A New O-Terpenoidal Coumarin from Clausena anisum-olens Merr.

A new O-terpenoidal coumarin 1, named hekumarone, was isolated from the leaves and twigs of Clausena anisum-olens Merr. (Rutaceae) collected in Hekou County in Yunnan Province, P. R. China. Structure elucidation and unambiguous NMR assignments for the title compound was carried out on the basis of 1D and 2D NMR experiments.


Introduction
The plants of the Rutaceae family are well-known to contain structurally diverse and biologically active coumarins [1][2][3][4][5][6]. Within this family, the plants of the genus Clausena are shrubs, widely distributed in South and Southeast Asia and many species are used in Chinese folk medicine for various indications [7]. Previous phytochemical studies have indicated that Clausena species are the OPEN ACCESS rich sources of carbazole alkaloids and coumarins [4][5][6][8][9][10]. Clausena anisum-olens Merr. is a shrub that both grows wild and is cultivated from Philippines and South China through Southeast Asia. The aerial parts of this plant have been used for the treatment of dysentery and arthritis [7]. Our previous phytochemical studies on C. anisum-olens Merr., collected in Hekou County in Yunnan Province, P. R. China, resulted in the isolation of new cyclic peptides and monoterpenoid coumarins [11][12][13]. In our ongoing search for bioactive compounds from this medicinally important genus, a new O-terpenoidal coumarin 1, which we have named hekumarone, was isolated from C. anisum-olens Merr. In this report, we describe the isolation and structure elucidation of 1 using spectroscopic data analysis, including 1D and 2D NMR techniques (COSY, HSQC and HMBC).

Results and Discussion
The powdered plant material of Clausena anisum-olens Merr. (22.5 kg) was repeatedly extracted with EtOH at room temperature. The extract was then concentrated under reduced pressure to give a brown syrup, which was suspended in water and successively partitioned with petroleum ether, ethyl acetate (EtOAc) and n-butanol (n-BuOH). The EtOAc fraction was subjected to silica gel column chromatography, Pharmadex LH-20 and RP C-18 to yield compound 1, which was isolated as a light   Key HMBC of 1 The 1 H-NMR spectrum (Table 1) showed resonances for two pairs of typical AB system characteristic doublets at δ H 6.32 and 7.64 (each J = 9.5 Hz) and δ H 6.98 and 7.20 (each J = 8.6 Hz), corresponding to H-3, H-4, H-5 and H-6 in the coumarin nucleus. Additional signals in the spectrum were consistent with three olefinic protons δ 6.37, 6.09 (each1H, s) and 7.01(1H, d, J =1.6 Hz), one oxymethylene group δ 5.57 (2H, s), two methylene protons δ 2.80, 2.62 and one olefinic methyl δ 1.77 could be seen. The 13 C-NMR spectrum (Table 1) showed, in addition to the resonances of the carbons belonging to the coumarin nucleus, 10 other signals arising from one methyl, one oxymethylene, one methylene, one oxygen-bearing methine, four olefinic and two carbonyl carbons that could only be located on the side-chain. Joint analysis of HSQC spectra and HMBC correlations (Figure 1) confirmed the presence of a C 10 terpenoid side-chain attached to the coumarin skeleton. The connection of the side chain to C-7 on the coumarin nucleus was revealed by observation of a three-bond correlation between the oxymethylene proton signals (H-1') and carbon C-7 at δ C 153.5s. The presence of only one methoxyl signal at δ H 4.05 and a significant HMBC correlation with a quaternary carbon signal at δ C 135.6s revealed that the methoxyl group must be unequivocally located on C-8. Meanwhile, the EI-MS spectra also showed characteristic 8-OMe coumarin fragment ion at m/z 193 corresponding to loss of side chain [10].
Carefully analysis of the 1 H and 13 C NMR data of 1 (Table 1), showed that the signal patterns were in good agreement with those of previously isolated compounds 2/3 [13], except for some chemical shift differences. IR bands at 1,753, 1,748 and 1,730 cm -1 were indicative of the presence of three carbonyl groups in 1, suggesting a ketonic group and a lactone in the side chain. The major difference between the 13 C-NMR spectra of 1 and 2/3 was the appearance of a characteristic keto quaternary carbon signal at δ C 193.8s (Table 1) in 1 and disappearance of oxygen-bearing carbons at δ C 72.7d/72.6d compared to 2/3. The proton signal at δ 5.57 (2H, H-1′) appeared as a singlet, revealing the ketone (δ C 193.8s) was located at C-2′. In the HMBC spectrum (Figure 1), an informative correlation between the oxymethylene proton signal at δ H 5.57 (2H, H-1′) and keto quaternary carbon signal at δ C 193.8s confirmed it. Compared to 2/3, because the C-2′ chiral center disappeared, there were no NMR signals pairs for C-2′, C-5′ and C-10′ in 1. All these suggested that 1 was the C-2′ oxygenation product of 2/3. To confirm the assigned structure, compound pair 2/3 was oxygenated to afford 1 with H 2 Cr 2 O 7 -2Pyr. (PDC) in CH 2 Cl 2 ( Figure 2). On the basis of these results, the structure of 1 as shown in Figure 1 is proposed.

Conclusions
As a continuation of our phytochemical investigation on Clausena, a new O-terpenoidal coumarin 1, named hekumarone, was isolated from the leaves and twigs of Clausena anisum-olens Merr., collected in Hekou County in Yunnan Province, P. R. China. It is documented that coumarins are one of the major constituents in plants belonging to the genus Clausena [4][5][6]9]. The result of the present study supports the conclusion that coumarins are characteristic and distinguishable chemical markers for the Rutaceae family, especially, the genus Clausena.

General
Commercial silica-gel plates (Qing Dao Marine Chemical Group Co.) were used for TLC analyses. UV/VIS Spectra was measured on a Shimadzu UV-2401PC spectrophotometer; λ max in nm. IR spectra were obtained on a Bio-Rad FTS-135 infrared spectrophotometer, ν max in cm -1 . 1 H-and 13 C-NMR as well as 2D-NMR spectra were recordered on a Bruker DRX-500 spectrometer with TMS as internal standard, coupling constant J are expressed in Hz. MS spectra were recorded on a VG Autospec-3000 mass spectrometer.

Plant material
The

Oxidation of 2/3
PDC (60 mg) was resolved in dry CH 2 Cl 2 (2 mL) under N 2 . The mixture was stirred 5 min at room temperature. Then a soln. of 2/3 (6 mg) in CH 2 Cl 2 (1 mL) was added. The reaction mixture was stirred overnight. The mixture was filtered and H 2 O (2 ml) was added, and then extracted with CH 2 Cl 2 . The org. phase dried (MgSO 4 ) and evaporated to afford 1 (3 mg) as a light yellow oil.