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Journal articles on the topic 'Saururus'

Author: Grafiati

Published: 29 July 2024

Last updated: 30 July 2024

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1

Song, MiKyung, Soon-Young Lee, Minhee Kim, Sangwoug Park, Juyeon Park, Yongbum Kwon, and Dae-Hun Park. "Saururus chinensis-controlled allergic pulmonary disease through NF-κB/COX-2 and PGE2 pathways." PeerJ 8 (September 24, 2020): e10043. http://dx.doi.org/10.7717/peerj.10043.

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Saururus chinensis is a perennial herb found in the northeastern regions of Asia, including Korea, China, and Japan, and is used in traditional medicine. Studies have identified the four major constituents in Saururus chinensis water extract (LHF618®) as miquelianin (11.75 ± 0.092 mg/g), rutin (1.20 ± 0.008 mg/g), quercitrin (2.38 ± 0.389 mg/g), and quercetin (0.068 ± 0.017 mg/g). Saururus chinensis can improve the symptoms of ovalbumin- or fine dust-induced allergic pulmonary disease by suppressing the effects of WBCs and neutrophils in BALF and IgE in the serum. Saururus chinensis dose-dependently recovered morphological changes such as mucous hyper secretion (from 2.7 ± 0.46 to 0.6 ± 0.65), pulmonary epithelial cell hyperplasia (from 2.4 ± 0.55 to 0.7 ± 0.67), and inflammatory cell infiltration (from 2.3 ± 0.45 to 0.6 ± 0.43), and effectively controlled cDNA levels and protein levels of IL-13. It inhibited NF-κB translocation and COX-2 protein synthesis and suppressed the expression of PGE2. Our results show that Saururus chinensis controlled allergic pulmonary disease via the anti-inflammatory pathways, NF-κB/COX-2 and PGE2. Saururus chinensis may be a promising drug candidate against fine dust-induced allergic pulmonary disease.

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2

Schneider, Edward L., and Sherwin Carlquist. "SEM STUDIES ON VESSEL ELEMENTS OF SAURURACEAE." IAWA Journal 22, no. 2 (2001): 183–93. http://dx.doi.org/10.1163/22941932-90000277.

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Vessel elements in Anemopsis have simple perforation plates and alternate (sometimes scalariform) lateral wall pitting; Anemopsis has tracheids with large, densely placed pits. These conditions are in contrast with tracheary element features of Gymnotheca, Houttuynia, and Saururus, in which perforation plates are scalariform (many with notably slender bars) and with scalariform lateral wall pitting. Porose pit membrane remnants, which cannot be seen with light microscopy, are newly reported in Houttuynia and Saururus. These porose pit membranes underline the primitive nature of vessels in Gymnotheca, Houttuynia, and Saururus. The highly specialized vessels of Anemopsis may relate to entry into seasonally dry habitats, whereas Gymnotheca, Houttuynia, and Saururus may have experienced unbroken occupancy of mesic habitats.

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3

Liu, Guangxin, Zefeng Zhao, Meilun Shen, Xue Zhao, Jing Xie, Xirui He, and Cuiqin Li. "A Review of Traditional Uses, Phytochemistry, and Pharmacological Properties of the Genus Saururus." American Journal of Chinese Medicine 48, no. 01 (January 2020): 47–76. http://dx.doi.org/10.1142/s0192415x20500032.

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The genus Saururus, belonging to Saururaceae, contains two species, S. cernuus L. and S. chinensis (Lour) Baill. with common utilization in traditional medicine from Asia to North America for the treatment of edema, beriberi, jaundice, leucorrhea, urinary tract infections, hypertension, hepatitis diseases, and tumors. An extensive review of literature was made on traditional uses, phytochemistry, and ethnopharmacology of Saururus using ethno-botanical books, published articles, and electronic databases. The 147 of chemical constituents have been isolated and identified from S. cernuus and S. chinensis, and lignans, flavonoids, alkaloids, anthraquinones, saponins, and phenols are the major constituents. Various pharmacological investigations in many in vitro and in vivo models have revealed the potential of the genus Saururus with anti-inflammatory, antitumor, anti-oxidant, hepatoprotective, antimelanogenic, lipid-lowering, and bone protective activities, supporting the rationale behind numerous of its traditional uses. Due to the noteworthy pharmacological properties, Saururus can be a better option for new drug discovery. Data regarding many aspects of this plant such as toxicology, pharmacokinetics, quality-control measures, and the clinical value of the active compounds is still limited which call for additional studies.

