Parietin (BioDeep_00000000367)

 

Secondary id: BioDeep_00000267309

PANOMIX_OTCML-2023 Marine Natural Products


代谢物信息卡片


1,8-Dihydroxy-3-methoxy-6-methylanthraquinone, Emodin-3-methyl ether

化学式: C16H12O5 (284.0685)
中文名称: 大黄素甲醚
谱图信息: 最多检出来源 Viridiplantae(plant) 8.46%

分子结构信息

SMILES: C12C(O)=CC(C)=CC=1C(=O)C1=C(C(O)=CC(OC)=C1)C2=O
InChI: InChI=1S/C16H12O5/c1-7-3-9-13(11(17)4-7)16(20)14-10(15(9)19)5-8(21-2)6-12(14)18/h3-6,17-18H,1-2H3

描述信息

Physcion is a dihydroxyanthraquinone that is 9,10-anthraquinone bearing hydroxy substituents at positions 1 and 8, a methoxy group at position 3, and a methyl group at position 6. It has been widely isolated and characterised from both terrestrial and marine sources. It has a role as an apoptosis inducer, an antineoplastic agent, a hepatoprotective agent, an anti-inflammatory agent, an antibacterial agent, an antifungal agent and a metabolite. It is functionally related to a 2-methylanthraquinone.
Physcion is a natural product found in Rumex dentatus, Ageratina altissima, and other organisms with data available.
See also: Reynoutria multiflora root (part of); Frangula purshiana Bark (part of).
A dihydroxyanthraquinone that is 9,10-anthraquinone bearing hydroxy substituents at positions 1 and 8, a methoxy group at position 3, and a methyl group at position 6. It has been widely isolated and characterised from both terrestrial and marine sources.
[Raw Data] CBA82_Physcion_pos_10eV.txt
[Raw Data] CBA82_Physcion_pos_30eV.txt
[Raw Data] CBA82_Physcion_pos_50eV.txt
[Raw Data] CBA82_Physcion_pos_40eV.txt
[Raw Data] CBA82_Physcion_pos_20eV.txt

同义名列表

56 个代谢物同义名

1,8-Dihydroxy-3-methoxy-6-methylanthraquinone, Emodin-3-methyl ether; 9,10-Anthracenedione, 1,8-dihydroxy-3-methoxy-6-methyl-; 1,8-dihydroxy-3-methoxy-6-methyl-anthracene-9,10-dione; 1,8-dihydroxy-3-methoxy-6-methylanthracene-9,10-dione; 7-methoxy-2-methyl-4,5-dihydroxyanthracene-9,10-dione; 1,8-Dihydroxy-3-methoxy-6-methyl-9,10-anthracenedione; 1,8-Dihydroxy-3-methoxy-6-methylanthra-9,10-quinone #; 8,9-dihydroxy-3-methyl-6-methoxy-1,10-anthraquinone; 8,9-dihydroxy-6-methyl-3-methoxy-1,10-anthraquinone; 1,8-Dihydroxy-3-methyl-6-methoxy-9,10-anthraquinone; ANTHRAQUINONE, 1,8-DIHYDROXY-3-METHOXY-6-METHYL-; 1,8-Dihydroxy-3-methoxy-6-methyl-anthraquinone; 1,8-Dihydroxy-3-methoxy-6-methylanthraquinone; Anthraquinone,8-dihydroxy-3-methoxy-6-methyl-; 1,8-Dihydroxy-3-methyl-6-methoxyanthraquinone; 1,8-dihydroxy-6-methoxy-3-methylanthraquinone; 1,8-dihydroxy-3-methoxy-6-methylanthracene-; 9, 1,8-dihydroxy-3-methoxy-6-methyl-; CHRYSOPHANIC ACID, 6-METHOXY-; Physcion, analytical standard; FFWOKTFYGVYKIR-UHFFFAOYSA-N; EMODIN 3-METHYL ETHER [MI]; Rheochrysidin (Physcione); Physcion, >=98.0\\% (TLC); Emodin monomethyl ether; Parietin;Rheochrysidin; emodin 3-methyl ether; Emodin-3-methyl ether; Spectrum3_001829; Spectrum4_000909; Spectrum2_000503; 6-O-METHYLEMODIN; Spectrum5_001742; UNII-H6PT94IV61; Emodin-3-methyl; Methoxyemodin; MEGxm0_000018; DivK1c_006567; Rheochrysidin; KBio1_001511; KBio2_004832; KBio2_007400; KBio2_002264; NCI60_002011; KBio3_002981; Physcion,(S); PHYSCIONE-; H6PT94IV61; 9,10-dione; Physcione; fischione; physcion; parietin; Parienin; Physcion; Physcion



数据库引用编号

23 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

BioCyc(0)

PlantCyc(0)

代谢反应

0 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(0)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(0)

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

152 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 13 AKT1, BCL2, CASP3, CASP9, CAT, MAPK14, PRKAA2, PTGS2, RELA, SP1, STAT3, TLR4, TP53
Peripheral membrane protein 2 ACHE, PTGS2
Endosome membrane 1 TLR4
Endoplasmic reticulum membrane 3 BCL2, BSG, PTGS2
Nucleus 12 ACHE, AKT1, BCL2, CASP3, CASP9, DNMT1, MAPK14, PRKAA2, RELA, SP1, STAT3, TP53
cytosol 10 AKT1, BCL2, CASP3, CASP9, CAT, MAPK14, PRKAA2, RELA, STAT3, TP53
dendrite 1 PRKAA2
centrosome 1 TP53
nucleoplasm 9 AKT1, CASP3, DNMT1, MAPK14, PRKAA2, RELA, SP1, STAT3, TP53
RNA polymerase II transcription regulator complex 1 STAT3
Cell membrane 5 ACHE, AKT1, BSG, TLR4, TNF
lamellipodium 1 AKT1
Synapse 1 ACHE
cell cortex 1 AKT1
cell surface 3 ACHE, TLR4, TNF
glutamatergic synapse 4 AKT1, CASP3, MAPK14, RELA
Golgi apparatus 2 ACHE, PRKAA2
Golgi membrane 1 BSG
neuromuscular junction 1 ACHE
neuronal cell body 3 CASP3, PRKAA2, TNF
postsynapse 1 AKT1
sarcolemma 1 BSG
endosome 1 BSG
plasma membrane 6 ACHE, AKT1, BSG, STAT3, TLR4, TNF
Membrane 8 ACHE, AKT1, BCL2, BSG, CAT, PRKAA2, TLR4, TP53
axon 2 CCK, PRKAA2
basolateral plasma membrane 1 BSG
caveola 1 PTGS2
extracellular exosome 2 BSG, CAT
endoplasmic reticulum 3 BCL2, PTGS2, TP53
extracellular space 5 ACHE, CCK, IL6, SP1, TNF
perinuclear region of cytoplasm 2 ACHE, TLR4
mitochondrion 7 BCL2, BSG, CASP9, CAT, DNMT1, MAPK14, TP53
protein-containing complex 6 AKT1, BCL2, CASP9, CAT, PTGS2, TP53
intracellular membrane-bounded organelle 2 BSG, CAT
Microsome membrane 1 PTGS2
postsynaptic density 1 CASP3
pericentric heterochromatin 1 DNMT1
Single-pass type I membrane protein 2 BSG, TLR4
Secreted 4 ACHE, CCK, IL6, SP1
extracellular region 7 ACHE, CAT, CCK, IL6, MAPK14, SP1, TNF
Mitochondrion outer membrane 1 BCL2
Single-pass membrane protein 1 BCL2
mitochondrial outer membrane 1 BCL2
Mitochondrion matrix 1 TP53
mitochondrial matrix 2 CAT, TP53
Extracellular side 1 ACHE
transcription regulator complex 3 RELA, STAT3, TP53
photoreceptor inner segment 1 BSG
photoreceptor outer segment 1 BSG
Cytoplasm, cytoskeleton, microtubule organizing center, centrosome 1 TP53
