Cipralisant maleate
Modify Date: 2025-08-26 22:59:17
Cipralisant maleate structure
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Common Name | Cipralisant maleate | ||
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| CAS Number | 223420-20-0 | Molecular Weight | 332.39 | |
| Density | N/A | Boiling Point | 386.7ºC at 760 mmHg | |
| Molecular Formula | C18H24N2O4 | Melting Point | N/A | |
| MSDS | N/A | Flash Point | 188.5ºC | |
Use of Cipralisant maleateCipralisant (GT-2331) (maleate) is an orally active, low-toxicity, potent, selective, high affinity histamine H3 receptor full antagonist in vivo, and an agonist in vitro, with a pKi of 9.9 for histamine H3 receptor and a Ki of 0.47 nM for rat histamine H3 receptor. Cipralisant (maleate) has the potential for attention-deficit hyperactivity disorder research[1][2][3][4]. |
| Name | (Z)-but-2-enedioic acid,5-[(1R,2R)-2-(5,5-dimethylhex-1-ynyl)cyclopropyl]-1H-imidazole |
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| Synonym | More Synonyms |
| Description | Cipralisant (GT-2331) (maleate) is an orally active, low-toxicity, potent, selective, high affinity histamine H3 receptor full antagonist in vivo, and an agonist in vitro, with a pKi of 9.9 for histamine H3 receptor and a Ki of 0.47 nM for rat histamine H3 receptor. Cipralisant (maleate) has the potential for attention-deficit hyperactivity disorder research[1][2][3][4]. |
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| Related Catalog | |
| Target |
H3 receptor:9.9 (pKi) rat H3 receptor:0.47 nM (Ki) |
| In Vitro | Cipralisant (maleate) behaves as a full agonist on adenylyl cyclase inhibition. Cipralisant (maleate) (HEK cells) potently inhibits forskolin-induced cAMP accumulation, showing that Cipralisant (maleate) works as a potent full histamine H3 receptor agonist. Cipralisant (maleate) increases the basal [35S]GTPγS binding activities in membranes from HEK cells expressing the rat histamine H3 receptor (EC50, 5.6 nM)[3]. |
| In Vivo | Cipralisant (maleate) (0.3~30 mg/kg; s.c.) enhances acquisition over five trials, reaching significance at 1 mg/kg[2]. Cipralisant (maleate) (10 mg/kg; p.o.) completely blocks R-α-methylhistamine-induced drinking[3]. Cipralisant (maleate) promotes wakefulness in the rat. Cipralisant (maleate) potently and significantly improves performance in the repeated acquisition model, in line with its high affinity for the rat H3 receptor and good CNS penetration. Cipralisant (maleate) does not appear to be as efficacious as 3 mg/kg ciproxifan at its maximally effective dose [2]. Cipralisant (maleate) behaves as a partial agonist in a rat brain synaptosome model[3]. Animal Model: Male SHR pups (35–50 g)[2] Dosage: 0.3~30 mg/kg Administration: S.c. Result: Significantly enhanced performance of the SHR pups in a dose-related manner at 1 mg/kg. Animal Model: Male Sprague-Dawley rats[3] Dosage: 10 and 30 mg/kg Administration: P.o. Result: Achieved greater brain exposure and water intake was monitored for 60 min after administration. |
| References |
| Boiling Point | 386.7ºC at 760 mmHg |
|---|---|
| Molecular Formula | C18H24N2O4 |
| Molecular Weight | 332.39 |
| Flash Point | 188.5ºC |
| Exact Mass | 332.17400 |
| PSA | 103.28000 |
| LogP | 3.05470 |
| Vapour Pressure | 7.72E-06mmHg at 25°C |
| Cipralisant maleate |
| 4-(2-(5,5-dimethylhex-1-ynyl)cyclopropyl)imidazole maleate |
| Perceptin (TN) |
| Cipralisant maleate (USAN) |
| GT 2331 |
| Perceptin |
| cipralisant |
| UNII-7ENI812SZS |