Synthesis and biological evaluation of a new series of ortho-carboranyl biphenyloxime derivatives

(Z,Z’)-1,1′-(4-ortho-Caboranyldimethyl)-bis(2-methoxyphenylethan-1-oxime) intermediate 3 was synthesized by a three-step reaction with a final treatment with base to give a new series of ortho-carboranyl biphenyloxime derivatives (4–8). Compounds 7 and 8 showed high solubility and the in vitro study results revealed high levels of accumulation in HeLa cells with higher cytotoxicity and boron uptake compared to l-boronphenylalanine. Electronic supplementary material The online version of this article (10.1186/s13065-018-0444-z) contains supplementary material, which is available to authorized users.


Introduction
Carborane (C 2 B 10 H 12 , Fig. 1) is a spherical compound formed by one or more boron peaks of polyhedral boron compounds, which is formed by carbon atoms. The volume is similar to that of a benzene ring [1][2][3][4][5]. This is a special large steric skeleton with a very strong hydrophobic structure. Therefore, improvement of the chemical structure can alter the stability, water solubility, and biological activity of compatibility and allow wider applications of carborane as a BNCT agent [6][7][8][9]. Boron neutron capture therapy (BNCT) was first proposed as a potential cancer therapy in 1936, based on the thermal neutron captured by 10 B atoms then produces a 4 He (α-particle) and a 7 Li ion [10,11]. However, its successful application in the treatment of cancer patients still presents a challenge in medical research [12]. A major challenge in designing boron containing drugs for BNCT of cancer is the selective delivery of 10 B to the tumor as well as water solubility [13]. Our synthetic strategy was to use heterocyclic alkyl chains as a boron delivery system, the target molecules being the heterocyclic alkyl oxime chains in which the boron functionality was present as a ortho-carborane. The large number of boron atoms has a clear advantage for BNCT [14]. This paper reports the hydrophilic carboranylbenzyloxime moiety, such as alkylmorpholine, alkylpiperidine, phenoxyalkyl, and pyridine, on carbon-oxygen combined with chemical bonding. These compounds have higher solubility in polar solvents and increased the boron uptake in tumor cells, highlighting the potential use of carborane as a hydrophilic carrier into the body that can pass the Blood Brain Barrier (BBB rule) to the cells within the organization for drug evaluation.

Experimental
All manipulations were performed under a dry nitrogen atmosphere using standard Schlenk techniques. Tetrahydrofuran (THF) was purchased from Aladdin Pure Chemical Company and dried over sodium metal distillation prior use. The reactions were monitored on Merck F-254 pre-coated TLC plastic sheets using hexane as the mobile phase. All yields refer to the isolated yields of the products after column chromatography using silica gel (200-230 mesh). All glassware, syringes, magnetic stirring bars, and needles were dried overnight in a convection oven. Ortho-carborane (C 2 H 2 B 10 H 10 ) was purchased from HENAN WANXIANG Fine Chemical Company and used after sublimation. The NMR spectra were recorded on a Bruker 300 spectrometer operated and the chemical shifts were measured relative to the internal residual peaks from the lock solvent (99.9% CDCl 3 and CD 3 COCD 3 ), and then referenced to Si(CH 3 ) 4 Open Access *Correspondence: organicboron@ujs.edu.cn School of Pharmacy, Jiangsu University, Zhenjiang 212013, People's Republic of China (0.00 ppm). The Fourier transform infrared (FTIR) spectra of the samples were recorded on an Agilent Cary 600 Series FT-IR spectrometer using KBr disks. Elemental analyses were performed using a Carlo Erba Instruments CHNS-O EA1108 analyzer (Additional file 1).
Synthesis of 1,1′-(4-caboranyldimethyl)-bis(2-methoxy-4,1-phenylene-ethan-1-one) (2). Acetyl chloride (1.4 mL, 20 mmol) was added via a syringe to a solution of aluminum chloride (2.6 g, 20 mmol) in 50 mL of methylene chloride at 0 °C and stirred for 30 min. A solution of compound 1 (3.5 g, 10 mmol) in methylene chloride 10 mL was added slowly to the reaction flask at 0 °C, and the reaction temperature was maintained at 0 °C for 30 min. The reaction mixture was then warmed slowly to room temperature, stirred for an additional 3 h, and quenched with a saturated NaHCO 3 (30 mL) solution. The crude product was then extracted, and the organic layer was washed with H 2 O, dried with anhydrous Na 2 SO 4 , and filtered then concentrated. The residue was purified by flash column chromatography (ethyl acetate/ hexane 1:8) to give compound 2 as a colorless oil: yield: 4.1 g (97%). IR (KBr pellet), cm −1 , ν: (B-H o-carborane ) 2602.