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4

Miller, Jim Wayne. "Rustlings Above Saururus Hollow." Appalachian Heritage 13, no. 1-2 (1985): 115–16. http://dx.doi.org/10.1353/aph.1985.0015.

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5

Wang, Lishu, Xuefeng Zhou, Tunhai Xu, Xianwen Yang, and Yonghong Liu. "Lignans from Saururus chinensis." Chemistry of Natural Compounds 46, no. 3 (July 2010): 450–51. http://dx.doi.org/10.1007/s10600-010-9640-3.

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6

Liu, Yonghong, Lishu Wang, Daqing Zhao, and Dongyan Cheng. "ent-Sauchinone from Saururus chinensis." HETEROCYCLES 75, no. 5 (2008): 1241. http://dx.doi.org/10.3987/com-07-11316.

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7

Gao, Xiu, Juan He, Xing-De Wu, Li-Yan Peng, Liao-Bin Dong, Xu Deng, Yan Li, Xiao Cheng, and Qin-Shi Zhao. "Further Lignans from Saururus chinensis." Planta Medica 79, no. 18 (December 19, 2013): 1720–23. http://dx.doi.org/10.1055/s-0033-1351053.

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8

Grímsson, Friðgeir, Guido W. Grimm, and Reinhard Zetter. "Tiny pollen grains: first evidence of Saururaceae from the Late Cretaceous of western North America." PeerJ 5 (June 13, 2017): e3434. http://dx.doi.org/10.7717/peerj.3434.

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Background The Saururaceae, a very small family of Piperales comprising only six species in four genera, have a relatively scanty fossil record outside of Europe. The phylogenetic relationships of the four genera to each other are resolved, with the type genus Saururus occurring in both eastern North America and East Asia. No extant species occurs in western Eurasia. The most exceptional find so far has been an inflorescence with in-situ pollen, Saururus tuckerae S.Y.Sm. & Stockey from Eocene of North America with strong affinities to extant species of Saururus. Recent dated trees suggest, however, an Eocene or younger crown age for the family. Methods Dispersed fossil pollen grains from the Campanian (82–81 Ma) of North America are compared to dispersed pollen grains from the Eocene strata containing S. tuckerae, the Miocene of Europe, and extant members of the family using combined LM and SEM imaging. Results The unambiguous fossil record of the Saururaceae is pushed back into the Campanian (82–81 Ma). Comparison with re-investigated pollen from the Eocene of North America, the Miocene of Europe, and modern species of the family shows that pollen morphology in Saururaceae is highly conservative, and remained largely unchanged for the last 80 million years. Discussion Campanian pollen of Saururaceae precludes young (Eocene or younger) estimates for the Saururaceae root and crown age, but is in-line with maximum age scenarios. Saururus-type pollen appear to represent the primitive pollen morphology of the family. Often overlooked because of its small size, dispersed Saururaceae pollen may provide a unique opportunity to map the geographic history of a small but old group of Piperales, and should be searched for in Paleogene and Cretaceous sediment samples.

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9

Carlquist, Sherwin, Karen Dauer, and Stefanie Y. Nishimura. "Wood and Stem Anatomy of Saururaceae with Reference to Ecology, Phylogeny, and Origin of the Monocotyledons." IAWA Journal 16, no. 2 (1995): 133–50. http://dx.doi.org/10.1163/22941932-90001400.

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Stern and rhizome anatomy is reported for Anemopsis californica Hook., Houttuynia cordata Thunb., and Saururus cernuus L. Secondary growth is reported for the first time in Saururaceae. Cambia function indefinitely in Anemopsis in both fascicular and interfascicular areas. Interfascicular cambium is minimal in Saururus and absent in Houttuynia; fascicular cambium is present in both genera and produces a finite quantity of vessels, fiber-tracheids, and axial parenchyma but no rays. Anemopsis has vessels with simple perforation plates plus tracheids in wood, suggestive of adaptation to fluctuating water availability. The scalariform perforation plates of Houttuynia and Saururus suggest an unbroken history of occupancy of mesic habitats. Ethereal oil cells are reported for rays of Anemopsis, and for pith and cortex of the three genera studied. Stern idioblasts and other histologieal details are ineluded along with wood data in anatomical deseriptions of sterns. DNA data as weIl as maeromorphologie al data implicate Saururaeeae, along with Aristolochiaceae, Lactoridaceae, and Piperaceae as paleoherbs elose to the origin of monoeotyledons. Key wood features that unite these families are cited. Chloranthaeeae, whieh share stern endodermis and sealariform perforation plates with Saururaeeae, are also considered elose. Features of Saururaceae that are analyzed with respeet to monoeotyledon origin inelude loss of interfaseieular cambium, minimization of faseieular cambium, lack of imperforate traeheary elements in monocotyledon bundles, trimery, the sympodial habit, and production of adventitious roots.

