Synthesis and Biological Evaluation of Benzo[f]indole-4,9-diones N-Linked to Carbohydrate Chains as New Type of Antitumor Agents

Abstract

In this work, we report the synthesis of three series of carbohydrate-based benzo[f]indole-4,9-diones and amino-1,4-naphthoquinone derivatives and evaluated their cytotoxic activity against eight human cancer cell lines. Several compounds showed a promising cytotoxic activity toward the tumor cell lines (half maximal inhibitory concentration (IC₅₀) < 10.0 μM). The importance of the substitution pattern of the quinone derivatives on the antitumor activity was also discussed. 3-Carboethoxy-2-methyl-benzo[f]indole-4,9-dione derivatives were more cytotoxic than their parent compounds and amino-1,4-naphthoquinones. Unlike clinically useful anticancer agent doxorubicin, the majority of synthesized compounds did not exhibit any lytic effects against erythrocytes or normal human leukocytes.

Keywords:
quinone; naphthoquinone; benzo[f]indole-4; 9-dione; carbohydrate; antitumor activity

Introduction

The quinone ring is a common structural motif found in many antitumor compounds.^1-4 For example, doxorubicin (1, Figure 1) is an anthracycline glycoconjugated antibiotic that exhibits biological activity against a wide variety of solid tumors in human patients.^5,6 The daunosamine carbohydrate attached to the quinone ring plays an important role in the formation of a ternary deoxyribonucleic acid (DNA)-topoisomerase-anthraquinone complex that results in the inhibition of DNA replication and subsequent induction of apoptosis.^7,8

Figure 1
Some examples of natural 1 and synthetic 2-4 antitumor quinones.

Quinone compounds can exert their toxic effects through two important mechanisms: (i) as prooxidant agents, reducing oxygen to reactive oxygen species (ROS), including superoxide, hydrogen peroxide and hydroxyl radicals, by redox cycling, which cause damage to proteins, nucleic acids, lipids, membranes and organelles; and (ii) as alkylating agents, forming covalent DNA adducts that lead to DNA fragmentation.^9-13

In addition to their ability to recognize a biological target, carbohydrates can improve the water-solubility of natural and synthetic compounds and decrease their toxicity side effects.¹⁴ Other relevant fact in sugar-conjugates area is related to high carbohydrate consumption by cancerous tissues compared to normal tissues due to the high rate of aerobic glycolysis, increasing the selectivity index of glycoconjugated compounds against cancer cells.¹⁵

With this goal in mind, we described the synthesis and pharmacological evaluation of carbohydrate-based 1,2-quinones 2a-2c and naphthotriazole derivatives 3a-3b (Figure 1).^16,17 From this study, we identified five glycoconjugated compounds 2a-2c and 3a-3b with promising cytotoxic profiles against different human cancer cells, with the half maximal inhibitory concentration (IC₅₀) values ranging from 0.29-1.22 and 0.64-3.66 µM, respectively.

Annulation of quinone with a series of functionalized pyrroles has been investigated by different research groups. The literature survey^18,19 reveals that naphthoquinone-annelated pyrrole (4) (Figure 1) is a promising molecule for the synthetic design of new antitumor compounds. This derivative exhibit high cytotoxic activity against several cancer cell lines with IC₅₀ values ranging from 0.3 to 1.5 μM, being comparable to the positive controls ellipticine and doxorubicin. Quinone 4 induced G2/M cell cycle arrest has been described as leading to apoptosis.^20-22

Numerous synthetic methods have been developed to prepare benzo[f]indole-4,9-dione derivatives (Figure 2) that include: oxidative free radical reaction between 2-amino-1,4-naphthoquinones and active methylene compounds, or carbonyl compound or ethyl nitroacetate mediated by transition metals (Figure 2a);^23-28 reaction of halo-quinones containing a carbonyl group with amines (Figure 2b);^21-29 ceric ammonium nitrate (CAN)-catalyzed three-component reaction between primary amines, β-dicarbonyl compounds and 2-bromonaphthoquinones (Figure 2c);³⁰ C,N-dialkylation of β-enaminones by 2,3-dichloronaphthoquinone (Figure 2d);³¹ oxidative copper(II)-mediated reaction between enaminones and 1,4-naphthoquinone (Figure 2e);^32,33 palladium-catalyzed cross-coupling of 3-amino-substituted-2-bromo-1,4-naphthoquinones with terminal acetylene derivatives (Figure 2f);³⁴ silver-catalyzed tandem reaction of tosylmethylisocyanide (TosMIC) with 2-methyleneindene-1,3-diones (Figure 2g);³⁵ Diels-Alder reaction of indole-4,7-dione with functionalized dienes (Figure 2h);³⁶ Mn^II-catalyzed reaction between vinyl azides and 2-hydroxynaphthoquinone (Figure 2i);³⁷ one-pot multicomponent domino reaction (MDR) between 2-amino-1,4-naphthoquinone, N-acylmethylpyridinium bromides and aromatic aldehydes (Figure 2j)²² and reaction of substituted α-bromonitroalkenes with various N-arylated aminonaphthoquinones (Figure 2k).³⁸

Figure 2
Different methods for the preparation of benzo[f]indole-4,9-dione derivatives. CAN: ceric ammonium nitrate; THF: tetrahydrofuran.

Here, our research focus is to develop a new class of benzo[f]indole-4,9-dione derivatives 5a-5c (Figure 3) N-linked to carbohydrate chains via reaction between halogenated naphthoquinone containing an α-methylene carbonyl functional group and amino-carbohydrates to act more selectively against tumor cells in vitro than the prototype compound 4. The choice of sugars containing cyclic acetal group was based on our previous works,^16,17 which have shown to add important structural features for the biological activity. It is important to note that there is a drug on the pharmaceutical market that contains two units of acetonides in its structure.³⁹ To investigate the effect of substitution pattern around the pyrrole core on antitumor activity, we have prepared the related compounds 6a-6c and 7a-7c by cerium(IV)-mediated oxidative free radical cyclization reaction of 2-amino-1,4-naphthoquinone glycoconjugates 8a-8c with β-dicarbonyl compounds.

Figure 3
Rational approach to the design of benzo[f]indole-4,9-dione glycoconjugates 5a-5c, 6a-6c and 7a-7c and 2-amino-1,4-naphthoquinone derivatives 8a-8c.

Results and Discussion

Chemistry

Aminocarbohydrates 9a-9c have been synthesized from their corresponding commercially reagents D-ribose (10a), D-galactose (10b) and D-xylose (10c) by using known methods (Scheme 1) of acetonization of hydrophilic groups, tosylation of partially protected carbohydrate derivatives, S_N2 (bimolecular nucleophilic substitution) of functionalized-sugars with sodium azide and catalytic hydrogenation of organic azides to amines using palladium catalyst.^9,40

Scheme 1
Preparation of aminocarbohydrate derivatives 9a-9c. (a) Acetone, H₂SO₄, MeOH, 25 °C, 48 h; (b) pyridine, TsCl, 25 °C, 20 h; (c) NaN₃/DMF, 120 °C, 20 h; (d) Pd/C, H₂, EtOH, 3 atm, 3 h; (e) acetone, H₂SO₄, CuSO₄, 25 °C, 24 h; (f) aqueous solution HCl 0.2%, Δ, 2 h.

