Comparison

SR 48692 European Partner

Item no. ALO-S-265-5mg
Manufacturer Alomone
CASRN 146362-70-1
Amount 5 mg
Quantity options 10 mg 25 mg 50 mg 5 mg
Category
Type Small Molecules
Format Lyophilized
Specific against other
Purity >98%
ECLASS 10.1 32160490
ECLASS 11.0 32160490
UNSPSC 12000000
Shipping Condition Room temperature
Available
Manufacturer - Type
Non Antibodies
Manufacturer - Category
S. Molecules
Manufacturer - Targets
Neurotensin Receptor 1
Country of Origin
Israel
Shipping Temperature
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
Storage Conditions
Storage as Solution: Store at -20°C. It is recommended to aliquot stock solutions to prevent repeated thawing and freezing. - 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.
Molecular Weight
587, 07
Manufacturer - Format
Lyophilized Powder
Short description
A Potent and Selective Antagonist of Neurotensin Receptor 1
Description
SR48692, Meclinertant, Reminertant - A Potent and Selective Antagonist of Neurotensin Receptor 1
Reconstitution
Soluble in DMSO. Centrifuge all products before handling (10000 x g 5 min).
PH
7, 4
UNSPSC
41116134
Effective Concentration
1 nM - 1 µM.
Activity
SR 48692 is a potent and selective non-peptide antagonist of NTS1 receptors, shown to inhibit neurotensin-stimulated IP production (Ki = 2.45 nM) and NTR1-mediated calcium mobilization1-3.
Solubility
Soluble in DMSO. Centrifuge all products before handling (10000 x g 5 min).
Bioassay tested
Yes
Chemical Name
2-[[1-(7-chloroquinolin-4-yl)-5-(2, 6-dimethoxyphenyl)pyrazole-3-carbonyl]amino]adamantane-2-carboxylic acid.
Scientific Background
SR 48692 is a potent and selective antagonist of neurotensin receptor 1 (NTR1/NTS1). The compound demonstrates hydrophobic and aromatic features1, 2. SR 48692 has been shown to antagonize neurotensin receptor actions in intestinal preparations, thus considered to be a useful tool in studying the physiological role of neurotensin receptor in the digestive tract. in vitro studies show that SR 48692 antagonizes NT-induced dopamine release in guinea pig striatal slices and NT-stimulated Ca2+ mobilization in HT29 cells1. In guinea pig ileum preparations, the compound displays an IC50 value of 33.5 nM1.The two neurotensin receptors, NTR1 and NTR2, belong to the family of G-protein-coupled receptors1, 2. The receptors are expressed in the brain and gastrointestinal tract where they play a role in pain transmission and intestinal motility.

Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.

All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

Amount: 5 mg
Available: In stock
available

Delivery expected until 1/8/2026 

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