Cell viability assay (MTT assay)
HeLa cells in a 3 × 10 4 /mL cell suspension per hole in 96 well plates were digested by adding 100 μL of a cell suspension and culturing for 24 h to absorb the original culture medium followed by the addition of 200 μL configured compounds-4, 5, 6, 7, 8 and BPA (l-boronphenylalanine). Each concentration was made from 4 compound holes, and the holes around the 96 well plates were sealed with PBS, the negative control. The blank control group lacked the compounds. After 24 h, 20 μL of a MTT solution was added to each hole, and cultured for 4 h. Subsequently, DMSO 150 μL was added to the medium through a suction hole and shaken for 10 min. The OD of each hole was determined at 490 nM, and the sample inhibition rate in different concentrations was calculated: inhibition rate = (Control OD value/Delivery OD value)/Control OD value × 100%. Finally, the IC 50 value of the sample was calculated using the related software.

Results and discussion
This paper reports the hydrophilic function of the orthocarboranylbenzyloxime moiety, such as alkylmorpholine, alkylpiperidine, phenoxyalkyl and pyridine, on carbon-oxygen combined with chemical bonding. These compounds have higher solubility in polar solvents and increasing boron uptake in tumor cells within the organization for a drug evaluation.
The major requirement of a BNCT agent is a high water solubility, high boron uptake, and low cytotoxicity. The HeLa cervical carcinoma cells were treated with the Scheme 1 Preparation of (Z,Z')-1, 1′-(4-Caboranyldimethyl)-bis(2-methoxyphenylethan-1-oxime) Scheme 2 Preparation of (Z,Z′)-1,1′-(4-Caboranyldimethyl)-bis (hydrophilic functional) derivatives(4- 8) candidate compounds 4-8 for 2 days, and the cell viability was determined by a MTT assay. Compounds 4-8 exhibited boron uptake in the range of 0.106-0.520 ppm (Table 1), and the cell cytotoxicity was in the range of 1.134-2.516 µM, as shown Fig. 2. In particular, compounds 7 and 8 showed high boron uptake in HeLa cells, and both compounds had higher cytotoxicity than BPA (l-boronphenylalanine). Morpholine and piperidine is a heterocyclic nitrogen and oxygen member six-ring reagent with a simple structure that improves the water solubility and bioactivity improvement. They are used in the preparation of pharmaceutical drugs for their antiinflammation, anticancer, and antiviral activity [24][25][26][27][28].

Conclusion
In conclusion, we reported the series of ortho-carborane substituted bipolar-function derivatives, such as alkyl pyridine, alkyl phenoxide, alkyl morpholine, and alkyl piperidine, were synthesized. The target compounds coupling of the aryl-oxime with chain functional group proceeded successfully for introduction of an ortho-carborane moiety in the molecules, which can easily be further four-step substituted to high yield final compound. The effects of synthesized compounds on biology activity were assay in HeLa cells. Both cyclic alkyl derivatives of ortho-carborane and oxime containing compounds, 7 and 8, respectively, were exhibit high boron uptake and higher cytotoxicity than BPA (l-boronphenylalanine). This resulted in carborane compounds with improved water solubility for the BNCT agent. The knowledge gained from modified bipolar groups could facilitate both drug selection and evaluations.