U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C19H24N2
Molecular Weight 280.4073
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of HISTAPYRRODINE

SMILES

C(CN1CCCC1)N(CC2=CC=CC=C2)C3=CC=CC=C3

InChI

InChIKey=MXHODDGKGSGCDI-UHFFFAOYSA-N
InChI=1S/C19H24N2/c1-3-9-18(10-4-1)17-21(19-11-5-2-6-12-19)16-15-20-13-7-8-14-20/h1-6,9-12H,7-8,13-17H2

HIDE SMILES / InChI

Molecular Formula C19H24N2
Molecular Weight 280.4073
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Histapyrrodine was investigated as a neuro-sedative drug for the treatment of anxiety and states of aggression.

Approval Year

PubMed

PubMed

TitleDatePubMed
Gas chromatographic determination of histapyrrodine hydrochloride in pharmaceutical preparations.
1986 Jul-Aug
Substance Class Chemical
Created
by admin
on Sat Dec 16 17:07:50 GMT 2023
Edited
by admin
on Sat Dec 16 17:07:50 GMT 2023
Record UNII
0FYM61NG4D
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
HISTAPYRRODINE
INN   MART.   MI   WHO-DD  
INN  
Official Name English
1-(2-N-BENZYLANILINOETHYL)PYRROLIDINE
Common Name English
HISTAPYRRODINE [MART.]
Common Name English
histapyrrodine [INN]
Common Name English
HISTAPYRRODINE [MI]
Common Name English
Histapyrrodine [WHO-DD]
Common Name English
Classification Tree Code System Code
WHO-ATC R06AC02
Created by admin on Sat Dec 16 17:07:51 GMT 2023 , Edited by admin on Sat Dec 16 17:07:51 GMT 2023
NCI_THESAURUS C29578
Created by admin on Sat Dec 16 17:07:51 GMT 2023 , Edited by admin on Sat Dec 16 17:07:51 GMT 2023
WHO-ATC R06AC52
Created by admin on Sat Dec 16 17:07:51 GMT 2023 , Edited by admin on Sat Dec 16 17:07:51 GMT 2023
WHO-VATC QR06AC52
Created by admin on Sat Dec 16 17:07:51 GMT 2023 , Edited by admin on Sat Dec 16 17:07:51 GMT 2023
WHO-VATC QR06AC02
Created by admin on Sat Dec 16 17:07:51 GMT 2023 , Edited by admin on Sat Dec 16 17:07:51 GMT 2023
Code System Code Type Description
ChEMBL
CHEMBL2105039
Created by admin on Sat Dec 16 17:07:51 GMT 2023 , Edited by admin on Sat Dec 16 17:07:51 GMT 2023
PRIMARY
INN
618
Created by admin on Sat Dec 16 17:07:51 GMT 2023 , Edited by admin on Sat Dec 16 17:07:51 GMT 2023
PRIMARY
FDA UNII
0FYM61NG4D
Created by admin on Sat Dec 16 17:07:51 GMT 2023 , Edited by admin on Sat Dec 16 17:07:51 GMT 2023
PRIMARY
EVMPD
SUB08044MIG
Created by admin on Sat Dec 16 17:07:51 GMT 2023 , Edited by admin on Sat Dec 16 17:07:51 GMT 2023
PRIMARY
SMS_ID
100000083982
Created by admin on Sat Dec 16 17:07:51 GMT 2023 , Edited by admin on Sat Dec 16 17:07:51 GMT 2023
PRIMARY
PUBCHEM
68122
Created by admin on Sat Dec 16 17:07:51 GMT 2023 , Edited by admin on Sat Dec 16 17:07:51 GMT 2023
PRIMARY
MESH
C049920
Created by admin on Sat Dec 16 17:07:51 GMT 2023 , Edited by admin on Sat Dec 16 17:07:51 GMT 2023
PRIMARY
MERCK INDEX
m762
Created by admin on Sat Dec 16 17:07:51 GMT 2023 , Edited by admin on Sat Dec 16 17:07:51 GMT 2023
PRIMARY Merck Index
WIKIPEDIA
HISTAPYRRODINE
Created by admin on Sat Dec 16 17:07:51 GMT 2023 , Edited by admin on Sat Dec 16 17:07:51 GMT 2023
PRIMARY
EPA CompTox
DTXSID20197764
Created by admin on Sat Dec 16 17:07:51 GMT 2023 , Edited by admin on Sat Dec 16 17:07:51 GMT 2023
PRIMARY
CAS
493-80-1
Created by admin on Sat Dec 16 17:07:51 GMT 2023 , Edited by admin on Sat Dec 16 17:07:51 GMT 2023
PRIMARY
DRUG CENTRAL
1376
Created by admin on Sat Dec 16 17:07:51 GMT 2023 , Edited by admin on Sat Dec 16 17:07:51 GMT 2023
PRIMARY
NCI_THESAURUS
C65855
Created by admin on Sat Dec 16 17:07:51 GMT 2023 , Edited by admin on Sat Dec 16 17:07:51 GMT 2023
PRIMARY
ECHA (EC/EINECS)
207-781-9
Created by admin on Sat Dec 16 17:07:51 GMT 2023 , Edited by admin on Sat Dec 16 17:07:51 GMT 2023
PRIMARY
DRUG BANK
DB13479
Created by admin on Sat Dec 16 17:07:51 GMT 2023 , Edited by admin on Sat Dec 16 17:07:51 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY