Cart
sales@molnova.com
Senkyunolide I
CAS No. 94596-28-8
Senkyunolide I( Senkyunolide I | Ligustilidiol, (Z)- | Ligustilidiol )
Catalog No. M19281 CAS No. 94596-28-8
Senkyunolide I has neuroprotective effect, associated with its anti-oxidation and anti-apoptosis properties.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 86 | In Stock |
|
| 5MG | 77 | In Stock |
|
| 10MG | 104 | In Stock |
|
| 25MG | 155 | In Stock |
|
| 50MG | 230 | In Stock |
|
| 100MG | 352 | In Stock |
|
| 200MG | 520 | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameSenkyunolide I
-
NoteResearch use only, not for human use.
-
Brief DescriptionSenkyunolide I has neuroprotective effect, associated with its anti-oxidation and anti-apoptosis properties.
-
DescriptionSenkyunolide I has antioxidant and anti-migraine activities; isolated from Ligusticum chuanxiong.
-
In Vitro——
-
In Vivo——
-
SynonymsSenkyunolide I | Ligustilidiol, (Z)- | Ligustilidiol
-
PathwayOthers
-
TargetOther Targets
-
RecptorOthers
-
Research AreaOthers-Field
-
Indication——
Chemical Information
-
CAS Number94596-28-8
-
Formula Weight224.25
-
Molecular FormulaC12H16O4
-
Purity>98% (HPLC)
-
SolubilityIn Vitro:?DMSO : 100 mg/mL (445.93 mM)
-
SMILESCCCC=C1C2=C(C(C(CC2)O)O)C(=O)O1
-
Chemical Name(6R,7R,Z)-3-butylidene-6,7-dihydroxy-4,5,6,7-tetrahydroisobenzofuran-1(3H)-one
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
molnova catalog
related products
-
Ethyl 2-ethylhexanoa...
Ethyl 2-ethylhexanoate is a RIFM fragrance and an active ingredient in mosquito repellents.
-
MTIC
MTIC is the active metabolite of Temozolomide (TMZ) with anticancer and antitumor activity and is used in the study of melanoma.3'-Sialyllactose (3'-SL) sodium is a prebiotic with anti-inflammatory activity.
-
Cephalandole B
cephalandole B, an indole alkaloid isolated from cyanide, significantly inhibited IL-17A gene expression and suppressed IL-17A luciferase reporter in Jukat cells in a dose-dependent manner.
