Luan, Zhen-jie team published research in Industrial Crops and Products in 2020 | 24034-73-9

Recommanded Product: (2E,6E,10E)-3,7,11,15-Tetramethylhexadeca-2,6,10,14-tetraen-1-ol, Geranylgeraniol is a diterpenoid that is hexadeca-2,6,10,14-tetraene substituted by methyl groups at positions 3, 7, 11 and 15 and a hydroxy group at position 1. It has a role as a plant metabolite, a volatile oil component and an antileishmanial agent. It is a diterpenoid and a polyprenol.

Geranylgeraniol, a precursor to geranylgeranylpyrophosphate, is an intermediate in the mevalonate pathway. Geranylgeraniol has been shown to prevent bone re-absorption, inhibition of osteoclast formation, and kinase activation in vitro. When working with statins, Geranylgeraniol can reduce the toxicity without inhibiting the cholesterol-producing effects. Geranylgeraniol has been documented to counteract the effects of fluvastatin by inhibiting activation of caspase-1 and production of IL-1. Additionally Geranylgeraniol has been found to induce apoptosis in HL-60 cells.
, 24034-73-9.

Recommanded Product: (2E,6E,10E)-3,7,11,15-Tetramethylhexadeca-2,6,10,14-tetraen-1-ol, In chemistry, an alcohol is a type of organic compound that carries at least one hydroxyl functional group (−OH) bound to a saturated carbon atom. 24034-73-9, name is (2E,6E,10E)-3,7,11,15-Tetramethylhexadeca-2,6,10,14-tetraen-1-ol, An important class of alcohols, of which methanol and ethanol are the simplest examples, includes all compounds which conform to the general formula CnH2n+1OH.

Luan, Zhen-jie;Li, Pei-pei;Li, Duo;Meng, Xiao-ping;Sun, Jing research published 《 Optimization of supercritical-CO2 extraction of Iris lactea seed oil: Component analysis and antioxidant activity of the oil》, the research content is summarized as follows. Iris lactea Pall. var. chinensis (Fisch.) Koidz. is a widely distributed species and the seeds of this species have been used as medicine. However, the chem. composition and biol. activities of the I. lactea seed oil (ILSO) have not been studied. In this present work, extraction time, temperature, and pressure were considered as variables and response surface methodol. based on the Box-Behnken design was utilized to identify the optimal conditions for supercritical fluid extraction of the ILSO. Furthermore, the main components (including fatty acids, unsaponifiables, and volatile components) in ILSO extracted with the above optimal conditions were identified by gas chromatog.-mass spectrometry. It was found that major fatty acids present in ILSO were linoleic acid (41.31%), oleic acid (34.74%), and docosahexaenoic acid (3.18%). The total content of sterols reached as high as the level of 87.44% in unsaponifiable matter and sterols with a content over 5% included β-sitosterol (27.14%) stigmasterol (18.38%), delta5-avenasterol (15.36%), campesterol (13.21%), and betulinicaldehyde (5.80%). The physicochem. properties of ILSO were analyzed according to Chinese national standards Total polyphenol content (TPC) and total tocopherol content of ILSO were also determined

Recommanded Product: (2E,6E,10E)-3,7,11,15-Tetramethylhexadeca-2,6,10,14-tetraen-1-ol, Geranylgeraniol is a diterpenoid that is hexadeca-2,6,10,14-tetraene substituted by methyl groups at positions 3, 7, 11 and 15 and a hydroxy group at position 1. It has a role as a plant metabolite, a volatile oil component and an antileishmanial agent. It is a diterpenoid and a polyprenol.

Geranylgeraniol, a precursor to geranylgeranylpyrophosphate, is an intermediate in the mevalonate pathway. Geranylgeraniol has been shown to prevent bone re-absorption, inhibition of osteoclast formation, and kinase activation in vitro. When working with statins, Geranylgeraniol can reduce the toxicity without inhibiting the cholesterol-producing effects. Geranylgeraniol has been documented to counteract the effects of fluvastatin by inhibiting activation of caspase-1 and production of IL-1. Additionally Geranylgeraniol has been found to induce apoptosis in HL-60 cells.
, 24034-73-9.

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts