Informational only. Not medical advice.INFORMATIONAL PLATFORM ONLY — NOT MEDICAL ADVICE, DIAGNOSIS, OR TREATMENT
(S)-CE-123 is a non-peptide small molecule belonging to the diphenylmethyl-sulfinyl-thiazole chemotype, structurally related to modafinil. It acts as an atypical, non-releasing dopamine transporter (DAT) inhibitor—blocking dopamine reuptake without triggering amphetamine-like transporter-mediated release. No human clinical data exist; all pharmacology, behavioral, and pharmacokinetic findings are preclinical (rodent in vivo and human-liver-microsome/HEK293-cell in vitro). The compound is not individually named on WADA's current Prohibited List, though modafinil (the parent compound) is a named S6 stimulant; no authoritative WADA ruling specific to CE-123 was found.
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No prices found for (S)-CE-123.
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Kimera Chems has the lowest single-vial (S)-CE-123 price at $0.018/mg among 2 COA-verified vendors on Disclosed Labs. Bulk or multi-vial deals may be lower.
What is the price range for (S)-CE-123?
Research-grade (S)-CE-123 is listed at $0.018/mg from 1 verified source on Disclosed Labs.
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No human data exist for (S)-CE-123. No registered ClinicalTrials.gov trials or DrugBank entries were found, and the primary source explicitly states that no human data are available. All pharmacology and behavioral data are preclinical. In rats, (S)-CE-123 at 24.0 mg/kg i.p. partially reversed tetrabenazine-induced deficits in effort-based lever pressing, increased progressive-ratio responding, and raised extracellular dopamine in the nucleus accumbens core. At 0.3–1.0 mg/kg i.p., CE-123 improved extra-dimensional set-shifting in an attentional task without the impulsivity-increasing effects observed with R-modafinil at 10 mg/kg. Daily dosing improved spatial memory acquisition and retrieval in a hole-board task and ameliorated maternal-separation-induced spatial learning deficits in adolescent rats, with sex-dependent effects. Pharmacokinetic studies in rats and human liver microsomes show that S-CE-123 achieves ~5-fold greater unbound brain penetration (Kp,uu,brain = 0.5) than R-modafinil but is metabolized 9.3-fold faster in human liver microsomes (t₁/₂ 39 min vs. 364 min).
This platform provides informational tools only, not medical advice.
The Novel Atypical Dopamine Uptake Inhibitor (S)-CE-123 Partially Reverses the Effort-Related Effects of the Dopamine Depleting Agent Tetrabenazine and Increases Progressive Ratio Responding
2019
A Novel Dopamine Transporter Inhibitor CE-123 Improves Cognitive Flexibility and Maintains Impulsivity in Healthy Male Rats
2017
A daily single dose of a novel modafinil analogue CE-123 improves memory acquisition and memory retrieval
Prices verified as of July 2026. Actual prices may vary. For research use only.
2018