product summary
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company name :
Alomone Labs
product type :
chemical
product name :
Clobenpropit dihydrobromide
catalog :
C-345
more info or order :
image
image 1 :

Cell surface detection of GPR91 in live intact mouse J774 macrophage cells: - ___Cells.___Cells + rabbit IgG isotype control-FITC.___Cells +Anti-GPR91 (SUCNR1) (extracellular)-FITC Antibody (#ASR-090-F) (2.5 g).
product information
CAT :
C-345
SKU :
C-345_10 mg
Product Name :
Clobenpropit dihydrobromide
Group Type :
Non Antibodies
Product Type :
S. Molecules
Storage After Reconstitution :
The reconstituted solution can be stored at 4°C for up to 1 week. For longer periods (up to 6 months), small aliquots should be stored at -20°C. We do not recommend storing the product in working solutions for longer than a few days. Avoid multiple freeze-thaw cycles.
Storage before Reconstitution :
The product is shipped as a lyophilized powder at room temperature. Upon receipt, store the product at -20°C. Protect from moisture.
Shipping and storage :
Shipped at room temperature. Product as supplied can be stored intact at room temperature for several weeks. For longer periods, it should be stored at -20°C
Product Page - Scientific background :
Clobenpropit dihydrobromide (VUF 9153) is a synthetic compound that acts as a potent, selective and competitive antagonist of the histamine H3 receptor and shows partial agonist activity towards the histamine H4 receptor. In addition, the compound acts as an antagonist of N-Methyl-d-aspartate (NMDA) receptors1 and displays IC50 values of 1 µM-14 µM2.NMDA receptors are heterotetrameric channels formed by the assembly of two obligatory GluN1 and two GluN2/GluN3 subunits. They play an important role in a variety of cellular processes and brain functions such as, synaptic plasticity, addiction and stroke, and mediate physiological functions such as learning and memory formation and participates in glutamate excitotoxicity2. Histamine H3 receptors are presynaptic G-protein coupled receptors that are expressed in the central nervous system. They regulate the release of several neurotransmitters, including biogenic amines, acetylcholine, GABA and glutamate3.
Supplier :
Alomone Labs
Target :
Histamine H3, Histamine H4, NMDA receptors
Long Description :
Clobenpropit dihydrobromide (#C-345) is a highly pure, synthetic, and biologically active compound.
Short Description :
A Potent and Selective Antagonist of Histamine H3 Receptors and an Antagonist of NMDA Receptors
MW :
470.65
Synonyms :
VUF 9153
Source :
Synthetic
Molecular formula :
C14H19Br2ClN4S.
Effective Concentration :
10 nM - 10 µM.
Activity :
Clobenpropit dihydrobromide is a potent and selective antagonist/inverse agonist of the histamine H3 receptors (pA2 = 9.93), with partial agonist activity at histamine H4 receptors1. It is also an antagonist of the NMDA receptors (IC50 1 µM - 14 µM)2.
Reconstitution and Solubility :
Up to 100 mM in water. Centrifuge all product preparations before use (10000 x g 5 min).
Solubility :
Up to 100 mM in water. Centrifuge all product preparations before use (10000 x g 5 min).
Storage of solutions :
Store at -20°C. It is recommended to prepare solutions afresh on the day of use, or aliquot stock solutions stored at -20°C to prevent repeated thawing and freezing.
Lead Time :
1-2 Business Days
Country of origin :
Israel/IL
Applications key :
Application key: FC- Flow cytometry, IFC- Indirect flow cytometry, IHC- Immunohistochemistry,LCI- Live cell imaging, Calcium imaging assay,Cell survival assay, Electrophysiology, Neurite outgrowth assay.
Purity :
>99%
CAS No :
145231-35-2
Form :
Lyophilized powder.
Comment :
Contact Alomone Labs for technical support and product customization
UNSPSC :
41116134
Bioassay Tested :
Yes
Chemical Name :
3-(1H-imidazol-5-yl)propyl N'-[(4-chlorophenyl)methyl]carbamimidothioate;dihydrobromide.
more info or order :
company information

Alomone Labs
Jerusalem BioPark (JBP), Hadassah Ein Kerem
P.O. Box 4287
Jerusalem 9104201
P.O. Box 4287
Jerusalem 9104201
info@alomone.com
http://www.alomone.com972 2 531 8002
headquarters: Israel
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