RGX-104 (DC10719) chemical structure
Chemical structureResearch use only
CAT. NO. DC10719Featured

RGX-104

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Product overview

Description & Application

RGX-104 is an LXR agonist for studying myeloid-derived suppressor cells, ApoE signaling and tumor immune responses.

ParameterValue
Chemical NameRGX-104 HCl
CAS No.610318-03-1
SynonymsRGX-104 hydrochloride; RGX-104 HCl; RGX-104; RGX104; RGX 104; SB742881; SB-742881; SB 742881
FormulaC34H34Cl2F3NO3
M.Wt632.56
SMILESC[C@H](CCOC1=CC=CC(=C1)CC(=O)O)N(CC2=C(C(=CC=C2)C(F)(F)F)Cl)CC(C3=CC=CC=C3)C4=CC=CC=C4.Cl
PurityOn request
Storage2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO
LXR / ApoE · Literature evidence

Biological Activity

RGX-104 is an LXR agonist for studying myeloid-derived suppressor cells, ApoE signaling and tumor immune responses. ApoE mediated the depletion of immunosuppressive myeloid cells and supported cytotoxic T-cell responses.

In Vitro

EndpointModel / conditions / sourceReported result
Mechanistic frameworkLXR/ApoE pathway interrogated using genetic and pharmacological approaches. [1]ApoE mediated the depletion of immunosuppressive myeloid cells and supported cytotoxic T-cell responses.

In Vivo

EndpointModel / conditions / sourceReported result
Preclinical pathway evidenceMultiple murine tumor models with LXR-directed interventions. [1]LXR/ApoE activation reduced MDSC abundance and enhanced antitumor immune responses. Compound and combination arms must be distinguished.

Clinical / Human Evidence

EndpointModel / conditions / sourceReported result
Human pharmacodynamicsFirst-in-human LXR-agonist dose-escalation study. [1]Lower circulating MDSC abundance was associated with activation of cytotoxic T-cell responses.

Compound and Evidence Context

EndpointModel / conditions / sourceReported result
RGX-104 attributionThe paper includes multiple pharmacological and genetic interventions. [1]The verified abstract does not resolve every animal dose or efficacy value to RGX-104. Those values are not attributed to this product here.

Interpretation

Human immune biomarker changes do not by themselves establish tumor-response or survival benefit.

Original studies

References

  1. Tavazoie MF, et al. LXR/ApoE Activation Restricts Innate Immune Suppression in Cancer. Cell (2018).

Product documentation

Refer to the certificate supplied with your lot for batch-specific release results.

Handling guide

2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO

For additional quantities or product documentation, contact info@dcchemicals.com.

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