Isoquercitrin (BioDeep_00000000179)

 

Secondary id: BioDeep_00000270288, BioDeep_00000275350, BioDeep_00000337862, BioDeep_00000408302, BioDeep_00000894603

natural product human metabolite PANOMIX_OTCML-2023 blood metabolite Chemicals and Drugs PANOMIX-Anthocyanidin BioNovoGene_Lab2019


代谢物信息卡片


2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)-4H-chromen-4-one

化学式: C21H20O12 (464.09547200000003)
中文名称: 槲皮素 3-β-D-葡萄糖甙, 槲皮素-3-葡萄糖苷, 异槲皮苷, 异懈皮苷, 槲皮素-3-O-葡萄糖苷, 槲皮素-3-β-D-葡萄糖苷、异槲皮苷
谱图信息: 最多检出来源 Viridiplantae(plant) 31.24%

Reviewed

Last reviewed on 2024-07-09.

Cite this Page

Isoquercitrin. BioDeep Database v3. PANOMIX ltd, a top metabolomics service provider from China. https://query.biodeep.cn/s/isoquercitrin (retrieved 2024-12-04) (BioDeep RN: BioDeep_00000000179). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

分子结构信息

SMILES: c1(cc(c2c(c1)oc(c(c2=O)O[C@H]1[C@@H]([C@@H]([C@@H]([C@H](O1)CO)O)O)O)c1ccc(c(c1)O)O)O)O
InChI: InChI=1/C21H20O12/c22-6-13-15(27)17(29)18(30)21(32-13)33-20-16(28)14-11(26)4-8(23)5-12(14)31-19(20)7-1-2-9(24)10(25)3-7/h1-5,13,15,17-18,21-27,29-30H,6H2/t13-,15-,17+,18-,21+/m1/s1

描述信息

Quercetin 3-O-beta-D-glucopyranoside is a quercetin O-glucoside that is quercetin with a beta-D-glucosyl residue attached at position 3. Isolated from Lepisorus contortus, it exhibits antineoplastic activityand has been found to decrease the rate of polymerization and sickling of red blood cells It has a role as an antineoplastic agent, a plant metabolite, a bone density conservation agent, an osteogenesis regulator, an antioxidant, a histamine antagonist, an antipruritic drug and a geroprotector. It is a quercetin O-glucoside, a tetrahydroxyflavone, a beta-D-glucoside and a monosaccharide derivative. It is functionally related to a beta-D-glucose. It is a conjugate acid of a quercetin 3-O-beta-D-glucopyranoside(1-).
Isoquercetin has been used in trials studying the treatment of Kidney Cancer, Renal cell carcinoma, Advanced Renal Cell Carcinoma, Thromboembolism of Vein in Pancreatic Cancer, and Thromboembolism of Vein VTE in Colorectal Cancer, among others.
Isoquercitrin is a natural product found in Ficus auriculata, Lotus ucrainicus, and other organisms with data available.
Isoquercetin is an orally bioavailable, glucoside derivative of the flavonoid quercetin and protein disulfide isomerase (PDI) inhibitor, with antioxidant and potential antithrombotic activity. As an antioxidant, isoquercetin scavenges free radicals and inhibits oxidative damage to cells. As a PDI inhibitor, this agent blocks PDI-mediated platelet activation, and fibrin generation, which prevents thrombus formation after vascular injury. In addition, isoquercetin is an alpha-glucosidase inhibitor. PDI, an oxidoreductase secreted by activated endothelial cells and platelets, plays a key role in the initiation of the coagulation cascade. Cancer, in addition to other thrombotic disorders, increases the risk of thrombus formation.

