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Cyanidin-3-O-[6-O-trans-caffeyl-(6-O-p-hydroxybenzoyl-2-O-β-glucopyranosyl)]-β-glucopyranoside)-5-O-β-glucopyranoside
Cyanidin-3-O-[6-O-trans-caffeyl-(6-O-p-hydroxybenzoyl-2-O-β-glucopyranosyl)]-β-glucopyranoside)-5-O-β-glucopyranoside
CAS No. 185044-11-5
Cyanidin-3-O-[6-O-trans-caffeyl-(6-O-p-hydroxybenzoyl-2-O-β-glucopyranosyl)]-β-glucopyranoside)-5-O-β-glucopyranoside( ——— )
Catalog No. M39760 CAS No. 185044-11-5
Cyanidin-3-O-[6-O-trans-caffeyl-(6-O-p-hydroxybenzoyl-2-O-β-glucopyranosyl)]-β-glucopyranoside)-5-O-β-glucopyranoside
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
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Biological Information
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Product NameCyanidin-3-O-[6-O-trans-caffeyl-(6-O-p-hydroxybenzoyl-2-O-β-glucopyranosyl)]-β-glucopyranoside)-5-O-β-glucopyranoside
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NoteResearch use only, not for human use.
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Brief DescriptionCyanidin-3-O-[6-O-trans-caffeyl-(6-O-p-hydroxybenzoyl-2-O-β-glucopyranosyl)]-β-glucopyranoside)-5-O-β-glucopyranoside
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DescriptionCyanidin-3-O-[6-O-trans-caffeyl-(6-O-p-hydroxybenzoyl-2-O-β-glucopyranosyl)]-β-glucopyranoside)-5-O-β-glucopyranoside
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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 Number185044-11-5
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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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Laurdan
Laurdan is a membrane-permeable fluorescent probe that displays spectral sensitivity to the phospholipid phase of the cell membrane to which it is bound.
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4-Nitrobenzoic acid
4-Nitrobenzoic acid (4Nitrobenzoic acid) is a pharmaceutical intermediate often found in the production of folic acid, DABA, PABA and dyes.
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PKC ζ pseudosubstrat...
Inhibitor of protein kinase C (PKC) ζ; attached to cell permeabilisation Antennapedia domain vector peptide. Consists of amino acids 113 - 129 of PKC ζ pseudosubstrate domain linked by a disulphide bridge to the Antennapedia domain vector peptide. The Antennapedia peptide is actively taken up by intact cells, at 4 or 37°C, ensuring rapid and effective uptake of the inhibitor peptide. Once inside the cell, the disulphide bonds are subjected to reduction in the cytoplasm leading to release of the inhibitor peptide. Induces mast cell degranulation by a PKC ζ-independent pathway.
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