research use only
Cat.No.S1029
| Related Targets | Proteasome E1 Activating E3 Ligase DUB SUMO p97 E2 conjugating |
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| Other E3 ligase Ligand Inhibitors | CC-99282 |
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In vitro |
DMSO
: 51 mg/mL
(196.71 mM)
Water : Insoluble Ethanol : Insoluble The solubility data above are all experimental results (not literature values). |
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In vivo |
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Step 1: Enter information below (Recommended: An additional animal making an allowance for loss during the experiment)
Step 2: Enter the in vivo formulation (This is only the calculator, not formulation. Please contact us first if there is no in vivo formulation at the solubility Section.)
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
Read more about CC-5013 (Lenalidomide) working concentrations for cell culture treatment
| 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. |
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Read more about CC-5013 (Lenalidomide) IC50 for cell-based and cell-free assays |
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| Primary Applications and Mechanism of Action | |
| Molecular Weight | 259.26 | Formula | C13H13N3O3 |
Storage (From the date of receipt) | |
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| CAS No. | 191732-72-6 | Download SDF | Storage of Stock Solutions |
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| Synonyms | CC-5013 | Smiles | C1CC(=O)NC(=O)C1N2CC3=C(C2=O)C=CC=C3N | ||
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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.