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Details

Stereochemistry ACHIRAL
Molecular Formula C23H32N2O2
Molecular Weight 368.5124
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CUTAMESINE

SMILES

COC1=CC=C(CCN2CCN(CCCC3=CC=CC=C3)CC2)C=C1OC

InChI

InChIKey=UVSWWUWQVAQPJR-UHFFFAOYSA-N
InChI=1S/C23H32N2O2/c1-26-22-11-10-21(19-23(22)27-2)12-14-25-17-15-24(16-18-25)13-6-9-20-7-4-3-5-8-20/h3-5,7-8,10-11,19H,6,9,12-18H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C23H32N2O2
Molecular Weight 368.5124
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Cutamesine, an agonsit of brain sigma 1 receptors, was developed by Santen Pharmaceutical for the treatment of cognitive diseases. The drug was tested in phase II in patients with major depressive disorders and for recovery of patients with stroke, however its development was terminated for the given conditions. Currently M's science corporation is developing cutamesine for Amyotrophic lateral sclerosis and Retinitis pigmentosa as more suitable target diseases.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
17.4 nM [IC50]
Conditions
Doses

Doses

DosePopulationAdverse events​
3 mg 1 times / day multiple, oral
Highest studied dose
Dose: 3 mg, 1 times / day
Route: oral
Route: multiple
Dose: 3 mg, 1 times / day
Sources:
unhealthy, ADULT
n = 19
Health Status: unhealthy
Condition: stroke
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Population Size: 19
Sources:
Sourcing

Sourcing

Vendor/AggregatorIDURL
PubMed

PubMed

TitleDatePubMed
Involvement of kappa-opioid and sigma receptors in short-term memory in mice.
2002 Oct 18
Sigma-1 receptor agonist fluvoxamine for delirium in intensive care units: report of five cases.
2010 Apr 24
Sigma-1 receptor agonist fluvoxamine for postoperative delirium in older adults: report of three cases.
2010 Jun 24
Patents

Patents

Sample Use Guides

Patients with stroke receive cutamesine at a dose of 1 mg/day or 3 mg/day for 28 days.
Route of Administration: Oral
Mice motor neuron cells were treated with cutamesine at concentration of 1-10 uM and the drug was shown to reduce SOD1(G93A)-induced cell death in a concentration-dependent manner.
Substance Class Chemical
Created
by admin
on Sat Dec 16 16:48:28 GMT 2023
Edited
by admin
on Sat Dec 16 16:48:28 GMT 2023
Record UNII
9J7A4144BX
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CUTAMESINE
INN   WHO-DD  
INN  
Official Name English
SA-4503
Common Name English
1-(2-(3,4-DIMETHOXYPHENYL)ETHYL)-4-(3-PHENYLPROPYL)PIPERAZINE
Systematic Name English
cutamesine [INN]
Common Name English
Cutamesine [WHO-DD]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C265
Created by admin on Sat Dec 16 16:48:28 GMT 2023 , Edited by admin on Sat Dec 16 16:48:28 GMT 2023
Code System Code Type Description
WIKIPEDIA
SA-4503
Created by admin on Sat Dec 16 16:48:28 GMT 2023 , Edited by admin on Sat Dec 16 16:48:28 GMT 2023
PRIMARY
EPA CompTox
DTXSID50167935
Created by admin on Sat Dec 16 16:48:28 GMT 2023 , Edited by admin on Sat Dec 16 16:48:28 GMT 2023
PRIMARY
CAS
165377-43-5
Created by admin on Sat Dec 16 16:48:28 GMT 2023 , Edited by admin on Sat Dec 16 16:48:28 GMT 2023
PRIMARY
DRUG BANK
DB06618
Created by admin on Sat Dec 16 16:48:28 GMT 2023 , Edited by admin on Sat Dec 16 16:48:28 GMT 2023
PRIMARY
NCI_THESAURUS
C83642
Created by admin on Sat Dec 16 16:48:28 GMT 2023 , Edited by admin on Sat Dec 16 16:48:28 GMT 2023
PRIMARY
FDA UNII
9J7A4144BX
Created by admin on Sat Dec 16 16:48:28 GMT 2023 , Edited by admin on Sat Dec 16 16:48:28 GMT 2023
PRIMARY
SMS_ID
100000178232
Created by admin on Sat Dec 16 16:48:28 GMT 2023 , Edited by admin on Sat Dec 16 16:48:28 GMT 2023
PRIMARY
PUBCHEM
9907323
Created by admin on Sat Dec 16 16:48:28 GMT 2023 , Edited by admin on Sat Dec 16 16:48:28 GMT 2023
PRIMARY
INN
9061
Created by admin on Sat Dec 16 16:48:28 GMT 2023 , Edited by admin on Sat Dec 16 16:48:28 GMT 2023
PRIMARY
Related Record Type Details
LABELED -> NON-LABELED
TARGET -> AGONIST
IC50
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY