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Details

Stereochemistry RACEMIC
Molecular Formula C12H18ClN
Molecular Weight 211.731
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MEFENOREX

SMILES

CC(CC1=CC=CC=C1)NCCCCl

InChI

InChIKey=XXVROGAVTTXONC-UHFFFAOYSA-N
InChI=1S/C12H18ClN/c1-11(14-9-5-8-13)10-12-6-3-2-4-7-12/h2-4,6-7,11,14H,5,8-10H2,1H3

HIDE SMILES / InChI

Molecular Formula C12H18ClN
Molecular Weight 211.731
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 17:19:58 UTC 2023
Edited
by admin
on Fri Dec 15 17:19:58 UTC 2023
Record UNII
K98M4N387W
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MEFENOREX
INN   MI   WHO-DD  
INN  
Official Name English
MEFENOREX [MI]
Common Name English
N-(3-CHLOROPROPYL)-.ALPHA.-METHYLPHENETHYLAMINE
Systematic Name English
mefenorex [INN]
Common Name English
PHENETHYLAMINE, N-(3-CHLOROPROPYL)-.ALPHA.-METHYL-
Systematic Name English
Mefenorex [WHO-DD]
Common Name English
BENZENEETHANAMINE, N-(3-CHLOROPROPYL)-.ALPHA.-METHYL
Common Name English
Classification Tree Code System Code
WHO-ATC A08AA09
Created by admin on Fri Dec 15 17:19:58 UTC 2023 , Edited by admin on Fri Dec 15 17:19:58 UTC 2023
NCI_THESAURUS C29728
Created by admin on Fri Dec 15 17:19:58 UTC 2023 , Edited by admin on Fri Dec 15 17:19:58 UTC 2023
DEA NO. 1580
Created by admin on Fri Dec 15 17:19:58 UTC 2023 , Edited by admin on Fri Dec 15 17:19:58 UTC 2023
WHO-VATC QA08AA09
Created by admin on Fri Dec 15 17:19:58 UTC 2023 , Edited by admin on Fri Dec 15 17:19:58 UTC 2023
Code System Code Type Description
MERCK INDEX
m7140
Created by admin on Fri Dec 15 17:19:58 UTC 2023 , Edited by admin on Fri Dec 15 17:19:58 UTC 2023
PRIMARY Merck Index
ChEMBL
CHEMBL2110962
Created by admin on Fri Dec 15 17:19:58 UTC 2023 , Edited by admin on Fri Dec 15 17:19:58 UTC 2023
PRIMARY
MESH
C000450
Created by admin on Fri Dec 15 17:19:58 UTC 2023 , Edited by admin on Fri Dec 15 17:19:58 UTC 2023
PRIMARY
ECHA (EC/EINECS)
241-279-0
Created by admin on Fri Dec 15 17:19:58 UTC 2023 , Edited by admin on Fri Dec 15 17:19:58 UTC 2023
PRIMARY
EPA CompTox
DTXSID6057665
Created by admin on Fri Dec 15 17:19:58 UTC 2023 , Edited by admin on Fri Dec 15 17:19:58 UTC 2023
PRIMARY
EVMPD
SUB08706MIG
Created by admin on Fri Dec 15 17:19:58 UTC 2023 , Edited by admin on Fri Dec 15 17:19:58 UTC 2023
PRIMARY
CAS
17243-57-1
Created by admin on Fri Dec 15 17:19:58 UTC 2023 , Edited by admin on Fri Dec 15 17:19:58 UTC 2023
PRIMARY
RXCUI
29444
Created by admin on Fri Dec 15 17:19:58 UTC 2023 , Edited by admin on Fri Dec 15 17:19:58 UTC 2023
PRIMARY RxNorm
DRUG BANK
DB13852
Created by admin on Fri Dec 15 17:19:58 UTC 2023 , Edited by admin on Fri Dec 15 17:19:58 UTC 2023
PRIMARY
PUBCHEM
21777
Created by admin on Fri Dec 15 17:19:58 UTC 2023 , Edited by admin on Fri Dec 15 17:19:58 UTC 2023
PRIMARY
INN
2494
Created by admin on Fri Dec 15 17:19:58 UTC 2023 , Edited by admin on Fri Dec 15 17:19:58 UTC 2023
PRIMARY
NCI_THESAURUS
C83915
Created by admin on Fri Dec 15 17:19:58 UTC 2023 , Edited by admin on Fri Dec 15 17:19:58 UTC 2023
PRIMARY
DRUG CENTRAL
1664
Created by admin on Fri Dec 15 17:19:58 UTC 2023 , Edited by admin on Fri Dec 15 17:19:58 UTC 2023
PRIMARY
WIKIPEDIA
MEFENOREX
Created by admin on Fri Dec 15 17:19:58 UTC 2023 , Edited by admin on Fri Dec 15 17:19:58 UTC 2023
PRIMARY
SMS_ID
100000081459
Created by admin on Fri Dec 15 17:19:58 UTC 2023 , Edited by admin on Fri Dec 15 17:19:58 UTC 2023
PRIMARY
FDA UNII
K98M4N387W
Created by admin on Fri Dec 15 17:19:58 UTC 2023 , Edited by admin on Fri Dec 15 17:19:58 UTC 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY