- Gamma-mangostin
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- $0.10 / 1KG
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2024-07-15
- CAS:31271-07-5
- Min. Order: 1KG
- Purity: 99.0%
- Supply Ability: 1000 tons
- Gamma-mangostin
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- $0.00 / 5mg
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2023-02-24
- CAS:31271-07-5
- Min. Order: 5mg
- Purity: ≥98%(HPLC)
- Supply Ability: 10 g
- Gamma-mangostin
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- $0.00 / 1g
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2021-07-20
- CAS:31271-07-5
- Min. Order: 5mg
- Purity: 99%HPLC
- Supply Ability: 2000tons
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| Product Name: | Gamma-mangostin | | Synonyms: | Gamma-mangostin;1,3,6,7-Tetrahydroxy-2,8-bis(3-methyl-2-butenyl)-9H-xanthen-9-one;Normangostin;r-Mangostin;1,3,6,7-Tetrahydroxy-2,8-bis(3-Methylbut-2-en-1-yl)-9H-xanthen-9-one;1,3,6,7-Tetrahydroxy-2,8-bis(3,3-dimethylallyl)xanthone;gamma-Mangostin (r-Mangostin);Nomangostin | | CAS: | 31271-07-5 | | MF: | C23H24O6 | | MW: | 396.43 | | EINECS: | | | Product Categories: | | | Mol File: | 31271-07-5.mol |  |
| | Gamma-mangostin Chemical Properties |
| Melting point | 206-208 °C | | Boiling point | 648.4±55.0 °C(Predicted) | | density | 1.326±0.06 g/cm3(Predicted) | | storage temp. | 2-8°C | | solubility | methanol: soluble1mg/mL, colorless to yellow | | form | powder | | pka | 7.05±0.20(Predicted) | | color | off-white to yellow | | InChI | InChI=1S/C23H24O6/c1-11(2)5-7-13-15(24)9-18-20(22(13)27)23(28)19-14(8-6-12(3)4)21(26)16(25)10-17(19)29-18/h5-6,9-10,24-27H,7-8H2,1-4H3 | | InChIKey | VEZXFTKZUMARDU-UHFFFAOYSA-N | | SMILES | C1(=O)C2=C(C=C(O)C(O)=C2C/C=C(/C)\C)OC2=C1C(O)=C(C/C=C(/C)\C)C(O)=C2 | | LogP | 5.744 (est) |
| Hazard Codes | Xn | | Risk Statements | 22 | | WGK Germany | 3 | | RTECS | ZD6122330 |
| | Gamma-mangostin Usage And Synthesis |
| Background |
Garcinia mangostana L., commonly known as mangosteen, is a tree mainly found in India, Myanmar, Sri Lanka and Thailand. The pericarp of mangosteen has been used in Thailand as an indigenous medicine for treating skin infections, wounds and diarrhea. The major bioactive compounds in mangosteen are xanthone derivatives, with α-mangostin (1, α-M) and Gamma-mangostin (4, γ-M) being the main derivatives isolated. α-M and γ-M possess not only antioxidant activity but also a wide range of biological activities, such as tumour cell-selective apoptosis and the attenuation of amyloid-β neurotoxicity and anti-inflammation. Gamma-mangostin strongly inhibited human colorectal adenocarcinoma cell proliferation. It was shown that γ-mangostin may mediate cytotoxicity via apoptosis in HT29 cells. Hence, it is a strong lead compound candidate in treating colon cancer cell growth and may directly affect colorectal adenocarcinoma cancer susceptibility through its modulation of cell proliferation and apoptosis[1].
| | Uses |
Gamma-Mangostin is a xanthones which displays anti-oxidant properties and could be a promising compound for the therapy of AlzheimerтАЩs disease.
| | Definition | ChEBI: A member of the class of xanthones that is 9H-xanthene substituted by hydroxy group at positions 1, 3, 6 and 7, an oxo group at position 9 and prenyl groups at positions 2 and 8. Isolated from the stems of Cratoxylum cochinchinense
/ital>, it exhibits antitumour activity. | | References |
[1] Takeshi Yokoyama. “Discovery of γ-Mangostin as an Amyloidogenesis Inhibitor.” Scientific Reports (2015): 13570.
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| | Gamma-mangostin Preparation Products And Raw materials |
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