118024-26-3
118024-26-3
Chemical Structure
Blumeatin
- CAS No.: 118024-26-3
- Formula:C16H14O6
- Molecular Weight:302.28
IUPAC Name: (S)-2-(3,5-dihydroxyphenyl)-5-hydroxy-7-methoxychroman-4-one
InChIKey: YEYLMQKEGSQNGZ-AWEZNQCLSA-N
SMILES: O=C1C[C@@H](C2=CC(O)=CC(O)=C2)OC3=CC(OC)=CC(O)=C13
Biological Activity: Blumeatin, isolated from Blumea balsamifera DC, could protect liver against injury induced by CCl4 and thioacetamide (TAA)[1].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Blumeatin | 99.90% | Blumeatin, isolated from Blumea balsamifera DC, could protect liver against injury induced by CCl4 and thioacetamide (TAA). | ||||||||||||||||||||
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(RS)-Sakuranetin | (RS)-Sakuranetin is the racemate of Sakuranetin (HY-N3006). | |||||||||||||||||||||
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Hesperetin | 99.12% | Hesperetin is a natural flavanone that can be found in citrus, and acts as a potent and orally active broad-spectrum inhibitor against human UGT activity. Hesperetin induces apoptosis via p38 MAPK activation. Hesperetin displays a range of bioactivities including antioxidant, anti-inflammatory, and anti-cancer. Hesperetin is found to induce cell-cycle arrest at G2/M phase. Hesperetin can reduce Bcl-2 and enhance BaxM. Hesperetin induces apoptosis through inhibiting NF-κB receptor. | ||||||||||||||||||||
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(Rac)-Hesperetin (Standard) | ≥98% | (Rac)-Hesperetin (Standard) is the analytical standard of (Rac)-Hesperetin. This product is intended for research and analytical applications. (Rac)-Hesperetin is the racemate of Hesperetin (HY-N0168), an orally active multi-target inhibitor. (Rac)-Hesperetin exhibits significant anti-tumor and anti-inflammatory activities by blocking the TGF-β1-mediated Fyn/RhoA signaling axis and the TLR4-MyD88-NF-κB inflammatory pathway. (Rac)-Hesperetin inhibits the formation of actin stress fibers and the migration and invasion of cancer cells, and is suitable for triple-negative breast cancer research. In inflammation models, (Rac)-Hesperetin effectively alleviates lung injury by reducing the release of pro-inflammatory mediators and regulating the activity of oxidative stress enzymes, and is suitable for acute lung injury research. (Rac)-Hesperetin also interferes with the entry and early replication processes of channel catfish virus, inhibits viral gene expression and progeny virus production, thereby protecting cells from virus-induced cytopathic effects. | ||||||||||||||||||||
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Sternbin | 99.98% | Sternbin (Eriodictyol 7-methyl ether) is a flavanone and antibacterial agent. Sternbin can be isolated from Heliotropium sinuatum. Sternbin has antibacterial activity against a wide range of bacteria. Sternbin has antiviral activity against infectious salmon anemia virus (ISAV). Sternbin inhibits the contraction of isolated rat smooth muscle. | ||||||||||||||||||||
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Sakuranetin (Standard) | ≥98% | Sakuranetin is a cherry flavonoid phytoalexin, shows strong antifungal activity. Sakuranetin has anti-inflammatory and antioxidative activities. Sakuranetin ameliorates LPS-induced acute lung injury. | ||||||||||||||||||||
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(2S)-5,7,3',5'-Tetrahydroxyflavanone | (2S)-5,7,3',5'-Tetrahydroxyflavanone ((2S)-3',5,5'7-Tetrahydroxyflavanone) is a porcine pancreatic lipase modulator with an IC50 of >200 μM against porcine pancreatic lipase. (2S)-5,7,3',5'-Tetrahydroxyflavanone interacts with an enzyme involved in triglyceride hydrolysis. | |||||||||||||||||||||
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Persicogenin | 98.55% | Persicogenin, isolated from Rhus retinorrhoea, possesses anti-cancer activity. | ||||||||||||||||||||
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Homoeriodictyol | 99.86% | Homoeriodictyol is an orally active, bitter-tasting flavanone that can penetrate the blood-brain barrier. Homoeriodictyol enhances synaptic-related protein expression through NCOA4-mediated ferritin autophagy. Homoeriodictyol improves memory impairment in mice by inhibiting the NLRP3 inflammasome. Homoeriodictyol protects human endothelial cells from oxidative damage by activating Nrf2 and inhibiting mitochondrial dysfunction. Homoeriodictyol enhances ROS activity and induces apoptosis, exhibiting anticancer effects. Homoeriodictyol inhibits the survival and migration of androgen-resistant prostate cancer cells in vitro. Homoeriodictyol exerts antinociceptive activity in mice in vivo. | ||||||||||||||||||||
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Eriodictyol 7, 3'-dimethyl ether | Eriodictyol 7, 3'-dimethyl ether (compound 11) is the first flavonoid extract from B. riparia with antioxidant and antibacterial activity. | |||||||||||||||||||||
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(±)Homoeriodictyol | (±) Homoeriodictyol is a Aromatase/CYP19 inhibitor that can be used in breast cancer research. | |||||||||||||||||||||
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