Safrole
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Basic Info
Common Name | Safrole(F05284) |
2D Structure | |
Description | Safrole is found in anise. Safrole occurs in nutmeg. Banned by FDA for use in food. Safrole is formerly used as a food flavour It is a precursor in the synthesis of the insecticide synergist piperonyl butoxide and the recreational drug MDMA (Ecstacy). Safrole is a natural plant constituent, found in oil of sassafras and certain other essential oils. It is a member of the methylenedioxybenzene group of compounds, many of which (e.g. piperonyl butoxide) are extensively used as insecticide synergists. Safrole is a major source of human exposure to safrole is through consumption of spices, such as nutmeg, cinnamon and black pepper, in which safrole is a constituent. Safrole is also present in root beer, and has been used as an additive in chewing gum, toothpaste, soaps and certain pharmaceutical preparations. Safrole is a weak hepatocarcinogen and it is a matter of considerable interest whether the ally1 moiety or the methylenedioxy group, or both, are involved in the mechanism of its carcinogenesis. Safrole is extensively metabolized, giving rise to a large number of metabolites. Metabolism involves essentially two major routes, oxidation of the ally1 side chain, and oxidation of the methylenedioxy group with subsequent cleavage to form the catechol. Safrole undergoes oxidation of the allylic group to yield the 2, 3-epoxide (safrole epoxide). The dihydrodiol is one of the metabolites of safrole, and presumably arises from the hydration of the 2, 3-epoxide. The principal route of metabolism of safrole is through cleavage of the methylenedioxy group, the major metabolites being allylcatechol and its isomer, propenylcatechol. Eugenol and its isomer I-methoxy- 2-hydroxy-4-allylbenzene have been detected as minor metabolites in the rat, mouse and man. ; Safrole, also known as shikimol, is a colorless or slightly yellow oily liquid. It is typically extracted from the root-bark or the fruit of sassafras plants in the form of sassafras oil, or synthesized from other related methylenedioxy compounds. It is the principal component of brown camphor oil, and is found in small amounts in a wide variety of plants, where it functions as a natural pesticide. The Ocotea cymbarum[verification needed] oil made of the Ocotea pretiosa[verification needed], a plant growing in Brazil, and sassafras oil made of Sassafras albidum, a tree growing in eastern North America, are the main natural sources for safrole. It has a characteristic candy-shop aroma. Safrole has been shown to exhibit antibiotic and anti-angiogenic functions (A3314, A3315, A3316). |
FRCD ID | F05284 |
CAS Number | 94-59-7 |
PubChem CID | 5144 |
Formula | C10H10O2 |
IUPAC Name | 5-prop-2-enyl-1,3-benzodioxole |
InChI Key | ZMQAAUBTXCXRIC-UHFFFAOYSA-N |
InChI | InChI=1S/C10H10O2/c1-2-3-8-4-5-9-10(6-8)12-7-11-9/h2,4-6H,1,3,7H2 |
Canonical SMILES | C=CCC1=CC2=C(C=C1)OCO2 |
Isomeric SMILES | C=CCC1=CC2=C(C=C1)OCO2 |
Wikipedia | Safrole |
Synonyms | 5-Allyl-1,3-benzodioxole safrole 94-59-7 Safrol Shikimole Shikomol Safrene Sassafras Rhyuno oil Safrole MF |
Classifies | Plant Toxin Pesticide |
Update Date | Nov 13, 2018 17:07 |
Chemical Taxonomy
Kingdom | Organic compounds |
Superclass | Organoheterocyclic compounds |
Class | Benzodioxoles |
Subclass | Not available |
Intermediate Tree Nodes | Not available |
Direct Parent | Benzodioxoles |
Alternative Parents | |
Molecular Framework | Aromatic heteropolycyclic compounds |
Substituents | Benzodioxole - Benzenoid - Oxacycle - Acetal - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Aromatic heteropolycyclic compound |
Description | This compound belongs to the class of organic compounds known as benzodioxoles. These are organic compounds containing a benzene ring fused to either isomers of dioxole. Dioxole is a five-membered unsaturated ring of two oxygen atoms and three carbon atoms. |
Properties
Property Name | Property Value |
---|---|
Molecular Weight | 162.188 |
Hydrogen Bond Donor Count | 0 |
Hydrogen Bond Acceptor Count | 2 |
Rotatable Bond Count | 2 |
Complexity | 167 |
Monoisotopic Mass | 162.068 |
Exact Mass | 162.068 |
XLogP | 3 |
Formal Charge | 0 |
Heavy Atom Count | 12 |
Defined Atom Stereocenter Count | 0 |
Undefined Atom Stereocenter Count | 0 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Isotope Atom Count | 0 |
Covalently-Bonded Unit Count | 1 |
ADMET
Model | Result | Probability |
---|---|---|
Absorption | ||
Blood-Brain Barrier | BBB+ | 0.9846 |
Human Intestinal Absorption | HIA+ | 0.9951 |
Caco-2 Permeability | Caco2+ | 0.6278 |
P-glycoprotein Substrate | Non-substrate | 0.7829 |
P-glycoprotein Inhibitor | Non-inhibitor | 0.7386 |
Non-inhibitor | 0.5800 | |
Renal Organic Cation Transporter | Non-inhibitor | 0.8177 |
Distribution | ||
Subcellular localization | Mitochondria | 0.4824 |
Metabolism | ||
CYP450 2C9 Substrate | Non-substrate | 0.8814 |
CYP450 2D6 Substrate | Non-substrate | 0.8577 |
CYP450 3A4 Substrate | Non-substrate | 0.7118 |
CYP450 1A2 Inhibitor | Inhibitor | 0.8554 |
CYP450 2C9 Inhibitor | Non-inhibitor | 0.6333 |
CYP450 2D6 Inhibitor | Inhibitor | 0.5435 |
CYP450 2C19 Inhibitor | Inhibitor | 0.6493 |
CYP450 3A4 Inhibitor | Non-inhibitor | 0.6972 |
CYP Inhibitory Promiscuity | High CYP Inhibitory Promiscuity | 0.7769 |
Excretion | ||
Toxicity | ||
Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9024 |
Non-inhibitor | 0.9577 | |
AMES Toxicity | Non AMES toxic | 0.9132 |
Carcinogens | Non-carcinogens | 0.8641 |
Fish Toxicity | High FHMT | 0.9255 |
Tetrahymena Pyriformis Toxicity | High TPT | 0.9883 |
Honey Bee Toxicity | High HBT | 0.7790 |
Biodegradation | Ready biodegradable | 0.6285 |
Acute Oral Toxicity | III | 0.8274 |
Carcinogenicity (Three-class) | Warning | 0.5214 |
Model | Value | Unit |
---|---|---|
Absorption | ||
Aqueous solubility | -2.5001 | LogS |
Caco-2 Permeability | 1.5491 | LogPapp, cm/s |
Distribution | ||
Metabolism | ||
Excretion | ||
Toxicity | ||
Rat Acute Toxicity | 1.9517 | LD50, mol/kg |
Fish Toxicity | 0.9028 | pLC50, mg/L |
Tetrahymena Pyriformis Toxicity | 0.6903 | pIGC50, ug/L |
References
Title | Journal | Date | Pubmed ID |
---|---|---|---|
Identification and analysis of the reactive metabolites related to the hepatotoxicity of safrole. | Xenobiotica | 2018 Nov | 29082813 |
Determination and risk assessment of naturally occurring genotoxic and carcinogenic alkenylbenzenes in nutmeg-based plant food supplements. | J Appl Toxicol | 2017 Oct | 28556924 |
Risk assessment of combined exposure to alkenylbenzenes through consumption of plant food supplements containing parsley and dill. | Food Addit Contam Part A Chem Anal Control Expo Risk Assess | 2017 Dec | 28580843 |
Level of Alkenylbenzenes in Parsley and Dill Based Teas and Associated Risk Assessment Using the Margin of Exposure Approach. | J Agric Food Chem | 2016 Nov 16 | 27771948 |
Acaricidal activity of Asarum heterotropoides root-derived compounds and hydrodistillate constitutes toward Dermanyssus gallinae (Mesostigmata: Dermanyssidae). | Exp Appl Acarol | 2016 Apr | 26708137 |
Structure-Activity Relationships for DNA Damage by Alkenylbenzenes in Turkey Egg Fetal Liver. | Toxicol Sci | 2016 Apr | 26719370 |
Analysis of the essential oil of Illicium henryi Diels root bark and itsinsecticidal activity against Liposcelis bostrychophila Badonnel. | J Food Prot | 2015 Apr | 25836404 |
Quantitation of tr-cinnamaldehyde, safrole and myristicin in cola-flavoured soft drinks to improve the assessment of their dietary exposure. | Food Chem Toxicol | 2013 Sep | 23845511 |
Biological reactive intermediates (BRIs) formed from botanical dietary supplements. | Chem Biol Interact | 2011 Jun 30 | 20970412 |
