Dihydroactinidiolide Chemical Properties

Melting point:

70-71°

alpha 

D24 -121.0° (c = 1.05 in CHCl3)

Boiling point:

296.1±9.0 °C(Predicted)

Density 

1.05±0.1 g/cm3(Predicted)

FEMA 

4020 | (+/-)-(2,6,6-TRIMETHYL-2-HYDROXYCYCLOHEXYLIDENE)ACETIC ACID GAMMA-LACTONE

storage temp. 

Sealed in dry,Room Temperature

Odor

musk coumarin

JECFA Number

1164

LogP

2.600

NIST Chemistry Reference

2(4H)-benzofuranone, 5,6,7,7a-tetrahydro-4,4,7a-trimethyl-, (r)-(17092-92-1)

Safety Information

Safety Statements 

24/25

HS Code 

29329990

Dihydroactinidiolide Usage And Synthesis

Biological activity

Dihydroactinidiolide is present in plant leaves and fruits, is a potent plant growth inhibitor, a regulator of gene expression, and is also responsible for light adaptation in Arabidopsis. Dihydroactinidiolide has antioxidant activity, antibacterial activity, anticancer activity and neuroprotection.

Use

Dihydroactinidiolide is an ester organic matter, which can be used as a food flavor.

Uses

Dihydroactinidiolide, existing in plant leaves and fruits, is a potent plant growth inhibitor, a regulator of gene expression and is responsible for photo acclimation in Arabidopsis. Dihydroactinidiolide has antioxidant activity, antibacterial activity, anticancer activity and neuroprotective effect[1]. Dihydroactinidiolide is also an inhibitor of AChE (IC50=34.03 nM) and has scavenging activities for DPPH and (.NO). Dihydroactinidiolide is present in plant leaves and fruits and is a potent plant growth inhibitor, regulator of gene expression, and responsible for light adaptation in Arabidopsis.

Definition

ChEBI: Dihydroactinidiolide is a member of benzofurans.

References

[1] Das M, et al. Dihydroactinidiolide, a natural product against Aβ25-35 induced toxicity in Neuro2a cells: Synthesis, in silico and in vitro studies. Bioorg Chem. 2018 Dec;81:340-349. DOI:10.1016/j.bioorg.2018.08.037
[2] Das M, et al. Dihydroactinidiolide, a natural product against Aβ25-35 induced toxicity in Neuro2a cells: Synthesis, in silico and in vitro studies. Bioorg Chem. 2018 Dec;81:340-349. DOI:10.1016/j.bioorg.2018.08.037

Dihydroactinidiolide(17092-92-1)Related Product Information

• Tetrahydrofuran
• Ethyl 2-(Chlorosulfonyl)acetate
• TRIOXSALEN
• Citric acid
• Terpineol
• Di-tert-butyl peroxide
• Di-tert-butyl dicarbonate
• gamma-Nonanolactone
• 4-Hexanolide
• Polycaprolactone
• Ethanol
• Glycerol
• DIHYDROACTINIDIOLIDE
• Acetic anhydride
• Phenylacetic acid
• POLY(TETRAHYDROFURAN) STANDARD 20000
• Dihydroactinidiolide