Nucleus membrane 1 BCL2
Bcl-2 family protein complex 1 BCL2
nuclear membrane 1 BCL2
external side of plasma membrane 2 TLR4, TNF
microtubule cytoskeleton 1 AKT1
nucleolus 1 TP53
Early endosome 1 TLR4
cell-cell junction 1 AKT1
recycling endosome 1 TNF
Single-pass type II membrane protein 1 TNF
vesicle 1 AKT1
Membrane raft 1 TNF
pore complex 1 BCL2
Cytoplasm, cytoskeleton 1 TP53
focal adhesion 2 BSG, CAT
spindle 1 AKT1
Peroxisome 1 CAT
basement membrane 1 ACHE
Peroxisome matrix 1 CAT
peroxisomal matrix 1 CAT
peroxisomal membrane 1 CAT
Nucleus, PML body 1 TP53
PML body 1 TP53
Mitochondrion intermembrane space 1 AKT1
mitochondrial intermembrane space 1 AKT1
lateral plasma membrane 1 BSG
nuclear speck 2 MAPK14, PRKAA2
Nucleus inner membrane 1 PTGS2
Nucleus outer membrane 1 PTGS2
nuclear inner membrane 1 PTGS2
nuclear outer membrane 1 PTGS2
Cell projection, ruffle 1 TLR4
ruffle 1 TLR4
receptor complex 1 TLR4
neuron projection 1 PTGS2
ciliary basal body 1 AKT1
chromatin 4 RELA, SP1, STAT3, TP53
phagocytic cup 2 TLR4, TNF
Cell projection, cilium, photoreceptor outer segment 1 BSG
spindle pole 1 MAPK14
Basolateral cell membrane 1 BSG
Lipid-anchor, GPI-anchor 1 ACHE
[Isoform 2]: Cell membrane 1 BSG
site of double-strand break 1 TP53
female germ cell nucleus 1 DNMT1
Melanosome 1 BSG
cytoplasmic stress granule 1 PRKAA2
euchromatin 1 SP1
side of membrane 1 ACHE
germ cell nucleus 1 TP53
replication fork 2 DNMT1, TP53
myelin sheath 1 BCL2
lipopolysaccharide receptor complex 1 TLR4
ficolin-1-rich granule lumen 2 CAT, MAPK14
secretory granule lumen 2 CAT, MAPK14
endoplasmic reticulum lumen 2 IL6, PTGS2
nuclear matrix 1 TP53
transcription repressor complex 2 SP1, TP53
apoptosome 1 CASP9
[Isoform 1]: Nucleus 1 TP53
synaptic cleft 1 ACHE
protein-DNA complex 1 SP1
death-inducing signaling complex 1 CASP3
[Isoform 1]: Cell membrane 1 BSG
nucleotide-activated protein kinase complex 1 PRKAA2
acrosomal membrane 1 BSG
[Isoform 3]: Cell membrane 1 BSG
[Tumor necrosis factor, soluble form]: Secreted 1 TNF
catalase complex 1 CAT
interleukin-6 receptor complex 1 IL6
BAD-BCL-2 complex 1 BCL2
[Isoform 4]: Cell membrane 1 BSG
NF-kappaB p50/p65 complex 1 RELA
[Isoform H]: Cell membrane 1 ACHE
NF-kappaB complex 1 RELA
caspase complex 1 CASP9
[C-domain 2]: Secreted 1 TNF
[Tumor necrosis factor, membrane form]: Membrane 1 TNF
[C-domain 1]: Secreted 1 TNF