The ultrasound-accelerated Michael addition type reaction of aminocarbohydrates 9a-9c with 1,4-naphthoquinone (12) produced the corresponding amino sugar quinones 8a-8c (Scheme 2), according to the method outlined in our previous reports^41,42 (Supplementary Information (SI) section).

Scheme 2
Preparation of glycoconjugated aminoquinones 8a-8c.

The structural characterization of the aminoquinone 8a-8c was performed by using one- and two-dimensional nuclear magnetic resonance (NMR) spectroscopy.

In the ¹³C NMR spectra of substances 8a-8c, two downfield signals observed at δ_C 183.2 and 181.8 (8a), 183.0 and 181.7 (8b) and 182.9 and 180.7 (8c) were attributed to the carbonyl carbons C-1 and C-4, respectively. The chemical shifts of C-1 and C-4 were differentiated on the basis of the analysis of the resonance effect caused by amino group attached to the C-2 position of the quinone ring, which makes the C-4 carbonyl group less electrophilic. The assignments of these carbons C-1 and C-4 were also supported by heteronuclear multiple bond correlation (HMBC) experiments. In their spectra it was observed long-range correlation (³J_CH) between H-3 and carbonyl carbon C-4 signals.

In the ¹H NMR spectra of these substances the doublet of doublets in the range of 8.07-8.10 ppm was attributed to hydrogen H-8, due to its proximity to the more electrophilic carbonyl group (C-1).

In the ¹H-¹H correlation spectroscopy (COSY) spectra of 8a-8c, the correlation of the H-8 signal led to assign H-7 hydrogen as the triplet of doublets in the range of 7.68-7.85 ppm. Correlation of this hydrogen led to the subsequent assignment of H-6, allowing, subsequently, the assignment of H-5. The singlet signal between 5.73-5.89 ppm was correlated to H-3.

In the HMBC spectra of 8a-8c, long-range correlations (³J_CH) between C-4a and C-8a and H-6 and H-7 signals support the assignments of these carbons.

Table S1 (SI section) shows ¹H and ¹³C assignments of quinonoid moiety of these compounds 8a-8c.

Spectroscopic analysis of the carbohydrate groups of 1,4-naphthoquinone derivatives 8a-8c

In the ¹H-¹H COSY spectrum of compound 8a, the methylene signal in the range 3.23-3.33 ppm (2H, m, H-5’ and H-5”) showed correlation to H-4’ (δ_H 4.49, dd, J 6.0, 6.0 Hz). The ¹H NMR spectrum of 8a, the singlet signal of anomeric proton H-1’ was found at δ_H 5.03. This proton could be easily identified based on the electron-attracting effect caused by two oxygen atoms attached to the carbon of the anomeric position C-1’. Two doublet signals at δ_H 4.64 (J 6.0 Hz) and 4.62 (J 6.0 Hz) were attributed to corresponding protons H-2’ and H-3’. The absence of vicinal coupling indicated a trans relationship between protons H-1’ and H-2’ and the β-anomeric configuration for the sugar ring. Further, in the HMBC spectrum, it was found that protons H-1’ and H-5’/H-5”showed three long-range correlations to quaternary carbon C-3’ (δ 82.3 ppm).

H-1’ signal of compound 8b at δ_H 5.54 (d, J 5.0 Hz) showed COSY correlation to H-2’ (δ_H 4.33, dd, J 5.0 and 2.5 Hz). The correlation observed between the H-2’ proton and doubled doublet signal at δ_H 4.63 (J 8.0, 2.5 Hz) permitted the identification of H-3’. COSY correlations between H-4’/H-3’, H-4’/H-5’ and between proton H-5’ and methylene protons H-6’ and H-6” were also observed. The twist-boat conformation of the D-galactose ring in 8b was confirmed by the ¹H-¹H vicinal coupling constants values J_{H-1’,H-2’}, J_{H-2’,H-3’}, J_{H-3’,H-4’} and J_{H-4’,H-5’} (5.0, 2.5, 8.0 and 1.5 Hz, respectively) of the ring protons.⁴⁰

The ¹H-¹H COSY spectrum of quinone derivative 8c showed connectivity among H-1’ (δ_H 6.02, J 3.5 Hz) and H-2’ (δ_H 4.61, J 3.5 Hz) protons. The H-4’ signal at 4.47 (ddd, J 9.5, 5.0, 3.0 Hz) showed COSY correlations to H-3’ (δ_H 4.24, d, J 3.0 Hz) and non-equivalent protons H-5’ (δ_H 3.58, dd, J 15.0, 9.5 Hz) and H-5” (δ_H 3.67, dd, J 15.0, 5.0 Hz).

Table S1 (SI section) shows ¹H and ¹³C assignments of sugar groups of the compounds 8a-8c.

Synthesis of benzo[f]indole-4,9-dione glycoconjugates 5a-5c, 6a-6c and 7a-7c

The cerium(IV)-mediated oxidative free radical cyclization reaction between 1,4-amino-naphthoquinones 8a-8c and ethyl cyanoacetate (13) (Scheme 3)²¹ resulted in a complex mixture of products in which the ring products 5a-5c could not be identified. However, the polyfunctionalized benzo[f]indole-4,9-diones 6a-6c and 7a-7c were successfully obtained under the same conditions, by reacting the corresponding β-dicarbonyl compounds 14a-14b with the amino derivatives 8a-8c.

Scheme 3
The synthetic routes used to prepare the annulated quinones 6-7.

In this reaction, electrophilic intermediates 15a and 15b were produced from the oxidative step with cerium(IV) of the corresponding 1,3-dicarbonyl compounds 14a and 14b, which underwent to an intermolecular addition involving the C-C double bond of aminoquinone derivatives 8a-8c followed by a second oxidation step to give 16a-16c and 17a-17c. These latter substances underwent intramolecular cyclization producing the annulated naphthoquinones 6a-6c and 7a-7c, respectively.

An alternative synthetic route to prepare the naphthoquinone compounds 5a-5c (Scheme 4) involved the nucleophilic substitution reaction between 2,3-dichloronaphthoquinone (20)²¹ with ethyl cyanoacetate carbanion, formed in situ by reaction of ethyl cyanoacetate (21) with potassium carbonate.

Scheme 4
Preparation of benzo[f]indole-4,9-dione derivatives 5a-5c.

The formation of the glycoconjugated quinones 5a-5c can be rationalized from compound 22 which results from the replacement of a chlorine atom of 20. The nucleophilic substitution of the second chlorine atom by aminocarbohydrates 9a-9c leads to the intermediate 23a-23c which spontaneously cyclize and then tautomerize to the respective glycoconjugated quinones 5a-5c (Scheme 4).

