Naringenin trimethyl ether
CAS No. 38302-15-7
Naringenin trimethyl ether( —— )
Catalog No. M18499 CAS No. 38302-15-7
Naringenin trimethyl ether shows significant molluscicidal activity with a median lethal concentration (LC(5)) of 3.9 μg/mL.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 37 | In Stock |
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| 5MG | 33 | In Stock |
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| 10MG | 59 | In Stock |
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| 100MG | Get Quote | In Stock |
|
| 200MG | Get Quote | In Stock |
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| 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 NameNaringenin trimethyl ether
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NoteResearch use only, not for human use.
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Brief DescriptionNaringenin trimethyl ether shows significant molluscicidal activity with a median lethal concentration (LC(5)) of 3.9 μg/mL.
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DescriptionNaringenin trimethyl ether shows significant molluscicidal activity with a median lethal concentration (LC(5)) of 3.9 μg/mL.
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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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RecptorOthers
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Research AreaOthers-Field
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Indication——
Chemical Information
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CAS Number38302-15-7
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Formula Weight314.33
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Molecular FormulaC18H18O5
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Purity>98% (HPLC)
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Solubility——
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SMILESCOC1=CC=C(C=C1)C2CC(=O)C3=C(C=C(C=C3O2)OC)OC
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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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TriMetazidine EP IMp...
It is an organic compounds with molecular fomula C10H14O4.
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BDC2.5 mimotope 1040...
BDC2.5 mimotope 1040-51 is a mimotope peptide for diabetogenic T cell clone BDC2.5. isolated from non-obese diabetic mice.This is a effectively agonistic peptide (mimotope) for diabetogenic T cell clone BDC2.5. from non-obese diabetic (NOD) mice. T cells from prediabetic and diabetic NODs respond to BDC2.5 mimotope peptides.
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Aschantin
Aschantin, a bisepoxylignan, can be isolated from Magnolia biondii. Aschantin has antiplasmodial, Ca2+-antagonistic, platelet activating factor-antagonistic, and chemopreventive activities. Aschantin is a mTOR kinase inhibitor. Aschantin is also an inhibitor of Cytochrome P450 and UGT enzyme.
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