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Details

Stereochemistry RACEMIC
Molecular Formula C15H23N.ClH
Molecular Weight 253.811
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PROLINTANE HYDROCHLORIDE

SMILES

Cl.CCCC(CC1=CC=CC=C1)N2CCCC2

InChI

InChIKey=FKOFBBOQSMUYHD-UHFFFAOYSA-N
InChI=1S/C15H23N.ClH/c1-2-8-15(16-11-6-7-12-16)13-14-9-4-3-5-10-14;/h3-5,9-10,15H,2,6-8,11-13H2,1H3;1H

HIDE SMILES / InChI

Molecular Formula C15H23N
Molecular Weight 217.3498
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

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

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 15:05:39 UTC 2023
Edited
by admin
on Fri Dec 15 15:05:39 UTC 2023
Record UNII
YEG124534B
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PROLINTANE HYDROCHLORIDE
MART.   MI   USAN   WHO-DD  
USAN  
Official Name English
PROLINTANE HYDROCHLORIDE [USAN]
Common Name English
PYRROLIDINE, 1-(1-(PHENYLMETHYL)BUTYL)-, HYDROCHLORIDE
Systematic Name English
VILESCON
Brand Name English
KATOVIT
Brand Name English
Prolintane hydrochloride [WHO-DD]
Common Name English
KATOVIT N
Brand Name English
PROMOTIL
Brand Name English
PROLINTANE HYDROCHLORIDE [MART.]
Common Name English
PROLINTANE HYDROCHLORIDE [MI]
Common Name English
1-(α-Propylphenethyl)pyrrolidine hydrochloride
Systematic Name English
SP-732
Code English
CATOVITAN
Brand Name English
VILLESCON
Brand Name English
NSC-169914
Code English
PYRROLIDINE, 1-(1-BENZYLBUTYL)-, HYDROCHLORIDE
Systematic Name English
Code System Code Type Description
RXCUI
235831
Created by admin on Fri Dec 15 15:05:39 UTC 2023 , Edited by admin on Fri Dec 15 15:05:39 UTC 2023
PRIMARY RxNorm
NSC
169914
Created by admin on Fri Dec 15 15:05:39 UTC 2023 , Edited by admin on Fri Dec 15 15:05:39 UTC 2023
PRIMARY
EVMPD
SUB04064MIG
Created by admin on Fri Dec 15 15:05:39 UTC 2023 , Edited by admin on Fri Dec 15 15:05:39 UTC 2023
PRIMARY
CAS
1211-28-5
Created by admin on Fri Dec 15 15:05:39 UTC 2023 , Edited by admin on Fri Dec 15 15:05:39 UTC 2023
PRIMARY
PUBCHEM
14591
Created by admin on Fri Dec 15 15:05:39 UTC 2023 , Edited by admin on Fri Dec 15 15:05:39 UTC 2023
PRIMARY
MESH
C005598
Created by admin on Fri Dec 15 15:05:39 UTC 2023 , Edited by admin on Fri Dec 15 15:05:39 UTC 2023
PRIMARY
FDA UNII
YEG124534B
Created by admin on Fri Dec 15 15:05:39 UTC 2023 , Edited by admin on Fri Dec 15 15:05:39 UTC 2023
PRIMARY
SMS_ID
100000085104
Created by admin on Fri Dec 15 15:05:39 UTC 2023 , Edited by admin on Fri Dec 15 15:05:39 UTC 2023
PRIMARY
ChEMBL
CHEMBL2111047
Created by admin on Fri Dec 15 15:05:39 UTC 2023 , Edited by admin on Fri Dec 15 15:05:39 UTC 2023
PRIMARY
NCI_THESAURUS
C170357
Created by admin on Fri Dec 15 15:05:39 UTC 2023 , Edited by admin on Fri Dec 15 15:05:39 UTC 2023
PRIMARY
ECHA (EC/EINECS)
214-917-0
Created by admin on Fri Dec 15 15:05:39 UTC 2023 , Edited by admin on Fri Dec 15 15:05:39 UTC 2023
PRIMARY
MERCK INDEX
m9166
Created by admin on Fri Dec 15 15:05:39 UTC 2023 , Edited by admin on Fri Dec 15 15:05:39 UTC 2023
PRIMARY Merck Index
CAS
141996-82-9
Created by admin on Fri Dec 15 15:05:39 UTC 2023 , Edited by admin on Fri Dec 15 15:05:39 UTC 2023
SUPERSEDED
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PARENT -> SALT/SOLVATE
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ACTIVE MOIETY