Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C22H32N4O |
| Molecular Weight | 368.5157 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 3 / 3 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCN1C[C@H](C[C@H]2[C@H]1CC3=CNC4=C3C2=CC=C4)NC(=O)N(CC)CC
InChI
InChIKey=FCRJELOYDVBTGW-ILZDJORESA-N
InChI=1S/C22H32N4O/c1-4-10-26-14-16(24-22(27)25(5-2)6-3)12-18-17-8-7-9-19-21(17)15(13-23-19)11-20(18)26/h7-9,13,16,18,20,23H,4-6,10-12,14H2,1-3H3,(H,24,27)/t16-,18+,20+/m0/s1
Proterguride is a highly potent dopamine receptor agonist with a long duration of action patented by Schering A.-G. for the treatment of Parkinsonism, restless leg syndrome, or the prophylaxis of migraine. According to preclinical studies, Proterguride, unlike most dopamine receptor agonist, is suitable for transdermal administration. Especially in the case of dopamine agonists, the transdermal route of administration might become of great clinical importance due to the ability to achieve constant plasma levels and, thus, to imitate the physiological continuous release profile of dopamine. Pulsatile stimulation of dopaminergic receptors as it occurs with oral administration of dopaminergic drugs is considered the cause of treatment-associated motor complications.
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/16109623
10 mkg
Route of Administration:
Intravenous
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NCI_THESAURUS |
C66884
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CHEMBL2106986
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SUB10136MIG
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5438
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71999
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C055236
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10661OD4VE
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C73309
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100000080834
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ACTIVE MOIETY