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A histamine H1 receptor antagonist (Ki = 15 nM), selective for the histamine H1 receptor over mAChRs (Ki = 263 nM) but also inhibits 5-HT2 (Ki = 7 nM), inhibits histamine release induced by an anti-IgE antibody in isolated human lung fragments (IC50 = 4.5 nM), inhibits A23187-induced degranulation of RBL-2H3 mast cells, inhibits LPS-induced NO production in RAW 264.7 cells at 50 µM and fMLP- or PMA-induced superoxide production in isolated rat neutrophils, reduces histamine-induced vascular permeability in mice (ED50 = 2.9 mg/kg). Formulation: A solid. InChI: InChI=1S/C27H30N4O/c32-27-28-24-14-7-8-15-25(24)31(27)17-9-16-29-18-20-30(21-19-29)26(22-10-3-1-4-11-22)23-12-5-2-6-13-23/h1-8,10-15,26H,9,16-21H2,(H,28,32). InChIKey: BAINIUMDFURPJM-UHFFFAOYSA-N. SMILES: O=C(NC1=C2C=CC=C1)N2CCCN3CCN(CC3)C(C4=CC=CC=C4)C5=CC=CC=C5
Keywords:
KW 4354, NSC 309710, R 35443, 1-[3-[4-(diphenylmethyl)-1-piperazinyl]propyl]-1,3-dihydro-2H-benzimidazol-2-one
This website uses cookies, which are necessary for the technical operation of the website and are always set. Other cookies, which increase the usability of this website, serve for direct advertising or simplify interaction with other websites and social networks, will only be used with your consent.
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