Diosmin (BioDeep_00000270488)
Main id: BioDeep_00000000373
natural product PANOMIX_OTCML-2023 BioNovoGene_Lab2019
代谢物信息卡片
化学式: C28H32O15 (608.1741122)
中文名称: 地奥司明, 地奥斯明
谱图信息:
最多检出来源 Chinese Herbal Medicine(otcml) 6.45%
分子结构信息
SMILES: c1(cc(c2c(c1)oc(cc2=O)c1ccc(c(c1)O)OC)O)O[C@H]1[C@@H]([C@H]([C@@H]([C@H](O1)CO[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)C)O)O)O)O)O)O
InChI: InChI=1S/C28H32O15/c1-10-21(32)23(34)25(36)27(40-10)39-9-19-22(33)24(35)26(37)28(43-19)41-12-6-14(30)20-15(31)8-17(42-18(20)7-12)11-3-4-16(38-2)13(29)5-11/h3-8,10,19,21-30,32-37H,9H2,1-2H3/t10-,19+,21-,22+,23+,24-,25+,26+,27+,28+/m0/s1
描述信息
Diosmin is a disaccharide derivative that consists of diosmetin substituted by a 6-O-(alpha-L-rhamnopyranosyl)-beta-D-glucopyranosyl moiety at position 7 via a glycosidic linkage. It has a role as an antioxidant and an anti-inflammatory agent. It is a glycosyloxyflavone, a rutinoside, a disaccharide derivative, a monomethoxyflavone and a dihydroxyflavanone. It is functionally related to a diosmetin.
Chronic venous insufficiency is a common condition the western population. Compression and pharmacotherapy are frequently used to manage chronic venous insufficiency, improving circulation and symptoms of venous disease. Diosmin is a bioflavonoid isolated from various plants or synthesized from [hesperidin]. It is used for the improvement of capillary fragility or venous insufficiency, including chronic venous insufficiency (CVI) and hemorrhoids. Diosmin is widely available over-the-counter and demonstrates a favourable a favorable safety profile.
Diosmin is a natural product found in Asyneuma argutum, Citrus hystrix, and other organisms with data available.
A bioflavonoid that strengthens vascular walls.
See also: Agathosma betulina leaf (part of).
C - Cardiovascular system > C05 - Vasoprotectives > C05C - Capillary stabilizing agents > C05CA - Bioflavonoids
C26170 - Protective Agent > C275 - Antioxidant > C306 - Bioflavonoid
Diosmin is a flavonoid found in a variety of citrus fruits and also an agonist of the aryl hydrocarbon receptor (AhR).
Diosmin is a flavonoid found in a variety of citrus fruits and also an agonist of the aryl hydrocarbon receptor (AhR).
同义名列表
95 个代谢物同义名
5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-7-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-((((2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)methyl)tetrahydro-2H-pyran-2-yl)oxy)-4H-chromen-4-one; 5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-7-((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(((2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yloxy)methyl)tetrahydro-2H-pyran-2-yloxy)-4H-chromen-4-one; 5-hydroxy-2-(3-hydroxy-4-methoxy-phenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyl-tetrahydropyran-2-yl]oxymethyl]tetrahydropyran-2-yl]oxy-chromen-4-one; 5-HYDROXY-2-(3-HYDROXY-4-METHOXYPHENYL)-7-{[(2S,3R,4S,5S,6R)-3,4,5-TRIHYDROXY-6-({[(2R,3R,4R,5R,6S)-3,4,5-TRIHYDROXY-6-METHYLOXAN-2-YL]OXY}METHYL)OXAN-2-YL]OXY}-4H-CHROMEN-4-ONE; 5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one; 5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one; 4H-1-Benzopyran-4-one, 7-((6-O-(6-deoxy-.alpha.-L-mannopyranosyl)-.beta.-D-glucopyranosyl)oxy)-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-; 4H-1-Benzopyran-4-one, 7-[[6-O-(6-deoxy-.alpha.-L-mannopyranosyl)-.beta.