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 | 149 | Get Quote |
|
| 5MG | 250 | Get Quote |
|
| 10MG | 399 | Get Quote |
|
| 25MG | 651 | Get Quote |
|
| 50MG | 888 | Get Quote |
|
| 100MG | Get Quote | Get Quote |
|
| 200MG | Get Quote | Get Quote |
|
| 500MG | Get Quote | Get Quote |
|
| 1G | Get Quote | Get Quote |
|
Biological Information
-
Product NameMethyl Kakuol
-
NoteResearch use only, not for human use.
-
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.
-
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.
-
In Vitro——
-
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.
-
Synonyms-(6-methoxy-1,3-benzodioxol-5-yl)propan-1-one
-
PathwayMembrane Transporter/Ion Channel
-
TargetTRP/TRPV Channel
-
RecptorTRP/TRPV Channel
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number70342-29-9
-
Formula Weight208.213
-
Molecular FormulaC11H12O4
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESCCC(=O)c1cc2OCOc2cc1OC
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
molnova catalog
related products
-
MK6-83
MK6-83 is the transient receptor potential channel ML3 agonist.
-
Pinokalant
Pinokalant (LOE-908) is a novel non-selective cation channel inhibitor.Pinokalant significantly reduces cortical infarct volume in in vivo experiments, improves the metabolic and electrophysiological status of the ischemic penumbra region.
-
BI-749327
BI-749327 is a high selectivity and orally bioavailable antagonist of TRPC6 (IC50s: 13 nM, 19 nM and 15 nM for mouse, human and guinea pig TRPC6).
Cart
sales@molnova.com