GLPBio

Deschloroclozapine dihydrochloride

Catalog No.: GC74124Purity:>98.00%
Deschloroclozapine dihydrochloride is a high-affinity, selective, and metabolically stable muscarinic DREADD agonist. Deschloroclozapine dihydrochloride can rapidly cross the blood-brain barrier and effectively activate both excitatory hM3Dq and inhibitory hM4Di DREADD receptors.

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Deschloroclozapine dihydrochloride
10mM (in 1mL DMSO)In Stock
$56.00
1
1mgIn Stock
$17.00
1
5mgIn Stock
$48.00
1
10mgIn Stock
$77.00
1
25mgIn Stock
$124.00
1
50mgIn Stock
$175.00
1
100mgIn Stock
$263.00
1

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Description

Deschloroclozapine dihydrochloride is a high-affinity, selective, and metabolically stable muscarinic DREADD agonist. Deschloroclozapine dihydrochloride can rapidly cross the blood-brain barrier and effectively activate both excitatory hM3Dq and inhibitory hM4Di DREADD receptors[1-2]. Deschloroclozapine dihydrochloride is primarily used in neuroscience for chemogenetic research to precisely modulate neuronal activity[3-4].

In vivo, In transgenic neuropathic pain model rats expressing hM3Dq, subcutaneous injection of Deschloroclozapine dihydrochloride (0.1mg/kg) for 120 minutes significantly increased serum OXT levels and rapidly raised the rats' mechanical pain threshold[5]. In transgenic mice expressing hM3Dq, intraperitoneal administration of Deschloroclozapine dihydrochloride (1mg/kg) for 5–10 minutes rapidly enhanced neuronal activity via hM3Dq, with an efficacy more than 2.5 times greater than that of Clozapine N-oxide (CNO; 100μg/kg), and brain concentrations of Deschloroclozapine dihydrochloride reached approximately 100 nM at 30 minutes[6].

References:
[1] Maggs JL, Williams D, Pirmohamed M, et al. The metabolic formation of reactive intermediates from clozapine, a drug associated with agranulocytosis in man. J Pharmacol Exp Ther. 1995 Dec;275(3):1463-75.
[2] Zhang S, Gumpper RH, Huang XP, et al. Molecular basis for selective activation of DREADD-based chemogenetics. Nature. 2022 Dec;612(7939):354-362.
[3] Nentwig TB, Obray JD, Vaughan DT, et al. Behavioral and slice electrophysiological assessment of DREADD ligand, Deschloroclozapine dihydrochloride (DCZ) in rats. Sci Rep. 2022 Apr 21;12(1):6595.
[4] Hu F, Morris PJ, Bonaventura J, et al. 18F-labeled radiotracers for in vivo imaging of DREADD with positron emission tomography. Eur J Med Chem. 2021 Mar 5;213:113047.
[5] Nagai Y, Miyakawa N, Takuwa H, et al. Deschloroclozapine dihydrochloride, a potent and selective chemogenetic actuator enables rapid neuronal and behavioral modulations in mice and monkeys. Nat Neurosci. 2020 Sep;23(9):1157-1167.
[6] Shimizu M, Yoshimura M, Baba K, et al. Deschloroclozapine dihydrochloride exhibits an exquisite agonistic effect at lower concentration compared to clozapine-N-oxide in hM3Dq expressing chemogenetically modified rats. Front Neurosci. 2023 Nov 30;17:1301515.

Protocol

Animal experiment [1]:

Animal models

OXT-hM3Dq-mCherry transgenic rats (adult male).

Preparation Method

Rats were subcutaneously (s.c.) administered a single dose of Deschloroclozapine dihydrochloride (0.1mg/kg). Serum oxytocin (OXT) concentrations were measured at 0, 10, 30, 60, 120, and 180 minutes post-injection. Brain neuronal activity (Fos expression) was assessed 120 minutes post-injection. In a neuropathic pain model (Seltzer model), behavioral tests (von Frey test, Rat Grimace Scale, hot plate test) were conducted at 0, 10, 30, 60, 120, and 180 minutes post-Deschloroclozapine dihydrochloride administration.

Dosage form

0.1mg/kg; s.c.; Single injection.

Applications

Deschloroclozapine dihydrochloride administration induced a rapid and robust increase in serum OXT levels, Deschloroclozapine dihydrochloride significantly enhanced neuronal activation (Fos expression) in brain regions including the SON, PVN, and PAG comparable to a 10-fold higher dose of CNO, and produced rapid analgesic effects in a neuropathic pain model (significantly increasing mechanical nociceptive threshold and reducing pain scores within 10 minutes).

References:
[1] Shimizu M, Yoshimura M, Baba K, et al. Deschloroclozapine dihydrochloride exhibits an exquisite agonistic effect at lower concentration compared to clozapine-N-oxide in hM3Dq expressing chemogenetically modified rats. Front Neurosci. 2023 Nov 30;17:1301515.

Product Documents

Purity:>98.00%Appearance:A solid

Chemical Properties

Molecular Formula
C18H22Cl2N4
Molecular Weight
365.3
Solubility
H2O : 100 mg/mL (273.75 mM; Need ultrasonic); DMSO : 80 mg/mL (219.00 mM; ultrasonic and adjust pH to 7 with 1 M NaOH)
Storage
-20°C, sealed storage, away from moisture
General tips
Select a suitable solvent according to the product solubility data. Once prepared, aliquot the stock solution to avoid repeated freeze-thaw cycles.
Use stock solutions within 6 months when stored at -80°C or within 1 month when stored at -20°C.
To improve solubility, warm the tube to 37°C and sonicate it for an appropriate period.
Shipping Condition
Evaluation samples are shipped with blue ice. Other available sizes are shipped at room temperature or with blue ice upon request.

CalculatorsMolarity / Dilution / Molecular Weight / Unit Conversion / In Vivo Formulation / Solubility

g/mol

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