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
化学式: C21H20O12 (464.0955)
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) 32.7%
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
2024-12-22) (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
- ChEBI: CHEBI:68352
- KEGG: C05623
- PubChem: 5280804
- HMDB: HMDB0037362
- Metlin: METLIN64227
- DrugBank: DB12665
- ChEMBL: CHEMBL250450
- Wikipedia: Isoquercetin
- LipidMAPS: LMPK12112086
- MeSH: isoquercitrin
- ChemIDplus: 0000482359
- MetaCyc: CPD1F-437
- KNApSAcK: C00005373
- foodb: FDB016389
- chemspider: 4444361
- CAS: 21637-25-2
- CAS: 482-35-9
- MoNA: PS043312
- MoNA: FIO00164
- MoNA: PS043302
- MoNA: PS043307
- MoNA: PS043303
- MoNA: FIO00168
- MoNA: RP017111
- MoNA: PR040186
- MoNA: PR040187
- MoNA: PR040185
- MoNA: PS043306
- MoNA: PR100254
- MoNA: PR040184
- MoNA: FIO00162
- MoNA: PR040182
- MoNA: PS043310
- MoNA: PS043311
- MoNA: RP017102
- MoNA: FIO00161
- MoNA: FIO00160
- MoNA: PR100677
- MoNA: PR020078
- MoNA: PS043309
- MoNA: FIO00163
- MoNA: FIO00165
- MoNA: FIO00167
- MoNA: RP017101
- MoNA: RP017113
- MoNA: RP017103
- MoNA: FIO00169
- MoNA: PR040188
- MoNA: PR040181
- MoNA: PS043304
- MoNA: PS043305
- MoNA: PS043301
- MoNA: RP017112
- MoNA: PR040183
- MoNA: FIO00166
- MoNA: PS043308
- medchemexpress: HY-N1445
- medchemexpress: HY-N0768
- MetaboLights: MTBLC68352
- ChEBI: CHEBI:28299
- PDB-CCD: HW2
- 3DMET: B01878
- NIKKAJI: J11.252F
- RefMet: Isoquercitrin
- BioNovoGene_Lab2019: BioNovoGene_Lab2019-699
- PubChem: 7940
- KNApSAcK: 28299
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)
- Flavone and Flavonol Biosynthesis:
Phosphoadenosine phosphosulfate + Quercetin ⟶ Adenosine 3',5'-diphosphate + Hydrogen Ion + Quercetin 3'-sulfate
PharmGKB(0)
347 个相关的物种来源信息
- 183220 - Abelmoschus manihot (L)Medic.: -
- 97171 - Abies nephrolepis: 10.1002/CBDV.201000373
- 281911 - Acaena magellanica: 10.1211/0022357021779014
- 720869 - Acalypha australis: 10.1007/S10600-012-0285-2
- 478095 - Acalypha indica: 10.1002/JCCS.199700075
- 171204 - Acer barbinerve: 10.1007/S10600-011-0016-0
- 168564 - Acer mandshuricum: 10.5012/BKCS.2010.31.04.929
- 165710 - Actinidia kolomikta: 10.1007/S10600-010-9569-6
- 4243 - Adenothamnus validus: 10.1016/0031-9422(88)87035-3
- 290911 - Aesculus chinensis: 10.1021/NP030470H
- 49175 - Agarista salicifolia: 10.1016/J.CHROMA.2007.03.038
- 57912 - Agrimonia eupatoria: 10.1271/BBB.100200
- 74656 - Agrimonia pilosa: 10.1016/J.PHYTOCHEM.2010.08.007
- 16897 - Alangium chinense: 10.1021/NP990391Z
- 60116 - Alangium platanifolium: 10.1016/0031-9422(93)85414-M
- 4679 - Allium cepa:
- 74896 - Allium neapolitanum: 10.1016/S0031-9422(96)00663-2
- 88845 - Allium victorialis: 10.1016/J.BMCL.2012.10.043
- 56196 - Amaranthus viridis: 10.1055/S-0033-1352389
- 386051 - Ammoides pusilla: 10.1007/S10600-005-0085-Z
- 1209471 - Anaphalis sinica: 10.1002/JCCS.200400063
- 256470 - Anchusa azurea: 10.1002/HLCA.200900230
- 13339 - Apocynum cannabinum:
- 377125 - Apocynum venetum:
- 3702 - Arabidopsis thaliana: 10.1104/PP.109.148031
