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TCS-1205

From Wikipedia, the free encyclopedia
TCS-1205
Names
IUPAC name
2-(5-nitro-1H-indol-3-yl)-2-oxo-N-[(1R)-1-phenylethyl]acetamide
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
  • Key: VCKKJKQZHHPPDR-LLVKDONJSA-N
  • InChI=1S/C18H15N3O4/c1-11(12-5-3-2-4-6-12)20-18(23)17(22)15-10-19-16-8-7-13(21(24)25)9-14(15)16/h2-11,19H,1H3,(H,20,23)/t11-/m1/s1
  • CC(C1=CC=CC=C1)NC(=O)C(=O)C2=CNC3=C2C=C(C=C3)[N+](=O)[O-]
Properties
C18H15N3O4
Molar mass 337.335g·mol−1
Except where otherwise noted, data are given for materials in theirstandard state(at 25 °C [77 °F], 100 kPa).

TCS 1205is an organic chemical compound. It is abenzodiazepine siteagonist selective for certain sub-units.

Pharmacology

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TCS 1205acts at thebenzodiazepinebinding site, it is selective for thea1anda2subunits of theGABAAreceptor.[1]In vivo,it hasanxiolyticeffects but no sedative effects.[2][3]

Chemistry

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Despite acting at thebenzodiazepine receptor,it does not contain thebenzodiazepinestructure, it could therefore be classed as aNonbenzodiazepine.

References

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  1. ^https://documents.tocris /pdfs/tocris_coa/3941_1_coa.pdf?1706728634
  2. ^"TCS 1205 | CAS 355022-97-8 | AbMole BioScience | TCS 1205 Price".
  3. ^Taliani, Sabrina; Cosimelli, Barbara; Da Settimo, Federico; Marini, Anna Maria; La Motta, Concettina; Simorini, Francesca; Salerno, Silvia; Novellino, Ettore; Greco, Giovanni; Cosconati, Sandro; Marinelli, Luciana; Salvetti, Francesca; L’Abbate, Gianluca; Trasciatti, Silvia; Montali, Marina; Costa, Barbara; Martini, Claudia (25 June 2009). "Identification of Anxiolytic/Nonsedative Agents among Indol-3-ylglyoxylamides Acting as Functionally Selective Agonists at the γ-Aminobutyric Acid-A (GABA A ) α 2 Benzodiazepine Receptor".Journal of Medicinal Chemistry.52(12): 3723–3734.doi:10.1021/jm9001154.