VOMIFOLIOL
VOMIFOLIOL Basic information
- Product Name:
- VOMIFOLIOL
- Synonyms:
-
- VOMIFOLIOL
- (1S)-1-Hydroxy-1-[(1E,3R)-3-hydroxy-1-butenyl]-2,6,6-trimethyl-2-cyclohexene-4-one
- (S)-4-Hydroxy-4-[(R,E)-3-hydroxy-1-butenyl]-3,5,5-trimethyl-2-cyclohexen-1-one
- Blumenol A
- 2-Cyclohexen-1-one,4-hydroxy-4-[(1E,3R)-3-hydroxy-1-buten-1-yl]-3,5,5-triMethyl-, (4S)-
- (6S,9R)-vomifoliol
- CAS:
- 23526-45-6
- MF:
- C13H20O3
- MW:
- 224.3
- Mol File:
- 23526-45-6.mol
VOMIFOLIOL Chemical Properties
- Melting point:
- 115 °C
- Boiling point:
- 362.3±42.0 °C(Predicted)
- Density
- 1.130±0.06 g/cm3(Predicted)
- solubility
- Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
- form
- Powder
- pka
- 12.72±0.60(Predicted)
- color
- White to off-white
- LogP
- 1.479 (est)
VOMIFOLIOL Usage And Synthesis
Uses
Vomifoliol, a compound related to abscisie acid (ABA), has a modified 2,4-pentadiene side chain and has activity equal to that displayed by ABA. Vomifoliol exhibits antiacetylcholinesterase activity and displays moderate antileishmanial activity[1][2].
Definition
ChEBI: (6S,9R)-vomifoliol is a (6S)-vomifoliol with a R configuration for the hydroxy group at position 9. It has a role as a phytotoxin and a metabolite. It is an enantiomer of a (6R,9S)-vomifoliol.
target
NF-kB | HIF | VEGFR
References
[1] Stuart KL, et al. The effect of vomifoliol on stomatal aperture. Planta. 1975;122(3):307-310. DOI:10.1007/BF00385281
[2] Mogana R, et al. The antiacetylcholinesterase and antileishmanial activities of Canarium patentinervium Miq. Biomed Res Int. 2014;2014:903529. DOI:10.1155/2014/903529
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