Skip to content
Pergolid

Structure via PubChem · Public domain (PubChem)

EntityQ415752· pop 12· linked from 1,801 articles

Also known as LY-127809, Permax®, Pergolida, Pergolidum, Pergolide, Prascend

Arzneistoff

Key facts

Drug.Verifiedfields
changed
Drug.verifiedrevid
464199003
Drug.image
Pergolide structure.svg
Drug.image_class
skin-invert-image
Drug.width
165px
Drug.image2
PergolideMV.png
Drug.image_class2
bg-transparent
Drug.width2
225px
Drug.tradename
Permax, Prascend (veterinary), others
Drug.pregnancy_category
B
Drug.routes_of_administration
Oral
Drug.class
Dopamine receptor agonist; Antiparkinsonian agent
Drug.ATC_prefix
N04
Drug.ATC_suffix
BC02
Drug.legal_BR
C1
Drug.legal_CA
Rx-only
Drug.legal_US_comment
Veterinary use only, withdrawn for human use
Drug.protein_bound
90%

via Wikipedia infobox

Chemical data

Formula
C19H26N2S
Molecular weight
314.5 g/mol
IUPAC name
(6aR,9R,10aR)-9-(methylsulfanylmethyl)-7-propyl-6,6a,8,9,10,10a-hexahydro-4H-indolo[4,3-fg]quinoline
SMILES
CCCN1C[C@@H](C[C@H]2[C@H]1CC3=CNC4=CC=CC2=C34)CSC
InChIKey
YEHCICAEULNIGD-MZMPZRCHSA-N
XLogP
4.2
Polar surface area
44.3 Ų
H-bond donors
1
H-bond acceptors
2
Formal charge
0

via PubChem

Drug data · ChEMBL

Withdrawn
Max clinical phase
Approved
Molecule type
Small molecule
First approval
1988
Admin. routes
oral
Indications
cocaine dependence, Parkinson disease, drug dependence

via ChEMBL · EBI

Wikidata facts

Subclass of
ergot alkaloids
Mass
314.18167
Has use
medication
Show 10 more facts
chemical formula
C₁₉H₂₆N₂S
medical condition treated
Tourette syndrome
isomeric SMILES
CCCN1C[C@@H](C[C@H]2[C@H]1CC3=CNC4=CC=CC2=C34)CSC
canonical SMILES
CCCN1CC(CC2C1CC3=CNC4=CC=CC2=C34)CSC
World Health Organisation international non-proprietary name
pergolide
defined daily dose
3
subject has role
antiparkinson
Commons category
Pergolide
legal status (medicine)
boxed warning
significant drug interaction
(RS)-sulpiride
Sources (6)

via Wikidata · CC0

Article · Deutsch

Pergolid ist ein Arzneistoff, der zur Therapie der Parkinson-Krankheit eingesetzt wird. Seine pharmakologischen Effekte vermittelt dieser von Mutterkornalkaloiden abgeleitete Arzneistoff über eine Aktivierung von Dopamin-Rezeptoren (Dopaminagonist).

Abstract from DBpedia / Wikipedia · CC BY-SA