δC 31.5), H-17 to C-18 (δC 35.0) and C-19 (δC 25.8) and OH-17 to C-18. The 1H−1H COSY cross-peaks of H-17/H-11/H-6 as well as the HMBC correlations from H-11 to C-17 (δC 69.4), C-5 (δC 34.0), C-6 (δC 41.3) and C-12 (δC 174.7) revealed that the 1-hydroxyhexyl side chain was connected with a γ-lactone (ring C). The HMBC correlations of H-1b to C-3 (δC 73.4), C-9 (δC 151.6) and C-10 (δC 129.6), H-3 to C-1 and C-10, H-4a to C-9 and C-10, H-4b to C-3, C-9 and C-10, H-5 to C-6 (δC 41.3), C-7 (δC 82.9), C-9 and C-10, H-6 to C-5 (δC 34.0), C-7 and C-8 (δC 192.4), H3-16 to C-7 and C-8 displayed the connection of ring A with ring B. Ring C was combined with ring B by the HMBC the correlations from H-6 to C-5, C-7, C-8 and C-11 (δC 174.7), H-11 to C-5, C-6 and C-12, H3-16 to C-7 and C-8 and was supported by the 1H−1H COSY correlations of H-11/H-6/H2-5 (Figure 2 and Supplementary Figures S44 and S45). Therefore, the planar structure of 13 was established and given the name monarubin C.
The relative stereochemistry of 13 was identified by the NOESY data. The large coupling constant (13.2 Hz) of the proton H-6 [δH 3.04 (ddd, 13.2, 9.6, 6.0 Hz)] with the proton H-11 [δH 2.75 (dd, 13.2, 3.0 Hz)] indicated that they were in opposite position on the ring. The NOESY cross peaks of H3-16 (δH 1.42) and H-11 (δH 2.75), H3-16 and H-1b (δH 4.44), H-1b and H-13 (δH 5.52) suggested that these protons were cofacial and assigned as β-orientation. The correlation between H-3 and H-1a (δH 4.37) suggested both of them having the α-orientation. The proton H-6 was determined as having an α-orientation because no NOESY correlation between H3-16 and H-6 was observed (Figure 2 and Supplementary Figure S46). Its absolute configuration was defined by calculated ECD. After calculation, it was found that the absolute configuration of C-17 was difficult to determine, 3S,6R,7R,11S,17R-13 and 3S,6R,7R,11S,17S-13 had almost the same result, which may be related to the fact that C-17 is too flexible in the branch, so only the absolute configuration of the remaining several chiral centers could be determined. By comparing the calculated curves with the experimental curve, the absolute configuration of compound 13 was defined as 3S,6R,7R,11S (Figure 3).
Deoxyhydroxyaspergillic acid (3) was obtained as white needles. The molecular formula was established as C12H20N2O2 by HR-(+) ESI-MS molecular ion peak at m/z 225.16019 [M + H]+ (calcd. for C12H21N2O2, 225.15975) (Supplementary Figure S11), implying four degrees of unsaturation. This is the first report of its NMR data (Table 1 and Supplementary Figures S12 and S13) and absolute configuration, although its structure was reported by James D. Dutcher in 1957 [27]. Its absolute configuration was defined as 11R by comparison of the experimental and ECD curves (Figure 4).
2-Hydroxy-6-(1-hydroxy-1-methylpropyl)-3-sec-buthylpyrazine (4) was afforded as white needles. The molecular formula was determined as C12H20N2O2 by HR-(+) ESI-MS at m/z 225.15967 [M + H]+ (calcd. for C12H21N2O2, 225.15975) (Supplementary Figure S14), which has four degrees of unsaturation. Fortunately, we obtained a single crystal of 4 from a MeOH solution. The absolute configuration was unambiguously determined as 11S by single-crystal X-ray diffraction (Figure 5). Although its planar structure was reported by Sasaki et al. in 1968 [28], its NMR data (Table 1 and Supplementary Figures S15 and S16) and absolute configuration are reported for the first time.
Compounds 2, 5 and 7–12 were elucidated as 3,6-diisobutyl-2(1H)-pyrazinone (2) [29], pulchellalactam (5) [30], lunatinin [also named 6, 8-dihydroxy-3-(2-hydroxypropyl)-7-methyl-1H-isochromen-1-one, 7] [31], 6,8-dimethoxy-3-methylisocoumarin (8) [32], monaspurpurone (9) [33], 5-amino-2,6-dimethyl-6-hydroxy-4-(2′-methyl-1-oxobutyl)-3-methoxy-2,4-cyclohexadien-1-one (10) [34], phomaligol A (11) [35] and monascuspiloin (12) [36], respectively, by comparing their spectroscopic data (Supplementary Figures S9, S10, S17, S18 and S27–S38) with the literature values. Some of the known compounds also showed various bioactivities. For example, pulchellalactam (5) exhibited potent CD45 protein tyrosine phosphatase inhibitor activity [30], lunatinin (7) was found to have a significant antibiofilm activity [37], monaspurpurone (9) showed strong DPPH radical scavenging activity [17], and monascuspiloin (12) showed effective inhibitory activity against both androgen-dependent LNCaP and androgen-independent PC-3 human prostate cancer cells [38,39].

