Zuclopenthixol

• Description:

  Zuclopenthixol ((Z) -Clopenthixol) is a thioxanthene derivative which acts as a mixed dopamine D1/D2 receptor antagonist[1][2].

• Product Name Alternative:

  (Z) -Clopenthixol

• UNSPSC:

  12352005

• Hazard Statement:

  H315, H319, H320

• Target:

  Dopamine Receptor

• Type:

  Reference compound

• Related Pathways:

  GPCR/G Protein; Neuronal Signaling

• Applications:

  Neuroscience-Neuromodulation

• Field of Research:

  Neurological Disease

• Assay Protocol:

  https://www.medchemexpress.com/Zuclopenthixol.html

• Purity:

  98.08

• Solubility:

  DMSO : 200 mg/mL (ultrasonic)

• Smiles:

  OCCN1CCN(CC/C=C2C3=C(SC4=C\2C=CC=C4)C=CC(Cl)=C3)CC1

• Molecular Formula:

  C22H25ClN2OS

• Molecular Weight:

  400.96

• Precautions:

  H315, H319, H320

• References & Citations:

  [1]Manzaneque JM, et al. An ethopharmacological assessment of the effects of zuclopenthixol on agonistic interactions in male mice. Methods Find Exp Clin Pharmacol. 1999 Jan-Feb;21 (1) :11-5.|[2]Khalifa AE, et al. Pro-oxidant activity of zuclopenthixol in vivo: differential effect of the drug on brain oxidative status of scopolamine-treated rats. Hum Exp Toxicol. 2004 Aug;23 (9) :439-45.

• Shipping Conditions:

  Room Temperature

• Storage Conditions:

  -20°C, 3 years; 4°C, 2 years (Powder)

• Scientific Category:

  Reference compound1

• Clinical Information:

  Launched

• Isoform:

  D2 Receptor

• CAS Number:

  [53772-83-1]