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qinyangshengenin-3-O-β-D-oleandropyranosyl-(1-4)-β-D-cymaropyranosyl-(1-4)-β-D-digitoxopyranosi
qinyangshengenin-3-O-β-D-oleandropyranosyl-(1-4)-β-D-cymaropyranosyl-(1-4)-β-D-digitoxopyranosi
CAS No. 1186628-88-5
qinyangshengenin-3-O-β-D-oleandropyranosyl-(1-4)-β-D-cymaropyranosyl-(1-4)-β-D-digitoxopyranosi( ——— )
Catalog No. M39686 CAS No. 1186628-88-5
qinyangshengenin-3-O-β-D-oleandropyranosyl-(1→4)-β-D-cymaropyranosyl-(1→4)-β-D-digitoxopyranosi
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 25MG | Get Quote | Get Quote |
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| 50MG | Get Quote | Get Quote |
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| 100MG | Get Quote | Get Quote |
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| 200MG | Get Quote | Get Quote |
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| 500MG | Get Quote | Get Quote |
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| 1G | Get Quote | Get Quote |
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Biological Information
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Product Nameqinyangshengenin-3-O-β-D-oleandropyranosyl-(1-4)-β-D-cymaropyranosyl-(1-4)-β-D-digitoxopyranosi
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NoteResearch use only, not for human use.
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Brief Descriptionqinyangshengenin-3-O-β-D-oleandropyranosyl-(1→4)-β-D-cymaropyranosyl-(1→4)-β-D-digitoxopyranosi
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Descriptionqinyangshengenin-3-O-β-D-oleandropyranosyl-(1→4)-β-D-cymaropyranosyl-(1→4)-β-D-digitoxopyranosi
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In Vitro———
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In Vivo———
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Synonyms———
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PathwayOthers
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TargetOther Targets
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Recptor———
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Research Area———
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Indication———
Chemical Information
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CAS Number1186628-88-5
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Formula Weight———
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Molecular Formula———
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Purity>98% (HPLC)
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Solubility———
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SMILES———
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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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Illudin M
Illudin M is a cytotoxic sesquiterpene from the fungus O. illudens that alkylates DNA. It has a cytotoxicity of 6-100 nM against HL-60 human leukemia cells.Illudin M has anticancer activity and is a pre-drug for the synthesis of anticancer compounds.
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Rose bengal lactone
Rose bengal lactone (C.I. Solvent Red 141) is a rose bengal lactone stain commonly used to stain the nuclei of plant and animal cells.
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Pyrocatechol
Pyrocatechol its sulfonic acid is often present in the urine of many mammals. Small amounts of catechol occur naturally in fruits and vegetables along with the enzyme polyphenol oxidase. Upon mixing the enzyme with the substrate and exposure to oxygen (as when a potato or apple is cut) the colorless catechol oxidizes to reddish-brown benzoquinone derivatives.