2.2. Biological Activity

Compounds 1–13 were evaluated for their cytotoxic activity against six cancer cell lines, including four human nasopharyngeal carcinoma cell lines CNE1, CNE2, SUNE1 and HONE1 and two human hepatocellular cancer cell lines HepG2 and QGY7701. As a result, compound 6 displayed potent cytotoxicities against the hepatocellular cancer cell lines HepG2 and QGY7701 with the IC50 values of 1.72 and 0.71 μΜ, respectively (Table 3 and Supplementary Tables S2 and S3). Compound 7 showed moderate inhibitory effects against the cancer cell lines HepG2, QGY7701 and SUNE1 with the IC50 values of 9.60, 7.12 and 28.12 μΜ, respectively (Table 3, Supplementary Tables S4–S6). Compound 8 exhibited weak cytotoxic activities against the cancer cell lines HepG2, QGY7701 and SUNE1 with the IC50 values of 46.10, 31.62 and 39.38 μΜ (Table 3). The new compounds monarubins A and C (1 and 13) and known compounds 2–5 and 9–12 were apparently inactive (IC50 values > 100 μΜ) in this assay. Hirsutanol A was used as a positive control [18,40,41].

3. Materials and Methods

3.1. General Procedures

Silica gel (SiO2, 200–300 mesh, Qingdao Puke parting Materials Co., Ltd. Qingdao, China) was used for the column chromatography. Preparative HPLC was performed using a Shimadzu LC-20AT HPLC pump (Shimadzu Corporation, Nakagyo-ku, Kyoto, Japan) equipped with a SPD-20A dual λ absorbance detector (Shimadzu Corporation, Nakagyo-ku, Kyoto, Japan) and a Capcell-Pak C18 UG80 HPLC column (250 × 20 mm, Shiseido Co., Ltd., Minato-ku, Tokyo, Japan). UV spectra were measured using Shimadzu UV–Vis–NIR spectrophotometer (Shimadzu Corporation, Nakagyo-ku, Kyoto, Japan). IR data were obtained on a PerkinElmer Frontier FT-IR spectrophotometer (PerkinElmer Inc., Waltham, MA, USA). CD spectra were measured on a J1700 circular dichroism spectrometer (Jasco, Kyoto, Japan). The high-resolution ESI-MS spectra were obtained on Thermo Fisher LTQ Orbitrap Elite High-Resolution liquid chromatography–mass spectrometer (Thermo Fisher Scientific Inc., Waltham, MA, USA). 1D and 2D NMR spectra were recorded on Bruker Avance Ⅲ 400, Avance 500 and Avance 600 spectrometers (Bruker Bio Spin AG, Industriestrasse 26, Fällanden, Switzerland). The chemical shifts corresponding to the residual solvent signals were the following (CDCl3: δH 7.260 and δC 77.000; acetone-d6: δH 2.050 and δC 29.840).

3.2. Fungal Strain and Culture Method

The marine fugus Monascus ruber BB5 was isolated from Meretrix meretrix collected from Hailing Island, Yangjiang, China. This fungal strain was conserved in 15% (v/v) glycerol aqueous solution at −80 °C. A voucher specimen (code name 2019FBB5) was deposited in the School of Chemistry, Sun Yat-sen University, Guangzhou, China. Analysis of the ITS rDNA by BLAST database screening provided 99.9% match with Monascus ruber.
The fermentation medium was glucose 20 g, peptone 10 g, yeast extract 2 g, Na2HPO4 2 g, sea salt 25 g and water 1 L. Fungal mycelia were cut and transferred aseptically to 1000 mL conical flasks each containing 400 mL sterilized liquid medium. The flasks were static incubated at 28 °C for 30 d.

