- *Corresponding Author:
- Kalpana P. Rahate
Department Pharmaceutical Chemistry, Smt. Kishoritai Bhoyar College of Pharmacy, Kamptee-441 002, India
E-mail: [email protected]
|Date of Submission||21 September 2016|
|Date of Revision||19 August 2017|
|Date of Acceptance||04 April 2018|
|Indian J Pharm Sci 2018;80(3):551-556|
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Roots of Desmostachya bipinnata Stapf are used in the treatment of jaundice and asthma in Indian traditional medicine. Phytochemical investigation of the methanol extract of the roots of this plant led to isolation of three flavonols. The structures of these compounds were assigned on the basis of elemental analysis and spectroscopic evidences as apigenin, luteolin and quercetin, of which apigenin and luteolin were isolated for the first time. The yield of these compounds was 0.0034, 0.0026 and 0.0042 % w/w, respectively. These findings suggested the possibility that the three flavonoids isolated from the roots of Desmostachya bipinnata could be responsible for the benefits to human health offered by these roots.
Apigenin, Desmostachya bipinnata Stapf, flavonols, luteolin, quercetin
Desmostachya bipinnata (L.) Stapf (family: Poaceae), is an official drug of Ayurvedic Pharmacopoeia. This perennial grass well-known as sacrificial grass is native to northeast and west tropical, northern Africa, countries in the Middle East and temperate and tropical Asia. It is a rhizomatous perennial of dry areas with an extensive system of rhizomes 2-3 mm thick at 20- 30 cm depth. Leaves are coarse, narrow, and tough, up to 50 cm long, 3-19 mm wide, often rolled. Ligule is a very short ring of hairs, 1-2 mm. Culms are with glossy yellow leaf sheaths at the base, up to 1 m high with a conspicuous inflorescence 30-60 cm long. Spikelets are carried in two dense rows on short branches 2-3 cm long arranged in whorls of 2-4 racemes. Glumes are one-nerved, 1-2 mm long, lemmas are 2-3 mm long, often purplish. Seed are ovoid, 1 mm long, narrow, grooved. Flowering is during August-November and fruiting later in cold season. Roots are bitter, sweet, cooling, diuretic, emollient, galactogogue and astringent, which are used in asthma, jaundice, vitiated conditions of ‘pitta’ and hyperdipsia . It has long been used in various traditions as a sacred plant. It was used by Buddha for his meditation seat when he attained enlightenment . During eclipses, its roots are kept in the houses by Hindus in the belief that edible things will not be affected by harmful radiations . It is reported that the aerial part exhibit antiulcerogenic  and antihelicobacter  activity and the whole plant found to be analgesic, antipyretic and antiinflammatory . In order to reveal the intrinsic constituents responsible for these major activities of the extract, a few phytochemical investigations and instrumental analyses were carried out. Studies have showed that the flavonols like quercetin, its glycosides and kaempferol and various compounds such as tricin and its glycoside and xanthene had been isolated and identified from the aerial part extracts. However, no flavonoids have been isolated so far from the root extracts. In the present study, three flavonoids were isolated from the polyphenolic fraction of roots of D. bipinnata, which were characterised using spectroscopic methods and identified as apigenin, luteolin and quercetin, among which apigenin and luteolin have been reported for the first time in this plant. In the present study, isolation, purification and structure elucidation of these compounds were described.
The plant D. bipinnata was collected in the month of October from different regions of Tuticorin in Tamilnadu. The plant was authenticated by the Botanical Survey of India, Coimbatore, India (authentication no: BSI/SRC/5/23/Tech.681). The roots were separated, dried and pulverized. Reference materials apigenin, luteolin were procured from Natural Remedies Pvt. Ltd, India and quercetin from Sigma-Aldrich, St. Louis, MO, USA. Chromatographic column (600×30 mm, Borosil, Magnum, India), silica gel (60:20 mesh, Qualigens Fine Chemicals, Mumbai), were used for fractionation. Camag Linomat V applicator, Camag TLC Scanner 3, CAMAG glass twin through chamber, precoated silica gel plate 60F 254 (10×5 cm with 0.2 mm thickness, E. Merck) were used for highperformance thin-layer chromatography (HPTLC) fingerprinting. Elemental analysis was carried on C-H-N analyser (Elementar Vario EL III). Ultraviolet (UV) measurements were performed on UV double beam spectrophotometer (UV 1800-240 V, Shimadzu). Infrared (IR) spectra were recorded in KBr pellets on a Fourier-transform Infrared spectrophotometer (IR Affinity I, Shimadzu). 1H-nuclear magnetic resonance spectroscopy (NMR) and 13C-NMR spectra were obtained on a Bruker AV-400 (Biospin) spectrometer using dimethyl sulfoxide-d6 (DMSO-d6) as solvent. Chemical shift was recorded in δ (ppm) with tetramethylsilane used as an internal reference. All mass spectra (MS) were taken under electronic spray ionization mode on API 2000 MS/MS (AB Sciex, Canada) and analysed on negative mode. In addition, analytical balance (High precision Axis LCGC AGN 204), rotary vacuum evaporator (RV10 Digital, IKA® India Pvt. Ltd.), Soxhlet apparatus (Borosil, Magnum, India), ultra sonicator (CD-4800, Shenzhen Codyson Electrical Co., Ltd., China) were used in this study.
