Comparison

APG-115

Item no. CS-0021621-1mg
Manufacturer ChemScene
Amount 1mg
Category
Type Molecules
Specific against other
ECLASS 10.1 32169090
ECLASS 11.0 32169090
UNSPSC 12000000
Alias 1818393-16-6
Similar products 1818393-16-6
Available
Alternative Names
AA-115
CAS
1818393-16-6
Purity
>98%
MWt
642.59
Formula
C34H38Cl2FN3O4
Solubility
10 mM in DMSO
Clinical Information
Phase 2
Pathway
Apoptosis; Metabolic Enzyme/Protease; Apoptosis
Target
Apoptosis; E1/E2/E3 Enzyme; MDM-2/p53
Biological Activity
APG-115 (AA-115) is an orally active MDM2 protein inhibitor binding to MDM2 protein with IC50 and Ki values of 3.8 nM and 1 nM, respectively[1]. APG-115 blocks the interaction of MDM2 and p53 and induces cell-cycle arrest and apoptosis in a p53-dependent manner[2][3]. IC50 & Target: IC50: 3.8 nm (APG-115)[1] In Vitro: APG-115 (0.001-100 uM; 72 hours) inhibits cell proliferation in concentration-dependent manner, with IC50s of 18.9?+/-?15.6 nM and 103.5?+/-?18.3 nM respectively in AGS and MKN45 cells[3].
APG-115 (0.02 uM, 0.2 uM; 48 hours) enhances the anti-proliferative effect of radiotherapy at different radiation dose[3].
APG-115 (0.02 uM, 0.2 uM; 48 hours) affects progression by inducing cells arrested at G0/G1 phase in AGS and MKN45 cell with wild p53[3].
APG-115 (0.02 uM, 0.2 uM; 24 hours) activates p53 to enhance radiosensitivity in AGS and MKN45 cells; stable knockout of p53 abrogates expression of MDM2, p53, p21, PUMA, BAX, Cleaved-caspase3, gammaH2AX[3].
APG-115 (0.3 uM, 1 uM, 3 uM, 10 uM; 24 hours) leads to a concentration-dependent cell cycle arrest in G2/M phases and a decreasing in S-phase in p53 wide-type cell lines (TPC-1, KTC-1)[4]. In Vivo: APG-115 (Delivered orally; 100 mg/kg; once daily; 10 days) enhances radiation antitumor effect in gastric adenocarcinoma in vivo[3].
Research Area
Cancer

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All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

Amount: 1mg
Available: In stock
available

Delivery expected until 9/6/2024 

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