3.3. Extraction and Isolation

The fungal strain was fermented in total 200 L. The culture broth was filtered by cheesecloth and successively extracted three times with EtOAc. The extract was concentrated by low-temperature rotary evaporation to obtain a crude extract (46.7 g).
The extract was separated on silica gel column (diameter: 6 cm, length: 100 cm, silica gel: 200 g) with a gradient of petroleum ether–EtOAc (10:0–0:10, v/v) followed by EtOAc–MeOH (10:0–0:10) to give 15 fractions (Fr.1–Fr.15). Fr.10 was purified by silica gel column using a step gradient elution with petroleum ether–EtOAc (10:0–0:10) to get 12 subfractions (Fr.10-1–Fr.10-12). HPLC purification of Fr.10-2 with a solvent system CH3OH–H2O (70:30, v/v) gave compound 1 (RT = 55 min, 1 mg). Fr.7 was purified by C-18 reversed-phase column to get 9 subfractions (Fr.7-1–Fr.7-9). Fr.7-3 was eluted with CH3OH–H2O (60:40, v/v) by preparative HPLC to obtain compounds 2 (RT = 49 min, 11.2 mg) and 10 (RT = 44 min, 22.9 mg). Fr.11 was chromatographed by silica gel column using a step gradient elution with petroleum ether–EtOAc (10:0–0:10) to get 25 subfractions (Fr.11-1–Fr.11-25). Fr.11-11 was purified with a solvent system CH3OH–H2O (65:35, v/v) by preparation HPLC to obtain compounds 3 (RT = 57 min, 5.5 mg), 4 (RT = 61 min, 6 mg), 6 (RT = 132 min, 6.6 mg) and 8 (RT = 51 min, 5.3 mg). Compound 11 (RT = 57 min, 1 mg) was obtained from the Fr.11-13 by preparation HPLC using CH3OH–H2O (60:40, v/v) as elution. Fr.11-14 was purified by preparative HPLC (CH3OH–H2O, 70:30, v/v) to obtain compounds 7 (RT = 53 min, 1.6 mg) and 9 (RT = 35 min, 1 mg). Fr.8 was separated by silica gel column using a step gradient elution with petroleum ether EtOAc (10:0-10:0) to get 7 subfractions (Fr.8-1–Fr.8-7), and compound 5 (RT = 37 min, 23 mg) was obtained from Fr.8-2 by preparative HPLC using CH3OH–H2O (80:20, v/v) as eluent. Fr.8-4 was purified by preparative HPLC (CH3OH–H2O, 80:20, v/v) to obtain compounds 12 (RT = 47 min, 10 mg) and 13 (RT = 42 min, 1.5 mg).
Monarubin A (1). UV (MeOH) λmax (logε) 330 (3.69), 239 (3.71), 202 (3.90). IR υmax 3405, 2963, 1639, 1583, 1411, 1265, 1096, 1044, 801 cm−1. 1H and 13C NMR data, see Table 1; HR-(+) ESI-MS m/z 207.14923 [M + H]+ (calcd. for C12H19N2O, 207.14919).
Deoxyhydroxy aspergillic acid (3). ECD (0.4 mM, MeOH) λmax (Δε) 211 (+0.51), 228 (+4.24), 309 (−2.63) nm. 1H and 13C NMR data, see Table 1; HR-(+) ESI-MS m/z 225.16019 [M + H]+ (calcd. for C12H21N2O2, 225.15975).
2-Hydroxy-6-(1-hydroxy-1-methylpropyl)-3-sec-buthylpyrazine (4). 1H and 13C NMR data, see Table 1; HR-(+) ESI-MS m/z 225.15967 [M + H]+ (calcd. for C12H21N2O2, 225.15975).
Monarubin B (6). [α]25 D + 19 (c = 0.001, MeOH), UV (MeOH) λmax (logε) 331 (3.62), 280 (3.71), 241 (4.49). ECD (0.7 mM, MeOH) λmax (Δε) 289 (+3.79) nm. IR υmax 3380, 2927, 1673, 1634, 1566, 1520, 1423, 1348, 1252, 1124, 939, 796 cm−1. 1H and 13C NMR data, see Table 2; HR-(+) ESI-MS m/z 265.10703 [M + H]+ (calcd. for C14H17O5, 265.10705).
Monarubin C (13). [α]25 D + 43 (c = 0.001, MeOH), UV (MeOH) λmax (logε) 243 (3.89). ECD (0.5 mM, MeOH) λmax (Δε) 246 (20.99) nm. IR υmax 3422, 2934, 1781, 1695, 1631, 1392, 1261, 1209, 1094, 1051, 965, 804 cm−1. 1H and 13C NMR data, see Table 3; HR-(+) ESI-MS m/z 363.21664 [M + H]+ (calcd. for C21H31O5, 363.21664).

3.4. Computational Methods

The absolute configurations of compounds 3, 6 and 13 were determined by ECD calculations using Gaussian 09 software. Conformational searches were carried out by means of the Spartan’14 software using a Molecular Merck force field (MMFF). The conformers with a Boltzmann distribution over 2% were chosen for ECD calculations by TD-DFT method at the B3LYP/6-311+G (d, p) level in methanol (Supplementary Figures S47–S54). The ECD spectra were generated by the SpecDis 3.0 using a Gaussian band shape with a 0.3 eV exponential half-width from dipole-length dipolar and rotational strengths.

3.5. X-ray Crystallographic Analysis for 4

Crystals of 4 were obtained from MeOH solution. X-ray diffraction data were collected on a Bruker SMART APEX CCD diffractometer with Cu Kα radiation (λ = 1.54184 Å). The structure was solved by direct methods using SHELXS-97, and refined through the program and full-matrix least-squares calculations. Hydrogen atoms were refined at calculated positions, and all non-hydrogen atoms were fixed anisotropically. Crystallographic data of 4 have been deposited at the Cambridge Crystallographic Data Centre (CCDC number: 1958991).
Crystal data of 4: monoclinic, C12H20N2O2, a = 11.77370(10) Å, b = 6.91360(10) Å, c = 16.5776(2) Å, α = γ = 90°, β = 91.3700(10)°, V = 1349.01(3) Å3, space group P21, Z = 2, Dc = 1.104 g/cm3, μ = 0.607 mm−1, and F(000) = 488.0. Independent reflections: 5242 (Rint = 0.0525). The final R1 value was 0.0570, wR2 = 0.1619 (I > 2σ(I)). The goodness of fit on F2 was 1.039. Flack parameter = −0.04(7) (Supplementary Table S1).