-D-glucopyranosyl]oxy]-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-; 4H-1-Benzopyran-4-one, 7-((6-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranosyl)oxy)-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-; 7-((6-O-(6-DEOXY-GA-L-MANNOPYRANOSYL)-.BETA.-D-GLUCOPYRANOSYL)OXY)-5-HYDROXY-2-(3-HYDROXY-4-METHOXYPHENYL)-4H-1-BENZOPYRAN-4-ONE; 7-((6-O-(6-Deoxy-ga-L-mannopyranosyl)-beta-D-glucopyranosyl)oxy)-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-4H-1-benzopyran-4-one; 5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-4-oxo-4H-1-benzopyran-7-yl 6-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranoside; 4H-1-Benzopyran-4-one,7-[[6-O-(6-deoxy-a-L-mannopyranosyl)-b-D-glucopyranosyl]oxy]-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-; 5-Hydroxy-2-(3-hydroxy-4-methoxyphenyl)-7-((6-O-alpha-L-rhamnopyranosyl-beta-D-glycopyranosyl)oxy)-4-chromenon; 5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-7-(O6-alpha-L-rhamnopyranosyl-beta-D-glucopyranosyloxy)chromen-4-one; 3,5,7-Trihydroxy-4-methoxyflavone-7-(6-O-(-deoxy-alpha-L-mannopyraonsyl)-beta-D-glucopyranoside; Diosmin for system suitability, European Pharmacopoeia (EP) Reference Standard; 3,5-Dihydroxy-4-methoxy-4-oxo-4H-chromen-7-ylrutosid (IUPAC); Diosmin, United States Pharmacopeia (USP) Reference Standard; 3,5-Dihydroxy-4-methoxy-4-oxo-4H-chromen-7-ylrutosid [IUPAC]; Diosmin, European Pharmacopoeia (EP) Reference Standard; 3,5-Dihydroxy-4-methoxy-4-oxo-4H-chromen-7-ylrutosid; 3,5,7-trihydroxy-4-methoxyflavone 7-rhamnoglucoside; 3,5,7-Trihydroxy-4-methoxyflavone 7-rutinoside;; 3,5,7-trihydroxy-4-methoxy flavone-7-rutinoside; 3,5,7-trihydroxy-4-methoxyflavone-7-rutinoside; 3,5,7-Trihydroxy-4-methoxyflavone 7-rutinoside; Luteolin 4-methyl ether 7-rutinoside; Diosmin, analytical standard; Diosmetin-7-O-rutinoside; Diosmetin 7-O-rutinoside; DIOSMIN [EP MONOGRAPH]; Diosmetin 7-rutinoside; DIOSMIN (EP MONOGRAPH); Diosmine [INN-French]; Diosminum [INN-Latin]; Diosmin [INN-Spanish]; Diosmin [INN:BAN]; DIOSMIN (USP-RS); DIOSMIN [WHO-DD]; DIOSMIN [USP-RS]; DIOSMINE [INCI]; UNII-7QM776WJ5N; DIOSMIN [MART.]; DIOSMIN (MART.); Tox21_111392_1; Diosmin [INN]; Diosmin (INN); DIOSMIN [DSC]; Tox21_111392; DIOSMIN [MI]; Resin, Buchu; Diosmin (8); SMP1_000183; Daflon (TN); Buchu Resin; Ven-Detrex; 7QM776WJ5N; Flebosten; Venosmine; Diosminum; Flebavena; flebosmil; Diosmina; Diosmine; Litosmil; Flebaven; Barosmin; Diosimin; Diovenor; Hemerven; Diosmin; Diosmil; Insuven; Varinon; Diosven; C05CA03; Rioven; Dioven; Daflon; Veno-V; Tovene; 5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-7-[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyl-2-tetrahydropyranyl]oxymethyl]-2-tetrahydropyranyl]oxy]-4-chromenone; 5-hydroxy-2-(3-hydroxy-4-methoxy-phenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyl-tetrahydropyran-2-yl]oxymethyl]tetrahydropyran-2-yl]oxy-chromone; 5-hydroxy-2-(3-hydroxy-4-methoxy-phenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyl-oxan-2-yl]oxymethyl]oxan-2-yl]oxy-chromen-4-one; 4H-1-Benzopyran-4-one, 7-((6-O-(6-deoxy-.alpha.-L-mannopyranosyl)-.beta.- D-glucopyranosyl)oxy)-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-; EINECS 208-289-7; STOCK1N-14729; AIDS-059330; CCRIS 7915; AIDS059330; 520-27-4; C10039; 5,7,3-Trihydroxy-4-methoxyflavone 7-rhamnosyl- (1->6) -glucoside; 5,7,3-Trihydroxy-4-methoxyflavone 7-O-rutinoside
数据库引用编号
53 个数据库交叉引用编号
- ChEBI: CHEBI:4631
