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Biological Data Biological description Histamine H1 antagonist. Potently activates the modified hM4Di "GRANPA" (G protein Receptor Activated by Non-Presciption Agents) DREADD receptor in vitro and in vivo.
Solubility & Handling Storage instructions Room temperature, desiccate.
Solubility overview Soluble in water (100 mM)
Important This product is for RESEARCH USE ONLY and is not intended for therapeutic or diagnostic use. Not for human or veterinary use
Chemical Data Chemical name 2-Diphenylmethoxy-N,N-dimethylethanamine hydrochloride
Chemical structure
Molecular Formula C17 H21 NO.HCl
SMILES CN(C)CCOC(C1=CC=CC=C1)C2=CC=CC=C2.Cl
InChi InChI=1S/C17H21NO.ClH/c1-18(2)13-14-19-17(15-9-5-3-6-10-15)16-11-7-4-8-12-16;/h3-12,17H,13-14H2,1-2H3;1H
InChiKey PCHPORCSPXIHLZ-UHFFFAOYSA-N
References for Diphenhydramine hydrochloride (DPH) References are publications that support the biological activity of the product
Improving the suitability of chemogenetic gene therapies by repurposing non-prescription agents as actuators Devenish et al (2022) Ucl Neuroscience Symposium 2022 :
Classic histamine H1 receptor antagonists: a critical review of their metabolic and pharmacokinetic fate from a bird's eye view. Sharma A et al (2003) Current drug metabolism 4 : 105-29
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Histamine H1 antagonist. Potent actuator of a modified hM4Di "GRANPA" DREADD receptor.