Lenalidomide

ArtNr	HY-A0003-5g
Hersteller	MedChem Express
CAS-Nr.	191732-72-6
Menge	5 g
Quantity options	100 mg 10 mM/1 mL 1 g 500 mg 5 g
Kategorie	Oncology Neuroscience Neuroinflammation Metabolism Diabetes Glucose Homeostasis Neural Development Inhibitors & Compound Libraries Small Molecules By Organ Heart & Blood Cancer Lymphatic System Cancer Bone Cancer
Typ	Inhibitors
Specific against	other
Purity	99.98
Citations	[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]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.\|[6]Nagashima, Takeyuki, et al. PHARMACEUTICAL COMPOSITION COMPRISING BICYCLIC NITROGEN-CONTAINING AROMATIC HETEROCYCLIC AMIDE COMPOUND AS ACTIVE INGREDIENT. Patent. 20170360780A1.\|[7]Krönke J, et al. Lenalidomide induces degradation of IKZF1 and IKZF3. Oncoimmunology. 2014 Jul 3;3(7):e941742. ACS Omega. 2024 Dec 3;9(50):49739-49748. ACS Pharmacol Transl Sci. 2021 Feb 26;4(2):941-952. Acta Pharmacol Sin. 2020 Sep;41(9):1246-1254. Acta Pharmacol Sin. 2025 Aug;46(8):2296-2309. Am J Pathol. 2015 Jun;185(6):1783-94. Biochim Biophys Acta Mol Basis Dis. 2022 Oct 1;1868(10):166472. Bioengineering (Basel). 2025 Oct 19;12(10):1121. bioRxiv. 2024 June 12. bioRxiv. 2024 October 19. bioRxiv. April. Cancer Cell. 2022 Nov 14;40(11):1294-1305.e4. Cancer Res. 2025 Jan 2;85(1):101-117. Cancer Sci. 2019 Dec;110(12):3802-3810. Cancers (Basel). 2024 Mar 28, 16(7), 1319. Cell Rep Med. 2024 Mar 19;5(3):101472. Cell Rep Med. 2025 Apr 2:102053. Cell Rep Methods. 2023 Oct 23;3(10):100599. Cell Rep. 2024 May 8;43(5):114211. Cell Syst. 2018 Apr 25;6(4):424-443.e7. Cell. 2018 Sep 20;175(1):171-185.e25. Chemrxiv. 2025 Nov 17. Clin Chim Acta. 2024 Jan 15:553:117707. Elife. 2018 Aug 1;7:e38430. Eur J Pharmacol. 2025 Dec 5:1008:178303. 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 Jul:203:86-101. Front Cell Infect Microbiol. 2022 Jul 28;12:954814. Harvard Medical School LINCS LIBRARY Harvard University. 2025. Inflammation. 2019 Feb;42(1):221-234. Int Immunopharmacol. 2025 May 14:158:114831. Int J Mol Sci. 2023 Sep 14;24(18):14097. iScience. 2022 Jul 19;25(8):104781. J Transl Med. 2024 Dec 3;22(1):1095. Leukemia. 2025 Mar;39(3):720-733. Microbiome. 2025 Feb 28;13(1):56. Mol Ther Oncol. 2025 Feb 20;33(1):200952. Nat Cancer. 2022 May;3(5):595-613. Nat Chem Biol. 2021 Jun;17(6):711-717. Nat Commun. 2017 May 22;8:15398. Nat Commun. 2025 Nov 6;16(1):9805. Nat Commun. 2025 Sep 1;16(1):8155. Nature. 2024 Sep;633(8030):670-677. Neoplasia. 2025 Oct 27:70:101243. Oncol Rep. 2018 Jun;39(6):2873-2880. Oxid Med Cell Longev. 2021 Dec 29:2021:8302831. Patent. US20170360780A1. Patent. US20180263995A1. Patent. US20210379039A1. Patent. US20220332776A1. Patent. US20240261246A1. Universidad de Navarra. 2024 Feb 28. University of Washington. The Columbian College of Arts and Sciences. August 31, 2021. Cell Commun Signal. 2025 May 7;23(1):216. Food Chem Toxicol. 2019 Mar:125:392-402.
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
Versandbedingung	Raumtemperatur
Lieferbar
Manufacturer - Type	Reference compound
Manufacturer - Applications	Cancer-Kinase/protease
Manufacturer - Category	Reference compound / Active compounds; API
Manufacturer - Targets	Apoptosis; Ligands for E3 Ligase; Molecular Glues
Manufacturer - HS Code	H361, H373
Shipping Temperature	Room Temperature
Storage Conditions	-20°C, 3 years; 4°C, 2 years (Powder)
Molecular Weight	259.26
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].
Manufacturer - Research Area	Cancer; Inflammation/Immunology
Solubility	DMSO : 100 mg/mL (ultrasonic)
Manufacturer - Pathway	Apoptosis; PROTAC
Clinical information	Launched
Isoform	Cereblon
UNSPSC Code	12352005
Precautionary	H361, H373

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