- KEGG: C10039
- KEGGdrug: D07858
- PubChem: 5281613
- DrugBank: DB08995
- ChEMBL: CHEMBL231884
- Wikipedia: Diosmin
- LipidMAPS: LMPK12110814
- MeSH: Diosmin
- ChemIDplus: 0000520274
- KNApSAcK: C00004362
- chemspider: 4444932
- CAS: 28680-33-3
- CAS: 520-27-4
- MoNA: VF-NPL-QTOF007520
- MoNA: VF-NPL-QTOF007519
- MoNA: VF-NPL-QTOF007518
- MoNA: VF-NPL-QTOF007517
- MoNA: VF-NPL-QTOF007516
- MoNA: VF-NPL-QTOF007515
- MoNA: VF-NPL-QTOF007514
- MoNA: VF-NPL-QTOF007513
- MoNA: VF-NPL-QTOF007512
- MoNA: VF-NPL-LTQ006696
- MoNA: VF-NPL-LTQ006694
- MoNA: VF-NPL-LTQ006693
- MoNA: VF-NPL-QEHF011460
- MoNA: VF-NPL-QEHF011459
- MoNA: VF-NPL-QEHF011458
- MoNA: VF-NPL-QEHF011457
- MoNA: VF-NPL-QEHF011456
- MoNA: VF-NPL-QEHF011455
- MoNA: VF-NPL-QEHF011454
- MoNA: VF-NPL-QEHF011453
- MoNA: VF-NPL-QEHF011452
- MoNA: VF-NPL-QEHF011451
- MoNA: VF-NPL-QEHF011450
- MoNA: VF-NPL-QEHF011449
- MoNA: VF-NPL-QEHF011448
- MoNA: VF-NPL-QEHF011447
- MoNA: VF-NPL-QEHF011446
- MoNA: PM009108
- MoNA: MetaboBASE0260
- MoNA: MetaboBASE0259
- MoNA: MetaboBASE0258
- medchemexpress: HY-N0178
- PMhub: MS000057620
- Flavonoid: FL3FAEGS0006
- PubChem: 12225
- 3DMET: B03482
- NIKKAJI: J6.600A
- RefMet: Diosmin
- BioNovoGene_Lab2019: BioNovoGene_Lab2019-855
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)
43 个相关的物种来源信息
- 97171 - Abies nephrolepis: 10.1002/CBDV.201000373
- 501610 - Agathosma betulina: 10.1016/S0731-7085(01)00476-9
- 85712 - Angelica gigas: 10.1016/S0031-9422(98)00342-2
- 1241007 - Asyneuma argutum: 10.1007/BF00570867
- 361369 - Asyneuma campanuloides: 10.1007/BF00570867
- 440359 - Campanula patula: 10.1007/BF01134637
- 239416 - Campanula persicifolia: 10.1007/BF00598373
- 558547 - Citrus deliciosa:
- 1766678 - Citrus excelsa: 10.1016/0031-9422(93)85237-L
- 76963 - Citrus glauca: 10.1016/0031-9422(93)85237-L
- 170989 - Citrus hystrix: 10.1016/0031-9422(93)85237-L
- 64884 - Citrus jambhiri: 10.1016/0031-9422(93)85237-L
- 481548 - Citrus longispina: 10.1016/0031-9422(93)85237-L
- 37334 - Citrus maxima: 10.1016/0021-9673(94)89051-X
- 171251 - Citrus medica: 10.1016/0031-9422(93)85237-L
- 171251 - Citrus medica L.var.sarcodactylis Swingle: -
- 85571 - Citrus reticulata:
- 488172 - Citrus tamurana: 10.1016/0031-9422(93)85237-L
- 55188 - Citrus unshiu: 10.1016/0021-9673(94)89051-X
- 481550 - Citrus webberi: 10.1016/0031-9422(93)85237-L
- 261776 - Helichrysum arenarium: 10.1007/S10600-010-9462-3
- 39324 - Hyssopus officinalis:
- 2500775 - Linaria macroura: 10.1007/BF00579788
- 672825 - Meehania urticifolia: 10.1007/S11418-010-0501-Y
- 21819 - Mentha:
- 29719 - Mentha spicata: 10.1016/S0031-9422(00)90052-9
- 33090 - Plants: -
- 368691 - Pratia nummularia: 10.5772/INTECHOPEN.75648
- 21880 - Salvia: 10.1021/JF040078P
- 184140 - Sicyos edulis: 10.1021/JF040214Q
- 2839963 - Zanthoxylum asiaticum: 10.1016/S0031-9422(00)97163-2
- 354528 - Zanthoxylum Nitidum: -
- 354528 - 两面针: -
- 380129 - 佛手: -
- 33090 - 半边莲: -
- 33090 - 海金沙: -
- 33090 - 玄参: -
- 4047 - 芫荽: -
- 33090 - 花椒: -
- 33090 - 荠菜: -
- 13422 - 菊花: -
- 33090 - 薄荷: -
- 569774 - 金线莲: -
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
- Yinai Deng, Peng Yang, Qianle Zhang, Qingwen Wu, Lingfang Feng, Wenjing Shi, Qian Peng, Li Ding, Xukai Tan, Ruoting Zhan, Dongming Ma. Genomic insights into the evolution of flavonoid biosynthesis and O-methyltransferase and glucosyltransferase in Chrysanthemum indicum.
