Bulletin of the Korean Chemical Society

  • 제35권5호
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  • Pages.1556-1558
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  • 2014
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  • 0253-2964(pISSN)
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  • 1229-5949(eISSN)
대한화학회 (Korean Chemical Society)
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A New Halimane Diterpenoid from Croton crassifolius

  • Zhang, Zhan-Xin (School of Pharmacy, Lanzhou University) ;
  • Li, Hui-Hong (School of Pharmacy, Lanzhou University) ;
  • Qi, Feng-Ming (State Key Laboratory of Applied Organic Chemistry, College of Chemistry and Chemical Engineering, Lanzhou University) ;
  • Xiong, Hui-Yan (Agriculture and Animal Husbandry College, Qinghai University) ;
  • Dong, Le-Le (School of Pharmacy, Lanzhou University) ;
  • Fan, Gai-Xia (School of Pharmacy, Lanzhou University) ;
  • Fei, Dong-Qing (School of Pharmacy, Lanzhou University)
  • 투고 : 2013.12.09
  • 심사 : 2014.01.13
  • 발행 : 2014.05.20
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초록

키워드

Experimental Section

General Experimental Procedures. Melting points were determined on an X-4 digital display micromelting point apparatus, and are uncorrected. UV spectra were recorded on a Shimadzu UV-2550 UV-Vis spectrophotometer. Optical rotations were measured on a Perkin Elmer 341 polarimeter. IR spectra were taken on a Nicolet NEXUS 670 FT-IR spectrometer. NMR spectra were recorded on a Varian Mercury-600BB NMR spectrometers with TMS as internal standard. HR-ESI-MS data were recorded on a Thermo LTQ Orbitrap Elite mass spectrometer. Sephadex LH-20 were supplied by Amersham Pharmacia Biotech. Silica gel (200-300 mesh) used for column chromatography and silica gel GF254 (10-40 μM) used for TLC were supplied by the Qingdao Marine Chemical Factory, Qingdao, China. Spots were detected on TLC under UV light or by heating after spraying with 5% H2SO4 in C2H5OH (v/v).

Plant Material. The roots of C. crassifolius were pur-chased from Hebei Anguo Medicine Market, and were originally collected from Fujian province of China in September 2012. A voucher specimen (No. 201209CC) was deposited at the School of Pharmacy, Lanzhou University and was identified by Dr. Jian-Yin Li.

Extraction and Isolation. The air-dried and powdered roots of C. crassifolius (9.5 kg) were extracted four times with 95% aqueous EtOH at room temperature to give a residue (962 g) after evaporation. The residue was suspend-ed in H2O and extract with EtOAc and n-BuOH. The EtOAc partition (731 g) was applied to silica gel CC, eluting with petroleum ether-acetone (40:1–0:1 gradient system). Then six crude fractions (A-F) were obtained by TLC analysis. Fraction B was subjected to silica gel CC eluting with petro-leum ether-acetone (50:1 to 10:1) to give two subfractions (Fr.B1 and Fr.B2). The subfration Fr.B2 (6.5 g) was further applied to silica gel CC, and eluted with petroleum ether-EtOAc (20:1, 10:1, 5:1, 3:1) to give Fr.B2.1–Fr.B2.4. The Fr.B2.2 was subjected to CC on Sephadex LH-20 (CHCl3-MeOH, 1:1) and silica gel (petroleum ether-acetone, 15:1 to 2:1) to yield compound 1 (5 mg). Fraction D was subjected to silica gel CC eluting with petroleum ether-acetone (20:1 to 3:1) to give two subfractions (Fr.D1 and Fr.D2). The subfration Fr.D2 (55 g) was further applied to silica gel CC, and eluted with petroleum ether-acetone (10:1, 5:1, 3:1) to give compound 2 (10 g).

Crassifoliusin A (1): Yellow crystals (acetone); mp 126-129 °C; –20° (c 0.1, CHCl3); UV (CH3OH) λmax (log ε) 216.2 (3.69) nm; IR (KBr) νmax cm−1: 3467, 2932, 2873, 1722, 1682, 1505, 1458, 1257, 1231, 1123, 870, 757; HR-ESI- MS m/z: 357.1688 [M + H]+ (calcd for C21H25O5, 357.1697); 1H-NMR (600 MHz, CDCl3) and 13C-NMR (150 MHz, CDCl3) spectral data are listed in Table 1.

X-ray Crystallographic Analysis of Compound 1. C21H24O5, molecular weight (Mw) = 356.40, orthorhombic, space group P212121, a = 8.8900 (12) Å, b = 9.7794 (8) Å, c = 21.473 (3) Å, α = b = γ = 90°, V = 1866.9 (4) Å3, Z = 4, Dc = 1.268 mg/m3, μ(Mo Kα) = 0.090 mm−1, F(000) = 760, and T = 292 K, crystal dimensions 0.35 × 0.31 × 0.11 mm was selected for X-ray analysis. The reflection data were collected on an Agilent Technologies SuperNova, Dual source, EOS CCD with mirror optics, using graphite-monochromated Mo-Ka radiation (λ = 0.7107 Å). A total of 3310 reflections were collected in the range 3.0° ≤ θ ≤ 25.7°, of which 2108 unique reflections with I > 2σ (I) were collected for the analysis. The structure was solved by direct methods using SHELXS97 and refined by full matrix least-squares on F2. The final R and RW factors were 0.060 and 0.128, respectively.

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