Methyl Kakuol
CAS No. 70342-29-9
Methyl Kakuol( -(6-methoxy-1,3-benzodioxol-5-yl)propan-1-one )
Catalog No. M29193 CAS No. 70342-29-9
Methyl Kakuol is an agonist of TRPA1 with an EC50 of 0.27 μM and can be used in studies about acting as an active ingredient in MBST constituent Asiasari Radix.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 93 | In Stock |
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| 5MG | 158 | In Stock |
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| 10MG | 252 | In Stock |
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| 25MG | 411 | In Stock |
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| 100MG | Get Quote | In Stock |
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| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
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Biological Information
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Product NameMethyl Kakuol
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NoteResearch use only, not for human use.
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Brief DescriptionMethyl Kakuol is an agonist of TRPA1 with an EC50 of 0.27 μM and can be used in studies about acting as an active ingredient in MBST constituent Asiasari Radix.
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DescriptionMethyl Kakuol is an agonist of TRPA1 with an EC50 of 0.27 μM and can be used in studies about acting as an active ingredient in MBST constituent Asiasari Radix.
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In Vitro——
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In VivoThe maximum concentration (Cmax) of Methyl kakuol at a dose of 2 g/kg (containing 1156 μg/kg, 294 μg/kg, 452 μg/kg, 852 μg/kg asarinin, sesamin, methyl kakuol, and amide A, respectively) is 98.2 ng/mL.
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Synonyms-(6-methoxy-1,3-benzodioxol-5-yl)propan-1-one
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PathwayMembrane Transporter/Ion Channel
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TargetTRP/TRPV Channel
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RecptorTRP/TRPV Channel
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Research Area——
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Indication——
Chemical Information
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CAS Number70342-29-9
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Formula Weight208.213
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Molecular FormulaC11H12O4
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Purity>98% (HPLC)
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Solubility——
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SMILESCCC(=O)c1cc2OCOc2cc1OC
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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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n-Butylidenephthalid...
(Z)-3-butylidenephthalide has antihyperglycemic effect is due to inhibition of α-glucosidase at the intestinal level, inhibited the activity of yeast-α-glucosidase (IC(5) 2.35 mM) in a noncompetitive fashion with a K(i) of 4.86 mM.
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AMTB hydrochloride
AMTB is a novel TRPM8 channel blocker and is effective for pain and urinary diseases.
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Pyr10
Pyr10 is a pyrazole derivative and a selective TRP cation 3 inhibitor. Pyr10 has the ability to distinguish between receptor-operated TRPC3 and native stromal interaction molecule 1 (STIM1)/Orai1 channels. Pyr10 inhibits Ca2+ influx in carbachol-stimulated TRPC3-transfected HEK293 cells (IC50: 0.72 μM) (IC50 of 13.08 μM for store-operated Ca2+ entry in BRL-2H3 cells) .
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