WEHI-539WEHI-539 - High-quality laboratory reagent available from Gentaur. Catalog: 804-HY-15607-01.804-HY-15607-01804-HY-15607-01Business & Industrial > Science & LaboratoryWEHI-539
Gentaur
EUR12027-02-24

WEHI-539

CAT:
804-HY-15607-01
Size:
1 mg
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
WEHI-539 - image 1

WEHI-539

  • Description:

    WEHI-539 is a selective inhibitor of Bcl-XL with an IC50 of 1.1 nM.
  • UNSPSC:

    12352005
  • Hazard Statement:

    H302, H312, H332
  • Target:

    Bcl-2 Family
  • Type:

    Reference compound
  • Related Pathways:

    Apoptosis
  • Applications:

    Cancer-programmed cell death
  • Field of Research:

    Cancer
  • Assay Protocol:

    https://www.medchemexpress.com/WEHI-539.html
  • Purity:

    95.05
  • Solubility:

    10 mM in DMSO
  • Smiles:

    OC(C1=C(CCCOC2=CC=C(CN)C=C2)SC(C3=CC4=C(CCC/C4=N\NC5=NC(C=CC=C6)=C6S5)C=C3)=N1)=O
  • Molecular Formula:

    C31H29N5O3S2
  • Molecular Weight:

    583.72
  • Precautions:

    H302, H312, H332
  • References & Citations:

    [1]Lessene G, et al. Structure-guided design of a selective BCL-X (L) inhibitor. Nat Chem Biol. 2013 Jun;9 (6) :390-7.|[2]Abed MN, et al. Antagonism of Bcl-XL is necessary for synergy between carboplatin and BH3 mimetics in ovarian cancer cells. J Ovarian Res. 2016 Apr 14;9:25.
  • Shipping Conditions:

    Room Temperature
  • Storage Conditions:

    -20°C, 3 years; 4°C, 2 years (Powder)
  • Scientific Category:

    Reference compound1
  • Clinical Information:

    No Development Reported
  • Isoform:

    Bcl-xL
  • Citation 01:

    Am J Cancer Res. 2019 Dec 1;9 (12) :2580-2598.|Breast Cancer Res Treat. 2019 Feb;173 (3) :585-596.|Cancer Biology. 2020 May.|Cell Death Differ. 2014 Jul;21 (7) :1170-7. |Cell Death Differ. 2017 Jan;24 (1) :111-119. |Cell Death Dis. 2017 Dec 13;8 (12) :3216.|Cell Death Dis. 2023 Oct 28;14 (10) :705.|Cell. 2014 Dec 18;159 (7) :1549-62.|Clin Cancer Res. 2019 Dec 1;25 (23) :7139-7150. |J Ovarian Res. 2016 Apr 14;9 (1) :25. |Nat Commun. 2016 Mar 9;7:10916.|Nature. 2017 Nov 9;551 (7679) :247-250. |Oncol Rep. 2019 Dec;42 (6) :2416-2425.|Pharmacol Res. 2023 Jan:187:106628.|Acta Pharmacol Sin. 2024 Nov;45 (11) :2420-2431.|bioRxiv. 2023 Aug 5.|Blood. 2014 Dec 4;124 (24) :3587-96. |Cell Death Dis. 2018 Jan 19;9 (2) :42.|Cell Rep. 2023 Mar 30;42 (4) :112324.|Cell. 2014 Dec 18;159 (7) :1549-62.|Immunity. 2024 Jun 11;57 (6) :1289-1305.e9.|Int J Cancer. 2018 Feb 1;142 (3) :584-596.|Malays Appl Biol. (2020) 49 (1) : 193-197.|Methods Mol Biol. 2018:1711:351-398.|Mol Cancer Ther. 2025 Jul 10.|Nat Biotechnol. 2018 Feb;36 (2) :179-189.|Nat Cancer. 2024 Jul;5 (7) :1082-1101.|Nat Chem Biol. 2022 Jun;18 (6) :615-624.|Nature. 2017 Nov 9;551 (7679) :247-250. |Oncotarget. 2018 May 25;9 (40) :26046-26063.|The Department of Medical Sciences, Harvard University. 2019 Dec.
  • CAS Number:

    [1431866-33-9]