Pinoresinol (BioDeep_00000000431)

 

Secondary id: BioDeep_00000017492, BioDeep_00000178742, BioDeep_00000398760

PANOMIX_OTCML-2023 Marine Natural Products natural product


代谢物信息卡片


PHENOL, 4,4-(TETRAHYDRO-1H,3H-FURO(3,4-C)FURAN-1,4-DIYL)BIS(2-METHOXY-, (1S-(1.ALPHA.,3A.ALPHA.,4.BETA.,6A.ALPHA.))-

化学式: C20H22O6 (358.1416)
中文名称: (+)-表松脂素, 表松脂酚, (+)-松脂酚, 松脂醇, 松脂素, (+)-表松脂酚
谱图信息: 最多检出来源 Viridiplantae(plant) 21.24%

分子结构信息

SMILES: COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O
InChI: InChI=1S/C20H22O6/c1-23-17-7-11(3-5-15(17)21)19-13-9-26-20(14(13)10-25-19)12-4-6-16(22)18(8-12)24-2/h3-8,13-14,19-22H,9-10H2,1-2H3/t13-,14-,19+,20+/m0/s1

描述信息

Epipinoresinol is an enantiomer of pinoresinol having (+)-(1R,3aR,4S,6aR)-configuration. It has a role as a plant metabolite and a marine metabolite.
Epipinoresinol is a natural product found in Pandanus utilis, Abeliophyllum distichum, and other organisms with data available.
An enantiomer of pinoresinol having (+)-(1R,3aR,4S,6aR)-configuration.
(+)-pinoresinol is an enantiomer of pinoresinol having (+)-1S,3aR,4S,6aR-configuration. It has a role as a hypoglycemic agent, a plant metabolite and a phytoestrogen.
Pinoresinol is a natural product found in Pandanus utilis, Zanthoxylum beecheyanum, and other organisms with data available.
See also: Acai fruit pulp (part of).
An enantiomer of pinoresinol having (+)-1S,3aR,4S,6aR-configuration.
relative retention time with respect to 9-anthracene Carboxylic Acid is 0.907
relative retention time with respect to 9-anthracene Carboxylic Acid is 0.905
relative retention time with respect to 9-anthracene Carboxylic Acid is 0.897
relative retention time with respect to 9-anthracene Carboxylic Acid is 0.895
Pinoresinol is a lignol of plant origin serving for defense in a caterpillar. Pinoresinol drastically sensitizes cancer cells against TNF-related apoptosis-inducing ligand (TRAIL) -induced apoptosis[1][2].
Pinoresinol is a lignol of plant origin serving for defense in a caterpillar. Pinoresinol drastically sensitizes cancer cells against TNF-related apoptosis-inducing ligand (TRAIL) -induced apoptosis[1][2].

