For research use only. Not for therapeutic Use.
5-HT<sub>1A</sub> receptor partial agonist (K<sub>i</sub> = 27 nM) that displays selectivity over 5-HT<sub>2</sub>, 5-HT<sub>1C</sub>, <span class=/’symbol/’>α</span><sub>1</sub>, <span class=/’symbol/’>α</span><sub>2</sub>, D<sub>1</sub> and D<sub>2</sub> receptors (K<sub>i</sub> values ranging from 1300 – 41000 nM). Inactive at 5-HT uptake sites, 5-HT<sub>1B</sub>, <span class=/’symbol/’>β</span>-adrenergic, muscarinic and benzodiazepine receptors. Displays anxiolytic activity.
| Catalog Number | I010279 |
| CAS Number | 99095-10-0 |
| Synonyms | Alternative Name: SM-3997 |
| Molecular Formula | C21H30ClN5O2 |
| Purity | ≥95% |
| Target | Neuronal Signaling |
| Solubility | Soluble to 100 mM in DMSO and to 100 mM in water |
| Storage | Store at +4C |
| InChI | InChI=1S/C21H29N5O2.ClH/c27-19-17-15-4-5-16(14-15)18(17)20(28)26(19)9-2-1-8-24-10-12-25(13-11-24)21-22-6-3-7-23-21;/h3,6-7,15-18H,1-2,4-5,8-14H2;1H/t15-,16+,17+,18-; |
| InChIKey | ACVFJYKNBOHIMH-DPFKZJTMSA-N |
| SMILES | C1CC2CC1C3C2C(=O)N(C3=O)CCCCN4CCN(CC4)C5=NC=CC=N5.Cl |
