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ChemicalBook--->CAS DataBase List--->2369979-68-8

2369979-68-8

2369979-68-8 Structure

2369979-68-8 Structure
IdentificationBack Directory
[Name]

5H-Dibenzo[b,e][1,4]diazepine, 8-chloro-11-(4-ethyl-1-piperazinyl)-4-fluoro-
[CAS]

2369979-68-8
[Synonyms]

8-chloro-11-(4-ethyl-1-piperazinyl)-4-fluoro-5H-Dibenzo[b,e][1,4]diazepine
5H-Dibenzo[b,e][1,4]diazepine, 8-chloro-11-(4-ethyl-1-piperazinyl)-4-fluoro-
[Molecular Formula]

C19H20ClFN4
[MDL Number]

MFCD34167517
[MOL File]

2369979-68-8.mol
[Molecular Weight]

358.84
Chemical PropertiesBack Directory
[Boiling point ]

493.0±55.0 °C(Predicted)
[density ]

1.34±0.1 g/cm3(Predicted)
[storage temp. ]

Store at RT
[solubility ]

DMSO|17.94|50|
[form ]

solid
[pka]

7.63±0.10(Predicted)
[color ]

Yellow
Hazard InformationBack Directory
[Uses]

JHU37160 is a potent and brain-penetrant DREADD agonist, with EC50s of 18.5?nM and 0.2?nM for hM3Dq and hM4Di DREADDs in HEK-293 cells, respectively. JHU37160 exhibits selective [3H]Clozapine displacement from DREADDs and not from other Clozapine-binding sites in mice brain tissue[1].
[Biological Activity]

JHU37160 (J60) is a potent DREADDs (Designer Receptors Exclusively Activated by Designer Drugs) ligand (hM3Dq/hM4Di Ki = 1.9/3.6 nM using mouse brain tissue18.5/0.2 nM by celluar BRET assays) with ~25-fold improved affinity than C21 and high in vivo potency for CNS applications. J60 selectively competes against clozapine at DREADDsbut not other clozapine-binding sites in mouse brain tissue ex vivo (10 nM)increases hM3Dq-stimulated locomotion in TH-hM3Dq rats (0.01-0.3 mg/kg i.p.) and selectively inhibits locomotor activity of D1-hM3Dq and D1-hM4Di transgenicbut not wild-typemice (0.01-1 mg/kg i.p.).
[in vivo]

JHU37160 (0.1 mg/kg; i.p.) exhibits high DREADD occupancy in mice and rats[1].
JHU37160 (0.01-1 mg/kg; i.p.) selectively inhibits locomotor activity in D1-hM3Dq and D1-hM4Di mice without any significant locomotor effects observed in WT mice[1].

[IC 50]

mAChR3; mAChR4
[storage]

Room temperature
[References]

[1] Bonaventura J, et, al. High-potency ligands for DREADD imaging and activation in rodents and monkeys. Nat Commun. 2019 Oct 11;10(1):4627. DOI:10.1038/s41467-019-12236-z
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