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10

Wang, Eie-Ching, Ming-Huei Shih, Mon-Chun Liu, Ming-Tyan Chen, and Gene-Hsiang Lee. "Studies of Constituents of Saururus chinensis." HETEROCYCLES 43, no. 5 (1996): 969. http://dx.doi.org/10.3987/com-95-7370.

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11

Park, Shin-Young, Sung Lee, Woo Choi, Eun Koh, Jee Seo, Shi Ryu, Young Kim, Dae Kwon, and Woo Koh. "Immunosuppressive Lignans Isolated from Saururus chinensis." Planta Medica 73, no. 7 (June 2007): 674–78. http://dx.doi.org/10.1055/s-2007-981525.

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12

Li, Cuibai, Ningxin Li, Jiarui Yue, Qishi Song, and Qingfei Fan. "Two new lignans from Saururus chinensis." Natural Product Research 31, no. 14 (February 6, 2017): 1598–603. http://dx.doi.org/10.1080/14786419.2017.1286483.

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13

Liu, Jianbin, Lishu Wang, Daqing Zhao, Dongyan Cheng, Tunhai Xu, Xuefeng Zhou, Xianwen Yang, and Yonghong Liu. "A new lignan from Saururus chinensis." Chemistry of Natural Compounds 46, no. 4 (August 28, 2010): 631–33. http://dx.doi.org/10.1007/s10600-010-9695-1.

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14

Bennett, D. J. "Propagation Protocol for Lizard's Tail (Saururus cernuus)." Native Plants Journal 2, no. 1 (March 1, 2001): 44–45. http://dx.doi.org/10.3368/npj.2.1.44.

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15

Vallejo, M. G., M. G. Ortega, J. L. Cabrera, V. P. Carlini, S. Rubiales de Barioglio, and A. M. Agnese. "Huperzia saururus increases memory retention in rats." Journal of Ethnopharmacology 111, no. 3 (May 2007): 685–87. http://dx.doi.org/10.1016/j.jep.2007.01.012.

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16

Sung, Sang Hyun. "A new dineolignan from Saururus chinensis root." Fitoterapia 77, no. 6 (September 2006): 487–88. http://dx.doi.org/10.1016/j.fitote.2006.05.021.

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17

Kang, Chang-Soo, Min-Joo Lee, Cheol-Bem Park, and In-Seok Bang. "Study on the Antioxidative and Physiological Activities of Saururus chinensis Extract." Journal of Life Science 22, no. 6 (June 30, 2012): 807–14. http://dx.doi.org/10.5352/jls.2012.22.6.807.

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18

Chin, Young-Won, Xing-Fu Cai, Kyung-Seop Ahn, Hyeong-Kyu Lee, and Sei-Ryang Oh. "Cytotoxic Sesquilignans from the Roots of Saururus chinensis." Bulletin of the Korean Chemical Society 31, no. 7 (July 20, 2010): 2088–90. http://dx.doi.org/10.5012/bkcs.2010.31.7.2088.

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19

Ortega, Marı́a Gabriela, Alicia Mariel Agnese, and José Luis Cabrera. "Sauroine—a novel Lycopodium alkaloid from Huperzia saururus." Tetrahedron Letters 45, no. 38 (September 2004): 7003–5. http://dx.doi.org/10.1016/j.tetlet.2004.07.149.

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20

Rao, Koppaka V., and N. S. Prakasa Rao. "Chemistry of Saururus cernuus, VI: Three New Neolignans." Journal of Natural Products 53, no. 1 (January 1990): 212–15. http://dx.doi.org/10.1021/np50067a036.

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21

Oh, Kwang-Seok, Yeon Choi, Shi Ryu, Byung Oh, Ho Seo, Gyu Yon, Young Kim, and Byung Lee. "Cardiovascular Effects of Lignans Isolated from Saururus chinensis." Planta Medica 74, no. 3 (February 2008): 233–38. http://dx.doi.org/10.1055/s-2008-1034310.

