Name | Epinastine hydrochloride |
Synonyms | Elestat Alesion WAL-801CL EPINASTIN HCL Epinastin Hcl EPINASTINE HCL Epinastine hcl Epinastine hydrochloride Epinastine Hydrochloride f)imidazo(1,5-a)azepin-3-amine,9,13b-dihydro-ih-dibenz(hydrochloride 9,13b-Dihydro-1H-Dibenz[c,f]imidazo[1,5-α]azepin-3-amine Hydrochloride 3-Amino-9,13b-Dihydro-1h-Dibenz[C,F]Imidazo[1,5-A]Azepine Hydrochloride 3-AMINO-9,13B-DIHYDRO-1H-DIBENZ[C,F]IMIDAZO[1,5-A]AZEPINE HYDROCHLORIDE |
CAS | 108929-04-0 80012-44-8 |
EINECS | 629-843-8 |
InChI | InChI=1/C16H15N3.ClH/c17-16-18-10-15-13-7-3-1-5-11(13)9-12-6-2-4-8-14(12)19(15)16;/h1-8,15H,9-10H2,(H2,17,18);1H |
InChIKey | VKXSGUIOOQPGAF-UHFFFAOYSA-N |
Molecular Formula | C16H16ClN3 |
Molar Mass | 285.77 |
Melting Point | 273-275°C |
Boling Point | 428°C at 760 mmHg |
Flash Point | 212.7°C |
Solubility | H2O: soluble38mg/mL |
Vapor Presure | 1.56E-07mmHg at 25°C |
Appearance | solid |
Color | white |
Storage Condition | 2-8°C |
MDL | MFCD00933434 |
In vitro study | In the guinea pig ileum, receptor binding studies showed that Epinastine has a high affinity for H1-receptors. At low concentrations, Epinastine was able to displace specific [Epinastine inhibited the release of histamine from rat peritoneal mast cells elicited by the antigen-antibody reaction and Compound 48/80 in Locust neural tissue. Epinastine was similarly effective in inhibiting Compound 48/80-induced histamine release from isolated rat peritoneal mast cells, or rat septal membranes. Epinastin not only can effectively inhibit Ca Epinastine show time-and dose-dependent inhibitory effect on IL-8, IL-8 is one of the Eosinophil chemotactic factors released by eosinophils isolated from allergic diseases. |
In vivo study | Epinastine inhibits histamine-induced skin or lung responses in rats, dogs, and guinea pigs. |
Hazard Symbols | T - Toxic |
Risk Codes | 25 - Toxic if swallowed |
Safety Description | 45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.) |
UN IDs | UN 2811 6.1/PG 3 |
WGK Germany | 3 |
RTECS | HO4360000 |
HS Code | 2933992600 |
Toxicity | LD50 in male, female rats (mg/kg): 314, 192 orally; 17, 22 i.v. (Nishikawa) |