Lenalidomide (hemihydrate)
Lenalidomide (hemihydrate)
CAS: 847871-99-2
Molecular Formula: C26H28N6O7
Lenalidomide (hemihydrate) - Names and Identifiers
| Name | Lenalidomide (hemihydrate) |
| Synonyms | CC-5013 hemihydrate LenalidoMide (heMihydrate) Lenalidomide (hemihydrate) Lenalidomide hemihydrate (Revlimid, CC 5013) |
| CAS | 847871-99-2 |
Lenalidomide (hemihydrate) - Physico-chemical Properties
| Molecular Formula | C26H28N6O7 |
| Molar Mass | 536.53652 |
| Solubility | 10 mM in DMSO |
| Storage Condition | -20℃ |
| In vitro study | Lenalidomide is potent in stimulating T cell proliferation and IFN-γ and IL-2 production. Lenalidomide has been shown to inhibit production of pro inflammatory cytokines TNF-α, IL-1, IL-6, IL-12 and elevate the production of anti-inflammatory cytokine IL-10 from human PBMCs. Lenalidomide downregulates the production of IL-6 directly and also by inhibiting multiple myeloma (MM) cells and bone marrow stromal cells (BMSC) interaction, which augments the apoptosis of myeloma cells. Dose-dependent interaction with the CRBN-DDB1 complex is observed with Thalidomide, Lenalidomide and Pomalidomide, with IC 50 values of ~30 μM, ~3 μM and ~3 μM, respectively, These reduced CRBN expression cells (U266-CRBN 60 and U266-CRBN 75 ) are less responsive than the parental cells to antiproliferative effects Lenalidomide across a dose-response range of 0.01 to 10 μM. Lenalidomide, a thalidomide analog, functions as a molecular glue between the human E3 ubiquitin ligase cereblon and CKIα is shown to induce the ubiquitination and degradation of this kinase, thus presumably killing leukemic cells by p53 activation. |
| In vivo study | The toxicity of Lenalidomide doses up to 15, 22.5, and 45 mg/kg via IV, IP, and PO routes of administration. Limited by solubility in our PBS dosing vehicle, these maximum achievable Lenalidomide doses are well tolerated with the exception of one mouse death (of four total dosed) at the 15 mg/kg IV dose. Notably, no other toxicities are observed in the study at IV doses of 15 mg/kg (n=3) or 10 mg/kg (n=45) or at any other dose level through IV, IP, and PO routes. |
Lenalidomide (hemihydrate) - Preparation solution concentration reference
| 1mg | 5mg | 10mg | |
|---|---|---|---|
| 1 mM | 3.728 ml | 18.638 ml | 37.276 ml |
| 5 mM | 0.746 ml | 3.728 ml | 7.455 ml |
| 10 mM | 0.373 ml | 1.864 ml | 3.728 ml |
| 5 mM | 0.075 ml | 0.373 ml | 0.746 ml |
Last Update：2024-01-02 23:10:35
Lenalidomide (hemihydrate) - Reference Information
| biological activity | lenlidomide hydrate (CC-5013 hemihydrate) is a derivative of alidomide and an orally active immunomodulator. Lenalidomide hemihydrate (CC-5013 hemihydrate) is a ligand for the ubiquitin E3 ligase cereblon (CRBN), two lymphatic transcription factors IKZF1 and IKZF3 were selectively ubiquitinated and degraded by CRBN-CRL4 ubiquitin ligase. Lenalidomide hydrate (CC-5013 hemihydrate) specifically inhibits the growth of mature B- cell lymphomas, including multiple myeloma, and induces the release of interleukin-2 from T cells (IL-2). |
Last Update：2024-04-10 22:29:15
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View History
Lenalidomide (hemihydrate)
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Z-3-氨基丁酸
对溴茴香醚
2-氨基-8-乙基-4-甲基-6-(1H-吡唑-3-基)吡啶并[2,3-D]嘧啶-7(8H)-酮
Nortriptyline Hydrochloride Impurity J as Hydrochloride
N-叔丁氧羰基-3-哌啶酮
CARBONIC ACID BIS(2-METHOXYPHENYL) ESTER
RS-4-氟苯甘氨酸甲酯盐酸盐
4-chlorocinnamic acid
METHYL (S)-2-AMINO-3,3-DIMETHYLBUTYRATE HYDROCHLORIDE
Z-3-氨基丁酸
对溴茴香醚