Synthesis and Cytotoxic Evaluation of Alkoxylated Chalcones

Bai, Xiao-Guang; Xu, Chang-Liang; Zhao, Shuang-Shuang; He, Hong-Wei; Wang, Yu-Cheng; Wang, Ju-Xian

doi:10.3390/molecules191117256

Open AccessArticle

Synthesis and Cytotoxic Evaluation of Alkoxylated Chalcones

Institute of Medicinal Biotechnology, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China

^*

Author to whom correspondence should be addressed.

^†

These authors contributed equally to this work.

Molecules 2014, 19(11), 17256-17278; https://doi.org/10.3390/molecules191117256

Submission received: 25 July 2014 / Revised: 26 September 2014 / Accepted: 17 October 2014 / Published: 28 October 2014

(This article belongs to the Section Medicinal Chemistry)

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Abstract

:

A series of chalcones a1–20 bearing a 4-OMe groups on the A-ring were initially synthesized and their anticancer activities towards HepG2 cells evaluated. Subsequently, a series of chalcones b1–42 bearing methoxy groups at the 2' and 6'-positions of the B-ring were synthesized and their anticancer activities towards five human cancer cell lines (HepG2, HeLa, MCF-7, A549 and SW1990) and two non-tumoral human cell lines evaluated. The results showed that six compounds (b6, b8, b11, b16, b18, b22, b23 and b29) displayed promising activities, with compounds b22 and b29 in particular showing higher levels of activity than etoposide against all five cancer cell lines. Compound b29 showed a promising SI value compared with both HMLE and L02 (2.1–6.5 fold in HMLE and > 33 > 103.1 fold in L02, respectively).

Keywords:

alkoxylated chalcones; synthesis; cytotoxicity

1. Introduction

Chalcones (1,3-diaryl-2-propen-1-ones, Figure 1) are naturally occurring compounds that are widely distributed in a variety of plant species. Compounds belonging to this structural class have been identified as both intermediates and end products in the biosynthesis of flavonoids, and make significant contributions to the medicinal value of herbs. The ease of preparation of these compounds, as well as their potential for oral administration and safety, make them good candidates for use as therapeutic agents in drug discovery [1]. For these reasons, chalcones have attracted considerable attention from chemists and pharmacologists, and a large number of results have been reported in the literature pertaining to the biological activities of both naturally occurring and synthetic chalcone compounds, including their anti-inflammatory [2,3], antimicrobial [4,5,6], antifungal [7,8], antioxidant [9] and anticancer activities [10,11,12,13,14,15].

Figure 1. General structure of chalcones.

The antitumor properties of chalcones have received considerable attention during the last few years, because they operate via a similar mode of action to the structurally related combretastatin [16]. The frequent occurrence of polymethoxyphenyl-type moieties in naturally occurring anticancer agents, such as colchicine and combretastatin, has inspired scientists to investigate the synthesis and biological evaluation of methoxylated chalcones, and the results of these studies have shown that methoxy groups generally make a significant contribution to the cytotoxicity of these compounds [17,18,19].

To develop potential anticancer drugs based on chalcones, as well as improve our understanding of the structure-activity relationships (SARs) of these compounds, we report herein the synthesis of a series of alkoxylated chalcones. The cytotoxic activities of these 62 compounds have also been evaluated against a panel of five cancer cell lines and two normal human cell lines, including HepG2, HeLa, MCF-7, A549, SW1990, HMLE and L02 cells.

2. Results and Discussion

Compounds a1–20 bearing a 4-OMe on their A-ring (i.e., their 1-phenyl moiety) were initially synthesized and evaluated in terms of their activity towards human liver carcinoma HepG2 cells using a SRB assay. This evaluation was conducted to develop a better understanding of the structural-activity relationship (SAR) of the B-ring of these compounds and the activity results (percentage rates at concentration of 10 μM) are shown in Table 1.

Table 1. Inhibitory activities of the 4-methoxyl chalcones a1–20 against HepG2 cells (10 μM). Molecules 19 17256 i001

**Table 1.** Inhibitory activities of the 4-methoxyl chalcones a1–20 against HepG2 cells (10 μM).
Compound	R¹	R²	R³	R⁴	R⁵	Inhibition (%) **
a1	H	H	H	H	H	42.4 ± 2.0
a2	H	H	Br	H	H	37.6 ± 4.4
a3	F	H	Br	H	H	41.8 ± 5.9
a4 *	Br	H	F	H	H	41.2 ± 4.6
a5 *	Cl	H	Br	H	H	9.0 ± 5.6
a6	H	H	NO₂	H	H	9.8 ± 5.0
a7	H	H	COOH	H	H	32.7 ± 3.0
a8	OCH₃	H	H	H	H	61.4 ± 3.4
a9	H	OCH₃	H	H	H	59.0 ± 2.9
a10	H	H	OCH₃	H	H	27.7 ± 17.7
a11	H	H	OCH₂CH₃	H	H	13.1 ± 8.4
a12	OCH₃	OCH₃	H	H	H	66.3 ± 4.2
a13	OCH₃	H	H	OCH₃	H	77.0 ± 2.2
a14 *	OCH₃	H	H	H	OCH₃	78.1 ± 4.7
a15	H	OCH₃	OCH₃	H	H	65.0 ± 17.6
a16	H	OCH₃	H	OCH₃	H	70.6 ± 2.0
a17	H	OCH₂Ph	OCH₃	H	H	44.1 ± 6.2
a18	OCH₃	OCH₃	OCH₃	H	H	31.8 ± 7.3
a19	OCH₃	H	OCH₃	OCH₃	H	38.1 ± 10.3
a20	H	OCH₃	OCH₃	OCH₃	H	71.1 ± 1.3
Etoposide						63.9 ± 0.1

*: Novel compound; **: The results are shown as the average percentage of the individual mean (±SD, standard deviation) for three independent experiments.

The introduction of halogen atoms (i.e., compounds a2–5), a NO₂ substituent (a6) and a COOH group (a7) on the B-ring led to a decrease in the activity of these compounds compared with the parent compound a1.Contrary to a2–7, compounds a8–20 which were substituted with electron donating groups (i.e., OMe, OEt and OBn), generally exhibited moderate to high levels of inhibition. A single OMe group substituted at the 2'-position (a8) or 3'-position (a9) led to much better inhibition than that of the 4'-position (a10). A comparison of a10 vs. a11 and a15 vs. a17 revealed that bulky substituents seemed to be poorly tolerated at the 3' and 4'-position. Interestingly, the substitution of the B ring with two OMe groups (compounds a12–16) led to a general increase in the activity (inhibition 65.0%–78.1%), with bis-substitution at the 2' and 6' positions (a14) providing the best results. The trimethoxy- substituted chalcones synthesized in the current study (i.e., compound a18–20) showed weak anti-proliferative activity towards HepG2 cells, except for the 3',4',5'-trimethoxy compound a20.

It is possible to draw some conclusions from the results in Table 1, including: (1) the introduction of electron donating groups to the B-ring generally made a positive contribution to the cytotoxicity, whereas electron withdrawing groups tended to have an adverse impact on the cytotoxicity; (2) the position and size of the substituents might have a specific impact on the activity of these compounds; and (3) the presence of two OMe moiety on the B-ring led to an remarkable increase in the cytotoxic activity.

With a aim of identifying potential anticancer agents with enhanced levels of activity, as well as verifying the conclusions provided above, we took a14 as a starting compound, and then designed and synthesized a series of chalcones b1–42 bearing methoxy groups at the 2' and 6'-positions of the B-ring, whilst varying the substituents on the A-ring. The cytotoxicities of the resulting chalcones were evaluated in vitro against five human cancer cell lines and other two non-tumoral cell lines, including HepG2, HeLa, MCF-7, A549, SW1990, HMLE and L02, and the results are shown in Table 2.

Compounds bearing electron donating groups (i.e., Me, OMe, OEt, OBn, OCH₂O, CH₂CH₂O, Ph, NH₂ and OH) generally exhibited higher levels of anticancer activity than those with electron withdrawing groups (i.e., F, Cl, Br, NO₂, CN and CF₃). Furthermore, chalcones substituted with alkoxyl groups exhibited greater cytotoxic activities than those substituted with methyl, amino or hydroxyl groups (e.g., the IC₅₀ values of b6–11 were lower than those of b2–5 and b23–27). A comparison of b2–4, b6–13 and b24–26 revealed that both the position and the size of the substituents had a significant impact on the cytotoxic activities of the compounds, with the position effect appearing to be of the order o > m > p (confirmed by b30–33), and the size contribution following the order OMe > OEt > OBn (b11 is an exception to this order).

A review of compounds b30 to b42 revealed that those with electron withdrawing groups exhibited weak cytotoxic activity, and that the cytotoxic activities of these compounds were related to the electrophilic nature of their substituents. For example, nearly all of the IC₅₀ values for compounds b30 and b39–42, which had a CN, NO₂ or CF₃ group on their A-ring, were greater than 30 µM.

It’s noteworthy that compound b6, b8, b11, b16, b18, b22, b23 and b29 exhibited the most outstanding activities among all the compounds tested in this study, with most of their in vitro IC₅₀ values against the five human cancer lines being less than 10 µM. Compound b22 was 20.4- and 23.6-fold as potent than etoposide against HepG2 and SW1990 cells, respectively, and compound b29 was 11.5-fold more potent than etoposide against A549 cells. These two compounds displayed the best activity and therefore are deserving of further investigation.

All compounds were also evaluated for their cytotoxic activity against two non-tumoral human cell lines named human mammary epithelial cell (HMLE) and L02 (a human liver cell line) in Table 2 and SI values between the CC₅₀ in non-tumoral cell lines and IC₅₀ in tumoral cells calculated. The data indicate that about one third of the compounds (b8, b11–13, b16, b18–24, b28–29, b31–32, b34, b36–38) exhibit more than 2-fold better SI between the CC₅₀ in L02 and IC₅₀ in tumoral cells, which is similar to the value of etoposide. Among them, compounds b11, b16, b22, b23 exhibited over 5-fold better SI toward L02. However, most compounds’ SI values between the CC₅₀ in HMLE and IC₅₀ in tumoral cells are unsatisfactory, except for b11, b27, b29 and b31 (2–7 fold), which is also similar to etoposide. Fortunately, compound b11, and especially b29, showed promising SI values compared with both HMLE and L02 (2.1–6.5 fold in HMLE and >33–>103.1 fold, respectively).

Table 2. Cytotoxicities of the 2',6'-dimethoxyl chalcones b1–b42 against five human cancer cell lines and two non-tumoral cell lines. Molecules 19 17256 i002

**Table 2.** Cytotoxicities of the 2',6'-dimethoxyl chalcones b1–**b42** against five human cancer cell lines and two non-tumoral cell lines.
Compound	R¹	R²	R³	R⁴	Human Cancer Cell Lines, IC₅₀ (µM) & SI										Normal Human Cell Lines, CC₅₀ (µM)^b
					HepG2		HeLa		MCF7		A549		SW1990		HMLE	L02
					IC₅₀ ^a		IC₅₀ ^a		IC₅₀ ^a		IC₅₀ ^a		IC₅₀ ^a
					SI ^c	SI ^d	SI ^e	SI ^f	SI ^g	SI ^h	SI ⁱ	SI ^j	SI ^k	SI ^l
b1 ^#	H	H	H	H	20.98 ± 1.75		>30		28.18 ± 0.04		>30		>30		9.47 ± 0.39	33.340.39e
b1 ^#	H	H	H	H	0.5	1.6	<0.3	<1.1	0.3	1.2	<0.3	<1.1	<0.3	<1.1	9.47 ± 0.39	33.340.39e
b2	CH₃	H	H	H	14.07 ± 1.84		18.40 ± 0.75		19.08 ± 2.11		25.47 ± 4.14		>30		14.98 ± 0.78	35.87 ± 3.40
b2	CH₃	H	H	H	1.1	2.5	0.8	1.9	0.8	1.9	0.6	1.4	<0.5	<1.2	14.98 ± 0.78	35.87 ± 3.40
b3	H	CH₃	H	H	12.81 ± 0.50		13.28 ± 2.14		26.78 ± 4.26		20.69 ± 0.59		25.23 ± 2.00		16.20 ± 0.19	33.26 ± 1.61
b3	H	CH₃	H	H	1.3	2.6	1.2	2.5	0.6	1.2	0.8	1.6	0.6	1.3	16.20 ± 0.19	33.26 ± 1.61
b4	H	H	CH₃	H	19.51 ± 1.28		18.60 ± 0.36		25.44 ± 0.15		22.07 ± 0.60		>30		13.77 ± 1.69	59.59 ± 5.56
b4	H	H	CH₃	H	0.7	3.1	0.7	3.2	0.5	2.3	0.6	2.7	<0.5	<2.0	13.77 ± 1.69	59.59 ± 5.56
b5	H	CH₃	CH₃	H	26.79 ± 0.30		20.33 ± 1.01		30.31 ± 0.29		>30		>30		15.66 ± 0.76	25.15 ± 2.71
b5	H	CH₃	CH₃	H	0.6	0.9	0.8	1.2	0.5	0.8	<0.5	<0.8	<0.5	<0.8	15.66 ± 0.76	25.15 ± 2.71
b6 ^#	OCH₃	H	H	H	2.05 ± 0.22		5.00 ± 0.03		5.60 ± 0.17		6.35 ± 0.32		10.02 ± 0.14		4.01 ± 0.05	8.78 ± 1.21
b6 ^#	OCH₃	H	H	H	2.0	4.3	0.8	1.8	0.7	1.6	0.6	1.4	0.4	0.9	4.01 ± 0.05	8.78 ± 1.21
b7	H	OCH₃	H	H	6.97 ± 0.55		9.98 ± 0.37		6.37 ± 0.05		14.02 ± 0.19		15.62		8.14 ± 0.53	18.08 ± 5.82
b7	H	OCH₃	H	H	1.2	2.6	0.8	1.8	1.3	2.8	0.6	1.3	0.5	1.2	8.14 ± 0.53	18.08 ± 5.82
a16			OCH₃		9.20 ± 0.31		12.42 ± 0.34		23.10 ± 0.79		21.18 ± 0.55		17.80 ± 0.07		3.28 ± 0.31	8.87 ± 1.83
a16			OCH₃		0.4	1.0	0.3	0.7	0.1	0.4	0.2	0.4	0.2	0.5	3.28 ± 0.31	8.87 ± 1.83
b8	OCH₂CH₃	H	H	H	4.23 ± 0.09		8.72 ± 0.07		8.56 ± 0.17		7.36 ± 0.37		8.20 ± 0.12		0.83 ± 0.21	39.55 ± 7.53
b8	OCH₂CH₃	H	H	H	0.2	9.3	0.1	4.5	0.1	4.6	0.1	5.4	0.1	4.8	0.83 ± 0.21	39.55 ± 7.53
b9	H	OCH₂CH₃	H	H	7.71 ± 0.21		12.16 ± 0.25		11.59 ± 0.07		13.22 ± 0.43		10.68 ± 0.08		9.58 ± 0.44	17.42 ± 5.96
b9	H	OCH₂CH₃	H	H	1.2	2.3	0.8	1.4	0.8	1.5	0.7	1.3	0.9	1.6	9.58 ± 0.44	17.42 ± 5.96
b10	H	H	OCH₂CH₃	H	10.92 ± 0.46		14.36 ± 0.15		19.76 ± 0.69		22.72 ± 0.57		19.47 ± 0.23		13.81 ± 3.77	36.66 ± 3.41
b10	H	H	OCH₂CH₃	H	1.3	3.4	1.0	2.6	0.7	1.9	0.6	1.6	0.7	1.9	13.81 ± 3.77	36.66 ± 3.41
b11	OCH₂Ph	H	H	H	2.76 ± 0.04		3.62 ± 0.07		4.15 ± 0.2		3.63 ± 0.13		7.43 ± 0.56		20.99 ± 1.26	38.28 ± 5.63
b11	OCH₂Ph	H	H	H	7.6	13.9	5.8	10.6	5.1	9.2	5.8	10.5	2.8	5.2	20.99 ± 1.26	38.28 ± 5.63
b12	H	OCH₂Ph	H	H	23.59 ± 0.84		25.59 ± 1.16		29.03 ± 0.09		13.25 ± 0.02		22.30 ± 0.07		31.40 ± 1.12	>100
b12	H	OCH₂Ph	H	H	1.3	>4.2	1.2	>3.9	1.1	>3.4	2.4	>7.5	1.4	>7.5	31.40 ± 1.12	>100
b13 ^#	H	H	OCH₂Ph	H	21.75 ± 0.62		>30		>30		>30		>30		>100	>100
b13 ^#	H	H	OCH₂Ph	H	>4.6	>4.6	-	-	-	-	-	-	-	-	>100	>100
b14	OCH₂Ph	H	OCH₃	H	>30		>30		>30		>30		>30		>100	>100
b14	OCH₂Ph	H	OCH₃	H	-	-	-	-	-	-	-	-	-	-	>100	>100
b15	H	OCH₃	OCH₂Ph	H	>30		>30		>30		>30		>30		>100	>100
b15	H	OCH₃	OCH₂Ph	H	-	-	-	-	-	-	-	-	-	-	>100	>100
b16	H	OCH₃	OCH₂CH₃	H	4.14 ± 0.11		5.02 ± 0.09		4.79 ± 0.13		5.78 ± 0.11		7.67 ± 0.04		9.15 ± 1.33	44.70 ± 8.15
b16	H	OCH₃	OCH₂CH₃	H	2.2	10.8	1.8	8.9	1.9	9.3	1.6	7.7	1.2	5.8	9.15 ± 1.33	44.70 ± 8.15
b17	OCH₂CH₃	H	OCH₃	H	11.97 ± 0.23		8.54 ± 0.14		7.74 ± 0.10		9.33 ± 0.30		10. 80 ± 0.50		9.03 ± 0.80	10.92 ± 0.42
b17	OCH₂CH₃	H	OCH₃	H	0.8	0.9	1.1	1.3	1.2	1.4	1.0	1.2	0.8	1.0	9.03 ± 0.80	10.92 ± 0.42
b18	OCH₃	H	H	OCH₃	1.59 ± 0.15		4.56 ± 0.22		5.60 ± 0.06		4.16 ± 0.72		9.64 ± 0.18		2.48 ± 0.34	16.97 ± 2.73
b18	OCH₃	H	H	OCH₃	1.6	10.7	0.5	3.7	0.4	3.0	0.6	4.1	0.3	1.8	2.48 ± 0.34	16.97 ± 2.73
b19 ^#	H	OCH₃	OCH₃	H	7.12 ± 0.67		9.26 ± 0.04		19.67 ± 0.20		13.62 ± 0.85		13.84 ± 0.06		10.53 ± 0.41	39.75 ± 6.32
b19 ^#	H	OCH₃	OCH₃	H	1.5	5.6	1.1	4.3	0.5	2.0	0.8	2.9	0.8	2.9	10.53 ± 0.41	39.75 ± 6.32
b20 ^#	H	OCH₂O		H	17.46 ± 0.54		16.23 ± 0.95		22.54 ± 0.37		19.50 ± 0.90		25.85 ± 0.65		14.21 ± 1.06	60.90 ± 5.61
b20 ^#	H	OCH₂O		H	0.8	3.5	0.9	3.8	0.6	2.7	0.7	3.1	0.5	2.4	14.21 ± 1.06	60.90 ± 5.61
b21	H	CH₂CH₂O		H	17.34 ± 0.23		21.57 ± 0.43		22.62 ± 2.10		22.26 ± 0.99		24.37 ± 0.60		14.58 ± 0.81	57.48 ± 13.57
b21	H	CH₂CH₂O		H	0.8	3.3	0.7	2.7	0.6	2.5	0.7	2.6	0.6	2.4	14.58 ± 0.81	57.48 ± 13.57
b22	H	H	Ph	H	0.25 ± 0.03		0.87 ± 0.25		2.40 ± 0.08		1.75 ± 0.15		1.24 ± 0.08		2.21 ± 0.09	14.54 ± 6.58
b22	H	H	Ph	H	8.8	58.2	2.5	16.7	0.9	6.1	1.3	8.3	1.8	11.7	2.21 ± 0.09	14.54 ± 6.58
b23 ^#	H	NH₂	H	H	5.70 ± 0.09		7.23 ± 0.07		8.56 ± 0.75		7.32 ± 0.29		10.07 ± 0.03		11.41 ± 0.76	43.18 ± 11.74
b23 ^#	H	NH₂	H	H	2.0	7.6	1.6	6.0	1.3	5.0	1.6	5.9	1.1	4.3	11.41 ± 0.76	43.18 ± 11.74
b24 ^#	OH	H	H	H	7.77 ± 0.08		13.38 ± 0.74		10.68 ± 0.38		8.64 ± 0.31		16.11 ± 0.32		8.96 ± 0.44	24.22 ± 2.71
b24 ^#	OH	H	H	H	1.2	3.1	0.7	1.8	0.8	2.3	1.0	2.8	0.6	1.5	8.96 ± 0.44	24.22 ± 2.71
b25	H	OH	H	H	7.27 ± 0.13		9.56 ± 0.33		8.92 ± 0.25		12.73 ± 0.28		21.03 ± 0.43		6.31 ± 0.13	19.64 ± 1.29
b25	H	OH	H	H	0.9	2.7	0.7	2.1	0.7	2.2	0.5	1.5	0.3	0.9	6.31 ± 0.13	19.64 ± 1.29
b26 ^#	H	H	OH	H	14.38 ± 0.81		12.73 ± 0.81		20.24 ± 0.30		23.75 ± 1.56		20.76 ± 0.54		12.55 ± 2.82	28.16 ± 1.69
b26 ^#	H	H	OH	H	0.9	2.0	1.0	2.2	0.6	1.4	0.5	1.2	0.6	1.4	12.55 ± 2.82	28.16 ± 1.69
b27	OH	H	OH	H	17.39 ± 1.01		24.84 ± 0.17		23.08 ± 0.82		17.27 ± 0.76		>30		>100	35.46 ± 5.72
b27	OH	H	OH	H	>5.8	2.0	>4.0	1.4	>4.3	1.5	>5.8	2.1	-	<1.2	>100	35.46 ± 5.72
b28 ^#	OH	H	OCH₃	H	19.52 ± 0.79		17.02 ± 0.65		28.37 ± 1.25		17.37 ± 0.97		28.30 ± 0.26		16.25 ± 2.48	>100
b28 ^#	OH	H	OCH₃	H	0.8	>5.1	1.0	>5.9	0.6	>3.5	0.9	>5.8	0.6	>3.5	16.25 ± 2.48	>100
b29	H	OCH₃	OH	H	0.97 ± 0.04		1.83 ± 0.08		1.79 ± 0.20		1.50 ± 0.07		3.03 ± 0.05		6.31 ± 0.13	>100
b29	H	OCH₃	OH	H	6.5	>103.1	3.4	>54.6	3.5	>55.9	4.2	>66.7	2.1	>33.0	6.31 ± 0.13	>100
b30	H	H	CN	H	20.45 ± 0.21		>30		>30		>30		>30		12.55 ± 2.82	>100
b30	H	H	CN	H	0.6	>4.9	<0.4	-	<0.4	-	<0.4	-	<0.4	-	12.55 ± 2.82	>100
b31	F	H	H	H	17.98 ± 0.88		23.33 ± 0.42		23.51 ± 0.98		27.44 ± 0.67		>30		>100	>100
b31	F	H	H	H	>5.6	>5.6	>4.3	>4.3	>4.3	>4.3	>3.6	>3.6	-	-	>100	>100
b32	H	F	H	H	21.56 ± 0.97		20.67 ± 0.78		25.52 ± 0.78		27.15 ± 1.39		28.38 ± 0.27		11.91 ± 1.28	72.01 ± 12.10
b32	H	F	H	H	0.6	3.3	0.6	3.5	0.5	2.8	0.4	2.7	0.4	2.5	11.91 ± 1.28	72.01 ± 12.10
b33	H	H	F	H	24.55 ± 0.36		17.41 ± 0.39		32.22 ± 1.34		>30		>30		12.73 ± 2.35	63.86 ± 13.78
b33	H	H	F	H	0.5	2.6	0.7	3.7	0.4	2.0	<0.4	<2.1	<0.4	<2.1	12.73 ± 2.35	63.86 ± 13.78
b34	H	Cl	H	H	13.45		16.55		21.97		16.08		21.44		9.42 ± 1.21	46.87 ± 13.91
b34	H	Cl	H	H	0.7	3.5	0.6	2.8	0.4	2.1	0.6	2.9	0.4	2.2	9.42 ± 1.21	46.87 ± 13.91
b35 ^#	H	H	Cl	H	27.09 ± 0.88		18.40 ± 0.06		29.76 ± 0.80		>30		>30		17.71 ± 1.35	85.43 ± 6.86
b35 ^#	H	H	Cl	H	0.7	3.2	1.0	4.6	0.6	2.9	<0.6	<2.8	<0.6	<2.8	17.71 ± 1.35	85.43 ± 6.86
b36	H	Br	H	H	11.30 ± 1.45		13.38 ± 0.44		23.33 ± 0.79		25.03 ± 3.17		17.13 ± 0.57		13.07 ± 1.21	61.24 ± 12.11
b36	H	Br	H	H	1.2	5.4	1.0	4.6	0.6	2.6	0.5	2.4	0.8	3.6	13.07 ± 1.21	61.24 ± 12.11
b37	Cl	H	Cl	H	11.73 ± 0.18		15.69 ± 1.09		30.35 ± 0.71		>30		15.36 ± 0.83		19.82 ± 1.44	>100
b37	Cl	H	Cl	H	1.7	>8.5	1.3	>6.4	0.7	>3.3	<0.7	-	1.3	>6.5	19.82 ± 1.44	>100
b38	H	Cl	Cl	H	18.58 ± 1.24		17.55 ± 2.01		29.58 ± 2.13		27.63 ± 0.58		26.16 ± 0.08		28.34 ± 3.74	>100
b38	H	Cl	Cl	H	1.5	>5.4	1.6	>5.7	1.0	>3.4	1.0	>3.6	1.1	>3.8	28.34 ± 3.74	>100
b39	H	NO₂	H	H	>30		>30		>30		>30		>30		>100	>100
b39	H	NO₂	H	H	-	-	-	-	-	-	-	-	-	-	>100	>100
b40	H	H	NO₂	H	>30		>30		>30		>30		>30		>100	>100
b40	H	H	NO₂	H	-	-	-	-	-	-	-	-	-	-	>100	>100
b41	H	CF₃	H	H	24.37 ± 5.87		29.07 ± 3.06		>30		>30		>30		>100	>100
b41	H	CF₃	H	H	>4.1	>4.1	>3.4	>3.4	-	-	-	-	-	-	>100	>100
b42	H	CF₃	H	CF₃	>30		>30		>30		>30		>30		>100	>100
b42	H	CF₃	H	CF₃	-	-	-	-	-	-	-	-	-	-	>100	>100
Etoposide					5.11 ± 0.45		3.96 ± 0.17		20.57 ± 0.34		3.23 ± 0.28		29.32 ± 1.73		6.42 ± 0.39	>100
Etoposide					1.3	>19.6	1.6	>25.3	0.3	>4.9	2.0	>31	0.2	>3.4	6.42 ± 0.39	>100