文献列表

  • Lu Liu, Sen Sun, Xiaohua Li. Physcion inhibition of CYP2C9, 2D6 and 3A4 in human liver microsomes. Pharmaceutical biology. 2024 Dec; 62(1):207-213. doi: 10.1080/13880209.2024.2314089. [PMID: 38353248]
  • Huang-Fei Jin, Qian-Xue Shen, Ying Shi, Fang-Ming Liu, Bin Wang, Jun Cao, Li-Hong Ye. Magnetic-stirring-enhanced mechanical amorphous dispersion extraction for the hydrophobic phytochemical constituents using an aqueous solution from a medicinal plant. Journal of pharmaceutical and biomedical analysis. 2024 Aug; 245(?):116191. doi: 10.1016/j.jpba.2024.116191. [PMID: 38728950]
  • Ruojun Du, Lichun Ye, Xinyan Chen, Yan Meng, Lei Zhou, Qiao Chen, Guohua Zheng, Junjie Hu, Zhaohua Shi. Screening of Key Components for Melanogenesis Inhibition of Polygonum cuspidatum Extract Based on the Spectrum-Effect Relationship and Molecular Docking. Molecules (Basel, Switzerland). 2024 Feb; 29(4):. doi: 10.3390/molecules29040857. [PMID: 38398609]
  • Fang Zhang, Rui Wu, Yanfang Liu, Shu Dai, Xinyan Xue, Xiaohong Gong, Yunxia Li. Comparative Pharmacokinetic Study of Rhubarb Anthraquinones in Normal and Nonalcoholic Fatty Liver Disease Rats. European journal of drug metabolism and pharmacokinetics. 2024 Jan; 49(1):111-121. doi: 10.1007/s13318-023-00875-z. [PMID: 38112917]
  • Mohamed Mendili, Ayda Khadhri, Francesca Sabatini, Ilaria Degano, Samira Aschi-Smiti. Parietin, the Vibrant Natural Dye in Xanthoria parietina. Chemistry & biodiversity. 2024 Jan; 21(1):e202301357. doi: 10.1002/cbdv.202301357. [PMID: 38072912]
  • Jan Schulze, Lisa Schöne, Abdallah M Ayoub, Damiano Librizzi, Muhammad Umair Amin, Konrad Engelhardt, Behrooz H Yousefi, Lena Bender, Jens Schaefer, Eduard Preis, Michaela Schulz-Siegmund, Christian Wölk, Udo Bakowsky. Modern Photodynamic Glioblastoma Therapy Using Curcumin- or Parietin-Loaded Lipid Nanoparticles in a CAM Model Study. ACS applied bio materials. 2023 Dec; 6(12):5502-5514. doi: 10.1021/acsabm.3c00695. [PMID: 38016693]
  • Shuxiang Zhang, Zhongdi Huang, Huanhuan Xu, Qihua Liu, Zhou Jiang, Caiping Yin, Guomin Han, Wei Zhang, Yinglao Zhang. Biological control of wheat powdery mildew disease by the termite-associated fungus Aspergillus chevalieri BYST01 and potential role of secondary metabolites. Pest management science. 2023 Dec; ?(?):. doi: 10.1002/ps.7938. [PMID: 38105413]
  • Martyna Nowak-Perlak, Piotr Ziółkowski, Marta Woźniak. A promising natural anthraquinones mediated by photodynamic therapy for anti-cancer therapy. Phytomedicine : international journal of phytotherapy and phytopharmacology. 2023 Oct; 119(?):155035. doi: 10.1016/j.phymed.2023.155035. [PMID: 37603973]
  • ShengHao Chen, YanLan Liang, YuanYuan Li, Yue Sun, Yang He. Determination of rhein and physcion in rhubarb by microchip capillary electrophoresis in mixed hydro-organic solvent combined with laser-induced fluorescence detection. Journal of separation science. 2023 Jul; ?(?):e2300192. doi: 10.1002/jssc.202300192. [PMID: 37507831]
  • H Wang, M Li, S Li, J Shi, L Huang, S Cheng, C Zou, H Yan. [Spectrum-effect relationship of total anthraquinone extract of Cassia seeds against fluorouracil-induced liver injury in mice]. Nan fang yi ke da xue xue bao = Journal of Southern Medical University. 2023 May; 43(5):825-831. doi: 10.12122/j.issn.1673-4254.2023.05.19. [PMID: 37313825]
