Anthraquinone (BioDeep_00000395818)

Main id: BioDeep_00000004265

 

PANOMIX_OTCML-2023 natural product


代谢物信息卡片


9,10-anthraquinone;9,10-anthracenedione;anthraquinone;anthracene-9,10-dione;9,10-anthraquinone 9,10-anthracenedione anthraquinone anthracene-9,10-dione

化学式: C14H8O2 (208.0524)
中文名称: 蒽醌
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C1=CC=C2C(=C1)C(=O)C3=CC=CC=C3C2=O
InChI: InChI=1S/C14H8O2/c15-13-9-5-1-2-6-10(9)14(16)12-8-4-3-7-11(12)13/h1-8H

描述信息

Anthraquinone appears as yellow crystals or powder. (NTP, 1992)
9,10-anthraquinone is an anthraquinone that is anthracene in which positions 9 and 10 have been oxidised to carbonyls.
Anthraquinone is a natural product found in Annona muricata, Casearia membranacea, and other organisms with data available.
Anthraquinone is a polycyclic aromatic hydrocarbon derived from anthracene or phthalic anhydride. Anthraquinone is used in the manufacture of dyes, in the textile and pulp industries, and as a bird repellant.
Compounds based on ANTHRACENES which contain two KETONES in any position. Substitutions can be in any position except on the ketone groups.
Anthraquinone is used as a precursor for dye formation.
Anthraquinone is used as a precursor for dye formation.

同义名列表

79 个代谢物同义名

9,10-anthraquinone;9,10-anthracenedione;anthraquinone;anthracene-9,10-dione;9,10-anthraquinone 9,10-anthracenedione anthraquinone anthracene-9,10-dione; InChI=1/C14H8O2/c15-13-9-5-1-2-6-10(9)14(16)12-8-4-3-7-11(12)13/h1-8; 1,4-bis-[2-(2-hydroxy-ethylamino)-ethylamino]-anthraquinone; Anthraquinone, PESTANAL(R), analytical standard; Anthraquinone, Vetec(TM) reagent grade, 97\\%; Anthraquinone, purum, >=99.0\\% (HPLC); Anthracene, 9,10-dihydro-9,10-dioxo-; 9,10-Dihydro-9,10-diketoanthracene; Anthraquinone, analytical standard; 9,10-dihydro-9,10-dioxoanthracene; 9,10-dihydroanthracene-9,10-dione; Anthracene,10-dihydro-9,10-dioxo-; an anthraquinone derivative; Derivatives, Anthraquinone; Derivative, Anthraquinone; 9,10-Anthrachinon [Czech]; Anthraquinone Derivatives; Anthraquinone Derivative; Compounds, Anthraquinone; Anthracene-9,10-quinone; Compound, Anthraquinone; Anthraquinone Compounds; Anthraquinone [BSI:ISO]; Anthraquinone Compound; Anthra-9,10-quinone #; anthracene-9,10-dione; ANTHRAQUINONE (IARC); ANTHRAQUINONE [HSDB]; 9,10-Dioxoanthracene; ANTHRAQUINONE [INCI]; ANTHRAQUINONE [IARC]; 9,10-Anthracenedione; ANTHRAQUINONE [ISO]; 9,10-Anthracendione; Anthraquinone, 97\\%; Anthra-9,10-quinone; ANTHRAQUINONE [MI]; 9,10-Anthracendion; 9,10-Anthraquinone; anthracenequinones; 9,10-Anthraguinone; 9,10-Anthrachinon; Spectrum2_000405; Spectrum4_000907; Spectrum3_001501; Spectrum5_001897; Anthracenediones; dioxoanthracene; Anthracenedione; FLIGHT CONTROL; Anthraquinones; Tox21_111369_1; Anthraquinone; DivK1c_006741; (p) Anthrapel; Kawasaki saq; KBio2_007143; KBio1_001685; KBio2_004575; KBio3_002641; 9,10-quinone; Tox21_111369; Anthrachinon; KBio2_002007; Anthranoids; Anthradione; CAS-84-65-1; Anthranoid; AI3-09073; Anthrapel; Hoelite; Corbit; Avipel; Morkit; Az-Q; SAQ; 9TA; Anthraquinone; Anthraquinone



