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danthron

Structure via PubChem · Public domain (PubChem)

EntityQ5221244· pop 9· linked from 67 articles

Also known as Dorbane, Istizin, 1,8-dihydroxy-9,10-anthracenedione, 1,8-dihydroxyanthra-9,10-quinone, 1,8-dihydroxy-9,10-anthraquinone, 1,8-Dihydroxyanthraquinone, Chrysazin

Dantron (INN), also known as chrysazin or 1,8-dihydroxyanthraquinone, is an orange-colored organic substance. Many structurally-related compounds are known. In terms of its molecular structure, it is related anthraquinone by the replacement of two hydrogen atoms by hydroxyl groups (–OH). It is used in some countries as a stimulant laxative.

In the Vinony graph

Within Vinony's link graph, danthron is referenced by 67 other articles, and connects out to laxative, United States and United Kingdom.

It is catalogued under topics including 3-Hydroxypropenals within hydroxyquinones, Dihydroxyanthraquinones and Drugboxes which contain changes to verified fields.

Its subject is documented across 9 Wikipedia language editions.

Chemical data

Formula
C14H8O4
Molecular weight
240.21 g/mol
IUPAC name
1,8-dihydroxyanthracene-9,10-dione
SMILES
C1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=CC=C3O
InChIKey
QBPFLULOKWLNNW-UHFFFAOYSA-N
XLogP
3.2
Polar surface area
74.6 Ų
H-bond donors
2
H-bond acceptors
4
Formal charge
0

via PubChem

Drug data · ChEMBL

Withdrawn
Max clinical phase
Approved
Molecule type
Small molecule
Indications
Constipation

via ChEMBL · EBI

Research

194 papers

via PubMed

Wikidata facts

Mass
240.042
Has use
medication
Show 6 more facts
chemical formula
C₁₄H₈O₄
canonical SMILES
C1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=CC=C3O
World Health Organisation international non-proprietary name
dantron
found in taxon
Asphodelus fistulosus
defined daily dose
50
subject has role
carcinogen
Sources (4)

via Wikidata · CC0

~1 min read

Encyclopedic overview

4 sections
Contents
  • Medical uses
  • Side effects
  • See also
  • References

Dantron (INN), also known as chrysazin or 1,8-dihydroxyanthraquinone, is an orange-colored organic substance. Many structurally-related compounds are known. In terms of its molecular structure, it is related anthraquinone by the replacement of two hydrogen atoms by hydroxyl groups (–OH). It is used in some countries as a stimulant laxative.

It should not be confused with ondansetron, an unrelated drug that was marketed in South Africa under the trade name "Dantron".

Excerpted from Wikipedia’s “danthron” article, available under the CC BY-SA 4.0 licence.

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