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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.