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escitalopram + RT2CK17
- Development stage
- Unknown
- Lead developer
- Laureate Institute for Brain Research
- Modality
- Small Molecules
- Administration
- Oral
01
Overview
Escitalopram + RT2CK17 appears to be a combination drug consisting of escitalopram and an agent designated as RT2CK17. Escitalopram is a selective serotonin reuptake inhibitor (SSRI) used primarily for the treatment of major depressive disorder and generalized anxiety disorder. It works by selectively inhibiting the reuptake of serotonin in the central nervous system, thereby increasing serotonergic activity[6][7][8]. The mechanism of action for RT2CK17 is not established in available literature or databases as of June 2025; no information about its pharmacology or clinical use could be found. Therefore, this combination may represent an investigational product or a non-standard formulation.
- Brand names
- Lexapro
- Other names
- escitalopramS-citalopram(S)-citalopramescitalopramumS(+)-citalopram
02
Targets
mAChR (Muscarinic acetylcholine receptors)HTR2A (Serotonin receptor 5-HT2A)ADRA1A (α1A)DRD2 (Dopamine D2 Receptor)SERT (Sodium-dependent serotonin transporter)KCNH2 (Voltage-gated potassium channel subfamily H member 2)HTR2C (5-hydroxytryptamine 2C receptor)HRH1 (Histamine H1 Receptor)DAT (Dopamine plasma membrane transport protein)NET (Norepinephrine Transporter)HTR1A (Serotonin receptor 1A (5-hydroxytryptamine receptor 1A))
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