AZABUPERONE

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National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	RACEMIC
Molecular Formula	C17H23FN2O
Molecular Weight	290.3757
Optical Activity	( + / - )
Defined Stereocenters	0 / 1
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of AZABUPERONE

Structure Search

SMILES

FC1=CC=C(C=C1)C(=O)CCCN2CCN3CCCC3C2

InChI

InChIKey=PQLYZHNINGGVMB-UHFFFAOYSA-N

InChI=1S/C17H23FN2O/c18-15-7-5-14(6-8-15)17(21)4-2-9-19-11-12-20-10-1-3-16(20)13-19/h5-8,16H,1-4,9-13H2

HIDE SMILES / InChI

Molecular Formula	C17H23FN2O
Molecular Weight	290.3757
Charge	0
Count

Stereochemistry	RACEMIC
Additional Stereochemistry	No
Defined Stereocenters	0 / 1
E/Z Centers	0
Optical Activity	( + / - )

Description
Sources: https://books.google.ru/books?id=0vXTBwAAQBAJ&pg=PA110&lpg=PA110&dq=AZABUPERONE&source=bl&ots=6JTmn4Txxt&sig=ACfU3U2NjvAXBvG3-18hweSkAKs7H7Uldw&hl=ru&sa=X&ved=2ahUKEwjjpI-Yg6HiAhWplosKHXJTDuU4FBDoATAAegQIBhAB#v=onepage&q=AZABUPERONE&f=false

Azabyperone was developed as tranquilizer and neuroleptic and has never been marketed.

Approval Year

Patents

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 18:03:46 GMT 2025` Edited by `admin` on `Mon Mar 31 18:03:46 GMT 2025`
Record UNII	9P043590EX
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

azabuperone [INN]

Preferred Name

English

AZABUPERONE

Official Name

English

4'-FLUORO-4-(HEXAHYDROPYRROLO(1,2-A)PYRAZIN-2(1H)-YL)BUTYROPHENONE

Systematic Name

English

Classification Tree Code System Code

NCI_THESAURUS

C29710

Created by admin on Mon Mar 31 18:03:46 GMT 2025 , Edited by admin on Mon Mar 31 18:03:46 GMT 2025

Code System Code Type Description

SMS_ID

100000086885

Created by admin on Mon Mar 31 18:03:46 GMT 2025 , Edited by admin on Mon Mar 31 18:03:46 GMT 2025

PRIMARY

PUBCHEM

18484

Created by admin on Mon Mar 31 18:03:46 GMT 2025 , Edited by admin on Mon Mar 31 18:03:46 GMT 2025

PRIMARY

MESH

C011672

Created by admin on Mon Mar 31 18:03:46 GMT 2025 , Edited by admin on Mon Mar 31 18:03:46 GMT 2025

PRIMARY

NCI_THESAURUS

C73282

Created by admin on Mon Mar 31 18:03:46 GMT 2025 , Edited by admin on Mon Mar 31 18:03:46 GMT 2025

PRIMARY

ChEMBL

CHEMBL1965536

Created by admin on Mon Mar 31 18:03:46 GMT 2025 , Edited by admin on Mon Mar 31 18:03:46 GMT 2025

PRIMARY

EVMPD

SUB05623MIG

Created by admin on Mon Mar 31 18:03:46 GMT 2025 , Edited by admin on Mon Mar 31 18:03:46 GMT 2025

PRIMARY

CAS

2856-81-7

Created by admin on Mon Mar 31 18:03:46 GMT 2025 , Edited by admin on Mon Mar 31 18:03:46 GMT 2025

PRIMARY

INN

3881

Created by admin on Mon Mar 31 18:03:46 GMT 2025 , Edited by admin on Mon Mar 31 18:03:46 GMT 2025

PRIMARY

FDA UNII

9P043590EX

Created by admin on Mon Mar 31 18:03:46 GMT 2025 , Edited by admin on Mon Mar 31 18:03:46 GMT 2025

PRIMARY

EPA CompTox

DTXSID1046186

Created by admin on Mon Mar 31 18:03:46 GMT 2025 , Edited by admin on Mon Mar 31 18:03:46 GMT 2025

PRIMARY

Related Record Type Details


					306O5MRM12

AZABUPERONE, (R)-

ENANTIOMER -> RACEMATE


					WX783YBJ7A

AZABUPERONE, (S)-

ENANTIOMER -> RACEMATE

Related Record Type Details


					9P043590EX

ACTIVE MOIETY