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

Details

Stereochemistry RACEMIC
Molecular Formula C23H25N.ClH
Molecular Weight 351.912
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FENDILINE HYDROCHLORIDE

SMILES

Cl.CC(NCCC(C1=CC=CC=C1)C2=CC=CC=C2)C3=CC=CC=C3

InChI

InChIKey=NJXWZWXCHBNOOG-UHFFFAOYSA-N
InChI=1S/C23H25N.ClH/c1-19(20-11-5-2-6-12-20)24-18-17-23(21-13-7-3-8-14-21)22-15-9-4-10-16-22;/h2-16,19,23-24H,17-18H2,1H3;1H

HIDE SMILES / InChI

Molecular Formula C23H25N
Molecular Weight 315.4513
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 17:24:16 UTC 2023
Edited
by admin
on Fri Dec 15 17:24:16 UTC 2023
Record UNII
HEM3Z10IIK
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FENDILINE HYDROCHLORIDE
MART.   MI   WHO-DD  
Common Name English
FENDILAR
Brand Name English
SENSIT
Brand Name English
BENZENEPROPANAMINE, .GAMMA.-PHENYL-N-(1-PHENYLETHYL)-, HYDROCHLORIDE (1:1)
Systematic Name English
FENDILINE HYDROCHLORIDE [MART.]
Common Name English
NSC-757826
Code English
BENZYLAMINE, N-(3,3-DIPHENYLPROPYL)-.ALPHA.-METHYL-, HYDROCHLORIDE
Systematic Name English
BENZENEPROPANAMINE, .GAMMA.-PHENYL-N-(1-PHENYLETHYL)-, HYDROCHLORIDE
Systematic Name English
FENDILINE HYDROCHLORIDE [MI]
Common Name English
CORDAN
Brand Name English
Fendiline hydrochloride [WHO-DD]
Common Name English
N-(2-BENZHYDRYLETHYL)-.ALPHA.-METHYLBENZYLAMINE HYDROCHLORIDE
Systematic Name English
PHENOXAN
Brand Name English
SENSITE
Brand Name English
FENDILINE HCL
Common Name English
Code System Code Type Description
SMS_ID
100000092346
Created by admin on Fri Dec 15 17:24:16 UTC 2023 , Edited by admin on Fri Dec 15 17:24:16 UTC 2023
PRIMARY
CAS
13636-18-5
Created by admin on Fri Dec 15 17:24:16 UTC 2023 , Edited by admin on Fri Dec 15 17:24:16 UTC 2023
PRIMARY
MERCK INDEX
m5272
Created by admin on Fri Dec 15 17:24:16 UTC 2023 , Edited by admin on Fri Dec 15 17:24:16 UTC 2023
PRIMARY Merck Index
PUBCHEM
26154
Created by admin on Fri Dec 15 17:24:16 UTC 2023 , Edited by admin on Fri Dec 15 17:24:16 UTC 2023
PRIMARY
EVMPD
SUB02113MIG
Created by admin on Fri Dec 15 17:24:16 UTC 2023 , Edited by admin on Fri Dec 15 17:24:16 UTC 2023
PRIMARY
NSC
757826
Created by admin on Fri Dec 15 17:24:16 UTC 2023 , Edited by admin on Fri Dec 15 17:24:16 UTC 2023
PRIMARY
ECHA (EC/EINECS)
237-121-5
Created by admin on Fri Dec 15 17:24:16 UTC 2023 , Edited by admin on Fri Dec 15 17:24:16 UTC 2023
PRIMARY
EPA CompTox
DTXSID2045860
Created by admin on Fri Dec 15 17:24:16 UTC 2023 , Edited by admin on Fri Dec 15 17:24:16 UTC 2023
PRIMARY
RXCUI
236767
Created by admin on Fri Dec 15 17:24:16 UTC 2023 , Edited by admin on Fri Dec 15 17:24:16 UTC 2023
PRIMARY RxNorm
FDA UNII
HEM3Z10IIK
Created by admin on Fri Dec 15 17:24:16 UTC 2023 , Edited by admin on Fri Dec 15 17:24:16 UTC 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
PARENT -> SALT/SOLVATE
Related Record Type Details
ACTIVE MOIETY