# Known compound; ^a IC₅₀ values were calculated by SigmaPlot 10.0 as the compounds concentrations producing half maximal inhibition after incubating the cells with increasing concentrations up to 30 μM. Data are the mean ± SD of at least three independent experiments; ^b CC₅₀ values were calculated by SigmaPlot 10.0 as the compounds concentrations producing half maximal inhibition after incubating the cells with increasing concentrations up to 100 μM. Data are the mean ± SD of at least three independent experiments. SI = selectivity index, given by ^c (CC₅₀^HMLE/IC₅₀^HepG2); ^d (CC₅₀^L02/IC₅₀^HepG2); ^e (CC₅₀^HMLE/IC₅₀^Hela); ^f (CC₅₀^L02/IC₅₀^Hela); ^g (CC₅₀^HMLE/IC₅₀^MCF7); ^h (CC₅₀^L02/IC₅₀^MCF7); ⁱ (CC₅₀^HMLE/IC₅₀^A549); ^j (CC₅₀^L02/IC₅₀^A549); ^k (CC₅₀^HMLE/IC₅₀^SW1990) or ^l (CC₅₀^L02/IC₅₀^SW1990); “-” means SI value can’t be calculated.

3. Experimental

3.1. Chemistry

3.1.1. General Methods

All of the solvents and reagents used in the current study were purchased from commercial suppliers and used without further purification. Melting points were determined in open capillaries and are uncorrected. The reaction products were purified by crystallization or flash column chromatography using a mixture of petroleum ether and ethyl acetate as the eluent. ¹H-NMR spectra were recorded on Varian Inova-400 MHz, Varian Inova-500 MHz and SYS-600 MHz instruments (Varian, Palo Alto, CA, USA). ¹³C-NMR spectra were recorded on a 600 MHz Bruker ARX-600 spectrometer (Bruker Bioscience, Billerica, MA, USA). The chemical shifts (δ) are reported in ppm relative to the internal reference standard tetramethylsilane (TMS) and the coupling constants (J values) have been reported in Hertz (Hz). MS data were obtained using time-of-flight mass spectrometer (TOF-MS) or Bruker microTOF-Q instrument (Bruker, Billerica, MA, USA). High resolution mass spectra (HRMS) were obtained on a Q-TOF Ultima ESI instrument (micrOTOF-Q II, Bruker Daltonics, Leipzig, Germany). Analysis by thin layer chromatography (TLC) was performed on silica gel plates (Merck, Billerica, MA, USA). Automated column chromatography was conducted over silica gel using a Companion Rf 200 automated chromatography system (Teledyne ISCO, Lincoln, NE, USA). The chalcones were prepared according to methods previously described in the literature 6, 13–15 [20,21,22].

The chalcones evaluated in the current study were synthesized by the base catalyzed Claisen-Schmidt condensation reaction of the appropriately substituted acetophenones and aldehydes (Scheme 1). The chalcones prepared according to this method were formed predominantly with the (E)-configuration (J_H2-H3 = 15–16 Hz).

Scheme 1. Synthesis of compounds a1–20 and b1–42.

3.1.2. General Procedure for Synthesis of Chalcones

A 50 mL flask was charged with substituted acetophenone (5 mmol) and a solution of sodium hydroxide (10 mmol) in a 4:1 (v/v) mixture of ethanol/H₂O (25 mL), and the resulting mixture was stirred at room temperature for 5 min. A substituted benzaldehyde (5 mmol) was then added to the reaction, and the resulting mixture was stirred at room temperature. The reaction was then monitored by TLC using ethyl acetate/petroleum ether (1:4 or 1:2 v/v) as the solvent system. Upon completion of the reaction, the crude product was filtered off and recrystallized from a mixture of dichloromethane and ethanol or purified by column chromatography over silica gel eluting with a mixture of petroleum ether and ethyl acetate to give the pure product.

3.1.3. Characterization Data

(E)-1-(4-Methoxyphenyl)-3-phenylprop-2-en-1-one (a1). White solid (76%), mp: 104.1–105.3 °C ([23] 103–105 °C). ¹H-NMR (400 MHz, DMSO-d₆) δ 8.19–8.17 (m, 2H), 7.95 (d, J = 15.6 Hz, 1H), 7.91–7.86 (m, 2H), 7.72 (d, J = 15.6 Hz, 1H), 7.47–7.45 (m, 3H), 7.11–7.09 (m, 2H), 3.88 (s, 3H); MS (ESI) m/z = 261 (M+Na)⁺; HRMS (ESI) m/z calcd. for C₁₆H₁₄O₂ [M+Na] 261.0896, found 261.0875 [M+Na].

(E)-1-(4-Methoxyphenyl)-3-(4-bromophenyl)prop-2-en-1-one (a2). Yellow solid (84%), mp: 153.7–155.1 °C ([24] 157 °C). ¹H-NMR (400 MHz, DMSO-d₆) δ 8.18 (d, J = 8.8 Hz, 2H), 7.99 (d, J = 15.6 Hz, 1H), 7.86 (d, J = 8.4 Hz, 2H), 7.68 (d, J = 15.6 Hz, 1H), 7.66 (d, J = 8.4 Hz, 2H), 7.09 (d, J = 8.8 Hz, 2H), 3.88 (s, 3H); MS (ESI) m/z = 339 (M+Na)⁺; HRMS (ESI) m/z calcd. for C₁₆H₁₃BrO₂ [M+Na] 338.9991, found 338.9980 [M+Na].

(E)-1-(4-Methoxyphenyl)-3-(4-bromo-2-fluorophenyl)prop-2-en-1-one (a3). White solid (99%), mp: 122.2–123.6 °C. ¹H-NMR (500 MHz, DMSO-d₆) δ 8.16 (d, J = 9.0 Hz, 2H), 8.11 (m, 1H), 8.03 (d, J = 15.5 Hz, 1H), 7.73 (d, J = 15.5 Hz, 1H), 7.71–7.68 (m, 1H), 7.56–7.54 (m, 1H), 7.10 (d, J = 9.0 Hz, 2H), 3.88 (s, 3H); MS (ESI) m/z = 357 (M+Na)⁺.

(E)-1-(4-Methoxyphenyl)-3-(2-bromo-4-fluorophenyl)prop-2-en-1-one (a4). White solid (63%), mp: 98.7–101.0 °C. ¹H-NMR (400 MHz, DMSO-d₆) δ 8.31–8.27 (m, 1H), 8.19 (d, J = 9.2 Hz, 2H), 7.96 (d, J = 15.6 Hz, 1H), 7.92 (d, J = 15.6 Hz, 1H), 7.75–7.72 (m, 1H), 7.44–7.39 (m, 1H), 7.10 (d, J = 9.2 Hz, 2H), 3.88 (s, 3H); ¹³C-NMR (150 MHz, DMSO-d₆): 187.5, 163.9, 139.8, 131.6, 131.4, 130.9, 130.6, 126.2, 125.3, 120.9, 116.2, 114.6, 56.1; MS (ESI) m/z = 357 (M+Na)⁺; HRMS (ESI) m/z calcd. for C₁₆H₁₂BrFO₂ [M+Na] 356.9897, found 356.9889 [M+Na].

(E)-1-(4-Methoxyphenyl)-3-(4-bromo-2-chlorophenyl)prop-2-en-1-one (a5). White solid (86%), mp: 145.3–146.4 °C. ¹H-NMR (500 MHz, DMSO-d₆) δ 8.20–8.18 (m, 3H), 8.05 (d, J = 15.5 Hz, 1H), 7.92 (d, J = 15.5 Hz, 1H), 7.87 (s, 1H), 7.68–7.67 (m, 1H), 7.10 (m, 2H), 3.88 (s, 3H); ¹³C-NMR (150 MHz, DMSO-d₆): δ 187.4, 164.0, 137.1, 135.6, 132.7, 132.3, 131.6, 131.2, 130.5, 130.4, 125.8, 124.4, 114.6, 56.1; MS (ESI) m/z = 351/353 (M+H)⁺.

(E)-1-(4-Methoxyphenyl)-3-(4-nitrophenyl)prop-2-en-1-one (a6).Yellow solid (63%), mp: 170.2–171.5 °C ([25] 168–169 °C). ¹H-NMR (500 MHz, DMSO-d₆) δ 8.30–8.28 (m, 2H), 8.21 (d, J = 9.0 Hz, 2H), 8.16–8.13 (m, 3H), 7.79 (d, J = 16.0 Hz, 1H), 7.11 (d, J = 9.0 Hz, 2H), 3.89 (s, 3H); MS (ESI) m/z = 284 (M+H)⁺; HRMS (ESI) m/z calcd. for C₁₆H₁₃NO₄ [M+H] 284.0917, found 284.0916 [M+H].

(E)-1-(4-Methoxyphenyl)-3-(4-carbonylphenyl)prop-2-en-1-one (a7) [26]. Yellow solid (40%), mp: >350 °C. ¹H-NMR (400 MHz, DMSO-d₆) δ 8.18 (d, J = 8.8 Hz, 2H), 7.92 (d, J = 15.6 Hz, 1H), 7.90 (d, J = 8.0 Hz, 2H), 7.77 (d, J = 8.0 Hz, 2H), 7.71 (d, J = 15.6 Hz, 1H), 7.09 (d, J = 8.8 Hz, 2H), 3.88 (s, 3H); MS (ESI) m/z = 321 (M+K)⁺.

(E)-1-(4-Methoxyphenyl)-3-(2-methoxyphenyl)prop-2-en-1-one (a8). Yellow solid (82%). mp: 43.2–45.5 °C ([27] 44–45 °C). ¹H-NMR (500 MHz, DMSO-d₆) δ 8.16–8.14 (m, 2H), 8.05 (d, J = 15.5 Hz, 1H), 7.99–7.97 (m, 1H), 7.89 (d, J = 15.5 Hz, 1H), 7.47–7.44 (m, 1H), 7.13–7.09 (m, 3H), 7.06–7.03 (m, 1H), 3.91 (s, 3H), 3.88 (s, 3H); MS (ESI) m/z = 269 (M+H)⁺; HRMS (ESI) m/z calcd. for C₁₇H₁₆O₃ [M+H] 269.1172, found 269.1177 [M+H].

(E)-1-(4-Methoxyphenyl)-3-(3-methoxyphenyl)prop-2-en-1-one (a9). Yellow solid (78%), mp: 95.7–97.0 °C ([28] 103–104 °C). ¹H-NMR (500 MHz, DMSO-d₆) δ 8.18 (d, J = 9.0 Hz, 2H), 7.95 (d, J = 15.5 Hz, 1H), 7.68 (d, J = 15.5 Hz, 1H), 7.48 (s, 1H), 7.44–7.43 (m, 1H), 7.38–7.35 (m, 1H), 7.10 (d, J = 9.0 Hz, 2H), 7.03–7.01 (m, 1H), 3.88 (s, 3H), 3.84 (s, 3H); MS (ESI) m/z = 269 (M+H)⁺; HRMS (ESI) m/z calcd. for C₁₇H₁₆O₃ [M+H] 269.1172, found 269.1179 [M+H].

(E)-1,3-bis(4-Methoxyphenyl)prop-2-en-1-one (a10). Yellow solid (72%), mp: 97.8–100.5 °C ([28] 103–104 °C). ¹H-NMR (400 MHz, DMSO-d₆) δ 8.16 (d, J = 9.2 Hz, 2H), 7.85 (d, J = 8.8 Hz, 2H), 7.81 (d, J = 15.6 Hz, 1H), 7.69 (d, J = 15.6 Hz, 1H), 7.08 (d, J = 9.2 Hz, 2H), 7.02 (d, J = 8.8 Hz, 2H), 3.87 (s, 3H), 3.83 (s, 3H); MS (ESI) m/z = 291 (M+Na)⁺; HRMS (ESI) m/z calcd. for C₁₇H₁₆O₃ [M+Na] 291.0992, found 291.0998 [M+Na].

(E)-1-(4-Methoxyphenyl)-3-(4-ethoxyphenyl)prop-2-en-1-one (a11). White solid (83%), mp: 106.3–107.9 °C ([29] 109 °C). ¹H-NMR (500 MHz, DMSO-d₆) δ 8.15 (d, J = 8.5 Hz, 2H), 7.84–7.78 (m, 3H), 7.68 (d, J = 15.5 Hz, 1H), 7.08 (d, J = 9.0 Hz, 2H), 7.00 (d, J = 8.5 Hz, 2H), 4.10 (q, J = 7.0 Hz, 2H), 3.87 (s, 3H), 1.35 (t, J = 7.0 Hz, 3H); MS (ESI) m/z = 283 (M+H)⁺; HRMS (ESI) m/z calcd. for C₁₈H₁₈O₃ [M+H] 283.1329, found 283.1347 [M+H].

(E)-1-(4-Methoxyphenyl)-3-(2,3-dimethoxyphenyl)prop-2-en-1-one (a12).White solid (91%), mp: 99.8–102.0 °C ([30] 99.0–99.5 °C). ¹H-NMR (500 MHz, DMSO-d₆) δ 8.15 (d, J = 9.0 Hz, 2H), 7.96 (d, J = 15.5 Hz, 1H), 7.89 (d, J = 15.5 Hz, 1H), 7.63–7.61 (m, 1H), 7.16–7.15 (m, 2H), 7.09 (d, J = 9.0 Hz, 2H), 3.88 (s, 3H), 3.85 (s, 3H), 3.80 (s, 3H); MS (ESI) m/z = 299 (M+H)⁺; HRMS (ESI) m/z calcd. for C₁₈H₁₈O₄ [M+H] 299.1278, found 299.1300 [M+H].

(E)-1-(4-methoxyphenyl)-3-(2,5-dimethoxyphenyl)prop-2-en-1-one (a13) [31]. Yellow solid (87%), mp: 54.7–56.3 °C. ¹H-NMR (400 MHz, DMSO-d₆) δ 8.16 (d, J = 8.8 Hz, 2H), 8.01 (d, J = 15.6 Hz, 1H), 7.91 (d, J = 15.6 Hz, 1H), 7.56–7.55 (m, 1H), 7.09 (d, J = 8.8 Hz, 2H), 7.07–7.00 (m, 2H), 3.87 (s, 3H), 3.85 (s, 3H), 3.80 (s, 3H); MS (ESI) m/z = 321 (M+Na)⁺; HRMS (ESI) m/z calcd. for C₁₈H₁₈O₄ [M+Na] 321.1097, found 321.1098 [M+Na].

(E)-1-(4-Methoxyphenyl)-3-(2,6-dimethoxyphenyl)prop-2-en-1-one (a14). Yellow solid (70%), mp: 123.7–125.7 °C. ¹H-NMR (400 MHz, DMSO-d₆) δ 8.10 (d, J = 15.6 Hz, 1H), 8.04–7.99 (m, 3H), 7.42–7.38 (m, 1H), 7.10–7.08 (m, 2H), 6.77–6.75 (m, 2H), 3.92 (s, 6H), 3.87 (s, 3H); ¹³C-NMR (150 MHz, DMSO-d₆): δ188.9, 163.4, 160.4, 134.5, 132.6, 131.4, 130.9, 124.1, 114.5, 112.1, 104.6, 56.5, 56.0; MS (ESI) m/z = 321 (M+Na)⁺; HRMS (ESI) m/z calcd. for C₁₈H₁₈O₄ [M+Na] 321.1097, found 321.1104 [M+Na].

(E)-1-(4-Methoxyphenyl)-3-(3,4-dimethoxyphenyl)prop-2-en-1-one (a15). Yellow solid (72%), mp: 104.9–106.4 °C ([32] 93–98 °C). ¹H-NMR (400 MHz, DMSO-d₆) δ 8.17 (d, J = 8.8 Hz, 2H), 7.83 (d, J = 15.6 Hz, 1H), 7.68 (d, J = 15.6 Hz, 1H), 7.54–7.53 (m, 1H), 7.40–7.37 (m, 1H), 7.09 (d, J = 8.8 Hz, 2H), 7.03–7.01 (m, 1H), 3.87 (s, 6H), 3.82 (s, 3H); MS (ESI) m/z = 321 (M+Na)⁺; HRMS (ESI) m/z calcd. for C₁₈H₁₈O₄ [M+Na] 321.1097, found 321.1083 [M+Na].

(E)-1-(4-Methoxyphenyl)-3-(3,5-dimethoxyphenyl)prop-2-en-1-one (a16) [33]. Yellow solid (85%), mp: 87.6–89.1 °C. ¹H-NMR (500 MHz, DMSO-d₆) δ 8.19 (d, J = 9.0 Hz, 2H), 7.94 (d, J = 15.5 Hz, 1H), 7.64 (d, J = 15.5 Hz, 1H), 7.09 (d, J = 9.0 Hz, 2H), 7.07–7.06 (m, 2H), 6.59–6.58 (m, 1H), 3.88 (s, 3H), 3.82 (s, 6H); ¹³C-NMR (150 MHz, DMSO-d₆): 187.9, 163.7, 161.2, 143.8, 137.2, 131.5, 130.9, 123., 114.5, 107.1, 103.1, 56.0, 55.9; MS (ESI) m/z = 299 (M+H)⁺; HRMS (ESI) m/z calcd. for C₁₈H₁₈O₄ [M+H]⁺ 299.1278, found 299.1298 [M+H].

(E)-1-(4-Methoxyphenyl)-3-(3-(benzyloxy)-4-methoxyphenyl)prop-2-en-1-one (a17). Yellow solid (97%), mp: 115.0–118.2 °C. ¹H-NMR (400 MHz, DMSO-d₆) δ 8.17 (d, J = 8.8 Hz, 2H), 7.82 (d, J = 15.2 Hz, 1H), 7.68–7.64 (m, 2H), 7.52–7.50 (m, 2H), 7.44–7.34 (m, 4H), 7.10 (d, J = 8.8 Hz, 2H), 7.06–7.04 (m, 1H), 5.19 (s, 2H), 3.87 (s, 3H), 3.83 (s, 3H); MS (ESI) m/z = 397 (M+Na)⁺; HRMS (ESI) m/z calcd. for C₂₂H₂₄O₄ [M+Na]⁺ 397.1410, found 397.1407 [M+Na].

(E)-1-(4-Methoxyphenyl)-3-(2,3,4-trimethoxyphenyl)prop-2-en-1-one (a18). Yellow solid (99%), mp: 94.4–96.5 °C ([34] 94 °C). ¹H-NMR (500 MHz, DMSO-d₆) δ 8.13 (d, J = 9.0 Hz, 2H), 7.88 (d, J = 15.5 Hz, 1H), 7.81 (d, J = 15.5 Hz, 1H), 7.79–7.77 (m, 1H), 7.09 (d, J = 9.0 Hz, 2H), 6.94–6.92 (m, 1H), 3.88 (s, 3H), 3.87 (s, 3H), 3.87 (s, 3H), 3.78 (s, 3H); MS (ESI) m/z = 351 (M+Na)⁺; HRMS (ESI) m/z calcd. for C₁₉H₂₀O₅ [M+Na]⁺ 351.1203, found 351.1216 [M+Na].

(E)-1-(4-Methoxyphenyl)-3-(2,4,5-trimethoxyphenyl)prop-2-en-1-one (a19). Yellow solid (94%), mp: 122.1–123.7 °C ([35] 107–110 °C). ¹H-NMR (400 MHz, DMSO-d₆) δ 8.14 (d, J = 8.8 Hz, 2H), 8.03 (d, J = 15.6 Hz, 1H), 7.76 (d, J = 15.6 Hz, 1H), 7.52 (s, 1H), 7.08 (d, J = 8.8 Hz, 2H), 6.75 (s, 1H), 3.90 (s, 3H), 3.87 (s, 3H), 3.87 (s, 3H), 3.83 (s, 3H); MS (ESI) m/z = 351 (M+Na)⁺; HRMS (ESI) m/z calcd. for C₁₉H₂₀O₅ [M+Na]⁺ 351.1203, found 351.1194 [M+Na].

