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Lenalidomide

Lenalidomide

€72.00

Excl. VAT

Item no.	HY-A0003-10mM
Manufacturer	MedChem Express
CASRN	191732-72-6
Amount	10 mM/1 mL
Category	Oncology Neuroscience Neuroinflammation Metabolism Diabetes Glucose Homeostasis Neural Development Inhibitors & Compound Libraries Small Molecules By Organ Heart & Blood Cancer Lymphatic System Cancer Bone Cancer
Type	Inhibitors
Clone	N/A
Specific against	other
Purity	99.98
Formula	C13H13N3O3
Citations	ACS Pharmacol Transl Sci. 2021 Feb 26. Acta Pharmacol Sin. 2020 Sep;41(9):1246-1254. Am J Pathol. 2015 Jun;185(6):1783-94. Biochim Biophys Acta Mol Basis Dis. 2022 Jun 22;166472. bioRxiv. April. Cancer Cell. 2022 Aug 26;S1535-6108(22)00372-5. Cancer Sci. 2019 Dec;110(12):3802-3810. Cell Syst. 2018 Apr 25;6(4):424-443.e7. Cell. 2018 Sep 20;175(1):171-185.e25. Clin Chim Acta. 2023 Dec 14:117707. Elife. 2018 Aug 1;7:e38430. Exp Cell Res. 2020 Aug 1;393(1):112054. Faculty of Science, Masaryk University. Department of Experimental Biology.2014. Food Chem Toxicol. 2019 Mar;125:392-402. Free Radic Biol Med. 2023 Apr 10;S0891-5849(23)00373-8. Front Cell Infect Microbiol. 2022 Jul 28;12:954814. Harvard Medical School LINCS LIBRARY Inflammation. 2019 Feb;42(1):221-234. Int J Mol Sci. 2023 Sep 14, 24(18), 14097. iScience. 19 July 2022, 104781. Nat Cancer. 2022 May;3(5):595-613. Nat Chem Biol. 2021 Jun;17(6):711-717. Nat Commun. 2017 May 22;8:15398. Oncol Rep. 2018 Jun;39(6):2873-2880. Oxid Med Cell Longev. 29 Dec 2021. Patent. US20170360780A1. Patent. US20180263995A1. Patent. US20210379039A1. Patent. US20220332776A1. University of Washington. The Columbian College of Arts and Sciences. August 31, 2021. Food Chem Toxicol. 2019 Mar;125:392-402. [1]Omran A, et al. Effects of MRP8, LPS, and lenalidomide on the expressions of TNF-α , brain-enriched, and inflammation-related microRNAs in the primary astrocyte culture. ScientificWorldJournal. 2013 Sep 21;2013:208309. [2]Kotla V, et al. Mechanism of action of lenalidomide in hematological malignancies. J Hematol Oncol. 2009 Aug 12;2:36. [3]Lopez-Girona A, et al. Cereblon is a direct protein target for immunomodulatory and antiproliferative activities of lenalidomide and pomalidomide. Leukemia. 2012 Nov;26(11):2326-35. [4]Rozewski DM, et al. Pharmacokinetics and tissue disposition of lenalidomide in mice. AAPS J. 2012 Dec;14(4):872-82. [5]Nagashima, Takeyuki, et al. PHARMACEUTICAL COMPOSITION COMPRISING BICYCLIC NITROGEN-CONTAINING AROMATIC HETEROCYCLIC AMIDE COMPOUND AS ACTIVE INGREDIENT. Patent. 20170360780A1. [6]Minzel W, et al. Small Molecules Co-targeting CKIα and the Transcriptional Kinases CDK7/9 Control AML in Preclinical Models. Cell. 2018 Sep 20;175(1):171-185.e25. [7]Krönke J, et al. Lenalidomide induces degradation of IKZF1 and IKZF3. Oncoimmunology. 2014 Jul 3;3(7):e941742.
Smiles	O=C1C2=CC=CC(N)=C2CN1C(C(N3)=O)CCC3=O
ECLASS 10.1	32160490
ECLASS 11.0	32160490
UNSPSC	12000000
Alias	CC-5013
Available
Product Description	Lenalidomide (CC-5013), a derivative of Thalidomide, acts as molecular glue. Lenalidomide is an orally active immunomodulator. 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 (CC-5013) specifically inhibits growth of mature B-cell lymphomas, including multiple myeloma, and induces IL-2 release from T cells[1][2].
StorageTemperature	-20°C, 3 years; 4°C, 2 years (Powder)
Shipping	Room Temperature
Manufacturers Applications	Cancer-Kinase/protease
Molecular Weight	259.26062
Clinical Information	Launched
Solubility	DMSO : 100 mg/mL (ultrasonic)
Isoform	Cereblon
Pathway	Apoptosis; PROTAC
Manufacturers Product type	Reference compound

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HY-A0003-10mM-safety-datasheet.pdf