References
- Bruhn T, Schaumlöffel A, Hemberger Y, Bringmann G. 2013. SpecDis: quantifying the comparison of calculated and experimental electronic circular dichroism spectra. Chirality. 25:243–249.10.1002/chir.v25.4
- Chen K-S, Wu Y-C, Teng C-M, Ko F-N, Wu T-S. 1997. Bioactive alkaloids from Illigera luzonensis. J Nat Prod. 60:645–647.10.1021/np9700735
- Chen J-J, Hung H-C, Sung P-J, Chen I-S, Kuo W-L. 2011. Aporphine alkaloids and cytotoxic lignans from the roots of Illigera luzonensis. Phytochem. 72:523–532.10.1016/j.phytochem.2010.12.015
- Chen J-J, Lee T-H, Kuo W-L, Sung P-J, Chen I-S, Shu C-W, Cheng M-J, Wang T-C, Lim Y-P, Xu R. 2015. (+)-(6aR,7R)-7-hydroxy-N-butyrylcaaverine, a new aporphine alkaloid from the roots of Illigera luzonensis with cytotoxic activity. Chem Nat Compd. 51:739–742.10.1007/s10600-015-1397-2
- Devi P, Wahidullah S, Rodrigues C, Souza LD. 2010. The sponge-associated bacterium Bacillus licheniformis SAB1: a source of antimicrobial compounds. Mar Drugs. 8:1203–1212.10.3390/md8041203
- Dong J-W, Cai L, Li X-J, Wang J-P, Mei R-F, Ding Z-T. 2017a. Monoterpene esters and aporphine alkaloids from Illigera aromatica with inhibitory effects against cholinesterase and NO production in LPS-stimulated RAW264.7 macrophages. Arch Pharm Res. 40:1394–1402.10.1007/s12272-016-0860-3
- Dong J-W, Cai L, Li X-J, Mei R-F, Wang J-P, Luo P, Shu Y, Ding Z-T. 2017b. Fermentation of Illigera aromatica with Clonostachys rogersoniana producing novel cytotoxic menthane-type monoterpenoid dimers. RSC Adv. 7:38956–38964.10.1039/C7RA06078E
- Flora of China Editorial Committee. 1982. Flora Reipublicae Popularis Sinicae. Vol. 30. Beijing: Science Press.
- Haruna M, Koube T, Ito K, Murata H. 1982. Balanophonin, a new neo-lignan from Balanophora japonica Makino. Chem Pharm Bull. 30:1525–1527.10.1248/cpb.30.1525
- Huang SZ. 1985. A new species and some medicinal plants of Illigera BL. from Guangxi. Guihaia. 5:17–20.
- Huang JH, Lei XG. 2013. A nature-inspired concise synthesis of (+)-ent-chromazonarol. Sci China Chem. 56:349–353.10.1007/s11426-012-4826-0
- Huang C-H, Chan Y-Y, Kuo P-C, Chen Y-F, Chang R-J, Chen I-S, Wu S-J, Wu T-S. 2014. The constituents of roots and stems of Illigera luzonensis and their anti-platelet aggregation effects. Int J Mol Sci. 15:13424–13436.10.3390/ijms150813424
- Li W, Mei WL, Wang H, Zuo WJ, Yang DL, Dai HF. 2013. Chemical constituents from stems of Aquilaria sinensis. Chin J Chin Mater Med. 38:2826–2831.
- Liao Y, Liu X, Yang J, Lao YZ, Yang XW, Li XN, Zhang JJ, Ding ZJ, Xu HX, Xu G. 2015. Hypersubones A and B, new polycyclic acylphloroglucinols with intriguing adamantane type cores from Hypericum subsessile. Org Lett. 17:1172–1175.10.1021/acs.orglett.5b00100
- Moridi Farimani M, Abbas-Mohammadi M. 2016. Two new polyhydroxylated triterpenoids from Salvia urmiensis and their cytotoxic activity. Nat Prod Res. 30:2648–2654.10.1080/14786419.2016.1138299
- Ohishi T, Zhang L, Nishiura M, Hou Z. 2011. Carboxylation of alkylboranes by N-heterocyclic carbene copper catalysts: synthesis of carboxylic acids from terminal alkenes and carbon dioxide. Angew Chem Int Ed. 50:8114–8117.10.1002/anie.v50.35
- Polatoğlu K, Karakoç ÖC, Gökçe A, Gören N. 2011. Insecticidal activity of Tanacetum chiliophyllum (Fisch. & Mey.) var. monocephalum grierson extracts and a new sesquiterpene lactone. Phytochem Lett. 4:432–435.10.1016/j.phytol.2011.06.005
- Polavarapu PL, Frelek J, Woźnica M. 2011. Determination of the absolute configurations using electronic and vibrational circular dichroism measurements and quantum chemical calculations. Tetrahedron: Asymmetry. 22:1720–1724.10.1016/j.tetasy.2011.09.008
- Wang F, Hua H, Pei Y, Chen D, Jing Y. 2006. Triterpenoids from the resin of Styrax tonkinensis and their antiproliferative and differentiation effects in human leukemia HL-60 cells. J Nat Prod. 69:807–810.10.1021/np050371z
- Wang KB, Di YT, Bao Y, Yuan CM, Chen G, Li DH, Bai J, He HP, Hao XJ, Pei YH, et al. 2014. Peganumine A, a β-carboline dimer with a new octacyclic scaffold from Peganum harmala. Org Lett. 16:4028–4031.10.1021/ol501856v
- Xie L, Li P, Gong Z, Ou Y. 2011. Study on chemical consituents of Illigera aromatica S. Z. Huang et S. L. Mo. Contemp Med. 17:31–32.
- Xue Z, Li S, Wang SJ, Yang YC, He DX, Ran GL, Kong LZ, Shi JG. 2005. Studies on chemical constituents from corn of Cremastra appendiculata. Chin J Chin Mater Med. 30:511–513.
- Yang J, Wang WG, Wu HY, Du X, Li XN, Li Y, Pu JX, Sun HD. 2016. Bioactive enmein-type ent-kaurane diterpenoids from Isodon phyllostachys. J Nat Prod. 79:132–140.10.1021/acs.jnatprod.5b00802
- Yuan T, Zhang C, Qiu C, Xia G, Wang F, Lin B, Li H, Chen L. 2017. Chemical constituents from Curcuma longa L. and their inhibitory effects of nitric oxide production. Nat Prod Res. doi:10.1080/14786419.2017.1354185.