(E)-1-(4-Methoxyphenyl)-3-(3,4,5-trimethoxyphenyl)prop-2-en-1-one (a20). Yellow solid (84%), mp: 109.7–111.5 °C ([36] 125 °C). ¹H-NMR (500 MHz, DMSO-d₆) δ 8.18 (d, J = 9.0 Hz, 2H), 7.88 (d, J = 15.5 Hz, 1H), 7.66 (d, J = 15.5 Hz, 1H), 7.22 (m, 2H), 7.10 (d, J = 9.0 Hz, 2H), 3.88 (s, 3H), 3.87 (s, 6H), 3.72 (s, 3H); MS (ESI) m/z = 351 (M+Na)⁺; HRMS (ESI) m/z calcd. for C₁₉H₂₀O₅ [M+Na]⁺ 351.1203, found 351.1183 [M+Na].

(E)-1-Phenyl-3-(2,6-dimethoxyphenyl)prop-2-en-1-one (b1). Yellow solid (84%), mp: 52.6–54.7 °C ([37] 80 °C). ¹H-NMR (500 MHz, DMSO-d₆) δ 8.13 (d, J = 16.0 Hz, 1H), 8.03–7.98 (m, 3H), 7.67–8.65 (m, 1H), 7.59–7.56 (m, 2H), 7.43–7.39 (m, 1H), 6.77–6.75 (m, 2H), 3.92 (s, 6H); MS (ESI) m/z = 291 (M+Na)⁺; HRMS (ESI) m/z calcd. for C₁₇H₁₆O₃ [M+Na] 291.0992, found 291.1007 [M+Na].

(E)-1-(2-Methylphenyl)-3-(2,6-dimethoxyphenyl)prop-2-en-1-one (b2). Yellow solid (91%), mp: 79.8–81.4 °C. ¹H-NMR (500 MHz, DMSO-d₆) δ 7.86 (d, J = 16.0 Hz, 1H), 7.51 (d, J = 16.0 Hz, 1H), 7.49–7.47 (m, 1H), 7.44–7.38 (m, 2H), 7.34–7.31 (m, 2H), 6.74–6.73 (m, 2H), 3.85 (s, 6H), 2.36 (s, 3H); ¹³C-NMR (150 MHz, DMSO-d₆): 196.8, 160.3, 140.0, 136.4, 136.3, 133.0, 131.6, 130.8, 128.7, 128.3, 126.2, 111.6, 104.7, 56.5, 20.34; MS (ESI) m/z = 305 (M+Na)⁺; HRMS (ESI) m/z calcd. for C₁₈H₁₈O₄ [M+Na] 305.1148, found 305.1134 [M+Na].

(E)-1-(3-Methylphenyl)-3-(2,6-dimethoxyphenyl)prop-2-en-1-one (b3). Yellow solid (94%), mp: 102.5–103.8 °C. ¹H-NMR (500 MHz, DMSO-d₆) δ 8.12 (d, J = 16.0 Hz, 1H), 7.98 (d, J = 16.0 Hz, 1H), 7.81–7.77 (m, 2H), 7.48–7.44 (m, 2H), 7.42–7.39 (m, 1H), 6.77–6.75 (m, 2H), 3.92 (s, 6H), 2.42 (s, 3H); ¹³C-NMR (150 MHz, DMSO-d₆): 190.9, 160.5, 138.7, 138.6, 135.3, 133.9, 132.8, 129.2, 128.9, 125.9, 124.3, 112.0, 104.6, 56.5, 21.41; MS (ESI) m/z = 305 (M+Na)⁺; HRMS (ESI) m/z calcd. for C₁₈H₁₈O₄ [M+Na] 305.1148, found 305.1155 [M+Na].

(E)-1-(4-Methylphenyl)-3-(2,6-dimethoxyphenyl)prop-2-en-1-one (b4). Yellow solid (74%), mp: 82.7–84.5 °C. ¹H-NMR (500 MHz, DMSO-d₆) δ 8.10 (d, J = 16.0 Hz, 1H), 7.99 (d, J = 16.0 Hz, 1H), 7.91–7.89 (m, 2H), 7.42–7.37 (m, 3H), 6.77–6.75 (m, 2H), 3.92 (s, 6H), 2.40 (s, 3H); ¹³C-NMR (150 MHz, DMSO-d₆): 190.2, 160.4, 143.6, 136.1, 135.0, 132.8, 129.9, 128.7, 124.1, 112.0, 104.7, 56.5, 21.64; MS (ESI) m/z = 305 (M+Na)⁺; HRMS (ESI) m/z calcd. for C₁₈H₁₈O₄ [M+Na] 305.1148, found 305.1135 [M+Na].

(E)-1-(3,4-Dimethylphenyl)-3-(2,6-dimethoxyphenyl)prop-2-en-1-one (b5). Yellow solid (90%), mp: 98.9–101.1 °C. ¹H-NMR (500 MHz, DMSO-d₆) δ 8.08 (d, J = 16.0 Hz, 1H), 7.98 (d, J = 16.0 Hz, 1H), 7.75–7.72 (m, 2H), 7.41–7.38 (m, 1H), 7.33–7.32 (m, 1H), 6.77–6.75 (m, 2H), 3.92 (s, 6H), 2.32 (s, 3H), 2.31 (s, 3H); ¹³C-NMR (150 MHz, DMSO-d₆): 190.3, 160.4, 142.5, 137.4, 136.5, 134.9, 132.7, 130.3, 129.5, 126.4, 124.3, 112.0, 104.7, 56.6, 20.1, 19.9; MS (ESI) m/z = 319 (M+Na)⁺; HRMS (ESI) m/z calcd. for C₁₉H₂₀O₃ [M+Na] 319.1305, found 319.1302 [M+Na].

(E)-1-(2-Methoxyphenyl)-3-(2,6-dimethoxyphenyl)prop-2-en-1-one (b6) [38]. Yellow solid (84%), mp: 109.0–111.4 °C. ¹H-NMR (500 MHz, DMSO-d₆) δ 7.91 (d, J = 16.5 Hz, 1H), 7.71 (d, J = 16.5 Hz, 1H), 7.56–7.46 (m, 2H), 7.39–7.18 (m, 2H), 7.07–7.04 (m, 1H), 6.74–6.72 (m, 2H), 3.88 (s, 3H), 3.86 (s, 6H); MS (ESI) m/z = 321 (M+Na)⁺; HRMS (ESI) m/z calcd. for C₁₈H₁₈O₄ [M+Na] 321.1097, found 321.1080 [M+Na].

(E)-1-(3-Methoxyphenyl)-3-(2,6-dimethoxyphenyl)prop-2-en-1-one (b7). Yellow solid (93%), mp: 93.5–95.6 °C. ¹H-NMR (400 MHz, DMSO-d₆) δ 8.12 (d, J = 16.0 Hz, 1H), 7.97 (d, J = 16.0 Hz, 1H), 7.58–7.51 (m, 1H), 7.49–7.45 (m, 1H), 7.44–7.41 (m, 2H), 7.25–7.22 (m, 1H), 6.77–6.75 (m, 2H), 3.92 (s, 6H), 3.85 (s, 3H); ¹³C-NMR (150 MHz, DMSO-d₆): 190.5, 160.5, 160.0, 140.1, 135.5, 132.9, 130.5, 124.2, 121.1, 119.3, 113.0, 111.9, 104.7, 56.6, 55.7; MS (ESI) m/z = 321 (M+Na)⁺. HRMS (ESI) m/z calcd. for C₁₈H₁₈O₄ [M+Na] 321.1097, found 321.1098 [M+Na].

(E)-1-(2-Ethoxyphenyl)-3-(2,6-dimethoxyphenyl)prop-2-en-1-one (b8). Yellow solid (94%). mp: 48.8–50.4 °C. ¹H-NMR (400 MHz, DMSO-d₆) δ 7.93 (d, J = 16.0 Hz, 1H), 7.74 (d, J = 16.0 Hz, 1H), 7.53–7.44 (m, 2H), 7.39–7.35 (m, 1H), 7.17–7.15 (m, 1H), 7.05–7.02 (m, 1H), 6.74–6.72 (m, 2H), 4.16 (q, J = 7.2 Hz, 2H), 3.86 (s, 6H), 1.31 (t, J = 7.2 Hz, 3H); ¹³C-NMR (150 MHz, DMSO-d₆): 193.8, 160.3, 157.4, 133.5, 133., 132.5, 130.1, 130.0, 129.5, 121.0, 113.7, 111.9, 104.7, 64.4, 56.4, 14.9; MS (ESI) m/z = 335 (M+Na)⁺; HRMS (ESI) m/z calcd. for C₁₉H₂₀O₄ [M+Na] 335.1254, found 335.1248 [M+Na].

(E)-1-(3-Ethoxyphenyl)-3-(2,6-dimethoxyphenyl)prop-2-en-1-one (b9). Yellow solid (42%), mp: 63.1–64.8 °C. ¹H-NMR (400 MHz, DMSO-d₆) δ 8.11 (d, J = 16.0 Hz, 1H), 7.95 (d, J = 16.0 Hz, 1H), 7.57–7.55 (m, 1H), 7.50–7.46 (m, 1H), 7.44–7.38 (m, 2H), 7.24–7.18 (m, 1H), 6.77–6.75 (m, 2H), 4.12 (q, J = 7.2 Hz, 2H), 3.92 (s, 6H), 1.36 (t, J = 7.2 Hz, 3H); ¹³C-NMR (150 MHz, DMSO-d₆): 190.5, 160.5, 159.2, 140.1, 135.5, 132.8, 130.4, 124.3, 120.9, 119.7, 113.5, 112.0, 104.6, 63.7, 56.5, 15.0; MS (ESI) m/z = 335 (M+Na)⁺; HRMS (ESI) m/z calcd. for C₁₉H₂₀O₄ [M+Na] 335.1254, found 335.1255 [M+Na].

(E)-1-(4-Ethoxyphenyl)-3-(2,6-dimethoxyphenyl)prop-2-en-1-one (b10). White solid (82%), mp: 99.0–101.2 °C. ¹H-NMR (500 MHz, DMSO-d₆) δ 8.09 (d, J = 15.5 Hz, 1H), 8.03–7.98 (m, 3H), 7.41–7.38 (m, 1H), 7.09–7.07 (m, 2H), 6.77–6.75 (m, 2H), 4.14 (q, J = 7.0 Hz, 2H), 3.92 (s, 6H), 1.37 (t, J = 7.0 Hz, 3H); ¹³C-NMR (150 MHz, DMSO-d₆): 188.9, 162.7, 160.4, 134.5, 132.6, 131.2, 130.9, 124.0, 114.9, 112.1, 104.6, 64.0, 56.5, 15.0; MS (ESI) m/z = 335 (M+Na)⁺; HRMS (ESI) m/z calcd. for C₁₉H₂₀O₄ [M+Na] 335.1254, found 335.1256 [M+Na].

(E)-1-(2-(Benzyloxy>)phenyl)-3-(2,6-dimethoxyphenyl)prop-2-en-1-one (b11). Yellow solid (20%), mp: 94.6–97.9 °C. ¹H-NMR (400 MHz, DMSO-d₆) δ 7.92 (d, J = 16.0 Hz, 1H), 7.76 (d, J = 16.0 Hz, 1H), 7.53–7.47 (m, 2H), 7.45–7.35 (m, 3H), 7.25–7.21(m, 4H), 7.09–7.05 (m, 1H), 6.73–6.71 (m, 2H), 5.24 (s, 2H), 3.78 (s, 6H); ¹³C-NMR(150 MHz, DMSO-d₆): 193.1, 157.6, 157.4, 137.4, 133.4, 131.7, 130.6, 129.9, 129.8, 128.9, 128.8, 128.1, 127.7, 120.7, 114.0, 113.7, 104.0, 70.11, 55.7; MS (ESI) m/z = 397 (M+Na)⁺; HRMS (ESI) m/z calcd. for C₂₄H₂₂O₄ [M+Na] 397.1410, found 397.1395 [M+Na].

