1,3,7-Trichlorodibenzofuran
(right click,save link as to download,it is a temp file,please download as soon as possible, you can also use CTRL+S to save the whole html page)
Basic Info
| Common Name | 1,3,7-Trichlorodibenzofuran(F04592) |
| 2D Structure | |
| Description | Chlorinated dibenzofurans (CDFs) are a family of chemical that contain one to eight chlorine atoms attached to the carbon atoms of the parent chemical, dibenzofuran. The CDF family contains 135 individual compounds (known as congeners) with varying harmful health and environmental effects. Of these 135 compounds, those that contain chlorine atoms at the 2,3,7,8-positions of the parent dibenzofuran molecule are especially harmful. Other than for laboratory use of small amounts of CDFs for research and development purposes, these chemicals are not deliberately produced by industry. Most CDFs are produced in very small amounts as unwanted impurities of certain products and processes utilizing chlorinated compounds. Only a few of the 135 CDF compounds have been produced in large enough quantities so that their properties, such as color, smell, taste, and toxicity could be studied. (L952) |
| FRCD ID | F04592 |
| CAS Number | 64560-16-3 |
| PubChem CID | 47426 |
| Formula | C12H5Cl3O |
| IUPAC Name | 1,3,7-trichlorodibenzofuran |
| InChI Key | INRBXOGZPDFCLQ-UHFFFAOYSA-N |
| InChI | InChI=1S/C12H5Cl3O/c13-6-1-2-8-10(4-6)16-11-5-7(14)3-9(15)12(8)11/h1-5H |
| Canonical SMILES | C1=CC2=C(C=C1Cl)OC3=CC(=CC(=C23)Cl)Cl |
| Isomeric SMILES | C1=CC2=C(C=C1Cl)OC3=CC(=CC(=C23)Cl)Cl |
| Synonyms |
Dibenzofuran, 1,3,7-trichloro-
1,3,7-TRICHLORODIBENZOFURAN
UNII-1R4XK91XYI
Dibenzofuran, 1,3,7-trichloro
1R4XK91XYI
64560-16-3
AC1L2I2O
Dibenzofuran,1,3,7-trichloro-
CTK5C1406
DTXSID00214827
|
| Classifies |
Pollutant
Pesticide
|
| Update Date | Nov 13, 2018 17:07 |
Chemical Taxonomy
| Kingdom | Organic compounds |
| Superclass | Organoheterocyclic compounds |
| Class | Benzofurans |
| Subclass | Dibenzofurans |
| Intermediate Tree Nodes | Chlorinated dibenzofurans |
| Direct Parent | Polychlorinated dibenzofurans |
| Alternative Parents | |
| Molecular Framework | Aromatic heteropolycyclic compounds |
| Substituents | Polychlorinated dibenzofuran - Benzenoid - Aryl halide - Aryl chloride - Heteroaromatic compound - Furan - Oxacycle - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Organochloride - Organohalogen compound - Aromatic heteropolycyclic compound |
| Description | This compound belongs to the class of organic compounds known as polychlorinated dibenzofurans. These are organic compounds containing two or more chlorine atoms attached to a dibenzofuran moiety. |
Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 271.521 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 0 |
| Complexity | 273 |
| Monoisotopic Mass | 269.941 |
| Exact Mass | 269.941 |
| XLogP | 5.6 |
| Formal Charge | 0 |
| Heavy Atom Count | 16 |
| 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+ | 0.9926 |
| Human Intestinal Absorption | HIA+ | 1.0000 |
| Caco-2 Permeability | Caco2+ | 0.6924 |
| P-glycoprotein Substrate | Non-substrate | 0.7478 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.8608 |
| Non-inhibitor | 0.5944 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.7546 |
| Distribution | ||
| Subcellular localization | Lysosome | 0.5772 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.7971 |
| CYP450 2D6 Substrate | Non-substrate | 0.8699 |
| CYP450 3A4 Substrate | Non-substrate | 0.6903 |
| CYP450 1A2 Inhibitor | Inhibitor | 0.8845 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.7284 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.8273 |
| CYP450 2C19 Inhibitor | Inhibitor | 0.8539 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.8142 |
| CYP Inhibitory Promiscuity | High CYP Inhibitory Promiscuity | 0.7929 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.7775 |
| Non-inhibitor | 0.8279 | |
| AMES Toxicity | AMES toxic | 0.7890 |
| Carcinogens | Non-carcinogens | 0.7782 |
| Fish Toxicity | High FHMT | 0.9123 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.9992 |
| Honey Bee Toxicity | High HBT | 0.7931 |
| Biodegradation | Not ready biodegradable | 0.9679 |
| Acute Oral Toxicity | I | 0.5001 |
| Carcinogenicity (Three-class) | Danger | 0.4960 |
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -4.6776 | LogS |
| Caco-2 Permeability | 1.6021 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 3.5696 | LD50, mol/kg |
| Fish Toxicity | -0.1863 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | 1.3473 | pIGC50, ug/L |
References
| Title | Journal | Date | Pubmed ID |
|---|---|---|---|
| Lead and cadmium contamination in a large sample of United States infant formulas and baby foods. | Sci Total Environ | 2019 Feb 15 | 30253364 |
| Liver histopathological alteration after repeated intra-tracheal instillation of titanium dioxide in male rats. | Gastroenterol Hepatol Bed Bench | 2018 Spring | 29910858 |
| Citrus peel polymethoxyflavones, sudachitin and nobiletin, induce distinct cellular responses in human keratinocyte HaCaT cells. | Biosci Biotechnol Biochem | 2018 Sep 5 | 30185129 |
| Isolation, identification and in silico toxicity predictions of two isomers from cefotiam hydrochloride. | J Pharm Biomed Anal | 2018 Sep 5 | 29945059 |
| Synephrine Hydrochloride Suppresses Esophageal Cancer Tumor Growth and Metastatic Potential through Inhibition of Galectin-3-AKT/ERK Signaling. | J Agric Food Chem | 2018 Sep 5 | 30113849 |
| Effects of aged ZnO NPs and soil type on Zn availability, accumulation and toxicity to pea and beet in a greenhouse experiment. | Ecotoxicol Environ Saf | 2018 Sep 30 | 29807295 |
| Rationale and design of the Caloric Restriction and Exercise protection from Anthracycline Toxic Effects (CREATE) study: a 3-arm parallel group phase II randomized controlled trial in early breast cancer. | BMC Cancer | 2018 Sep 3 | 30176834 |
| Application of bacteriophages in simultaneously controlling Escherichia coli O157:H7 and extended-spectrum beta-lactamase producing Escherichia coli. | Appl Microbiol Biotechnol | 2018 Sep 29 | 30267128 |
| In vitro antiplasmodial, antitrypanosomal and antileishmanial activities of selected medicinal plants from Ugandan flora: Refocusing into multi-component potentials. | J Ethnopharmacol | 2018 Sep 28 | 30273736 |
| Simultaneous determination of trace Aflatoxin B<sub>1</sub> and Ochratoxin A by aptamer-based microchip capillary electrophoresis in food samples. | J Chromatogr A | 2018 Sep 28 | 30037541 |
| Sensitive, simple and rapid colorimetric detection of Malachite green in water, salmon and canned tuna samples based on gold nanoparticles. | J Sci Food Agric | 2018 Sep 28 | 30267409 |
| A NEW PAPER SENSOR METHOD FOR FIELD ANALYSIS OF ACID VOLATILE SULFIDES (AVS) IN SOILS. | Environ Toxicol Chem | 2018 Sep 26 | 30259571 |
| Clinical and Morphological Aspects in Assessing the Safety of OSPL-502 with Repeated Dose Administration. | Open Access Maced J Med Sci | 2018 Sep 25 | 30337969 |
| Evaluation of chemical extractants to assess metals phytoavailability in Brazilian municipal solid waste composts. | Environ Pollut | 2018 Sep 21 | 30267920 |
