JP-153 (DC11954) chemical structure
Chemical structureResearch use only
CAT. NO. DC11954Featured

JP-153

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Product overview

Description & Application

JP-153 is a focal-adhesion-signaling modulator for VEGF-dependent retinal endothelial-cell and angiogenesis research.

ParameterValue
Chemical Name4-(3,4,5-trimethoxyphenyl)-1,4-dihydro-2H-naphtho[1,2-d][1,3]oxazin-2-one
CAS No.1802937-26-3
SynonymsJP 153; JP153
FormulaC21H19NO5
M.Wt365.385
SMILESO1C(C2=CC(OC)=C(OC)C(OC)=C2)C2=CC=C3C(=C2NC1=O)C=CC=C3
Purity>98%
Storage2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO
FAK / paxillin signaling · Literature evidence

Biological Activity

JP-153 is a focal-adhesion-signaling modulator for VEGF-dependent retinal endothelial-cell and angiogenesis research. JP-153 disrupted FAK–paxillin interactions and reduced paxillin Tyr118 and Akt Ser473 phosphorylation.

In Vitro

EndpointModel / conditions / sourceReported result
Focal-adhesion signalingHuman retinal endothelial cells stimulated with VEGF. [1]JP-153 disrupted FAK–paxillin interactions and reduced paxillin Tyr118 and Akt Ser473 phosphorylation.
Functional readoutsRetinal endothelial migration and proliferation assays. [1]Both responses decreased; initial Src and FAK activation were not prevented, distinguishing complex modulation from simple Src/FAK inhibition.

In Vivo

EndpointModel / conditions / sourceReported result
Retinal angiogenesisMouse oxygen-induced retinopathy; topical JP-153 microemulsion. [1]Pathological neovascular tuft formation decreased in a dose-dependent manner.
Important accompanying effectSame retinal model. [1]Avascular area increased. Reduced tuft formation should not be described as uniform restoration of normal retinal vasculature.

Interpretation

Formulated ocular efficacy cannot be directly assigned to unformulated JP-153 or a different route of administration.

Original studies

References

  1. Toutounchian JJ, et al. Novel Small Molecule JP-153 Targets the Src-FAK-Paxillin Signaling Complex to Inhibit VEGF-Induced Retinal Angiogenesis. Molecular pharmacology (2017).

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

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