About: 1,3,6,7-Tetrahydroxy-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]xanthen-9-one

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About: 1,3,6,7-Tetrahydroxy-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]xanthen-9-one Goto Sponge NotDistinct Permalink

An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

group of stereoisomers

Attributes	Values
rdf:type	Item
description	group of stereoisomers (en) група стереоізомерів (uk) groep van stereo-isomeren (nl)
rdfs:label	1,3,6,7-Tetrahydroxy-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]xanthen-9-one (en)
skos:prefLabel	1,3,6,7-Tetrahydroxy-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]xanthen-9-one (en)
name	1,3,6,7-Tetrahydroxy-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]xanthen-9-one (en)
instance of	wds:Q104085142-A779176A-B0B4-4E4C-886B-DFE4549E13CC
instance of	group of stereoisomers
subclass of	wds:Q104085142-409F2A72-3FE2-4D1E-B080-8DF19B68EE09
subclass of	biogenic xanthone
found in taxon	wds:Q104085142-051589AD-EA91-4980-A231-48DF2AF94F98 wds:Q104085142-0B0D87CE-C9E0-498D-972D-D50C20A230DF wds:Q104085142-21E4FFC4-CAEC-4469-9027-119A61B6F584 wds:Q104085142-25B0460B-95C8-43DA-B124-47D7949A6258 wds:Q104085142-37932011-F20D-4A99-BCAD-000E12E120A9 wds:Q104085142-3FD7F7AF-543F-49EE-B65B-EB3ABC4D4B8D wds:Q104085142-413B8153-E297-4B4D-B944-2E7327FF8842 wds:Q104085142-46E2D1C1-1818-4C25-8FBB-43365A9667C7 wds:Q104085142-5971A096-154B-4E9C-9B27-669389DCEB19 wds:Q104085142-5EC196F2-7FEE-40B6-9524-647F7D8A3F6E wds:Q104085142-63F86C3A-FA97-4618-A800-0DFF512AF939 wds:Q104085142-7AF843A3-616B-4A16-8832-86218A28F339 wds:Q104085142-9027B7E8-21D7-4D03-95B7-AD0E2758EA72 wds:Q104085142-9700FE1C-D189-4E4D-9D82-06F0130FDA89 wds:Q104085142-E7B8DE47-F9D1-47BF-9938-4D2773696F7E wds:Q104085142-EE4A2187-4751-400E-9270-7AAF795F4BEF wds:Q104085142-F021736F-08B0-4597-A4D3-D5280C680BF3 wds:Q104085142-F48B818E-19AD-4B5D-A6AD-90F1130E42BF
found in taxon	Anemarrhena asphodeloides Kothala himbutu Iris domestica Bombax ceiba Mangifera indica Smilax Hypericum perforatum Salacia chinensis Polygala sibirica Great yellow gentian Bombax malabaricum Gentiana cruciata Swertia punicea Metagentiana rhodantha Hedysarum denticulatum Tripterospermum lanceolatum Pterospermum lanceolatum Polygala telephioides
UniChem compound ID	wds:Q104085142-7CB64D27-9192-495E-9B20-51B8CD4E685D
Probes And Drugs ID	wds:Q104085142-BE1C80D0-6327-46A4-91F0-F18563D95D74
Human Metabolome Database ID	wds:Q104085142-A2ACB868-2134-470E-97EA-5D31189D5B66
canonical SMILES	wds:Q104085142-A29C461C-C595-4874-83D7-2606378A432D
InChI	wds:Q104085142-2BE8283D-9899-45AA-8FF7-C5CC7860F226
InChIKey	wds:Q104085142-D8B0FD75-8DA7-47E9-90C4-5B5D04A89CBE
chemical formula	wds:Q104085142-54AAFA56-996C-4157-B14F-E1CF1D5494DA
PubChem CID	wds:Q104085142-70F7D981-4EA7-460C-AB01-EBA9C07ECC61
PubChem CID	http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID5358385
UniChem compound ID	980937
Probes And Drugs ID	PD056524
Human Metabolome Database ID	HMDB0034410
canonical SMILES	O=C1C2=CC(O)=C(O)C=C2OC3=CC(O)=C(C(O)=C13)C4OC(CO)C(O)C(O)C4O
InChI	InChI=1S/C19H18O11/c20-4-11-15(25)17(27)18(28)19(30-11)12-8(23)3-10-13(16(12)26)14(24)5-1-6(21)7(22)2-9(5)29-10/h1-3,11,15,17-23,25-28H,4H2
InChIKey	AEDDIBAIWPIIBD-UHFFFAOYSA-N
chemical formula	C₁₉H₁₈O₁₁
PubChem CID	5358385
mass	wds:Q104085142-BA0C6CAC-F09A-438A-92C2-04FCECA004DC
mass	422.084911396 (xsd:decimal)
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q104085142
is subclass of of	mangiferin 1,3,6,7-tetrahydroxy-2-[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]xanthen-9-one 1,3,6,7-tetrahydroxy-2-[(2S,3R,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]xanthen-9-one
is subclass of of	wds:Q104910001-DA962230-B6AF-4428-9CDC-1F45B83C1E36 wds:Q104909988-AF708818-CC53-42F3-B7F8-99FA8B9C5592 wds:Q1074417-36EABFDC-74DA-4CA8-B365-A69DDC4015DD
is main subject of	Structures of new friedelane- and norfriedelane-type triterpenes and polyacylated eudesmane-type sesquiterpene from Salacia chinensis LINN. (S. prinoides DC., Hippocrateaceae) and radical scavenging activities of principal constituents Flavonoids ofHedysarum sericeum andH. caucasicum New phenolic principles from Hypericum sampsonii Phenolic compounds from Hypericum perforatum Studies on the constituents of Iris florentina L. II. C-Glucosides of xanthones and flavones from the leaves. Biological activities of Salacia chinensis originating in Thailand: the quality evaluation guided by alpha-glucosidase inhibitory activity Isolation of mangiferin from Bombax malabaricum and structure revision of shamimin. Phenolic compounds from the whole plants of Gentiana rhodantha (Gentianaceae). Biosynthesis of mangiferin in Anemarrhena asphodeloides Bunge. I. The origin of the xanthone nucleus. Antioxidant C-glucosylxanthones from the leaves of Arrabidaea patellifera. Two new xanthone glycosides from Tripterospermum lanceolatum Neuroprotective xanthone glycosides from Swertia punicea A Mangiferin Monomethyl Ether from Mangifera indica L. Five New XanthenoneO-Glycosides from the Roots ofPolygala sibirica L. New Oligosaccharide Esters and XanthoneC-Glucosides fromPolygala telephioides Studies on Constituents of Iris Genus Plants. IV. The Constituents of Iris florentina L. (2) C-Glycosyl Compounds in the Leaves ofGemmingia chinensisO. Kuntze Campestroside, a new tetrahydroxanthone glucoside from Gentiana campestris
is main subject of	wds:Q44570795-2B1BCD3B-50F5-40C7-A8AF-32A7D3B85170 wds:Q44631035-F3A38EF4-5736-4788-93E7-B60745B53B38 wds:Q104909998-A331B1ED-02A9-4C1B-BD09-D893147A5AA5 wds:Q104385702-80873FB2-6607-41BC-A515-FE5688C71E34 wds:Q105386507-D04BFC6D-4C61-4B86-B964-A00B03127B38 wds:Q104909992-BB97BEB4-9BD5-4412-9FA7-3E3F272C3E7D wds:Q104908783-19D15AB6-A44F-4923-B205-A846B181AF85 wds:Q44736397-D51E6670-507A-4CC6-914D-1A232C734804 wds:Q43884597-298D0064-37FB-4EDB-A178-B5453CBFA265

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