LY 393558

Modify Date: 2025-09-13 14:13:36

LY 393558 Structure
LY 393558 structure
Common Name LY 393558
CAS Number 271780-64-4 Molecular Weight 546.67700
Density N/A Boiling Point N/A
Molecular Formula C26H31FN4O4S2 Melting Point N/A
MSDS N/A Flash Point N/A

 Use of LY 393558


LY393558 is a potent and orally active inhibitor of the 5-HT transporter and an antagonist of 5-HT1B and 5-HT1D receptors. LY393558 increase the extracellular levels of 5-HT in mice model frontal cortex. LY393558 can be used for researching depression[1].

 Names

Name 1-[2-[4-(6-fluoro-1H-indol-3-yl)-3,6-dihydro-2H-pyridin-1-yl]ethyl]-6-methylsulfonyl-3-propan-2-yl-4H-2λ6,1,3-benzothiadiazine 2,2-dioxide

 LY 393558 Biological Activity

Description LY393558 is a potent and orally active inhibitor of the 5-HT transporter and an antagonist of 5-HT1B and 5-HT1D receptors. LY393558 increase the extracellular levels of 5-HT in mice model frontal cortex. LY393558 can be used for researching depression[1].
Related Catalog
In Vivo LY393558 (1-20 mg/kg; p.o., single) raises extracellular levels of 5-HT to 200-250% at 1 mg/kg in guinea pigs model, while levels of 5-HT to approximately 1500% at the highest dose 20 mg/kg[1]. LY393558 (20 mg/kg; p.o., single) completely abolishes the reduction of levels of 5-HT induced by tetrodotoxin (1μM) in guinea pigs model[1]. LY393558 (1-20 mg/kg; p.o., single) significantly increases extracellular levels of 5-HT in rats model[1]. LY393558 (5 mg/kg/day; p.o., 21 days) can still elicit a further increase in extracellular 5-HT in chronic treatment[1]. Animal Model: Female Dunkin Hartley guinea pigs (350-400 g)[1] Dosage: 1-20 mg/kg Administration: p.o., single Result: Extracellular levels of 5-HT reached 200-250% at 1 mg/kg, while levels of 5-HT reached approximately 1500% at the highest dose 20 mg/kg. Animal Model: Female Dunkin Hartley guinea pigs (350-400 g)[1] Dosage: 20 mg/kg Administration: p.o., single Result: Completely abolished the reduction of levels of 5-HT induced by tetrodotoxin (1μM). Animal Model: Male Lister Hooded rats (290-320 g)[1] Dosage: 1-20 mg/kg Administration: p.o., single Result: Significantly increased extracellular levels of 5-HT. Animal Model: Male Lister Hooded rats (290-320 g)[1] Dosage: 5 mg/kg/day Administration: p.o., 21 days Result: Still elicited a further increase in extracellular 5-HT in chronic treatment.
References

[1]. Mitchell SN, et al. LY393558, a 5-hydroxytryptamine reuptake inhibitor and 5-HT(1B/1D) receptor antagonist: effects on extracellular levels of 5-hydroxytryptamine in the guinea pig and rat. Eur J Pharmacol. 2001;432(1):19-27.

 Chemical & Physical Properties

Molecular Formula C26H31FN4O4S2
Molecular Weight 546.67700
Exact Mass 546.17700
PSA 110.55000
LogP 5.87740
InChIKey QUSLYAPLTMMCFE-UHFFFAOYSA-N
SMILES CC(C)N1Cc2cc(S(C)(=O)=O)ccc2N(CCN2CC=C(c3c[nH]c4cc(F)ccc34)CC2)S1(=O)=O
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