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M3824

Sigma-Aldrich

α-Mangostin

≥98% (HPLC)

Sinonimo/i:

α-MG, alpha-Mangostin

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About This Item

Formula empirica (notazione di Hill):
C24H26O6
Numero CAS:
6147-11-1
Peso molecolare:
410.46
Numero CE:
448-420-7
Numero MDL:
MFCD00135200
Codice UNSPSC:
12352212
ID PubChem:
329817982
NACRES:
NA.25
Prezzi e disponibilità al momento non sono disponibili

Saggio

≥98% (HPLC)

Stato

powder

Solubilità

methanol: 1 mg/mL, clear, very light yellow

applicazioni

metabolomics
vitamins, nutraceuticals, and natural products

Temperatura di conservazione

2-8°C

Stringa SMILE

COc1c(O)cc2Oc3cc(O)c(C\C=C(\C)C)c(O)c3C(=O)c2c1C\C=C(/C)C

InChI

1S/C24H26O6/c1-12(2)6-8-14-16(25)10-19-21(22(14)27)23(28)20-15(9-7-13(3)4)24(29-5)17(26)11-18(20)30-19/h6-7,10-11,25-27H,8-9H2,1-5H3
GNRIZKKCNOBBMO-UHFFFAOYSA-N

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Categorie correlate

Descrizione generale

α-Mangostin (α-MG) is the most abundant phytochemical derived from the pericarp of Garcinia mangostana L..[1] It is a tetraoxygenated diprenylated xanthone.[2] The chemical structure of α-MG molecule is 1,3,6-trihydroxy-7-methoxy-2,8-bis(3-methyl-2-butenyl)- 9H-xanthen-9-one.[2]

Applicazioni

α-Mangostin has been used:
  • to study its protective effect against oxidative stress mediated-retinal cell death[3]
  • to study its role as an antigenotoxic agent in DNA protection against oxidative damage[4]
  • to understand its anti-bacterial activity against Staphylococcus epidermidis RP62A[5]

Azioni biochim/fisiol

α-Mangostin displays various pharmacological properties both in in vitro and in vivo studies.[6] These include antimicrobial, anticarcinogenic, antidiabetic, neuroprotective, hepatoprotective[1] and anti-inflammatory properties.[7]
Xanthone derivative isolated from mangosteen (Garcinia mangostana). Antioxidant and anti-inflammatory.
Xanthone derivative isolated from mangosteen (Garcinia mangostana). Antioxidant and anti-inflammatory. α-mangostin has been shown to induce apoptosis via the mitochondrial pathway, reduce cell proliferation and inhibit tumorigenesis.

Pittogrammi

Exclamation mark
GHS07

Avvertenze

Warning

Indicazioni di pericolo

H302

Classi di pericolo

Acute Tox. 4 Oral

Codice della classe di stoccaggio

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

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Certificati d'analisi (COA)

Lot/Batch Number
WXBF2536V
WXBF0975V
WXBD6883V
WXBD5557V
WXBD2826V

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Aungkana Krajarng et al.
Research in veterinary science, 93(2), 788-794 (2012-02-22)
Osteosarcoma is the most frequently diagnosed primary bone tumor in dog. Since chemotherapeutics are quite limited due to high cost and severe toxicity, therefore, the ultimate goal is to discover cost-effective therapeutics with less toxicity. We have studied the effect
Murugesan Sivaranjani et al.
Frontiers in microbiology, 10, 150-150 (2019-02-23)
Background: Alpha-mangostin (α-MG) is a natural xanthone reported to exhibit rapid bactericidal activity against Gram-positive bacteria, and may therefore have potential clinical application in healthcare sectors. This study sought to identify the impact of α-MG on Staphylococcus epidermidis RP62A through
Xiaofang Quan et al.
PloS one, 7(3), e33376-e33376 (2012-03-20)
α-Mangostin, isolated from the hulls of Garcinia mangostana L., was found to have in vitro cytotoxicity against 3T3-L1 cells as well as inhibiting fatty acid synthase (FAS, EC 2.3.1.85). Our studies showed that the cytotoxicity of α-mangostin with IC(50) value
alpha-Mangostin from Garcinia mangostana Linn: an updated review of its pharmacological properties
Ibrahim MY, et al.,
Arabian Journal of Chemistry, 317-329 (2016)
Ali Ghasemzadeh et al.
Molecules (Basel, Switzerland), 23(8) (2018-07-26)
Since α-mangostin in mangosteen fruits was reported to be the main compound able to provide natural antioxidants, the microwave-assisted extraction process to obtain high-quality α-mangostin from mangosteen pericarp (Garcinia mangostana L.) was optimized using a central composite design and response
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