Nilotinib (monohydrochloride monohydrate)

CAT:
804-HY-10159A-01
Size:
100 mg

For Laboratory Research Only. Not for Clinical or Personal Use.

  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
Nilotinib (monohydrochloride monohydrate) - image 1

Nilotinib (monohydrochloride monohydrate)

  • UNSPSC Description:

    Nilotinib monohydrochloride monohydrate is a second generation tyrosine kinase inhibitor (TKI), is significantly potent against BCR-ABL, and is active against many BCR-ABL mutants.
  • Target Antigen:

    Autophagy; Bcr-Abl
  • Type:

    Reference compound
  • Related Pathways:

    Autophagy;Protein Tyrosine Kinase/RTK
  • Applications:

    Cancer-Kinase/protease
  • Field of Research:

    Cancer
  • Assay Protocol:

    https://www.medchemexpress.com/Nilotinib-monohydrochloride-monohydrate.html
  • Purity:

    99.97
  • Solubility:

    DMSO : 33.33 mg/mL (ultrasonic)|H2O : < 0.1 mg/mL (ultrasonic)
  • Smiles:

    O=C(NC1=CC(C(F)(F)F)=CC(N2C=NC(C)=C2)=C1)C3=CC=C(C)C(NC4=NC=CC(C5=CC=CN=C5)=N4)=C3.[H]Cl.O
  • Molecular Weight:

    583.99
  • References & Citations:

    [1]Weisberg E, et al. Beneficial effects of combining nilotinib and imatinib in preclinical models of BCR-ABL+ leukemias. Blood. 2007 Mar 1;109(5):2112-20.|[2]Sako H, et al. Antitumor effect of the tyrosine kinase inhibitor Nilotinib on gastrointestinal stromal tumor (GIST) and Imatinib-resistant GIST cells. PLoS One. 2014 Sep 15;9(9):e107613.|[3]Dervis Hakim G, et al. Mucosal healing effect of nilotinib in indomethacin-induced enterocolitis: A rat model. World J Gastroenterol. 2015 Nov 28;21(44):12576-85.bioRxiv. January 25, 2022.|Cell Rep Methods. 2023 Oct 23;3(10):100599.|Drug Metab Pharmacokinet. 2020 Feb;35(1):102-110.|ACS Chem Biol. 2016 Apr 15;11(4):992-1000.|Biomaterials. 16 September 2022.|Biomed Chromatogr. 2019 Dec;33(12):e4674.|Biomolecules. 2022 Jun 11;12(6):819.|bioRxiv. 2024 May 8:2024.05.07.592424.|Br J Cancer. 2021 Nov 24.|Breast Cancer Res. 2023 May 5;25(1):51.|Cancer Biol Ther. 2019;20(6):877-885.|Cancer Lett. 2024 Aug 1:217150.|Cancer Med. 2016 Nov;5(11):3223-3234.|Cancer Res. 2024 Oct 22.|Cell Death Dis. 2021 Sep 25;12(10):875.|Cell Mol Immunol. 2024 Aug;21(8):856-872.|Cell Syst. 2018 Apr 25;6(4):424-443.e7.|Diseases. 2023 Oct 23;11(4):147.|Eur J Pharmacol. 2021 Feb 10;173944.|Glia. 2022 Feb 13.|Harvard Medical School LINCS LIBRARY|Int J Mass Spectrom. 442 (2019) 44-50.|J Pharm Sci. 2017 Sep;106(9):2632-2641.|Leuk Lymphoma. 2015;56(8):2416-23. |Oncotarget. 2018 Apr 24;9(31):22158-22183. |Patent. US20190084960A1|Patent. US20210299273A1.|Sci Transl Med. 2018 Jul 18;10(450):eaaq1093.|Stem Cell Reports. 2019 May 14;12(5):996-1006. |Target Oncol. 2020 Oct;15(5):659-671.|Technical University of Munich. 24.01.2018.|Toxicol Lett. 2022 Jun 6;S0378-4274(22)00117-5.|Toxicology. 2024 May 15:505:153830.|Xenobiotica. 2018 Oct;48(10):1059-1071.
  • Shipping Conditions:

    Room Temperature
  • Storage Conditions:

    4°C (Powder, sealed storage, away from moisture)
  • Clinical Information:

    Launched
  • CAS Number:

    923288-90-8