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E7820

Catalog No. T4435   CAS 289483-69-8
Synonyms: ER68203-00

E7820 (ER68203-00) is an angiogenesis inhibitor by suppressing integrin a2 (a cell adhesion molecule expressed on endothelial cells).

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E7820 Chemical Structure
E7820, CAS 289483-69-8
Pack Size Availability Price/USD Quantity
1 mg In stock $ 30.00
2 mg In stock $ 44.00
5 mg In stock $ 63.00
10 mg In stock $ 80.00
25 mg In stock $ 147.00
50 mg In stock $ 222.00
100 mg In stock $ 357.00
200 mg In stock $ 529.00
1 mL * 10 mM (in DMSO) In stock $ 77.00
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Purity: 99.11%
Purity: 98.48%
Purity: 98.31%
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Biological Description
Chemical Properties
Storage & Solubility Information
Description E7820 (ER68203-00) is an angiogenesis inhibitor by suppressing integrin a2 (a cell adhesion molecule expressed on endothelial cells).
In vitro E7820 inhibits proliferation of HUVEC induced by either bFGF (IC50: 0.10 μg/mL) and VEGF (IC50: 0.081 μg/mL) in serum-free medium. E7820 also inhibits both bFGF- (IC50: 0.20 μg/mL) and VEGF-driven (IC50: 0.24 μg/mL) tube formation of HUVEC in this assay[3].
In vivo E7820 (50 mg/kg) with erlotinib has a significantly synergistic antitumor effect in three xenograft models without severe body weight loss. E7820 (50 mg/kg) and erlotinib decrease MVD and enhance apoptosis in tumor-associated endothelial cells, inhibit tumor cell proliferation and enhanced apoptosis, and enhance inhibition of cell proliferation and apoptosis through activation of both intrinsic and extrinsic apoptosis pathways in human NSCLC xenograft models[1]. E7820 shows anti-tumor activity at doses of 50, 100, and 200 mg/kg in the tumor growth and α2-integrin expression experiments[2]. E7820 (50, 100, and 200 mg/kg) inhibits tumor growth in a dose-dependent manner in all s.c. xenograft models. E7820 completely inhibits s.c. tumor growth of LoVo tumor cells and also regresses the tumor mass of KP-1 tumor cells at the dosages of both 100 and 200 mg/kg[3].
Synonyms ER68203-00
Molecular Weight 336.37
Formula C17H12N4O2S
CAS No. 289483-69-8

Storage

store at low temperature

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

Solubility Information

H2O: Insoluble

DMSO: 33 mg/mL

TargetMolReferences and Literature

1. Ito K, Semba T, Uenaka T, et al. Enhanced anti‐angiogenic effect of E7820 in combination with erlotinib in epidermal growth factor receptor–tyrosine kinase inhibitor‐resistant non‐small‐cell lung cancer xenograft models[J]. Cancer science, 2014, 105(8): 1023-1031. 2. Keizer R J, Funahashi Y, Semba T, et al. Evaluation of α 2-Integrin Expression as a Biomarker for Tumor Growth Inhibition for the Investigational Integrin Inhibitor E7820 in PreClinicalal and Clinicalal Studies[J]. The AAPS journal, 2011, 13(2): 230-239. 3. Semba T, Funahashi Y, Ono N, et al. An angiogenesis inhibitor E7820 shows broad-spectrum tumor growth inhibition in a xenograft model: possible value of integrin α2 on platelets as a biological marker[J]. Clinicalal Cancer Research, 2004, 10(4): 1430-1438.

Related compound libraries

This product is contained In the following compound libraries:
Inhibitor Library Anti-Cancer Drug Library Drug Repurposing Compound Library Anti-Cancer Clinical Compound Library Anti-Cancer Active Compound Library Clinical Compound Library Anti-COVID-19 Compound Library NO PAINS Compound Library Orally Active Compound Library Angiogenesis related Compound Library

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Keywords

E7820 289483-69-8 Cytoskeletal Signaling Integrin cell tumor E 7820 WiDr derivative colorectal LoVo inhibit Inhibitor sulfonamide HUVEC ER68203-00 E-7820 endothelium inhibitor

 

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