同义名列表

46 个代谢物同义名

PHENOL, 4,4-(TETRAHYDRO-1H,3H-FURO(3,4-C)FURAN-1,4-DIYL)BIS(2-METHOXY-, (1S-(1.ALPHA.,3A.ALPHA.,4.BETA.,6A.ALPHA.))-; 4-[(3R,3aR,6S,6aR)-6-(4-hydroxy-3-methoxy-phenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxy-phenol; 4-[(3R,3aR,6S,6aR)-6-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxyphenol; PHENOL, 4,4-(3A.BETA.,4,6,6A.BETA.-TETRAHYDRO-1H,3H-FURO(3,4-C)FURAN-1.ALPHA.,4.BETA.-DIYL)BIS(2-METHOXY-; PHENOL, 4,4-((1R,3AR,4S,6AR)-TETRAHYDRO-1H,3H-FURO(3,4-C)FURAN-1,4-DIYL)BIS(2-METHOXY-; 4,4-((1R,3AR,4S,6AR)-TETRAHYDRO-1H,3H-FURO(3,4-C)FURAN-1,4-DIYL)BIS(2-METHOXYPHENOL); 4,4-(1R,3aR,4S,6aR)-tetrahydro-1H,3H-furo[3,4-c]furan-1,4-diylbis(2-methoxyphenol); HGXBRUKMWQGOIE-WZBLMQSHSA-N; (+)-epi-pinoresinol; (+)-Epipinoresinol; UNII-6YKG9JJC1S; epi-pinoresinol; Epipinoresinol; pino-resinol; Pinoresinol; 6YKG9JJC1S; PHENOL, 4,4-(TETRAHYDRO-1H,3H-FURO(3,4-C)FURAN-1,4-DIYLBIS(2-METHOXY-, (1S-(1.ALPHA.,3A.ALPHA.,4.ALPHA.,6A.ALPHA.))-; 4-[(3S,3aR,6S,6aR)-6-(3-methoxy-4-oxidanyl-phenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxy-phenol; 4-[(3S,3aR,6S,6aR)-6-(4-hydroxy-3-methoxy-phenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxy-phenol; Phenol, 4,4-(tetrahydro-1H,3H-furo(3,4-c)furan-1,4-diylbis(2-methoxy-, (1S-(1alpha,3aalpha,4alpha,6aalpha))-; Phenol, 4,4-[(1S,3aR,4R,6aS)-tetrahydro-1H,3H-furo[3,4-c]furan-1,4-diyl]bis[2-methoxy-; PHENOL, 4,4-((1S,3AR,4S,6AR)-TETRAHYDRO-1H,3H-FURO(3,4-C)FURAN-1,4-DIYL)BIS(2-METHOXY-; Phenol,4,4-[(1S,3aR,4R,6aS)-tetrahydro-1H,3H-furo[3,4-c]furan-1,4-diyl]bis[2-methoxy-; 4,4-(1s,3ar,4s,6ar)-tetrahydro-1h,3h-furo[3,4-c]furan-1,4-diylbis(2-methoxyphenol); 4,4-((1S,3aR,4S,6aR)-Hexahydrofuro[3,4-c]furan-1,4-diyl)bis(2-methoxyphenol); (7alpha,7alpha,8alpha,8alpha)-3,3-dimethoxy-7,9:7,9-diepoxylignane-4,4-diol; Pinoresinol, analytical reference material; ( inverted exclamation markA)-Pinoresinol; Pinoresinol, >=95.0\\% (HPLC); Pinoresinol, >=95\\% (HPLC); PINORESINOL, (+)-; UNII-V4N1UDY811; (+)-Pinoresinol; D-PINORESINOL; MEGxp0_000829; ACon1_001809; V4N1UDY811; CHEBI:40; 4-[(1S,3aR,4S,6aR)-4-(4-hydroxy-3-methoxy-phenyl)-1,3,3a,4,6,6a-hexahydrofuro[4,3-c]furan-1-yl]-2-methoxy-phenol; 4-[(1S,3aR,4S,6aR)-4-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[4,3-c]furan-1-yl]-2-methoxyphenol; AIDS-012018; AIDS012018; NSC 35444; 487-36-5; C10872; (+)-Pinoresinol



数据库引用编号

48 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

BioCyc(3)

PlantCyc(2)

代谢反应

254 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(6)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(248)

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

1124 个相关的物种来源信息

在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有：

  • PubMed: 来源于PubMed文献库中的文献信息，我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表，这个列表按照代谢物同时出现的文献数量降序排序，取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
  • NCBI Taxonomy: 通过文献数据挖掘，得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序，取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
  • Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
  • Chemical Reaction: 在化学反应过程中，存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。

