Iodophenpropit dihydrobromide

Pricing Availability   Qty
Description: Potent, selective H3 antagonist
Chemical Name: N-[2-(4-Iodophenyl)ethyl]-S-[3-(4(5)-imidazolyl)propyl]isothiourea dihydrobromide
Purity: ≥98% (HPLC)
Datasheet
Citations (2)
Reviews
Literature (2)

Biological Activity for Iodophenpropit dihydrobromide

Iodophenpropit dihydrobromide is a selective H3 antagonist with high affinity (KD = 0.3 nM).

Licensing Information

Sold with the permission of SCI, Amsterdam

Technical Data for Iodophenpropit dihydrobromide

M. Wt 576.13
Formula C15H19IN4S.2HBr
Storage Desiccate at +4°C
Purity ≥98% (HPLC)
CAS Number 145196-87-8
PubChem ID 24978528
InChI Key BOSOGNBLIWPCMS-UHFFFAOYSA-N
Smiles Br.Br.IC1=CC=C(CCNC(=N)SCCCC2=CNC=N2)C=C1

The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.

Tocris products are intended for laboratory research use only, unless stated otherwise.

Solubility Data for Iodophenpropit dihydrobromide

Solvent Max Conc. mg/mL Max Conc. mM
Solubility
water 14.4 25

Preparing Stock Solutions for Iodophenpropit dihydrobromide

The following data is based on the product molecular weight 576.13. Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Select a batch to recalculate based on the batch molecular weight:
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
0.25 mM 6.94 mL 34.71 mL 69.43 mL
1.25 mM 1.39 mL 6.94 mL 13.89 mL
2.5 mM 0.69 mL 3.47 mL 6.94 mL
12.5 mM 0.14 mL 0.69 mL 1.39 mL

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Product Datasheets for Iodophenpropit dihydrobromide

References for Iodophenpropit dihydrobromide

References are publications that support the biological activity of the product.

Jansen et al (1992) The first radiolabelled histamine H3 receptor antagonist, [125I]iodophenpropit: saturable and reversible binding to rat cortex membranes. Eur.J.Pharmacol. 217 203 PMID: 1330590

Jansen et al (1994) Characterisation of the binding of the first selective radiolabelled histamine H3 receptor antagonist, [125I]-iodophenpropit, to rat brain. Br.J.Pharmacol. 113 355 PMID: 7834183

Menge et al (1992) Synthesis of S-[3-(4(5)-imidazolyl)propyl]-N-[2-(4-[125I]-iodophenylethyl]isothiourea sulfate [125I]-iodophenpropit), a new probe for histamine H3 receptor binding sites. J.Labelled Comp.Radiopharm. XXXI 10 781

Shahid et al (2009) Histamine, histamine receptors, and their role in immunomodulation: An updated systematic review. Open Immunol.J. 2 9


If you know of a relevant reference for Iodophenpropit dihydrobromide, please let us know.

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Keywords: Iodophenpropit dihydrobromide, Iodophenpropit dihydrobromide supplier, Potent, selective, H3, antagonists, Receptors, Histamine, histaminergic, 0779, Tocris Bioscience

2 Citations for Iodophenpropit dihydrobromide

Citations are publications that use Tocris products. Selected citations for Iodophenpropit dihydrobromide include:

Otvos et al (2015) Development of Plate Reader and On-Line Microfluidic Screening to Identify Ligands of the 5-Hydroxytryptamine Binding Protein in Venoms. BMC Neurosci 7 2336 PMID: 26114334

Spaethling et al (2014) Serotonergic neuron regulation informed by in vivo single-cell transcriptomics. Toxins (Basel) 28 771 PMID: 24192459


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Literature in this Area

Tocris offers the following scientific literature in this area to showcase our products. We invite you to request* your copy today!

*Please note that Tocris will only send literature to established scientific business / institute addresses.


Histamine Receptors Scientific Review

Histamine Receptors Scientific Review

Written by Iwan de Esch and Rob Leurs, this review provides a synopsis of the different histamine receptor subtypes and the ligands that act upon them; compounds available from Tocris are listed.

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Alzheimer's disease (AD) is a debilitating and progressive neurodegenerative disease and the most common cause of dementia, affecting approximately 30% of individuals aged over 85 years. This poster summarizes the cellular and molecular mechanisms of AD.