Eugenol 4-O-beta-D-(6-O-galloyl) glucopyranoside
CAS No. 152041-15-1
Eugenol 4-O-beta-D-(6-O-galloyl) glucopyranoside( ——— )
Catalog No. M39259 CAS No. 152041-15-1
Eugenol 4-O-beta-D-(6'-O-galloyl) glucopyranoside
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
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Biological Information
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Product NameEugenol 4-O-beta-D-(6-O-galloyl) glucopyranoside
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NoteResearch use only, not for human use.
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Brief DescriptionEugenol 4-O-beta-D-(6'-O-galloyl) glucopyranoside
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DescriptionEugenol 4-O-beta-D-(6'-O-galloyl) 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 Number152041-15-1
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Formula Weight478.5
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Molecular FormulaC23H26O11
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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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(3Z)-1-methyl-3-[2-(...
(3Z)-1-methyl-3-[2-(4-methylphenyl)-2-oxo-ethylidene]piperazin-2-one is a chemical agent.
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Schnurri-3 inhibitor...
Schnurri-3 inhibitor-1, a potent inhibitor of schnurri-3, is an essential regulator of bone formation in adults that can be used in osteoporosis research. Schnurri-3 inhibitor-1 can inhibit Shn3 with EF1alpha promoter in osteoblast cell line Shn3FFL (AC50 = 2.09 μM) .
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Compound K
HIV-IN-11 is part of the hydroxylaminoglutaramide (HAPA) transition state isomeric series of HIV protease inhibitors and is a potent and selective inhibitor of HIV-1 protease. HIV-IN-11 competitively inhibits HIV-1 PR (Ki: 0.049 nM) and potently inhibits replication of HIV(IIIb)-infected MT4 lymphocytes at concentrations of 25.0-50.0 nM. HIV-IN-11 displays a longer half-life than indinavir sulfate in animal models and serves as a promising second-generation HIV protease inhibitor.
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