3.6. Cytotoxicity Assay

Human nasopharyngeal carcinoma cell lines CNE1, CNE2, SUNE1 and HONE1 and hepatocellular carcinoma cell lines QGY-7701 and HepG2 were generously provided by Professor Mu-Sheng Zeng (Cancer Center, Sun Yat-sen University, Guangzhou, China) and conserved in the State Key Laboratory of Oncology in South China, Cancer Center, Sun Yat-sen University. The culture medium was DMEM (Gibco®, Suzhou, China) with 10% fetal bovine serum (FBS) (Gibco®). All of the cells were authenticated using short tandem repeat profiling, tested for Mycoplasma contamination, and cultured for less than 2 months.
The in vitro cytotoxic activities of 1–13 were determined by means of the colorimetric 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) assays and the assays were performed in triplicate. The cells were maintained at 37 °C with 5% CO2 and were seeded in 96-well plates. The volume and number of cells seeded was 0.2 mL and 3 × 103 per well. Compounds 1–13 were added to the cultures at different concentrations (1.5625–100 μM); moreover, compound 6 was tested at additional different concentrations (0.037–27 μM). Solvent DMSO was added as the control. After 72 h, 0.5 mg/mL MTT was added to the culture medium, and the plates were incubated for 4 h at 37 °C. The supernatant was removed. The formazan crystals were dissolved in DMSO (150 µL), the absorbance was measured at 570 nm by using a microplate reader (Bio-Rad, Hercules, CA, USA), and the data were analyzed with the CalcuSystem software package. Hirsutanol A, a potent anticancer agent isolated from marine fungal metabolites, was used as a positive control, and its cytotoxic activities against the tested cancer cell lines were shown in Table 3.

4. Conclusions

Three new metabolites, monarubins A–C, together with ten known compounds containing alkaloids, isocoumarins and polyketides were isolated from the fungal strain Monascus ruber BB5. Monarubin B (6) showed potent cytotoxic activities against the human hepatocellular cancer cell lines HepG2 and QGY7701 with IC50 values of 1.72 and 0.71 μΜ, and lunatinin (7) exhibited moderate inhibitory effects against the human hepatocellular cancer cell lines HepG2, QGY7701, and nasopharyngeal carcinoma cancer cell line SUNE1 with IC50 values of 9.60, 7.12 and 28.12 μΜ, respectively. Compound 8 exhibited weak cytotoxic activities against the cancer cell lines HepG2, QGY7701 and SUNE1 with IC50 values in the range of 30–50 μΜ. Compounds 6–8 have the same isocoumarin skeleton. By comparing their structures and activities, we can preliminarily conclude that 8-OH is an essential active functional group. Our finding once again demonstrates that Monascus are genius strains with the ability to produce chemodiverse bioactive compounds.

Supplementary Materials

The following are available online at https://www.mdpi.com/1660-3397/18/2/100/s1. Figures S1–S45: The HR-(+)ESI-MS and NMR spectra of compounds 1–13, Figures S46–S53: the most stable conformers of 3, 6 and 13, Table S1 and CIF file: the X-ray crystallography data of 4 and Tables S2–S6: the cytotoxic activities data of 6 and 7.

Author Contributions

Conceived and designed the experiments: J.D., H.-J.L. and W.-J.L. Performed the experiments: Y.-Q.R., Y.Q. and Q.G., G.-K.F., R.D. and X.-F.Z. Wrote the paper: Y.-Q.R., J.D., H.-J.L. and W.-J.L. All authors have read and agreed to the published version of the manuscript.

Funding

This work was financially supported by the National Natural Science Foundation of China (No. 81872795), Guangdong Provincial Science and Technology Research Program (Nos. 2016A020222004 and 2019B070702003), Natural Science Foundation of Guangdong Province (No. 2018A030313157), and the National Science and Technology Major Project for New Drug Innovation and Development (No. 2017ZX09305010).

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Zhao, W.W.; Shen, H.H. A statistical analysis of China’s fisheries in the 12th five-year period. Aquac. Fish. 2016, 1, 41–49. [Google Scholar] [CrossRef]
  2. Ferreira, J.G.; Sequeira, A.; Hawkins, A.J.S.; Newton, A.; Nickell, T.D.; Pastres, R.; Forte, J.; Bodoy, A.; Bricker, S.B. Analysis of coastal and offshore aquaculture: Application of the FARM model to multiple systems and shellfish species. Aquaculture 2009, 289, 32–41. [Google Scholar] [CrossRef]
  3. Shapiro, K.; Silver, M.; Byrne, B.A.; Berardi, T.; Aguilar, B.; Melli, A.; Smith, W.A. Fecal indicator bacteria and zoonotic pathogens in marine snow and California mussels (Mytilus californianus). FEMS Microbiol. Ecol. 2018, 94, 172. [Google Scholar] [CrossRef] [PubMed]
  4. Salam, M.A.; Paul, S.C.; Noor, S.N.B.M.; Siddiqua, S.A.; Aka, T.D.; Wahab, R.; Aweng, E.R. Contamination profile of heavy metals in marine fish and shellfish. Glob. J. Environ. Sci. Manag. 2019, 5, 225–236. [Google Scholar]
  5. Hallegaeff, G.M. A review of harmful algal blooms and their apparent global increase. Phycologia 1993, 2, 79–99. [Google Scholar] [CrossRef] [Green Version]
  6. Natarajan, S.B.; Kim, Y.S.; Hwang, J.W.; Park, P.J. Immunomodulatory properties of shellfish derivatives associated with human health. RSC Adv. 2016, 6, 26163–26177. [Google Scholar] [CrossRef]
  7. Ma, J.Y.; Li, Y.G.; Ye, Q.; Li, J.; Hua, Y.J.; Ju, D.J.; Zhang, D.C.; Cooper, R.; Chang, M. Constituents of red yeast rice, a traditional Chinese food and medicine. J. Agric. Food Chem. 2000, 48, 5220–5225. [Google Scholar] [CrossRef]
  8. Wu, H.C.; Cheng, M.J.; Wu, M.D.; Chen, J.J.; Chen, Y.L.; Chang, H.S. Three new constituents from the fungus of Monascus purpureus and their anti-inflammatory activity. Phytochem. Lett. 2019, 31, 242–248. [Google Scholar] [CrossRef]
  9. Akihisa, T.; Tokuda, H.; Yasukawa, K.; Ukiya, M.; Kiyota, A.; Sakamoto, N.; Suzuki, T.; Tanabe, N.; Nishino, H. Azaphilones, furanoisophthalides, and amino acids from the extracts of Monascus pilosus-fermented rice red-mold rice and their chemopreventive effects. J. Agric. Food Chem. 2005, 53, 562–565. [Google Scholar] [CrossRef]
  10. Wei, W.D.; Lin, S.; Chen, M.H.; Liu, T.X.; Wang, A.; Li, J.J.; Guo, Q.L.; Shang, X.Y. Monascustin, an unusual γ-lactam from red yeast rice. J. Nat. Prod. 2017, 80, 201–204. [Google Scholar] [CrossRef]
  11. Huang, Z.B.; Xu, Y.; Li, L.S.; Li, Y.P. Two new Monascus metabolites with strong blue fluorescence isolated from red yeast rice. J. Agric. Food Chem. 2008, 56, 112–118. [Google Scholar] [CrossRef] [PubMed]
  12. Patakova, P. Monascus secondary metabolites: Production and biological activity. J. Ind. Microbiol. Biot. 2013, 40, 169–181. [Google Scholar] [CrossRef] [PubMed]
  13. Hong, M.Y.; Seeram, N.P.; Zhang, Y.J.; Heber, D. Anticancer effects of Chinese red yeast rice versus monacolin K alone on colon cancer cells. J. Nutr. Biochem. 2008, 19, 448–458. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  14. Cheng, M.J.; Wu, M.D.; Chen, I.S.; Tseng, M.; Yuan, G.F. Chemical constituents from the fungus Monascus purpureus and their antifungal activity. Phytochem. Lett. 2011, 4, 372–376. [Google Scholar] [CrossRef]
  15. Hsu, L.C.; Liang, Y.H.; Hsu, Y.W.; Kuo, Y.H.; Pan, T.M. Anti-inflammatory properties of yellow and orange pigments from Monascus purpureus NTU 568. J. Agric. Food Chem. 2013, 61, 2796–2802. [Google Scholar] [CrossRef]
  16. Lee, C.L.; Wang, J.J.; Pan, T.M. Red mold rice extract represses amyloid beta peptide-induced neurotoxicity via potent synergism of anti-inflammatory and antioxidative effect. Appl. Microbiol. Biotechnol. 2008, 79, 829–841. [Google Scholar] [CrossRef]