Cell reports.
2024 Jan; 43(2):113725. doi:
10.1016/j.celrep.2024.113725
. [PMID: 38300800] - Kaushal Vyas, Supraja Prabaker, Dhamodharan Prabhu, Meenakumari Sakthivelu, Sundararaj Rajamanikandan, Palaniyandi Velusamy, Chia-Hung Su, Subash C B Gopinath, Raman Pachaiappan. Study of an inhibitory effect of plant polyphenolic compounds against digestive enzymes using bench-working experimental evidence predicted by molecular docking and dynamics.
International journal of biological macromolecules.
2024 Jan; 259(Pt 1):129222. doi:
10.1016/j.ijbiomac.2024.129222
. [PMID: 38185307] - Jingwei Zhao, Mingming Zhang, Huamin Zhang, Ying Wang, Bingyu Chen, Jing Shao. Diosmin ameliorates LPS-induced depression-like behaviors in mice: Inhibition of inflammation and oxidative stress in the prefrontal cortex.
Brain research bulletin.
2024 Jan; 206(?):110843. doi:
10.1016/j.brainresbull.2023.110843
. [PMID: 38092305] - Clare Njoki Kimani, Helmuth Reuter, Sanet Henriët Kotzé, Pieter Venter, Pritika Ramharack, Christo John Frederick Muller. Pancreatic beta cell regenerative potential of Zanthoxylum chalybeum Engl. Aqueous stem bark extract.
Journal of ethnopharmacology.
2023 Nov; ?(?):117374. doi:
10.1016/j.jep.2023.117374
. [PMID: 37944876] - Mehdi Rahimmalek, Antoni Szumny, Shima Gharibi, Natalia Pachura, Mehran Miroliaei, Jacek Łyczko. Chemical Investigations in Kelussia odoratissima Mozaff. Leaves Based on Comprehensive Analytical Methods: LC-MS, SPME, and GC-MS Analyses.
Molecules (Basel, Switzerland).
2023 Aug; 28(16):. doi:
10.3390/molecules28166140
. [PMID: 37630391] - Marcin Feldo, Magdalena Wójciak, Sławomir Dresler, Paweł Sowa, Bartosz J Płachno, Dariusz Samborski, Ireneusz Sowa. Effect of Diosmin on Selected Parameters of Oxygen Homeostasis.
International journal of molecular sciences.
2023 Aug; 24(16):. doi:
10.3390/ijms241612917
. [PMID: 37629098] - K S Kiran, Vivek Hamse Kameshwar, Kiran Kumar Munakudu-Nagaraju, P Nagalambika, R Kavitha, Avathade Karthick, D Guru Kumar, S Nanjunda Swamy, K L Krishna, J R Kumar. Diosmin: A Daboia russelii venom PLA2s inhibitor- purified, and characterized from Oxalis corniculata L medicinal plant.
Journal of ethnopharmacology.
2023 Aug; ?(?):116977. doi:
10.1016/j.jep.2023.116977
. [PMID: 37544341] - Lukasz Gwozdzinski, Joanna Bernasinska-Slomczewska, Anna Wiktorowska-Owczarek, Edward Kowalczyk, Anna Pieniazek. Diosmin and Bromelain Stimulate Glutathione and Total Thiols Production in Red Blood Cells.
Molecules (Basel, Switzerland).
2023 Mar; 28(5):. doi:
10.3390/molecules28052291
. [PMID: 36903535] - Tarique Anwer, Saeed Alshahrani, Ahmad M H Somaili, Abdullah H Khubrani, Rayan A Ahmed, Abdulmajeed M Jali, Ayed Alshamrani, Hina Rashid, Yousra Nomeir, Mohammad Khalid, Mohammad Firoz Alam. Nephroprotective Effect of Diosmin against Cisplatin-Induced Kidney Damage by Modulating IL-1β, IL-6, TNFα and Renal Oxidative Damage.
Molecules (Basel, Switzerland).
2023 Jan; 28(3):. doi:
10.3390/molecules28031302
. [PMID: 36770968] - Seyed Sajad Hossieni Geshnigani, Masoud Mahdavinia, Mojtaba Kalantar, Mehdi Goudarzi, Layasadat Khorsandi, Hadi Kalantar. Diosmin prophylaxis reduces gentamicin-induced kidney damage in rats.
Naunyn-Schmiedeberg's archives of pharmacology.
2023 01; 396(1):63-71. doi:
10.1007/s00210-022-02295-3
. [PMID: 36121447] - Qing-Wen Wu, Min Wei, Ling-Fang Feng, Li Ding, Wu-Ke Wei, Jin-Fen Yang, Xiao-Jing Lin, Hui-Lin Liang, Ruo-Ting Zhan, Dong-Ming Ma. Rhamnosyltransferases involved in the biosynthesis of flavone rutinosides in Chrysanthemum species.
Plant physiology.
2022 11; 190(4):2122-2136. doi:
10.1093/plphys/kiac371
. [PMID: 35947689] - Magdalena Wójciak, Marcin Feldo, Grzegorz Borowski, Tomasz Kubrak, Bartosz J Płachno, Ireneusz Sowa. Antioxidant Potential of Diosmin and Diosmetin against Oxidative Stress in Endothelial Cells.
Molecules (Basel, Switzerland).
2022 Nov; 27(23):. doi:
10.3390/molecules27238232
. [PMID: 36500323] - Johirul Islam, Alpa Shree, Haider Ali Khan, Sarwat Sultana. Chemopreventive potential of Diosmin against benzo[a]pyrene induced lung carcinogenesis in Swiss Albino mice.
Journal of biochemical and molecular toxicology.
2022 Nov; 36(11):e23187. doi:
10.1002/jbt.23187
. [PMID: 35920545] - Piyush Kashyap, Mamta Thakur, Nidhi Singh, Deep Shikha, Shiv Kumar, Poonam Baniwal, Yogender Singh Yadav, Minaxi Sharma, Kandi Sridhar, Baskaran Stephen Inbaraj. In Silico Evaluation of Natural Flavonoids as a Potential Inhibitor of Coronavirus Disease.
Molecules (Basel, Switzerland).
2022 Sep; 27(19):. doi:
10.3390/molecules27196374
. [PMID: 36234910] - Rosa Martha Pérez Gutiérrez, Julio Téllez Gómez, Raúl Borja Urby, José G Contreras Soto, Héctor Romo Parra. Evaluation of Diabetes Effects of Selenium Nanoparticles Synthesized from a Mixture of Luteolin and Diosmin on Streptozotocin-Induced Type 2 Diabetes in Mice.
Molecules (Basel, Switzerland).
2022 Sep; 27(17):. doi:
10.3390/molecules27175642
. [PMID: 36080407] - Hasnaa Osama, Ehdaa O Hamed, Muhammed A Mahmoud, Mohamed E A Abdelrahim. The Effect of Hesperidin and Diosmin Individually or in Combination on Metabolic Profile and Neuropathy among Diabetic Patients with Metabolic Syndrome: A Randomized Controlled Trial.
Journal of dietary supplements.
2022 Aug; ?(?):1-14. doi:
10.1080/19390211.2022.2107138
. [PMID: 35946912] - Marcin Feldo, Magdalena Wójciak, Aleksandra Ziemlewska, Sławomir Dresler, Ireneusz Sowa. Modulatory Effect of Diosmin and Diosmetin on Metalloproteinase Activity and Inflammatory Mediators in Human Skin Fibroblasts Treated with Lipopolysaccharide.
Molecules (Basel, Switzerland).
2022 Jul; 27(13):. doi:
10.3390/molecules27134264
. [PMID: 35807509] - Jiuhong Deng, Chao Zheng, Zhou Hua, Haideng Ci, Guiying Wang, Lijing Chen. Diosmin mitigates high glucose-induced endoplasmic reticulum stress through PI3K/AKT pathway in HK-2 cells.
BMC complementary medicine and therapies.
2022 Apr; 22(1):116. doi:
10.1186/s12906-022-03597-y
. [PMID: 35477428] - Dinesh Kumar, M S Ladaniya, Manju Gurjar, Sunil Kumar. Impact of drying methods on natural antioxidants, phenols and flavanones of immature dropped Citrus sinensis L. Osbeck fruits.
Scientific reports.
2022 04; 12(1):6684. doi:
10.1038/s41598-022-10661-7
. [PMID: 35461355] - Shivani Sharma, Konica Porwal, Chirag Kulkarni, Subhashis Pal, Praveer Sihota, Saroj Kumar, Mahesh Chandra Tiwari, Roshan Katekar, Ashish Kumar, Priya Singh, Swati Rajput, Rajdeep Guha, Navin Kumar, Jiaur R Gayen, Naibedya Chattopadhyay. Diosmin, a citrus fruit-derived phlebotonic bioflavonoid protects rats from chronic kidney disease-induced loss of bone mass and strength without deteriorating the renal function.
