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Medicarpin (b)
CAS No. 33983-39-0
Medicarpin (b)( —— )
Catalog No. M26573 CAS No. 33983-39-0
(+)-Medicarpin potently inhibits osteoclastogenesis and promotes bone healing and increases bone mass by osteoblast differentiation with estrogen receptor (ER) β-mediated osteogenic action.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 840 | Get Quote |
|
| 10MG | 1143 | Get Quote |
|
| 25MG | 1692 | Get Quote |
|
| 50MG | 2277 | Get Quote |
|
| 100MG | 3087 | Get Quote |
|
| 200MG | Get Quote | Get Quote |
|
| 500MG | Get Quote | Get Quote |
|
| 1G | Get Quote | Get Quote |
|
Biological Information
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Product NameMedicarpin (b)
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NoteResearch use only, not for human use.
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Brief Description(+)-Medicarpin potently inhibits osteoclastogenesis and promotes bone healing and increases bone mass by osteoblast differentiation with estrogen receptor (ER) β-mediated osteogenic action.
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Description(+)-Medicarpin potently inhibits osteoclastogenesis and promotes bone healing and increases bone mass by osteoblast differentiation with estrogen receptor (ER) β-mediated osteogenic action. (+)-Medicarpin, a pterocarpan, is a type of isoflavonoid isolated from several medicinal plant species with various biological effects, including Sophora japonica, Zollernia paraensis and Platymiscium yucatamun, Machaerium aristulatum, Platymiscium floribundum, and so on.
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In Vitro——
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In Vivo——
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Synonyms——
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PathwayEndocrinology/Hormones
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TargetEstrogen Receptor/ERR
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RecptorHIV-1| TLR7| TLR8
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Research Area——
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Indication——
Chemical Information
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CAS Number33983-39-0
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Formula Weight270.284
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Molecular FormulaC16H14O4
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Purity>98% (HPLC)
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Solubility——
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SMILES[H][C@]12COc3cc(O)ccc3[C@@]1([H])Oc1cc(OC)ccc21
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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
1.Buitendijk M, et al. Gardiquimod: a Toll-like receptor-7 agonist that inhibits HIV type 1 infection of human macrophages and activated T cells. AIDS Res Hum Retroviruses. 2013 Jun;29(6):907-18.
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