数据库引用编号

18 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)

38 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 11 ABCB1, ANG, ANXA5, BCL2, CASP3, CASP8, CAT, NLRP3, PRKX, PTGS2, TP53
Peripheral membrane protein 5 ACHE, ANXA5, CYP1B1, HSD17B6, PTGS2
Endoplasmic reticulum membrane 3 BCL2, CYP1B1, PTGS2
Nucleus 8 ACHE, ANG, BCL2, CASP3, CASP8, NLRP3, PRKX, TP53
cytosol 9 ANG, ANXA5, BCL2, CASP3, CASP8, CAT, GPT, NLRP3, TP53
centrosome 1 TP53
nucleoplasm 4 CASP3, CASP8, PRKX, TP53
Cell membrane 3 ABCB1, ACHE, TNF
lamellipodium 1 CASP8
Early endosome membrane 1 HSD17B6
Multi-pass membrane protein 1 ABCB1
Golgi apparatus membrane 1 NLRP3
Synapse 1 ACHE
cell surface 3 ABCB1, ACHE, TNF
glutamatergic synapse 1 CASP3
Golgi apparatus 1 ACHE
Golgi membrane 2 INS, NLRP3
growth cone 1 ANG
lysosomal membrane 1 GAA
neuromuscular junction 1 ACHE
neuronal cell body 3 ANG, CASP3, TNF
sarcolemma 1 ANXA5
Cytoplasm, cytosol 1 NLRP3
Lysosome 1 GAA
plasma membrane 4 ABCB1, ACHE, GAA, TNF
Membrane 9 ABCB1, ACHE, ANXA5, BCL2, CAT, CYP1B1, GAA, NLRP3, TP53
apical plasma membrane 1 ABCB1
caveola 1 PTGS2
extracellular exosome 5 ABCB1, ANXA5, CAT, GAA, GPT
Lysosome membrane 1 GAA
Lumenal side 1 HSD17B6
endoplasmic reticulum 5 BCL2, HSD17B6, NLRP3, PTGS2, TP53
extracellular space 6 ACHE, ANG, CXCL8, IL6, INS, TNF
lysosomal lumen 1 GAA
perinuclear region of cytoplasm 1 ACHE
mitochondrion 6 BCL2, CASP8, CAT, CYP1B1, NLRP3, TP53
protein-containing complex 5 BCL2, CASP8, CAT, PTGS2, TP53
intracellular membrane-bounded organelle 4 CAT, CYP1B1, GAA, HSD17B6
Microsome membrane 3 CYP1B1, HSD17B6, PTGS2
postsynaptic density 1 CASP3
Secreted 7 ACHE, ANG, CXCL8, GAA, IL6, INS, NLRP3
extracellular region 10 ACHE, ANG, ANXA5, CAT, CXCL8, GAA, IL6, INS, NLRP3, TNF
Mitochondrion outer membrane 1 BCL2
Single-pass membrane protein 1 BCL2
mitochondrial outer membrane 2 BCL2, CASP8
Mitochondrion matrix 1 TP53
mitochondrial matrix 2 CAT, TP53
Extracellular side 1 ACHE
transcription regulator complex 1 TP53
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 ANXA5, TNF
actin cytoskeleton 1 ANG
nucleolus 2 ANG, TP53
recycling endosome 1 TNF
Single-pass type II membrane protein 1 TNF
