MedKoo Cat#: 466265 | Name: RAGE 229
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Description:

WARNING: This product is for research use only, not for human or veterinary use.

RAGE 229 is an antagonist of the interaction between the cytoplasmic tail of the receptor for advanced glycation end products (ctRAGE) and the formin, Diaphanous-1 (DIAPH1) (KD for binding to ctRAGE = 2 nM). RAGE 229 inhibits the migration of human aortic smooth muscle cells in an in vitro wound healing assay (IC50 = 120 nM). RAGE 229 reduces short- and long-term complications of diabetes in mouse models, without lowering blood glucose concentrations. RAGE 229 also reduces plasma concentrations of TNF-α, IL-6, and CCL2/JE-MCP1 and attenuates inflammatory signaling in diabetic mice.

Chemical Structure

RAGE 229
RAGE 229
CAS#2143072-85-7

Theoretical Analysis

MedKoo Cat#: 466265

Name: RAGE 229

CAS#: 2143072-85-7

Chemical Formula: C23H22N4O2

Exact Mass: 386.1743

Molecular Weight: 386.46

Elemental Analysis: C, 71.48; H, 5.74; N, 14.50; O, 8.28

Price and Availability

Size Price Availability Quantity
5mg USD 575.00 2 Weeks
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Related CAS #
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Synonym
RAGE 229; RAGE229; RAGE-229;
IUPAC/Chemical Name
N-(4-(7-cyano-4-(morpholinomethyl)quinolin-2-yl)phenyl)acetamide
InChi Key
VDYYVNHJRNDKDO-UHFFFAOYSA-N
InChi Code
InChI=1S/C23H22N4O2/c1-16(28)25-20-5-3-18(4-6-20)22-13-19(15-27-8-10-29-11-9-27)21-7-2-17(14-24)12-23(21)26-22/h2-7,12-13H,8-11,15H2,1H3,(H,25,28)
SMILES Code
N#CC1=CC2=NC(C3=CC=C(NC(C)=O)C=C3)=CC(CN4CCOCC4)=C2C=C1
Appearance
Solid powder
Purity
>98% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
Solubility
To be determined
Shelf Life
>2 years if stored properly
Drug Formulation
To be determined
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.9001
More Info
Solvent mg/mL mM
Solubility
DMSO 38.7 100.00
Note: There can be variations in solubility for the same chemical from different vendors or different batches from the same vendor. The following factors can affect the solubility of the same chemical: solvent used for crystallization, residual solvent content, polymorphism, salt versus free form, degree of hydration, solvent temperature. Please use the solubility data as a reference only. Warming and sonication will facilitate dissolving. Still have questions? Please contact our Technical Support scientists.

Preparing Stock Solutions

The following data is based on the product molecular weight 386.46 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.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
1: Manigrasso MB, Rabbani P, Egaña-Gorroño L, Quadri N, Frye L, Zhou B, Reverdatto S, Ramirez LS, Dansereau S, Pan J, Li H, D'Agati VD, Ramasamy R, DeVita RJ, Shekhtman A, Schmidt AM. Small-molecule antagonism of the interaction of the RAGE cytoplasmic domain with DIAPH1 reduces diabetic complications in mice. Sci Transl Med. 2021 Nov 24;13(621):eabf7084. doi: 10.1126/scitranslmed.abf7084. Epub 2021 Nov 24. PMID: 34818060; PMCID: PMC8669775. 2: Carr, K. D., Weiner, S. P., Vasquez, C., & Schmidt, A. M. (2023). Involvement of the Receptor for Advanced Glycation End Products (RAGE) in high fat-high sugar diet-induced anhedonia in rats. Physiology & Behavior, 271, 114337. 3: Gu, M. J., Lee, Y. R., Kim, D., Kim, Y., & Ha, S. K. (2024). Comprehensive research on the properties of advanced glycation end products in food and biological samples and their harmful role in inducing metabolic diseases. Comprehensive Reviews in Food Science and Food Safety, 23(5), e13412.