analytical standard, Moligand™, ≥98% Analytischer Standard,Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at 2-8°C Ships Wet ice Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 16 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Übersicht

Mangiferin is an Nrf2 activator. It inhibits the nuclear translocation of NF-κB subunits p65 and p50. Mangiferin exhibits antioxidant, anti-diabetic, anti-hyperuricemic, antiviral, anti-cancer and anti-inflammatory activities.

Specifications

Synonyme

Spezifikationen & Reinheit

analytical standard, Moligand™, ≥98%

Anmeldung

Mangiferin may be used as an analytical standard for the determination of the analyte in rat plasma, traditional Chinese medicines and honeybush tea (Cyclopia spp.) by chromatography based techniques.

Storage

Store at 2-8°C

Verschickt in

Wet ice

Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.

Note

Analytischer Standard, Moligand™

Aktionsart

INHIBITOR

Reinheit

≥98%

Namen und Kennungen

Pubchem Sid

528775099

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/528775099

Kanonisches Lächeln

C1=C2C(=CC(=C1O)O)OC3=C(C2=O)C(=C(C(=C3)O)C4C(C(C(C(O4)CO)O)O)O)O

IUPAC Name

1,3,6,7-tetrahydroxy-2-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]xanthen-9-one

InChIKey

AEDDIBAIWPIIBD-ZJKJAXBQSA-N

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/t11-,15-,17+,18-,19+/m1/s1

Isomere SMILES

C1=C2C(=CC(=C1O)O)OC3=C(C2=O)C(=C(C(=C3)O)[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O)O

Molekulargewicht

422.34

Reaxy-Rn

1359328

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1359328&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organoheterocyclic compounds
  - Klasse Benzopyrans
    - Subclass 1-benzopyrans
      - Ebene5 Dibenzopyrans
        Ebene6 Xanthenes
        Ebene7 Xanthones

Kingdom	Organic compounds
Superclass	Organoheterocyclic compounds
Klasse	Benzopyrans
Subclass	1-benzopyrans
Intermediate Tree Nodes	Dibenzopyrans - Xanthenes
Direct Parent	Xanthones
Alternative Parents	Phenolic glycosides Hexoses C-glycosyl compounds Chromones Pyranones and derivatives 1-hydroxy-2-unsubstituted benzenoids 1-hydroxy-4-unsubstituted benzenoids Oxanes Vinylogous acids Heteroaromatic compounds Secondary alcohols Polyols Oxacyclic compounds Dialkyl ethers Organic oxides Primary alcohols Hydrocarbon derivatives
Molecular Framework	Aromatic heteropolycyclic compounds
Substituents	Phenolic glycoside - Xanthone - Hexose monosaccharide - C-glycosyl compound - Chromone - Glycosyl compound - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Pyranone - Benzenoid - Pyran - Oxane - Monosaccharide - Heteroaromatic compound - Vinylogous acid - Secondary alcohol - Oxacycle - Polyol - Dialkyl ether - Ether - Hydrocarbon derivative - Organic oxygen compound - Organic oxide - Organooxygen compound - Primary alcohol - Alcohol - Aromatic heteropolycyclic compound
Beschreibung	This compound belongs to the class of organic compounds known as xanthones. These are polycyclic aromatic compounds containing a xanthene moiety conjugated to a ketone group at carbon 9. Xanthene is a tricyclic compound made up of two benzene rings linearly fused to each other through a pyran ring.
External Descriptors	xanthenes
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

3D-Struktur

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AKR1B1 Tclin Aldose reductase (1404 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

MMP1 Tchem Matrix metalloproteinase-1 (7046 Activities)

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U2OS (164939 Activities)

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NUDT1 Tchem 7,8-dihydro-8-oxoguanine triphosphatase (280 Activities)

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Zugehörige Ziele (nicht menschlich)

NA Neuraminidase (1107 Activities)

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Gusb Beta-glucuronidase (17 Activities)

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Mmp9 Matrix metalloproteinase 9 (38 Activities)

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Plasmodium falciparum (966862 Activities)

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Rattus norvegicus (775804 Activities)

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Human alphaherpesvirus 1 (11089 Activities)

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3T3-L1 (3664 Activities)

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BHK-21 (725 Activities)

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Vero (26788 Activities)

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BV-2 (3710 Activities)

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Genome polyprotein (620 Activities)

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rep Replicase polyprotein 1ab (378 Activities)

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nanH Sialidase (337 Activities)

Discover Target: nanH

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Glyceraldehyde-3-phosphate dehydrogenase, glycosomal (75 Activities)

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Danio rerio (3092 Activities)

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Plasma (328 Activities)

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SARS-CoV-2 (38078 Activities)

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Wirkungsmechanismen

Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

4 results found

Lot Number	Certificate Type	Datum	Artikel
D2324660	Certificate of Analysis	Sep 22, 2026	M114062
D2629022	Certificate of Analysis	May 11, 2026	M114062
I2118371	Certificate of Analysis	Jun 15, 2023	M114062
A2305564	Certificate of Analysis	Nov 11, 2022	M114062

Chemische und physikalische Eigenschaften

Empfindlichkeit	Heat sensitive
Schmelzpunkt (°C)	270 °C
Molekulargewicht	422.300 g/mol
XLogP3	-0.400
Hydrogen Bond Donor Count	8
Hydrogen Bond Acceptor Count	11
Rotatable Bond Count	2
Exact Mass	422.085 Da
Monoisotopic Mass	422.085 Da
Topological Polar Surface Area	197.000 Å²
Heavy Atom Count	30
Formal Charge	0
Complexity	646.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	5
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

FAQs und Artikel

Glycosidic Bond Structure and Cleavage Mechanisms—Chemical and Enzymatic Cleavage of O-, N-, S-, and C-Glycosides

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

O-glycosides C-glycosides Glycosides

Citations of This Product

How to Cite Aladdin Scientific Products? Citations Search

Lösungsrechner

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Bewertungen

📚 Citations by Application

Controlled-release & nanoparticle carrier2

Other applications10

Extraction & workup solvent4

Spectroscopy sample preparation1

Organic synthesis — reaction medium3

Drug / compound screening3

Topical & ophthalmic formulation1

Polymer synthesis & polymerization1

IC50 determination1

View all 16 citations →

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Mangiferin - analytical standard,Moligand™,≥98% , CAS No.4773-96-0

Storage & shipping

Quality documents

Literature proof

Übersicht

Specifications

Documentation

📋 Safety Data Sheet (SDS)

✅ Certificate of Analysis (COA)

📊 Datasheet

🔬 Specification Sheet

Advanced Data

Molarity Calculator

Dilution Calculator

Reconstitution Calculator

Kundenbewertungen

📚 Citations by Application

Need help choosing the grade?

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