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Details

Stereochemistry RACEMIC
Molecular Formula C24H32N2.2ClH
Molecular Weight 421.446
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MT-45 hydrochloride

SMILES

Cl.Cl.C(C(N1CCN(CC1)C2CCCCC2)C3=CC=CC=C3)C4=CC=CC=C4

InChI

InChIKey=PDTBWROWBIVSFO-UHFFFAOYSA-N
InChI=1S/C24H32N2.2ClH/c1-4-10-21(11-5-1)20-24(22-12-6-2-7-13-22)26-18-16-25(17-19-26)23-14-8-3-9-15-23;;/h1-2,4-7,10-13,23-24H,3,8-9,14-20H2;2*1H

HIDE SMILES / InChI

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
44.0 nM [Ki]
606.0 nM [Ki]
204.0 nM [Ki]
PubMed

PubMed

TitleDatePubMed
Chondrocyte-derived ezrin-like domain containing protein (CDEP), a rho guanine nucleotide exchange factor, is inducible in chondrocytes by parathyroid hormone and cyclic AMP and has transforming activity in NIH3T3 cells.
2001
Patents

Patents

Name Type Language
MT-45 hydrochloride
Common Name English
NSC-299236
Preferred Name English
1-Cyclohexyl-4-(1,2-diphenylethyl)piperazine dihydrochloride
Systematic Name English
(±)-1-Cyclohexyl-4-(1,2-diphenylethyl)piperazine dihydrochloride
Systematic Name English
I-C6 hydrochloride
Common Name English
Piperazine, 1-cyclohexyl-4-(1,2-diphenylethyl)-, hydrochloride (1:2)
Common Name English
Piperazine, 1-cyclohexyl-4-(1,2-diphenylethyl)-, dihydrochloride, (±)-
Common Name English
1-cyclohexyl-4-(1,2-diphenylethyl)-piperazine dihydrochloride
Systematic Name English
Piperazine, 1-cyclohexyl-4-(1,2-diphenylethyl)-, dihydrochloride
Common Name English
Code System Code Type Description
CAYMAN
14082
Created by admin on Wed Apr 02 20:39:36 GMT 2025 , Edited by admin on Wed Apr 02 20:39:36 GMT 2025
PRIMARY
PUBCHEM
3044473
Created by admin on Wed Apr 02 20:39:36 GMT 2025 , Edited by admin on Wed Apr 02 20:39:36 GMT 2025
PRIMARY
CAS
57314-55-3
Created by admin on Wed Apr 02 20:39:36 GMT 2025 , Edited by admin on Wed Apr 02 20:39:36 GMT 2025
PRIMARY
FDA UNII
EB2C2TKJ67
Created by admin on Wed Apr 02 20:39:36 GMT 2025 , Edited by admin on Wed Apr 02 20:39:36 GMT 2025
PRIMARY