CLOMINOREX

U.S. Department of Health & Human Services Divider Arrow

National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	RACEMIC
Molecular Formula	C9H9ClN2O
Molecular Weight	196.634
Optical Activity	( + / - )
Defined Stereocenters	0 / 1
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of CLOMINOREX

Structure Search

SMILES

NC1=NCC(O1)C2=CC=C(Cl)C=C2

InChI

InChIKey=HAHOPPGVHWVBRR-UHFFFAOYSA-N

InChI=1S/C9H9ClN2O/c10-7-3-1-6(2-4-7)8-5-12-9(11)13-8/h1-4,8H,5H2,(H2,11,12)

HIDE SMILES / InChI

Molecular Formula	C9H9ClN2O
Molecular Weight	196.634
Charge	0
Count

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

Description
Sources: https://patents.google.com/patent/US3278382A/en | https://www.ncbi.nlm.nih.gov/pubmed/5351864

Clominorex is an appetite suppressant, developed in the 1950s by McNeil Laboratories. The compound is claimed to possess the central nervous system stimulant action. Administration of clominorex to mice led to a strong increase in activity and decrease in food intake.

Originator

Approval Year

PubMed

PubMed

Title	Date	PubMed

Patents

Patents

Substance Class	Chemical Created by `admin` on `Fri Dec 15 15:08:35 UTC 2023` Edited by `admin` on `Fri Dec 15 15:08:35 UTC 2023`
Record UNII	O1R2462WA0
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

CLOMINOREX

Official Name

English

2-OXAZOLAMINE, 5-(4-CHLOROPHENYL)-4,5-DIHYDRO-

Systematic Name

English

clominorex [INN]

Common Name

English

NSC-139299

Code

English

CLOMINOREX [USAN]

Common Name

English

MCN-1107

Code

English

Classification Tree Code System Code

NCI_THESAURUS

C29728

Created by admin on Fri Dec 15 15:08:35 UTC 2023 , Edited by admin on Fri Dec 15 15:08:35 UTC 2023

Code System Code Type Description

SMS_ID

100000084526

Created by admin on Fri Dec 15 15:08:35 UTC 2023 , Edited by admin on Fri Dec 15 15:08:35 UTC 2023

PRIMARY

PUBCHEM

19752

Created by admin on Fri Dec 15 15:08:35 UTC 2023 , Edited by admin on Fri Dec 15 15:08:35 UTC 2023

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ChEMBL

CHEMBL2104179

Created by admin on Fri Dec 15 15:08:35 UTC 2023 , Edited by admin on Fri Dec 15 15:08:35 UTC 2023

PRIMARY

CAS

3876-10-6

Created by admin on Fri Dec 15 15:08:35 UTC 2023 , Edited by admin on Fri Dec 15 15:08:35 UTC 2023

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INN

1653

Created by admin on Fri Dec 15 15:08:35 UTC 2023 , Edited by admin on Fri Dec 15 15:08:35 UTC 2023

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NSC

139299

Created by admin on Fri Dec 15 15:08:35 UTC 2023 , Edited by admin on Fri Dec 15 15:08:35 UTC 2023

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NCI_THESAURUS

C72177

Created by admin on Fri Dec 15 15:08:35 UTC 2023 , Edited by admin on Fri Dec 15 15:08:35 UTC 2023

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EVMPD

SUB06724MIG

Created by admin on Fri Dec 15 15:08:35 UTC 2023 , Edited by admin on Fri Dec 15 15:08:35 UTC 2023

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EPA CompTox

DTXSID30863286

Created by admin on Fri Dec 15 15:08:35 UTC 2023 , Edited by admin on Fri Dec 15 15:08:35 UTC 2023

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WIKIPEDIA

CLOMINOREX

Created by admin on Fri Dec 15 15:08:35 UTC 2023 , Edited by admin on Fri Dec 15 15:08:35 UTC 2023

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FDA UNII

O1R2462WA0

Created by admin on Fri Dec 15 15:08:35 UTC 2023 , Edited by admin on Fri Dec 15 15:08:35 UTC 2023

PRIMARY

Related Record Type Details


					N0BX071LZN

CLOMINOREX, (R)-

ENANTIOMER -> RACEMATE


					88UN493A8V

CLOMINOREX, (S)-

ENANTIOMER -> RACEMATE

Related Record Type Details


					O1R2462WA0

ACTIVE MOIETY