- 3818 - Arachis hypogaea: 10.1021/JF703652A
- 13345 - Ardisia crenata: 10.3389/FMOLB.2021.683671
- 1006429 - Ardisia sanguinolenta: 10.1248/CPB.50.1484
- 99325 - Argemone platyceras: 10.1016/J.EJPHAR.2005.08.046
- 149410 - Arnica longifolia: 10.1016/S0031-9422(00)89581-3
- 436215 - Arnica viscosa: 10.1002/J.1537-2197.1987.TB12148.X
- 35608 - Artemisia annua: 10.1016/0031-9422(94)00591-G
- 35608 - Artemisia Annua L.: -
- 992876 - Artemisia armeniaca: 10.1002/CBDV.201000284
- 401898 - Artemisia gmelinii: 10.1155/2014/673286
- 265784 - Artemisia iwayomogi: 10.1155/2014/673286
- 32220 - Aruncus dioicus: 10.1016/J.BMCL.2011.04.043
- 947972 - Aster koraiensis:
- 1197409 - Astragalus arguricus: 10.1007/BF00574227
- 1080390 - Astragalus asper: 10.1007/S10600-010-9597-2
- 20410 - Astragalus cicer: 10.1007/BF00602480
- 1197414 - Astragalus goktschaicus: 10.1007/BF00574227
- 1906524 - Astragalus lagurus: 10.1007/BF00580090
- 1091133 - Astragalus onobrychis: 10.1007/BF00574227
- 1264832 - Astragalus saganlugensis: 10.1007/BF00602480
- 1197423 - Astragalus sevangensis: 10.1007/BF00574227
- 1080395 - Astragalus varius: 10.1007/BF00596666
- 1215405 - Atraphaxis frutescens: 10.1007/BF00571235
- 103964 - Austrocedrus chilensis: 10.1016/0031-9422(90)85105-O
- 124943 - Azadirachta indica:
- 1620022 - Baccharis angustifolia: 10.1016/S0031-9422(00)90045-1
- 72900 - Baccharis dracunculifolia: 10.1248/CPB.49.1388
- 2707479 - Baccharis ochracea: 10.1016/S0031-9422(96)00565-1
- 258209 - Berberis vulgaris: 10.1007/BF00579837
- 53576 - Berlandiera pumila: 10.1016/S0031-9422(00)90045-1
- 284673 - Betula alnoides: 10.1016/J.PHYTOL.2011.02.011
- 1527831 - Bidens bipinnata: 10.3987/COM-03-S31
- 36774 - Brassica oleracea var. italica: 10.1002/(SICI)1097-0010(199808)77:4<468::AID-JSFA66>3.0.CO;2-B
- 319147 - Bridelia ferruginea:
- 56523 - Buphthalmum salicifolium: 10.1016/S0031-9422(99)00082-5
- 52451 - Bupleurum chinense DC.: -
- 1027102 - Byrsonima coccolobifolia: 10.1021/NP400717M
- 4270 - Byrsonima crassifolia: 10.1016/S0031-9422(96)00842-4
- 41496 - Calendula officinalis:
- 3431 - Calycanthus chinensis: 10.1016/J.BMC.2011.03.055
- 4442 - Camellia sinensis:
- 239399 - Campanula barbata: 10.1016/S0031-9422(00)00423-4
- 1238577 - Campanula kemulariae: 10.1007/BF00579158
- 239408 - Campanula kolenatiana: 10.1007/BF00579158
- 239416 - Campanula persicifolia: 10.1007/BF00607553
- 239420 - Campanula raddeana: 10.1007/BF00579158
- 16922 - Camptotheca acuminata: 10.1055/S-2004-835854
- 300208 - Canarium album: 10.1007/S10600-010-9543-3
- 20484 - Caragana arborescens: 10.1007/BF00598323
- 41502 - Carthamus lanatus: 10.1007/BF02329612
- 167387 - Castanopsis fissa: 10.1016/J.PHYTOCHEM.2011.07.007
- 46112 - Celosia argentea: 10.1080/10286020.2010.503652
- 48106 - Centella asiatica: 10.1016/J.BMCL.2011.01.066
- 49801 - Cercis canadensis: 10.1021/JA01176A016
- 228520 - Cheniella glauca: 10.1016/J.BMCL.2015.05.089
- 46091 - Chenopodiastrum murale: 10.1007/S10600-007-0056-7
- 3559 - Chenopodium album:
- 221251 - Chrysophyllum cainito: 10.1021/JF011178N
- 337469 - Cinnamomum philippinense: 10.1002/JCCS.201190020
- 165299 - Cissus discolor: 10.1248/CPB.57.1089
- 191224 - Cistus creticus: 10.1016/0031-9422(92)80355-I
- 335173 - Cistus ladanifer: 10.1016/0031-9422(92)80355-I
- 43366 - Clitoria ternatea:
- 401069 - Coleogyne ramosissima: 10.1016/S0031-9422(00)00192-8
- 93759 - Corchorus olitorius: 10.1038/192288B0
- 4285 - Cornus mas: 10.1016/J.FOODCHEM.2009.07.063
- 459758 - Cosmos sulphureus:
- 1851000 - Cotoneaster orbicularis: 10.1016/S0031-9422(99)00598-1
- 49140 - Craibiodendron yunnanense: 10.1007/S10600-008-0012-1
- 189211 - Crassocephalum crepidioides: 10.1248/BPB.28.19
- 1465651 - Cressa cretica: 10.1016/J.FITOTE.2004.05.008
- 1345247 - Cryptocarya moschata: 10.1021/NP400717M
- 87530 - Cyclamen persicum: 10.1016/S0031-9422(99)00297-6
- 107308 - Dalbergia sissoo: 10.1016/J.BMCL.2011.12.036
- 89411 - Descurainia sophia: 10.1248/CPB.52.1483
- 89411 - Descurainia sophia (L.) Webb. ex Prantl: -
- 37229 - Dicranopteris linearis: 10.1248/CPB.43.1800
- 298346 - Dictamnus albus: 10.1007/BF00579494
- 714465 - Dictamnus dasycarpus: 10.1007/BF00575725
- 35874 - Dioscorea bulbifera: 10.1002/CBDV.201000279
- 665996 - Diospyros cathayensis: 10.1248/CPB.53.591
- 35925 - Diospyros kaki:
- 35925 - Diospyros kaki Thunb.: -
- 171822 - Draba nemorosa: 10.1007/S12272-010-0806-0
- 39297 - Dracocephalum ruyschiana: 10.1021/NP300609U
- 240045 - Dysphania botrys: 10.1007/BF00563912
- 191066 - Empetrum nigrum:
- 3258 - Equisetum arvense: 10.1248/YAKUSHI1881.60.8_449
- 270432 - Erica cinerea: 10.1016/0031-9422(92)83305-I
- 34316 - Eucalyptus camaldulensis: 10.1016/0031-9422(93)85448-Z
- 627158 - Eucalyptus robusta: 10.1016/0031-9422(93)85448-Z
- 4392 - Eucommia ulmoides:
- 526193 - Euphorbia ebracteolata: 10.1016/J.CARRES.2003.12.017
- 212301 - Euphorbia humifusa: 10.1016/J.FITOTE.2010.04.012
- 1091645 - Euphorbia retusa: 10.1016/S0031-9422(00)83562-1
- 1091647 - Euphorbia sulcata: 10.1016/S0031-9422(00)83562-1
- 210332 - Euscaphis japonica: 10.1055/S-2007-981551
- 439689 - Evolvulus alsinoides:
- 241838 - Excoecaria agallocha: 10.1016/J.BMCL.2011.11.109
- 164500 - Fadogia ancylantha: 10.1021/NP900466X
- 66629 - Fagonia indica: 10.1016/0305-1978(88)90012-9
- 291474 - Fagonia paulayana: 10.1016/0305-1978(88)90012-9
- 76028 - Fallopia multiflora var. ciliinervis: 10.1002/JCCS.200700015
- 1009471 - Ficus pandurata: 10.1080/14786410902757899
- 479338 - Ficus ruficaulis: 10.1021/NP0401056
- 3746 - Fragaria: 10.1021/JF049450R
- 114476 - Gardenia jasminoides: 10.1021/NP050447R
- 49826 - Genista tricuspidata:
- 49810 - Genista tridentata: 10.1002/PTR.2403
- 554690 - Geranium carolinianum: 10.1248/BPB.31.743
- 314613 - Geranium tuberosum: 10.1002/HLCA.200800346
- 3311 - Ginkgo biloba:
- 3311 - Ginkgo biloba L.: -
- 1007786 - Gladiolus italicus: 10.1007/S13369-010-0015-7
- 99038 - Glebionis coronaria: 10.1007/S10600-007-0222-Y
- 48119 - Glehnia littoralis: 10.1248/CPB.50.73
- 49827 - Glycyrrhiza glabra:
- 49827 - Glycyrrhiza glabra L.: -
- 74614 - Glycyrrhiza inflata Bat.: -
- 74613 - Glycyrrhiza uralensis: 10.3987/COM-04-10150
- 74613 - Glycyrrhiza uralensis Fisch.: -
- 3635 - Gossypium hirsutum: 10.1007/S10600-008-9067-2
- 648866 - Grona styracifolia: 10.1007/S10600-010-9746-7
- 321551 - Haematoxylum campechianum: 10.1016/0031-9422(95)00924-8
- 239185 - Halocnemum strobilaceum: 10.1007/BF02238224
- 365472 - Halostachys belangeriana: 10.3390/MOLECULES15117933
- 282322 - Halostachys caspica: 10.3390/MOLECULES15117933
- 261776 - Helichrysum arenarium:
- 261805 - Helichrysum stoechas:
- 34190 - Hemerocallis fulva: 10.1016/J.LFS.2004.07.001
- 60145 - Heterophyllaea pustulata: 10.1021/NP050181O
- 71056 - Heterotheca: 10.1016/S0968-0896(00)00102-4
- 9606 - Homo sapiens: -
- 16752 - Houttuynia cordata Thunb.: -
- 282542 - Hypericum japonicum:
- 65561 - Hypericum perforatum:
- 673934 - Hypericum richeri: 10.1080/14786410802401390
- 282553 - Hypericum sampsonii: 10.1248/CPB.52.866
- 282556 - Hypericum sikokumontanum: 10.1016/J.PHYTOCHEM.2008.11.006
- 1321357 - Hypericum thasium: 10.1016/J.PHYTOCHEM.2008.10.006
- 185166 - Ichthyothere terminalis: 10.1016/0031-9422(82)83123-3
- 2033736 - Ilex dunniana: 10.1002/HLCA.201000385
- 1043421 - Ilex hainanensis: 10.1080/14786410802044885
- 453958 - Inula japonica Thunb.: -
- 362360 - Iochroma gesnerioides: 10.1016/0031-6865(94)90049-3
- 211591 - Iphiona scabra: 10.1016/S0031-9422(00)81848-8
- 4120 - Ipomoea batatas: 10.1271/BBB1961.55.613
- 389181 - Jasminum grandiflorum: 10.1055/S-2006-957419
- 2116407 - Kali collina:
- 2116407 - Kali collinum:
- 61147 - Kandelia candel: 10.1016/J.BMCL.2015.02.048
- 240080 - Krascheninnikovia ceratoides: 10.1007/S10600-009-9247-8
- 75953 - Lactuca indica: 10.1016/J.BMCL.2007.10.046
- 53159 - Lamium album: 10.1016/0031-9422(94)00727-B
- 62751 - Larix sibirica: 10.1007/BF00564611
- 254779 - Lathyrus pratensis: 10.1007/BF00607555
- 85223 - Laurus nobilis: 10.1248/BPB.25.102
- 141191 - Lawsonia inermis: 10.1016/J.BMCL.2015.04.052
- 4138 - Leonurus japonicus: 10.3136/FSTI9596T9798.4.278
- 153459 - Lepidium apetalum Willd: -
- 699669 - Lepisorus contortus: 10.1021/NP100373F
- 556514 - Lespedeza bicolor: 10.1016/S0031-9422(00)90131-6
- 151069 - Litchi chinensis: 10.1021/JF000815R
- 105884 - Lonicera japonica:
- 47247 - Lotus corniculatus: 10.1007/S10600-009-9362-6
- 1006353 - Lotus ucrainicus: 10.1007/S10600-009-9362-6
- 260603 - Lycopus europaeus: 10.1055/S-2006-958151
- 109849 - Macaranga tanarius: 10.1016/J.PHYTOCHEM.2009.07.020
- 325535 - Machilus japonica: 10.1021/NP9000653
- 3750 - Malus domestica:
- 283210 - Malus pumila:
- 75425 - Mayaca fluviatilis: 10.1016/0031-9422(85)80068-6
- 248847 - Meconopsis quintuplinervia: 10.1016/J.PHYTOCHEM.2005.12.002
- 861159 - Melilotus sulcatus: 10.3390/12020263
- 477031 - Miconia cabucu: 10.1016/J.PHYTOCHEM.2007.04.020
- 1049779 - Mikania laevigata: 10.1016/J.TETLET.2010.10.102
- 43522 - Morinda citrifolia: 10.1021/JF010492E
- 3735 - Moringa oleifera: 10.1016/J.PHYTOCHEM.2011.02.021
- 3498 - Morus alba:
- 3498 - Morus alba L.: -
- 1031565 - Morus insignis: 10.1248/CPB.41.1238
- 85232 - Morus nigra: 10.1021/JF703709R
- 59982 - Myrsine africana: 10.1016/S0031-9422(96)00329-9
- 4432 - Nelumbo nucifera:
- 299116 - Nymphaea ampla: 10.1016/J.PHYTOCHEM.2005.02.027
- 1616377 - Nymphaea nouchali var. caerulea: 10.1016/J.PHYTOCHEM.2008.04.009
- 4419 - Nymphaea odorata: 10.1016/J.PHYTOCHEM.2008.04.009
- 2699572 - Ochna obtusata: 10.1021/NP9604590
- 238830 - Onychium contiguum: 10.1016/0031-9422(74)85048-X
- 164276 - Onychium lucidum: 10.1016/0031-9422(74)85048-X
- 671264 - Oxytropis racemosa: 10.1248/CPB.58.1587
- 106693 - Paliurus spina-christi: 10.1007/BF00599276
- 4054 - Panax ginseng: 10.1248/YAKUSHI1947.89.1_122
- 103977 - Papuacedrus papuana: 10.1016/0031-9422(90)85105-O
- 59871 - Pelargonium reniforme: 10.1016/S0031-9422(01)00403-4
- 190712 - Periploca sepium: 10.1007/S10600-010-9646-X
- 254780 - Persicaria amphibia: 10.1021/NP9900674
- 580470 - Persicaria decipiens:
- 46901 - Persicaria hydropiper: 10.1007/BF00580088
- 430754 - Persicaria lapathifolia:
- 186965 - Petasites japonicus: 10.1271/BBB.66.1571
- 49563 - Peucedanum japonicum: 10.1021/JF0262458
- 2338973 - Phedimus stoloniferus: 10.1016/0031-9422(93)85416-O
- 68554 - Phellodendron amurense:
- 697203 - Phellodendron amurense var. wilsonii: 10.1021/NP030034V
- 354509 - Phellodendron chinense var. glabriusculum: 10.1021/NP030034V
- 1403168 - Philadelphus coronarius: 10.1007/0-387-28822-8_5
- 113250 - Phoenix canariensis: 10.1248/CPB.39.2053
- 293060 - Phyllanthus amarus: 10.1016/0031-9422(93)85545-3
- 296036 - Phyllanthus emblica: 10.1016/J.FOODCHEM.2011.09.063
- 296034 - Phyllanthus niruri: 10.1515/ZNB-2006-0111
- 3329 - Picea abies: 10.1016/0031-9422(95)00383-I
- 49509 - Pilularia globulifera: 10.1016/0031-9422(88)80645-9
- 500174 - Pilularia minuta: 10.1016/0031-9422(88)80645-9
- 191075 - Planchonella obovata: 10.1002/HLCA.200900264
- 33090 - Plants: -
- 375264 - Plinia cauliflora: 10.1021/NP0600999
- 120615 - Podocarpus fasciculus: 10.1248/CPB.56.585
- 1769194 - Polygonatum glaberrimum: 10.1007/S10600-011-0072-5
- 2259079 - Polygonatum orientale: 10.1007/S10600-011-0072-5
- 83819 - Polygonum cuspidatum Sieb. et Zucc.: -
- 73824 - Populus balsamifera: 10.1016/S0031-9422(00)97307-2
- 1616482 - Populus candicans: 10.1016/S0031-9422(00)97307-2
- 36596 - Prunus armeniaca: 10.1016/0003-9861(53)90127-1
- 140311 - Prunus cerasus: 10.1021/JF0734727
- 102107 - Prunus mume: 10.1016/J.BMCL.2014.01.028
- 3760 - Prunus persica: 10.1021/JF0104681
- 323851 - Prunus persica var. nucipersica: 10.1021/JF0104681
- 88123 - Prunus salicina: 10.1021/JA01113A529
- 120290 - Psidium guajava:
- 180039 - Psychotria punctata: 10.3389/FMOLB.2021.683671
- 265703 - Pteris linearis: 10.1248/CPB.43.1800
- 162890 - Pterogyne nitens: 10.1016/J.PHYTOCHEM.2008.01.006
- 193309 - Pyracantha coccinea: 10.1016/0031-9422(93)85108-4
- 642526 - Pyrola calliantha H.AndreS: -
- 642527 - Pyrola decorata H. Andres: -
- 93825 - Pyrola elliptica: 10.1016/S0031-9422(97)00878-9
- 187374 - Pyrrosia lingua: 10.1177/1934578X1501000714
- 187374 - Pyrrosia lingua (Thunb.) Farwell: -
- 746522 - Pyrrosia petiolosa (Christ) Ching: -