(E)-1-(3-(Benzyloxy)phenyl)-3-(2,6-dimethoxyphenyl)prop-2-en-1-one (b12). Yellow solid (81%), mp: 108.8–110.2 °C. ¹H-NMR (400 MHz, DMSO-d₆) δ 8.11 (d, J = 16.0 Hz, 1H), 7.95 (d, J = 16.0 Hz, 1H), 7.60–7.58 (m, 1H), 7.54–7.47 (m, 4H), 7.43–7.38 (m, 3H), 7.37–7.33 (m, 1H), 7.32–7.29 (m, 1H), 6.77–7.75 (m, 2H), 5.21 (s, 2H), 3.91 (s, 6H); ¹³C-NMR (150 MHz, DMSO-d₆): 190.5, 160.5, 159.1, 140.1, 137.3, 135.5, 132.9, 130.5, 128.9, 128.4, 128.2, 124.2, 121.3, 120.2, 114.0, 111.9, 104.7, 69.8, 56.6; MS (ESI) m/z = 397 (M+Na)⁺; HRMS (ESI) m/z calcd. for C₂₄H₂₂O₄ [M+Na] 397.1410, found 397.1394 [M+Na].

(E)-1-(4-(Benzyloxy)phenyl)-3-(2,6-dimethoxyphenyl)prop-2-en-1-one (b13) [39]. White solid (97%), mp: 96.6–97.8 °C. ¹H-NMR (500 MHz, DMSO-d₆) δ 8.10 (d, J = 16.0 Hz, 1H), 8.04–7.98 (m, 3H), 7.49–7.47 (m, 2H), 7.44–7.33 (m, 4H), 7.18–7.16 (m, 2H), 6.77–6.75 (m, 2H), 5.23 (s, 2H), 3.92 (s, 6H); MS (ESI) m/z = 375 (M+H)⁺; HRMS (ESI) m/z calcd. for C₂₄H₂₂O₄ [M+H] 375.1591, found 375.1591 [M+H].

(E)-1-(2-(Benzyloxy)-4-methoxyphenyl)-3-(2,6-dimethoxyphenyl)prop-2-en-1-one (b14). Yellow solid (75%), mp: 82.2–83.6 °C. ¹H-NMR (400 MHz, DMSO-d₆) δ 7.94 (d, J = 16.0, 1H), 7.90 (d, J = 16.0, 1H), 7.59–7.57 (m, 1H), 7.45–7.43 (m, 2H), 7.38–7.34 (m, 1H), 7.24–7.22 (m, 3H), 6.76–6.75 (m, 1H), 6.72–6.70 (m, 2H), 6.67–6.64 (m, 1H), 5.27 (s, 2H), 3.83 (s, 3H), 3.76 (s, 6H); MS (ESI) m/z = 427 (M+Na)⁺; HRMS (ESI) m/z calcd. for C₂₅H₂₄O₅ [M+Na] 427.1516, found 427.1512 [M+Na].

(E)-1-(4-(Benzyloxy)-3-methoxyphenyl)-3-(2,6-dimethoxyphenyl)prop-2-en-1-one (b15). Yellow solid (80%), mp: 112.8–114.1 °C. ¹H-NMR (400 MHz, DMSO-d₆) δ 8.09 (d, J = 16.0 Hz, 1H), 8.02 (d, J = 16.0 Hz, 1H), 7.67–7.65 (m, 1H), 7.55–7.54 (m, 1H), 7.51–7.45 (m, 2H), 7.45–7.32 (m, 4H), 7.21–7.19 (m, 1H), 6.77–6.75 (m, 2H), 5.21 (s, 2H), 3.92 (s, 6H), 3.87 (s, 3H); ¹³C-NMR (150 MHz, DMSO-d₆): 188.9, 160.4, 152.4, 149.5, 137.0, 134.5, 132.6, 131.7, 129.0, 128.5, 128.4, 124.1, 123.0, 112.9, 112.1, 111.2, 104.7, 70.4, 56.5, 56.0; MS (ESI) m/z = 405 (M+H)⁺; HRMS (ESI) m/z calcd. for C₂₅H₂₄O₅ [M+H] 405.1697, found 405.1693 [M+H].

(E)-1-(4-Ethoxy-3-methoxyphenyl)-3-(2,6-dimethoxyphenyl)prop-2-en-1-one (b16). Yellow solid (91%), mp: 105.3–107.2 °C. ¹H-NMR (400 MHz, DMSO-d₆) δ 8.08 (d, J = 16.0 Hz, 1H), 8.02 (d, J = 16.0 Hz, 1H), 7.68–7.65 (m, 1H), 7.52–7.51 (m, 1H), 7.41–7.37 (m, 1H), 7.11–7.09 (m, 1H), 6.77–6.75 (m, 2H), 4.14 (q, J = 7.2 Hz, 2H), 3.92 (s, 6H), 3.86 (s, 3H), 1.38 (t, J = 7.2 Hz, 3H); ¹³C-NMR (150 MHz, DMSO-d₆): 188.9, 160.4, 152.7, 149.3, 134.3, 132.5, 131.3, 124.1, 123.1, 112.1, 112.0, 111.0, 104.7, 64.4, 56.5, 55.8, 15.0; MS (ESI) m/z = 365 (M+Na)⁺; HRMS (ESI) m/z calcd. for C₂₀H₂₂O₅ [M+Na] 365.1359, found 365.1350 [M+Na].

(E)-1-(2-Ethoxy-4-methoxyphenyl)-3-(2,6-dimethoxyphenyl)prop-2-en-1-one (b17). Yellow solid (65%), mp: 98.7–100.2 °C. ¹H-NMR (400 MHz, DMSO-d₆) δ 7.95 (d, J = 16.0 Hz, 1H), 7.89 (d, J = 16.0 Hz, 1H), 7.57–7.55 (m, 1H), 7.38–7.33 (m, 1H), 6.74–6.72 (m, 2H), 6.68–6.59 (m, 2H), 4.18 (q, J = 7.2 Hz, 2H), 3.87 (s, 6H), 3.84 (s, 3H), 1.34 (t, J = 7.2 Hz, 3H); ¹³C-NMR (150 MHz, DMSO-d₆): 191.3, 164.1, 160.3, 159.7, 132.4, 132.3, 132.1, 129.8, 122.7, 112.3, 106.5, 104.6, 99.8, 64.5, 56.4, 56.0, 14.8; MS (ESI) m/z = 365 (M+Na)⁺; HRMS (ESI) m/z calcd. for C₂₀H₂₂O₅ [M+Na] 365.1359, found 365.1357 [M+Na].

(E)-1-(2,5-Dimethoxyphenyl)-3-(2,6-dimethoxyphenyl)prop-2-en-1-one (b18). White solid (92%), mp: 121.0–122.0 °C. ¹H-NMR (400 MHz, DMSO-d₆) δ 7.91 (d, J = 16.0 Hz, 1H), 7.72 (d, J = 16.0 Hz, 1H), 7.40–7.36 (m, 1H), 7.16–7.08 (m, 2H), 7.02–7.01 (m, 1H), 6.73–6.71 (m, 2H), 3.87 (s, 6H), 3.82 (s, 3H), 3.75 (s, 3H); ¹³C-NMR (150 MHz, DMSO-d₆): 193.1, 160.3, 153.6, 152.4, 134.1, 132.6, 130.3, 129.3, 118.8, 114.5, 114.4, 112.0, 104.7, 56.8, 56.5, 56.0; MS (ESI) m/z = 351 (M+Na)⁺; HRMS (ESI) m/z calcd. for C₁₉H₂₀O₅Na [M+Na] 351.1203, found 351.1189 [M+Na].

(E)-1-(3,4-Dimethoxyphenyl)-3-(2,6-dimethoxyphenyl)prop-2-en-1-one (b19) [15]. Yellow solid (80%), mp: 120.5–122.7 °C. ¹H-NMR (500 MHz, DMSO-d₆) δ 8.08 (d, J = 16.0 Hz, 1H), 8.03 (d, J = 16.0 Hz, 1H), 7.69–7.67 (m, 1H), 7.52–7.51 (m, 1H), 7.40–7.38 (m, 1H), 7.13–7.11 (m, 1H), 6.77–7.75 (m, 2H), 3.92 (s, 6H), 3.87 (s, 3H), 3.85 (s, 3H); MS (ESI) m/z = 329 (M+H)⁺.

(E)-1-(Benzo[d][1,3]dioxol-5-yl)-3-(2,6-dimethoxyphenyl)prop-2-en-1-one (b20) [40]. White solid (95%), mp: 138.6–140.4 °C. ¹H-NMR (500 MHz, DMSO-d₆) δ 8.08 (d, J = 16.0 Hz, 1H), 7.96 (d, J = 16.0 Hz, 1H), 7.66–7.64 (m, 1H), 7.47–7.46 (m, 1H), 7.40–7.38 (m, 1H), 7.08–7.06 (m, 1H), 6.76–7.75 (m, 2H), 6.16 (s, 2H), 3.92 (s, 6H); MS (ESI) m/z = 313 (M+H)⁺; HRMS (ESI) m/z calcd. for C₁₈H₁₆O₅ [M+H] 313.1071, found 313.1068 [M+H].

(E)-1-(2,3-Dihydrobenzofuran-5-yl)-3-(2,6-dimethoxyphenyl)prop-2-en-1-one (b21). Yellow solid (99%), mp: 118.8–120.2 °C. ¹H-NMR (400 MHz, DMSO-d₆) δ 8.07 (d, J = 15.6 Hz, 1H), 7.98 (d, J = 15.6 Hz, 1H), 7.91–7.90 (m, 1H), 7.87–7.84 (m, 1H), 7.41–7.37 (m, 1H), 6.91–6.89 (m, 1H), 6.77–6.75 (m, 2H), 4.65 (t, J = 8.8 Hz, 2H), 3.92 (s, 6H), 3.27 (t, J = 8.8 Hz, 2H); ¹³C-NMR (150 MHz, DMSO-d₆): 188.7, 164.3, 160.3, 134.3, 132.5, 131.7, 130.4, 128.9, 126.0, 124.2, 112.1, 109.4, 104.7, 72.6, 56.5, 28.9; MS (ESI) m/z = 333 (M+Na)⁺; HRMS (ESI) m/z calcd. for C₁₉H₁₈O₄ [M+Na] 333.1097, found 333.1098 [M+Na].

(E)-1-([1,1'-Biphenyl]-4-yl)-3-(2,6-dimethoxyphenyl)prop-2-en-1-one (b22). Yellow solid (70%), mp: 121.7–123.5 °C. ¹H-NMR (500 MHz, DMSO-d₆) δ 8.17 (d, J = 16.0 Hz, 1H), 8.10–8.08 (m, 2H), 8.06 (d, J = 16.0 Hz, 1H), 7.88–7.86 (m, 2H), 7.78–7.76 (m, 2H), 7.54–7.51 (m, 2H), 7.46–7.40 (m, 2H), 6.78–6.76 (m, 2H), 3.94 (s, 6H); ¹³C-NMR (150 MHz, DMSO-d₆): 190.1, 160.5, 144.7, 139.5, 137.4, 135.4, 132.9, 129.6, 129.3, 128.8, 127.5, 127.4, 124.1, 112.0, 104.7, 56.6; MS (ESI) m/z = 345 (M+H)⁺; HRMS (ESI) m/z calcd. for C₂₃H₂₀O₃ [M+H] 345.1485, found 345.1478 [M+H].