Apical cell membrane 1 ABCB1
Cell projection, lamellipodium 1 CASP8
Membrane raft 1 TNF
pore complex 1 BCL2
Cytoplasm, cytoskeleton 1 TP53
focal adhesion 2 ANXA5, CAT
Peroxisome 1 CAT
basement membrane 2 ACHE, ANG
Peroxisome matrix 1 CAT
peroxisomal matrix 1 CAT
peroxisomal membrane 1 CAT
Nucleus, PML body 1 TP53
PML body 1 TP53
collagen-containing extracellular matrix 1 ANXA5
Cytoplasm, cytoskeleton, microtubule organizing center 1 NLRP3
Inflammasome 1 NLRP3
interphase microtubule organizing center 1 NLRP3
NLRP3 inflammasome complex 1 NLRP3
Nucleus inner membrane 1 PTGS2
Nucleus outer membrane 1 PTGS2
nuclear inner membrane 1 PTGS2
nuclear outer membrane 1 PTGS2
Zymogen granule membrane 1 ANXA5
neuron projection 1 PTGS2
chromatin 1 TP53
phagocytic cup 1 TNF
Chromosome 1 ANG
cytoskeleton 1 CASP8
Nucleus, nucleolus 1 ANG
Lipid-anchor, GPI-anchor 1 ACHE
site of double-strand break 1 TP53
Endomembrane system 1 NLRP3
endosome lumen 1 INS
microtubule organizing center 1 NLRP3
tertiary granule membrane 1 GAA
Cytoplasm, Stress granule 1 ANG
cytoplasmic stress granule 1 ANG
cell body 1 CASP8
side of membrane 1 ACHE
germ cell nucleus 1 TP53
replication fork 1 TP53
myelin sheath 1 BCL2
ficolin-1-rich granule lumen 1 CAT
secretory granule lumen 2 CAT, INS
Golgi lumen 1 INS
endoplasmic reticulum lumen 3 IL6, INS, PTGS2
nuclear matrix 1 TP53
transcription repressor complex 1 TP53
endocytic vesicle 1 ANG
transport vesicle 1 INS
azurophil granule membrane 1 GAA
Endoplasmic reticulum-Golgi intermediate compartment membrane 1 INS
vesicle membrane 1 ANXA5
[Isoform 1]: Nucleus 1 TP53
synaptic cleft 1 ACHE
ficolin-1-rich granule membrane 1 GAA
external side of apical plasma membrane 1 ABCB1
CD95 death-inducing signaling complex 1 CASP8
death-inducing signaling complex 2 CASP3, CASP8
ripoptosome 1 CASP8
[Tumor necrosis factor, soluble form]: Secreted 1 TNF
angiogenin-PRI complex 1 ANG
catalase complex 1 CAT
interleukin-6 receptor complex 1 IL6
endothelial microparticle 1 ANXA5
autolysosome lumen 1 GAA
BAD-BCL-2 complex 1 BCL2
[Isoform H]: Cell membrane 1 ACHE
[C-domain 2]: Secreted 1 TNF
[Tumor necrosis factor, membrane form]: Membrane 1 TNF
[C-domain 1]: Secreted 1 TNF


文献列表

  • 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]
  • Xun Li, Minghe Yao, Lingling Li, Huifen Ma, Yiran Sun, Xiangpeng Lu, Weipeng Jing, Shanshan Nie. Aloe-emodin alleviates cerebral ischemia-reperfusion injury by regulating microglial polarization and pyroptosis through inhibition of NLRP3 inflammasome activation. Phytomedicine : international journal of phytotherapy and phytopharmacology. 2024 Jul; 129(?):155578. doi: 10.1016/j.phymed.2024.155578. [PMID: 38621328]
  • Qi Qiu, Fei Fu, Yaling Wu, Chenxia Han, Weiling Pu, Li Wen, Qing Xia, Dan Du. Rhei Radix et Rhizoma and its anthraquinone derivatives: Potential candidates for pancreatitis treatment. Phytomedicine : international journal of phytotherapy and phytopharmacology. 2024 Jul; 129(?):155708. doi: 10.1016/j.phymed.2024.155708. [PMID: 38733906]
  • Hafidha Mehallah, Noureddine Djebli, Pham Ngoc Khanh, Nguyen Xuan Ha, Vu Thi Ha, Tran Thu Huong, Do Dinh Tung, Nguyen Manh Cuong. In silico and in vivo study of anti-inflammatory activity of Morinda longissima (Rubiaceae) extract and phytochemicals for treatment of inflammation-mediated diseases. Journal of ethnopharmacology. 2024 Jun; 328(?):118051. doi: 10.1016/j.jep.2024.118051. [PMID: 38493905]
  • Susana Tavares Cotrim Ribeiro, Naiara Cássia Gancedo, Arildo José Braz de Oliveira, Regina Aparecida Correia Gonçalves. A comprehensive review of Pfaffia glomerata botany, ethnopharmacology, phytochemistry, biological activities, and biotechnology. Journal of ethnopharmacology. 2024 Jun; 328(?):118003. doi: 10.1016/j.jep.2024.118003. [PMID: 38484957]
  • Jing Sun, Linying Zhong, Ling Dong, Jianbo Chen. Mid-infrared spectroscopic identification of the right-baked rhubarb for ulcerative colitis therapy. Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy. 2024 Jun; 314(?):124244. doi: 10.1016/j.saa.2024.124244. [PMID: 38579425]
  • Min-Min Gu, Qing Li, Yu Zhang, Hong-Wei Wu, Yuan-Ling Shao, Hong-Ping Han, Zhi-Xin Liao. Chemical constituents of Rubia tibetica Hook. f. from Tibetan medicine and cytotoxic activity evaluation. Fitoterapia. 2024 Jun; 175(?):105961. doi: 10.1016/j.fitote.2024.105961. [PMID: 38626855]
  • Ting Han, Wenjuan Xu, Xuan Wang, Jiahui Gao, Shuyan Zhang, Linlin Yang, Min Wang, Chunshuai Li, Xiangri Li. Emodin-8-O-β-D-glucopyranoside-induced hepatotoxicity and gender differences in zebrafish as revealed by integration of metabolomics and transcriptomics. Phytomedicine : international journal of phytotherapy and phytopharmacology. 2024 Jun; 128(?):155411. doi: 10.1016/j.phymed.2024.155411. [PMID: 38518638]
  • Yue Zeng, Xingyu Liu, Qing Yi, Gan Qiao, Lulu Wang, Li Chen, Ling Fan, Yao Li, Lingjing Duan, Liqiang Huang, Qian Zhuang, Yejiang Zhou, Yuxia Xiong. Free total rhubarb anthraquinones protect intestinal mucosal barrier of SAP rats via inhibiting the NLRP3/caspase-1/GSDMD pyroptotic pathway. Journal of ethnopharmacology. 2024 May; 326(?):117873. doi: 10.1016/j.jep.2024.117873. [PMID: 38346523]
  • Fangyuan Wang, Jingyin Mai, Haoyi Wang, Ying Xu, Xianglu Zhou, Zhishen Xie, Bao Yu, Ping Liu, Wei Liu, Yang Cheng. Identification of Erzhu Jiedu Recipe and its molecular mechanism underlying inhibited human hepatoma cells by UHPLC-Q-Exactive Orbitrap HRMS and network pharmacology. Journal of ethnopharmacology. 2024 May; 325(?):117893. doi: 10.1016/j.jep.2024.117893. [PMID: 38336184]
  • Zhoukang Zhuang, Wenping Kong, Zhongqing Wen, Nian Tong, Jing Lin, Fan Zhang, Zhiying Fan, Liwei Yi, Yong Huang, Yanwen Duan, Xiaohui Yan, Xiangcheng Zhu. Combinatorial metabolic engineering of Streptomyces sp. CB03234-S for the enhanced production of anthraquinone-fused enediyne tiancimycins. Microbial cell factories. 2024 May; 23(1):128. doi: 10.1186/s12934-024-02399-w. [PMID: 38704580]
  • Xueqiong Feng, Zhongqing Wen, Xiangcheng Zhu, Xiaohui Yan, Yanwen Duan, Yong Huang. Anti-HER2 Immunoliposomes: Antitumor Efficacy Attributable to Targeted Delivery of Anthraquinone-Fused Enediyne. Advanced science (Weinheim, Baden-Wurttemberg, Germany). 2024 May; 11(17):e2307865. doi: 10.1002/advs.202307865. [PMID: 38355309]
  • Shujun Xu, Shuang Zheng, Ninghui Ma, Hongyan Zhang, Jingbin Shi, Jingyi Huang, Ninghchao Luo, Menglin Wang, Yang Xiong. Rhein potentiates doxorubicin in treating triple negative breast cancer by inhibiting cancer-associated fibroblasts. Biochemical pharmacology. 2024 May; 223(?):116139. doi: 10.1016/j.bcp.2024.116139. [PMID: 38499109]
  • Jin-Ling Chang, Yu-Tian Gan, Yin-Hui Zhou, Xiao-Gang Peng, Zuo-Ye Xie, Xianggao Meng, Shu-Ming Li, Han-Li Ruan. Asperustins A-J: Austocystins with Immunosuppressive and Cytotoxic Activities from Aspergillus ustus NRRL 5856. Journal of natural products. 2024 Apr; 87(4):966-975. doi: 10.1021/acs.jnatprod.3c01243. [PMID: 38441877]
  • Tianyi Zhang, Lipan Zhou, Yang Pu, Yadi Tang, Jie Liu, Li Yang, Tao Zhou, Li Feng, Xumei Wang. A chromosome-level genome reveals genome evolution and molecular basis of anthraquinone biosynthesis in Rheum palmatum. BMC plant biology. 2024 Apr; 24(1):261. doi: 10.1186/s12870-024-04972-2. [PMID: 38594606]
  • Fang Zhang, Rui Wu, Yanfang Liu, Shu Dai, Xiaohong Gong, Yunxia Li. Integration of pharmacodynamics and metabolomics to reveal rhubarb anthraquinone protection against nonalcoholic fatty liver disease rat model. The Journal of pharmacy and pharmacology. 2024 Apr; 76(4):381-390. doi: 10.1093/jpp/rgae014. [PMID: 38349666]
  • Zhongqing Wen, Zhoukang Zhuang, Huiming Liu, Zilong Wang, Xueqiong Feng, Xiangcheng Zhu, Xiaohui Yan, Yanwen Duan, Yong Huang. DNA Interaction and Cleavage Modes of Anthraquinone-Fused Enediynes: A Study on Tiancimycins, Yangpumicins, and Their Semisynthetic Analogues. Journal of medicinal chemistry. 2024 Mar; 67(6):4624-4640. doi: 10.1021/acs.jmedchem.3c02049. [PMID: 38483132]
  • Lingling Wang, Shuo Zhao, Jianan Li, Guoying Zhou. Metabolomics analysis reveals the metabolite profiles of Rheum tanguticum grown under different altitudinal gradients. BMC plant biology. 2024 Mar; 24(1):226. doi: 10.1186/s12870-024-04933-9. [PMID: 38539101]
  • Tianyi Zhao, Shiyi Lun, Maoying Yan, JongPil Park, Shumin Wang, Changbao Chen. 6,7-Dimethoxycoumarin, Gardenoside and Rhein combination improves non-alcoholic fatty liver disease in rats. Journal of ethnopharmacology. 2024 Mar; 322(?):117646. doi: 10.1016/j.jep.2023.117646. [PMID: 38135236]
  • 吉 Deji, Jun Lan, Basangyangzong, Dawazhuoma. [Establishment and Optimization of Quality Standards for the Traditional Tibetan Medicine Preparation of Liuwei Nengxiao Pills]. Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition. 2024 Mar; 55(2):425-432. doi: 10.12182/20240360102. [PMID: 38645843]
  • Ahmad Nasir Labaran, Zakariyya Uba Zango, Giriraj Tailor, Ahmed Alsadig, Fahad Usman, Muhammad Tukur Mukhtar, Alhassan Muhammad Garba, Raed Alhathlool, Khalid Hassan Ibnaouf, Osamah A Aldaghri. Biosynthesis of copper nanoparticles using Alstonia scholaris leaves and its antimicrobial studies. Scientific reports. 2024 03; 14(1):5589. doi: 10.1038/s41598-024-56052-y. [PMID: 38453990]
  • Bi Wang, Jingjing Yang, Xingzeng Zhao, Xu Feng, Shu Xu, Pirui Li, Linwei Li, Yu Chen. Antifungal activity of the botanical compound rhein against Phytophthora capsici and the underlying mechanisms. Pest management science. 2024 Mar; 80(3):1228-1239. doi: 10.1002/ps.7852. [PMID: 37897133]
  • Jiang-Bo He, Ying Wang, Gao-Hong Zhang, Ji-Ai Wang, Yi-Shu Chen, Jing Jia, Xiao-Man Lv, Fu-Cai Ren, Bing Chen, Yan-Ru Cao. Secondary metabolites from the Actinomadura sp. and their cytotoxic activity. Fitoterapia. 2024 Mar; 173(?):105806. doi: 10.1016/j.fitote.2023.105806. [PMID: 38181893]
  • Tao Zhou, Yadi Tang, Lipan Zhou, Jie Liu, Yang Pu, Fan Jiang, Jian Wang, Xumei Wang. Transcriptomic divergence of the Rheum palmatum complex derived from top-geoherb and non-geoherb areas provides the insights into geoherbalism properties of rhubarb. BMC genomics. 2024 Feb; 25(1):212. doi: 10.1186/s12864-024-10142-3. [PMID: 38408895]
  • Jiali Wu, Yaokun Pang, Dan Liu, Jianxia Sun, Weibin Bai. Photodynamic Inactivation of Staphylococcus aureus Using Aloe-emodin as Photosensitizer. Food research international (Ottawa, Ont.). 2024 Feb; 178(?):113959. doi: 10.1016/j.foodres.2024.113959. [PMID: 38309912]
  • Zhongjing Jiang, Linhua Deng, Mengjun Li, Emmanuel Alonge, Yanling Wang, Yunjia Wang. Ginsenoside Rg1 modulates PI3K/AKT pathway for enhanced osteogenesis via GPER. Phytomedicine : international journal of phytotherapy and phytopharmacology. 2024 Feb; 124(?):155284. doi: 10.1016/j.phymed.2023.155284. [PMID: 38176267]
  • Li-Jun Wang, Feng Wen, Li-Xia Li, Zhan-Feng Xia. Antifungal activity and mechanism of oxanthromicin against Verticillium dahliae. Archives of microbiology. 2024 Jan; 206(2):83. doi: 10.1007/s00203-023-03815-2. [PMID: 38296859]
  • Lifang Wang, Haijao Wang, Jingjing Niu, Honggang Chen, Meng Wang, Zhigang Yang, Shaohua Wang, Xiuxia Sun, Yanbin Shi. Cholesterol-lowering effects of rhubarb free anthraquinones and their mechanism of action. European journal of pharmacology. 2024 Jan; ?(?):176348. doi: 10.1016/j.ejphar.2024.176348. [PMID: 38286356]