In the ¹³C NMR spectra of substances 5a-5c, 6a-6c and 7a-7c, the chemical shifts of the C-4 and C-9 carbonyl carbons were attributed based on those of the corresponding carbons in the spectra of the quinones 8a-8c and also on long range correlations observed in their HMBC spectra (Tables S2, S3, S4, in the SI section). In HMBC spectra of 5a-5c, 6a-6c and 7a-7c the hydrogens H-5 correlated with the C-4 (³J_CH) carbon signals and these latter showed correlation to H-5 signals (²J_CH).

The long-range correlations ²J_CH and ³J_CH of the C-2 carbon with the methylene and methyl hydrogens of the carbohydrate groups (Tables S2, S3, S4 in the SI section) clearly confirmed the presence of the fused pyrrolic ring to the naphthoquinone framework. The HMBC spectra were also important for the assignment of C-9a carbon. ¹H and ¹³C NMR data of quinone derivatives 5a-5c, 6a-6c and 7a-7c are listed in Tables S2, S3 and S4 (SI section).

Biological analysis

The cancer cell lines used in this study were MCF-7 (human mammary gland/breast epithelial adenocarcinoma); MDA-MB 231 (human mammary gland/breast epithelial adenocarcinoma); A549 (human lung carcinoma); HT-29 (human epithelial colorectal adenocarcinoma); Hep G2 (human liver hepatocellular carcinoma); SH-SY5Y (human bone marrow neuroblastoma); HT-1080 (human connective tissue epithelial fibrosarcoma) and DMS 79 (human lung pleural fluid carcinoma) and normal human blood peripheral leukocytes and erythrocytes. The compounds 5a-5c, 6a-6c, 7a-7c and 8a-8c were tested in vitro by the MTT (3-(4,5-dimethyl-2-thiazyl)-2,5-diphenyl-2H-tetrazolium bromide) assay to evaluate the cytotoxicity after 24 h of treatment. Lytic effect was evaluated against human erythrocytes. Doxorubicin (an antitumor drug) was used as positive control. Data is expressed as concentration that induced 50% cytotoxic effect (IC₅₀) (Table 1).

Table 1
Cytotoxicity expressed as 50% cytotoxic effect (IC₅₀) of compounds 5a-5c, 6a-6c, 7a-7c and 8a-8c against different cell lines

Compound	IC50 / µM
	MCF-7	MDA-MB 231	A549	HT-29	HepG2	SH-SY5Y	HT-1080	DMS 79	Human blood leukocyte	Erythrocytea
5a	> 30	22.4	20.9	18.8	17.9	> 30	21.1	17.0	> 100	> 150
5b	9.7	> 30	12.7	21.8	29.6	> 30	15.7	13.8	> 100	> 150
5c	11.9	> 30	8.8	18.7	14.8	> 30	21.1	12.1	> 100	> 150
6a	9.9	> 30	5.4	6.3	11.8	28.4	15.6	11.1	> 100	> 150
6b	9.9	> 30	6.8	11.6	19.6	13.5	27.7	7.7	> 100	> 150
6c	> 30	> 30	> 30	> 30	> 30	> 30	> 30	> 30	> 100	> 150
7a	27.8	> 30	21.8	22.6	20.3	> 30	20.4	21.7	> 100	> 150
7b	> 30	28	25.4	28.8	21.3	> 30	22.5	22.9	> 100	> 150
7c	> 30	> 30	> 30	> 30	> 30	> 30	> 30	> 30	> 100	> 150
8a	25.6	8.9	13.8	19.4	17.7	> 30	20	21.7	> 100	> 150
8b	> 30	> 30	20.4	18.8	13.4	> 30	> 30	17.7	> 100	> 150
8c	> 30	18.9	23.6	27.5	17.7	> 30	29.9	13.8	> 100	> 150
Doxorubicinb	1.8	0.7	0.47	0.33	0.58	0.77	1.1	0.08	3.41	> 25

• ^a
  Concentration of compound that induced erythrocyte lysis;
• ^b
  doxorubicin was used as positive control. Only compounds with an IC₅₀ value lower than 10 mM for at least one cell line were considered active; Data are presented as IC₅₀ values obtained by nonlinear regression for all cell lines from three independent experiments. MCF-7: human mammary gland/breast epithelial adenocarcinoma; MDA-MB 231: human mammary gland/breast epithelial adenocarcinoma; A549: human lung carcinoma; HT-29: human epithelial colorectal adenocarcinoma; Hep G2: human liver hepatocellular carcinoma; SH-SY5Y: human bone marrow neuroblastoma; HT-1080: human connective tissue epithelial fibrosarcoma; DMS 79: human lung pleural fluid carcinoma.

The compounds were classified according to their activity as highly active (IC₅₀ < 2 μM), moderately active (2 μM < IC₅₀ < 10 μM) or inactive (IC₅₀ > 10 μM).⁴³

The quinone glycoconjugates 5a-5c, 6a-6c, 7a-7c and 8a-8c (Table 1) did not exhibit any lytic effects against normal human erythrocytes or leukocytes. Among the pyrrolo-annelated naphthoquinones 5a-5c, only derivatives 5b-5c showed selective cytotoxicity against MCF-7 and A549 cancer cell lines, respectively, with IC₅₀ values of 9.7 and 8.8 μM, respectively (Table 1).

The nature of the substituents attached to the pyrrole nucleus influenced the antitumor activity of the naphthoquinone derivatives 5a-5c, 6a-6c and 7a-7c. It was observed that the replacement of a free primary amino group at C-2 position of the pyrrole ring of 5a-5b by methyl group made the naphthoquinone derivatives 6a-6b more cytotoxic than the related parent compounds against three tumor cell lines (Table 1). These results suggest that the hydrophobic effect of methyl group attached to the naphthoquinone nucleus of substances 6a and 6b plays an important role for improvement of their potency and broader their spectrum of antitumor activity.

For derivative 6c, the presence of a methyl group attached at C-2 position of the pyrrole ring resulted in the loss of antitumor activity, while its analogous compound 5c exhibited selective cytotoxicity against A549 cell lines. The compounds 7a-7c bearing acetyl group at the C-3 position of the pyrrole ring did not cause any cytotoxic effect on all cell lines tested.

Among the carbohydrate-based 1,4-naphthoquinones 8a-8c, only amino derivative 8a displayed selective cytotoxicity toward MDA-MB 231 cell line, with an IC₅₀ value of 8.9 μM. The antitumor activity of this compound can be related to the chemical properties (e.g., conformation and intermolecular interactions) of the ribofuranosyl ring. Major number of annelated glycoconjugated compounds displayed better cytotoxicity than 2-amino-1,4-naphthoquinones glycoconjugates. In addition, the series of quinones 6a-6b displayed greater activity in three tested cancer cell lines than their parent compounds. It is noteworthy that the compounds 6a-6b can serve as available inspiration in the search for new effective antitumoral agents.

