Record Information |
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Version | 1.0 |
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Created at | 2020-04-27 17:10:10 UTC |
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Updated at | 2021-01-06 19:06:59 UTC |
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CannabisDB ID | CDB005924 |
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Secondary Accession Numbers | Not Available |
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Cannabis Compound Identification |
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Common Name | indeno[1,2,3,-c d] fluoranthene |
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Description | Indeno[1,2,3-cd]fluoranthene belongs to the class of organic compounds known as Fluoranthene is a polycyclic aromatic hydrocarbon (PAH) that consists of a naphthalene moiety connected by a five membered ring to a benzene. Fluoranthene is a colorless solid, although samples may appear as pale yellow. Fluoranthene is an isomer of pyrene and it results from the incomplete combustion of organic compounds, in a wide array of conditions. However, fluoranthene is less stable than pyrene and thus, less abundant. PAH metabolism occurs in all tissues, usually by cytochrome P-450, specifically by its associated enzymes CYP1A1 and CYP1B1 (PMID: 14720319 ). These enzymes metabolize PAH's into their toxic intermediates. The metabolites of pyrene, such as phenols, quinones, and dihydrodiols, can all be conjugated to glucuronides and sulfate esters; the quinones also form glutathione conjugates. PAHs are generally considered as cancerogenic to varying degrees. Benzo[j]fluoranthene is formed during the combustion of cannabis and is therefore a constituent of cannabis smoke ( Ref:DOI ). |
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Structure | |
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Synonyms | Value | Source |
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Indeno(1,2,3-CD)fluoranthene | MeSH |
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Chemical Formula | C22H12 |
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Average Molecular Weight | 276.34 |
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Monoisotopic Molecular Weight | 276.0939 |
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IUPAC Name | hexacyclo[9.9.2.0^{2,7}.0^{8,21}.0^{12,17}.0^{18,22}]docosa-1(20),2,4,6,8,10,12,14,16,18,21-undecaene |
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Traditional Name | hexacyclo[9.9.2.0^{2,7}.0^{8,21}.0^{12,17}.0^{18,22}]docosa-1(20),2,4,6,8,10,12,14,16,18,21-undecaene |
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CAS Registry Number | 193-43-1 |
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SMILES | C1=CC=C2C(=C1)C1=CC=C3C4=CC=CC=C4C4=CC=C2C1=C34 |
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InChI Identifier | InChI=1S/C22H12/c1-2-6-14-13(5-1)17-9-10-19-15-7-3-4-8-16(15)20-12-11-18(14)21(17)22(19)20/h1-12H |
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InChI Key | XAKRHFYJDSMEMI-UHFFFAOYSA-N |
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Chemical Taxonomy |
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Description | Belongs to the class of organic compounds known as naphthalenes. Naphthalenes are compounds containing a naphthalene moiety, which consists of two fused benzene rings. |
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Kingdom | Organic compounds |
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Super Class | Benzenoids |
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Class | Naphthalenes |
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Sub Class | Not Available |
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Direct Parent | Naphthalenes |
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Alternative Parents | |
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Substituents | - Naphthalene
- Aromatic hydrocarbon
- Polycyclic hydrocarbon
- Unsaturated hydrocarbon
- Hydrocarbon
- Aromatic homopolycyclic compound
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Molecular Framework | Aromatic homopolycyclic compounds |
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External Descriptors | Not Available |
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Ontology |
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Not Available | Physical Properties |
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State | Not Available |
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Experimental Properties | Property | Value | Reference |
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Melting Point | Not Available | Not Available | Boiling Point | Not Available | Not Available | Water Solubility | Not Available | Not Available | logP | Not Available | Not Available |
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Predicted Properties | [] |
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