点击图上的相关代谢物的名称，可以跳转到相关代谢物的信息页面。

亚细胞结构定位 关联基因列表
Cytoplasm 9 ABCB1, AKR1B1, EGFR, FASN, MAPK14, MTOR, PPARG, PTGS2, RUNX2
Peripheral membrane protein 4 ACHE, CYP1B1, MTOR, PTGS2
Endosome membrane 1 EGFR
Endoplasmic reticulum membrane 4 CYP1B1, EGFR, MTOR, PTGS2
Nucleus 7 ACHE, EGFR, GABPA, MAPK14, MTOR, PPARG, RUNX2
cytosol 6 AKR1B1, FASN, MAPK14, MTOR, PPARG, RUNX2
dendrite 1 MTOR
phagocytic vesicle 1 MTOR
nucleoplasm 6 AKR1B1, GABPA, MAPK14, MTOR, PPARG, RUNX2
RNA polymerase II transcription regulator complex 1 PPARG
Cell membrane 5 ABCB1, ACHE, EGFR, MGAM, TNF
Cytoplasmic side 1 MTOR
ruffle membrane 1 EGFR
Early endosome membrane 1 EGFR
Multi-pass membrane protein 1 ABCB1
Golgi apparatus membrane 1 MTOR
Synapse 1 ACHE
cell junction 1 EGFR
cell surface 5 ABCB1, ACHE, BMP2, EGFR, TNF
glutamatergic synapse 2 EGFR, MAPK14
Golgi apparatus 2 ACHE, FASN
Golgi membrane 3 EGFR, INS, MTOR
lysosomal membrane 1 MTOR
neuromuscular junction 1 ACHE
neuronal cell body 1 TNF
Lysosome 2 MTOR, SGSH
endosome 1 EGFR
plasma membrane 7 ABCB1, ACHE, BMP2, EGFR, FASN, MGAM, TNF
Membrane 7 ABCB1, ACHE, CYP1B1, EGFR, FASN, MGAM, MTOR
apical plasma membrane 3 ABCB1, EGFR, MGAM
basolateral plasma membrane 1 EGFR
caveola 1 PTGS2
extracellular exosome 5 ABCB1, AKR1B1, FASN, MGAM, SGSH
Lysosome membrane 1 MTOR
endoplasmic reticulum 1 PTGS2
extracellular space 9 ACHE, AKR1B1, BMP2, CCL2, CXCL8, EGFR, IL6, INS, TNF
lysosomal lumen 1 SGSH
perinuclear region of cytoplasm 3 ACHE, EGFR, PPARG
mitochondrion 3 AKR1B1, CYP1B1, MAPK14
protein-containing complex 2 EGFR, PTGS2
intracellular membrane-bounded organelle 3 BMP2, CYP1B1, PPARG
Microsome membrane 3 CYP1B1, MTOR, PTGS2
TORC1 complex 1 MTOR
TORC2 complex 1 MTOR
Single-pass type I membrane protein 1 EGFR
Secreted 7 ACHE, BMP2, CCL2, CXCL8, IL6, INS, MGAM
extracellular region 9 ACHE, BMP2, CCL2, CXCL8, IL6, INS, MAPK14, MGAM, TNF
Mitochondrion outer membrane 1 MTOR
Single-pass membrane protein 1 MGAM
mitochondrial outer membrane 1 MTOR
Extracellular side 1 ACHE
transcription regulator complex 1 RUNX2
nuclear membrane 1 EGFR
external side of plasma membrane 1 TNF
recycling endosome 1 TNF
Single-pass type II membrane protein 1 TNF
Apical cell membrane 1 ABCB1
Membrane raft 2 EGFR, TNF
focal adhesion 1 EGFR
basement membrane 1 ACHE
intracellular vesicle 1 EGFR
Nucleus, PML body 1 MTOR
PML body 1 MTOR
nuclear speck 1 MAPK14
Nucleus inner membrane 1 PTGS2
Nucleus outer membrane 1 PTGS2
nuclear inner membrane 1 PTGS2
nuclear outer membrane 1 PTGS2
receptor complex 2 EGFR, PPARG
neuron projection 1 PTGS2
chromatin 3 GABPA, PPARG, RUNX2
phagocytic cup 1 TNF
spindle pole 1 MAPK14
Lipid-anchor, GPI-anchor 1 ACHE
nuclear envelope 1 MTOR
Endomembrane system 1 MTOR
endosome lumen 1 INS
tertiary granule membrane 1 MGAM
Melanosome 1 FASN
side of membrane 1 ACHE
basal plasma membrane 1 EGFR
synaptic membrane 1 EGFR
ficolin-1-rich granule lumen 1 MAPK14
secretory granule lumen 2 INS, MAPK14
Golgi lumen 1 INS
endoplasmic reticulum lumen 3 IL6, INS, PTGS2
transport vesicle 1 INS
Endoplasmic reticulum-Golgi intermediate compartment membrane 1 INS
clathrin-coated endocytic vesicle membrane 1 EGFR
synaptic cleft 1 ACHE
ficolin-1-rich granule membrane 1 MGAM
external side of apical plasma membrane 1 ABCB1
Cytoplasmic vesicle, phagosome 1 MTOR
multivesicular body, internal vesicle lumen 1 EGFR
Shc-EGFR complex 1 EGFR
[Tumor necrosis factor, soluble form]: Secreted 1 TNF
interleukin-6 receptor complex 1 IL6
BMP receptor complex 1 BMP2
[Isoform H]: Cell membrane 1 ACHE
glycogen granule 1 FASN
[C-domain 2]: Secreted 1 TNF
[Tumor necrosis factor, membrane form]: Membrane 1 TNF
[C-domain 1]: Secreted 1 TNF


