Basic information Safety Supplier Related

TC-2153

Basic information Safety Supplier Related

TC-2153 Basic information

Product Name:
TC-2153
Synonyms:
  • benzopentathiepin 8-(trifluoromethyl)-1,2,3,4,5-benzopentathiepin-6-amine hydrochloride
  • TC-2153
  • TC-2153 >=95% (HPLC)
  • TC-2153 hydrochloride
CAS:
1381769-23-8
MF:
C7H5ClF3NS5
MW:
355.87
Mol File:
1381769-23-8.mol
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TC-2153 Chemical Properties

storage temp. 
-20°C
solubility 
DMSO: 5mg/mL, clear
form 
powder
color 
white to beige
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Safety Information

WGK Germany 
WGK 3
Storage Class
11 - Combustible Solids
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TC-2153 Usage And Synthesis

Uses

TC-2153 is a selective inhibitor of striatal-enriched protein tyrosine phosphatase (STEP), with psychotropic activity and low acute toxicity. TC-2153 increases the expression of brain-derived neurotropic factor (BDNF) in the brain. And it decreases MAOA and 5-HT1A receptors mRNA level in midbrain. TC-2153 also inhibits 5-HT2A receptor-mediated signaling[1].

Biochem/physiol Actions

TC-2153 is a potent inhibitor of STEP (STriatal-Enriched protein tyrosine Phosphatase) that forms a reversible covalent bond with the catalytic cysteine in STEP. TC-2153 increases tyrosine phosphorylation of STEP substrates ERK1/2, Pyk2, and GluN2B in cell cultures. TC-2153 improves cognitive function in transgenic AD mice.

in vivo

Chronic TC-2153 treatment: TC-2153 (20 mg/kg; i.p.; once daily for 7 d) shows antidepressant-like effect without altering locomotor, exploratory activity and anxiety[1].
Acute TC-2153 treatment: TC-2153 (10 mg/kg and 20 mg/kg; p.o.; single dose) inhibits the functional activity of 5-HT2A receptors in vivo in mice[1].

Animal Model:SPF-state adult mouse males[1]
Dosage:10 mg/kg and 20 mg/kg; with or without 1 mg/kg DOI i.p. at 3 h after final treatment
Administration:Oral gavage or intraperitoneal injection; single dose or once daily for 7 d
Result:Showed antidepressant-like effect in the forced swim test without any adverse side effects on locomotor activity, anxiety, exploration, motor skill and obsessive-compulsive-like behavior.
Both acute and chronic methods inhibited the functional activity of 5-HT2A receptors.

IC 50

5-HT1A Receptor; 5-HT2A Receptor; MAO-A

References

[1] Walters JM, et al. Pharmacological inhibition of STriatal-Enriched protein tyrosine Phosphatase by TC-2153 reduces hippocampal excitability and seizure propensity. Epilepsia. 2022 May;63(5):1211-1224. DOI:10.1111/epi.17192

TC-2153Supplier

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