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22

SUNG, Sang Hyun, Myoung Sook HUH, and Young Choong KIM. "New Tetrahydrofuran-Type Sesquilignans of Saururus chinensis Root." CHEMICAL & PHARMACEUTICAL BULLETIN 49, no. 9 (2001): 1192–94. http://dx.doi.org/10.1248/cpb.49.1192.

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23

Yoo, Sae-Rom, Hyekyung Ha, Hyeun-Kyoo Shin, and Chang-Seob Seo. "Anti-Inflamatory Activity of Neolignan Compound Isolated from the Roots of Saururus chinensis." Plants 9, no. 8 (July 23, 2020): 932. http://dx.doi.org/10.3390/plants9080932.

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Saururus chinensis (Lour.) Baill. is a perennial herb and grows in Korea, China, and Japan. Interestingly, (7S,8S)-Δ8′-3,4-methylenedioxy-3′,5,5′-trimethoxy-7-monoacetate-8.O.4′-neolignan (MTMN), one of the active neolignans, was first isolated from the roots of Saururus chinensis. The compound was screened for anti-inflammatory activity using a RAW264.7 murine macrophage cell line. The dried roots of S. chinensis (9.7 kg) were extracted with 70% methanol and then solvent fractionation. From the ethyl acetate fraction, MTMN was purified through silica gel column and reverse-phase column chromatography and its structure was identified by spectroscopic analysis with nuclear magnetic resonance, circular dichroism, and mass spectrometry. RAW264.7 cells were induced using lipopolysaccharide (LPS) and treated with or without MTMN. Production of nitric oxide (NO) and prostaglandin E2 (PGE2) levels were measured and protein expressions of nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2) were analyzed by immunoblotting. The isolated neolignan was (7S,8S)-Δ8′-3,4-methylenedioxy-3′,5,5′-trimethoxy-7-monoacetate-8.O.4′-neolignan. This compound suppressed the LPS-induced iNOS and COX-2 protein expressions, which led to a decrease in the production of NO and PGE2 levels. Further studies, including in animal models, will be required to establish the precise pharmacological effect of MTMN.

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24

Kubanek, Julia, William Fenical, Mark E. Hay, Pam J. Brown, and Niels Lindquist. "Two antifeedant lignans from the freshwater macrophyte Saururus cernuus." Phytochemistry 54, no. 3 (June 2000): 281–87. http://dx.doi.org/10.1016/s0031-9422(00)00076-5.

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25

Ortega, M. G., A. M. Agnese, and J. L. Cabrera. "Anticholinesterase activity in an alkaloid extract of Huperzia saururus." Phytomedicine 11, no. 6 (September 2004): 539–43. http://dx.doi.org/10.1016/j.phymed.2003.07.006.

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26

Ortega, M. G., M. G. Vallejo, J. L. Cabrera, M. F. Pérez, R. S. Almirón, O. A. Ramírez, and A. M. Agnese. "Huperzia saururus, activity on synaptic transmission in the hippocampus." Journal of Ethnopharmacology 104, no. 3 (April 2006): 374–78. http://dx.doi.org/10.1016/j.jep.2005.11.002.

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27

Zhuang, Tao, Jing-Yu Liang, Jian-Bo Sun, Yi Wu, Li-Ru Huang, and Wei Qu. "Secondary metabolites from Saururus chinensis and their chemotaxonomic significance." Biochemical Systematics and Ecology 56 (October 2014): 95–98. http://dx.doi.org/10.1016/j.bse.2014.04.002.

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28

Kubanek, Julia, Mark E. Hay, Pam J. Brown, Niels Lindquist, and William Fenical. "Lignoid chemical defenses in the freshwater macrophyte Saururus cernuus." Chemoecology 11, no. 1 (March 2001): 1–8. http://dx.doi.org/10.1007/pl00001826.

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29

Sung, Mi Jeong, Munkhtugs Davaatseren, Haeng Jeon Hur, Hyun Jin Kim, Shi-Yong Ryu, Yeon Hee Choi, Mi Ran Cha, and Dae Young Kwon. "Antiosteoporotic Activity of Saururus chinensis Extract in Ovariectomized Rats." Phytotherapy Research 26, no. 8 (January 4, 2012): 1182–88. http://dx.doi.org/10.1002/ptr.3714.

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30

Lim, Chae-Jin, To Dao Cuong, Tran Manh Hung, Sung-Woo Ryoo, Jeong-Hyung Lee, Eun-Hee Kim, Mi-Hee Woo, Jae-Sue Choi, and Byung-Sun Min. "Arginase II Inhibitory Activity of Phenolic Compounds from Saururus chinensis." Bulletin of the Korean Chemical Society 33, no. 9 (September 20, 2012): 3079–82. http://dx.doi.org/10.5012/bkcs.2012.33.9.3079.

