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Details

Stereochemistry ACHIRAL
Molecular Formula C11H16N2O3S
Molecular Weight 256.321
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CALDARET

SMILES

CC1=CC=C(N2CCNCC2)C(=C1)S(O)(=O)=O

InChI

InChIKey=DCDFLGVJWQIRGH-UHFFFAOYSA-N
InChI=1S/C11H16N2O3S/c1-9-2-3-10(11(8-9)17(14,15)16)13-6-4-12-5-7-13/h2-3,8,12H,4-7H2,1H3,(H,14,15,16)

HIDE SMILES / InChI

Molecular Formula C11H16N2O3S
Molecular Weight 256.321
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Caldaret is intracardiac calcium (Ca2+) handling modulator whose cardioprotective actions are presumed to be due to inhibition of the NCX exchanger and increasing the uptake of Ca2+ via the sarcoplasmic reticulum (SR). Unfortunately, Caldaret failed to demonstrate efficacy in Phase II clinical trials as an adjunct to standard therapy with primary percutaneous coronary intervention patients diagnosed as having an acute myocardial infarction

Approval Year

PubMed

PubMed

TitleDatePubMed
Breast-feeding may reduce later blood pressure.
2004 Mar 16
Effect of caldaret on the incidence of severe left ventricular dysfunction in patients with ST-elevation myocardial infarction undergoing primary coronary intervention.
2009 Jan 1
Patents

Sample Use Guides

4.5 mg/kg/48 hours
Route of Administration: Intravenous
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:39:12 GMT 2023
Edited
by admin
on Fri Dec 15 16:39:12 GMT 2023
Record UNII
9L3Y3IJ2HI
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CALDARET
INN  
INN  
Official Name English
caldaret [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C333
Created by admin on Fri Dec 15 16:39:12 GMT 2023 , Edited by admin on Fri Dec 15 16:39:12 GMT 2023
Code System Code Type Description
SMS_ID
300000036945
Created by admin on Fri Dec 15 16:39:12 GMT 2023 , Edited by admin on Fri Dec 15 16:39:12 GMT 2023
PRIMARY
FDA UNII
9L3Y3IJ2HI
Created by admin on Fri Dec 15 16:39:12 GMT 2023 , Edited by admin on Fri Dec 15 16:39:12 GMT 2023
PRIMARY
DRUG BANK
DB06231
Created by admin on Fri Dec 15 16:39:12 GMT 2023 , Edited by admin on Fri Dec 15 16:39:12 GMT 2023
PRIMARY
EPA CompTox
DTXSID80158376
Created by admin on Fri Dec 15 16:39:12 GMT 2023 , Edited by admin on Fri Dec 15 16:39:12 GMT 2023
PRIMARY
NCI_THESAURUS
C77830
Created by admin on Fri Dec 15 16:39:12 GMT 2023 , Edited by admin on Fri Dec 15 16:39:12 GMT 2023
PRIMARY
ChEMBL
CHEMBL2106572
Created by admin on Fri Dec 15 16:39:12 GMT 2023 , Edited by admin on Fri Dec 15 16:39:12 GMT 2023
PRIMARY
INN
8113
Created by admin on Fri Dec 15 16:39:12 GMT 2023 , Edited by admin on Fri Dec 15 16:39:12 GMT 2023
PRIMARY
MESH
C487217
Created by admin on Fri Dec 15 16:39:12 GMT 2023 , Edited by admin on Fri Dec 15 16:39:12 GMT 2023
PRIMARY
PUBCHEM
6433076
Created by admin on Fri Dec 15 16:39:12 GMT 2023 , Edited by admin on Fri Dec 15 16:39:12 GMT 2023
PRIMARY
CAS
133804-44-1
Created by admin on Fri Dec 15 16:39:12 GMT 2023 , Edited by admin on Fri Dec 15 16:39:12 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
SOLVATE->ANHYDROUS
TARGET -> INHIBITOR
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ACTIVE MOIETY