30861-27-9
30861-27-9
Chemical Structure
Aloesin
Synonym(s): Aloeresin
- CAS No.: 30861-27-9
- Formula:C19H22O9
- Molecular Weight:394.37
IUPAC Name: 7-hydroxy-5-methyl-2-(2-oxopropyl)-8-((2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)-4H-chromen-4-one
InChIKey: HKIKAXXIWJHWLY-ZIIYPAMZSA-N
SMILES: OC1=CC(C)=C(C(C=C(CC(C)=O)O2)=O)C2=C1[C@@H]3O[C@@H]([C@@H](O)[C@H](O)[C@H]3O)CO
Biological Activity: Aloesin (Aloeresin) is a tyrosinase inhibitor, and shows anti-inflammatory activity, ultraviolet protection, and antibacterium effects. Aloesin can induce apoptosis and be used in ovarian cancer research[1][2][3].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Aloesin | 99.81% | Aloesin (Aloeresin) is a tyrosinase inhibitor, and shows anti-inflammatory activity, ultraviolet protection, and antibacterium effects. Aloesin can induce apoptosis and be used in ovarian cancer research. | ||||||||||||||||||||
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Structural Analogs
-
Similarity Score 0.87
HY-N118938-C-Glucosyl-(R)-aloesol -
Similarity Score 0.77
HY-N118927-O-Methylaloesinol -
Similarity Score 0.75
HY-N12693Isobiflorin -
Similarity Score 0.75
HY-N89678-Glucosyl-5,7-dihydroxy-2-(1-methylpropyl)chromone -
Similarity Score 0.74
HY-N97648-Glucosyl-5,7-dihydroxy-2-isopropylchromone -
Similarity Score 0.72
HY-N12447C-2′-Decoumaroylaloeresin G -
Similarity Score 0.72
HY-N17768Obtusichromoneside B -
Similarity Score 0.71
HY-N7219Aloeresin A -
Similarity Score 0.67
HY-N15726Obtusichromoneside C -
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References
- [1]. Zhang LQ, et al. Aloesin Suppresses Cell Growth and Metastasis in Ovarian Cancer SKOV3 Cells through the Inhibition of the MAPK Signaling Pathway. Anal Cell Pathol (Amst). 2017;2017:8158254. [Content Brief]
- [2]. Wahedi HM, et al. Aloesin from Aloe vera accelerates skin wound healing by modulating MAPK/Rho and Smad signaling pathways in vitro and in vivo. Phytomedicine. 2017 May 15;28:19-26. [Content Brief]
- [3]. Y H Jin, et al. Aloesin and arbutin inhibit tyrosinase activity in a synergistic manner via a different action mechanism. Arch Pharm Res. 1999 Jun;22(3):232-6. [Content Brief]