Isoquercitrin is found in alcoholic beverages. Isoquercitrin occurs widely in plants. Isoquercitrin is present in red wine.Isoquercitin can be isolated from mangoes and from Rheum nobile, the Noble rhubarb or Sikkim rhubarb, a giant herbaceous plant native to the Himalaya. Quercetin glycosides are also present in tea. (Wikipedia
A quercetin O-glucoside that is quercetin with a beta-D-glucosyl residue attached at position 3. Isolated from Lepisorus contortus, it exhibits antineoplastic activityand has been found to decrease the rate of polymerization and sickling of red blood cells

[Raw Data] CB053_Isoquercitrin_pos_10eV_CB000025.txt
[Raw Data] CB053_Isoquercitrin_pos_30eV_CB000025.txt
[Raw Data] CB053_Isoquercitrin_pos_50eV_CB000025.txt
[Raw Data] CB053_Isoquercitrin_pos_40eV_CB000025.txt
[Raw Data] CB053_Isoquercitrin_pos_20eV_CB000025.txt
[Raw Data] CB053_Isoquercitrin_neg_40eV_000017.txt
[Raw Data] CB053_Isoquercitrin_neg_20eV_000017.txt
[Raw Data] CB053_Isoquercitrin_neg_50eV_000017.txt
[Raw Data] CB053_Isoquercitrin_neg_30eV_000017.txt
[Raw Data] CB053_Isoquercitrin_neg_10eV_000017.txt

Quercetin 3-glucoside. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=482-35-9 (retrieved 2024-07-09) (CAS RN: 482-35-9). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
Isoquercetin (Quercetin 3-glucoside) is a naturally occurring polyphenol that has antioxidant, anti-proliferative, and anti-inflammatory properties. Isoquercetin alleviates ethanol-induced hepatotoxicity, oxidative stress, and inflammatory responses via the Nrf2/ARE antioxidant signaling pathway[1]. Isoquercetin regulates the expression of nitric oxide synthase 2 (NO2) via modulating the nuclear factor-κB (NF-κB) transcription regulation system. Isoquercetin has high bioavailability and low toxicity, is a promising candidate agent to prevent birth defects in diabetic pregnancies[2].
Isoquercetin (Quercetin 3-glucoside) is a naturally occurring polyphenol that has antioxidant, anti-proliferative, and anti-inflammatory properties. Isoquercetin alleviates ethanol-induced hepatotoxicity, oxidative stress, and inflammatory responses via the Nrf2/ARE antioxidant signaling pathway[1]. Isoquercetin regulates the expression of nitric oxide synthase 2 (NO2) via modulating the nuclear factor-κB (NF-κB) transcription regulation system. Isoquercetin has high bioavailability and low toxicity, is a promising candidate agent to prevent birth defects in diabetic pregnancies[2].
Isoquercitrin (Isoquercitroside) is an effective antioxidant and an eosinophilic inflammation suppressor.
Isoquercitrin (Isoquercitroside) is an effective antioxidant and an eosinophilic inflammation suppressor.

