n-Butylidenephthalide
CAS No. 551-08-6
n-Butylidenephthalide( Butylidenephthalide | BP | 3-Butylidene Phthalide )
Catalog No. M18790 CAS No. 551-08-6
(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.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 35 | In Stock |
|
| 5MG | 29 | In Stock |
|
| 10MG | 46 | In Stock |
|
| 25MG | 72 | In Stock |
|
| 50MG | 100 | In Stock |
|
| 100MG | 145 | In Stock |
|
| 200MG | 212 | In Stock |
|
| 500MG | 362 | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product Namen-Butylidenephthalide
-
NoteResearch use only, not for human use.
-
Brief Description(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.
-
DescriptionButylidenephthalide is an inhibitor of platelet-derived growth factor (PDGF). Butylidenephthalide activity leads to the reduction of liver fibrosis, increased Nur77 (NR4A1) expression, and downregulation of EMT-related genes such as Snail (Snail/SNAI1) and Slug (Slug/SNAI2).
-
In Vitro3-Butylidenephthalide (Butylidenephthalide) abrogates the myofibroblasts activation and mesenchymal transdifferentiation in oral submucous fibrosis.
-
In Vivo——
-
SynonymsButylidenephthalide | BP | 3-Butylidene Phthalide
-
PathwayMembrane Transporter/Ion Channel
-
TargetTRP/TRPV Channel
-
Recptorα-glucosidase
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number551-08-6
-
Formula Weight188.22
-
Molecular FormulaC12H12O2
-
Purity>98% (HPLC)
-
SolubilityIn Vitro:?DMSO : 250 mg/mL (1328.23 mM)
-
SMILESCCCC=C1C2=CC=CC=C2C(=O)O1
-
Chemical Name3-Butylidene-2-benzofuran-1-one
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
molnova catalog
related products
-
TRPM4-IN-1
TRPM4-IN-1 is a potent and selective inhibitor of TRPM4 with an IC50 of 1.5 μM.
-
TC-I2000
TC-I2000 is an TRPM8 channel blocker. Inhibits?icilin-induced TRPM8 channel activation in rTRPM8-expressing CHO cells with IC50?of 53 nM.
-
AC1903
AC1903 is a specific inhibitor of TRPC5 channel, and has been shown to suppress severe proteinuria and prevent podocyte loss.AC1903, that specifically blocks TRPC5 channel activity in glomeruli of proteinuric rats.?
Cart
sales@molnova.com