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Trimipramine (maleate)

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    Trimipramine (maleate)
  • Trimipramine (maleate)
Cat No: 15921
Biochemicals - Receptor Pharmacology
Cayman

Trimipramine is a tricyclic antidepressant.{25914,40358,30236} It selectively binds the serotonin (5-HT) transporter (SERT) over the norepinephrine transporter (NET) and dopamine transporter (DAT; Kds = 149, 2,450, and 3,780 nM, respectively) and acts...

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Territorial Availability: Available through Bertin Technologies only in France
Synonyms:
  • 10,11-dihydro-N,N,?-trimethyl-5H-dibenz[b,f]azepine-5-propanamine, (2Z)-2-butenedioate
Correlated keywords:
  • 739-71-9 117848-?51-?8 138145-?72-?9 1202867-?12-?6 Surmontil anti-depressant 5HT
Product Overview:
Trimipramine is a tricyclic antidepressant.{25914,40358,30236} It selectively binds the serotonin (5-HT) transporter (SERT) over the norepinephrine transporter (NET) and dopamine transporter (DAT; Kds = 149, 2,450, and 3,780 nM, respectively) and acts as a histamine H1 receptor antagonist (Ki = 0.02 µM) that is selective for histamine H1 over H2, H3, and H4 receptors (Kis = 0.04, >100, and 43.6 µM, respectively).{25914,40358} Trimipramine binds to muscarinic acetylcholine and α1- and α2-adrenergic receptors (Kds = 58, 24, and 580 nM, respectively), as well as dopamine D1 and D2 receptors and 5-HT receptor subtypes 5-HT1C and 5-HT2 (Kis = 346.7, 57.5, 537, and 19.5 nM, respectively).{25914,30236} It reduces immobility time in the forced swim test in rats when administered at a dose of 10 mg/kg.{59740} Formulations containing trimipramine have previously been used in the treatment of depression.
Size 1 g
Shipping dry ice
CAS Number 521-78-8
Molecular Formula C20H26N2 • C4H4O4
SMILES CN(C)CC(C)CN1C2=C(C=CC=C2)CCC3=C1C=CC=C3.OC(/C=C\C(O)=O)=O
Molecular Weight 410,5
Formulation A crystalline solid
Purity ≥95%
Custom Code 2933.49
UNSPSC code 12352300

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Our scientists are experts in the synthesis, purification, and characterization of biochemicals ranging from small drug-like heterocycles to complex biolipids, fatty acids, and many others. We are also highly skilled in all aspects of assay and antibody development, protein expression, crystallization, and structure determination.

Over the past thirty years, Cayman developed a deep knowledge base in lipid biochemistry, including research involving the arachidonic acid cascade, inositol phosphates, and cannabinoids. This knowledge enabled the production of reagents of exceptional quality for cancer, oxidative injury, epigenetics, neuroscience, inflammation, metabolism, and many additional lines of research.

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