  • Adam Yasgar, Danielle Bougie, Richard T Eastman, Ruili Huang, Misha Itkin, Jennifer Kouznetsova, Caitlin Lynch, Crystal McKnight, Mitch Miller, Deborah K Ngan, Tyler Peryea, Pranav Shah, Paul Shinn, Menghang Xia, Xin Xu, Alexey V Zakharov, Anton Simeonov. Quantitative Bioactivity Signatures of Dietary Supplements and Natural Products. ACS pharmacology & translational science. 2023 May; 6(5):683-701. doi: 10.1021/acsptsci.2c00194. [PMID: 37200814]
  • Hanaa M Sayed, Mahmoud A Ramadan, Heba H Salem, Iqrar Ahmad, Harun Patel, Marwa A A Fayed. Phytochemical Investigation, In silico/In vivo Analgesic, and Anti-inflammatory Assessment of the Egyptian Cassia occidentalis L. Steroids. 2023 May; 196(?):109245. doi: 10.1016/j.steroids.2023.109245. [PMID: 37141980]
  • Dongpeng Wang, Jufeng Duan, Xiao-Jing Chen, Kaiqi Liu, Yingying Guo, Run Shi, Sha Li, Ming Liu, Lijun Zhao, Bei Li, Hongtao Liu, Minglun Li, Yibin Feng, Hongliang Li, Xuanbin Wang. Pharmacokinetic characteristics of emodin in polygoni Multiflori Radix Praeparata. Journal of ethnopharmacology. 2023 Mar; 303(?):115945. doi: 10.1016/j.jep.2022.115945. [PMID: 36435407]
  • Yongpeng Yao, ErLan Yang, Yuanyuan Pan, Xian Shu, Gang Liu. Mining an O-methyltransferase for de novo biosynthesis of physcion in Aspergillus nidulans. Applied microbiology and biotechnology. 2023 Feb; 107(4):1177-1188. doi: 10.1007/s00253-023-12373-y. [PMID: 36648527]
  • Feifei Qi, Wei Zhang, Yingying Xue, Ce Geng, Zhigang Jin, Jibin Li, Qiang Guo, Xuenian Huang, Xuefeng Lu. Microbial production of the plant-derived fungicide physcion. Metabolic engineering. 2022 11; 74(?):130-138. doi: 10.1016/j.ymben.2022.10.007. [PMID: 36328293]
  • Bo Yuan, Nancy P Keller, Berl R Oakley, Jason E Stajich, Clay C C Wang. Manipulation of the Global Regulator mcrA Upregulates Secondary Metabolite Production in Aspergillus wentii Using CRISPR-Cas9 with In Vitro Assembled Ribonucleoproteins. ACS chemical biology. 2022 10; 17(10):2828-2835. doi: 10.1021/acschembio.2c00456. [PMID: 36197945]
  • Xiaolei Du, Lili Xu, Zhe Zhang, Yang Wang, Huifen Li, Weiliang Cui, Huibin Lin. Analyze the Effect of Steaming on the Chemical Constituents, Defecation and Liver Injury of Polygonum Multiflorum Radix (Heshouwu) by Multiple Analysis Techniques Combined with Multivariate Statistics. Molecules (Basel, Switzerland). 2022 Sep; 27(19):. doi: 10.3390/molecules27196284. [PMID: 36234820]
  • Chwan-Fwu Lin, Shih-Yi Chuang, Tse-Hung Huang, Thi My Huyen Nguyen, Pei-Wen Wang, Ahmed Alalaiwe, Jia-You Fang. A systematic comparison of the effect of topically applied anthraquinone aglycones to relieve psoriasiform lesion: The evaluation of percutaneous absorption and anti-inflammatory potency. Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie. 2022 Jan; 145(?):112482. doi: 10.1016/j.biopha.2021.112482. [PMID: 34915669]
