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Details

Stereochemistry ACHIRAL
Molecular Formula C16H24N4O2
Molecular Weight 304.3874
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TRACAZOLATE

SMILES

CCCCNC1=C2C=NN(CC)C2=NC(C)=C1C(=O)OCC

InChI

InChIKey=PCTRYMLLRKWXGF-UHFFFAOYSA-N
InChI=1S/C16H24N4O2/c1-5-8-9-17-14-12-10-18-20(6-2)15(12)19-11(4)13(14)16(21)22-7-3/h10H,5-9H2,1-4H3,(H,17,19)

HIDE SMILES / InChI
Tracazolate (ICI 136,753), a pyrazolopyridine, is a non-benzodiazepine with anxiolytic-like activity in animal models. It is known to interact with gamma-aminobutyric acid (GABA)(A) receptors, adenosine receptors, and phosphodiesterases. Its intrinsic efficacy, potentiation, or inhibition is determined by the nature of the third subunit (gamma1-3, delta, or epsilon) within the GABA(A) receptor complex.

CNS Activity

Curator's Comment: Tracazolate is CNS active in animals. No human data available.

Approval Year

PubMed

PubMed

TitleDatePubMed
Dihydropyrimidinone positive modulation of delta-subunit-containing gamma-aminobutyric acid type A receptors, including an epilepsy-linked mutant variant.
2010-06-15
Kinetic and structural determinants for GABA-A receptor potentiation by neuroactive steroids.
2010-03
Limiting activity at beta1-subunit-containing GABAA receptor subtypes reduces ataxia.
2010-03
alpha1beta2delta, a silent GABAA receptor: recruitment by tracazolate and neurosteroids.
2008-03
Role of the alpha subunit in the modulation of GABA(A) receptors by anabolic androgenic steroids.
2005-09
Tracazolate reveals a novel type of allosteric interaction with recombinant gamma-aminobutyric acid(A) receptors.
2002-04
Name Type Language
ICI 136,753
Preferred Name English
TRACAZOLATE
INN   USAN  
INN   USAN  
Official Name English
ETHYL 4-(BUTYLAMINO)-1-ETHYL-6-METHYL-1H-PYRAZOL(3,4-B)PYRIDINE-5-CARBOXYLATE
Common Name English
ICI-136,753
Common Name English
1H-PYRAZOLO(3,4-B)PYRIDINE-5-CARBOXYLIC ACID, 4-(BUTYLAMINO)-1-ETHYL-6-METHYL-, ETHYL ESTER
Common Name English
TRACAZOLATE [USAN]
Common Name English
ICI-136753
Code English
tracazolate [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C28197
Created by admin on Mon Mar 31 21:28:20 GMT 2025 , Edited by admin on Mon Mar 31 21:28:20 GMT 2025
NCI_THESAURUS C264
Created by admin on Mon Mar 31 21:28:20 GMT 2025 , Edited by admin on Mon Mar 31 21:28:20 GMT 2025
Code System Code Type Description
SMS_ID
100000077196
Created by admin on Mon Mar 31 21:28:20 GMT 2025 , Edited by admin on Mon Mar 31 21:28:20 GMT 2025
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INN
4959
Created by admin on Mon Mar 31 21:28:20 GMT 2025 , Edited by admin on Mon Mar 31 21:28:20 GMT 2025
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EPA CompTox
DTXSID3046956
Created by admin on Mon Mar 31 21:28:20 GMT 2025 , Edited by admin on Mon Mar 31 21:28:20 GMT 2025
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ChEMBL
CHEMBL84567
Created by admin on Mon Mar 31 21:28:20 GMT 2025 , Edited by admin on Mon Mar 31 21:28:20 GMT 2025
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WIKIPEDIA
Tracazolate
Created by admin on Mon Mar 31 21:28:20 GMT 2025 , Edited by admin on Mon Mar 31 21:28:20 GMT 2025
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NCI_THESAURUS
C152706
Created by admin on Mon Mar 31 21:28:20 GMT 2025 , Edited by admin on Mon Mar 31 21:28:20 GMT 2025
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FDA UNII
NH0HPL3U1T
Created by admin on Mon Mar 31 21:28:20 GMT 2025 , Edited by admin on Mon Mar 31 21:28:20 GMT 2025
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PUBCHEM
5522
Created by admin on Mon Mar 31 21:28:20 GMT 2025 , Edited by admin on Mon Mar 31 21:28:20 GMT 2025
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CAS
41094-88-6
Created by admin on Mon Mar 31 21:28:20 GMT 2025 , Edited by admin on Mon Mar 31 21:28:20 GMT 2025
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EVMPD
SUB11206MIG
Created by admin on Mon Mar 31 21:28:20 GMT 2025 , Edited by admin on Mon Mar 31 21:28:20 GMT 2025
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ECHA (EC/EINECS)
255-214-9
Created by admin on Mon Mar 31 21:28:20 GMT 2025 , Edited by admin on Mon Mar 31 21:28:20 GMT 2025
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