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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
Structure of DIPROBUTINE

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

HIDE SMILES / InChI

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

PubMed

PubMed

TitleDatePubMed
Determination of diprobutine in human plasma using gas-liquid chromatography with nitrogen-selective detection.
1985 Apr 12
Allosteric effects of diprobutine on acetylcholine receptors.
1985 Nov 5
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:21:22 GMT 2023
Edited
by admin
on Fri Dec 15 16:21:22 GMT 2023
Record UNII
5XE7IWD0JX
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DIPROBUTINE
INN  
INN  
Official Name English
1,1-DIPROPYLBUTYLAMINE
Systematic Name English
diprobutine [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C38149
Created by admin on Fri Dec 15 16:21:22 GMT 2023 , Edited by admin on Fri Dec 15 16:21:22 GMT 2023
Code System Code Type Description
EPA CompTox
DTXSID70210811
Created by admin on Fri Dec 15 16:21:22 GMT 2023 , Edited by admin on Fri Dec 15 16:21:22 GMT 2023
PRIMARY
ChEMBL
CHEMBL2104369
Created by admin on Fri Dec 15 16:21:22 GMT 2023 , Edited by admin on Fri Dec 15 16:21:22 GMT 2023
PRIMARY
EVMPD
SUB07221MIG
Created by admin on Fri Dec 15 16:21:22 GMT 2023 , Edited by admin on Fri Dec 15 16:21:22 GMT 2023
PRIMARY
FDA UNII
5XE7IWD0JX
Created by admin on Fri Dec 15 16:21:22 GMT 2023 , Edited by admin on Fri Dec 15 16:21:22 GMT 2023
PRIMARY
MESH
C045947
Created by admin on Fri Dec 15 16:21:22 GMT 2023 , Edited by admin on Fri Dec 15 16:21:22 GMT 2023
PRIMARY
NCI_THESAURUS
C65430
Created by admin on Fri Dec 15 16:21:22 GMT 2023 , Edited by admin on Fri Dec 15 16:21:22 GMT 2023
PRIMARY
PUBCHEM
41701
Created by admin on Fri Dec 15 16:21:22 GMT 2023 , Edited by admin on Fri Dec 15 16:21:22 GMT 2023
PRIMARY
INN
4367
Created by admin on Fri Dec 15 16:21:22 GMT 2023 , Edited by admin on Fri Dec 15 16:21:22 GMT 2023
PRIMARY
CAS
61822-36-4
Created by admin on Fri Dec 15 16:21:22 GMT 2023 , Edited by admin on Fri Dec 15 16:21:22 GMT 2023
PRIMARY
SMS_ID
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
PRIMARY
Related Record Type Details
ACTIVE MOIETY