  • Young-Seon Kim, Ji-Hye Han, Chang-Hoon Lim, Xue-Quan Fang, Hyeock-Soon Jang, Sang-Yun Lee, Woo-Jong Yim, Ji-Hong Lim. Effects of Fermented Polygonum cuspidatum on the Skeletal Muscle Functions. Nutrients. 2024 Jan; 16(2):. doi: 10.3390/nu16020305. [PMID: 38276543]
  • Jingna Li, Yaming Sun, Yong Man, Tao Zhang, Xiaxing Feng, Zhen Yang, Hailiang Zhao, Renyong Zhao, Lijun He. A Novel and Highly Efficient Microextraction Method for the Determination of Aflatoxin Precursor Averantin in Fatty Grain Samples. Journal of agricultural and food chemistry. 2024 Jan; 72(2):1330-1338. doi: 10.1021/acs.jafc.3c06572. [PMID: 38173280]
  • Qiang Huang, Meiling Fan, Fenglan Ji, Yuqi Wang, Hongyue Ding, Jie Xu, Xin Wang, Bo Liu, Bei Wang, Xinmiao Yu, Zhidong Qiu, Fan Yao. The safety evaluation of Shenze Shugan capsule and mechanism of apoptosis induced by five potentially nephrotoxic components. Journal of ethnopharmacology. 2024 Jan; 324(?):117777. doi: 10.1016/j.jep.2024.117777. [PMID: 38219879]
  • Nadja Meier, Beat Meier, Alexander Schenk, Le Nhung Ziegler, Samuel Peter, Evelyn Wolfram. Photostability of sennosides and their aglycones in solution. Phytochemical analysis : PCA. 2024 Jan; ?(?):. doi: 10.1002/pca.3308. [PMID: 38198752]
  • Hongyu Zhang, Qiang He, Longsheng Xing, Ruyu Wang, Yu Wang, Yu Liu, Qinghong Zhou, Xuanzhao Li, Zheng Jia, Ze Liu, Yuqing Miao, Tao Lin, Wei Li, Huilong Du. The haplotype-resolved genome assembly of autotetraploid rhubarb Rheum officinale provides insights into its genome evolution and massive accumulation of anthraquinones. Plant communications. 2024 Jan; 5(1):100677. doi: 10.1016/j.xplc.2023.100677. [PMID: 37634079]
  • 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]
  • Xin-Shu Ji, De-Cai Dai, Yi-Tong Wang, Jing-Yi Cui, Hai-Xiang Li, Xin-Ming Song, Ji-Ling Yi, Xue-Ming Zhou. Two new anthraquinone derivatives from Saprosma crassipes H. S. Lo. Natural product research. 2024 Jan; 38(1):91-96. doi: 10.1080/14786419.2022.2106483. [PMID: 35921492]
  • Razieh Amini, Shadi Moradi, Rezvan Najafi, Mehrdokht Mazdeh, Amir Taherkhani. BACE1 Inhibition Utilizing Organic Compounds Holds Promise as a Potential Treatment for Alzheimer's and Parkinson's Diseases. Oxidative medicine and cellular longevity. 2024; 2024(?):6654606. doi: 10.1155/2024/6654606. [PMID: 38425997]
  • A F Serain, A J Buitrago-Mejia, G C A de Souza, W R Corrêa, M E A Stefanello, M J Salvador. Antitumoral photoinduced effects of crude extract, fractions, and naphthoquinones from Sinningia magnifica (Otto & A. Dietr.) Wiehler (Gesneriaceae) in a bioguided study. Photochemistry and photobiology. 2024 Jan; 100(1):190-203. doi: 10.1111/php.13830. [PMID: 37395166]
  • Yichao Wu, Fen Leng, Mingli Liao, Yan Yu, Zhenyong Chen, Shuhong Wei, Zaijun Yang, Qi Wu. Characterization of the physiological parameters, effective components, and transcriptional profiles of Polygonum multiflorum Thunb. Under pH stress. Plant physiology and biochemistry : PPB. 2024 Jan; 206(?):108279. doi: 10.1016/j.plaphy.2023.108279. [PMID: 38128226]
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