It is well-known that the cytotoxic assay, MTT, is considered a metabolic assay and can result in variable results.⁴³ The morphology-based evaluation of viability/cytotoxicity by phase-contrast microscopy and DAPI (4’,6-diamidino-2-phenylindole) staining are greatly useful to explain the apoptotic effects.

Breast cancer is composed of multiple subtypes, with distinct morphologies and clinical implications, including triple-negative breast cancer (TNBC), which refers to estrogen receptor, progesterone receptor and HER2 (human epidermal growth factor receptor-type 2) negative. Without available targeted therapy options, the standard of care for TNBC remains chemotherapy. The recurrence and mortality in the TNBC is significantly higher than the other subtypes.⁴⁴ Many TNBC exhibit resistance to chemotherapy and all metastatic TNBC eventually develop resistance.⁴⁵ Han et al.⁴⁶ showed that chemoresistance can be acquired rapidly in MDA-MB 231 cells under a doxorubicin concentration gradient. So we decided to investigate the potential apoptotic effects of four synthesized compounds, 5b, 5c, 6a and 6b in MDA-MB 231, a TNBC cell line.

The apoptogenic property of the compounds was verified through the analysis of morphological changes in MDA-MB 231 cells. Apoptotic cells exhibit typical features such as nuclear condensation, cytoplasm shrinkage, membrane blebs, formation of pyknotic bodies (this is the most characteristic feature of apoptosis) and energy-dependent biochemical mechanisms.⁴⁷

After incubation with tested compounds for 24 h, morphological alterations in MDA-MB 231 cells were observed (Figure 4) in comparison to control cells. 0.5 μM doxorubicin (1) was used as positive control. Visualization of the control (untreated) cells showed that the cells maintained their original morphology form. In contrast, exposure of MDA-MB 231 cells treated with 30 µM of compounds 5b, 5c, 6a and 6b for 24 h revealed typical apoptotic features such as shrinkage, membrane blebbing, and losing contact with adjacent cells, which can also be seen in the positive control.

Figure 4
Morphological changes of MDA-MB 231 (human mammary gland/breast epithelial adenocarcinoma) cells. (a) Nontreated, control cells; and treated cells (30 µM) with compounds (b) 5b; (c) 5c; (d) 6a; (e) 6b and (f) 0.5 µM doxorubicin (1) for 24 h and imaged by phase-contrast microscope (magnification 40×). Arrows indicate apoptotic bodies.

Apoptotic cells were defined exhibiting condensed chromatin and fragmented nuclei, while nonapoptotic cells showed a fine network of chromatin in the entire nuclear area. To examine whether the cytotoxicity of these compounds was mediated through apoptosis, MDA-MB 231 cells treated with 30 µM of the selected compounds for 24 h were stained with DAPI, and the appearance of chromatin condensation and fragmentation of nuclei were analyzed (Figure 5). The morphological observation in the cell nuclei of MDA-MB 231 with or without tested compounds showed significant morphological alterations when compared to untreated control. 0.5 μM doxorubicin (1) was used as positive control. No apoptotic nuclei were observed in control cells (Figure 5a) and apoptotic nuclei, indicated by arrows, were significantly increased in cells exposed to 30 µM of the compounds (Figures 5b, 5c, 5d, 5e). The results indicate that these four compounds induce apoptotic cell death in MDA-MB 231 cells.

Figure 5
Representative images show morphological changes of MDA-MB 231 (human mammary gland/breast epithelial adenocarcinoma) cells detected with DAPI (4’,6-diamidino-2-phenylindole) staining. (a) Nontreated, control cells; and treated cells (30 µM) with compounds (b) 5b; (c) 5c; (d) 6a; (e) 6b and (f) 0.5 µM doxorubicin (1) for 24 h and imaged by fluorescence microscope (magnification 40×). Arrows indicate live cells with apoptotic nuclei.

All bioactive compounds were found to be less cytotoxic active against cancer cells than the clinically useful anticancer agent doxorubicin. Although doxorubicin is considered an important drug for the chemotherapy, it has several clinical limitations, such as cardiotoxic effects and a high incidence of multi-drug resistance.⁴⁸ Furthermore, the normal cells, erythrocytes, were more sensitive to treatment with doxorubicin (1), reducing cell viability with lower concentrations, than with all the test compounds, suggesting that the effect of these test compounds was selected for cancer cell lines.

Conclusions

In summary, three classes of benzo[f]indole-4,9-dione glycoconjugates 5a-5c, 6a-6c and 7a-7c and amino-naphthoquinones 8a-8c have been synthesized and evaluated for antitumoral activity against eight human cancer cell lines. None of these compounds exhibited lytic effects against normal human erythrocytes or leukocytes. The compounds 5b-5c, 6a-6b and 8a exhibited significant cytotoxic activity. The quinone derivatives bearing carbetoxy moiety at the position of pyrrole ring 6a-6b were the most potent of these families, with IC₅₀ values below 7.8 μM against two tumor cell lines. The influence of carbohydrates can be better evidenced for the series 6a-6c. The enhanced anticancer activity of 6a-6b in most of the tested cancer cell lines may be related to the chemical structures (e.g., conformation and intermolecular interactions) of the corresponding furanose and pyranose rings. The derivatives 6a-6b can be considered as promising lead compounds for the development of more potent anticancer agents. Furthermore, morphological analysis using phase contrast microscope and DAPI staining procedures by fluorescence microscope indicate that the compounds 5b, 5c, 6a and 6b were able to trigger cell death of triple negative breast cancer cells, MDA-MB 231, through apoptosis. Nevertheless, further investigations are necessary to validate its therapeutic claims and to determine the mode of action of these compounds.

Experimental

Cell culture

Compounds (0.15-30 μM) were tested for cytotoxic activity against MCF-7 (human mammary gland/breast epithelial adenocarcinoma, American Type Culture Collection (ATCC) No. HTB-22), A549 (human lung carcinoma, ATCC No. CCL-185), MDA-MB 231 (human mammary gland/breast epithelial adenocarcinoma, ATCC No. HTB-26), HT-29 (human epithelial colorectal adenocarcinoma, ATCC No. HTB-38), Hep G2 (human liver hepatocellular carcinoma, ATCC No. HB-8065), SH-SY5Y (human bone marrow neuroblastoma, ATCC No. CRL-2266), HT-1080 (human connective tissue epithelial fibrosarcoma, ATCC No. CCL-212), DMS 79 (human lung pleural fluid carcinoma, ATCC No. CRL-2049), freshly prepared human blood leukocytes and erythrocytes. All cell lines were maintained in Roswell Park Memorial Institute (RPMI) 1640 medium supplemented with 10% fetal bovine serum (FBS), 2 mM glutamine, 100 U mL^-1 penicillin and 100 mg mL^-1 streptomycin at 37 °C with 5% CO₂. Media were changed every two or three days.

