MedKoo Cat#: 463180 | Name: Deschloroclozapine
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Description:

WARNING: This product is for research use only, not for human or veterinary use.

Deschloroclozapine is a high affinity and highly potent activator of muscarinic DREADDs. It is a derivative of clozapine, and exhibits 100-fold greater affinity for hM3Dq and hM4Di compared to clozapine N-oxide, and 50-fold greater affinity compared to DREADD agonist 21. Deschloroclozapine displays low 'off-target' receptor binding and rapid binding and activation of hM3Dq and hM4Di in mice and non-human primates. It also induces spatial memory deficits in non-human primates expressing hM4Di in the prefrontal cortex.

Chemical Structure

Deschloroclozapine
Deschloroclozapine
CAS#1977-07-7

Theoretical Analysis

MedKoo Cat#: 463180

Name: Deschloroclozapine

CAS#: 1977-07-7

Chemical Formula: C18H20N4

Exact Mass: 292.1688

Molecular Weight: 292.39

Elemental Analysis: C, 73.94; H, 6.89; N, 19.16

Price and Availability

Size Price Availability Quantity
200mg USD 550.00 2 Weeks
500mg USD 1,150.00 2 Weeks
1g USD 1,950.00 2 Weeks
2g USD 3,650.00 2 Weeks
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Related CAS #
Synonym
Deschloroclozapine; DCZ;
IUPAC/Chemical Name
11-(4-methylpiperazin-1-yl)-5H-dibenzo[b,e][1,4]diazepine
InChi Key
VQHITFFJBFOMBG-UHFFFAOYSA-N
InChi Code
InChI=1S/C18H20N4/c1-21-10-12-22(13-11-21)18-14-6-2-3-7-15(14)19-16-8-4-5-9-17(16)20-18/h2-9,19H,10-13H2,1H3
SMILES Code
CN1CCN(CC1)C2=NC3=C(NC4=CC=CC=C24)C=CC=C3
Appearance
Solid powder
Purity
>98% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Room Temperature
Solubility
Soluble in DMSO
Shelf Life
>3 years if stored properly
Drug Formulation
This drug may be formulated in DMSO
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.9001
More Info

Preparing Stock Solutions

The following data is based on the product molecular weight 292.39 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
1: Nagai Y, Miyakawa N, Takuwa H, Hori Y, Oyama K, Ji B, Takahashi M, Huang XP, Slocum ST, DiBerto JF, Xiong Y, Urushihata T, Hirabayashi T, Fujimoto A, Mimura K, English JG, Liu J, Inoue KI, Kumata K, Seki C, Ono M, Shimojo M, Zhang MR, Tomita Y, Nakahara J, Suhara T, Takada M, Higuchi M, Jin J, Roth BL, Minamimoto T. Deschloroclozapine, a potent and selective chemogenetic actuator enables rapid neuronal and behavioral modulations in mice and monkeys. Nat Neurosci. 2020 Sep;23(9):1157-1167. doi: 10.1038/s41593-020-0661-3. Epub 2020 Jul 6. PMID: 32632286. 2: Upright NA, Baxter MG. Effect of chemogenetic actuator drugs on prefrontal cortex-dependent working memory in nonhuman primates. Neuropsychopharmacology. 2020 Oct;45(11):1793-1798. doi: 10.1038/s41386-020-0660-9. Epub 2020 Mar 19. PMID: 32193513. 3: Zhang GO, McKay G, Hubbard JW, Midha KK. Application of electrospray mass spectrometry in the identification of intact glucuronide and suplate conjugates of clozapine in rat. Xenobiotica. 1996 May;26(5):541-50. doi: 10.3109/00498259609046730. PMID: 8736064. 4: Maggs JL, Williams D, Pirmohamed M, Park BK. 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. PMID: 8531117.