  17. Pandey, V.V.; Varshney, V.K.; Pandey, A. Lovastatin: A journey from ascomycetes to basidiomycetes fungi. J. Biol. Act. Product. Nat. 2019, 9, 162–178. [Google Scholar] [CrossRef]
  18. Li, H.J.; Lan, W.J.; Lam, C.K.; Yang, F.; Zhu, X.F. Hirsutane sesquiterpenoids from the marine-derived fungus Chondrostereum sp. Chem. Biodivers. 2011, 8, 317–324. [Google Scholar] [CrossRef]
  19. Li, H.J.; Chen, T.; Xie, Y.L.; Chen, W.D.; Zhu, X.F.; Lan, W.J. Isolation and structure elucidation of chondrosterins F–H from the marine fungus Chondrostereum sp. Mar. Drugs 2013, 11, 551–558. [Google Scholar] [CrossRef] [Green Version]
  20. Li, H.J.; Xie, Y.L.; Xie, Z.L.; Chen, Y.; Lam, C.K.; Lan, W.J. Chondrosterins A–E, triquinane-type sesquiterpenoids from soft coral-associated fungus Chondrostereum sp. Mar. Drugs 2012, 10, 627–638. [Google Scholar] [CrossRef] [Green Version]
  21. Li, H.J.; Jiang, W.H.; Liang, W.L.; Huang, J.X.; Mo, Y.F.; Ding, Y.Q.; Lam, C.K.; Qian, X.J.; Zhu, X.F.; Lan, W.J. Induced marine fungus Chondrostereum sp. as a means of producing new sesquiterpenoids chondrosterins I and J by using glycerol as the carbon source. Mar. Drugs 2014, 12, 167–175. [Google Scholar] [CrossRef] [PubMed]
  22. Huang, L.; Lan, W.J.; Deng, R.; Feng, G.K.; Xu, Q.Y.; Hu, Z.Y.; Zhu, X.F.; Li, H.J. Additional new cytotoxic triquinane-type sesquiterpenoids chondrosterins K–M from the marine fungus Chondrostereum sp. Mar. Drugs 2016, 14, 157. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  23. Lan, W.J.; Liu, W.; Liang, W.L.; Xu, Z.; Le, X.; Xu, J.; Lam, C.K.; Yang, D.P.; Li, H.J.; Wang, L.Y. Pseudaboydins A and B, novel isobenzofuranone derivatives from marine fungus Pseudallescheria boydii associated with starfish Acanthaster planci. Mar. Drugs 2014, 12, 4188–4199. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  24. Huang, L.H.; Xu, M.Y.; Li, H.J.; Li, J.Q.; Chen, Y.X.; Ma, W.Z.; Li, Y.P.; Xu, J.; Yang, D.P.; Lan, W.J. Amino acid-directed strategy for inducing the marine-derived fungus Scedosporium apiospermum F41–1 to maximize alkaloid diversity. Org. Lett. 2017, 19, 4888–4891. [Google Scholar] [CrossRef]
  25. Cao, Q.X.; Wei, J.H.; Deng, R.; Feng, G.K.; Zhu, X.F.; Lan, W.J.; Li, H.J. Two new pyripyropenes from the marine fungus Fusarium sp. 2016F18-1. Chem. Biodivers. 2017, 14, e1600298. [Google Scholar] [CrossRef]
  26. Yuan, M.X.; Qiu, Y.; Ran, Y.Q.; Feng, G.K.; Deng, R.; Zhu, X.F.; Lan, W.J.; Li, H.J. Exploration of indole alkaloids from marine fungus Pseudallescheria boydii F44-1 using an amino acid-directed strategy. Mar. Drugs 2019, 17, 77. [Google Scholar] [CrossRef] [Green Version]
  27. Dutcher, J.D. Aspergillic acid: An antibiotic substance produced by Aspergillus flavus. III. Structure of hydroxyaspergillic acid. J. Biol. Chem. 1958, 232, 785–795. [Google Scholar]
  28. Sasaki, M.; Asao, Y.; Yokotsuka, T. Compounds produced by molds. III. Fluorescent compounds produced by Japanese commercial molds. Nippon Nogeikagaku Kaishi 1968, 42, 288–293. [Google Scholar] [CrossRef] [Green Version]
  29. Li, H.J.; Cai, Y.T.; Chen, Y.Y.; Lam, C.K.; Lan, W.J. Metabolites of marine fungus Aspergillus sp. collected from soft coral Sarcophyton tortuosum. Chem. Res. Chin. Univ. 2010, 26, 415–419. [Google Scholar]
  30. Alvi, K.A.; Casey, A.; Nair, B.G. Pulchellalactam: A CD45 protein tyrosine phosphatase inhibitor from the marine fungus Corollospora pulchella. J. Antibiot. 1997, 51, 515–517. [Google Scholar] [CrossRef] [Green Version]
  31. Yamaguchi, Y.; Masuma, R.; Kim, Y.P.; Uchida, R.; Tomoda, H.; Omura, S. Taxonomy and secondary metabolites of Pseudobotrytis sp. FKA-25. Mycoscience 2004, 45, 9–16. [Google Scholar] [CrossRef]