Food & function.
2022 Feb; 13(4):2184-2199. doi:
10.1039/d1fo03867b
. [PMID: 35119062] - Samar H Gerges, Sara A Wahdan, Doaa A Elsherbiny, Ebtehal El-Demerdash. Pharmacology of Diosmin, a Citrus Flavone Glycoside: An Updated Review.
European journal of drug metabolism and pharmacokinetics.
2022 Jan; 47(1):1-18. doi:
10.1007/s13318-021-00731-y
. [PMID: 34687440] - Nicolas Monjotin, Guillaume Tenca. Lymphotonic activity of Ruscus extract, hesperidin methyl chalcone and vitamin C in human lymphatic smooth muscle cells.
Microvascular research.
2022 01; 139(?):104274. doi:
10.1016/j.mvr.2021.104274
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Methods (San Diego, Calif.).
2021 11; 195(?):44-56. doi:
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Proteins.
2021 11; 89(11):1425-1441. doi:
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Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.
2021 Sep; 141(?):111903. doi:
10.1016/j.biopha.2021.111903
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Experimental parasitology.
2021 Jul; 226-227(?):108124. doi:
10.1016/j.exppara.2021.108124
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Life sciences.
2021 Jun; 275(?):119349. doi:
10.1016/j.lfs.2021.119349
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Environmental science and pollution research international.
2021 Apr; 28(13):15890-15908. doi:
10.1007/s11356-020-11277-y
. [PMID: 33242198] - Michèle Cazaubon, Jean-Patrick Benigni, Marcio Steinbruch, Violaine Jabbour, Christelle Gouhier-Kodas. Is There a Difference in the Clinical Efficacy of Diosmin and Micronized Purified Flavonoid Fraction for the Treatment of Chronic Venous Disorders? Review of Available Evidence.
Vascular health and risk management.
2021; 17(?):591-600. doi:
10.2147/vhrm.s324112
. [PMID: 34556990] - Kushagra Dubey, Raghvendra Dubey, Revathi Gupta, Arun Gupta. Exploration of Diosmin to Control Diabetes and Its Complications-an In Vitro and In Silico Approach.
Current computer-aided drug design.
2021; 17(2):307-313. doi:
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BioMed research international.
2021; 2021(?):3508281. doi:
10.1155/2021/3508281
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The journal of physical chemistry letters.
2020 Nov; 11(21):9272-9281. doi:
10.1021/acs.jpclett.0c02203
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The Cochrane database of systematic reviews.
2020 11; 11(?):CD003229. doi:
10.1002/14651858.cd003229.pub4
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Medical hypotheses.
2020 Nov; 144(?):109957. doi:
10.1016/j.mehy.2020.109957
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Food & function.
2020 Oct; 11(10):8472-8492. doi:
10.1039/d0fo01598a
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Investigational new drugs.
2020 10; 38(5):1303-1315. doi:
10.1007/s10637-020-00905-6
. [PMID: 32048108] - Samar H Gerges, Sara A Wahdan, Doaa A Elsherbiny, Ebtehal El-Demerdash. Diosmin ameliorates inflammation, insulin resistance, and fibrosis in an experimental model of non-alcoholic steatohepatitis in rats.
Toxicology and applied pharmacology.
2020 08; 401(?):115101. doi:
10.1016/j.taap.2020.115101
. [PMID: 32512072] - Johirul Islam, Alpa Shree, Shekh M Afzal, Abul Vafa, Sarwat Sultana. Protective effect of Diosmin against benzo(a)pyrene-induced lung injury in Swiss Albino Mice.
Environmental toxicology.
2020 Jul; 35(7):747-757. doi:
10.1002/tox.22909
. [PMID: 32061149] - Shahenda Mahgoub, Anas O Sallam, Hazem K A Sarhan, Amal A A Ammar, Sameh H Soror. Role of Diosmin in protection against the oxidative stress induced damage by gamma-radiation in Wistar albino rats.
Regulatory toxicology and pharmacology : RTP.
2020 Jun; 113(?):104622. doi:
10.1016/j.yrtph.2020.104622
. [PMID: 32087353] - Sara Mahmmoud El-Dakhly, Abeer Abdallah Ali Salama, Soha Osama Mahmoud Hassanin, Noha Nazeeh Yassen, Alaaeldin Ahmed Hamza, Amr Amin. Aescin and diosmin each alone or in low dose- combination ameliorate liver damage induced by carbon tetrachloride in rats.