Physiologically based biokinetic (PBBK) model for safrole bioactivation anddetoxification in rats. | Chem Res Toxicol | 2011 Jun 20 | 21446753 |
Genotoxic and apoptotic activities of the food flavourings myristicin and eugenolin AA8 and XRCC1 deficient EM9 cells. | Food Chem Toxicol | 2011 Feb | 21087650 |
Toxicity of the essential oil of Illicium difengpi stem bark and its constituent compounds towards two grain storage insects. | J Insect Sci | 2011 | 22236213 |
Predicting the hepatocarcinogenic potential of alkenylbenzene flavoring agentsusing toxicogenomics and machine learning. | Toxicol Appl Pharmacol | 2010 Mar 15 | 20004213 |
Toxicity of Myristica fagrans seed compounds against Blattella germanica (Dictyoptera: Blattellidae). | J Med Entomol | 2007 May | 17547241 |
Human cytochrome p450 enzyme specificity for the bioactivation of estragole andrelated alkenylbenzenes. | Chem Res Toxicol | 2007 May | 17407329 |
Metabolic activation of herbal and dietary constituents and its clinical and toxicological implications: an update. | Curr Drug Metab | 2007 Aug | 17691916 |
Quantification of flavor-related compounds in the unburned contents of bidi and clove cigarettes. | J Agric Food Chem | 2006 Nov 1 | 17061837 |
Genotoxicity and endoreduplication inducing activity of the food flavouringeugenol. | Mutagenesis | 2006 May | 16595588 |
Molecular mechanisms of toxicity of important food-borne phytotoxins. | Mol Nutr Food Res | 2005 Feb | 15635687 |
Human consumption of methyleugenol and its elimination from serum. | Environ Health Perspect | 2004 May | 15121510 |
Targets
- General Function:
- Zinc ion binding
- Specific Function:
- Ligand-activated transcription factor. Key regulator of lipid metabolism. Activated by the endogenous ligand 1-palmitoyl-2-oleoyl-sn-glycerol-3-phosphocholine (16:0/18:1-GPC). Activated by oleylethanolamide, a naturally occurring lipid that regulates satiety. Receptor for peroxisome proliferators such as hypolipidemic drugs and fatty acids. Regulates the peroxisomal beta-oxidation pathway of fatty acids. Functions as transcription activator for the ACOX1 and P450 genes. Transactivation activity requires heterodimerization with RXRA and is antagonized by NR2C2. May be required for the propagation of clock information to metabolic pathways regulated by PER2.
- Gene Name:
- PPARA
- Uniprot ID:
- Q07869
- Molecular Weight:
- 52224.595 Da
References
- Sipes NS, Martin MT, Kothiya P, Reif DM, Judson RS, Richard AM, Houck KA, Dix DJ, Kavlock RJ, Knudsen TB: Profiling 976 ToxCast chemicals across 331 enzymatic and receptor signaling assays. Chem Res Toxicol. 2013 Jun 17;26(6):878-95. doi: 10.1021/tx400021f. Epub 2013 May 16. [23611293 ]
- General Function:
- Zinc ion binding
- Specific Function:
- Nuclear receptor. Interaction with RXR shifts RXR from its role as a silent DNA-binding partner to an active ligand-binding subunit in mediating retinoid responses through target genes defined by LXRES. LXRES are DR4-type response elements characterized by direct repeats of two similar hexanuclotide half-sites spaced by four nucleotides. Plays an important role in the regulation of cholesterol homeostasis, regulating cholesterol uptake through MYLIP-dependent ubiquitination of LDLR, VLDLR and LRP8. Interplays functionally with RORA for the regulation of genes involved in liver metabolism (By similarity). Exhibits a ligand-dependent transcriptional activation activity (PubMed:25661920).
- Gene Name:
- NR1H3
- Uniprot ID:
- Q13133
- Molecular Weight:
- 50395.34 Da
References
- Sipes NS, Martin MT, Kothiya P, Reif DM, Judson RS, Richard AM, Houck KA, Dix DJ, Kavlock RJ, Knudsen TB: Profiling 976 ToxCast chemicals across 331 enzymatic and receptor signaling assays. Chem Res Toxicol. 2013 Jun 17;26(6):878-95. doi: 10.1021/tx400021f. Epub 2013 May 16. [23611293 ]