  32. Kendall, J.K.; Fisher, T.H. An improved synthesis of 6,8-dimethoxy-3-methylisocoumarin, a fungal metabolite precursor. J. Org. Chem. 1989, 54, 4218–4220. [Google Scholar] [CrossRef]
  33. Cheng, M.J.; Wu, M.D.; Chen, I.S.; Chen, C.Y.; Lo, W.L.; Yuan, G.F. Secondary metabolites from the red mould rice of Monascus purpureus BCRC 38113. Nat. Prod. Res. 2010, 24, 1719–1725. [Google Scholar] [CrossRef] [PubMed]
  34. Pedras, M.S.C.; Taylor, J.L.; Morales, V.M. Phomaligin A and other yellow pigments in Phoma lingam and P. wasabiae. Phytochemistry 1995, 38, 1215–1222. [Google Scholar] [CrossRef]
  35. Elbandy, M.; Shinde, P.B.; Hong, J.; Bae, K.S.; Kim, M.A.; Lee, S.M.; Jung, J.H. α-Pyrones and yellow pigments from the sponge-derived fungus Paecilomyces lilacinus. Bull. Korean Chem. Soc. 2009, 30, 188–192. [Google Scholar]
  36. Wu, M.D.; Cheng, M.J.; Liu, T.W.; Chen, Y.L.; Chan, H.Y.; Chen, H.P.; Wu, W.J.; Chen, K.P.; Yuan, G.F. Chemical constituents of the fungus Monascus pilosus BCRC 38093-fermented rice. Chem. Nat. Compd. 2015, 51, 554–556. [Google Scholar] [CrossRef]
  37. Zin, W.W.M.; Buttachon, S.; Dethoup, T.; Pereira, J.A.; Gales, L.; Inacio, A.; Costa, P.M.; Lee, M.; Sekeroglu, N.; Silva, A.M.S.; et al. Antibacterial and antibiofilm activities of the metabolites isolated from the culture of the mangrove-derived endophytic fungus Eurotium chevalieri KUFA 0006. Phytochemistry 2017, 141, 86–97. [Google Scholar] [CrossRef]
  38. Chiu, H.W.; Fang, W.H.; Chen, Y.L.; Wu, M.D.; Yuan, G.F.; Ho, S.Y.; Wang, Y.J. Monascuspiloin enhances the radiation sensitivity of human prostate cancer cells by stimulating endoplasmic reticulum stress and inducing autophagy. PLoS ONE 2012, 7, e40462. [Google Scholar] [CrossRef] [Green Version]
  39. Chen, R.J.; Hung, C.M.; Chen, Y.L.; Wu, M.D.; Yuan, G.F.; Wang, Y.J. Monascuspiloin induces apoptosis and autophagic cell death in human prostate cancer cells via the Akt and AMPK signaling pathways. J. Agric. Food Chem. 2012, 60, 7185–7193. [Google Scholar] [CrossRef]
  40. Yang, F.; Chen, W.D.; Deng, R.; Zhang, H.; Tang, J.; Wu, K.W.; Li, D.D.; Feng, G.K.; Lan, W.J.; Li, H.J.; et al. Hirsutanol A, a novel sesquiterpene compound from fungus Chondrostereum sp., induces apoptosis and inhibits tumor growth through mitochondrial-independent ROS production: Hirsutanol A inhibits tumor growth through ROS production. J. Transl. Med. 2013, 11, 32. [Google Scholar] [CrossRef] [Green Version]
  41. Yang, F.; Chen, W.D.; Deng, R.; Li, D.D.; Wu, K.W.; Feng, G.K.; Li, H.J.; Zhu, X.F. Hirsutanol A induces apoptosis and autophagy via reactive oxygen species accumulation in breast cancer MCF-7 cells. J. Pharmacol. Sci. 2012, 119, 214–220. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Marinedrugs 18 00100 g001 550
Figure 1. Chemical structures of compounds 1–13.
Figure 1. Chemical structures of compounds 1–13.
Marinedrugs 18 00100 g001
Marinedrugs 18 00100 g002 550
Figure 2. 1H–1H COSY, key HMBC and key NOESY correlations of 1, 6 and 13.
Figure 2. 1H–1H COSY, key HMBC and key NOESY correlations of 1, 6 and 13.
Marinedrugs 18 00100 g002
Marinedrugs 18 00100 g003 550
Figure 3. Comparison of the experimental and calculated ECD spectra of 6 and 13.
Figure 3. Comparison of the experimental and calculated ECD spectra of 6 and 13.
Marinedrugs 18 00100 g003
Marinedrugs 18 00100 g004 550
Figure 4. Comparison of the experimental and calculated ECD spectra of 3.
Figure 4. Comparison of the experimental and calculated ECD spectra of 3.
Marinedrugs 18 00100 g004
Marinedrugs 18 00100 g005 550
Figure 5. ORTEP diagram for the single-crystal X-ray structure of 4.
Figure 5. ORTEP diagram for the single-crystal X-ray structure of 4.
Marinedrugs 18 00100 g005
Table
Table 1. 1H and 13C NMR data for compounds 1, 3 and 4 in CDCl3 (δ in ppm).
