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CC-5013 (Lenalidomide) Immunomodulator

Cat.No.S1029

Lenalidomide is a TNF-α secretion inhibitor with IC50 of 13 nM in PBMCs. Lenalidomide (CC-5013) is a ligand of ubiquitin E3 ligase cereblon (CRBN), and it causes selective ubiquitination and degradation of two lymphoid transcription factors, IKZF1 and IKZF3, by the CRBN-CRL4 ubiquitin ligase. Lenalidomide promotes cleaved caspase-3 expression and inhibit VEGF expression and induces apoptosis.
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Quality Control

Batch: Purity: 99.97%
99.97

Solubility in DMSO or Water

In vitro
Batch:

DMSO : 51 mg/mL (196.71 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO.)

Water : Insoluble

Ethanol : Insoluble

The solubility data above are all experimental results (not literature values).

Molarity Calculator

Mass Concentration Volume Molecular Weight
Dilution Calculator Molecular Weight Calculator

In vivo
Batch:

In vivo Formulation Calculator (Clear solution)

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Calculation results:

Working concentration: mg/ml;

Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

Note: 1. Please make sure the liquid is clear before adding the next solvent.
2. Be sure to add the solvent(s) in order. You must ensure that the solution obtained, in the previous addition, is a clear solution before proceeding to add the next solvent. Physical methods such
as vortex, ultrasound or hot water bath can be used to aid dissolving.

Read more about CC-5013 (Lenalidomide) solubility in DMSO or water

Working Concentrations for Cell Culture Treatment

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Mechanism of Action

Information CC-5013 (Lenalidomide) is a potent immunomodulatory CRBN E3 ligase modulator. It affects NF-κB, ERK, and MYC signaling pathways, by inducing CRBN-dependent ubiquitination and proteasomal degradation of IKZF1/3 and CK1α, inhibiting tumor proliferation and promoting NK/T cell-mediated cytotoxicity.

Read more about CC-5013 (Lenalidomide) IC50 for cell-based and cell-free assays

Primary Applications and Mechanism of Action

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Chemical Information, Storage & Stability

Molecular Weight 259.26 Formula

C13H13N3O3

Storage (From the date of receipt)
CAS No. 191732-72-6 Download SDF Storage of Stock Solutions

Synonyms CC-5013 Smiles C1CC(=O)NC(=O)C1N2CC3=C(C2=O)C=CC=C3N

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Read more comparative analysis about CC-5013 (Lenalidomide)

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Handling Instructions

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Frequently Asked Questions

Question 1:
What is the formulation for its injection (i.p.) in mice?

Answer:
This paper has the information you need: http://link.springer.com/article/10.1208/s12248-012-9401-2. Add it to the appropriate volume of sterile phosphate-buffered saline (PBS) containing 1% hydrochloric acid (HCl). The pH of this preparation was adjusted to 7.0–7.6 using sodium hydroxide and sterile filtered using a 0.22 μm Steriflip filter.

Question 2:
what is the procedure to resuspend it?

Answer:
This compound can be resuspended by DMSO, with a solubility of about 52 mg/mL (200.57 mM). For in vivo study, the working solution can be prepared with the vehicle of: 30% PEG400/0.5% Tween80/5% propylene glycol for oral administration.