MedKoo Cat#: 126969 | Name: EP26

Description:

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

EP26 is a potent PD-L1/EGFR Dual Inhibitor with High Druggability for Glioblastoma Immunotherapy. EP26 exhibited the inhibitory activity against EGFR (IC50 = 37.5 nM) and PD-1/PD-L1 interaction (IC50 = 1.77 μM). EP26 displayed superior in vitro antiproliferative activities and in vitro immunomodulatory effects by promoting U87MG cell death in a U87MG/Jurkat cell coculture model. Furthermore, EP26 Possessed favorable pharmacokinetic properties (F = 22%) and inhibited tumor growth (TGI = 92.0%) in a GBM mouse model more effectively than Gefitinib (77.2%) and NP19 (82.8%).

Chemical Structure

EP26
EP26
CAS#N/A

Theoretical Analysis

MedKoo Cat#: 126969

Name: EP26

CAS#: N/A

Chemical Formula: C42H42ClFN4O5

Exact Mass: 736.2828

Molecular Weight: 737.27

Elemental Analysis: C, 68.42; H, 5.74; Cl, 4.81; F, 2.58; N, 7.60; O, 10.85

Price and Availability

This product is currently not in stock but may be available through custom synthesis. To ensure cost efficiency, the minimum order quantity is 1 gram. The estimated lead time is 2 to 4 months, with pricing dependent on the complexity of the synthesis (typically high for intricate chemistries). Quotes for quantities below 1 gram will not be provided. To request a quote, please click the button below. Note: If this product becomes available in stock in the future, pricing will be listed accordingly.
Bulk Inquiry
Related CAS #
No Data
Synonym
EP26; EP-26; EP 26
IUPAC/Chemical Name
N-(3-chloro-2-fluorophenyl)-6-(4-((2,6-dimethoxy-4-((2-methyl-[1,1'-biphenyl]-3-yl)methoxy)benzyl)amino)butoxy)-7-methoxyquinazolin-4-amine
InChi Key
UNVKVCJYTQIHSW-UHFFFAOYSA-N
InChi Code
InChI=1S/C42H42ClFN4O5/c1-27-29(14-10-15-31(27)28-12-6-5-7-13-28)25-53-30-20-37(49-2)33(38(21-30)50-3)24-45-18-8-9-19-52-40-22-32-36(23-39(40)51-4)46-26-47-42(32)48-35-17-11-16-34(43)41(35)44/h5-7,10-17,20-23,26,45H,8-9,18-19,24-25H2,1-4H3,(H,46,47,48)
SMILES Code
CC1=C(COC2=CC(OC)=C(CNCCCCOC3=C(OC)C=C(N=CN=C4NC5=CC=CC(Cl)=C5F)C4=C3)C(OC)=C2)C=CC=C1C6=CC=CC=C6
Appearance
To be determined
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

Preparing Stock Solutions

The following data is based on the product molecular weight 737.27 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
Yang Z, Liu Z, Wan S, Xu J, Huang Y, He H, Liu T, Li L, Ren Y, Zhang J, Chen J. Discovery of Novel Small-Molecule-Based Potential PD-L1/EGFR Dual Inhibitors with High Druggability for Glioblastoma Immunotherapy. J Med Chem. 2024 May 13. doi: 10.1021/acs.jmedchem.4c00128. Epub ahead of print. PMID: 38739112.