同义名列表

123 个代谢物同义名

2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)-4H-chromen-4-one; 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-((2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)-tetrahydro-2H-pyran-2-yloxy)-4H-chromen-4-one; 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)-tetrahydro-2H-pyran-2-yloxy)-4H-chromen-4-one; 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yloxy)-4H-chromen-4-one; 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-chromen-4-one; 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-4H-chromen-4-one; 2-(3,4-Dihydroxy-phenyl)-5,7-dihydroxy-3-(3,4,5-trihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxy)-chromen-4-one; 4H-1-Benzopyran-4-one, 2-(3,4-dihydroxy-phenyl)-3-(.beta.-D-glucofuranosyloxy)-5,7-dihydroxy-; 4H-1-BENZOPYRAN-4-ONE, 2-(3,4-DIHYDROXYPHENYL)-3-(.BETA.-D-GLUCOPYRANOSYLOXY)-5,7-DIHYDROXY-; 2-(3,4-Dihydroxyphenyl)-3-(b-D-glucopyranosyloxy)-5,7-dihydroxy-4H-1-benzopyran-4-one, 9CI; 4H-1-BENZOPYRAN-4-ONE, 2- (3,4-DIHYDROXYPHENYL)-3- (SS-D-GLUCOFURANOSYLOXY)-5,7-DIHYDROXY-; 4H-1-benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-3-(beta-D-glucopyranosyloxy)-5,7-dihydroxy-; 4H-1-Benzopyran-4-one, 5,7-dihydroxy-2-(3,4-dihydroxyphenyl)-3-(beta-D-glucopyranosyloxy)-; 4H-1-benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-3-(beta-D-glucofuranosyloxy)-5,7-dihydroxy; 2-(3,4-Dihidroxyphenyl)-3-(beta-D-glucofuranosyloxy)-5,7-dihydroxy-4H-1-benzopyran-4-one; 4H-1-BENZOPYRAN-4-ONE, 2-(3,4-DIHYDROXYPHENYL)-3-(SS-D-GLUCOFURANOSYLOXY)-5,7-DIHYDROXY-; 2-(3,4-dihydroxyphenyl)-3-(beta-D-glucopyranosyloxy)-5,7-dihydroxy-4H-1-benzopyran-4-one; 2-(3,4-dihydroxyphenyl)-3-(beta-D-glucofuranosyloxy)-5,7-dihydroxy-4H-1-benzopyran-4-one; 4H-1-Benzopyran-4-one,2-(3,4-dihydroxyphenyl)-3-(b-D-glucopyranosyloxy)-5,7-dihydroxy-; 2-(3,4-Dihidroxyphenyl)-3-(β-D-glucofuranosyloxy)-5,7-dihydroxy-4H-1-benzopyran-4-one; 2-(3,4-Dihydroxyphenyl)-3-(b-D-glucopyranosyloxy)-5,7-dihydroxy-4H-1-benzopyran-4-one; 2-(3,4-Dihydroxyphenyl)-3-(β-D-glucopyranosyloxy)-5,7-dihydroxy-4H-1-benzopyran-4-one; 2-(3,4-Dihidroxyphenyl)-3-(b-D-glucofuranosyloxy)-5,7-dihydroxy-4H-1-benzopyran-4-one; 2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4H-chromen-3-yl beta-D-glucopyranoside; flavone, 3,3,4,5,7-pentahydroxy-, 3-beta-D-glucofuranoside; Isoquercitrin, primary pharmaceutical reference standard; 3,4,5,7-TETRAHYDROXYFLAVONE-3-.BETA.-D-GLUCOPYRANOSIDE; QUERCETIN 3-O-GLUCOSIDE (CONSTITUENT OF GINKGO) [DSC]; 3,4,5,7-TETRAHYDROXYFLAVONE-3-beta-D-GLUCOPYRANOSIDE; 3’,4’,5,7-Tetrahydroxyflavone-3-β-D-glucopyranoside; 3,4,5,7-Tetrahydroxyflavone-3-β-D-glucopyranoside; 3,3,4,5,7-pentahydroxyflavone-3-beta-O-glucoside; QUERCETIN 3-O-GLUCOSIDE (CONSTITUENT OF GINKGO); 3-Glucopyranosyloxy-3,4,5,7-tetrahydroxyflavone; 3,3,4,5,7-Pentahydroxyflavone 3-beta-glucoside; 4-18-00-03493 (Beilstein Handbook Reference); Quercetin 3-beta-D-glucoside, >=90\\% (HPLC); 3,3,4,5,7-Pentahydroxyflavone 3-A-glucoside; Quercetin 3-glucoside, analytical standard; (-)-Quercetin-3-O-beta-D-glucopyranoside; quercetin -3-O-beta-D-galactopyranoside; QUERCETIN 3-O-GLUCOPYRANOSIDE [WHO-DD]; Quercetin-3-O-beta-D-galactopyranoside; Quercetin 3-O-.beta.-D-glucopyranoside; quercetin-3-O-beta-D-glucopyranoside; quercetin 3-(beta-D-glucofuranoside); quercetin 3-O-beta-D-glucopyranoside; 3-O-.BETA.-D-GLUCOPYRANOSYLQUERCETIN; quercetin 3-O-beta-D-glucofuranoside; Quercetin 3-beta-D-glucopyranoside; QUERCETIN-3-.BETA.-GLUCOPYRANOSIDE; quercetin-3-o-beta-glucopyranoside; 3-o-beta-d-glucopyranosylquercetin; Quercetin 3-O-β-D-glucopyranoside; Quercetin 3-O-b-D-glucopyranoside; quercetin-3-beta-glucopyranoside; QUERCETIN-3-O-.BETA.-D-GLUCOSIDE; 3-O-β-D-Glucopyranosylquercetin; Quercetin 3-β-D-glucopyranoside; Quercetin 3- beta -D-glucoside; quercetin 3-O-beta-D-glucoside; Quercetin-3-O-glucopyranoside; Quercetin-3-β-glucopyranoside; Quercetin 3-o-glucopyranoside; Quercetin 3-beta-O-glucoside; Quercetin 3-mono-D-glucoside; Quercetin 3-O-beta-glucoside; Quercetin 3-beta-D-glucoside; quercetin-3-O-beta-glucoside; Quercetin 3-O-β-D-glucoside; Quercetin 3beta-O-glucoside; Quercetin 3.beta.-glucoside; Quercetin 3-glucopyranoside; OVSQVDMCBVZWGM-QSOFNFLRSA-N; Quercetin 3-beta-glucoside; Quercetin 3-ss-D-glucoside; 3-beta-D-Glucosylquercetin; QUERCETIN 3beta-GLUCOSIDE; Quercetin 3-β-D-glucoside; Quercetol 3-monoglucoside; Quercetin 3-O-β-glucoside; 3-glucoside isoquercitrin; Quercetin 3-monoglucoside; Quercetin 3β-O-glucoside; Quercetin 3-D-glucoside; Quercetin 3-O-glucoside; quercetin-3-O-glucoside; 3-β-D-Glucosylquercetin; Quercetin 3β-glucoside; Ronacare isoquercetin; Quercetin 3-glucoside; Quercetol 3-glucoside; quercetin-3-glucoside; Glucosyl 3-quercetin; Glucosyl-3-quercetin; Quercetin-3-glucose; ISOQUERCETIN [INCI]; 3-Glucosylquercetin; quercetin glucoside; ISOQUERCITRIN [MI]; Isoquercetin, (-)-; (-)-Isoquercetrin; Isoquercitrin (6); isoquercitroside; UNII-6HN2PC637T; CONTIGOSIDE B; Isoquercetrin; Isoquercitrin; isoquercitin; PDSP1_001363; isotrifoliin; PDSP2_001347; Isoquercetin; ACon1_002134; trifoliin A; 6HN2PC637T; Hirsutrin; hydroside; trifoliin; Q 5; HW2; 2-(3,4-Dihidroxyphenyl)-3-(β-D-glucofuranosyloxy)-5,7-dihydroxy- 4H-1-benzopyran-4-one; Quercetin 3-O-glucoside



