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Found to be the most potent and selective H1 histamine receptor agonist of a panel of compounds in functional in vitro studies on histamine H2, H3, and other neurotransmitter receptors. It showed better potency at the guinea pig H1 histamine receptor than at the human H1 histamine receptor (pKi : 5.9). The selectivity of 2-((3-Trifluoromethyl)phenyl)histamine dimaleate was found to be 2138 (H1:H2), > 64 (H1:H3), 1000 (H1:M3), 105 (H1: a1), 708 (H1:β1), and 71 (H1:5HT2A). This substance does not cross the blood-brain barrier.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
2-((3-Trifluoromethyl)phenyl)histamine dimaleate, 5 mg | sc-251656 | 5 mg | $99.00 |