文献列表

  • Jingxian Feng, Yuan Yao, Yuqi Qiao, Xueqi Ma, Zongtai Wu, Yonghao Duan, Peng Di, Wansheng Chen, Ying Xiao. Effect of pinoresinol-lariciresinol reductases on biosynthesis of lignans with substrate selectivity in Schisandra chinensis. Phytochemistry. 2024 May; 221(?):114053. doi: 10.1016/j.phytochem.2024.114053. [PMID: 38479587]
  • Mona Soltani, Reza Fotovat, Mohsen Sharifi, Najmeh Ahmadian Chashmi, Mehrdad Behmanesh. In Vitro Comparative Study on Antineoplastic Effects of Pinoresinol and Lariciresinol on Healthy Cells and Breast Cancer-Derived Human Cells. Iranian journal of medical sciences. 2024 Jan; 49(1):30-39. doi: 10.30476/ijms.2023.94805.2611. [PMID: 38322161]
  • Mareia Ahmed-M Elgaleidh, Hafize Dilek Tepe, Fatma Doyuk, Talip Çeter, İdris Yazgan. Identification of Marker Molecules in Aqueous Plant Extracts Affecting the Gold Nanostructures' Morphology and Size. Chemistry & biodiversity. 2023 Dec; ?(?):e202301349. doi: 10.1002/cbdv.202301349. [PMID: 38108659]
  • Fabiola Muro-Villanueva, Leonard D Pysh, Hoon Kim, Tyler Bouse, John Ralph, Zhiwei Luo, Bruce R Cooper, Amber S Jannasch, Zeyu Zhang, Chong Gu, Clint Chapple. Pinoresinol rescues developmental phenotypes of Arabidopsis phenylpropanoid mutants overexpressing FERULATE 5-HYDROXYLASE. Proceedings of the National Academy of Sciences of the United States of America. 2023 08; 120(31):e2216543120. doi: 10.1073/pnas.2216543120. [PMID: 37487096]
  • Meng-Ting Li, He-Jia Hu, Yang Jin, Yi Chen, Si-Ying Chen, Yue-Ting Li, Yong Huang, Lin Zheng, Jing Huang, Zi-Peng Gong. [Content determination of seven active components of Eucommiae Cortex in aortic vascular endothelial cells of spontaneously hypertensive rats by UPLC-MS/MS]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 2023 Jul; 48(13):3623-3632. doi: 10.19540/j.cnki.cjcmm.20230224.202. [PMID: 37474995]
  • Yakun Pei, Wenhan Cao, Wenwen Yu, Chaoyang Peng, Wenhao Xu, Yayun Zuo, Wenjun Wu, Zhaonong Hu. Identification and functional characterization of the dirigent gene family in Phryma leptostachya and the contribution of PlDIR1 in lignan biosynthesis. BMC plant biology. 2023 May; 23(1):291. doi: 10.1186/s12870-023-04297-6. [PMID: 37259047]
  • Niamh M O'Boyle, Ida B Niklasson, David J Ponting, Miguel A Ortega, Tina Seifert, Andreas Natsch, Kristina Luthman, Ann-Therese Karlberg. Nature-derived epoxy resins: Synthesis, allergenicity, and thermosetting properties of pinoresinol diglycidyl ether. Toxicology and industrial health. 2022 May; 38(5):259-269. doi: 10.1177/07482337221089595. [PMID: 35465773]
  • Ying Xiao, Kai Shao, Jingwen Zhou, Lian Wang, Xueqi Ma, Di Wu, Yingbo Yang, Junfeng Chen, Jingxian Feng, Shi Qiu, Zongyou Lv, Lei Zhang, Peng Zhang, Wansheng Chen. Structure-based engineering of substrate specificity for pinoresinol-lariciresinol reductases. Nature communications. 2021 05; 12(1):2828. doi: 10.1038/s41467-021-23095-y. [PMID: 33990581]
  • Li Yang, Ronghua Liu, Yiwei Fang, Junwei He. Anti-inflammatory effect of phenylpropanoids from Dendropanax dentiger in TNF-α-induced MH7A cells via inhibition of NF-κB, Akt and JNK signaling pathways. International immunopharmacology. 2021 May; 94(?):107463. doi: 10.1016/j.intimp.2021.107463. [PMID: 33618295]
  • Davide Decembrino, Esther Ricklefs, Stefan Wohlgemuth, Marco Girhard, Katrin Schullehner, Guido Jach, Vlada B Urlacher. Assembly of Plant Enzymes in E. coli for the Production of the Valuable (-)-Podophyllotoxin Precursor (-)-Pluviatolide. ACS synthetic biology. 2020 11; 9(11):3091-3103. doi: 10.1021/acssynbio.0c00354. [PMID: 33095000]
  • Zsuzsanna Hajdú, Peter Forgo, Gergely Király, Gyula Pinke, István Zupkó, Judit Hohmann. Isolation of chemical constituents from Filago vulgaris and antiproliferative activity of the plant extract and its flavonoid against human tumor cell lines. Pakistan journal of pharmaceutical sciences. 2020 Jul; 33(4):1593-1597. doi: . [PMID: 33583792]
  • Madhura Shettigar, Sahil Balotra, Annette Kasprzak, Stephen L Pearce, Michael J Lacey, Matthew C Taylor, Jian-Wei Liu, David Cahill, John G Oakeshott, Gunjan Pandey. Oxidative Catabolism of (+)-Pinoresinol Is Initiated by an Unusual Flavocytochrome Encoded by Translationally Coupled Genes within a Cluster of (+)-Pinoresinol-Coinduced Genes in Pseudomonas sp. Strain SG-MS2. Applied and environmental microbiology. 2020 05; 86(10):. doi: 10.1128/aem.00375-20. [PMID: 32198167]
  • Hejia Hu, Linlin Wu, Mei Li, Cun Xue, Guangcheng Wang, Siying Chen, Yong Huang, Lin Zheng, Aimin Wang, Yueting Li, Zipeng Gong. Comparative absorption kinetics of seven active ingredients of Eucommia ulmoides extracts by intestinal in situ circulatory perfusion in normal and spontaneous hypertensive rats. Biomedical chromatography : BMC. 2020 Jan; 34(1):e4714. doi: 10.1002/bmc.4714. [PMID: 31633806]
  • Sun Young Kim, Joo Young Lee, Changho Jhin, Ji Min Shin, Myungsuk Kim, Hong Ruyl Ahn, Gyhye Yoo, Yang-Ju Son, Sang Hoon Jung, Chu Won Nho. Reduction of Hepatic Lipogenesis by Loliolide and Pinoresinol from Lysimachia vulgaris via Degrading Liver X Receptors. Journal of agricultural and food chemistry. 2019 Nov; 67(45):12419-12427. doi: 10.1021/acs.jafc.9b01488. [PMID: 31610126]
  • Ji-Won Choi, Joon Yeon Shin, Il-Joo Jo, Dong-Gu Kim, Ho-Joon Song, Chi-Su Yoon, Hyuncheol Oh, Youn-Chul Kim, Gi-Sang Bae, Sung-Joo Park. 8α-Hydroxypinoresinol isolated from Nardostachys jatamansi ameliorates cerulein-induced acute pancreatitis through inhibition of NF-κB activation. Molecular immunology. 2019 10; 114(?):620-628. doi: 10.1016/j.molimm.2019.09.002. [PMID: 31542607]
  • So-Ra Lee, Khong Trong Quan, Hee Sun Byun, InWha Park, Kidong Kang, Xuezhe Piao, Eunjin Ju, Hyunju Ro, MinKyun Na, Gang Min Hur. Accelerated degradation of cFLIPL and sensitization of the TRAIL DISC-mediated apoptotic cascade by pinoresinol, a lignan isolated from Rubia philippinensis. Scientific reports. 2019 09; 9(1):13505. doi: 10.1038/s41598-019-49909-0. [PMID: 31534206]
  • Lucija Markulin, Cyrielle Corbin, Sullivan Renouard, Samantha Drouet, Laurent Gutierrez, Ivan Mateljak, Daniel Auguin, Christophe Hano, Elisabeth Fuss, Eric Lainé. Pinoresinol-lariciresinol reductases, key to the lignan synthesis in plants. Planta. 2019 Jun; 249(6):1695-1714. doi: 10.1007/s00425-019-03137-y. [PMID: 30895445]
  • Yingling Wu, Dawei Xing, Guoliang Ma, Xinlong Dai, Liping Gao, Tao Xia. A variable loop involved in the substrate selectivity of pinoresinol/lariciresinol reductase from Camellia sinensis. Phytochemistry. 2019 Jun; 162(?):1-9. doi: 10.1016/j.phytochem.2019.02.003. [PMID: 30844490]
  • Yang Ning, Yue Ling Fu, Qing Hua Zhang, Chun Zhang, Ying Chen. Inhibition of in vitro and in vivo ovarian cancer cell growth by pinoresinol occurs by way of inducing autophagy, inhibition of cell invasion, loss of mitochondrial membrane potential and inhibition Ras/MEK/ERK signalling pathway. Journal of B.U.ON. : official journal of the Balkan Union of Oncology. 2019 Mar; 24(2):709-714. doi: . [PMID: 31128027]
  • Jing Li, Xiaoli Liang, Beixian Zhou, Xiaowei Chen, Peifang Xie, Haiming Jiang, Zhihong Jiang, Zifeng Yang, Xiping Pan. (+)‑pinoresinol‑O‑β‑D‑glucopyranoside from Eucommia ulmoides Oliver and its anti‑inflammatory and antiviral effects against influenza A (H1N1) virus infection. Molecular medicine reports. 2019 01; 19(1):563-572. doi: 10.3892/mmr.2018.9696. [PMID: 30483751]
  • Joséphine Ottavioli, Mathieu Paoli, Joseph Casanova, Félix Tomi, Ange Bighelli. Identification and Quantitative Determination of Resin Acids from Corsican Pinus pinaster Aiton Oleoresin Using 13 C-NMR Spectroscopy. Chemistry & biodiversity. 2019 Jan; 16(1):e1800482. doi: 10.1002/cbdv.201800482. [PMID: 30632681]