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31

THIEN, LEONARD B., ERIK G. ELLGAARD, MARGARET S. DEVALL, SARA E. ELLGAARD, and PAUL F. RAMP. "Population Structure and Reproductive Biology of Saururus cernuus L. (Saururaceae)." Plant Species Biology 9, no. 1 (April 1994): 47–55. http://dx.doi.org/10.1111/j.1442-1984.1994.tb00082.x.

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32

Hwang, Bang Yeon, Jeong-Hyung Lee, Jeong Bum Nam, Young-Soo Hong, and Jung Joon Lee. "Lignans from Saururus chinensis inhibiting the transcription factor NF-κB." Phytochemistry 64, no. 3 (October 2003): 765–71. http://dx.doi.org/10.1016/s0031-9422(03)00391-1.

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33

Lee, Eunkyung, Kyungmi Haa, Ju Min Yook, Mei Hua Jin, Chang Seob Seo, Kun Ho Son, Hyun Pyo Kim, et al. "Anti-asthmatic Activity of an Ethanol Extract from Saururus chinensis." Biological & Pharmaceutical Bulletin 29, no. 2 (2006): 211–15. http://dx.doi.org/10.1248/bpb.29.211.

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34

Quan, Zhejiu, Youn Ju Lee, Ju Hye Yang, Yue Lu, Ying Li, Yeun-Kyung Lee, Meihua Jin, et al. "Ethanol extracts of Saururus chinensis suppress ovalbumin-sensitization airway inflammation." Journal of Ethnopharmacology 132, no. 1 (October 2010): 143–49. http://dx.doi.org/10.1016/j.jep.2010.08.002.

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35

Qu, Wei, Jiao Xue, Fei Hua Wu, and Jing Yu Liang. "Lignans from Saururus chinensis with Antiplatelet Aggregation and Neuroprotective Activities." Chemistry of Natural Compounds 50, no. 5 (October 30, 2014): 814–18. http://dx.doi.org/10.1007/s10600-014-1090-x.

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36

Rao, Koppaka V., and G. C. S. Reddy. "Chemistry of Saururus cernuus, V. Sauristolactam and Other Nitrogenous Constituents." Journal of Natural Products 53, no. 2 (March 1990): 309–12. http://dx.doi.org/10.1021/np50068a006.

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37

Kang, T. H., H. Cho, H. Oh, D. H. Sohn, and Y. C. Kim. "Flavonol glycosides with free radical-scavenging activity of Saururus chinensis." Fitoterapia 76, no. 1 (January 2005): 115–17. http://dx.doi.org/10.1016/j.fitote.2004.10.011.

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38

Sung, Sang Hyun, Myoung Sook Huh, and Young Choong Kim. "ChemInform Abstract: New Tetrahydrofuran-Type Sesquilignans of Saururus chinensis Root." ChemInform 33, no. 6 (May 22, 2010): no. http://dx.doi.org/10.1002/chin.200206260.

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39

Chin, Young-Won, Xing-Fu Cai, Kyung-Seop Ahn, Hyeong-Kyu Lee, and Sei-Ryang Oh. "ChemInform Abstract: Cytotoxic Sesquilignans from the Roots of Saururus chinensis." ChemInform 41, no. 48 (November 4, 2010): no. http://dx.doi.org/10.1002/chin.201048218.

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40

Zhao, Yin-He, Xue-Mei Zhang, and De-Zhu Li. "Development of the petaloid bracts of a paleoherb species, Saururus chinensis." PLOS ONE 16, no. 9 (September 2, 2021): e0255679. http://dx.doi.org/10.1371/journal.pone.0255679.

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Saururus chinensis is a core member of Saururaceae, an ancient, perianthless (lacking petals or sepals) family of the magnoliids in the Mesangiospermae, which is important for understanding the origin and evolution of early flowers due to its unusual floral composition and petaloid bracts. To compare their transcriptomes, RNA-seq abundance analysis identified 43,463 genes that were found to be differentially expressed in S. chinensis bracts. Of these, 5,797 showed significant differential expression, of which 1,770 were up-regulated and 4,027 down-regulated in green compared to white bracts. The expression profiles were also compared using cDNA microarrays, which identified 166 additional differentially expressed genes. Subsequently, qRT-PCR was used to verify and extend the cDNA microarray results, showing that the A and B class MADS-box genes were up-regulated in the white bracts. Phylogenetic analysis was performed on putative S. chinensis A and B-class of MADS-box genes to infer evolutionary relationships within the A and B-class of MADS-box gene family. In addition, nature selection and protein interactions of B class MADS-box proteins were inferred that B-class genes free from evolutionary pressures. The results indicate that petaloid bracts display anatomical and gene expression features normally associated with petals, as found in petaloid bracts of other species, and support an evolutionarily conserved developmental program for petaloid bracts.

