RO4929097

SKU: orb1300914

Description

RO4929097

Research Area

Neuroscience, Protein Biochemistry, Stem Cell & Developmental Biology

Key Properties

• CAS Number: 847925-91-1
• MW: 469.4
• Purity: 98.50%
• Formula: C₂₂H₂₀F₅N₃O₃
• SMILES: CC(C)(C(=O)NCC(F)(F)C(F)(F)F)C(=O)N[C@H]1c2ccccc2-c2ccccc2NC1=O
• Target: Gamma-secretase,Beta Amyloid
• Solubility: H2O:Insoluble;10% DMSO+40% PEG300+5% Tween 80+45% Saline:3.3 mg/mL (7.03 mM);Ethanol:13 mg/mL (27.69 mM);DMSO:122.5 mg/mL (260.97 mM)

Bioactivity

• Target IC50:
  γ-secretase:4 nM|Notch:5 nM (EC50)|β-Amyloid (1-40):14 nM (EC50)
• In Vivo:
  Oral injection of 3 to 60 mg/kg RO4929097 once daily or twice daily to nude mice bearing A549 NSCLC xenografts for either 7, 14, or 21 days of a 21-day schedule results in significant tumor growth Inhibition compared with Vehicle-treated animals the tumor growth Inhibition Values ranges from 66% to 91%. When mice are treated with 60 mg/kg RO4929097 twice daily wit the 7+/14- schedule, treatment initially arouses regression of established A549 tumors. At the end of the 21-day cycle (day 47), tumor growth prevention is still 91% compared with Vehicle control mice. Inhibition of tumor growth remains prolonged and sustained up to 34 days post-treatment (day 67). On day 67, these mice are retreated wit the same dose of RO4929097 for a second cycle (7 days) until day 74. Importantly the antitumor effects are sustained after dosing is completed. RO4929097 leads to reduced expression of genes associated with angiogenesis in A549 xenograft model. In contrast the RO4929097-resistant H460a xenograft displays little change in expression of these genes, underscorin the in vivo anti-angiogenesis mechanism of action of RO4929097 For IL6 and IL8 overexpressing tumors, RO4929097 no longer impacts angiogenesis o the infiltration of tumor associated fibroblasts.
• In Vitro:
  RO4929097 strongly inhibited γ-secretase enzyme activity with a 4 nMol/L potency IC50 . Treatment of cells caused a dose-dependent decrease in the amount of Aβ peptides secreted int the culture medium (EC50, 14 nMol/L) the potent in vitro activity of RO4929097 translated into strong dose-dependent Inhibition of Notch processing in the Notch cell-based Reporter assay (EC50, 5 nMol/L) the potency of RO4929097 in cell-free and cellular assays was in the low nanomolar range with >100-fold selectivity observed with respect to 75 Other proteins of various types including receptors, ion channels, and enzymes. RO4929097 downregulate the Notch target genes Hes1, Hey1, and HeyL, and showed a significant reduction in anchorage-independent growth in SUM190 and SUM149. however the putative self-renewal assay mammosphere formation efficiency was increased wit the drug. in the conventional 2D clonogenic assay, RO4929097 (1 μM) significantly sensitized SUM190 cells to ionizing radiation and has a modest radiosensitization effect in SUM149 cells. In human Primary melanoma cell lines, RO4929097 decrease the levels of NOTCH transcriptional target HES1. This was accompanied by reduced proliferation and impaired ability to form colonies in soft agar and to organize in tridimensional spheres.
• Cell Research:
  Monolayer cultures of both IBC cell lines were trypsinized into Single cells and were seeded into individual wells of a 6-well tissue culture plate (for 2D) or ultralow attachment plates (for 3D, 20,000 cells/ml) in the presence or absence of 1 μM RO4929097. the The 2D and 3D 6-well plates containing seeded Single cells were exposed to increasing doses of irradiation (0, 2, 4, or 6 Gy) 4 hrs after plating. however, SUM149 2D monolayer cells were also pre-treated with 1 μM RO4929097 or Vehicle for 24 hours to see if cell contact had an effect. 2D plates were incubated for 14 days and colonies were stained with crystal violet while 3D cells were incubated in mammosphere media for 7 days the spheres were assessed for proliferation usin the MTT assay and those with a size of 50 μM were counted using a Gelcount colony counter. For secondary mammosphere assay, cells from Primary mammospheres were dispersed with 0.05% trypsin, seeded in 6-well ultra-low attachment plates (10,000 cells/ml) in mammosphere media and counted after a week. Survival curves were generated using Sigmaplot 8.0.
• Animal Research:
  RO4929097 was formulated as a suspension in 1.0% Klucel in water with 0.2% Tween 80 for oral administration. RO4929097-treated mice were orally dosed with suspensions at 3 to 60 mg/kg RO4929097 according to the indicated regimens. In the Calu-6 xenograft model, RO4929097 was dosed at 60 mg/kg/d every other week for 4 weeks (7 days on/7 days off × 2 cycles). For all other xenograft models, RO4929097 was dosed once daily at 10 mg/kg for 21 days. Statistical analysis was determined by Mann-Whitney rank-sum test, one-way ANOVA, and post hoc Bonferroni t-test. Differences between groups were considered significant when P ≤ 0.05. A549 tumors from vehicle-treated and selected RO4929097-treated groups were collected and fixed in 10% zinc-formalin overnight, processed, paraffin-embedded, sectioned at 5 μm, and stained with H&E for histopathology assessment. An Olympus BX51 microscope (with a ×10 objective) mounted with a Nikon DS-Fi1 using the NIS-Elements F2.20 program collected the histology pictures. For Western blot analysis, three A549 tumors from each group, after 7 days (60 mg/kg) or 21 days (3 and 30 mg/kg), were flash-frozen. Collagen type V was detected using the H-200 antibody at a dilution of 1:1,000, and MFAP5 was detected using the antibody at a dilution of 1:1,000.

Storage & Handling

• Storage: Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
• Disclaimer: For research use only

Alternative Names

Beta Amyloid, BetaAmyloid, bAmyloid, b Amyloid, Aβ40, Notch, inhibit, Inhibitor, Gamma secretase, Gammasecretase, RG 4733, RG4733, RG-4733, RO 4929097, RO4929097, RO-4929097, γ secretase, γ-secretase, βAmyloid, β Amyloid

Compound Identifiers

PubChem CID

49867930