
Thiethylperazine dimaleate
CAS No. 1179-69-7
Thiethylperazine dimaleate( Toresten | Norzine | Thiethylperazine maleate )
Catalog No. M26844 CAS No. 1179-69-7
Thiethylperazine dimaleate is an antagonist of the D2 receptor and H1 receptor.
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
5MG | 72 | Get Quote |
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10MG | 110 | Get Quote |
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25MG | 200 | Get Quote |
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50MG | 335 | Get Quote |
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100MG | 515 | Get Quote |
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500MG | 1071 | Get Quote |
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1G | Get Quote | Get Quote |
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Biological Information
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Product NameThiethylperazine dimaleate
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NoteResearch use only, not for human use.
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Brief DescriptionThiethylperazine dimaleate is an antagonist of the D2 receptor and H1 receptor.
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DescriptionThiethylperazine dimaleate is an antagonist of the D2 receptor and H1 receptor. Thiethylperazine dimaleate is an activator of ABCC1 and possesses antimicrobial, anti-emetic, and antipsychotic effects.(In Vitro):Thiethylperazine dimaleate dimaleate is an antagonist of the D2 receptor and H1 receptor. Thiethylperazine dimaleate dimaleate is an activator of ABCC1 and possesses antimicrobial, anti-emetic, and antipsychotic effects.(In Vivo):In APP/PS1 mice, Thiethylperazine dimaleate (3 mg/kg; intramuscular injection) causes a significant reduction of Aβ42 levels.
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In VitroThiethylperazine could enhance the antibiotic (Vancomycin) activity at a concentration as low as 2 μg/mL. Thiethylperazine inhibits Vancomycin-sensitive E. faecalis ATCC 29212, Vancomycin-resistant E. faecalis ATCC 51299 and vancomycin-resistant E. faecalis (VREF) isolates with MIC values of 8 μg/mL, 16 μg/mL and 8 μg/mL, respectively.
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In VivoThiethylperazine (3 mg/kg; intramuscular injection; twice daily; for 30 days; young APP/PS1 mice) treatment significantly reduces Aβ42 levels in APP/PS1 mice. Animal Model:Young Aβ precursor protein (APPswe) and mutant presenilin-1 (PS1) (APP/PS1) mice Dosage:3 mg/kg Administration:Intramuscular injection; twice daily; for 30 days Result:Significantly reduced Aβ42 levels in APP/PS1 mice.
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SynonymsToresten | Norzine | Thiethylperazine maleate
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PathwayGPCR/G Protein
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TargetDopamine Receptor
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Recptor——
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Research Area——
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Indication——
Chemical Information
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CAS Number1179-69-7
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Formula Weight631.76
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Molecular FormulaC30H37N3O8S2
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 125 mg/mL (197.86 mM)
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SMILESOC(=O)\C=C/C(O)=O.OC(=O)\C=C/C(O)=O.CCSc1ccc2Sc3ccccc3N(CCCN3CCN(C)CC3)c2c1
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Otsuka M, et al. Reduction of bleomycin induced lung fibrosis by candesartan cilexetil, an angiotensin II type 1 receptor antagonist. Thorax. 2004 Jan;59(1):31-8.
molnova catalog



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