BMC research notes.
2020 May; 13(1):259. doi:
10.1186/s13104-020-05094-2
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Naunyn-Schmiedeberg's archives of pharmacology.
2020 04; 393(4):639-649. doi:
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. [PMID: 31792554] - Mengxia Wei, Ru Zhao, Xiaojin Peng, Chunte Feng, Huiyan Gu, Lei Yang. Ultrasound-Assisted Extraction of Taxifolin, Diosmin, and Quercetin from Abies nephrolepis (Trautv.) Maxim: Kinetic and Thermodynamic Characteristics.
Molecules (Basel, Switzerland).
2020 Mar; 25(6):. doi:
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The American journal of the medical sciences.
2020 01; 359(1):32-41. doi:
10.1016/j.amjms.2019.10.005
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Pakistan journal of pharmaceutical sciences.
2020 Jan; 33(1):33-40. doi:
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Environmental science and pollution research international.
2019 Dec; 26(34):35151-35162. doi:
10.1007/s11356-019-06660-3
. [PMID: 31686333] - Sirus Mirzaee, Esrafil Mansouri, Maryam Shirani, Marzieh Zeinvand-Lorestani, Mohammad Javad Khodayar. Diosmin ameliorative effects on oxidative stress and fibrosis in paraquat-induced lung injury in mice.
Environmental science and pollution research international.
2019 Dec; 26(36):36468-36477. doi:
10.1007/s11356-019-06572-2
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Naunyn-Schmiedeberg's archives of pharmacology.
2019 12; 392(12):1523-1536. doi:
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Molecules (Basel, Switzerland).
2019 Sep; 24(18):. doi:
10.3390/molecules24183316
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Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.
2019 Aug; 1124(?):58-71. doi:
10.1016/j.jchromb.2019.05.030
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Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy.
2019 Aug; 219(?):1-7. doi:
10.1016/j.saa.2019.04.026
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Current topics in medicinal chemistry.
2019; 19(29):2658-2675. doi:
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Molecular and cellular biochemistry.
2018 Dec; 449(1-2):27-37. doi:
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Journal of controlled release : official journal of the Controlled Release Society.
2018 10; 287(?):78-93. doi:
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Molecules (Basel, Switzerland).
2018 Aug; 23(9):. doi:
10.3390/molecules23092174
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Pakistan journal of pharmaceutical sciences.
2018 Jul; 31(4):1191-1201. doi:
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Revista brasileira de enfermagem.
2018 Jul; 71(4):1921-1927. doi:
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. [PMID: 30156678] - Rania El-Fawal, Hassan M El Fayoumi, Mona F Mahmoud. Diosmin and crocin alleviate nephropathy in metabolic syndrome rat model: Effect on oxidative stress and low grade inflammation.
Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.
2018 Jun; 102(?):930-937. doi:
10.1016/j.biopha.2018.03.162
. [PMID: 29710548] - S Sharmila Queenthy, P Stanely Mainzen Prince, Babu John. Diosmin Prevents Isoproterenol-Induced Heart Mitochondrial Oxidative Stress in Rats.
Cardiovascular toxicology.
2018 04; 18(2):120-130. doi:
10.1007/s12012-017-9422-2
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Ultrasound in medicine & biology.
2018 02; 44(2):359-367. doi:
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Naunyn-Schmiedeberg's archives of pharmacology.
2018 Feb; 391(2):115-121. doi:
10.1007/s00210-017-1439-3
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Oxidative medicine and cellular longevity.
2018; 2018(?):2561705. doi:
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Angiologiia i sosudistaia khirurgiia = Angiology and vascular surgery.
2018 ; 24(4):72-74. doi:
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Molecules (Basel, Switzerland).
2017 Dec; 22(12):. doi:
10.3390/molecules22122251
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Environmental science and pollution research international.
2017 Dec; 24(36):27931-27941. doi:
10.1007/s11356-017-0232-7
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International journal of biological macromolecules.
2017 Nov; 104(Pt A):778-787. doi:
10.1016/j.ijbiomac.2017.06.045
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Xenobiotica; the fate of foreign compounds in biological systems.
2017 Oct; 47(10):879-884. doi:
10.1080/00498254.2016.1244368
. [PMID: 27690733] - Weronika Wojnar, Ilona Kaczmarczyk-Sedlak, Maria Zych. Diosmin ameliorates the effects of oxidative stress in lenses of streptozotocin-induced type 1 diabetic rats.
Pharmacological reports : PR.
2017 Oct; 69(5):995-1000. doi:
10.1016/j.pharep.2017.04.005
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Nutrients.
