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Details

Stereochemistry RACEMIC
Molecular Formula C27H32N2O3
Molecular Weight 432.5546
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TAMOLARIZINE

SMILES

COC1=C(OC)C=C(C=C1)C(O)CN2CCN(CC2)C(C3=CC=CC=C3)C4=CC=CC=C4

InChI

InChIKey=PIKMDZDCXCAPEF-UHFFFAOYSA-N
InChI=1S/C27H32N2O3/c1-31-25-14-13-23(19-26(25)32-2)24(30)20-28-15-17-29(18-16-28)27(21-9-5-3-6-10-21)22-11-7-4-8-12-22/h3-14,19,24,27,30H,15-18,20H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C27H32N2O3
Molecular Weight 432.5546
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Tamolarizine (also known as NC-1100), an organic Ca2+ channel blocker, was studied in clinical trials phase II in patients with neurological disorders. However, these studies were discontinued. In addition, experiments on rodents have shown that tamolarizine treatment protected the hippocampus from ischemic brain damage and ameliorated place learning impairment. Tamolarizine was also able to reverse the multidrug-resistance phenotype in human leukemia K562 cells through direct interaction with P-glycoprotein.

Approval Year

PubMed

PubMed

TitleDatePubMed
Reversal of multidrug resistance in human leukemia K562 by tamolarizine, a novel calcium antagonist.
2000-03
Ameliorative effects of tamolarizine on place learning impairment induced by transient forebrain ischemia in rats.
2000-01-17
A new type of Ca2+ channel blocker, NC-1100, inhibits the low- and high-threshold Ca2+ currents in the rat CNS neurons.
1992-12-11
Selectivity of cerebral vasodilators on basilar arteries.
1986
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:25:07 GMT 2025
Edited
by admin
on Mon Mar 31 18:25:07 GMT 2025
Record UNII
0PG3PMK9YA
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
tamolarizine [INN]
Preferred Name English
TAMOLARIZINE
INN  
INN  
Official Name English
Classification Tree Code System Code
NCI_THESAURUS C333
Created by admin on Mon Mar 31 18:25:07 GMT 2025 , Edited by admin on Mon Mar 31 18:25:07 GMT 2025
Code System Code Type Description
CAS
128229-52-7
Created by admin on Mon Mar 31 18:25:07 GMT 2025 , Edited by admin on Mon Mar 31 18:25:07 GMT 2025
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EVMPD
SUB10824MIG
Created by admin on Mon Mar 31 18:25:07 GMT 2025 , Edited by admin on Mon Mar 31 18:25:07 GMT 2025
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INN
6849
Created by admin on Mon Mar 31 18:25:07 GMT 2025 , Edited by admin on Mon Mar 31 18:25:07 GMT 2025
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NCI_THESAURUS
C76583
Created by admin on Mon Mar 31 18:25:07 GMT 2025 , Edited by admin on Mon Mar 31 18:25:07 GMT 2025
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FDA UNII
0PG3PMK9YA
Created by admin on Mon Mar 31 18:25:07 GMT 2025 , Edited by admin on Mon Mar 31 18:25:07 GMT 2025
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ChEMBL
CHEMBL2074664
Created by admin on Mon Mar 31 18:25:07 GMT 2025 , Edited by admin on Mon Mar 31 18:25:07 GMT 2025
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MESH
C050134
Created by admin on Mon Mar 31 18:25:07 GMT 2025 , Edited by admin on Mon Mar 31 18:25:07 GMT 2025
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SMS_ID
100000082421
Created by admin on Mon Mar 31 18:25:07 GMT 2025 , Edited by admin on Mon Mar 31 18:25:07 GMT 2025
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EPA CompTox
DTXSID20869757
Created by admin on Mon Mar 31 18:25:07 GMT 2025 , Edited by admin on Mon Mar 31 18:25:07 GMT 2025
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PUBCHEM
146396
Created by admin on Mon Mar 31 18:25:07 GMT 2025 , Edited by admin on Mon Mar 31 18:25:07 GMT 2025
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY