Mangiferin
- Mangiferin
- 4773-96-0
- Chinonin
- Alpizarin
- Hedysarid
- Create:2005-06-24
- Modify:2025-01-04
- 2-beta-D-glucopyranosyl-1,3,6,7-tetrahydroxy-9H-xanthen-9-one
- 9H-xanthen-9-one, 2-beta-D-glucopyranosyl-1,3,6,7-tetrahydroxy-
- alpizarin
- chinonin
- mangiferin
- Mangiferin
- 4773-96-0
- Chinonin
- Alpizarin
- Hedysarid
- Aphloiol
- Chinomin
- Alpizarine
- UNII-1M84LD0UMD
- 1M84LD0UMD
- CHEBI:6682
- MFCD00075656
- 2-beta-D-glucopyranosyl-1,3,6,7-tetrahydroxy-9H-xanthen-9-one
- 9H-Xanthen-9-one, 2-b-D-glucopyranosyl-1,3,6,7-tetrahydroxy-
- Mangiferin Mangifera indica
- NSC 248870
- (1S)-1,5-anhydro-1-(1,3,6,7-tetrahydroxy-9-oxo-9H-xanthen-2-yl)-D-glucitol
- 1,3,6,7-Tetrahydroxy-2-((2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)-9H-xanthen-9-one
- DTXSID60197263
- 9H-Xanthen-9-one, 2-beta-D-glucopyranosyl-1,3,6,7-tetrahydroxy-
- NSC-248870
- 1,3,6,7-tetrahydroxy-2-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]xanthen-9-one
- 9H-Xanthen-9-one, 2-.beta.-D-glucopyranosyl-1,3,6,7-tetrahydroxy-
- MANGIFERIN (USP-RS)
- MANGIFERIN [USP-RS]
- Chinoinin
- Shamimin
- 9H-Xanthen-9-one, 2-beta-D-glucopyranosyl-1,3,6,7-tetrahydroxy- (9CI)
- cid_5358385
- Mangiferol
- NSC248870
- Mangiferin,(S)
- Xanthone-c-glucoside
- Mangiferin (Standard)
- 1,3,6,7-tetrahydroxyxanthone C2-beta-D-glucoside
- 1,3,6,7-Tetrahydroxyxanthone-C2-b-D-glucoside
- MANGIFERIN [WHO-DD]
- SCHEMBL556844
- Mangiferin (Many other names)
- Mangiferin, analytical standard
- CHEMBL464825
- BCBcMAP01_000240
- HY-N0290R
- DTXCID70119754
- GLXC-03051
- HY-N0290
- BDBM50248691
- s3808
- STL564509
- AKOS015896788
- CCG-268909
- CS-4663
- SMP1_000290
- AC-34484
- AS-15337
- DA-75300
- 1ST158066
- M2886
- NS00074224
- AN-668/21203018
- Q-100508
- Q1074417
- c2-beta-d-glucopyranosyl-1,3,6,7-tetrahydroxyxanthone
- Mangiferin, European Pharmacopoeia (EP) Reference Standard
- 1,3,6,7-tetrahydroxy-2-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]xanthen-9-one
- HZI
198.18 Ų [M+Na]+ [CCS Type: TW; Method: calibrated with polyalanine and drug standards]
189.35 Ų [M+H]+ [CCS Type: TW; Method: calibrated with polyalanine and drug standards]
201.27 Ų [M+K]+ [CCS Type: TW; Method: calibrated with polyalanine and drug standards]
185.6 Ų [M+H-H2O]+ [CCS Type: TW; Method: calibrated with polyalanine and drug standards]
195.81 Ų [M-H]- [CCS Type: DT; Method: stepped-field]
196.62 Ų [M+H]+ [CCS Type: DT; Method: stepped-field]
195.1 Ų [M-H]-
195.4 Ų [M+H]+
423 999
423.2 879
422.7 560
423.1 533
422.6 523
273.1 99
273 96
273.2 90
272.9 80
273.3 70
273.032410 100
303.043396 90.68
327.045135 53.65
369.054047 27.23
339.043518 23.27
301.049622 100
331.056488 66.80
272.040497 40.77
259.035675 35.29
271.033783 35.02
P264, P270, P301+P317, P330, and P501
(The corresponding statement to each P-code can be found at the GHS Classification page.)
Aggregated GHS information provided per 43 reports by companies from 2 notifications to the ECHA C&L Inventory.
Information may vary between notifications depending on impurities, additives, and other factors. The percentage value in parenthesis indicates the notified classification ratio from companies that provide hazard codes. Only hazard codes with percentage values above 10% are shown.
- CAS Common ChemistryLICENSEThe data from CAS Common Chemistry is provided under a CC-BY-NC 4.0 license, unless otherwise stated.https://creativecommons.org/licenses/by-nc/4.0/
- ChemIDplusChemIDplus Chemical Information Classificationhttps://pubchem.ncbi.nlm.nih.gov/source/ChemIDplus
- EPA DSSToxCompTox Chemicals Dashboard Chemical Listshttps://comptox.epa.gov/dashboard/chemical-lists/
- European Chemicals Agency (ECHA)LICENSEUse of the information, documents and data from the ECHA website is subject to the terms and conditions of this Legal Notice, and subject to other binding limitations provided for under applicable law, the information, documents and data made available on the ECHA website may be reproduced, distributed and/or used, totally or in part, for non-commercial purposes provided that ECHA is acknowledged as the source: "Source: European Chemicals Agency, http://echa.europa.eu/". Such acknowledgement must be included in each copy of the material. ECHA permits and encourages organisations and individuals to create links to the ECHA website under the following cumulative conditions: Links can only be made to webpages that provide a link to the Legal Notice page.https://echa.europa.eu/web/guest/legal-noticeXanthone-c-glucosidehttps://echa.europa.eu/substance-information/-/substanceinfo/100.153.319Xanthone-c-glucoside (EC: 624-757-7)https://echa.europa.eu/information-on-chemicals/cl-inventory-database/-/discli/details/157919
- FDA Global Substance Registration System (GSRS)LICENSEUnless otherwise noted, the contents of the FDA website (www.fda.gov), both text and graphics, are not copyrighted. They are in the public domain and may be republished, reprinted and otherwise used freely by anyone without the need to obtain permission from FDA. Credit to the U.S. Food and Drug Administration as the source is appreciated but not required.https://www.fda.gov/about-fda/about-website/website-policies#linking
- CCSbaseCCSbase Classificationhttps://ccsbase.net/
- NORMAN Suspect List ExchangeLICENSEData: CC-BY 4.0; Code (hosted by ECI, LCSB): Artistic-2.0https://creativecommons.org/licenses/by/4.0/MangiferinNORMAN Suspect List Exchange Classificationhttps://www.norman-network.com/nds/SLE/
- ChEBI
- LOTUS - the natural products occurrence databaseLICENSEThe code for LOTUS is released under the GNU General Public License v3.0.https://lotus.nprod.net/Mangiferinhttps://www.wikidata.org/wiki/Q1074417LOTUS Treehttps://lotus.naturalproducts.net/
- ChEMBLLICENSEAccess to the web interface of ChEMBL is made under the EBI's Terms of Use (http://www.ebi.ac.uk/Information/termsofuse.html). The ChEMBL data is made available on a Creative Commons Attribution-Share Alike 3.0 Unported License (http://creativecommons.org/licenses/by-sa/3.0/).http://www.ebi.ac.uk/Information/termsofuse.htmlChEMBL Protein Target Treehttps://www.ebi.ac.uk/chembl/g/#browse/targets
- Comparative Toxicogenomics Database (CTD)LICENSEIt is to be used only for research and educational purposes. Any reproduction or use for commercial purpose is prohibited without the prior express written permission of NC State University.http://ctdbase.org/about/legal.jsp
- Therapeutic Target Database (TTD)
- EPA Chemical and Products Database (CPDat)EPA CPDat Classificationhttps://www.epa.gov/chemical-research/chemical-and-products-database-cpdat
- FooDBLICENSEFooDB is offered to the public as a freely available resource. Use and re-distribution of the data, in whole or in part, for commercial purposes requires explicit permission of the authors and explicit acknowledgment of the source material (FooDB) and the original publication.https://foodb.ca/aboutMangiferolhttps://foodb.ca/compounds/FDB005974
- Human Metabolome Database (HMDB)LICENSEHMDB is offered to the public as a freely available resource. Use and re-distribution of the data, in whole or in part, for commercial purposes requires explicit permission of the authors and explicit acknowledgment of the source material (HMDB) and the original publication (see the HMDB citing page). We ask that users who download significant portions of the database cite the HMDB paper in any resulting publications.http://www.hmdb.ca/citing
- Japan Chemical Substance Dictionary (Nikkaji)
- KEGGLICENSEAcademic users may freely use the KEGG website. Non-academic use of KEGG generally requires a commercial licensehttps://www.kegg.jp/kegg/legal.htmlPhytochemical compoundshttp://www.genome.jp/kegg-bin/get_htext?br08003.keg
- Natural Product Activity and Species Source (NPASS)
- MassBank Europe
- MassBank of North America (MoNA)LICENSEThe content of the MoNA database is licensed under CC BY 4.0.https://mona.fiehnlab.ucdavis.edu/documentation/license
- Metabolomics Workbench
- NIST Mass Spectrometry Data CenterLICENSEData covered by the Standard Reference Data Act of 1968 as amended.https://www.nist.gov/srd/public-lawMangiferinhttp://www.nist.gov/srd/nist1a.cfm
- Protein Data Bank in Europe (PDBe)
- RCSB Protein Data Bank (RCSB PDB)LICENSEData files contained in the PDB archive (ftp://ftp.wwpdb.org) are free of all copyright restrictions and made fully and freely available for both non-commercial and commercial use. Users of the data should attribute the original authors of that structural data.https://www.rcsb.org/pages/policies
- SpectraBase
- Springer Nature
- The Cambridge Structural Database
- Thieme ChemistryLICENSEThe Thieme Chemistry contribution within PubChem is provided under a CC-BY-NC-ND 4.0 license, unless otherwise stated.https://creativecommons.org/licenses/by-nc-nd/4.0/
- Wikidatamangiferinhttps://www.wikidata.org/wiki/Q1074417
- Wikipedia5-Methoxy-7,N,N-trimethyltryptaminehttps://en.wikipedia.org/wiki/5-Methoxy-7,N,N-trimethyltryptamineMangiferinhttps://en.wikipedia.org/wiki/Mangiferin
- PubChem
- Medical Subject Headings (MeSH)LICENSEWorks produced by the U.S. government are not subject to copyright protection in the United States. Any such works found on National Library of Medicine (NLM) Web sites may be freely used or reproduced without permission in the U.S.https://www.nlm.nih.gov/copyright.html
- GHS Classification (UNECE)GHS Classification Treehttp://www.unece.org/trans/danger/publi/ghs/ghs_welcome_e.html
- MolGenieMolGenie Organic Chemistry Ontologyhttps://github.com/MolGenie/ontology/