Cart
sales@molnova.com
Diphenhydramine hydrochloride
CAS No. 147-24-0
Diphenhydramine hydrochloride( DPH )
Catalog No. M12021 CAS No. 147-24-0
Diphenhydramine HCl (Benadryl), a histamine H1 antagonist used as an antiemetic, antitussive.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 100MG | 31 | In Stock |
|
| 200MG | 43 | In Stock |
|
| 500MG | 52 | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameDiphenhydramine hydrochloride
-
NoteResearch use only, not for human use.
-
Brief DescriptionDiphenhydramine HCl (Benadryl), a histamine H1 antagonist used as an antiemetic, antitussive.
-
DescriptionDiphenhydramine HCl (Benadryl), a histamine H1 antagonist used as an antiemetic, antitussive, for dermatoses and pruritus, for hypersensitivity reactions, as a hypnotic, an antiparkinson, and as an ingredient in common cold preparations.
-
In Vitro——
-
In Vivo——
-
SynonymsDPH
-
PathwayGPCR/G Protein
-
TargetHistamine Receptor
-
RecptorH1 receptor
-
Research AreaInflammation/Immunology
-
Indication——
Chemical Information
-
CAS Number147-24-0
-
Formula Weight291.82
-
Molecular FormulaC17H22ClNO
-
Purity>98% (HPLC)
-
SolubilityEthanol: 58 mg/mL (198.75 mM); Water: 58 mg/mL (198.75 mM); DMSO: 58 mg/mL (198.75 mM)
-
SMILESCl.CN(C)CCOC(C1=CC=CC=C1)C1=CC=CC=C1
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Piao H, et al. Vascul Pharmacol. 2007 Apr;46(4):260-70.
molnova catalog
related products
-
Dimethindene maleate
Dimethindene maleate is a histamine H1 antagonist and can be used in studies about the treatment of hypersensitivity reactions, pruritus and rhinitis.
-
Thiethylperazine
Thiethylperazine (Tietilperazina) is an orally available, highly potent D2 receptor and H1 receptor antagonist and selective ABCC1 activator with antimicrobial and antiemetic activity that reduces amyloid β (Aβ) load in mice.
-
SUVN-G3031
SUVN-G3031 (SUVN-G 3031) is a potent, selective, orally active histamine H3 receptor (H3R) inverse agonist with Ki of 8.73 nM (hH3R).