The air-dried and powdered roots of D. bipinnata (1.4 kg) were extracted with 70 % methanol (MeOH; 2×3 l) in a Soxhlet apparatus at 40°. After filtration the extract was evaporated under reduced pressure to render methanol extract (125 g). This extract was initially chromatographed over silica gel column under gradient conditions using benzene, chloroform, ethyl acetate and MeOH (100:0, 80:20, 60:40, 40:60, 20:80, 0:100). The eluted fractions were collected and monitored on TLC. Similar fractions were pooled together to obtain three major fractions (E1, E2 and E3).
Fraction E2 (13.6 g) was rechromatographed on silica gel column eluting with chloroform, ethyl acetate and MeOH mixture (10:0, 8:2, 6:4, 4:6, 2:8, 0:10, gradient) to yield three subfractions. These fractions were purified over Sephadex LH20 with 100 % MeOH to produce compounds 1 (17 mg, 0.0034 % w/w), 2 (13 mg, 0.0026 % w/w) and 3 (21 mg, 0.0042 % w/w), respectively. Structures of these isolated compounds were established on the basis of elemental analysis and UV, IR, 1HNMR, 13CNMR, and MS data as well as by comparison with published data. The spectral data were as follows and the structures were shown in Figure 1.
Compound (1): elements %: (C 50.7, H 33.03, N<0.5) C15H10O5 (molecular weight: 270); MS/MS: m/z 269 (M-H); UVmax (MeOH) nm: 270.4, 337; NaOAc nm: 275.2, 325.8, 391.6; NaOAc+H3BO3 nm: 268.8, 341.2; AlCl3 nm: 276.8, 301.4, 343.6, 381; AlCl3+ HCl nm: 275.8, 301, 341.8; NaOH nm: 275.2, 325, 392.6; IR: 3284 cm-1: OH, 1649 cm-1: C=O, 1605, 1556 and 1497 cm-1: aromatic ring; 1H NMR (DMSO-d6, 400 MHz): δ 12.9, 10.9, 10.4 (1H, s, 5, 7, 4’-OH), 7.9 (2H, d, J 7.2 Hz, H-2’/H-6’), 6.9 (2H, d, J 7.2 Hz, H-3’/H-5’ ), 6.79 (1H, s, H-3), 6.49 (1H, d, J 2.1 Hz, H-8), 6.2 (1H, J 2.1 Hz, H-6); 13C NMR (100 MHz, DMSO-d6): δ 181.7 (s, C-4), 164.1 (s, C-2), 163.8 (s, C-7), 161.4 (s, C-5), 161.1 (s, C-4’), 157.4 (s, C-9), 128.5 (d, C-2’/C-6’), 121.1 (s, C-1’), 115.9 (d, C-3’/C-5’), 103.7 (s, C-10), 102.8 (d, C-3), 98.7 (s, C-6), 93.9 (d, C-8).
Compound (2): elements %: (C 48.09, H 32.76, N<0.5) C15H10O6 (mol. wt. 286); MS/MS: m/z 285 (M-H); UVmax (MeOH) nm: 254.4, 348.2; NaOAc nm: 268.2, 401; NaOAc+H3BO3 nm: 259.8, 371.8; AlCl3 nm: 272.8, 419.8; AlCl3+HCl nm: 262.8, 274.8, 296, 359.6296, 359.6; NaOH nm: 270.4, 407.8; IR: 3208 cm-1: -OH, 1661 cm-1: C=O, 1606, 1506 and 1441 cm-1: aromatic ring; 1H NMR (DMSO-d6, 400 MHz): δ 12.97 (1H, s, 5-OH), 7.43 (1H, dd, J 7.8 Hz, H-6’), 7.41 (1H, d, J 2.2 Hz, H-2’), 6.92 (1H, d, J 7.8 Hz, H-5’), 6.66 (1H, s, H-3), 6.47 (1H, d, J 2.2 Hz, H-8), 6.21 (1H, d, J 2.2 Hz, H-6). 13C NMR (100 MHz, DMSO d6): δ 181.5 (C-4), 163.9 (C-2), 163.8 (C-7), 161.1 (C-5), 157.3 (C-9), 149.4 (C-4’), 145.5 (C-3’), 121.5 (C-1’), 118.8 (C-6’), 115.8 (C-5’), 113.1 (C-2’), 103.6 (C-10), 102.8 (C-3), 98.6 (C-6), 93.7 (C-8).
