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bromadiolone

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EntityQ423091· pop 17· linked from 48 articles

bromadiolone

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thumb|right|Warning label on a tube of rat poison containing bromadiolone on a Levee|dike of the [[Scheldt river in Steendorp, Belgium]] Bromadiolone is a potent anticoagulant rodenticide. It is a second-generation 4-hydroxycoumarin derivative and vitamin K antagonist, often called a "super-warfarin" for its added potency and tendency to accumulate in the liver of the poisoned organism. When first introduced to the UK market in 1980, it was effective against rodent populations that had become resistant to first generation anticoagulants.

Chemical data

Formula
C30H23BrO4
Molecular weight
527.4 g/mol
IUPAC name
3-[3-[4-(4-bromophenyl)phenyl]-3-hydroxy-1-phenylpropyl]-4-hydroxychromen-2-one
SMILES
C1=CC=C(C=C1)C(CC(C2=CC=C(C=C2)C3=CC=C(C=C3)Br)O)C4=C(C5=CC=CC=C5OC4=O)O
InChIKey
OWNRRUFOJXFKCU-UHFFFAOYSA-N
XLogP
6.1
Polar surface area
66.8 Ų
H-bond donors
2
H-bond acceptors
4
Formal charge
0

via PubChem

Drug data · ChEMBL

Molecule type
Small molecule

via ChEMBL · EBI

Research

297 papers

via PubMed

Described at

Link to a page describing this subject · not written by Vinony

Wikidata facts

Mass
526.078
Image
Rattenvergifwaarschuwing edit.JPG
Show 5 more facts
chemical formula
C₃₀H₂₃BrO₄
canonical SMILES
C1=CC=C(C=C1)C(CC(C2=CC=C(C=C2)C3=CC=C(C=C3)Br)O)C4=C(C5=CC=CC=C5OC4=O)O
subject has role
anticoagulant
Commons category
Bromadiolone
Sources (2)

via Wikidata · CC0

~2 min read

Encyclopedic overview

5 sections
Contents
  • Toxicity
  • Chemistry
  • Antidote
  • See also
  • References

thumb|right|Warning label on a tube of rat poison containing bromadiolone on a Levee|dike of the [[Scheldt river in Steendorp, Belgium]] Bromadiolone is a potent anticoagulant rodenticide. It is a second-generation 4-hydroxycoumarin derivative and vitamin K antagonist, often called a "super-warfarin" for its added potency and tendency to accumulate in the liver of the poisoned organism. When first introduced to the UK market in 1980, it was effective against rodent populations that had become resistant to first generation anticoagulants.

The product may be used both indoors and outdoors for rats and mice.

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

Gallery (9)