CHEBI:23681 - dibenzothiophene

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ChEBI Name dibenzothiophene
ChEBI ID CHEBI:23681
Definition A mancude organic heterotricyclic parent that consists of a thiophene ring flanked by two benzene rings ortho-fused across the 2,3- and 4,5-positions.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information ChemicalBook:CB0128551, eMolecules:480663, eMolecules:491267
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Manganese(II) chloride is the dichloride salt of manganese, MnCl2. This inorganic chemical exists in the anhydrous form, as well as the dihydrate (MnCl2·2H2O) and tetrahydrate (MnCl2·4H2O), with the tetrahydrate being the most common form. Like many Mn(II) species, these salts are pink, with the paleness of the color being characteristic of transition metal complexes with high spin d5 configurations.
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Formula C12H8S
Net Charge 0
Average Mass 184.258
Monoisotopic Mass 184.03467
InChI InChI=1S/C12H8S/c1-3-7-11-9(5-1)10-6-2-4-8-12(10)13-11/h1-8H
InChIKey IYYZUPMFVPLQIF-UHFFFAOYSA-N
SMILES C1=2C=3C=CC=CC3SC1=CC=CC2
Roles Classification
Application(s): keratolytic drug
A drug that softens, separates, and causes desquamation of the cornified epithelium or horny layer of skin. Keratolytic drugs are used to expose mycelia of infecting fungi or to treat corns, warts, and certain other skin diseases.
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ChEBI Ontology
Outgoing dibenzothiophene (CHEBI:23681) has role keratolytic drug (CHEBI:50176)
dibenzothiophene (CHEBI:23681) is a dibenzothiophenes (CHEBI:23684)
dibenzothiophene (CHEBI:23681) is a mancude organic heterotricyclic parent (CHEBI:36416)
Incoming dibenzothiophene 5-oxide (CHEBI:23683) has functional parent dibenzothiophene (CHEBI:23681)
dibenzothiophene sulfone (CHEBI:90356) has functional parent dibenzothiophene (CHEBI:23681)
1,2-dihydroxydibenzothiophene (CHEBI:17212) has parent hydride dibenzothiophene (CHEBI:23681)
IUPAC Name
dibenzo[b,d]thiophene
Synonyms Sources
9-thiafluorene NIST Chemistry WebBook
[1,1'-biphenyl]-2,2'-diyl sulfide NIST Chemistry WebBook
α-thiafluorene NIST Chemistry WebBook
dibenzothiophene UniProt
dibenzothiophene ChemIDplus
diphenylene sulfide NIST Chemistry WebBook
Manual Xrefs Databases
c0118 UM-BBD
D03777 KEGG DRUG
Dibenzothiophene Wikipedia
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Registry Numbers Types Sources
121101 Reaxys Registry Number Reaxys
132-65-0 CAS Registry Number ChemIDplus
132-65-0 CAS Registry Number NIST Chemistry WebBook
83631 Gmelin Registry Number Gmelin
Citations Types Sources
15092946 PubMed citation Europe PMC
16232582 PubMed citation Europe PMC
16268154 PubMed citation Europe PMC
16391083 PubMed citation Europe PMC
17616875 PubMed citation Europe PMC
21750993 PubMed citation Europe PMC
Last Modified
12 January 2016