sameAs
Physcion inhibits the metastatic potential of human colorectal cancer SW620 cells in vitro by suppressing the transcription factor SOX2Physcion, a naturally occurring anthraquinone derivative, induces apoptosis and autophagy in human nasopharyngeal carcinomaSecondary Metabolites in Ramalina terebrata Detected by UHPLC/ESI/MS/MS and Identification of Parietin as Tau Protein InhibitorTranscriptomic analysis reveals distinct resistant response by physcion and chrysophanol against cucumber powdery mildewPreparative isolation of three anthraquinones from Rumex japonicus by high-speed counter-current chromatography.Antibacterial metabolites from Australian macrofungi from the genus Cortinarius.Antiproliferative, antibacterial and antifungal activity of the lichen Xanthoria parietina and its secondary metabolite parietin.Induction of Cell Cycle Arrest and Apoptosis by Physcion, an Anthraquinone Isolated From Rhubarb (Rhizomes of Rheum tanguticum), in MDA-MB-231 Human Breast Cancer Cells.Upregulation of Human ST8Sia VI (α2,8-Sialyltransferase) Gene Expression by Physcion in SK-N-BE(2)-C Human Neuroblastoma Cells.Upregulating miR-146a by physcion reverses multidrug resistance in human chronic myelogenous leukemia K562/ADM cells.Upregulation of miR-124 by physcion 8-O-β-glucopyranoside inhibits proliferation and invasion of malignant melanoma cells via repressing RLIP76.Anti-proliferative Effect of Physcion on Human Gastric Cell Line via Inducing ROS-Dependent Apoptosis.Hepatoxicity of major constituents and extractions of Radix Polygoni Multiflori and Radix Polygoni Multiflori Praeparata.A new phenolic compound with anticancer activity from the wood of Millettia leucantha.Regulation of human pregnane X receptor and its target gene cytochrome P450 3A4 by Chinese herbal compounds and a molecular docking study.Hypericins and thioredoxin reductase: Biochemical and docking studies disclose the molecular basis for effective inhibition by naphthodianthrones.Effective constituents in Xiexin Decoction for anti-inflammation.Phenols from the roots of Rheum palmatum attenuate chemotaxis in rat hepatic stellate cells.Correlation between reduction potentials and inhibitions of Epstein-Barr virus activation by anthraquinone derivatives.Comparison of the cytotoxic activities of naturally occurring hydroxyanthraquinones and hydroxynaphthoquinones.Estrogenic and anti-estrogenic activities of Cassia tora phenolic constituents.Anti-HIV-1 constituents from leaves and twigs of Cratoxylum arborescens.Antimutagenicity and cytotoxicity of the constituents from the aerial parts of Rumex acetosa.Physcion induces mitochondria-driven apoptosis in colorectal cancer cells via downregulating EMMPRIN.Structure and absolute configuration of toxic polyketide pigments from the fruiting bodies of the fungus Cortinarius rufo-olivaceusPhyscion, a natural anthraquinone derivative, enhances the gene expression of leaf-specific thionin of barley against Blumeria graminis.Comparison of three different extraction methods and HPLC determination of the anthraquinones aloe-emodine, emodine, rheine, chrysophanol and physcione in the bark of Rhamnus alpinus L. (Rhamnaceae).Antioxidant polyketide phenolic metabolites from the edible mushroom Cortinarius purpurascens.Physcion from marine-derived fungus Microsporum sp. induces apoptosis in human cervical carcinoma HeLa cells.High-affinity, non-nucleotide-derived competitive antagonists of platelet P2Y12 receptors.Ultrasonic extraction and HPLC determination of anthraquinones, aloe-emodine, emodine, rheine, chrysophanol and physcione, in roots of Polygoni multiflori.Prenylated anthraquinones and other constituents from the seeds of Vismia laurentii.Anthraquinones from the seeds of Cassia tora with inhibitory activity on protein glycation and aldose reductase.Chaetopyranin, a benzaldehyde derivative, and other related metabolites from Chaetomium globosum, an endophytic fungus derived from the marine red alga Polysiphonia urceolata.New anthraquinone dimer from the root bark of Cassia artemisioides (Gaudich. Ex. DC) Randell.Detection and aggregation of the antitumoral drug parietin in ethanol/water mixture and on plasmonic metal nanoparticles studied by surface-enhanced optical spectroscopy: Effect of pH and ethanol concentration.Synergistic interaction of physcion and chrysophanol on plant powdery mildewThe use of response surface methodology to optimize the ultrasound-assisted extraction of five anthraquinones from Rheum palmatum LA new polymorph of physcion
P921
Q28386917-D0B60A01-A0DB-43A5-8B3A-0F3F6E7E1C20Q28818357-6742B680-92CF-484C-9994-53D726446179Q28828799-35A4E5F4-E1F2-443A-A54D-02CB814AB193Q28833581-2D936A2D-C808-458F-955E-555CA1094D3EQ33805899-EA96F95A-C43E-4A74-9BED-B0B724FC92BEQ34110146-C050E92F-B8CC-4F08-AA78-1422F7CC5CADQ34471130-55BA704F-8605-48DE-A297-208CB8B9C293Q34853169-0D3330FF-88EB-4620-BFB5-1D82A17F8300Q37209960-774086CF-D8B3-4DFC-A118-3D1BF70D2CD8Q37447892-18D9FAD9-D9E7-4F7B-885C-DFA591E1057EQ38744389-54BCB68C-5FEF-4406-8D71-4C5C0ACB0294Q38761246-CFE63BA6-08B1-449D-9F97-3C09F8C8CAA4Q39490619-E7A6E2E3-01BF-4385-B5C4-A3BEC16BA6ECQ39513437-C5E3F39F-DC55-424F-8C5A-8B5A5BECA8A2Q39625852-384E22BF-6CFB-4D66-8B9D-3971B5B54A5BQ39813619-5CC26B8D-1180-4BF1-8E8D-5005950EFCFBQ39841297-6D6C3EEA-A0D8-491F-B36D-14FB422C8689Q39963459-25905833-4B61-42CD-B515-5141A7CBFB0FQ39972034-FDD463F9-BD79-4669-8D1B-C434E1BF4F76Q40065046-9D3AF028-BD11-43C0-B3B0-4A92484F9D64Q40071819-8B1710E1-9150-45A5-B842-B493D2C5DB68Q40210832-AD4C1319-7CBA-4A75-9A93-EDFC3191B88DQ40354132-5405E642-58F0-4132-BD5D-AEF8F6127F55Q40767732-B8294F97-683B-473E-B7A4-BAB52BFFAB29Q43039861-E33AAEA2-0814-4180-B713-F070A6BD319AQ43141998-62F16E71-EBE9-43BC-9718-63A0BE808032Q43213406-0C29E0A4-5107-4601-90C6-83687752398AQ44228716-4260AEA1-0078-4A32-86E4-E5749AAF293BQ45181455-09E169D4-0FBA-460D-8054-EE8554732DFFQ46000448-FEADABF6-C074-4682-9C19-0DBF787C2548Q46032509-DDFCFC8D-1AF2-4E6F-8CBC-98F93CC61034Q46917977-9F059F1F-20AA-453F-8A99-B0D3D60F743DQ46918041-0B80FCC8-C1BF-4B78-A4D1-73C81A9CD8F8Q50713920-03199A68-21DA-48B0-9614-5B7E71F77247Q51611273-46F4877F-B227-4383-A675-8DF96558375EQ53190035-28894E92-4C45-4415-BF24-AA9337101A31Q57134767-1552453E-06C6-4FB9-9C77-CC75438E0595Q84567207-AFB01689-3034-4020-951A-FF1FFF90BC52Q84693068-63578176-AE4E-45BE-A642-26CFE408C558
P921
description
chemesch Verbindung
@lb
chemical compound
@en
chemical compound
@en-ca
chemical compound
@en-gb
chemická sloučenina
@cs
chemická zlúčenina
@sk
chemiese verbinding
@af
chemische Verbindung
@de
chemische Verbindung
@de-ch
chemische verbinding
@nl
name
Parietin
@de
Parietin
@es
Parietin
@sh
Parietin
@sr
Parietín
@is
parietin
@en
pariétine
@fr
پاریتین
@azb
پاریتین
@fa
フィシオン
@ja
type
label
Parietin
@de
Parietin
@es
Parietin
@sh
Parietin
@sr
Parietín
@is
parietin
@en
pariétine
@fr
پاریتین
@azb
پاریتین
@fa
フィシオン
@ja
altLabel
physcione
@en
prefLabel
Parietin
@de
Parietin
@es
Parietin
@sh
Parietin
@sr
Parietín
@is
parietin
@en
pariétine
@fr
پاریتین
@azb
پاریتین
@fa
フィシオン
@ja
P592
P6366
P661
P662
P683
P117
P2067
P231
P232
P233
CC1=CC(=C2C(=C1)C(=O)C3=CC(=CC(=C3C2=O)O)OC)O
P234
1S/C16H12O5/c1-7-3-9-13(11(17) ...... 2)6-12(14)18/h3-6,17-18H,1-2H3
P235
FFWOKTFYGVYKIR-UHFFFAOYSA-N
P2566
100.007.561
P274
P2840
P3117
DTXSID20200101
P4964
splash10-0006-0090000000-c51cf2220ec9285a1711
splash10-0079-0090000000-5e0934d063bd6a571c02
P592
CHEMBL42624
P6366
2779151380
P652
H6PT94IV61