Details
Stereochemistry | ACHIRAL |
Molecular Formula | C10H23N |
Molecular Weight | 157.2963 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCC(N)(CCC)CCC
InChI
InChIKey=VQIAWQKBOAUGHE-UHFFFAOYSA-N
InChI=1S/C10H23N/c1-4-7-10(11,8-5-2)9-6-3/h4-9,11H2,1-3H3
Molecular Formula | C10H23N |
Molecular Weight | 157.2963 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Diprobutine, or tripropylmethylamine, is a pharmacological agent with rather unusual anti-Parkinsonian activity. In experimental animals, it causes general arousal with stimulation of locomotor activity, antagonizes neuroleptic-induced catatonia and blocks nicotine-elicited convulsions. In vitro, diprobutine does not interact directly with either dopaminergic, noradrenergic, serotonergic or muscarinic brain binding sites. Diprobutine binds to the high affinity allosteric site for noncompetitive blockers on T. marmorata acetylcholine receptor. Diprobutine blocks the tonic crisis induced by nicotine. A pharmacological action of diprobutine as blocker of the ionic channel associated with brain nicotinic receptors.
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 16:21:22 GMT 2023
by
admin
on
Fri Dec 15 16:21:22 GMT 2023
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Record UNII |
5XE7IWD0JX
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Record Status |
Validated (UNII)
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Record Version |
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NCI_THESAURUS |
C38149
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admin on Fri Dec 15 16:21:22 GMT 2023 , Edited by admin on Fri Dec 15 16:21:22 GMT 2023
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DTXSID70210811
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CHEMBL2104369
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SUB07221MIG
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5XE7IWD0JX
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C045947
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C65430
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41701
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4367
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61822-36-4
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100000082332
Created by
admin on Fri Dec 15 16:21:22 GMT 2023 , Edited by admin on Fri Dec 15 16:21:22 GMT 2023
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Related Record | Type | Details | ||
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ACTIVE MOIETY |