V-9302

CAT:
804-HY-112683-01
Size:
5 mg
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
V-9302 - image 1

V-9302

  • Description :

    V-9302 is a competitive antagonist of transmembrane glutamine flux. V-9302 selectively and potently targets the amino acid transporter ASCT2 (SLC1A5) not ASCT1. V-9302 inhibits ASCT2-mediated glutamine uptake (IC50=9.6 μM) in HEK-293 cells[1].
  • UNSPSC :

    12352005
  • Target :

    ASCT
  • Type :

    Reference compound
  • Related Pathways :

    Membrane Transporter/Ion Channel
  • Applications :

    Cancer-programmed cell death
  • Field of Research :

    Cancer
  • Assay Protocol :

    https://www.medchemexpress.com/v-9302.html
  • Purity :

    99.46
  • Solubility :

    DMSO : 25 mg/mL (ultrasonic; warming; heat to 80°C) |H2O : < 0.1 mg/mL (ultrasonic)
  • Smiles :

    O=C(O)[C@@H](N)CCN(CC1=CC=CC=C1OCC2=CC=CC(C)=C2)CC3=CC=CC=C3OCC4=CC=CC(C)=C4
  • Molecular Formula :

    C34H38N2O4
  • Molecular Weight :

    538.68
  • References & Citations :

    [1]Schulte ML, et al. Pharmacological blockade of ASCT2-dependent glutamine transport leads to antitumor efficacyin preclinical models. Nat Med. 2018 Feb;24 (2) :194-202.|[2]Jin H, et al. A powerful drug combination strategy targeting glutamine addiction for the treatment of human liver cancer. Elife. 2020;9:e56749. Published 2020 Oct 5.|[3]Edwards DN, et al. Selective glutamine metabolism inhibition in tumor cells improves antitumor T lymphocyte activity in triple-negative breast cancer. J Clin Invest. 2021;131 (4) :e140100.
  • Shipping Conditions :

    Room Temperature
  • Storage Conditions :

    4°C (Powder, sealed storage, away from moisture)
  • Scientific Category :

    Reference compound1
  • Clinical Information :

    No Development Reported
  • Isoform :

    ASCT2
  • Citation 01 :

    Adv Sci (Weinh) . 2024 Dec 16:e2411479.|Adv Sci (Weinh) . 2025 Aug 10:e07057.|Autophagy. 2025 Jul 23:1-16.|Biomaterials. 2025 Sep 17:326:123726.|bioRxiv. 2024 July 05.|bioRxiv. 2025 Jul 31:2025.07.28.667320.|Cell Death Dis. 2024 Feb 5;15 (2) :111.|Cell Metab. 2022 Dec 6;34 (12) :1999-2017.e10.|Cell. 2024 Oct 31;187 (22) :6251-6271.e20.|FASEB J. 2025 Jul 15;39 (13) :e70774.|Front Pharmacol. 2021 May 14;12:671328.|J Biol Chem. 2022 Apr;298 (4) :101753.|J Control Release. 2023 May:357:460-471.|J Gastroenterol. 2025 Oct 8.|J Virol. 2025 Nov 25;99 (11) :e0098525.|Magn Reson Imaging. 2022 Nov:93:189-194.|Nano Today. 2025 Apr.|Nat Immunol. 2024 Oct;25 (10) :1845-1857.|Npj Imaging. 2025 Aug 1;3 (1) :34.|Pharmaceutics. 2024 Jun 29;16 (7) :877.|Proc Natl Acad Sci U S A. 2024 Mar 26;121 (13) :e2319429121.|University of Maryland. 2024.|University of Regensburg. 2024 Jul 18.|Biochem Pharmacol. 2025 Feb 7:116796.|Biochem Pharmacol. 2025 Jun 7:117047.|J Nanobiotechnology. 2022 May 6;20 (1) :216.|Research Square Print. 2023 Jan 31.
  • CAS Number :

    [1855871-76-9]

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