- 746523 - Pyrrosia sheareri (Bak. ) Ching: -
- 58334 - Quercus ilex: 10.1016/J.TETLET.2009.01.158
- 38865 - Quercus petraea: 10.1007/BF00564461
- 58331 - Quercus suber: 10.1002/ARDP.2503240811
- 1442767 - Rhodiola coccinea: 10.1007/BF00564357
- 344754 - Rhododendron decorum: 10.1007/S10600-009-9245-X
- 134444 - Rhododendron ellipticum: 10.1016/0031-9422(94)00905-9
- 184576 - Rhododendron latoucheae: 10.1016/0031-9422(94)00905-9
- 49626 - Rhododendron moulmainense: 10.1016/0031-9422(94)00905-9
- 105903 - Rhododendron mucronulatum: -
- 182159 - Rhododendron spinuliferum: 10.1007/S10600-009-9410-2
- 78511 - Ribes nigrum:
- 175228 - Ribes rubrum: 10.1021/JF0347517
- 108447 - Ripariosida hermaphrodita: 10.1007/BF00607552
- 262050 - Rodgersia podophylla: 10.1248/CPB.54.234
- 74632 - Rosa gallica: 10.1021/JF903515F
- 74645 - Rosa rugosa Thunb.: -
- 23216 - Rubus: 10.1002/JSFA.1885
- 420769 - Rubus adenotrichos: 10.1021/JF071475D
- 57936 - Rubus chamaemorus: 10.1021/JF049450R
- 190226 - Rubus glaucus: 10.1021/JF071475D
- 32247 - Rubus idaeus:
- 59497 - Rubus rigidus: 10.1007/S12272-011-0404-9
- 52312 - Rudbeckia fulgida: 10.1016/S0031-9422(00)80813-4
- 525237 - Salsola collina:
- 933122 - Salvia blepharophylla: 10.1016/S0031-9422(99)00324-6
- 4202 - Sambucus nigra: 10.1016/S0031-9422(01)00401-0
- 316852 - Sapium haematospermum: 10.1021/NP0303411
- 54806 - Saururus chinensis (Lour.) Baill.: -
- 137893 - Saussurea medusa:
- 182070 - Saxifraga stolonifera: 10.1016/J.BMC.2007.10.072
- 691236 - Scandosorbus intermedia: 10.1007/S10600-009-9409-8
- 289766 - Sclerocarya birrea: 10.1021/JF030374M
- 4278 - Securidaca diversifolia: 10.1016/S0031-9422(00)80695-0
- 23028 - Sedum acre: 10.1016/0031-9422(88)83050-4
- 91146 - Sedum sarmentosum: 10.1248/BPB.27.2035
- 4722 - Serenoa repens: 10.1002/ARDP.19893220211
- 1055022 - Sibiraea angustata: 10.1007/S11418-009-0362-4
- 53588 - Silphium perfoliatum: 10.1016/S0031-9422(02)00133-4
- 91157 - Sinocrassula indica: 10.1248/CPB.55.1308
- 329779 - Solanum incanum: 10.1002/JCCS.200000029
- 4112 - Solanum nigrum L.: -
- 36599 - Sorbus aucuparia: 10.1007/S002170100328
- 211926 - Spathodea campanulata: 10.1177/1934578X0900400602
- 409506 - Spiraea canescens: 10.1016/J.PHYTOCHEM.2009.07.013
- 409510 - Spiraea formosana: 10.1248/CPB.52.1227
- 167472 - Stachyurus himalaicus: 10.1007/S10600-011-9847-Y
- 13274 - Stellaria media: 10.1016/J.HELIYON.2020.E04150
- 3897 - Styphnolobium japonicum:
- 53928 - Tachigali paniculata: 10.1021/NP0200764
- 1157238 - Tephrosia vogelii: 10.1016/S0031-9422(00)83511-6
- 1084670 - Thalictrum foetidum: 10.1007/BF00595063
- 121718 - Tilia tomentosa: 10.1016/S0968-0896(01)00321-2
- 2914000 - Torminalis glaberrima: 10.1016/J.PHYTOL.2011.02.005
- 361561 - Trifolium aureum: 10.1007/BF00579982
- 97022 - Trifolium echinatum: 10.1007/BF00630553
- 13306 - Tulipa gesneriana: 10.1016/0031-9422(91)84233-I
- 198266 - Ulmus pumila: 10.1007/BF00565315
- 91168 - Umbilicus rupestris: 10.1248/CPB.48.1768
- 69266 - Vaccinium corymbosum: 10.1002/JSFA.1885
- 13750 - Vaccinium macrocarpon: 10.1021/JF034970S
- 180763 - Vaccinium myrtillus: 10.1021/JA01097A013
- 180772 - Vaccinium vitis-idaea: 10.1021/JF0623687
- 23278 - Vahlia capensis: 10.1055/S-2006-957671
- 32250 - Vauquelinia corymbosa: 10.3390/MOLECULES200815330
- 386441 - Veratrum dahuricum: 10.1007/S10600-007-0233-8
- 237933 - Viburnum dilatatum: 10.1002/HLCA.200890199
- 237959 - Viburnum tinus: 10.1016/J.PHYTOCHEM.2005.07.019
- 1276853 - Vicia subvillosa: 10.1007/S10600-007-0058-5
- 3916 - Vigna radiata var. radiata: 10.1007/BF00633405
- 167923 - Vitex quinata: 10.1007/S10600-010-9645-Y
- 3605 - Vitis aestivalis:
- 226012 - Vitis cinerea: 10.1016/0305-1978(87)90085-8
- 96939 - Vitis riparia: 10.1016/0305-1978(87)90085-8
- 29760 - Vitis vinifera:
- 754105 - Vitis vulpina: 10.1016/0305-1978(87)90085-8
- 549618 - Warburgia stuhlmannii: 10.1016/S0031-9422(03)00105-5
- 224084 - Wikstroemia canescens: 10.1248/CPB.58.859
- 203955 - Xylonagra arborea: 10.1016/0031-9422(83)80111-3
- 3498 - 桑叶: -
- 33090 - 罗布麻叶: -
- 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
- 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:
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Toxicologic pathology.
2018 07; 46(5):530-539. doi:
10.1177/0192623318778508
. [PMID: 29843569] - Carmen Steinborn, Olivier Potterat, Ulrich Meyer, Rainer Trittler, Sven Stadlbauer, Roman Huber, Carsten Gründemann. In Vitro Anti-inflammatory Effects of Equisetum arvense Are Not Solely Mediated by Silica.
Planta medica.
2018 May; 84(8):519-526. doi:
10.1055/s-0043-123075
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Molecular nutrition & food research.
2018 05; 62(9):e1700729. doi:
10.1002/mnfr.201700729
. [PMID: 29396908] - Toshiyuki Nakamura, Chinatsu Kinjo, Yoshimasa Nakamura, Yoji Kato, Miyu Nishikawa, Masahiro Hamada, Noriyuki Nakajima, Shinichi Ikushiro, Kaeko Murota. Lymphatic metabolites of quercetin after intestinal administration of quercetin-3-glucoside and its aglycone in rats.
Archives of biochemistry and biophysics.
2018 05; 645(?):126-136. doi:
10.1016/j.abb.2018.03.024
. [PMID: 29574052] - Antonietta Cerulli, Milena Masullo, Angela Mari, Anna Balato, Rosanna Filosa, Serena Lembo, Assunta Napolitano, Sonia Piacente. Phenolics from Castanea sativa leaves and their effects on UVB-induced damage.
Natural product research.
2018 May; 32(10):1170-1175. doi:
10.1080/14786419.2017.1331225
. [PMID: 28539059] - Arnaud Gaudry, Sandra Bos, Wildriss Viranaicken, Marjolaine Roche, Pascale Krejbich-Trotot, Gilles Gadea, Philippe Desprès, Chaker El-Kalamouni. The Flavonoid Isoquercitrin Precludes Initiation of Zika Virus Infection in Human Cells.
International journal of molecular sciences.
2018 Apr; 19(4):. doi:
10.3390/ijms19041093
. [PMID: 29621184] - A Garbetta, L Nicassio, I D'Antuono, A Cardinali, V Linsalata, G Attolico, F Minervini. Influence of in vitro digestion process on polyphenolic profile of skin grape (cv. Italia) and on antioxidant activity in basal or stressed conditions of human intestinal cell line (HT-29).
Food research international (Ottawa, Ont.).
2018 04; 106(?):878-884. doi:
10.1016/j.foodres.2018.01.072
. [PMID: 29579999] - Fangbo Xia, Chenchen Li, Ning Zhao, He Li, Qi Chang, Xinmin Liu, Yonghong Liao, Ruile Pan. Rapid Determination of Active Compounds and Antioxidant Activity of Okra Seeds Using Fourier Transform Near Infrared (FT-NIR) Spectroscopy.
Molecules (Basel, Switzerland).
2018 Mar; 23(3):. doi:
10.3390/molecules23030550
. [PMID: 29498632] - Yunjeong Kim, Kyeong-Ok Chang. Protein disulfide isomerases as potential therapeutic targets for influenza A and B viruses.
Virus research.
2018 03; 247(?):26-33. doi:
10.1016/j.virusres.2018.01.010
. [PMID: 29382552] - JiEun Yun, Eun-Rhan Woo, Dong Gun Lee. Effect of isoquercitrin on membrane dynamics and apoptosis-like death in Escherichia coli.
Biochimica et biophysica acta. Biomembranes.
2018 Feb; 1860(2):357-363. doi:
10.1016/j.bbamem.2017.11.008
. [PMID: 29155212] - Yang Liu, Shengzuo Fang, Wanxia Yang, Xulan Shang, Xiangxiang Fu. Light quality affects flavonoid production and related gene expression in Cyclocarya paliurus.
Journal of photochemistry and photobiology. B, Biology.
2018 Feb; 179(?):66-73. doi:
10.1016/j.jphotobiol.2018.01.002
. [PMID: 29334625] - Rana Adhikary, Sahin Sultana, Biswadev Bishayi. Clitoria ternatea flower petals: Effect on TNFR1 neutralization via downregulation of synovial matrix metalloproteases.
Journal of ethnopharmacology.
2018 Jan; 210(?):209-222. doi:
10.1016/j.jep.2017.08.017
. [PMID: 28826781] - Jun Zhou, Jiang Bing Sun, Qiao Feng Wang. Determination of isoquercitrin in rat plasma by high performance liquid chromatography coupled with a novel synergistic cloud point extraction.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.
2018 Jan; 1072(?):136-141. doi:
10.1016/j.jchromb.2017.11.014
. [PMID: 29153998] - Misato Nakamura, Ayumi Eguchi, Mari Inohana, Rei Nagahara, Hirotada Murayama, Masashi Kawashima, Sayaka Mizukami, Mihoko Koyanagi, Shim-Mo Hayashi, Robert R Maronpot, Makoto Shibutani, Toshinori Yoshida. Differential impacts of mineralocorticoid receptor antagonist potassium canrenoate on liver and renal changes in high fat diet-mediated early hepatocarcinogenesis model rats.
The Journal of toxicological sciences.
2018; 43(10):611-621. doi:
10.2131/jts.43.611
. [PMID: 30298849] - Chang Won Lee, Jeong Yeon Seo, Jisun Lee, Ji Won Choi, Sarang Cho, Jae Youn Bae, Jae Kyung Sohng, Sung Oog Kim, Jihoon Kim, Yong Il Park. 3-O-Glucosylation of quercetin enhances inhibitory effects on the adipocyte differentiation and lipogenesis.
Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.
2017 Nov; 95(?):589-598. doi:
10.1016/j.biopha.2017.08.002
. [PMID: 28869898] - Ilyas Yildiz, Ozkan Sen, Ramazan Erenler, Ibrahim Demirtas, Lutfi Behcet. Bioactivity-guided isolation of flavonoids from Cynanchum acutum L. subsp. sibiricum (willd.) Rech. f. and investigation of their antiproliferative activity.
Natural product research.
2017 Nov; 31(22):2629-2633. doi:
10.1080/14786419.2017.1289201
. [PMID: 28278670] - Elina Karhu, Janne Isojärvi, Pia Vuorela, Leena Hanski, Adyary Fallarero. Identification of Privileged Antichlamydial Natural Products by a Ligand-Based Strategy.
Journal of natural products.
2017 10; 80(10):2602-2608. doi:
10.1021/acs.jnatprod.6b01052
. [PMID: 29043803] - Ping Wu, Siyuan Liu, Jianyu Su, Jianping Chen, Lin Li, Runguang Zhang, Tianfeng Chen. Apoptosis triggered by isoquercitrin in bladder cancer cells by activating the AMPK-activated protein kinase pathway.
Food & function.
2017 Oct; 8(10):3707-3722. doi:
10.1039/c7fo00778g
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