M3547

Mangiferin Mangifera indica

Manufacturer: Sigma Aldrich

CAS Number: 4773-96-0

Synonym(S): 1,3,6,7-Tetrahydroxyxanthone C2-β-D-glucoside

Select a Size

Pack Size SKU Availability Price
100 MG M3547-100-MG In Stock ₹ 8,854.85
1 G M3547-1-G In Stock ₹ 43,927.85

M3547 - 100 MG

₹ 8,854.85

In Stock

Quantity

1

Base Price: ₹ 8,854.85

GST (18%): ₹ 1,593.873

Total Price: ₹ 10,448.723

Assay

≥98% (TLC)

Quality Level

200

form

powder

application(s)

metabolomicsvitamins, nutraceuticals, and natural products

SMILES string

OC[C@H]1O[C@H]([C@H](O)[C@@H](O)[C@@H]1O)c2c(O)cc3Oc4cc(O)c(O)cc4C(=O)c3c2O

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

InChI key

AEDDIBAIWPIIBD-ZJKJAXBQSA-N

Other Options

Image Product Name Manufacturer Price Range
11-101-4250
Mangiferin, ≥98% (TLC), MilliporeSigma™ Supelco™
MilliporeSigma Supelco ₹ 16,256.40
06279
Mangiferin
Supelco ₹ 13,087.43
Y0001751
Mangiferin
Sigma Aldrich ₹ 16,085.95
PHL89729
Mangiferin
Sigma Aldrich ₹ 30,623.93

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Description

  • General description: Mangiferin (MGF) is a natural bioactive polyphenol predominantly isolated from the Mangifera indica (Mango) tree.[1] It has a xanthone glucoside structure.[2] Mangiferin can also be found in other angiosperm plants and herbs.[3]
  • Application: Mangiferin has been used:as a reference standard for the characterization of mangiferin from Mangifera indica using ultrasound with three-phase partitioning (UTPP)[4]to study its effects in promoting brown adipose phenotype murine C3H10T1/2 mesenchymal stem cells (MSCs) and its role in mitochondrial biogenesis and homeostasis[5]as a reference standard for the quantitative determination of markers compounds in the culture Swertia paniculata shoot culture using high-performance thin-layer chromatography (HPTLC)[6]
  • Biochem/physiol Actions: Mangiferin has various pharmacological properties including antioxidant, anti-diabetic, anti-bacterial, cardioprotective, neuroprotective, and immunomodulatory activities.[1] It has also displayed antidiabetic, antihyperlipidemic, and antiatherogenic properties in streptozotocin-induced diabetic rats.[2] MGF exerts chemotherapeutic and chemo-preventative activities.[7] It displays antioxidant, analgesic, and hepatoprotective activity against carbon tetrachloride-induced liver injury.[8] MGF is a known accelerator of gastrointestinal transit (GIT).[9]

SAFETY INFORMATION

Pictograms

GHS06

Signal Word

Danger

Hazard Statements

H300

Precautionary Statements

P264 - P270 - P301 + P310 - P405 - P501

Hazard Classifications

Acute Tox. 1 Oral

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Assay:
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powder

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metabolomicsvitamins, nutraceuticals, and natural products

SMILES string:
OC[C@H]1O[C@H]([C@H](O)[C@@H](O)[C@@H]1O)c2c(O)cc3Oc4cc(O)c(O)cc4C(=O)c3c2O

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

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AEDDIBAIWPIIBD-ZJKJAXBQSA-N

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C\C(=C/c1ccccc1)C(O)=O

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1S/C10H10O2/c1-8(10(11)12)7-9-5-3-2-4-6-9/h2-7H,1H3,(H,11,12)/b8-7+

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XNCRUNXWPDJHGV-BQYQJAHWSA-N

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1S/C10H10O2/c1-8-2-4-9(5-3-8)6-7-10(11)12/h2-7H,1H3,(H,11,12)/b7-6+

InChI key:
RURHILYUWQEGOS-VOTSOKGWSA-N