| Photosystem II Is More Sensitive than Photosystem I to Al<sup>3+</sup> Induced Phytotoxicity. | Materials (Basel) | 2018 Sep 19 | 30235794 |
| Genotypic variation and mechanism in uptake and translocation of perfluorooctanoic acid (PFOA) in lettuce (Lactuca sativa L.) cultivars grown in PFOA-polluted soils. | Sci Total Environ | 2018 Sep 15 | 29729517 |
| Prevalence of Enterotoxigenic Staphylococcus aureus and Shiga Toxin Producing Escherichia coli in Fish in Egypt: Quality Parameters and Public Health Hazard. | Vector Borne Zoonotic Dis | 2018 Sep 15 | 30222525 |
| Influence of Carbon Nanotubes and Its Derivatives on Tumor Cells In Vitro and Biochemical Parameters, Cellular Blood Composition In Vivo. | Nanoscale Res Lett | 2018 Sep 12 | 30209630 |
| Methyl-β-cyclodextrin potentiates the BITC-induced anti-cancer effect through modulation of the Akt phosphorylation in human colorectal cancer cells. | Biosci Biotechnol Biochem | 2018 Sep 10 | 30200817 |
| <i>Histophilus somni</i> Survives in Bovine Macrophages by Interfering with Phagosome-Lysosome Fusion, but Requires IbpA for Optimal Serum Resistance. | Infect Immun | 2018 Sep 10 | 30201700 |
Targets
- General Function:
- Temperature-gated cation channel activity
- Specific Function:
- Receptor-activated non-selective cation channel involved in detection of pain and possibly also in cold perception and inner ear function (PubMed:25389312, PubMed:25855297). Has a central role in the pain response to endogenous inflammatory mediators and to a diverse array of volatile irritants, such as mustard oil, cinnamaldehyde, garlic and acrolein, an irritant from tears gas and vehicule exhaust fumes (PubMed:25389312, PubMed:20547126). Is also activated by menthol (in vitro)(PubMed:25389312). Acts also as a ionotropic cannabinoid receptor by being activated by delta(9)-tetrahydrocannabinol (THC), the psychoactive component of marijuana (PubMed:25389312). May be a component for the mechanosensitive transduction channel of hair cells in inner ear, thereby participating in the perception of sounds. Probably operated by a phosphatidylinositol second messenger system (By similarity).
- Gene Name:
- TRPA1
- Uniprot ID:
- O75762
- Molecular Weight:
- 127499.88 Da
References
- Nilius B, Prenen J, Owsianik G: Irritating channels: the case of TRPA1. J Physiol. 2011 Apr 1;589(Pt 7):1543-9. doi: 10.1113/jphysiol.2010.200717. Epub 2010 Nov 15. [21078588 ]
- General Function:
- Transcription regulatory region dna binding
- Specific Function:
- Ligand-activated transcriptional activator. Binds to the XRE promoter region of genes it activates. Activates the expression of multiple phase I and II xenobiotic chemical metabolizing enzyme genes (such as the CYP1A1 gene). Mediates biochemical and toxic effects of halogenated aromatic hydrocarbons. Involved in cell-cycle regulation. Likely to play an important role in the development and maturation of many tissues. Regulates the circadian clock by inhibiting the basal and circadian expression of the core circadian component PER1. Inhibits PER1 by repressing the CLOCK-ARNTL/BMAL1 heterodimer mediated transcriptional activation of PER1.
- Gene Name:
- AHR
- Uniprot ID:
- P35869
- Molecular Weight:
- 96146.705 Da
- Mechanism of Action:
- Dibenzofurans bind the aryl hydrocarbon receptor, which increases its ability to activate transcription in the XRE promoter region. This alters the expression of a number of genes.
References
- Ni J, Pang ST, Yeh S: Differential retention of alpha-vitamin E is correlated with its transporter gene expression and growth inhibition efficacy in prostate cancer cells. Prostate. 2007 Apr 1;67(5):463-71. [17252538 ]