Compound (3): elements %: (C 46.17, H 31.15, N<0.5) C15H10O7 (mol. wt. 302); MS/MS: m/z 301 (M-H); UVmax (MeOH) nm: 256.2, 371.8; NaOAc nm: 279.4, 331.6, 395S; NaOAc+H3BO3 nm: 272.8, 387; AlCl3 nm: 278.5, 326, 438.3; AlCl3+HCl nm: 266.7, 372, 422S; NaOH nm: 329.2, 426.4; IR: 3277 cm-1: -OH, 1655 cm-1: C=O, 1610, 1522 and 1449 cm-1: aromatic ring; 1HNMR (DMSO-d6, 400 MHz): δ 12.5 (1H, s, 5-OH), 9.4 (1H, s, 4’-OH), 7.68 (1H, d, J 2.1 Hz, H-2’), 7.55 (1H, dd, J 7.4 Hz, H-6’), 6.9 (1H, d, J 7.4 Hz, H-5’), 6.41 (1H, d, J 2.1 Hz, H-8), 6.19 (1H, d, J 2.1 Hz, H-6); 13CNMR (100 MHz, DMSO-d6): d 175.8 (C-4), 163.9 (C-7), 160.7 (C-5), 156.1 (C-9), 147.7 (C-3’), 146.7 (C-2), 145.0 (C-4’), 135.7 (C-3), 121.9 (C-1’), 119.9 (C-6’), 115.6 (C-5’), 115.0 (C-2’), 103.0 (C-10), 98.1 (C-6), 93.3 (C-8).
Apigenin (1) was obtained as a pale yellow amorphous powder. The UV spectra (Table 1) in different shift reagents showed the pattern of a 4’,5,7-trihydroxy flavone, where the presence of 5-hydroxy group was indicated by AlCl3 spectrum, while the presence of 7-hydroxy group was deduced from NaOAc spectra. The NaOH spectrum indicated the presence of free 4’-hydroxy group. The negative atmospheric pressure ionization-tandem mass spectrometry (API-MS/MS) spectrum showed a quasimolecular ion peak [M-H]+ at m/z 268.9, corresponding to the molecular formula C15H10O5 (Figure 2A), which was supported by elemental analysis [7-9]. The IR spectra showed absorption bands for hydroxyl groups (3283.98 cm-1), aromatic ring (1604.8, 1555.9, 1497.4 cm-1), carbonyl group (1649.4 cm-1) and ketone group (1154.8 cm-1). The 1HNMR spectrum showed two meta coupled aromatic protons at δ 6.2 (d, J=2.1 Hz) and δ 6.49 (d, J=2.1 Hz), assigned for H-6 and H-8, respectively, confirming a 5,7-disubstituted ring A. The 4’-substituted ring B was deduced by the appearance of four protons with a typical doublet pattern for 2’,6’-H and 3’,5’-H at δ 7.9 (d, J=7.2 Hz) and at δ 6.9 (d, J=7.2 Hz), respectively. The 13CNMR spectrum indicated the presence of 15 signals corresponding to 15 carbons. Signals for C-7 at δ 163.8, C-4’ at δ 161.1 and C-5 at δ 161.4 confirmed the OH-bonded carbons. Thorough study of the homonuclear correlation spectroscopy (COSY) and the heteronuclear multiple quantum coherence (HMQC) spectra helped in full assignment of all protons to their carbon signals. Upon comparison of the spectral data with the earlier reported, the structure of compound 1 (Figure 1) was identified as apigenin, 2-(4-hydroxyphenyl)-5,7-dihydroxy-4-chromenone.