Cytotoxic assay

Cell viability was determined using 3-(4,5-dimethyl-2-thiazyl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) reagent (Sigma-Aldrich, Massachusetts, USA). Briefly, cells were plated at an initial density of 2.5 × 10⁴ cells per well in 96-well plates and incubated for 24 h at 37 °C and 5% CO₂. After 24 h cultures were treated with the compounds (0.15-30 μM) and further incubated for 24 h. Each compound was dissolved with dimethyl sulfoxide (DMSO) and diluted with cell culture medium to obtain a concentration of 100 μM. The negative control received the same amount of DMSO (0.005% in the highest concentration). Doxorubicin (1) was used as a positive control. After treatment, the supernatant of each well was removed, and cells were washed twice with medium. Then, 10 μL of MTT solution (5 mg mL^-1 in RPMI) and 100 μL of medium were added to each well and incubated for 3 h at 37 °C, 5% CO₂, as described by Denizot and Lang.⁴⁹ The resultant formazan crystals were dissolved in dimethyl sulfoxide (100 μL) and absorbance intensities were measured in a microplate reader (FlexStation Reader, Molecular Devices, USA) at 570 nm. All experiments were performed in triplicate.

Erythrocytes hemolysis

The test was performed as adapted from Malagoli,⁵⁰ in 96-well plates using a 2% human erythrocyte suspension in 0.85% NaCl containing 10 mM CaCl₂. The compounds diluted as mentioned above were tested at concentration of 150 μM. After incubation at room temperature for 30 min and centrifugation, the supernatant was removed, and the liberated hemoglobin was measured spectrophotometrically at 540 nm. DMSO was used as a negative control and Triton X-100 (1%) was used as positive control.

Cell morphological assessment of apoptosis

Cultured cells, MDA-MB 231, were incubated for 24 h with or without selected compounds at concentrations of 30 μM in a 12-wells plate cell culture dishes, were fixed with 2% formaldehyde in phosphate buffered saline (PBS) for 3 min after washing with PBS at 37 °C. The morphological changes of the apoptotic cells were observed using phase contrast microscope (Leica DMI 3000B, Germany) at 40× magnification.

Nuclei morphological changes

MDA-MB 231 cells were grown on cell culture dishes and treated with or without tested compounds at concentration of 30 μM. After 24 h, the cells were washed with cold PBS. The cells were fixed with 2% formaldehyde in PBS for 3 min after washing with PBS at 37 °C. Cells were permeabilized with 0.5% Triton X-100 in PBS for 10 min, three times. Nuclei were labelled with DAPI (0.1 μg mL^-1 in 0.9% NaCl) and cells were mounted in ProLong Gold antifade reagent (Molecular Probes, Eugene, Oregon, USA) and examined with an Axiovert 100 microscope (Carl Zeiss, Germany). Images were acquired with an Olympus DP71 digital camera (Olympus, Japan). Image processing was performed using Fiji software (based on ImageJ).⁵¹

Chemistry

Melting points (mp) were determined with a Fisher-Johns instrument and are uncorrected. Infrared (IR) spectra were recorded on PerkinElmer FT-IR, model 1600 series spectrophotometer in KBr pellets. NMR spectra were obtained in CDCl₃ or CD₃OD (Sigma-Aldrich, São Paulo, Brazil) using a Varian Unity Plus 500 MHz spectrometer. Chemical shifts (δ) are expressed in ppm and the coupling constant (J) in hertz. Column chromatography was performed on silica gel flash from Merck (Darmstadt, Germany). Reactions were routinely monitored by thin layer chromatography (TLC) on silica gel pre-coated F254 Merck plates. Microanalyses were performed using a PerkinElmer model 2400 instrument and all values were within ± 0.4% of the calculated compositions.

Synthesis of aminocarbohydrate 9a-9c and 2-amino-1,4-naphthoquinones 8a-8c

Aminocarbohydrate 9a-9c were prepared from their corresponding commercially available reagents D-ribose (10a), D-galactose (10b) and D-xylose (10c) using previously described methods for carbohydrate derivatization.^9,39 The general procedure for the synthesis of the aminonaphthoquinones derivatives 8a-8c has been performed according to Franco et al.⁴¹

Preparation of benzo[f]indole-4,9-diones 6a-6c and 7a-7c

In a 50 mL round bottom flask were added 0.064 mmol of the 2-amino-1,4-naphtoquinone 8a-8c, 2.56 mmol of active methylene compound (12a-12b), 10 mL of ethanol, 2 mL of dichloromethane and 2 mL of distilled water. Ceric sulfate (315 mg, 5 mmol) was added to the reaction mixture over a 2 h period. The reaction medium was kept under continuous stirring for 24 h at room temperature. Monitoring the reaction by TLC was performed using hexane:ethyl acetate (7:3) as the eluent. Compounds 6a-6c and 7a-7c were detected by a spray reagent consisting of 1% (m v^-1) vanillin with sulfuric acid after gentle heating or by viewing under short-wave UV light (254 nm). The mixture was filtered through a Buchner funnel and the filtrate was treated with saturated solution of sodium bisulfite. The organic phase was extracted with dichloromethane and dried with anhydrous sodium sulfate. The solvent was evaporated under reduced pressure and the crude product was purified by chromatography on a silica gel column, using a gradient elution of 90-70% (v/v) hexane in ethyl acetate.

2-Methyl-1-(methyl-5’-deoxy-2’,3’-O-isopropylidene-β-D-methylfuranosid-5’-yl)-4,9-dioxo-4,9-dihydro-1H-benzo[f]indole-3-ethyl carboxylate (6a)

The compound 6a was obtained as a yellow solid, mp 144-145 °C, with 51% yield. IR (KBr pellets) ν / cm^-1 1683 and 1601 (C=O), 1567 (C=C); ¹H NMR (500.00 MHz, CDCl₃) δ 1.27 (s, 3H, CH₃), 1.43 (s, 3H, CH₃), 1.44 (t, 3H, J 7.1 Hz, CH₂-CH₃), 2.54 (s, 3H, C₂-CH₃), 3.45 (s, 3H, OCH₃), 4.29 (dd, 1H, J 15.0, 5.0 Hz, H-5”), 4.44 (q, 2H, J 7.1 Hz, CH₂-CH₃), 4.50 (dd, 1H, J 10.0, 5.0 Hz, H-4’), 4.73 (d, 1H, J 5.0 Hz, H-3’), 4.78 (d, 1H, J 5.0 Hz, H-2’), 5.03 (s, 1H, H-1’), 5.05 (dd, 1H, J 15.0, 10.0 Hz, H-5’), 7.66-7.67 (m, 1H, H-7), 7.67-7.68 (m, 1H, H-6), 8.13-8.15 (m, 1H, H-5), 8.16-8.17 (m, 1H, H-8); ¹³C NMR APT (attached proton test) (125.0 MHz, CDCl₃) δ 11.0 (C₂-CH₃), 14.1 (CH₂-CH₃), 24.9 (CH₃), 26.4 (CH₃), 47.9 (C-5’), 55.6 (OCH₃), 61.1 (CH₂-CH₃), 81.6 (C-3’), 85.2 (C-2’), 85.5 (C-4’), 110.4 (C-1’), 112.7 (-OCO-), 114.6 (C-3), 126.2 (C-3a), 126.3 (C-5), 126.6 (C-8), 129.9 (C-9a), 132.9 (C-6), 133.0 (C-4a), 133.3 (C-7), 133.6 (C-8a), 141.8 (C-2), 164.3 (C=OOCH₂-CH₃), 176.2 (C-4), 179.2 (C-9); anal. calcd. for C₂₅H₂₇NO₈: C 63.96, H 5.89, N 2.98, found: C 63.09, H 6.29, N 3.26%.

2-Methyl-4-[(6’-deoxy-1’,2’:3’,4’-di-O-isopropylidene-D-galactopiranos-6’-yl)methyl]-4,9-dioxo-4,9-dihydro-1H-benzo[f]indole-3-ethyl carboxylate (6b)

The compound 6b was obtained as a yellow solid, mp 138-140 °C, with 56% yield. IR (film) ν / cm^-1 1609 and 1678 (C=O), 1572 (C=C); ¹H NMR (500.00 MHz, CDCl₃) δ 1.15 (s, 3H, CH₃), 1.18 (s, 3H, CH₃), 1.37 (s, 3H, CH₃), 1.41 (t, 3H, J 7.1 Hz, CH₂-CH₃), 1.50 (s, 3H, CH₃), 2.49 (s, 3H, C₂-CH₃), 4.24 (dt, 1H, J 9.5, 2.5 Hz, H-5’), 4.26 (dd, 1H, J 5.0, 2.5 Hz, H-2’), 4.32 (dd, 1H, J 14.0, 9.5 Hz, H-6”), 4.42-4.45 (m, 1H, H-4’), 4.43 (q, 2H, J 7.1 Hz, CH₂-CH₃), 4.64 (dd, 1H, J 8.0, 2.5 Hz, H-3’), 4.75 (dd, 1H, J 14.0, 2.5 Hz, H-6’), 5.41 (d, 1H, J 5.0 Hz, H-1’), 7.64 (td, 1H, J 6.0, 2.0 Hz, H-7), 7.67 (td, 1H, J 6.0, 2.0 Hz, H-6), 8.05 (dd, 1H, J 6.0, 2.0 Hz, H-5), 8.12 (dd, 1H, J 6.0, 2.0 Hz, H-8); ¹³C NMR APT (125.0 MHz, CDCl₃) δ 11.1 (C₂-CH₃), 14.1 (CH₂-CH₃), 24.4 (CH₃), 24.8 (CH₃), 25.4 (CH₃), 26.0 (CH₃), 46.3 (C-6’), 60.9 (CH₂-CH₃), 67.6 (C-5’), 70.3 (C-2’), 70.9 (C-3’), 71.5 (C-4’), 96.2 (C-1’), 108.6 (-OCO-), 109.5 (-OCO), 113.7 (C-3), 125.8 (C-5), 126.2 (C-3a), 126.7 (C-8), 129.8 (C-9a), 132.7 (C-6), 132.9 (C-4a), 133.1 (C-7), 133.8 (C-8a), 144.0 (C-2), 164.5 (C=OOCH₂-CH₃), 176.0 (C-4), 179.3 (C-9); anal. calcd. for C₂₈H₃₁NO₉: C 63.99, H 5.95, N 2.67%, found: C 63.94, H 6.62, N 2.43%.

2-Methyl-2-[(5’-deoxy-1’,2’-O-isopropylidene-D-xilofuranos-5’-yl)]-4,9-dioxo-4,9-dihydro-1H-benzo[f]indole-3-ethyl carboxylate (6c)

The compound 6c was obtained as a yellow solid, mp 161-163 °C, with 43% yield. IR (film) ν / cm^-1 1608 and 1679 (C=O), 1566 (C=C); ¹H NMR (500.00 MHz, CDCl₃) δ 1.18 (s, 3H, CH₃), 1.29 (s, 3H, CH₃), 1.32 (t, 3H, J 7.1 Hz, CH₂-CH₃), 2.45 (s, 3H, C₂-CH₃), 4.18-4.22 (m, 1H, H-5”), 4.22-4.26 (m, 2H, H-3’and H4’), 4.34 (q, 2H, J 7.1 Hz, CH₂-CH₃), 4.48 (d, 1H, J 3.5 Hz, H-2’), 5.03 (dd, 1H, J 14.0, 4.0 Hz, H-5’), 5.86 (d, 1H, J 3.5 Hz, H-1’), 7.55-7.57 (m, 2H, H-6 and H-7), 8.00 (dd, 1H, J 6.0, 2.0 Hz, H-5), 8.09 (dd, 1H, J 6.0, 2.0 Hz, H-8); ¹³C NMR APT (125.0 MHz, CDCl₃) δ 11.3 (C₂-CH₃), 14.3 (CH₂-CH₃), 26.3 (CH₃), 26.9 (CH₃), 44.3 (C-5’), 61.4 (CH₂-CH₃), 74.9 (C-4’), 80.7 (C-3’), 85.4 (C-2’), 104.8 (C-1’), 112.1 (-OCO-), 115.0 (C-3), 126.5 (C-5), 126.6 (C-3a), 127.0 (C-8), 129.9 (C-9a), 133.2 (C-6), 133.2 (C-4a), 133.7 (C-7), 133.9 (C-8a), 143.4 (C-2), 164.7 (C=OOCH₂-CH₃), 176.9 (C-4), 179.4 (C-9); anal. calcd. for C₂₄H₂₅NO₈: C 63.29, H 5.53, N 3.08%, found: C 62.46, H 5.70, N 3.28%.

3-Acetyl-2-methyl-1-(methyl-5’-deoxy-2’,3’-O-iso-propylidene-β-D-methylfuranosid-5’-yl)-4,9-dioxo-4,9-dihydro-1H-benzo[f]indole (7a)

The compound 7a was obtained as a yellow solid, mp 210-212 °C, with 54% yield. IR (KBr pellets) ν / cm^-1 1683 and 1601 (C=O), 1567 (C=C); ¹H NMR (500.00 MHz, CDCl₃) δ 1.27 (s, 3H, CH₃), 1.43 (s, 3H, CH₃), 2.48 (s, 3H, C₂-CH₃), 2.70 (s, 3H, C=OCH₃), 3.45 (s, 3H, OCH₃), 4.30 (dd, 1H, J 15.0, 5.0 Hz, H-5”), 4.50 (dd, 1H, J 10.0, 5.0 Hz, H-4’), 4.74 (d, 1H, J 5.0 Hz, H-3’), 4.78 (d, 1H, J 5.0 Hz, H-2’), 5.02-5.06 (m, 1H, H-5’), 5.03 (s, 1H, H-1’), 7.68-7.72 (m, 2H, H-6, H-7), 8.13 (d, 1H, J 9.0 Hz, H-5), 8.16 (d, 1H, J 9.0 Hz, H-8); ¹³C NMR APT (125.0 MHz, CDCl₃) δ 11.3 (C₂-CH₃), 25.2 (CH₃), 26.6 (CH₃), 31.8 (C=OCH₃), 48.3 (C-5’), 55.9 (OCH₃), 81.9 (C-3’), 85.4 (C-2’), 85.8 (C-4’), 110.7 (C-1’), 113.0 (-OCO-), 123.3 (C-3), 125.7 (C-3a), 126.6 (C-5), 126.8 (C-8), 129.7 (C-9a), 133.3 (C-6), 133.4 (C-4a), 133.5 (C-7), 141.8 (C-2), 176.3 (C-4), 180.7 (C-9), 199.2 (C=OCH₃); anal. calcd. for C₂₄H₂₅NO₇: C 65.59, H 5.73, N 3.19%, found: C 65.10, H 6.05, N 3.27%.

