118-34-3
118-34-3
Chemical Structure
Syringin
Synonym(s): Eleutheroside B
- CAS No.: 118-34-3
- Formula:C17H24O9
- Molecular Weight:372.37
IUPAC Name: (2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-(4-((E)-3-hydroxyprop-1-en-1-yl)-2,6-dimethoxyphenoxy)tetrahydro-2H-pyran-3,4,5-triol
InChIKey: QJVXKWHHAMZTBY-GCPOEHJPSA-N
SMILES: O[C@H]([C@@H](O)[C@@H]1O)[C@@H](O[C@@H]1CO)OC(C(OC)=CC(/C=C/CO)=C2)=C2OC
Biological Activity: Syringin (Eleutheroside B) is an active natural phenolic glycoside possessing various pharmacological activities, including anti-inflammatory, anti-irradiation, anti-osteoporosis and anticancer activities. Syringin also can be used to enhance memory, relieve fatigue, improve human cognition and protect ischemia heart against cerebrovascular damage, etc[1].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Syringin | 99.93% | Syringin (Eleutheroside B) is an active natural phenolic glycoside possessing various pharmacological activities, including anti-inflammatory, anti-irradiation, anti-osteoporosis and anticancer activities. Syringin also can be used to enhance memory, relieve fatigue, improve human cognition and protect ischemia heart against cerebrovascular damage, etc. | ||||||||||||||||||||
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Syringin (Standard) | 99.13% | Syringin (Standard) is the analytical standard of Syringin. This product is intended for research and analytical applications. Syringin (Eleutheroside B) is an active natural phenolic glycoside possessing various pharmacological activities, including anti-inflammatory, anti-irradiation, anti-osteoporosis and anticancer activities. Syringin also can be used to enhance memory, relieve fatigue, improve human cognition and protect ischemia heart against cerebrovascular damage, etc. | ||||||||||||||||||||
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Methylsyringin | 99.34% | Methylsyringin exhibits anti-inflammatory activity in the LPS-stimulated RAW264.7 cells. | ||||||||||||||||||||
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Erigeside II | Erigeside II is a sesquiterpene glycoside found in the root bark of Dictamnus dasycarpus. Erigeside II stimulates the proliferation of T-cells. | |||||||||||||||||||||
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trans-p-Sinapoyl-β-D-glucopyranoside | trans-p-Sinapoyl-β-D-glucopyranoside is a phenolic acid glycoside and Antibacterial agent. trans-p-Sinapoyl-β-D-glucopyranoside can be isolated from chili pepper (Capsicum annuum L.) and Sorbaria tomentosa. trans-p-Sinapoyl-β-D-glucopyranoside scavenges DPPH free radicals. trans-p-Sinapoyl-β-D-glucopyranoside exhibits anticancer, anti-inflammatory, antidiabetic and antihypertensive activities. trans-p-Sinapoyl-β-D-glucopyranoside exerts antioxidant activity by inhibiting the fading of β-Carotene (HY-N0411) emulsion. | |||||||||||||||||||||
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Sinapaldehyde glucoside | Sinapaldehyde glucoside is a phenolic compound that can be isolated from the bark of Phellodendron amurense. | |||||||||||||||||||||
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Pipercroside A | Pipercroside A is found in Piper crocatum Ruiz & Pav. Pipercroside A is a CYP51 inhibitor. Pipercroside A has antifungal activity. | |||||||||||||||||||||
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Acantrifoside E | Acantrifoside E (Compound 8) is a nature compound. Acantrifoside E can be isolated from the 90% ethanol extract of Salacia cochinchinensis. Acantrifoside E has none α-glucosidase inhibitory activity. | |||||||||||||||||||||
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Coniferin (Standard) | ≥98% | Coniferin (Standard) is an analytical standard for Coniferin. This product is intended for research and analytical applications. Coniferin (Laricin) is a glucoside of coniferyl alcohol. Coniferin inhibits fungal melanization. Coniferin inhibits the release of certain hormones from cells, including Prostaglandin E2 and Thromboxane B2. | ||||||||||||||||||||
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Di-O-methylcrenatin | Di-O-methylcrenatin is a secondary metabolite which can be isolated from S. trojana. Di-O-methylcrenatin has antioxidant and anti-cancer activity. | |||||||||||||||||||||
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Glucosyringic acid | 99.62% | Glucosyringic acid is a compound isolated from Saxifraga Montana H.. | ||||||||||||||||||||
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Leonuriside A | 99.79% | Leonuriside A is a phenolic compound that can be isolated from Leonurus japonicus. Leonuriside A exhibits anti-inflammatory activity, which inhibits the iNOS-related inflammatory pathway in LPS (HY-D1056)-stimulated macrophages, thereby suppressing the production of nitric oxide (NO) with an IC50 of 15.6 μM. Leonuriside A can be used in studies of anti-inflammatory natural products and the molecular mechanisms of inflammation. | ||||||||||||||||||||
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