数据库引用编号

67 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

1 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(1)

PharmGKB(0)

347 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。



文献列表

  • Qi-Yang Wang, Hao-Yu Wang, Wei-Guo Zhang, Jian-Zhong Xu. Economical one-pot synthesis of isoquercetin and D-allulose from quercetin and sucrose using whole-cell biocatalyst. Enzyme and microbial technology. 2024 May; 176(?):110412. doi: 10.1016/j.enzmictec.2024.110412. [PMID: 38402828]
  • Tengfei Niu, Chaokang Huang, Rufeng Wang, Li Yang, Shujuan Zhao, Zhengtao Wang. Combinatorial metabolic engineering of Bacillus subtilis enables the efficient biosynthesis of isoquercitrin from quercetin. Microbial cell factories. 2024 Apr; 23(1):114. doi: 10.1186/s12934-024-02390-5. [PMID: 38641799]
  • Hong-Liu Jin, Xiao-Ying Feng, Sen-Ling Feng, Ling Dai, Wen-Ting Zhu, Zhong-Wen Yuan. Isoquercitrin attenuates the progression of non-alcoholic steatohepatitis in mice by modulating galectin-3-mediated insulin resistance and lipid metabolism. Phytomedicine : international journal of phytotherapy and phytopharmacology. 2024 Jan; 123(?):155188. doi: 10.1016/j.phymed.2023.155188. [PMID: 38056146]
  • Meijuan Yi, Opeyemi B Fasina, Yajing Li, Lan Xiang, Jianhua Qi. Mixture of Peanut Skin Extract, Geniposide, and Isoquercitrin Improves the Hepatic Lipid Accumulation of Mice via Modification of Gut Microbiota Homeostasis and the TLR4 and AMPK Signaling Pathways. International journal of molecular sciences. 2023 Nov; 24(23):. doi: 10.3390/ijms242316684. [PMID: 38069009]
  • Xinggu Luo, Yongqian Gong, Qingshan Jiang, Qin Wang, Songtao Li, Lijun Liu. Isoquercitrin promotes ferroptosis and oxidative stress in nasopharyngeal carcinoma via the AMPK/NF-κB pathway. Journal of biochemical and molecular toxicology. 2023 Sep; ?(?):e23542. doi: 10.1002/jbt.23542. [PMID: 37712196]
  • Muxin Zheng, Shenghao Chen, Yi Liu, Yang He. α-Glucosidase inhibitory activities of constituents from Psidium guajava leaves. Natural product research. 2023 Jul; ?(?):1-4. doi: 10.1080/14786419.2023.2238113. [PMID: 37506309]
  • Ye-Jin Moon, Hee-Seong Kim, Min-Ji Kim, Hyeon-Yeong Im, Yun-Hee Lee. Synergistic Effects of Heat-Treated Green Tea Extract and Enzymatically-Modified Isoquercitrin in Preventing Obesity. Nutrients. 2023 Jun; 15(13):. doi: 10.3390/nu15132931. [PMID: 37447257]
  • Mohamad Fawzi Mahomoodally, Gokhan Zengin, Seebaluck-Sandoram Roumita, Giovanni Caprioli, Ahmed M Mustafa, Diletta Piatti, Evren Yıldıztugay, Gunes Ak, Ayşe Esra Karadağ, Asaad Khalid, Ashraf N Abdalla, Abdullahi Ibrahim Uba, Fatih Demirci. Chemical Characterization and Multidirectional Biological Effects of Different Solvent Extracts of Arum elongatum: in Vitro and in Silico Approaches. Chemistry & biodiversity. 2023 Mar; ?(?):e202201181. doi: 10.1002/cbdv.202201181. [PMID: 36891864]
  • Sou Hyun Kim, Chawon Yun, Doyoung Kwon, Yun-Hee Lee, Jae-Hwan Kwak, Young-Suk Jung. Effect of Isoquercitrin on Free Fatty Acid-Induced Lipid Accumulation in HepG2 Cells. Molecules (Basel, Switzerland). 2023 Feb; 28(3):. doi: 10.3390/molecules28031476. [PMID: 36771140]
  • Jiang Liu, LiJun Ren, HaoWen Wang, Zuowei Li. Isoquercitrin Induces Endoplasmic Reticulum Stress and Immunogenic Cell Death in Gastric Cancer Cells. Biochemical genetics. 2022 Dec; ?(?):. doi: 10.1007/s10528-022-10309-1. [PMID: 36480095]
  • Majid Manzoor, Makoto Muroi, Naoko Ogawa, Hiroki Kobayashi, Haruna Nishimura, Danni Chen, Opeyemi B Fasina, Jianyu Wang, Hiroyuki Osada, Minoru Yoshida, Lan Xiang, Jianhua Qi. Isoquercitrin from Apocynum venetum L. produces an anti-obesity effect on obese mice by targeting C-1-tetrahydrofolate synthase, carbonyl reductase, and glutathione S-transferase P and modification of the AMPK/SREBP-1c/FAS/CD36 signaling pathway in mice in vivo. Food & function. 2022 Oct; 13(21):10923-10936. doi: 10.1039/d2fo02438a. [PMID: 36205648]