3-Acetyl-2-methyl-4-[(6’-deoxy-1’,2’:3’,4’-di-O-iso-propylidene-D-galactopiranos-6’-yl)methyl]-4,9-dioxo-4,9-dihydro-1H-benzo[f]indole (7b)

The compound 7b was obtained as a yellow solid, mp 197-198 °C, with 44% yield. IR (film) ν / cm^-1 1609 and 1678 (C=O), 1572 (C=C); ¹H NMR (500.00 MHz, CDCl₃) δ 1.17 (s, 3H, CH₃), 1.19 (s, 3H, CH₃), 1.37 (s, 3H, CH₃), 1.50 (s, 3H, CH₃), 2.43 (s, 3H, C₂-CH₃), 2.70 (s, 3H, C=OCH₃), 4.23-4.24 (m, 1H, H-5’), 4.26-4.27 (m, 1H, H-2’), 4.32-4.37 (m, 1H, H-6”), 4.44 (dd, 1H, J 8.0, 1.0 Hz, H-4’), 4.65 (dd, 1H, J 8.0, 2.5 Hz, H-3’), 4.74 (dd, 1H, J 14.0, 2.5 Hz, H-6’), 5.41 (d, 1H, J 5.0 Hz, H-1’), 7.65-7.67 (m, 2H, H-6, H-7), 8.08 (d, 1H, J 9.0 Hz, H-5), 8.12 (d, 1H, J 9.0 Hz, H-8); ¹³C NMR APT (125.0 MHz, CDCl₃) δ 11.4 (C₂-CH₃), 24.7 (CH₃), 25.0 (CH₃), 25.6 (CH₃), 26.3 (CH₃), 31.9 (C=OCH₃), 46.4 (C-6’), 67.7 (C-5’), 70.5 (C-2’), 71.2 (C-3’), 71.7 (C-4’), 96.5 (C-1’), 108.8 (-OCO-), 109.8 (-OCO-), 122.7 (C-3), 125.8 (C-3a), 126.2 (C-5), 126.9 (C-8), 129.7 (C-9a), 133.3 (C-6), 133.4 (C-4a and C-8a), 133.8 (C-7), 143.9 (C-2), 176.2 (C-4), 180.9 (C-9), 199.4 (C=OCH₃); anal. calcd. for C₂₇H₂₉NO₈: C 65.44, H 5.90, N 2.83%, found: C 66.20, H 6.47, N 2.59%.

3-Methyl-2-methyl-2-[(5’-deoxy-1’,2’-O-isopropylidene-D-xilofuranos-5’-yl)]-4,9-dioxo-4,9-dihydro-1H-benzo[f]indole (7c)

The compound 7c was obtained as a yellow solid, mp 227-228 °C, with 48% yield. IR (film) ν / cm^-1 1608 and 1679 (C=O), 1566 (C=C); ¹H NMR (500.00 MHz, CDCl₃) δ 1.28 (s, 3H, CH₃), 1.40 (s, 3H, CH₃), 2.49 (s, 3H, C₂-CH₃), 2.71 (s, 3H, C=OCH₃), 4.35 (dd, 1H, J 15.0, 10.0 Hz, H-5”), 4.38-4.39 (m, 1H, H-3’), 4.40 (dd, 1H, J 10.0, 5.0 Hz, H-4’), 4.58 (d, 1H, J 5.0 Hz, H-2’), 5.09 (dd, 1H, J 15.0, 5.0 Hz, H-5’), 5.96 (d, 1H, J 5.0 Hz, H-1’), 7.67-7.69 (m, 2H, H-6, H-7), 8.09-8.11 (m, 1H, H-5), 8.12-8.13 (m, 1H, H-8); ¹³C NMR APT (125.0 MHz, CDCl₃) δ 11.0 (C₂-CH₃), 25.9 (CH₃), 26.6 (CH₃), 31.5 (C=OCH₃), 44.7 (C-5’), 74.8 (C-4’), 80.3 (C-3’), 85.2 (C-2’), 104.6 (C-1’), 111.8 (-OCO-), 123.2 (C-3), 125.7 (C-3a), 126.3 (C-5), 126.7 (C-8), 129.3 (C-9a), 133.0 (C-6), 133.2 (C-4a), 133.4 (C-8a), 133.5 (C-7), 142.9 (C-2), 176.5 (C-4), 180.4 (C-9), 199.3 (C=OCH₃); anal. calcd. for C₂₅H₂₇NO₈: C 64.93, H 5.45, N 3.29%, found: C 65.64, H 6.38, N 3.01%.

Synthesis of 2-chloro-3-(α-cyano-α-ethoxycarbonyl-methyl)-1,4-naphthoquinone (22)

To a 125 mL round bottom flask were added 1.0 mmol of ethyl cianoacetate (21), 2 mmol of K₂CO₃ and 100 mL of acetonitrile. The reaction was kept under stirring at room temperature for 10 min. Then 1.0 mmol of 2,3-dichloronaphthoquinone (20) was added and stirred for 20 min. The product 22 was purified by chromatography on a silica gel column using hexane/ethyl acetate (7:3) as eluent. This derivative was obtained as a brown solid in 73% yield.

Synthesis of benzo[f]indole-4,9-diones 5a-5c

To a 50 mL round bottom flask containing compound 22 (1.65 mmol) dissolved in 50 mL of ethanol were added 3.3 mmol of aminocarbohydrates 9a-9c. The reaction was kept under reflux for 20 h. The annelated product was purified by chromatography on a silica gel column, using a gradient elution of 90-80% (v/v) hexane in ethyl acetate.

