1. GPCR/G Protein Neuronal Signaling
  2. 5-HT Receptor Serotonin Transporter
  3. Zimelidine

Zimelidine is a potent and selective inhibitor of serotonin 5-HT uptake and SERT.

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Zimelidine Chemical Structure

Zimelidine Chemical Structure

CAS No. : 56775-88-3

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Description

Zimelidine is a potent and selective inhibitor of serotonin 5-HT uptake and SERT. Zimelidine is an antidepressant[1][2][3][4]. In Vivo: Zimelidine (15 mg/kg, IP, once) reduces the development of tolerance to morphine-induced antinociception in rats[3].
Zimelidine (5 mg/kg, IP, daily for 14 days) dose not modify the responsiveness of CA3 hippocampal pyramidal neurons to microiontophoreticahy applied 5-HT[2].
Zimelidine (0.2, 2 and 20 nmol/100 nL) in medial amygdaloid nucleus (MeA) evokes dose dependent hypophagic effects in fasted rats[4].

In Vivo
Animal Model: Male Wistar albino rats (160-180 g, n=72)[3]
Dosage: 15 mg/kg
Administration: IP, once
Result: Significantly attenuated the development and expression of morphine tolerance. The maximal antinociceptive effect of Zimelidine was obtained at the 60 minutes measurements in the zimelidine group and at the 30 minutes measurements in the morphine tolerant group by the tail-flick and hot-plate tests. Administration of zimelidine with morphine showed additive analgesic effect.
Animal Model: Sprague-Dawley rats (150 to 250 g, Ten, male)[2]
Dosage: 5 mg/kg
Administration: IP, daily for 14 days
Result: Did not modify the responsiveness of CA3 hippocampal pyramidal neurons to microiontophoreticahy applied 5-HT.
Molecular Weight

317.22

Formula

C16H17BrN2

CAS No.
SMILES

CN(C/C=C(C1=CC=CN=C1)/C2=CC=C(C=C2)Br)C

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  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Zimelidine
Cat. No.:
HY-118835
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