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Details

Stereochemistry ACHIRAL
Molecular Formula C22H23Cl2N3OS.ClH
Molecular Weight 484.869
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of ELZASONAN HYDROCHLORIDE

SMILES

Cl.CN1CCN(CC1)C2=CC=CC=C2\C=C3/SCCN(C3=O)C4=CC=C(Cl)C(Cl)=C4

InChI

InChIKey=NMTRXBJYASHMND-UXTSPRGOSA-N
InChI=1S/C22H23Cl2N3OS.ClH/c1-25-8-10-26(11-9-25)20-5-3-2-4-16(20)14-21-22(28)27(12-13-29-21)17-6-7-18(23)19(24)15-17;/h2-7,14-15H,8-13H2,1H3;1H/b21-14-;

HIDE SMILES / InChI

Molecular Formula C22H23Cl2N3OS
Molecular Weight 448.409
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 1
Optical Activity NONE

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

Elzasonan (CP 448187) is a serotonin 1B/1D receptor antagonist. Elzasonan was primarily metabolized via oxidative N‐demethylation, N‐oxidation, and aryl hydroxylation. Pfizer was developing elzasonan for the treatment of anxiety and affective disorders however development has been discontinued.

Approval Year

PubMed

PubMed

TitleDatePubMed
Profiling 976 ToxCast chemicals across 331 enzymatic and receptor signaling assays.
2013-06-17
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 18:02:04 GMT 2025
Edited
by admin
on Mon Mar 31 18:02:04 GMT 2025
Record UNII
X38F62RR8L
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CP-448,187-01
Preferred Name English
ELZASONAN HYDROCHLORIDE
USAN  
USAN  
Official Name English
CP-448187-01
Code English
3-THIOMORPHOLINONE, 4-(3,4-DICHLORPHENYL)-2-(((2-(4-METHYL-1-PIPERAZINYL)PHENYL)METHYLENE)- MONOHYDROCHLORIDE, (2Z)-
Common Name English
ELZASONAN HCL
Common Name English
ELZASONAN HYDROCHLORIDE [USAN]
Common Name English
(2Z)-4-(3,4-Dichlorophenyl)-2-[2-(4-methylpiperazin-1-yl)benzylidene]thiomorpholin-3-one monohydrochloride
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C66885
Created by admin on Mon Mar 31 18:02:04 GMT 2025 , Edited by admin on Mon Mar 31 18:02:04 GMT 2025
Code System Code Type Description
ChEMBL
CHEMBL2110932
Created by admin on Mon Mar 31 18:02:04 GMT 2025 , Edited by admin on Mon Mar 31 18:02:04 GMT 2025
PRIMARY
FDA UNII
X38F62RR8L
Created by admin on Mon Mar 31 18:02:04 GMT 2025 , Edited by admin on Mon Mar 31 18:02:04 GMT 2025
PRIMARY
NCI_THESAURUS
C73806
Created by admin on Mon Mar 31 18:02:04 GMT 2025 , Edited by admin on Mon Mar 31 18:02:04 GMT 2025
PRIMARY
CAS
220322-05-4
Created by admin on Mon Mar 31 18:02:04 GMT 2025 , Edited by admin on Mon Mar 31 18:02:04 GMT 2025
PRIMARY
SMS_ID
300000044593
Created by admin on Mon Mar 31 18:02:04 GMT 2025 , Edited by admin on Mon Mar 31 18:02:04 GMT 2025
PRIMARY
USAN
MM-16
Created by admin on Mon Mar 31 18:02:04 GMT 2025 , Edited by admin on Mon Mar 31 18:02:04 GMT 2025
PRIMARY
CAS
205683-38-1
Created by admin on Mon Mar 31 18:02:04 GMT 2025 , Edited by admin on Mon Mar 31 18:02:04 GMT 2025
NON-SPECIFIC STEREOCHEMISTRY
PUBCHEM
6506051
Created by admin on Mon Mar 31 18:02:04 GMT 2025 , Edited by admin on Mon Mar 31 18:02:04 GMT 2025
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE
Related Record Type Details
ACTIVE MOIETY