7-demethylsuberosin
CAS No. 21422-04-8
7-demethylsuberosin( Demethylsuberosin )
Catalog No. M20413 CAS No. 21422-04-8
7-demethylsuberosin is a coumarin compound isolated from Angelica gigas Nakaiand has anti-inflammatory activityand exhibited inhibitory effects on PGE2 production with the IC50 values of 9.42 μM.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 57 | In Stock |
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| 2MG | 33 | In Stock |
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| 5MG | 51 | In Stock |
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| 10MG | 85 | In Stock |
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| 25MG | 161 | In Stock |
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| 50MG | 235 | In Stock |
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| 100MG | 352 | In Stock |
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| 200MG | Get Quote | In Stock |
|
| 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 Name7-demethylsuberosin
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NoteResearch use only, not for human use.
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Brief Description7-demethylsuberosin is a coumarin compound isolated from Angelica gigas Nakaiand has anti-inflammatory activityand exhibited inhibitory effects on PGE2 production with the IC50 values of 9.42 μM.
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Description7-demethylsuberosin is a coumarin compound isolated from Angelica gigas Nakaiand has anti-inflammatory activityand exhibited inhibitory effects on PGE2 production with the IC50 values of 9.42 μM.
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In Vitro——
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In Vivo——
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SynonymsDemethylsuberosin
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PathwayGPCR/G Protein
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TargetProstaglandin Receptor
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RecptorPGE2
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Research Area——
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Indication——
Chemical Information
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CAS Number21422-04-8
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Formula Weight230.26
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Molecular FormulaC14H14O3
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 250 mg/mL (1085.73 mM)
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SMILESC\C(C)=C\Cc1cc2ccc(=O)oc2cc1O
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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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16-dimethyl PGE2
16,16-Dimethyl prostaglandin E2 (16,16-dimethyl PGE2) is an orally active vertebrate Hematopoietic stem cells (HSCs) homeostasis critical regulator. 16,16-Dimethyl prostaglandin E2 can act through EP2/EP4 and has an interaction with the Wnt pathway.
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MF-766
MF-766 is a highly potent, selective and orally active EP4 antagonist with a Ki of 0.23 nM. It behaves as a full antagonist with an IC50 of 1.4 nM (shifted to 1.8 nM in the presence of 10% HS) in the functional assay. It can be used for cancer and inflammation diseases research.
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ONO-1301
A stable, orally active, non-prostanoid prostacyclin I2 (PGI2) mimetic and prostacyclin agonist with inhibitory activity against thromboxane A2 synthase.
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