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
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)
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
Sources: https://www.ncbi.nlm.nih.gov/pubmed/2872613 | https://www.ncbi.nlm.nih.gov/pubmed/6121711
Curator's Comment: Tracazolate is CNS active in animals. No human data available.
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| 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 |
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NCI_THESAURUS |
C28197
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NCI_THESAURUS |
C264
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100000077196
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4959
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DTXSID3046956
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CHEMBL84567
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Tracazolate
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C152706
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NH0HPL3U1T
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5522
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41094-88-6
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SUB11206MIG
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255-214-9
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ACTIVE MOIETY