The MeOH-soluble fraction and EtOAc-soluble fraction of the MeOH extract of S. grandiflora root afforded four compounds 1–4, after repeated column chromatography purifications. Compound 1 was isolated as an amorphous powder, [α]_D²⁰: −66.6 (MeOH). The molecular formula of 1 was determined as C₁₆H₁₆O₄ ([M+H]⁺m/z 273.1) from the FAB mass spectrum. This compound was found to be an isoflavan on the basis of its characteristic spectral data: λ_max 227 and 284 nm in the UV spectrum and a set of aliphatic proton signals (δ 2.81, 2.98, 3.49, 3.99, and 4.25) in the ¹H-NMR spectrum, which in addition displayed three aromatic protons in an AMX system (δ 6.43, 6.51, and 7.06) and three aromatic protons in an ABM system (δ 6.29, 6.38, and 6.90). The ¹³C-NMR spectrum exhibited signals for 17 carbons which were distributed between one methoxyl, two methylenes, seven methines, and six quaternary carbons. The molecular structure of 1 was confirmed by a DEPT experiment. Further assignment was done by Heteronuclear Multiple Quantum Coherence (HMQC) and Heteronuclear Multiple Bond Correlation (HMBC) spectra. The placement of one methoxyl group and two hydroxyl groups at the C-2', C-4', and C-7 positions, respectively, were confirmed from the HMBC experiment, which revealed a correlation between the methoxyl group with a carbon at C-2' (δ 159.64), and a correlation between the hydroxyl group at C-4' (δ 155.64) and carbon at C-3' (δ 102.08) and C-5' (δ 102.08). The position of the other hydroxyl group was assigned at C-7. The HMBC spectrum exhibited a correlation between the hydroxyl group at C-7 (δ 157.03) and carbon at C-6 (δ 108.28), and C-8 (δ 103.99). On the basis of the spectroscopic evidence, compound 1 was characterised as 7,4'-dihydroxy-2'-methoxyisoflavan or isovestitol [11,12].

Compound 2 was obtained as an amorphous powder and its molecular formula was assigned as C₁₆H₁₄O₄ ([M-H]⁺m/z 269.0816) from the HRESI mass spectrum. The characteristic spectral data; λ_max 229 and 286 nm in the UV spectrum and a pair of four aliphatic protons (δ 3.61; 3.61; 4.28; and 5.52) in the ¹H-NMR spectrum revealed that compound 2 has a pterocarpan skeleton. The ¹H-NMR spectrum (Table 1) of compound 2 revealed two sets of the AMX type aromatic protons (δ 6.37, 6.57, and 7.33; and 6.39, 6.46, and 7.24), one methoxyl group (δ 3.76, 3H), and one hydroxyl group (δ 8.66). The location of the methoxyl group at C-9 and the hydroxyl group at C-3 position were assessed by a HMBC experiment. The structure of compound 2 was deduced from detailed analysis of ¹H-and ¹³C-NMR data aided by 2D-NMR experiments (COSY, HMQC, HMBC, and NOESY) and identified as 3-hydroxy-9-methoxypterocarpan or medicarpin [12].

Compound 3 was obtained as an amorphous powder and its molecular formula was analysed as C₁₇H₁₈O₄ ([M-H]⁺m/z 285.1119) from the HRESI mass spectrum. The spectral (IR, ¹H-NMR and ¹³C-NMR) data of compound 3 revealed that its structure was similar to that of the isolated compound 1 mentioned earlier in this paper. The hydroxyl group at the C-4' position of 1 is replaced by a methoxyl group in 3. It was also clearly observed that the ¹³C-NMR spectrum of 3 (Table 1) revealed two methoxyl carbons at δ 3.76 and 3.86. Thus, the structure of compound 3 was confirmed as 7-hydroxy-2',4'-dimethoxyisoflavan or sativan [13]. This structure was further confirmed from ¹H-¹H COSY and HMBC experiments.

Another known isolated compound, 3β-hydroxy-lup-20(29)-en-(28)-oic acid or betulinic acid (4) was readily identified based on its spectroscopy data (1D-and 2D-NMR) and also by comparing its physico-chemical, spectroscopic, and mass spectrometric data with literature values [14].All isolated compounds are known compounds, therefore, elucidation of their structures was confirmed by comparison of their spectral data with those reported earlier.

The crude extract of S. grandiflora root and the isolated compounds were assessed in vitro against M. tuberculosis H37Rv. The antituberculosis activity data are displayed in Table 2. A first-line antituberculosis drug, isoniazid, was used as a positive control. The methanol extract exhibited a moderate activity with MIC value of 625 µg/mL. Among the isolated chemical constituents, compounds 1, 2 and 3 showed similar antituberculosis activity, with MIC values of 50 µg/mL, while compound 4 exhibited a weaker activity, with a MIC value of 100 µg/mL. This is the first report on the antituberculosis activity of the tested compounds.

TLC was performed on pre-coated Merck 60 GF₂₅₄ silica gel plates (absorbent thickness, 0.25 mm) and sprayed with Ce (IV) sulphate solution for visualization of spots. Preparative plates TLC was performed on 20 cm × 20 cm glass plates coated with 0.5 mm Kieselgel F₂₅₄ (Merck), and were air-dried and used without prior activation. Column chromatography was performed on silica gel (Merck Kieselgel 60, 70-230 mesh ASTM). Melting points were recorded on a Stuart Scientific SMP1 apparatus. Optical rotations were determined using a JASCO DIP–370 digital polarimeter with a 0.5 cm microcell. NMR spectra were recorded in acetone-d₆, with TMS as internal standard, using either a Bruker Avance 300 or a Bruker Avance 400 spectrometer, HRESIMS spectra were using a Micro TOF-Q mass spectrometer in positive-ion mode. IR(KBr) spectra were recorded using a Perkin-Elmer system 2000 FT-IR spectrometer. UV spectra were recorded using a Perkin-Elmer Lambda 25 spectrometer. Blank discs and antibiotic discs were purchased from Oxoid, Middlebrook 7H9 broth from Difco, and Tetrazolium-Tween 80 mixture from Sigma.

The roots of Sesbania grandiflora were collected in September 2008 in the village of Sidosari, South Lampung, Indonesia. The identity of the plant specimen was authenticated by Harry Wiriadinata and a voucher specimen (No. N-III) was deposited at the Bogoriense Herbarium, Bogor, Indonesia.

Air-dried and powdered roots (1.5 kg) of S. grandiflora were extracted with 90% aqueous MeOH (3 × 5 L) at room temperature for a period of seven days. The extract was concentrated to a volume of 100 mL under reduced pressure using a rotatory evaporator at a bath temperature of 40 °C, and then partitioned with hexane to afford a hexane-soluble fraction (Fr. A, 1.9 g) and a MeOH-soluble fraction. The MeOH-soluble fraction was suspended in H₂O and partitioned sequentially with CHCl₃, and EtOAc, yielding a CHCl₃-soluble fraction (Fr. B, 0.9 g) and an EtOAc-soluble fraction (Fr. C, 4 g). Fr. C was separated by extensive centrifugal TLC (hexane-EtOAc gradient) to afford 7 major fractions, Fr. C1–C7. Fr. C2 (290 mg) was further fractionated by centrifugal TLC (CHCl₃-MeOH 95:5 v/v) to afford 8 sub-fractions, Fr. C2.1–Fr. C2.8. Fr. C2.6 (180 mg) was fractionated by column chromatography (hexane-EtOAc 95:5 v/v) to give 10 sub-fractions: Fr.C2.6.1–Fr. C2.6.10. Fr. C2.6.7 (40 mg) was purified by silica gel preparative TLC (hexane-CHCl₃-MeOH 5:99:1 v/v/v) to afford 1 (20 mg, R_f 0.25). Fr. C3 (250 g) was separated by centrifugal TLC (CHCl₃-MeOH gradient) to afford 7 sub-fractions, Fr.C3.1–Fr. C3.7. Fr.C3.4 (95 mg) was further purified by preparative silica gel TLC (toluene-EtOAc 99:1 v/v) to yield 2 (18.5 mg, R_f 0.45) and 3 (7 mg, R_f 0.47). Compound 4 (23.7 mg) was obtained by recrystallization from the MeOH-soluble fraction. The fractionation procedure is summarized in Figure 1. The isolated compounds 1–4 were readily identified based on their spectroscopic data (1D- and 2D-NMR) and also by comparing their physico-chemical, spectroscopic, and mass spectrometric data with those reported in the literature. All the isolated compounds are known compounds, and were confirmed as isovestitol (1), medicarpin (2), sativan (3) and betulinic acid (4), the structures of which are shown in Figure 2.

Assay was performed by the Tetrazolium Microplate Assay method as described previously [15], with minor modifications. A susceptible virulent strain of M. tuberculosis H37Rv ATCC 27294 was used in this study. The test concentrations of purified compounds and the extracts ranged from 200 to 0.391 μg/mL and 2,500 to 4.883 μg/mL, respectively. Each sample was tested in triplicates twice. The plates were sealed with Parafilm and incubated at 37 °C in 8% CO₂ for 5 days. On day 5, Tetrazolium-Tween 80 mixture {50 μL, 1.5 mL of tetrazolium bromide [3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-tetrazolium bromide] at a dilution of 1 mg/mL in absolute ethanol and 1.5 mL of sterile 10% Tween 80} was added to a control well and then reincubated at 37 °C for 24 h. Tetrazolium-Tween 80 mixture was added to all wells and the colour was recorded at 24 h. A colour change from yellow to purple indicated growth and the minimum inhibitory concentration (MIC) was interpreted as the lowest tested compound and extract concentration which prevented the colour change from yellow to purple.