CAS No. 413611-93-5

Batch: Purity:99.44
10074-G5 Chemical Structure
Chemical Structure
Check the 10074-G5 product page for in-depth specifications, including solubility, stock solutions, MOA, and working concentrations.

Chemical Information

IUPAC Name 4-nitro-N-(2-phenylphenyl)-2,1,3-benzoxadiazol-7-amine
CAS Number 413611-93-5
Molecular Formula

C18H12N4O3

Molecular Weight (MW) 332.31
SMILES C1=CC=C(C=C1)C2=CC=CC=C2NC3=CC=C(C4=NON=C34)[N+](=O)[O-]
InChIKey KMJPYSQOCBYMCF-UHFFFAOYSA-N

Ordering Information

Biological Activity

10074-G5 is a c-Myc inhibitor that binds to the bHLH-ZIP domain of c-Myc (Kd 2.8 µM) and inhibits c-Myc/Max transcriptional activity (IC50 146 µM). By disrupting c-Myc/Max heterodimer formation, 10074-G5 impairs c-Myc-driven transcriptional programs. Disruption of c-Myc pathway signaling leads to reduced cellular proliferation and the suppression of oncogenic phenotypes in c-Myc-dependent tumor cells.

How to Prepare Stock Solution?

Concentration Volume Mass
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Solubility

Batch:
All in vitro solubility values are batch-tested experimental data (non-literature values).
Solvent Solubility & Note
DMSO 66 mg/mL (198.6 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO. The recommended stock concentration is 10 mM in DMSO.)
Ethanol 8 mg/mL
Water Insoluble
FAQ
Q: Why does a DMSO stock precipitate in media/saline?
A: It is caused by unheated aqueous media (supersaturation), local solvent shock, or incorrect mixing sequence.
How to fix it?
  • Preheat media/saline to 37°C.
  • Mix rapidly (pipette/vortex) upon addition.
  • For complex mixes, always add the aqueous phase last.
  • Re-dissolve minor precipitates with a 37°C water bath and sonication (≤30 min).

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Note: Technical data last updated: Sep 1, 2026.