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and serves as a basis for new selective inhibitors of other HDAC isoforms
InChi: InChI=1S/C14H8FNO3S/c15-9-3-1-8(2-4-9)11-6-5-10(19-11)7-12-13(17)16-14(18)20-12/h1-7H
In the mouse model of airway epithelial remodeling that is inducible by viral infection and features a delayed but permanent switch to goblet cell metaplasia
Roberto GM
Ginsenoside Rh4 is a saponin isolated from the roots of Panax notoginseng (Burk
Doxepin Hydrochloride modelin hydrobromide and serves as a basisDoxepin hydrochloride is a highly potent Histamine H1 Receptor (histamine H1) antagonist. Doxepin hydrochloride also binds to histamine H4 receptor. Doxepin hydrochloride is an inhibitor of AR and mAChR. Doxepin Hydrochloride is a dibenzoxepin derivative and tricyclic antidepressant with antipruritic and sedative activities. Doxepin also has antagonistic effects on histamine (H1 and H2), 5 HT2, alpha 1 adrenergic, and muscarinic receptors. The
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