Table 1. 1H and 13C NMR data for compounds 1, 3 and 4 in CDCl3 (δ in ppm).
Position1 a3 b4 b
δC, typeδH, mult. (J, Hz)δC, typeδH, mult. (J, Hz)δC, typeδH, mult. (J, Hz)
1-NH 10.83, brs 11.53, brs 11.50, brs
2156.9, C 157.0, C 156.5, C
3159.5, C 157.6, C 161.7, C
5120.9, CH7.41, s120.0, CH7.30, s120.0, CH7.32, s
6135.1, C 142.5, C 142.0, C
741.8, CH22.69, d (7.0)41.5, CH22.68, dd (14.4, 7.6)
2.62, dd (14.4, 7.2)		36.6, CH3.24, ddq (6.8, 6.8, 6.8)
826.9, CH2.23, tqq (7.0, 7.0, 7.0)26.9, CH2.18, m27.6, CH21.53, ddq (13.6, 6.8, 6.8)
1.79, ddq (13.6, 6.8, 6.8)
922.7, CH30.98, d (7.0)22.6, CH30.95, d (6.6)11.9, CH30.89, t (8.4)
1022.7, CH30.98, d (7.0)22.6, CH30.95, d (6.6)17.6, CH31.21, d (6.8)
11140.8, C 72.1, C 72.2, C
1226.0, CH22.46, q (7.0)35.4, CH21.86, m35.3, CH21.87, m
1312.6, CH31.17, t (7.0)8.1, CH30.90, t (7.2)8.1, CH30.92, t (7.6)
14115.0, CH2a. 5.35, s
b. 5.66, s		27.1, CH31.57, s27.1, CH31.57, s
11-OH 3.77, brs 3.482, brs
a 1H (500 MHz) and 13C (125 MHz) NMR; b 1H (400 MHz) and 13C (100 MHz) NMR.
Table
Table 2. 1H and 13C NMR data for compounds 6 and 13 in CDCl3 (δ in ppm).
Table 2. 1H and 13C NMR data for compounds 6 and 13 in CDCl3 (δ in ppm).
6 a13 b
PositionδC, typeδH, mult. (J, Hz)PositionδC, typeδH, mult. (J, Hz)
1166.5, C 163.6, CH2a. 4.37, brd (16.2)
b. 4.44, brd (16.2)
3153.8, C 373.4, CH4.00, m
4106.3, CH6.30, s436.2, CH2a. 2.22, ddd (18.0, 3.0, 3.0)
b. 2.35, dd (18.0, 9.0)
4a136.5, C 534.0, CH22.58, m
597.2, CH6.32, s641.3, CH3.04, ddd (13.2, 9.6, 6.0)
6164.6, C 782.9, C
7112.6, C 8192.4, C
8159.9, C 9151.6, C
8a99.9, C 10129.6, C
943.0, CH22.59, dd (14.4, 8.0)
2.66, dd (14.4, 4.4)		1148.8, CH2.75, dd (13.2, 3.0)
1065.5, CH4.26, m12174.7, C
1123.2, CH31.30, d (6.0)13130.0, CH5.52, ddq (15.6, 6.6, 1.2)
127.9, CH32.12, s14129.0, CH5.78, dqd (15.6, 6.6, 1.2)
1355.8, CH33.90, s1517.8, CH31.73, ddd (6.6, 1.2, 0.6)
8-OH 11.15, brs1616.6, CH31.42, s
10-OH 1.71, brs1769.4, CH4.22, m
1835.0, CH21.55, m
1925.8, CH21.53, m
1.33, m
2031.5, CH21.33, m
2122.5, CH21.33, m
2214.0, CH30.91, t (7.2)
17-OH 2.07, d (4.8)
a 1H (400 MHz) and 13C (100 MHz) NMR; b 1H (600 MHz) and 13C (150 MHz) NMR.
Table
Table 3. Cytotoxic activities of compounds 1–13 (IC50 ± SD, μM, n = 3).
Table 3. Cytotoxic activities of compounds 1–13 (IC50 ± SD, μM, n = 3).
CompoundsHuman Nasopharyngeal Carcinoma Cell LinesHuman Hepatocellular Cancer Cell Lines
CNE1CNE2HONE1SUNE1HepG2QGY7701
1− a−−90.55 ± 1.58−−
2−−−92.53 ± 1.10−−
381.91 ±1.81−−−−−
463.88 ± 1.22−−92.78 ± 1.73−−
5−91.78 ± 1.90−64.35 ± 0.89−−
6−75.70 ± 1.09−72.07 ± 0.651.72 ± 0.350.71 ± 0.12
7−85.66 ± 1.69−28.12 ± 0.759.60 ± 0.467.12 ± 0.36
8−−−39.38 ± 0.5846.10 ± 0.9131.62 ± 1.23
970.96 ± 1.51−−−−−
1072.72 ± 1.36−−−−−
1192.87 ± 2.10−−−−−
12−−−−−−
1350.55 ± 0.88−−−−−
Hirsutanol A10.08 ± 0.9212.72 ± 0.8617.40 ± 0.523.50 ± 0.2810.11 ± 0.6921.12 ± 1.01
a In the table, “−” means IC50 value > 100 μΜ.

Share and Cite

MDPI and ACS Style

Ran, Y.-Q.; Lan, W.-J.; Qiu, Y.; Guo, Q.; Feng, G.-K.; Deng, R.; Zhu, X.-F.; Li, H.-J.; Dong, J. Monarubins A–C from the Marine Shellfish-Associated Fungus Monascus ruber BB5. Mar. Drugs 2020, 18, 100. https://doi.org/10.3390/md18020100

AMA Style

Ran Y-Q, Lan W-J, Qiu Y, Guo Q, Feng G-K, Deng R, Zhu X-F, Li H-J, Dong J. Monarubins A–C from the Marine Shellfish-Associated Fungus Monascus ruber BB5. Marine Drugs. 2020; 18(2):100. https://doi.org/10.3390/md18020100

Chicago/Turabian Style

Ran, Yan-Qin, Wen-Jian Lan, Yi Qiu, Qi Guo, Gong-Kan Feng, Rong Deng, Xiao-Feng Zhu, Hou-Jin Li, and Jun Dong. 2020. "Monarubins A–C from the Marine Shellfish-Associated Fungus Monascus ruber BB5" Marine Drugs 18, no. 2: 100. https://doi.org/10.3390/md18020100

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop