Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C20H25N.ClH |
| Molecular Weight | 315.88 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.CC(C)N1CCC(CC1)(C2=CC=CC=C2)C3=CC=CC=C3
InChI
InChIKey=ZFCBOUXJVGNRIF-UHFFFAOYSA-N
InChI=1S/C20H25N.ClH/c1-17(2)21-15-13-20(14-16-21,18-9-5-3-6-10-18)19-11-7-4-8-12-19;/h3-12,17H,13-16H2,1-2H3;1H
| Molecular Formula | C20H25N |
| Molecular Weight | 279.4192 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
| Molecular Formula | ClH |
| Molecular Weight | 36.461 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Prodipine (also known as BY-101) is diphenylpiperidines derivative patented by Chemische Fabrik Promonta G.m.b.H. as an anti parkinsonian agent. Prodipine showed monoamine oxidase inhibiting effects in vitro (liver and brain homogenates) similar to those of harmaline. In preclinical studies, Prodipine caused no tachyphylaxis, no increased salivation, or hyperthermia, and had lower toxicity in mice than amphetamine or pemoline. Prodipine decreased reserpine-induced ptosis, antagonized tremorine-induced seizures, and caused only mild hypertension in mice.
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:24:35 GMT 2025
by
admin
on
Mon Mar 31 22:24:35 GMT 2025
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| Record UNII |
89CCP8Z2PS
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| Record Status |
Validated (UNII)
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31314-39-3
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m1237
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89CCP8Z2PS
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admin on Mon Mar 31 22:24:35 GMT 2025 , Edited by admin on Mon Mar 31 22:24:35 GMT 2025
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3030531
Created by
admin on Mon Mar 31 22:24:35 GMT 2025 , Edited by admin on Mon Mar 31 22:24:35 GMT 2025
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