  • Zizhao Lao, Yaohua Fan, Yuhang Huo, Feng Liao, Rongwen Zhang, Bei Zhang, Ziyun Kong, Haishan Long, Jieliang Xie, Chuanlan Sang, Ludi Fu, Ji Lin, Yina Wu, Liangwen Yu, Geng Li. Physcion, a novel inhibitor of 5α-reductase that promotes hair growth in vitro and in vivo. Archives of dermatological research. 2022 Jan; 314(1):41-51. doi: 10.1007/s00403-021-02195-1. [PMID: 33635414]
  • Mark J Henderson, Kathleen A Trychta, Shyh-Ming Yang, Susanne Bäck, Adam Yasgar, Emily S Wires, Carina Danchik, Xiaokang Yan, Hideaki Yano, Lei Shi, Kuo-Jen Wu, Amy Q Wang, Dingyin Tao, Gergely Zahoránszky-Kőhalmi, Xin Hu, Xin Xu, David Maloney, Alexey V Zakharov, Ganesha Rai, Fumihiko Urano, Mikko Airavaara, Oksana Gavrilova, Ajit Jadhav, Yun Wang, Anton Simeonov, Brandon K Harvey. A target-agnostic screen identifies approved drugs to stabilize the endoplasmic reticulum-resident proteome. Cell reports. 2021 04; 35(4):109040. doi: 10.1016/j.celrep.2021.109040. [PMID: 33910017]
  • Xiao Wei Ji, Hang Ji Lyu, Guang Hai Zhou, Bo Wu, Yuan Yuan Zhu, Tian Hua Wu, Feng Zhang, Song Nan Jin, Kyung Woo Cho, Jin Fu Wen. Physcion, a tetra-substituted 9,10-anthraquinone, prevents homocysteine-induced endothelial dysfunction by activating Ca2+- and Akt-eNOS-NO signaling pathways. Phytomedicine : international journal of phytotherapy and phytopharmacology. 2021 Jan; 81(?):153410. doi: 10.1016/j.phymed.2020.153410. [PMID: 33285470]
  • Tobie D Lee, Olivia W Lee, Kyle R Brimacombe, Lu Chen, Rajarshi Guha, Sabrina Lusvarghi, Bethilehem G Tebase, Carleen Klumpp-Thomas, Robert W Robey, Suresh V Ambudkar, Min Shen, Michael M Gottesman, Matthew D Hall. A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein. Molecular pharmacology. 2019 11; 96(5):629-640. doi: 10.1124/mol.119.115964. [PMID: 31515284]
  • XunLi, Yingjiao Liu, Shifeng Chu, Songwei Yang, Ye Peng, Siyu Ren, Birui Wen, Naihong Chen. Physcion and physcion 8-O-β-glucopyranoside: A review of their pharmacology, toxicities and pharmacokinetics. Chemico-biological interactions. 2019 Sep; 310(?):108722. doi: 10.1016/j.cbi.2019.06.035. [PMID: 31226286]
  • Bing Yang, Li Xie, Siying Peng, Kanping Sun, Junjie Jin, Yanping Zhen, Kunming Qin, Baochang Cai. Nine components pharmacokinetic study of rat plasma after oral administration raw and prepared Semen Cassiae in normal and acute liver injury rats. Journal of separation science. 2019 Jul; 42(14):2341-2350. doi: 10.1002/jssc.201900007. [PMID: 31037812]
  • Rong-Rong Li, Xue-Fang Liu, Su-Xiang Feng, Sheng-Nan Shu, Pei-Yang Wang, Na Zhang, Jian-Sheng Li, Ling-Bo Qu. Pharmacodynamics of Five Anthraquinones (Aloe-emodin, Emodin, Rhein, Chysophanol, and Physcion) and Reciprocal Pharmacokinetic Interaction in Rats with Cerebral Ischemia. Molecules (Basel, Switzerland). 2019 May; 24(10):. doi: 10.3390/molecules24101898. [PMID: 31108858]
  • Phil-Dong Moon, Na-Ra Han, Jin Soo Lee, Sungwei Hong, Min-Sun Yoo, Hyeong-Jin Kim, Ji-Hyeon Kim, Soonsik Kang, Hyun-Woo Jee, Hyung-Min Kim, Hyun-Ja Jeong. Use of Physcion to Improve Atopic Dermatitis-Like Skin Lesions through Blocking of Thymic Stromal Lymphopoietin. Molecules (Basel, Switzerland). 2019 Apr; 24(8):. doi: 10.3390/molecules24081484. [PMID: 30991764]