  • Xue Li, Dongyue Zhou, Di Yang, Yunhua Fu, Xingyu Tao, Xuan Hu, Yulin Dai, Hao Yue. Isoquercitrin Attenuates Osteogenic Injury in MC3T3 Osteoblastic Cells and the Zebrafish Model via the Keap1-Nrf2-ARE Pathway. Molecules (Basel, Switzerland). 2022 May; 27(11):. doi: 10.3390/molecules27113459. [PMID: 35684398]
  • Daisuke Takahashi, Eri Matsunaga, Tomohiro Yamashita, Jose M M Caaveiro, Yoshito Abe, Tadashi Ueda. Compound screening identified gossypetin and isoquercitrin as novel inhibitors for amyloid fibril formations of Vλ6 proteins associated with AL amyloidosis. Biochemical and biophysical research communications. 2022 03; 596(?):22-28. doi: 10.1016/j.bbrc.2022.01.066. [PMID: 35108650]
  • Fatma Kübra Ata, Fahriye Ercan, Serap Yalcin Azarkan. In vivo, in vitro and Molecular Modelling Analysis of Isoquercetin, Roseoside, Coreximine, Anonaine, and Arianacin Molecules. Current computer-aided drug design. 2022; 18(3):168-184. doi: 10.2174/1573409918666220509213313. [PMID: 35538817]
  • Shi-Chang Cai, Chuan-An Yi, Xiang-Shang Hu, Gen-Yun Tang, Li-Ming Yi, Xiu-Ping Li. Isoquercitrin Upregulates Aldolase C Through Nrf2 to Ameliorate OGD/R-Induced Damage in SH-SY5Y Cells. Neurotoxicity research. 2021 Dec; 39(6):1959-1969. doi: 10.1007/s12640-021-00430-1. [PMID: 34773594]
  • Edward Owen Norman, Stuart Hombsch, James Lever, Robert Brkljača, Jonathan White, Robin B Gasser, Aya C Taki, Sylvia Urban. Phytochemical Profiling and Biological Testing of the Constituents of the Australian Plant Haemodorum brevisepalum. Journal of natural products. 2021 11; 84(11):2832-2844. doi: 10.1021/acs.jnatprod.1c00509. [PMID: 34780692]
  • John Paul Sese Tosoc, Olga Macas Nuñeza, Thangirala Sudha, Noureldien H E Darwish, Shaker A Mousa. Anticancer Effects of the Corchorus olitorius Aqueous Extract and Its Bioactive Compounds on Human Cancer Cell Lines. Molecules (Basel, Switzerland). 2021 Oct; 26(19):. doi: 10.3390/molecules26196033. [PMID: 34641577]
  • Arti Nile, Shivraj Hariram Nile, Juhyun Shin, Gyunseok Park, Jae-Wook Oh. Quercetin-3-Glucoside Extracted from Apple Pomace Induces Cell Cycle Arrest and Apoptosis by Increasing Intracellular ROS Levels. International journal of molecular sciences. 2021 Oct; 22(19):. doi: 10.3390/ijms221910749. [PMID: 34639090]
  • Małgorzata Kikowska, Barbara Thiem, Karolina Jafernik, Marta Klimek-Szczykutowicz, Elżbieta Studzińska-Sroka, Halina Ekiert, Agnieszka Szopa. Effect of Elicitation with (+)-Usnic Acid on Accumulation of Phenolic Acids and Flavonoids in Agitated Microshoots of Eryngium alpinum L. Molecules (Basel, Switzerland). 2021 Sep; 26(18):. doi: 10.3390/molecules26185532. [PMID: 34577004]
  • Chan-Su Rha, Cheon-Seok Park, Dae-Ok Kim. Optimized enzymatic synthesis of digestive resistant anomalous isoquercitrin glucosides using amylosucrase and response surface methodology. Applied microbiology and biotechnology. 2021 Sep; 105(18):6931-6941. doi: 10.1007/s00253-021-11532-3. [PMID: 34477942]
  • Xu Pang, Mei Wang, Shuang-Yan Wang, Jie Zhang, Ya-Peng Du, Ye Zhao, Xiao-Hui Zheng, Bai-Ping Ma. Phenolic compounds from the leaves of Crataegus pinnatifida Bge. var. major N.E.Br. And their lipid-lowering effects. Bioorganic & medicinal chemistry letters. 2021 09; 47(?):128211. doi: 10.1016/j.bmcl.2021.128211. [PMID: 34157392]
  • Francesca Guzzo, Rosita Russo, Cinzia Sanna, Odeta Celaj, Alessia Caredda, Angela Corona, Enzo Tramontano, Antonio Fiorentino, Francesca Esposito, Brigida D'Abrosca. Chemical Characterization and Anti-HIV-1 Activity Assessment of Iridoids and Flavonols from Scrophularia trifoliata. Molecules (Basel, Switzerland). 2021 Aug; 26(16):. doi: 10.3390/molecules26164777. [PMID: 34443358]
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