| Weight | 222.24 g/mol |
|---|---|
| Formula | C12H14O4 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 4 |
Dillapiole (8025-95-4, 484-31-1)
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- Chemical variation in Piper aduncum and biological properties of its dillapiole-rich essential oil. (Chemistry & Biodiversity, 2009)
- Psychotrophic phenylisopropylamines derived from apiole and dillapiole. (Nature, 1967)
- Synthesis and synergistic activity of dillapiole based pyrethrum synergists (Journal of Agricultural and Food Chemistry, 1979)
- The anti-inflammatory activity of dillapiole and some semisynthetic analogues (Pharmaceutical Biology, 2011)
- Dillapiole as Antileishmanial Agent: Discovery, Cytotoxic Activity and Preliminary SAR Studies of Dillapiole Analogues (Archiv Der Pharmazie, 2012)
- Cytotoxic effects of dillapiole on MDA-MB-231 cells involve the induction of apoptosis through the mitochondrial pathway by inducing an oxidative stress while altering the cytoskeleton network. (Biochimie, 2014)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCOC1=C(C2=C(C=C1CC=C)OCO2)OC
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InChIKeyLIKYNOPXHGPMIH-UHFFFAOYSA-N
- Pubchem - Dillapiole
- Wikipedia - dillapiole
Dillapiole is an organic chemical compound and essential oil commonly extracted from dill weed, though it can be found in a variety of other plants such as fennel root. This compound is closely related to apiole, having a methoxy group positioned differently on the benzene ring. No carcinogenicity was detected with parsley apiol or dill apiol in mice.
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