| Weight | 454.527 g/mol |
|---|---|
| Formula | C24H30N4O5 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 4 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 5 |
Cuvalit (19875-60-6)
Lisuride · Dopergin · Schering Brand 2 of Lisuride Maleate
Score:
#238 in Neurology
,
#1163 in Neuroscience
,
#5026 in Biology
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- Effect of repeated L-DOPA, bromocriptine, or lisuride administration on preproenkephalin-A and preproenkephalin-B mRNA levels in the striatum of the 6-hydroxydopamine-lesioned rat (Experimental Neurology, 1999)
- [11C]raclopride and positron emission tomography in previously untreated patients with Parkinson's disease Influence of Ldopa and lisuride therapy on striatal dopamine D2receptors (Neurology, 1994)
- Prospective randomized trial of lisuride infusion versus oral levodopa in patients with Parkinsons disease (Brain, 2002)
- Direct dopaminergic action of lisuride hydrogen maleate, an ergot derivative, in mice (European Journal of Pharmacology, 1976)
- Size reduction of macroprolactinomas by bromocriptine or lisuride treatment. (The Journal of Clinical Endocrinology and Metabolism, 1981)
- Effect of lisuride and other ergot derivatives on monoaminergic mechanisms in rat brain (European Journal of Pharmacology, 1977)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Lisuride
- Dopergin
- Schering Brand 2 of Lisuride Maleate
- Lisuride Maleate
- Roche Brand of Lisuride Maleate
- Lisuride Maleate (1:1)
- Revanil
- Lysuride Hydrogen Maleate
- Lisuride Hydrochloride
- Lisuride Phosphate (1:1)
- Lisuride Maleate, (8beta)-Isomer
- Schering Brand 1 of Lisuride Maleate
- Lisuride Mesylate
- Lysurid
- Lisuride, (8alpha)-(+-)-Isomer
- Lysenyl
- IPRAD Brand of Lisuride Maleate
- Dopergine
- Arolac
- Methylergol Carbamide
-
SMILESCCN(CC)C(=O)NC1CN(C2CC3=CNC4=CC=CC(=C34)C2=C1)C.C(=CC(=O)O)C(=O)O
-
InChIKeyCVQFAMQDTWVJSV-UHFFFAOYSA-N
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