2,3,7,8-Tetrachlorodibenzodioxin (BioCAD00000002965)
Metabolite Card
Formula: C12H4Cl4O2 (319.8965)
SMILES: [H]C1=C2OC3=C([H])C(Cl)=C(Cl)C([H])=C3OC2=C([H])C(Cl)=C1Cl
Synonyms [en]
2,3,7,8-Tetrachlorodibenzodioxin; TCDD; 2,3,7,8-Tetrachlorodibenzo-p-dioxin; PCDD 48; Tetrachlorodibenzodioxin; Dioxine
Last reviewed on 2024-06-28.
Cite this Page
2,3,7,8-Tetrachlorodibenzodioxin. 数据之源,洞见之始. SMRUCC genomics institute, a synthetic life researcher from China.
https://biocad_registry.innovation.ac.cn/s/(-)-arctiin
(retrieved
2026-01-03) (CAD Registry RN: BioCAD00000002965). Licensed
under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
Note
2,3,7,8-tetrachlorodibenzo-p-dioxin (tcdd) appears as white crystals or tan crystalline powder. (NTP, 1992) 2,3,7,8-tetrachlorodibenzodioxine is a polychlorinated dibenzodioxine. 2,3,7,8-Tetrachlorodibenzo-p-dioxin . 2,3,7,8-Tetrachlorodibenzo-P-dioxin is 2,3,7,8-Tetrachlorodibenzo-p-dioxin which is often referred to simply as dioxin and is the reference for a number of compounds which are similar structurally and have dioxin-like toxicity. A substance extremely toxic to mammals, with a wide variation in sensitivity among species. Longer-term exposure of test mammals to lesser amounts can affect reproduction, cause birth defects, damage the liver and suppress the immune system. Several studies suggest that exposure to TCDD increases the risk of several types of cancer in people. Animal studies have also shown an increased risk of cancer from exposure to TCDD. The WHO and the USA DHHS have determined that TCDD is a human carcinogen. (NCI) 2,3,7,8-Tetrachlorodibenzo-p-dioxin (TCDD) can cause cancer according to an independent committee of scientific and health experts. It can cause developmental toxicity according to The Environmental Protection Agency (EPA). 2,3,7,8-Tetrachlorodibenzo-p-dioxin is the most toxic of 75 chlorinated dibenzo-p-dioxin (CDD) congeners. CDDs are a class of manufactured chemicals that consist of dioxin skeletel structures with chlorine substituents. They are also persistent organic pollutants (POPs), thus their production is regulated in most areas. Dioxins occur as by-products from the manufacture of organochlorides, the bleaching of paper, chlorination by waste and drinking water treatment plants, municipal solid waste and industrial incinerators, and natural sources such as volcanoes and forest fires. (L177, L178) Dibenzodioxin derivatives that contain multiple chloride atoms bound to the benzene ring structures.
DBLinks
- CAS Registry Number: 1746-01-6
- PubChem CID: 15625
- ChEBI: 28119
- HMDB: HMDB0258755
- LipidMaps:
- KEGG: C07557
- BioCyc:
- NCBI MeSH: Polychlorinated Dibenzodioxins
- Wikipedia: 2,3,7,8-Tetrachlorodibenzo-P-Dioxin
Other DBLinks
- CAS Registry Number: 1746-01-6
- PubChem: 15625
- ChEBI: ChEBI:28119
- HMDB: HMDB0258755
- KEGG: C07557
- NCBI MeSH: Polychlorinated Dibenzodioxins
- Wikipedia: 2,3,7,8-Tetrachlorodibenzo-P-Dioxin
- Wikipedia: 2,3,7,8-Tetrachlorodibenzodioxin
- Wikipedia: 2\,3\,7\,8-Tetrachlorodibenzo-P-Dioxin
- Metlin: METLIN_66680
Class / Ontology
- WishartLab ClassyFire: [Benzo-p-dioxins] Benzo-p-dioxins
- ChEBI: [CHEBI:28119] 2,3,7,8-tetrachlorodibenzodioxine
Taxonomy Source
Pathway Synthetic
| pathway id | name |
|---|---|
| Reactome:R-BTA-1430728 | Metabolism |
| Reactome:R-BTA-211945 | Phase I - Functionalization of compounds |
| Reactome:R-BTA-211981 | Xenobiotics |
| Reactome:R-CEL-211859 | Biological oxidations |
| Reactome:R-CEL-8937144 | Aryl hydrocarbon receptor signalling |
| Reactome:R-CFA-1430728 | Metabolism |
| Reactome:R-CFA-211976 | Endogenous sterols |
| Reactome:R-DME-8937144 | Aryl hydrocarbon receptor signalling |
| Reactome:R-GGA-211976 | Endogenous sterols |
| Reactome:R-HSA-400206 | Regulation of lipid metabolism by PPARalpha |
| Reactome:R-HSA-211859 | Biological oxidations |
| Reactome:R-MMU-1430728 | Metabolism |
| Reactome:R-MMU-211859 | Biological oxidations |
| Reactome:R-RNO-211945 | Phase I - Functionalization of compounds |
| Reactome:R-RNO-211981 | Xenobiotics |
| Reactome:R-SSC-211945 | Phase I - Functionalization of compounds |
| Reactome:R-SSC-211981 | Xenobiotics |
| Reactome:R-XTR-8937144 | Aryl hydrocarbon receptor signalling |
| Reactome:R-BTA-211859 | Biological oxidations |
| Reactome:R-CFA-211897 | Cytochrome P450 - arranged by substrate type |