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553030 RAGE Antagonist, FPS-ZM1 - CAS 945714-67-0 - Calbiochem

Overview

Replacement Information

Key Specifications Table

CAS #Empirical Formula
945714-67-0C₂₀H₂₂ClNO

Products

Catalog NumberPackaging Qty/Pack
553030-25MG Glass bottle 25 mg
Description
OverviewA blood-brain-barrier-permeant, non-toxic, tertiary amide compound that acts as a high affinity, potent, multimodal blocker of RAGE (Receptor for Advanced Glycation End products) V domain-mediated ligand binding (Ki = 25, 148, and 230 nM, respectively, against Aβ40, HMGB1, and S100B, binding to sRAGE). Blocks RAGE-mediated influx of Aβ40 and Aβ42 into the brain. Also shown to suppress Aβ-RAGE induced NF-κB activation and NF-κB-dependent transcription of β-secretase. Daily treatment of APPsw/0 murine AD model (1 mg/kg/d via i.p.) is reported to greatly reduce Thioflavin S-positive amyloid plaques in cortex and hippocampus (by 70 to 80%) and restore congnitive performance to the level of non-AD mice.
Catalogue Number553030
Brand Family Calbiochem®
SynonymsReceptor for AGE Antagonist, FPS-ZM1, N-Benzyl-4-chloro-N-cyclohexylbenzamide
References
ReferencesDeane, R., et al. 2012. J. Clin. Invest. 122, 1377.
Product Information
CAS number945714-67-0
FormWhite to off-white semi-solid or viscous liquid
Hill FormulaC₂₀H₂₂ClNO
ReversibleY
Structure formula ImageStructure formula Image
Quality LevelMQ100
Applications
Biological Information
Primary TargetRAGE
Primary Target K<sub>i</sub>25, 148, and 230 nM, respectively, against A&beta
Purity≥98% by HPLC
Physicochemical Information
Cell permeableY
Dimensions
Materials Information
Toxicological Information
Safety Information according to GHS
Safety Information
Product Usage Statements
Storage and Shipping Information
Ship Code Ambient Temperature Only
Toxicity Standard Handling
Storage +2°C to +8°C
Protect from Light Protect from light
Do not freeze Ok to freeze
Special InstructionsFollowing reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 6 months at -20°C.
Packaging Information
Packaged under inert gas Packaged under inert gas
Transport Information
Supplemental Information
Specifications
Global Trade Item Number
Catalog Number GTIN
553030-25MG 04055977193466

Documentation

RAGE Antagonist, FPS-ZM1 - CAS 945714-67-0 - Calbiochem SDS

Title

Safety Data Sheet (SDS) 

RAGE Antagonist, FPS-ZM1 - CAS 945714-67-0 - Calbiochem Certificates of Analysis

TitleLot Number
553030

References

Reference overview
Deane, R., et al. 2012. J. Clin. Invest. 122, 1377.
Data Sheet

Note that this data sheet is not lot-specific and is representative of the current specifications for this product. Please consult the vial label and the certificate of analysis for information on specific lots. Also note that shipping conditions may differ from storage conditions.

Revision20-June-2017 JSW
SynonymsReceptor for AGE Antagonist, FPS-ZM1, N-Benzyl-4-chloro-N-cyclohexylbenzamide
DescriptionA blood-brain-barrier-permeant, non-toxic, tertiary amide compound that acts as a high affinity, potent, multimodal blocker of RAGE (Receptor for Advanced Glycation End products) V domain-mediated ligand binding (Ki = 25, 148, and 230 nM, respectively, against Aβ40, HMGB1, and S100B, binding to sRAGE). Blocks RAGE-mediated influx of Aβ40 and Aβ42 into the brain. Also shown to suppress Aβ-RAGE induced NF-κB activation and NF-κB-dependent transcription of β-secretase. Daily treatment of APPsw/0 murine AD model (1 mg/kg/d via i.p.) is reported to greatly reduce Thioflavin S-positive amyloid plaques in cortex and hippocampus (by 70 to 80%) and restore congnitive performance to the level of non-AD mice.
FormWhite to off-white semi-solid or viscous liquid
Intert gas (Yes/No) Packaged under inert gas
CAS number945714-67-0
Structure formulaStructure formula
Purity≥98% by HPLC
SolubilityDMSO (100 mg/ml)
Storage Protect from light
+2°C to +8°C
Do Not Freeze Ok to freeze
Special InstructionsFollowing reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 6 months at -20°C.
Toxicity Standard Handling
ReferencesDeane, R., et al. 2012. J. Clin. Invest. 122, 1377.