T123

Thioperamide maleate salt

≥98% (HPLC), histamine H3 receptor antagonist, solid

• Synonym(s): MR-12842, N-Cyclohexyl-4-(1H-imidazol-4-yl)-1-piperidinecarbothioamide maleate salt
• Empirical Formula (Hill Notation): C₁₅H₂₄N₄S · C₄H₄O₄
• CAS Number: 148440-81-7
• Molecular Weight: 408.52
• UNSPSC Code: 12352200
• PubChem Substance ID: 24277809
• NACRES: NA.77
• MDL number: MFCD00083209
• Assay: ≥98% (HPLC)
• Form: solid
• Storage condition: desiccated, under inert gas

Properties

• Product Name: Thioperamide maleate salt, solid
• assay: ≥98% (HPLC)
• Quality Segment: 200
• form: solid
• storage condition: desiccated, under inert gas
• color: white
• solubility: H₂O: >10 mg/mL, DMSO: 12 mg/mL, ethanol: 3 mg/mL
• SMILES string: OC(=O)\C=C/C(O)=O.S=C(CC1CCCCC1)N2CCC(CC2)c3c[nH]cn3
• InChI: 1S/C16H25N3S.C4H4O4/c20-16(10-13-4-2-1-3-5-13)19-8-6-14(7-9-19)15-11-17-12-18-15;5-3(6)1-2-4(7)8/h11-14H,1-10H2,(H,17,18);1-2H,(H,5,6)(H,7,8)/b;2-1-
• InChI key: REZRBLGMJZZSID-BTJKTKAUSA-N
• Gene Information: human ... HRH3(11255)

Description

Application

Thioperamide maleate salt was used to study the sympathetic[1] and autonomic[2] nerve activity in mammalian white adipose tissue.

Biochem/physiol Actions

Potent and selective H₃ histamine receptor antagonist that crosses the blood-brain barrier.

Thioperamide is a potent and selective H₃ histamine receptor antagonist that crosses the blood-brain barrier. It affects the central histaminergic system and decreases the duration of seizures and convulsions in mice.[3] It also improves learning deficit induced by other drugs such as scopolamine.[4]

Features and Benefits

This compound is featured on the Histamine Receptors page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.

Safety Information

• Storage Class: 11 - Combustible Solids
• wgk: WGK 3
• flash_point_f: Not applicable
• flash_point_c: Not applicable
• ppe: dust mask type N95 (US), Eyeshields, Gloves