(E)-1-(3-Aminophenyl)-3-(2,6-dimethoxyphenyl)prop-2-en-1-one (b23) [41]. Yellow solid (67%), mp: 148.6–150.3 °C. ¹H-NMR (600 MHz, DMSO-d₆) δ 8.06 (d, J = 16.2 Hz, 1H), 7.92 (d, J = 16.2 Hz, 1H), 7.41–7.38 (m, 1H), 7.21–7.17 (m, 2H), 7.13–7.12 (m, 1H), 6.84–6.80 (m, 1H), 6.77–6.75 (m, 2H), 5.39 (s, 2H), 3.92 (s, 6H); MS (ESI) m/z = 306 (M+Na)⁺; HRMS (ESI) m/z calcd. for C₁₇H₁₇NO₃ [M+Na] 306.1101, found 306.1097 [M+Na].

(E)-1-(2-Hydroxyphenyl)-3-(2,6-dimethoxyphenyl)prop-2-en-1-one (b24) [42]. Yellow solid (83%), mp: 114.2–115.9 °C. ¹H-NMR (400 MHz, DMSO-d₆) δ 12.55 (s, 1H), 8.25 (d, J = 15.6 Hz, 1H), 8.13 (d, J = 15.6 Hz, 1H), 7.96–7.94 (m, 1H), 7.59–7.52 (m, 1H), 7.45–7.41 (m, 1H), 7.03–6.99 (m, 2H), 6.78–6.76 (m, 2H), 3.94 (s, 6H); MS (ESI) m/z = 285 (M+H)⁺; HRMS (ESI) m/z calcd. for C₁₇H₁₆O₄ [M+H] 285.1121, found 285.1133 [M+H].

(E)-1-(3-Hydroxyphenyl)-3-(2,6-dimethoxyphenyl)prop-2-en-1-one (b25). Yellow solid (70%), mp: 138.1–139.7 °C. ¹H-NMR (400 MHz, DMSO-d₆) δ 9.79 (s, 1H), 8.09 (d, J = 16.0 Hz, 1H), 7.94 (d, J = 16.0 Hz, 1H), 7.46–7.33 (m, 4H), 7.05–7.02 (m, 1H), 6.77–6.75 (m, 2H), 3.92 (s, 6H); ¹³C-NMR (150 MHz, DMSO-d₆): 190.5, 160.5, 158.2, 140.0, 135.2, 132.8, 130.4, 124.2, 120.4, 119.5, 114.8, 112.0, 104.7, 56.6; MS (ESI) m/z = 307 (M+Na)⁺; HRMS (ESI) m/z calcd. for C₁₇H₁₆O₄ [M+Na] 307.0941, found 307.0939 [M+Na].

(E)-1-(4-Hydroxyphenyl)-3-(2,6-dimethoxyphenyl)prop-2-en-1-one (b26) [43]. Yellow solid (82%), mp: 189.6–191.4 °C. ¹H-NMR (500 MHz, DMSO-d₆) δ 10.35 (s, 1H), 8.06 (d, J = 16.0 Hz, 1H), 7.99 (d, J = 16.0 Hz, 1H), 7.92–7.90 (m, 2H), 7.40–7.36 (m, 1H), 6.91–6.89 (m, 2H), 6.76–6.74 (m, 2H), 3.92 (s, 6H); MS (ESI) m/z = 307 (M+Na)⁺; HRMS (ESI) m/z calcd. for C₁₇H₁₆O₄ [M+Na] 307.0941, found 307.0938 [M+Na].

(E)-1-(2,4-Dihydroxyphenyl)-3-(2,6-dimethoxyphenyl)prop-2-en-1-one (b27). Yellow solid (85%), mp: 218.7–220.2 °C. ¹H-NMR (600 MHz, DMSO-d₆) δ 13.51 (s, 1H), 10.70 (s, 1H), 8.21 (d, J = 15.6 Hz, 1H), 8.06 (d, J = 15.6 Hz, 1H), 7.88–7.86 (m, 1H), 7.43–7.40 (m, 1H), 6.77–6.76 (m, 2H), 6.46–6.44 (m, 1H), 6.30–6.29 (m, 1H), 3.93 (s, 6H); ¹³C-NMR (150 MHz, DMSO-d₆): 192.8, 166.2, 165.4, 160.5, 135.1, 133.1, 132.7, 122.7, 113.6, 111.9, 108.9, 104.7, 103.2, 56.6; MS (ESI) m/z = 323 (M+Na)⁺; HRMS (ESI) m/z calcd. for C₁₇H₁₆O₅ [M+Na] 323.0890, found 323.0876 [M+Na].

(E)-1-(2-Hydroxy-4-methoxyphenyl)-3-(2,6-dimethoxyphenyl)prop-2-en-1-one (b28) Yellow solid (74%), mp: 143.5–144.7 °Cs ([13] 140 °C). ¹H-NMR (500 MHz, DMSO-d₆) δ 13.55 (s, 1H), 8.21 (d, J = 15.5 Hz, 1H), 8.10 (d, J = 15.5 Hz, 1H), 7.93–7.91 (m, 1H), 7.42–7.40 (m, 1H), 6.77–6.75 (m, 2H), 6.57–6.47 (m, 2H), 3.93 (s, 6H), 3.83 (s, 3H); MS (ESI) m/z = 315 (M+H)⁺; HRMS (ESI) m/z calcd. for C₁₈H₁₈O₅ [M+H] 315.1227, found 315.1243 [M+H].

(E)-1-(4-Hydroxy-3-methoxyphenyl)-3-(2,6-dimethoxyphenyl)prop-2-en-1-one (b29). Yellow solid (40%), mp: 128.7–131.2 °C. ¹H-NMR (500 MHz, DMSO-d₆) δ 10.02 (s, 1H), 8.06 (d, J = 16.0 Hz, 1H), 8.01 (d, J = 16.0 Hz, 1H), 7.59–7.57 (m, 1H), 7.53–7.52 (m, 1H), 7.40–7.36 (m, 1H), 6.94–6.92 (m, 1H), 6–6.74 (m, 2H), 3.92 (s, 6H), 3.86 (s, 3H); ¹³C-NMR (150 MHz, DMSO-d₆): 188.6, 160.3, 152.1, 148.3, 134.0, 132.4, 130.4, 124.2, 123.5, 115.5, 112.2, 111.7, 104.6, 56.5, 56.0; MS (ESI) m/z = 337 (M+Na)⁺; HRMS (ESI) m/z calcd. for C₁₈H₁₈O₅ [M+Na] 337.1046, found 337.1042 [M+Na].

(E)-1-(4-Cyanophenyl)-3-(2,6-dimethoxyphenyl)prop-2-en-1-one (b30). Yellow solid (95%), mp: 144.3–145.9 °C. ¹H-NMR (500 MHz, DMSO-d₆) δ 8.16 (d, J = 16.0 Hz, 1H), 8.13–8.11 (m, 2H), 8.04–8.02 (m, 2H), 7.96 (d, J = 16.0 Hz, 1H), 7.45–7.42 (m, 1H), 6.78–6.76 (m, 2H), 3.92 (s, 6H); ¹³C-NMR (150 MHz, DMSO-d₆): 190.1, 160.7, 142.0, 136.8, 133.4, 133.3, 129.2, 123.6, 118.7, 115.2, 111.7, 104.7, 56.6; MS (ESI) m/z = 294 (M+H)⁺; HRMS (ESI) m/z calcd. for C₁₈H₁₅NO₃ [M+H] 294.1125, found 294.1130 [M+H].

(E)-1-(2-Fluorophenyl)-3-(2,6-dimethoxyphenyl)prop-2-en-1-one (b31). Yellow solid (93%), mp: 66.6–68.1 °C. ¹H-NMR (500 MHz, DMSO-d₆) δ 8.06–8.02 (m, 1H), 7.76–7.70 (m, 2H), 7.66–7.64 (m, 1H), 7.44–7.34 (m, 3H), 6.76–6.74 (m, 2H), 3.88 (s, 6H); 190.2, 160.52, 136.0, 134.5, 133.2, 130.9, 127.9, 125.3, 117.1, 111.6, 104.7, 56.5; MS (ESI) m/z = 287 (M+H)⁺; HRMS (ESI) m/z calcd. for C₁₇H₁₅FO₃ [M+H] 287.1078, found 287.1097 [M+H].

(E)-1-(3-Fluorophenyl)-3-(2,6-dimethoxyphenyl)prop-2-en-1-one (b32). Yellow solid (93%), mp: 105.4–107.3 °C. ¹H-NMR (500 MHz, DMSO-d₆) δ 8.15 (d, J = 16.0 Hz, 1H), 7.96 (d, J = 16.0 Hz, 1H), 7.86–7.84 (m, 1H), 7.72–7.70 (m, 1H), 7.64–7.62 (m, 1H), 7.53–7.51 (m, 1H), 7.43–7.41 (m, 1H), 6.78–7.76 (m, 2H), 3.93 (s, 6H); ¹³C-NMR (150 MHz, DMSO-d₆): 189.6, 160.6, 140.9, 136.2, 133.2, 131.5, 124.8, 123.7, 120.2, 115.0, 111.8, 104.6, 56.6; MS (ESI) m/z = 287 (M+H)⁺; HRMS (ESI) m/z calcd. for C₁₇H₁₅FO₃ [M+H] 287.1078, found 287.1086 [M+H].

(E)-1-(4-Fluorophenyl)-3-(2,6-dimethoxyphenyl)prop-2-en-1-one (b33). Yellow solid (89%), mp: 108.2–109.6 °C. ¹H-NMR (500 MHz, DMSO-d₆) δ 8.13 (d, J = 16.0 Hz, 1H), 8.10–8.06 (m, 2H), 7.99 (d, J = 16.0 Hz, 1H), 7.44–7.36 (m, 3H), 6.77–6.75 (m, 2H), 3.92 (s, 6H); ¹³C-NMR (150 MHz, DMSO-d₆): 189.2, 160.5, 135.6, 135.2, 133.0, 131.6, 123.7, 116.4, 111.9, 104.7, 56.5. MS (ESI) m/z = 309 (M+Na)⁺; HRMS (ESI) m/z calcd. for C₁₇H₁₅FO₃ [M+Na] 309.0897, found 309.0890 [M+Na].

(E)-1-(3-Chlorophenyl)-3-(2,6-dimethoxyphenyl)prop-2-en-1-one (b34). Yellow solid (96%), mp: 116.5–117.2 °C. ¹H-NMR (500 MHz, DMSO-d₆) δ 8.14 (d, J = 16.0 Hz, 1H), 7.96–7.92 (m, 3H), 7.75–7.71 (m, 1H), 7.63–7.60 (m, 1H), 7.44–7.41 (m, 1H), 6.77–6.75 (m, 2H), 3.92 (s, 6H); ¹³C-NMR (150 MHz, DMSO-d₆): 189.6, 160.6, 140.5, 136.3, 134.3, 133.2, 132.9, 131.3, 128.1, 127.3, 123.6, 111.8, 104.7, 56.6; MS (ESI) m/z = 303 (M+H)⁺; HRMS (ESI) m/z calcd. for C₁₇H₁₅ClO₃ [M+H] 303.0782, found 303.0782 [M+H].

(E)-1-(4-Chlorophenyl)-3-(2,6-dimethoxyphenyl)prop-2-en-1-one (b35) [44]. Yellow solid (92%), mp: 107.9–109.7 °C. ¹H-NMR (500 MHz, DMSO-d₆) δ 8.14 (d, J = 16.0 Hz, 1H), 8.02–7.99 (m, 2H), 7.97 (d, J = 16.0 Hz, 1H), 7.65–7.61 (m, 2H), 7.44–7.40 (m, 1H), 6.77–6.75 (m, 2H), 3.92 (s, 6H); MS (ESI) m/z = 325 (M+Na)⁺; HRMS (ESI) m/z calcd. for C₁₇H₁₅ClO₃ [M+Na] 325.0602, found 325.0597 [M+Na].

(E)-1-(3-Bromophenyl)-3-(2,6-dimethoxyphenyl)prop-2-en-1-one (b36). Yellow solid (98%), mp: 135.7–138.2 °C. ¹H-NMR (500 MHz, DMSO-d₆) δ 8.14 (d, J = 16.0 Hz, 1H), 8.06–8.05 (m, 1H), 8.01–7.97 (m, 1H), 7.93 (d, J = 16.0 Hz, 1H), 7.87–7.85 (m, 1H), 7.56–7.53 (m, 1H), 7.44–7.40 (m, 1H), 6.77–6.75 (m, 2H), 3.92 (s, 6H); ¹³C-NMR (150 MHz, DMSO-d₆): 189.5, 160.6, 140.7, 136.3, 135.8, 133.2, 131.6, 131.0, 127.7, 123.6, 122.8, 111.8, 104.7, 56.6; MS (ESI) m/z = 347 (M+H)⁺; HRMS (ESI) m/z calcd. for C₁₇H₁₅BrO₃ [M+H] 347.0277, found 347.0257 [M+H].

(E)-1-(2,4-Dichlorophenyl)-3-(2,6-dimethoxyphenyl)prop-2-en-1-one (b37). Yellow solid (99%), mp: 111.1–112.7 °C. ¹H-NMR (500 MHz, DMSO-d₆) δ 7.82 (d, J = 16.5 Hz, 1H), 7.78 (s, 1H), 7.59–7.54 (m, 2H), 7.45 (d, J = 16.5 Hz, 1H), 7.42–7.40 (m, 1H), 6.75–6.73 (m, 2H), 3.85 (s, 6H); ¹³C-NMR (150 MHz, DMSO-d₆): 193.6, 160.5, 138.5, 137.7, 135.9, 133.7, 131.6, 131.1, 130.1, 128.1, 128.0, 111.3, 104.7, 56.6; MS (ESI) m/z = 359 (M+Na)⁺; HRMS (ESI) m/z calcd. for C₁₇H₁₄Cl₂O₃ [M+Na] 359.0212, found 359.0215 [M+Na].

(E)-1-(3,4-Dichlorophenyl)-3-(2,6-dimethoxyphenyl)prop-2-en-1-one (b38). Yellow solid (98%), mp: 142.1–143.4 °C. ¹H-NMR (500 MHz, DMSO-d₆) δ 8.15 (d, J = 16.0 Hz, 1H), 8.12–8.10 (m, 1H), 7.97–7.95 (m, 1H), 7.93 (d, J = 16.0 Hz, 1H), 7.84–7.82 (m, 1H), 7.44–7.41 (m, 1H), 6.77–6.75 (m, 2H), 3.92 (s, 6H); ¹³C-NMR (150 MHz, DMSO-d₆): 188.7, 160.6, 138.8, 136.6, 136.0, 133.3, 132.4, 131.7, 130.3, 128.7, 123.3, 111.8, 104.7, 56.6; MS (ESI) m/z = 359 (M+Na)⁺; HRMS (ESI) m/z calcd. for C₁₇H₁₄Cl₂O₃ [M+Na] 359.0212, found 359.0189 [M+Na].

(E)-1-(3-Nitrophenyl)-3-(2,6-dimethoxyphenyl)prop-2-en-1-one (b39). Yellow solid (92%), mp: 172.3–173.7 °C. ¹H-NMR (500 MHz, DMSO-d₆) δ 8.66–8.63 (m, 1H), 8.49–8.47 (m, 1H), 8.44–8.42 (m, 1H), 8.20 (d, J = 16.0 Hz, 1H), 8.02 (d, J = 16.0 Hz, 1H), 7.89–7.86 (m, 1H), 7.46–7.42 (m, 1H), 6.77–6.75 (m, 2H), 3.93 (s, 6H); ¹³C-NMR (150 MHz, DMSO-d₆): 189.0, 160.7, 148.6, 139.7, 136.9, 134.7, 133.5, 131.2, 127.5, 123.2, 122.9, 111.7, 104.7, 56.6; MS (ESI) m/z = 336 (M+Na)⁺; HRMS (ESI) m/z calcd. for C₁₇H₁₅NO₅ [M+Na] 336.0842, found 336.0825 [M+Na].

(E)-1-(4-Nitrophenyl)-3-(2,6-dimethoxyphenyl)prop-2-en-1-one (b40). Yellow solid (97%), mp: 147.3–148.6 °C. ¹H-NMR (400 MHz, DMSO-d₆) δ 8.39–8.36 (m, 2H), 8.21–8.16 (m, 3H), 7.98 (d, J = 15.6 Hz, 1H), 7.46–7.42 (m, 1H), 6.78–6.76 (m, 2H), 3.93 (s, 6H); ¹³C-NMR (150 MHz, DMSO-d₆): 189.9, 160.7, 150.1, 143.5, 136.9, 133.5, 130.0, 124.4, 123.7, 111.7, 104.7, 56.6; MS (ESI) m/z = 314 (M+H)⁺; HRMS (ESI) m/z calcd. for C₁₇H₁₅NO₅ [M+H] 314.1023, found 314.1022 [M+H].

(E)-1-(3-(Trifluoromethyl)phenyl)-3-(2,6-dimethoxyphenyl)prop-2-en-1-one (b41). Yellow solid (97%), mp: 145.3–146.7 °C. ¹H-NMR (500 MHz, DMSO-d₆) δ 8.31–8.29 (m, 1H), 8.19 (s, 1H), 8.17 (d, J = 16.0 Hz, 1H), 8.04–8.02 (m, 1H), 7.99 (d, J = 16.0 Hz, 1H), 7.85–7.82 (m, 1H), 7.45–7.41 (m, 1H), 6.77–6.75 (m, 2H), 3.93 (s, 6H); ¹³C-NMR (150 MHz, DMSO-d₆): 189.7, 160.6, 139.3, 136.6, 133.3, 132.6, 130.8, 130.2, 129.9, 129.6, 124.8, 123.6, 111.8, 104.7, 56.6; MS (ESI) m/z = 337 (M+H)⁺; HRMS (ESI) m/z calcd. for C₁₈H₁₅F₃O₃ [M+H] 337.1046, found 337.1039 [M+H].

(E)-1-(3,5-bis(Trifluoromethyl)phenyl)-3-(2,6-dimethoxyphenyl)prop-2-en-1-one (b42). Yellow solid (99%), mp: 126.5–127.8 °C. ¹H-NMR (500 MHz, DMSO-d₆) δ 8.47 (s, 2H), 8.43 (s, 1H), 8.16 (d, J = 16.0 Hz, 1H), 7.95 (d, J = 16.0 Hz, 1H), 7.46–7.43 (m, 1H), 6.77–6.75 (m, 2H), 3.91 (s, 6H); ¹³C-NMR (150 MHz, DMSO-d₆): 188.9, 160.6, 140.6, 137.5, 133.6, 131.4, 131.2, 129.0, 126.4, 124.4, 123.6, 122.6, 111.7, 104.7, 56.6; MS (ESI) m/z = 405 (M+H)⁺; HRMS (ESI) m/z calcd. for C₁₉H₁₄F₆O₃ [M+H] 405.0920, found 405.0917 [M+H].

3.2. Biology

3.2.1. Cell Culture

HepG2 and MCF7 cells were grown in the Eagle’s minimum essential medium with Earle’s balanced salts (MEM-EBSS) medium, HeLa, A549 and L02 cells were grown in Dulbecco’s Modified Eagle Media (DMEM), SW1990 cells were grown in RPMI-1640 medium, and HMLE cell were grown in DMEM/F-12 medium. The media were supplemented with 100 U/mL penicillin, 100 mg/mL streptomycin and 10% fetal bovine serum (FBS), and incubated at 37 °C in a humidified atmosphere containing 5% CO₂.

3.2.2. In Vitro Anti-Proliferative Assay

Cells were seeded into 96-well plates (4000 cells/well) and incubated at 37 °C in a humidified 5% CO₂ atmosphere. After 24 h, the cells were treated with different concentrations of the compounds for 48 h in triplicate to generate dose-response curves. Cell viability was evaluated using the sulforhodamine B (SRB) assay as previous described [45]. The IC₅₀ values of the compounds were calculated using SigmaPlot10.0 software, which defined the IC₅₀ value as the concentration required to inhibit cell growth by 50%. Etoposide was used as the positive control.

4. Conclusions

In summary, we have developed a class of alkoxylated chalcones and evaluated their cytotoxicities in vitro against a panel of five different cancer cell lines and two non-tumoral cell lines. Most of the chalcones displayed potent cytotoxic activities. The results of this study also revealed that chalcones bearing electron donating alkoxy groups on their A- or B-ring generally exhibited good levels of cytotoxicity, and that the position and size of the substituents had a significant impact on the cytotoxic activity, with ortho and meta substituents being beneficial to the activity and large substituents having the opposite effect. The most potent compounds were b22 and b29, which had a 4-phenyl moiety and a 3-OMe-4-OH moiety, respectively. The SI values indicate that about one third of the compounds exhibit more than a 2-fold SI between the CC₅₀ in L02 and IC₅₀ in tumoral cells, which is similar with etoposide. Compounds b11, especially b29 showed promising SI values compared with both HMLE and L02 (2.1–6.5 fold in HMLE and over 33 fold in L02, respectively). These compounds are therefore worthy of further investigation.

Supplementary Materials

Supplementary materials can be accessed at: https://www.mdpi.com/1420-3049/19/11/17256/s1.

Supplementary Files

Supplementary File 1

Acknowledgments

This work was supported by the Natural Science Foundation of China (No. 81102376, 81302644), and the National S&T Major Special Project on Major New Drug Innovation (No. 2012ZX09301002-001-023-03).

Author Contributions

Yu-Cheng Wang and Ju-Xian Wang designed the research; Xiao-Guang Bai, Chang-Liang Xu, Shuang-Shuang Zhao and Hong-Wei He performed the experimental work; Xiao-Guang Bai and Chang-Liang Xu wrote the manuscript.

Conflicts of Interest

The authors declare no conflict of interest.

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Sample Availability: Samples of the compounds a1–20 and b1–42 are available from the authors.

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Bai, X.-G.; Xu, C.-L.; Zhao, S.-S.; He, H.-W.; Wang, Y.-C.; Wang, J.-X. Synthesis and Cytotoxic Evaluation of Alkoxylated Chalcones. Molecules 2014, 19, 17256-17278. https://doi.org/10.3390/molecules191117256

AMA Style

Bai X-G, Xu C-L, Zhao S-S, He H-W, Wang Y-C, Wang J-X. Synthesis and Cytotoxic Evaluation of Alkoxylated Chalcones. Molecules. 2014; 19(11):17256-17278. https://doi.org/10.3390/molecules191117256

Chicago/Turabian Style

Bai, Xiao-Guang, Chang-Liang Xu, Shuang-Shuang Zhao, Hong-Wei He, Yu-Cheng Wang, and Ju-Xian Wang. 2014. "Synthesis and Cytotoxic Evaluation of Alkoxylated Chalcones" Molecules 19, no. 11: 17256-17278. https://doi.org/10.3390/molecules191117256

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Synthesis and Cytotoxic Evaluation of Alkoxylated Chalcones

Abstract

1. Introduction

2. Results and Discussion

3. Experimental

3.1. Chemistry

3.1.1. General Methods

3.1.2. General Procedure for Synthesis of Chalcones

3.1.3. Characterization Data

3.2. Biology

3.2.1. Cell Culture

3.2.2. In Vitro Anti-Proliferative Assay

4. Conclusions

Supplementary Materials

Supplementary Files

Acknowledgments

Author Contributions

Conflicts of Interest

References

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