|Flavonoid 1||Flavonoid 2||Flavonoid 3|
|Band I||Band II||Band I||Band II||Band I||Band II|
|MeOH+NaOAc||275.2||325.8, 391.6S||268.2||401||279.4||331.6, 395S|
|MeOH+AlCl3||276.8||343.6, 381S||272.8||419.8||278.5||326, 438.3S|
|MeOH+AlCl3, HCl||275.8||341.8||262.8||296, 359.6S||266.7||372, 422S|
|MeOH+ NaOH||275.2||325, 392.6S||270.4||407.8||329.2||426.4|
Table 1: UV Spectral Data of Flavonoids 1, 2 and 3
Luteolin (2) was obtained as a cream coloured amorphous powder. The UV spectra in different shift reagents showed the pattern of 3’,4’,5,7-tetrahydroxy flavone, where the presence of 5-hydroxy group was indicated by AlCl3 spectrum, while the presence of 7-hydroxy group was deduced from NaOAc spectra. NaOAc/H3BO3 spectrum and AlCl3 spectrum gave evidence for the presence of ortho dihydroxy system in ring B. The NaOH spectrum indicated the presence of free hydroxy groups. The negative API-MS/MS spectrum showed a quasimolecular ion peak [M-H]+ at m/z 285 (Figure 2B), corresponding to the molecular formula C15H10O6, supported also by elemental analysis. The IR spectra showed absorption bands for hydroxyl groups (3207.65 cm-1), aromatic ring (1606, 1505.6, 1441.2 cm-1), carbonyl group (1661.05 cm-1) and ketone group (1153.7 cm-1). The 1H NMR spectrum showed two meta coupled aromatic protons at δ 6.21 (d, J=2.2 Hz) and δ 6.47 (d, J=2.2 Hz), assigned for H-6 and H-8, respectively, confirming a 5,7-disubstituted ring A. The 3’,4’-disubstituted ring B was deduced by the appearance of three protons with a typical doublet pattern for 2’,5’ and 6’-H at δ 7.41 (d, J=2.2 Hz), 6.92 (d, J=7.8 Hz) and at δ 7.43 (dd, J=7.8 Hz), respectively. The 13CNMR spectrum indicated the presence of 15 signals corresponding to 15 carbons. Signals for C-7 at δ 163.8, C-4’ at δ 149.38, C-5 at δ 161.1 and C-3’ at δ 145.47 confirmed the OH-bonded carbons. Thorough study of the COSY and the HMQC spectra helped in full assignment of all protons to their carbon signals. Upon comparison of the spectral data with the earlier reported, the structure of compound 2 (Figure 1) was identified as luteolin, 2-(3,4-dihydroxyphenyl)- 5,7-dihydroxy-4-chromenone.
Quercetin (3) was obtained as yellow amorphous powder. The UV spectra in different shift reagents showed the pattern of 3,3’,4’,5,7-pentahydroxy flavone, where the presence of 5-hydroxy group was indicated by AlCl3 spectrum, while the presence of 7-hydroxy group was deduced from NaOAc spectra. NaOAc/H3BO3 spectrum and AlCl3 spectrum gave evidence for the presence of ortho dihydroxy system in ring B. The NaOH spectrum indicated the presence of free 3’,4’-hydroxy groups. The negative API-MS/MS spectrum showed a quasimolecular ion peak [M-H]+ at m/z 301 (Figure 2C), corresponding to the molecular formula C15H10O7, supported also by elemental analysis. The IR spectra showed absorption bands for hydroxyl groups (3276.96 cm-1), aromatic ring (1610, 1522, 1449 cm-1), carbonyl group (1655.13 cm-1) and ketone group (1167.8 cm-1). The 1H NMR spectrum showed two meta coupled aromatic protons at δ 6.19 (d, J=2.1 Hz) and δ 6.41 (d, J=2.1 Hz), assigned for H-6 and H-8, respectively, confirming a 5,7-disubstituted ring A. The 3’,4’-disubstituted ring B was deduced by the appearance of three protons with a typical doublet pattern for 2’,5’ and 6’-H at δ 7.68 (d, J=2.1 Hz), 6.9 (d, J=7.4 Hz) and at δ 7.55 (dd, J=7.4 Hz), respectively. The 13CNMR spectrum indicated the presence of 15 signals corresponding to 15 carbons. Signals for C-3 at δ 135.68, C-7 at δ 163.86, C-3’ at δ 145, C-4’ at δ 147.65 and C-5 at δ 160.67 confirmed the OH-bonded carbons. Thorough study of the COSY and the HMQC spectra helped in full assignment of all protons to their carbon signals. Upon comparison of the spectral data with the earlier reported, the structure of compound 3 (Figure 1) was identified as quercetin, 2-(3,4- dihydroxyphenyl)-3,5,7-trihydroxy-4-chromenone.
The present investigation appears to be the first report of the isolation of apigenin and luteolin from the species D. bipinnata. Till date, the isolation of quercetin and its glycosides, tricin and its glycoside, xanthene and kaempferol were reported from D. bipinnata. These findings also suggested that D. bipinnata could be a promising natural source in health-related applications. Previous studies suggested that D. bipinnata was effective antioxidant, in vitro cytotoxic as well as in vitro and in vivo hepatoprotective [10-12]. These effects have been attributed to the presence of these flavonols in the plant.
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