(E)-Ligustilide

Modify Date: 2025-08-23 16:15:36

(E)-Ligustilide Structure
(E)-Ligustilide structure
Common Name (E)-Ligustilide
CAS Number 81944-08-3 Molecular Weight 190.23800
Density N/A Boiling Point N/A
Molecular Formula C12H14O2 Melting Point N/A
MSDS N/A Flash Point N/A

 Use of (E)-Ligustilide


(E)-Ligustilide is isolated from Angelica sinensis and has nephroprotective effects[1]。

 Names

Name trans-ligustilide
Synonym More Synonyms

 (E)-Ligustilide Biological Activity

Description (E)-Ligustilide is isolated from Angelica sinensis and has nephroprotective effects[1]。
Related Catalog
In Vitro (E)-Ligustilide (50 μM; 24-72 hours) decreases HK-2 cell survival to 86%, to 67% and to 49% for 24, 48 or 72 hours incubation, respectively[1]. (E)-Ligustilide (50 μM; 48-72 hours) alone decreases the metabolic activity to 87±6% and 71±8% after 48 and 72 h incubation, respectively, as compared to the control condition in HK-2 cells[1]. Cell Viability Assay[1] Cell Line: HK-2 cell Concentration: 50 μM Incubation Time: 24 hours, 48 hours and 72 hours Result: Decreased cell survival as a dose-dependent manner.
References

[1]. Bunel V, et al. Nephroprotective effects of ferulic acid, Z-ligustilide and E-ligustilide isolated from Angelica sinensis against cisplatin toxicity in vitro.Toxicol In Vitro. 2015 Apr;29(3):458-67.

 Chemical & Physical Properties

Molecular Formula C12H14O2
Molecular Weight 190.23800
Exact Mass 190.09900
PSA 26.30000
LogP 2.87380
Storage condition -20°C

 Synonyms

E-ligustilide
3-But-(E)-ylidene-4,5-dihydro-3H-isobenzofuran-1-one
(E)-Ligustilide
The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.
Top Suppliers:I want be here

Get all suppliers and price by the below link:

(E)-Ligustilide suppliers

(E)-Ligustilide price

Related Compounds: More...
(E,E)-2-<(4-methoxyphenyl)methylene>-3-(2-thienylmethylene)succinic anhydride
100047-10-7
(E)-N'-((1H-indol-3-yl)methylene)-2-((3,5-dihydroxy-1,2,4-triazin-6-yl)amino)acetohydrazide
307508-65-2
E-HYDROXYIMINO-PHENYLACETIC ACID
704-18-7
(E)-5-benzylidene-3-ethoxycarbonyl-4-hydroxyfuran-2(5H)-one
100074-98-4
(E)-N-[(E)-propylideneamino]propan-1-imine
15601-98-6
(e)-3-o-tolyl-acryloyl chloride
15873-40-2
E/Z-6-chloro-3-[1-(3-cyanophenyl)methylidene]-1,3-dihydroindol-2-one
1001331-99-2
(E)-N'-((1H-indol-3-yl)methylene)-3-((3,5-dihydroxy-1,2,4-triazin-6-yl)amino)propanehydrazide
307508-66-3
(E)-3-[N-(cyclopropylmethyl)-2,6-dinitro-4-(trifluoromethyl)anilino]prop-2-enal
116726-05-7
4-Phenyl-N-(1-thieno[3,2-d]pyrimidin-4-ylazetidin-3-yl)oxane-4-carboxamide
2380185-36-2
5-[[4-[6-(4-Chlorophenyl)pyridazin-3-yl]piperazin-1-yl]methyl]-3-propan-2-yl-1,2,4-oxadiazole
2380193-07-5
N-{[1-(1,3-benzothiazole-2-carbonyl)piperidin-4-yl]methyl}-3-methoxy-N-methylpyrazin-2-amine
2380185-28-2
4-Methyl-6-{5-[4-(pyrrolidine-1-sulfonyl)benzoyl]-octahydropyrrolo[3,4-c]pyrrol-2-yl}pyrimidine
2380177-02-4
1-{Pyrazolo[1,5-a]pyrazin-4-yl}-4-[3-(trifluoromethyl)-[1,2,4]triazolo[4,3-b]pyridazin-6-yl]piperazine
2380177-33-1
2-(1-{[1-(propan-2-yl)-1H-imidazol-4-yl]sulfonyl}azetidin-3-yl)-6-(pyridin-4-yl)-2,3-dihydropyridazin-3-one
2380186-16-1
5-(Furan-2-yl)-N-[(4-morpholin-4-ylthian-4-yl)methyl]-1,2-oxazole-3-carboxamide
2380188-23-6
(4E)-4-({[(3,4-dimethoxyphenyl)methyl]amino}methylidene)-2,5-dimethyl-3,4-dihydro-2H-1lambda6,2,6-thiadiazine-1,1,3-trione
2380195-72-0
N-(1-Thieno[3,2-d]pyrimidin-4-ylazetidin-3-yl)benzenesulfonamide
2380180-01-6
3-(4-Chlorophenyl)-6-(4-{[5-(oxan-4-yl)-1,3,4-oxadiazol-2-yl]methyl}piperazin-1-yl)pyridazine
2380194-43-2