  • Nadiah Syafiqah Nor Azman, Md Shahadat Hossan, Veeranoot Nissapatorn, Chairat Uthaipibull, Parichat Prommana, Khoo Teng Jin, Mohammed Rahmatullah, Tooba Mahboob, Chandramathi Samudi Raju, Hassan Mahmood Jindal, Banasri Hazra, Mohd Ridzuan Mohd Abd Razak, Vijay Kumar Prajapati, Rajan Kumar Pandey, Norhaniza Aminudin, Khozirah Shaari, Nor Hadiani Ismail, Mark S Butler, Vladimir V Zarubaev, Christophe Wiart. Anti-infective activities of 11 plants species used in traditional medicine in Malaysia. Experimental parasitology. 2018 Nov; 194(?):67-78. doi: 10.1016/j.exppara.2018.09.020. [PMID: 30268422]
  • Luca Pompermaier, Elke H Heiss, Mostafa Alilou, Fabian Mayr, Mawunu Monizi, Thea Lautenschlaeger, Daniela Schuster, Stefan Schwaiger, Hermann Stuppner. Dihydrochalcone Glucosides from the Subaerial Parts of Thonningia sanguinea and Their in Vitro PTP1B Inhibitory Activities. Journal of natural products. 2018 09; 81(9):2091-2100. doi: 10.1021/acs.jnatprod.8b00450. [PMID: 30207720]
  • Taewoong Rho, Kee Dong Yoon. Application of off-line two-dimensional high-performance countercurrent chromatography on the chloroform-soluble extract of Cuscuta auralis seeds. Journal of separation science. 2018 May; 41(10):2169-2177. doi: 10.1002/jssc.201701498. [PMID: 29450982]
  • Madhura Shettigar, Sahil Balotra, David Cahill, Andrew C Warden, Michael J Lacey, Hans-Peter E Kohler, Daniel Rentsch, John G Oakeshott, Gunjan Pandey. Isolation of the (+)-Pinoresinol-Mineralizing Pseudomonas sp. Strain SG-MS2 and Elucidation of Its Catabolic Pathway. Applied and environmental microbiology. 2018 02; 84(4):. doi: 10.1128/aem.02531-17. [PMID: 29222099]
  • En Gao, Zheng-Qun Zhou, Jian Zou, Yang Yu, Xiao-Lin Feng, Guo-Dong Chen, Rong-Rong He, Xin-Sheng Yao, Hao Gao. Bioactive Asarone-Derived Phenylpropanoids from the Rhizome of Acorus tatarinowii Schott. Journal of natural products. 2017 11; 80(11):2923-2929. doi: 10.1021/acs.jnatprod.7b00457. [PMID: 29116780]
  • Xiaojian Gong, Qingxiang Luan, Xin Zhou, Yang Zhao, Chao Zhao. UHPLC-ESI-MS/MS determination and pharmacokinetics of pinoresinol glucoside and chlorogenic acid in rat plasma after oral administration of Eucommia ulmoides Oliv extract. Biomedical chromatography : BMC. 2017 Nov; 31(11):. doi: 10.1002/bmc.4008. [PMID: 28493441]
  • Yan Song, Lan Pan, Wenjie Li, Yingying Si, Di Zhou, Chengjian Zheng, Xiaofang Hao, Xinyue Jia, Yuemei Jia, Minghui Shi, Xiaoguang Jia, Ning Li, Yue Hou. Natural neuro-inflammatory inhibitors from Caragana turfanensis. Bioorganic & medicinal chemistry letters. 2017 10; 27(20):4765-4769. doi: 10.1016/j.bmcl.2017.08.047. [PMID: 28911817]
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