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41

Lee, Ju-Hyun, Yeong-Ho Choe, Yoon-Jin Park, Xiao-Wan Zhang, and Byeong-Soo Kim. "Antimicrobial and antiviral activity of Saururus chinensis extract by n-Hexane." Korean Journal of Veterinary Service 36, no. 2 (June 30, 2013): 87–93. http://dx.doi.org/10.7853/kjvs.2013.36.2.87.

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42

Lee, You Jin, Jinhee Kim, Jin-Mu Yi, Se-Mi Oh, No Soo Kim, Haejin Kim, Dal-Seok Oh, Ok-Sun Bang, and Jun Lee. "Anti-proliferative Neolignans from Saururus chinensis against Human Cancer Cell Lines." Biological and Pharmaceutical Bulletin 35, no. 8 (2012): 1361–66. http://dx.doi.org/10.1248/bpb.b110670.

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43

Chattopadhyay, Sunil K., and Koppaka V. Rao. "Chemistry of saururus cernuus IV: cyclooctadiene systems derived from austrobailignan-5." Tetrahedron 43, no. 4 (1987): 669–78. http://dx.doi.org/10.1016/s0040-4020(01)90001-8.

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44

Birri, Marcela, Mariana Vallejo, Miguel Carro-Juárez, and A. Mariel Agnese. "Aphrodisiac activity of Phlegmariurus saururus in copulating and noncopulating male rats." Phytomedicine 24 (January 2017): 104–10. http://dx.doi.org/10.1016/j.phymed.2016.11.020.

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45

Jin, Qinghao, Jin Woo Lee, Jun Gu Kim, Dongho Lee, Jin Tae Hong, Youngsoo Kim, Mi Kyeong Lee, and Bang Yeon Hwang. "Lignans from Saururus chinensis with Inhibitory Effects on Nitric Oxide Production." Journal of Natural Products 82, no. 11 (October 23, 2019): 3002–9. http://dx.doi.org/10.1021/acs.jnatprod.9b00520.

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46

Vallejo, Mariana G., Maria Gabriela Ortega, José L. Cabrera, and Alicia Mariel Agnese. "N-Demethyl-sauroxine, a novel Lycodine Group alkaloid from Huperzia saururus." Tetrahedron Letters 54, no. 38 (September 2013): 5197–200. http://dx.doi.org/10.1016/j.tetlet.2013.07.068.

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47

Hwang, Dong Ryeol, Jin Boo Jeong, Hyun Ji Eo, Se Chul Hong, Ji Hyun Yoo, Kun Hee Lee, Bo Ram Kim, and Jin Suk Koo. "The effect of Saururus chinensis Baill against oxidative damage and inflammation." Korea Journal of Herbology 27, no. 6 (November 30, 2012): 1–6. http://dx.doi.org/10.6116/kjh.2012.27.6.1.

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48

Jin, Lei, Jin Yang, Changkun Liu, Mengling He, and Hanjing Yan. "Characterization of the complete plastome of medicinal plant Saururus chinensis (Saururaceae)." Mitochondrial DNA Part B 4, no. 2 (July 3, 2019): 3206–7. http://dx.doi.org/10.1080/23802359.2019.1667909.

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49

Qu, Wei, and Jing Yu Liang. "Two isomeric compounds of C13-norisoprenoids from Saururus chinensis (Lour.) Baill." Chinese Chemical Letters 20, no. 11 (November 2009): 1342–44. http://dx.doi.org/10.1016/j.cclet.2009.05.023.

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Li, Na, Zhen-Dong Tuo, Shi-Zhou Qi, Shan-Shan Xing, Hyun-Sun Lee, Jian-Guang Chen, and Long Cui. "Two new lignans from Saururus chinensis and their DGAT inhibitory activity." Fitoterapia 101 (March 2015): 46–50. http://dx.doi.org/10.1016/j.fitote.2014.12.011.

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