| Identification | Back Directory | [Name]
(4aR)-5β-[2-(3-Furyl)ethyl]-3,4,4aβ,5,6,7,8,8a-octahydro-5,6α,8aα-trimethyl-1-naphthalenecarboxylic acid | [CAS]
1782-65-6 | [Synonyms]
(-)-Hardwickiic acid
(4aR)-5β-[2-(3-Furyl)ethyl]-3,4,4aβ,5,6,7,8,8a-octahydro-5,6α,8aα-trimethyl-1-naphthalenecarboxylic acid
(4aR,5R,6R,8aR)-5-[2-(furan-3-yl)ethyl]-5,6,8a-trimethyl-3,4,4a,6,7,8-hexahydronaphthalene-1-carboxylicaci
1-Naphthalenecarboxylic acid, 5-(2-(3-furanyl)ethyl)-3,4,4A,5,6,7,8,8A-octahydro-5,6,8A-trimethyl-, (4ar-(4aalpha,5alpha,6beta,8abeta))- | [Molecular Formula]
C20H28O3 | [MDL Number]
MFCD17214876 | [MOL File]
1782-65-6.mol | [Molecular Weight]
316.435 |
| Hazard Information | Back Directory | [Uses]
Hardwickiic acid ((-)-Hardwikiic acid) is an antinociceptive compound that blocks Tetrodotoxin-sensitive voltage-dependent sodium channels. Hardwickiic acid shows insecticidal activity[1][2]. | [Biological Activity]
Hardwickiic acid ((-)-Hardwikiic acid) is an antinociceptive compound that blocks Tetrodotoxin-sensitive voltage-dependent sodium channels. Hardwickiic acid shows insecticidal activity[1][2]. | [References]
[1]. Cai S, et al. (-)-Hardwickiic Acid and Hautriwaic Acid Induce Antinociception via Blockade of Tetrodotoxin-Sensitive Voltage-Dependent Sodium Channels. ACS Chem Neurosci. 2019 Mar 20;10(3):1716-1728.
[2]. Bandara BM, et al. Isolation and Insecticidal Activity of (-)-Hardwickiic Acid from Croton aromaticus. Planta Med. 1987 Dec;53(6):575. |
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