Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C12H20N2 |
| Molecular Weight | 192.3006 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
C(C#CCN1CCCC1)N2CCCC2
InChI
InChIKey=JSUAJTLKVREZHV-UHFFFAOYSA-N
InChI=1S/C12H20N2/c1-2-8-13(7-1)11-5-6-12-14-9-3-4-10-14/h1-4,7-12H2
| Molecular Formula | C12H20N2 |
| Molecular Weight | 192.3006 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Loss of thalamic serotonin transporters in early drug-naïve Parkinson's disease patients is associated with tremor: an [(123)I]beta-CIT SPECT study. | 2008-05 |
|
| Antiparkinsonian-like effects of Plumbago scandens on tremorine-induced tremors methodology. | 2004-12 |
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| The spinal antinociceptive effects of cholinergic drugs in rats: receptor subtype specificity in different nociceptive tests. | 2002-11-19 |
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| Pimprinine, an extracellular alkaloid produced by Streptomyces CDRIL-312: fermentation, isolation and pharmacological activity. | 2001-06-01 |
|
| [Inhibition of harmaline induced tremor by L-threo-3, 4-dihydroxyphenylserine, an L-norepinephrine precursor]. | 1976-04 |
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| Tremorine-oxotremorine-induced tremor, hypothermia and analgesia, and physostigmine toxicity, in mice after pretreatment with beta-adrenoceptor antagonists. | 1976-04 |
|
| 1-Hydroxy-3-amino-pyrrolidone-2(HA-966): a new GABA-like compound, with potential use in extrapyramidal diseases. | 1971-11 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 21:21:01 GMT 2025
by
admin
on
Mon Mar 31 21:21:01 GMT 2025
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| Record UNII |
U817VZ1URQ
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| Record Status |
Validated (UNII)
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| Record Version |
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Tremorine
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m11014
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U817VZ1URQ
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407428
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51-73-0
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D014203
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DTXSID00199004
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