Fananserin
- Product Name
- Fananserin
- CAS No.
- 127625-29-0
- Chemical Name
- Fananserin
- Synonyms
- RP-62203;Fananserin;Fananserin, 10 mM in DMSO;2-[3-[4-(4-Fluorophenyl)piperazino]propyl]-2H-naphth[1,8-cd]isothiazole 1,1-dioxide;2-(3-(4-(4-fluorophenyl)piperazin-1-yl)propyl)-2H-naphtho[1,8-cd]isothiazole 1,1-dioxide;2-[3-[4-(4-Fluorophenyl)-1-piperazinyl]propyl]-2H-naphthyl[1,8-cd]isothiazole-1,1-dioxide;2H-Naphth[1,8-cd]isothiazole, 2-[3-[4-(4-fluorophenyl)-1-piperazinyl]propyl]-, 1,1-dioxide;Fananserin,Inhibitor,5-HT Receptor,inhibit,5-HT2,RP62203,RP-62203,dopamine,Dopamine Receptor,Serotonin Receptor,5-hydroxytryptamine Receptor
- CBNumber
- CB71073778
- Molecular Formula
- C23H24FN3O2S
- Formula Weight
- 425.52
- MOL File
- 127625-29-0.mol
Fananserin Property
- Melting point:
- 95-97 °C(Solv: acetonitrile (75-05-8))
- Boiling point:
- 641.1±65.0 °C(Predicted)
- Density
- 1.331±0.06 g/cm3(Predicted)
- storage temp.
- Store at RT
- solubility
- Soluble to 100 mM in DMSO
- form
- Powder
- pka
- 7.31±0.10(Predicted)
N-Bromosuccinimide Price
- Product number
- 2645
- Product name
- Fananserin
- Purity
- ≥99%(HPLC)
- Packaging
- 10
- Price
- $155
- Updated
- 2021/12/16
- Product number
- 2645
- Product name
- Fananserin
- Purity
- ≥99%(HPLC)
- Packaging
- 50
- Price
- $558
- Updated
- 2021/12/16
- Product number
- 255281
- Product name
- Fananserin
- Packaging
- 10mg
- Price
- $403
- Updated
- 2021/12/16
- Product number
- F102368
- Product name
- Fananserin
- Packaging
- 2.5mg
- Price
- $165
- Updated
- 2021/12/16
- Product number
- CS-0024310
- Product name
- Fananserin
- Purity
- 99.83%
- Packaging
- 5mg
- Price
- $188
- Updated
- 2021/12/16
Fananserin Chemical Properties,Usage,Production
Uses
Antipsychotic.
Uses
Fananserin is an antagonist of 5-HT2A.
Definition
ChEBI: LSM-2183 is a sulfonic acid derivative and a member of naphthalenes.
Biological Activity
5-HT 2A receptor antagonist that also displays high affinity at D 4 receptors (K i values are 0.26, 2.93, 25, 38, 70 and 726 nM for 5-HT 2A , D 4 , H 1 , α 1 , 5-HT 1A and D 2 receptors respectively). Inhibits inositol phosphate formation evoked by 5-HT in vitro (IC 50 = 7.76 nM) and antagonizes mescaline-induced head twitches in vivo .
in vivo
Fananserin displaces [125I]AMIK from 5-HT2 receptors with an IC50 of 0.21 nM in rat frontal cortex[2].
Fananserin shows moderate affinity for alpha 1-adrenoceptors in the rat thalamus (IC50 = 14 nM) and for histamine H1 receptors in the guinea-pig cerebellum (IC50 = 13 nM)[2].
Fananserin (0.5-4 mg/kg; p.o.) increases the duration of deep nonrapid eye movement (NREM) sleep at the expense of wakefulness in a dose-dependent manner[3].
| Animal Model: | Adult male Sprague Dawley rats (250-300 g)[3] |
| Dosage: | 0.5 mg/kg, 1 mg/kg,2 mg/kg, 4 mg/kg |
| Administration: | Oral administration |
| Result: | Increased the duration of deep nonrapid eye movement (NREM) sleep at the expense of wakefulness in a dose-dependent manner from 0.5 mg/kg. |
IC 50
5-HT2 Receptor: 0.37 nM (Ki); D4 Receptor: 2.93 nM (Ki)
Fananserin Preparation Products And Raw materials
Raw materials
Preparation Products
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