SEP-363856 HCl
- Product Name
- SEP-363856 HCl
- CAS No.
- 1310422-41-3
- Chemical Name
- SEP-363856 HCl
- Synonyms
- SEP-363856 HCl;SEP-856 hydrochloride;SEP-363856 hydrochloride;SEP-363856 HCl (Ulotaront);SEP-363856 (SEP-856) hydrochloride;SEP-363856 hydrochloride, 10 mM in DMSO;1-[(7S)-5,7-dihydro-4H-thieno[2,3-c]pyran-7-yl]-N-methylmethanamine;Inhibitor,SEP 856,SEP856,SEP363856,SEP 363856 hydrochloride,5-hydroxytryptamine Receptor,inhibit,Serotonin Receptor,SEP363856 hydrochloride,SEP-363856,SEP 363856,SEP-856,5-HT Receptor
- CBNumber
- CB26199351
- Molecular Formula
- C9H14ClNOS
- Formula Weight
- 219.73
- MOL File
- 1310422-41-3.mol
SEP-363856 HCl Property
- solubility
- DMSO:60.0(Max Conc. mg/mL);273.06(Max Conc. mM)
- form
- Solid
- color
- White to off-white
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H302Harmful if swallowed
H319Causes serious eye irritation
H336May cause drowsiness or dizziness
H373May cause damage to organs through prolonged or repeated exposure
- Precautionary statements
-
P260Do not breathe dust/fume/gas/mist/vapours/spray.
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
P264Wash hands thoroughly after handling.
P264Wash skin thouroughly after handling.
P270Do not eat, drink or smoke when using this product.
P271Use only outdoors or in a well-ventilated area.
P280Wear protective gloves/protective clothing/eye protection/face protection.
P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.
P304+P340IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
P312Call a POISON CENTER or doctor/physician if you feel unwell.
P314Get medical advice/attention if you feel unwell.
P330Rinse mouth.
P403+P233Store in a well-ventilated place. Keep container tightly closed.
P405Store locked up.
P501Dispose of contents/container to..…
N-Bromosuccinimide Price
- Product number
- CS-0119592
- Product name
- SEP-363856(hydrochloride)
- Purity
- 99.78%
- Packaging
- 5mg
- Price
- $300
- Updated
- 2021/12/16
- Product number
- CS-0119592
- Product name
- SEP-363856(hydrochloride)
- Purity
- 99.78%
- Packaging
- 10mg
- Price
- $500
- Updated
- 2021/12/16
- Product number
- CS-0119592
- Product name
- SEP-363856(hydrochloride)
- Purity
- 99.78%
- Packaging
- 50mg
- Price
- $1250
- Updated
- 2021/12/16
- Product number
- CS-0119592
- Product name
- SEP-363856(hydrochloride)
- Purity
- 99.78%
- Packaging
- 100mg
- Price
- $1800
- Updated
- 2021/12/16
- Product number
- 027606
- Product name
- SEP-363856(hydrochloride)
- Packaging
- 001
- Price
- $750
- Updated
- 2021/12/16
SEP-363856 HCl Chemical Properties,Usage,Production
Uses
SEP-363856 (SEP-856) hydrochloride, an orally active TAAR1 and 5-HT1A agonist and CNS active psychotropic agent with a unique, non-D2/5-HT2A mechanism of action, exerts its antipsychotic-like effects. SEP-363856 hydrochloride has the potential for the study of schizophrenia[1].
in vivo
SEP-856 (0.3, 1 and 10 mg/kg, i.p.) hydrochloride is CNS active and exhibits a behavioral signature similar to known antipsychotic drugs[1].
SEP-856 (0.3, 1 and 10 mg/kg, orally once) hydrochloride significantly reduces PCP-induced hyperactivity[1].
Oral SEP-856 hydrochloride administration (1, 3 and 10 mg/kg) produces a dosedependent decrease in REM sleep, increase in latency to REM sleep and increase in cumulative wake (W) time[1].
| Animal Model: | Acute treatment with phencyclidine (PCP), which induces robust hyperactivity in rodents[1]. |
| Dosage: | 0.3, 1 and 3 mg/kg. |
| Administration: | Orally once. |
| Result: | Resulted in a dose-dependent inhibition of PCP-induced hyperactivity responses in C57Bl/6J mice (1-way ANOVA F (5, 59) = 18.96, p < 0.0001; Tukey’s post-hoc test, p < 0.05) with a 50% effective dose (ED50) of approximately 0.3 mg/kg. |
| Animal Model: | Male Sprague Dawley rats[1]. |
| Dosage: | 1, 2, and 5 mg/kg. |
| Administration: | I.V. injection. (Pharmacokinetic Analysis). |
| Result: | Rapidly absorbed with maximum plasma and brain concentrations reached within 0.25 to 0.5 hours in mice and rats and maximum plasma concentrations reached within 6 ± 2.83 hours in monkeys. Penetrated mouse and rat brains after oral administration (10 mg/kg), with average brain-to-plasma AUC ratios of ~3 respectively. |
IC 50
TAAR1: 0.140 μM (EC50); 5-HT1A Receptor: 2.3 μM (EC50); 5-HT1B Receptor: 15.6 μM (EC50); 5-HT1D Receptor: 0.262 μM (EC50); 5-HT2A Receptor: >10 μM (EC50); 5-HT2C Receptor: 30 μM (EC50); 5-HT7 Receptor: 6.7 μM (EC50)
References
[1] Dedic N, et al. SEP-363856, a Novel Psychotropic Agent with a Unique, Non-D2 Receptor Mechanism of Action. J Pharmacol Exp Ther. 2019 Oct;371(1):1-14. DOI:10.1124/jpet.119.260281
SEP-363856 HCl Preparation Products And Raw materials
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