Description
Sclareol glycol is extracted from the plants of Salvia sclarea L. It has anxiogenic, adaptogenic and memory-facilitator effects and was mediated by different mechanisms of action such as interaction with GABA-ergic, stimulation of adenylate cyclase and dopaminergic transmitter. It inhibits clonidine-induced aggressive behavior via its effect on adenylate cyclase and perhaps involving synaptic transmitter action. It induces changes in core body temperature by interacting with the second messenger system of 3',5'-AMP in the brain thermoregulatory areas and with dopamine (DA) receptors.
Synonyms
1-Naphthaleneethanol, decahydro-2-hydroxy-2,5,5,8a-tetramethyl-, (1R,2R,4aS,8aS)-; (1R,2R,4aS,8aS)-Decahydro-2-hydroxy-2,5,5,8a-tetramethyl-1-naphthaleneethanol; 1-Naphthaleneethanol, decahydro-2-hydroxy-2,5,5,8a-tetramethyl-, [1R-(1α,2β,4aβ,8aα)]-; (-)-13,14,15,16-Tetranorlabdane-8α,12-diol; (-)-Sclareoldiol; 13,14,15,16-Tetranorlabdane-8,12-diol; 13,14,15,16-Tetranorlabdane-8α,12-diol; 8α,12-Dihydroxy-13,14,15,16-tetranorlabdane; Ambroxdiol; AT 1; Sukurarerin
IUPAC Name
(1R,2R,4aS,8aS)-1-(2-hydroxyethyl)-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-2-ol
Molecular Formula
C16H30O2
Canonical SMILES
CC1(CCCC2(C1CCC(C2CCO)(C)O)C)C
InChI
InChI=1S/C16H30O2/c1-14(2)8-5-9-15(3)12(14)6-10-16(4,18)13(15)7-11-17/h12-13,17-18H,5-11H2,1-4H3/t12-,13+,15-,16+/m0/s1
InChIKey
AIALTZSQORJYNJ-LQKXBSAESA-N
Boiling Point
315.3±10.0°C at 760 mmHg
Melting Point
132.2-133.0°C
Solubility
Soluble in Acetone, Chloroform, Dichloromethane, DMSO, Ethyl Acetate