Asperosaponin Ⅵ
CAS No. 39524-08-8
Asperosaponin Ⅵ( —— )
Catalog No. M18520 CAS No. 39524-08-8
Asperosaponin Ⅵ is extracted from Dipsacus asperoides.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 10MG | 88 | In Stock |
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| 25MG | 157 | In Stock |
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| 100MG | Get Quote | In Stock |
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| 200MG | Get Quote | In Stock |
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| 500MG | Get Quote | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product NameAsperosaponin Ⅵ
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NoteResearch use only, not for human use.
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Brief DescriptionAsperosaponin Ⅵ is extracted from Dipsacus asperoides.
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DescriptionAsperosaponin Ⅵ is extracted from Dipsacus asperoides.
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In Vitro——
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In Vivo——
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Synonyms——
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PathwayChromatin/Epigenetic
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TargetCOX
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RecptorOthers
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Research AreaOthers-Field
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Indication——
Chemical Information
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CAS Number39524-08-8
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Formula Weight929.1
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Molecular FormulaC47H76O18
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Purity>98% (HPLC)
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SolubilityIn Vitro:?H2O : 100 mg/mL (107.63 mM)
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SMILES[C@]1([C@H]2[C@](CC[C@@H]1O[C@@H]1OC[C@@H]([C@@H]([C@H]1O)O)O)([C@@H]1[C@@](CC2)([C@]2(C(=CC1)[C@H]1[C@@](CC2)(CCC(C1)(C)C)C(=O)O[C@@H]1O[C@@H]([C@H]([C@@H]([C@H]1O)O)O)CO[C@H]1[C@@H]([C@H]([C@@H]([C@H](O1)CO)O)O)O)C)C)C)(CO)C
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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4',7-Dihydroxyflavon...
4',7-Dihydroxyflavone can induce transcription of nodulation (nod) genes in Rhizobium meliloti. It has inhibitory activities against COX-2.Root exudate from 3-day-old alfalfa seedlings was purified and then assayed for biological activity with a nodABC-lacZ fusion in R. meliloti.
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SC 58125
SC-58125 is a selective cyclooxygenase 2 (COX-2) inhibitor,?with an IC50 of 0.04 μM. SC-58125 exhibits antitumor activity in vitro and in vivo, and it also can inhibit edema at the inflammatory site and is analgesicSC-58125 treatment on the growth of human colon carcinoma cells in nude mice.?
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Sasapyrine
Salsalate is a nonsteroidal anti-inflammatory agent for oral administration. Salsalate's mode of action as an anti-inflammatory and antirheumatic agent may be due to inhibition of synthesis and release of prostaglandins.
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