Names | |
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IUPAC name
2-(5-nitro-1H-indol-3-yl)-2-oxo-N-[(1R)-1-phenylethyl]acetamide
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Identifiers | |
3D model (
JSmol)
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ChEMBL | |
ChemSpider | |
PubChem
CID
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Properties | |
C18H15N3O4 | |
Molar mass | 337.335 g·mol−1 |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
TCS 1205 is an organic chemical compound. It is a benzodiazepine site agonist selective for certain sub-units.
TCS 1205 acts at the benzodiazepine binding site, it is selective for the a1 and a2 subunits of the GABAA receptor. [1] In vivo, it has anxiolytic effects but no sedative effects. [2] [3]
Despite acting at the benzodiazepine receptor, it does not contain the benzodiazepine structure, it could therefore be classed as a Nonbenzodiazepine.
Names | |
---|---|
IUPAC name
2-(5-nitro-1H-indol-3-yl)-2-oxo-N-[(1R)-1-phenylethyl]acetamide
| |
Identifiers | |
3D model (
JSmol)
|
|
ChEMBL | |
ChemSpider | |
PubChem
CID
|
|
| |
| |
Properties | |
C18H15N3O4 | |
Molar mass | 337.335 g·mol−1 |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
TCS 1205 is an organic chemical compound. It is a benzodiazepine site agonist selective for certain sub-units.
TCS 1205 acts at the benzodiazepine binding site, it is selective for the a1 and a2 subunits of the GABAA receptor. [1] In vivo, it has anxiolytic effects but no sedative effects. [2] [3]
Despite acting at the benzodiazepine receptor, it does not contain the benzodiazepine structure, it could therefore be classed as a Nonbenzodiazepine.