Name | N,N-dimethyl-2-[3-(1-pyridin-2-ylethyl)-1H-inden-2-yl]ethanamine |
---|---|
Synonyms |
Triten
Dimethpyrindene Dimetindeno N,N-dimethyl-3-[1-(2-pyridyl)ethyl]inden-2-ethylamine Dimetindene dimethyl-{2-[3-(1-pyridin-2-yl-ethyl)-inden-2-yl]-ethyl}-amine Pecofenil dimethindene Dimetindenum Foristal Fenistil Forhistal |
Description | Dimethindene is a potent, selective histamine H1 antagonist. Dimethindene impairs cutaneous wound healing (WH). Dimethindene can block K+ currents[1][2]. |
---|---|
Related Catalog | |
Target |
Human Endogenous Metabolite |
In Vitro | Dimethindene (5-500 μM; follicle-enclosed Xenopus oocytes) decreases Cromakalim cromakalim-induced K+ currents with an IC50 value of 29.5 μM[2]. |
In Vivo | Dimethindene (0.25 mg; i.p.; once; C57BL/6 mice with skin WH) impaires cutaneous wound healing (WH) and delays skin wound closure[1]. Animal Model: C57BL/6 mice with skin WH[1] Dosage: 0.25 mg Administration: intraperitoneal injection; once Result: Delayed skin wound closure as compared to vehicle treated mice. |
Density | 1.065 g/cm3 |
---|---|
Boiling Point | 416.3ºC at 760 mmHg |
Melting Point | 50 - 53 °C |
Molecular Formula | C20H24N2 |
Molecular Weight | 292.41800 |
Flash Point | 205.6ºC |
Exact Mass | 292.19400 |
PSA | 16.13000 |
LogP | 4.14670 |
Index of Refraction | 1.587 |
Storage condition | 2-8°C |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
|
Precursor 0 | |
---|---|
DownStream 1 | |