2-Amino-2-methyl-1-(methyl-5’-deoxy-2’,3’-O-iso-propylidene-β-D-methylfuranosid-5’-yl)-4,9-dioxo-4,9-dihydro-1H-benzo[f]indole-3-ethyl carboxylate (5a)

The compound 5a was obtained as a red solid, mp 154-155 °C, with 48% yield. IR (KBr pellets) ν / cm^-1 1683 and 1601 (C=O), 1567 (C=C); ¹H NMR (500.00 MHz, CDCl₃) δ 1.35 (s, 3H, CH₃), 1.46 (t, 3H, J 7.0 Hz, CH₂-CH₃), 1.47 (s, 3H, CH₃), 3.49 (s, 3H, OCH₃), 3.98 (dd, 1H, J 14.5, 9.5 Hz, H-5”), 4.40 (q, 2H, J 7.0 Hz, CH₂-CH₃), 4.70 (d, 1H, J 3.5 Hz, H-4’), 4.73 (d, 1H, J 6.0 Hz, H-2’), 4.82 (dd, 1H, J 6.0, 1.0 Hz, H-3’), 4.99 (dd, 1H, J 14.5, 3.5 Hz, H-5’), 5.03 (s, 1H, H-1’), 6.45 (s, 1H, NH₂), 7.60-7.62 (m, 2H, H-6, H-7), 8.05-8.06 (m, 1H, H-5), 8.09-8.11 (m, 1H, H-8); ¹³C NMR APT (125.0 MHz, CDCl₃) δ 14.6 (CH₂-CH₃), 25.2 (CH₃), 26.6 (CH₃), 48.3 (C-5’), 56.0 (OCH₃), 60.6 (CH₂-CH₃), 82.0 (C-3’), 84.3 (C-2’), 87.2 (C-4’), 94.0 (C-1’), 111.5 (-OCO-), 113.4 (C-3), 125.6 (C-5), 126.2 (C-3a, C-9a), 126.8 (C-8), 132.8 (C-6), 132.8 (C-7), 133.0 (C-4a), 134.0 (C-8a), 153.0 (C-2), 165.8 (C=OOCH₂-CH₃), 175.3 (C-4), 179.6 (C-9).

2-Amino-2-methyl-4-[(6’-deoxy-1’,2’:3’,4’-di-O-iso-propylidene-D-galactopiranos-6’-yl)methyl]-4,9-dioxo-4,9-dihydro-1H-benzo[f]indole-3-ethyl carboxylate (5b)

The compound 5b was obtained as a red solid, mp 178-180 °C, with 41% yield. IR (film) ν / cm^-1 1609 and 1678 (C=O), 1572 (C=C); ¹H NMR (500.00 MHz, CDCl₃) δ 1.18 (s, 3H, CH₃), 1.24 (s, 3H, CH₃), 1.30 (s, 3H, CH₃), 1.38 (t, 3H, J 7.0 Hz, CH₂-CH₃), 1.44 (s, 3H, CH₃), 4.14 (dd, 1H, J 14.5, 8.0 Hz, H-6”), 4.22-4.23 (m, 1H, H-5’), 4.24 (dd, 1H, J 4.5, 2.5 Hz, H-2’), 4.32 (q, 2H, J 7.0 Hz, CH₂-CH₃), 4.37 (dd, 1H, J 8.0, 2.0 Hz, H-4’), 4.59 (dd, 1H, J 8.0, 2.0 Hz, H-3’), 4.70 (dd, 1H, J 14.5, 3.5 Hz, H-6’), 5.44 (d, 1H, J 5.0 Hz, H-1’), 6.06 (s, 2H, NH₂), 7.51-7.55 (m, 2H, H-6, H-7), 7.94 (dd, 1H, J 5.5, 2.5 Hz, H-5), 8.01 (dd, 1H, J 5.5, 2.5 Hz, H-8); ¹³C NMR APT (125.0 MHz, CDCl₃) δ 14.6 (CH₂-CH₃), 24.4 (CH₃), 25.1 (CH₃), 26.0 (CH₃), 26.2 (CH₃), 45.9 (C-6’), 60.6 (CH₂-CH₃), 68.6 (C-5’), 70.7 (C-2’), 70.9 (C-3’), 71.5 (C-4’), 94.5 (C-3), 96.3 (C-1’), 109.3 (-OCO-), 109.8 (-OCO-), 125.4 (C-5), 126.6 (C-3a), 126.8 (C-8), 126.8 (C-9a), 132.7 (C-6), 132.8 (C-7), 132.9 (C-4a), 134.1 (C-8a), 153.5 (C-2), 165.6 (C=OOCH₂-CH₃), 175.3 (C-4), 179.6 (C-9); anal. calcd. for C₂₇H₃₀N₂O₉: C 61.59, H 5.74, N 5.32%, found: C 61.54, H 6.00, N 5.05%.

2-Amino-2-methyl-2-[(5’-deoxy-1’,2’-O-isopropylidene-D-xilofuranos-5’-yl)]-4,9-dioxo-4,9-dihydro-1H-benzo[f]indole-3-ethyl carboxylate (5c)

The compound 5c was obtained as a red solid, mp 163-166 °C, with 56% yield. IR (film) ν / cm^-1 1608 and 1679 (C=O), 1566 (C=C); ¹H NMR (500.00 MHz, CDCl₃) δ 1.29 (s, 3H, CH₃), 1.42 (s, 3H, CH₃), 1.44 (t, 3H, J 7.0 Hz, CH₂-CH₃), 4.22-4.26 (m, 1H, H-5”), 4.39 (q, 2H, J 7.0 Hz, CH₂-CH₃), 4.45 (d, 1H, J 3.0 Hz, H-4’), 4.52 (d, 1H, J 3.0 Hz, H-3’), 4.59 (d, 1H, J 3.5 Hz, H-2’), 5.10 (dd, 1H, J 15.0, 3.0 Hz, H-5’), 6.02 (d, 1H, J 3.5 Hz, H-1’), 7.60-7.62 (m, 2H, H-6, H-7), 8.00 (dd, 1H, J 5.5, 2.5 Hz, H-5), 8.09 (dd, 1H, J 5.5, 2.5 Hz, H-8); ¹³C NMR APT (125.0 MHz, CDCl₃) δ 14.6 (CH₂-CH₃), 26.3 (CH₃), 26.9 (CH₃), 44.6 (C-5’), 60.7 (CH₂-CH₃), 75.4 (C-4’), 81.0 (C-3’), 85.6 (C-2’), 94.8 (C-3), 105.0 (C-1’), 112.4 (-OCO-), 125.5 (C-5), 126.6 (C-3a), 126.9 (C-8), 127.0 (C-9a), 132.8 (C-6), 132.9 (C-4a), 133.0 (C-7), 133.9 (C-8a), 153.4 (C-2), 165.5 (C=OOCH₂-CH₃), 175.7 (C-4), 179.5 (C-9); anal. calcd. for C₂₃H₂₄N₂O₈: C 60.52, H 5.30, N 6.14%, found: C 59.51, H 5.60, N 5.88%.

Supplementary Information

Supplementary data are available free of charge at http://jbcs.sbq.org.br as PDF file.

Acknowledgments

We acknowledge CNPq/Universal (420491/2016-3), FIOCRUZ, CAPES (post-doctoral fellowship for F. S. G.), FAPERJ (CNE, E-26/202.955/2016; E-26/202.763/2018 and E-26/010.001837/2015 for P. D. F.) and CNPQ (405332/2016 and 304394/2017-3 for P. D. F.) for financial support and research fellowships.

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Publication Dates

• Publication in this collection
  01 Mar 2021
• Date of issue
  Mar 2021

History

• Received
  24 June 2020
• Accepted
  8 Oct 2020