2017 Jun; 9(7):. doi:
10.3390/nu9070684
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Clinical and experimental pharmacology & physiology.
2017 May; 44(5):549-555. doi:
10.1111/1440-1681.12739
. [PMID: 28218955] - Satish Kumar Bedada, Praveen Kumar Boga, Harish Kaushik Kotakonda. The effect of diosmin on the pharmacokinetics of fexofenadine in healthy human volunteers.
Xenobiotica; the fate of foreign compounds in biological systems.
2017 Mar; 47(3):230-235. doi:
10.1080/00498254.2016.1180564
. [PMID: 27151911] - Anna Lewinska, Jagoda Adamczyk-Grochala, Ewa Kwasniewicz, Anna Deregowska, Maciej Wnuk. Diosmin-induced senescence, apoptosis and autophagy in breast cancer cells of different p53 status and ERK activity.
Toxicology letters.
2017 Jan; 265(?):117-130. doi:
10.1016/j.toxlet.2016.11.018
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Annals of vascular surgery.
2017 Jan; 38(?):212-219. doi:
10.1016/j.avsg.2016.04.014
. [PMID: 27521821] - Mohamed M Abdel-Daim, Hesham A Khalifa, Abdelrahman Ibrahim Abushouk, Mohamed A Dkhil, Saleh A Al-Quraishy. Diosmin Attenuates Methotrexate-Induced Hepatic, Renal, and Cardiac Injury: A Biochemical and Histopathological Study in Mice.
Oxidative medicine and cellular longevity.
2017; 2017(?):3281670. doi:
10.1155/2017/3281670
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Inflammation.
2016 Oct; 39(5):1783-97. doi:
10.1007/s10753-016-0413-4
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Bioorganic & medicinal chemistry.
2016 09; 24(18):4108-4119. doi:
10.1016/j.bmc.2016.06.053
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Pharmaceutical biology.
2016 Sep; 54(9):1513-21. doi:
10.3109/13880209.2015.1107105
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The Cochrane database of systematic reviews.
2016 Apr; 4(?):CD003229. doi:
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Ginekologia polska.
2015 Dec; 86(12):962-5. doi:
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Natural product communications.
2015 Sep; 10(9):1569-72. doi:
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Chemical biology & drug design.
2015 May; 85(5):574-85. doi:
10.1111/cbdd.12445
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Pharmacological reports : PR.
2015 Apr; 67(2):339-44. doi:
10.1016/j.pharep.2014.09.010
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Toxicology in vitro : an international journal published in association with BIBRA.
2015 Apr; 29(3):417-25. doi:
10.1016/j.tiv.2014.12.005
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PloS one.
2015; 10(3):e0122417. doi:
10.1371/journal.pone.0122417
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International journal of pharmaceutics.
2014 Oct; 473(1-2):407-13. doi:
10.1016/j.ijpharm.2014.07.017
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Diabetes research and clinical practice.
2014 Sep; 105(3):373-81. doi:
10.1016/j.diabres.2014.04.029
. [PMID: 24956965] - Oomaidurai Senthamizhselvan, Jeganathan Manivannan, Thangarasu Silambarasan, Boobalan Raja. Diosmin pretreatment improves cardiac function and suppresses oxidative stress in rat heart after ischemia/reperfusion.
European journal of pharmacology.
2014 Aug; 736(?):131-7. doi:
10.1016/j.ejphar.2014.04.026
. [PMID: 24769512] - Giulia Milano, Silvia Leone, Carmen Fucile, Maria Laura Zuccoli, Andrea Stimamiglio, Antonietta Martelli, Francesca Mattioli. Uncommon serum creatine phosphokinase and lactic dehydrogenase increase during diosmin therapy: two case reports.
Journal of medical case reports.
2014 Jun; 8(?):194. doi:
10.1186/1752-1947-8-194
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Andrologia.
2014 May; 46(4):380-5. doi:
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Research in veterinary science.
2014 Feb; 96(1):139-42. doi:
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Journal of integrative medicine.
2014 Jan; 12(1):35-41. doi:
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Bosnian journal of basic medical sciences.
2013 Nov; 13(4):218-24. doi:
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Biochimie.
2013 Nov; 95(11):2042-9. doi:
10.1016/j.biochi.2013.07.014
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European journal of pharmacology.
2013 Oct; 718(1-3):213-8. doi:
10.1016/j.ejphar.2013.08.031
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Journal of ocular pharmacology and therapeutics : the official journal of the Association for Ocular Pharmacology and Therapeutics.
2013 Oct; 29(8):733-7. doi:
10.1089/jop.2013.0010
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The British journal of nutrition.
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