For research use only. Not for therapeutic Use.
Talopram(CAT: I036977) is a potent and selective inhibitor of the presynaptic norepinephrine transporter (NET), making it a valuable tool for research on mood disorders, particularly depression and anxiety. By modulating norepinephrine reuptake, Talopram enhances neurotransmitter availability, offering insights into the mechanisms of antidepressant activity and catecholaminergic signaling. Its high specificity for NET over other monoamine transporters ensures precise experimental outcomes. Widely utilized in neuropharmacological studies, Talopram supports the investigation of therapeutic strategies targeting norepinephrine modulation in mood and stress-related disorders.
Catalog Number | I036977 |
CAS Number | 7182-51-6 |
Synonyms | Talopram; Phthalapromine; Talopramum; Talopran |
Molecular Formula | C20H25NO |
Purity | 98% |
Solubility | Soluble in DMSO |
Appearance | Solid powder |
Storage | Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years). |
IUPAC Name | N,3,3-Trimethyl-1-phenyl-1-phthalanpropylamin |
InChI | InChI=1S/C20H25NO/c1-19(2)17-12-7-8-13-18(17)20(22-19,14-9-15-21-3)16-10-5-4-6-11-16/h4-8,10-13,21H,9,14-15H2,1-3H3 |
InChIKey | LJBBMCNHIUJBDU-UHFFFAOYSA-N |
SMILES | CC1(C)OC(CCCNC)(C2=CC=CC=C2)C3=CC=CC=C13 |