  • Kun-Ze Du, Ying Chen, Jin Li, Ge Tang, Fei Tian, Jun He, Yanxu Chang. Quantification of eight active ingredients in crude and processed radix polygoni multiflori applying miniaturized matrix solid-phase dispersion microextraction followed by UHPLC. Journal of separation science. 2018 Sep; 41(17):3486-3495. doi: 10.1002/jssc.201800342. [PMID: 30028075]
  • Ki Sun Kwon, Ju Hee Lee, Kyung Su So, Byung Kyu Park, Hyun Lim, Jae Sue Choi, Hyun Pyo Kim. Aurantio-obtusin, an anthraquinone from cassiae semen, ameliorates lung inflammatory responses. Phytotherapy research : PTR. 2018 Aug; 32(8):1537-1545. doi: 10.1002/ptr.6082. [PMID: 29675883]
  • Beatriz Fernández-Marín, Unai Artetxe, José María Becerril, Javier Martínez-Abaigar, Encarnación Núñez-Olivera, José Ignacio García-Plazaola. Can Parietin Transfer Energy Radiatively to Photosynthetic Pigments?. Molecules (Basel, Switzerland). 2018 Jul; 23(7):. doi: 10.3390/molecules23071741. [PMID: 30018202]
  • Guo Feng, Yun-Long Chen, Wei Li, Lai-Lai Li, Zeng-Guang Wu, Zi-Jun Wu, Yue Hai, Si-Chao Zhang, Chuan-Qi Zheng, Chang-Xiao Liu, Xin He. Exploring the Q-marker of "sweat soaking method" processed radix Wikstroemia indica: Based on the "effect-toxicity-chemicals" study. Phytomedicine : international journal of phytotherapy and phytopharmacology. 2018 Jun; 45(?):49-58. doi: 10.1016/j.phymed.2018.03.063. [PMID: 29691116]
  • Xiaotong Qin, Ying Peng, Jiang Zheng. In Vitro and in Vivo Studies of the Electrophilicity of Physcion and its Oxidative Metabolites. Chemical research in toxicology. 2018 05; 31(5):340-349. doi: 10.1021/acs.chemrestox.8b00026. [PMID: 29667811]
  • Ulrich Hildebrandt, Alexander Marsell, Markus Riederer. Direct Effects of Physcion, Chrysophanol, Emodin, and Pachybasin on Germination and Appressorium Formation of the Barley ( Hordeum vulgare L.) Powdery Mildew Fungus Blumeria graminis f. sp. hordei (DC.) Speer. Journal of agricultural and food chemistry. 2018 Apr; 66(13):3393-3401. doi: 10.1021/acs.jafc.7b05977. [PMID: 29554805]
  • Jing Zhang, Tenghua Wang, Zhiyao Ren, Lu Gong, Juan Huang, Junqi Bai, Xiaohui Qiu, Wen Xu. Application of HPLC-LTQ Orbitrap MS for metabolic profiles of Polygonum multiflora extract in rats. Biomedical chromatography : BMC. 2018 Feb; 32(2):. doi: 10.1002/bmc.4067. [PMID: 28833268]
  • Renato Sonchini Gonçalves, Expedito Leite Silva, Noboru Hioka, Celso Vataru Nakamura, Marcos Luciano Bruschi, Wilker Caetano. An optimized protocol for anthraquinones isolation from Rhamnus frangula L. Natural product research. 2018 Feb; 32(3):366-369. doi: 10.1080/14786419.2017.1356836. [PMID: 28745519]
  • Thais Fernanda Moreira, Juliana Maria Sorbo, Felipe de Oliveira Souza, Barbara Colatto Fernandes, Fernanda Maria Marins Ocampos, Daniella Maria Soares de Oliveira, Carlos Alberto Arcaro, Renata Pires Assis, Andersson Barison, Obdulio Gomes Miguel, Amanda Martins Baviera, Christiane Pienna Soares, Iguatemy Lourenço Brunetti. Emodin, Physcion, and Crude Extract of Rhamnus sphaerosperma var. pubescens Induce Mixed Cell Death, Increase in Oxidative Stress, DNA Damage, and Inhibition of AKT in Cervical and Oral Squamous Carcinoma Cell Lines. Oxidative medicine and cellular longevity. 2018; 2018(?):2390234. doi: 10.1155/2018/2390234. [PMID: 30057674]
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