Vatalanib

CAT:
804-HY-10203-01
Size:
5 mg
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
Vatalanib - image 1

Vatalanib

  • Description:

    Vatalanib (PTK787; ZK-222584; CGP-79787) is an inhibitor of VEGFR2/KDR with IC50 of 37 nM.
  • Product Name Alternative:

    PTK787; ZK-222584; CGP-79787
  • UNSPSC:

    12352005
  • Hazard Statement:

    H315, H319, H335
  • Target:

    VEGFR
  • Type:

    Reference compound
  • Related Pathways:

    Protein Tyrosine Kinase/RTK
  • Applications:

    Cancer-Kinase/protease
  • Field of Research:

    Cancer
  • Assay Protocol:

    https://www.medchemexpress.com/vatalanib.html
  • Purity:

    99.93
  • Solubility:

    DMSO : 62.5 mg/mL (ultrasonic)
  • Smiles:

    ClC1=CC=C(C=C1)NC2=NN=C(CC3=CC=NC=C3)C4=C2C=CC=C4
  • Molecular Formula:

    C20H15ClN4
  • Molecular Weight:

    346.81
  • Precautions:

    H315, H319, H335
  • References & Citations:

    [1]Wood JM, et al. PTK787/ZK 222584, a novel and potent inhibitor of vascular endothelial growth factor receptor tyrosine kinases, impairs vascular endothelial growth factor-induced responses and tumor growth after oral administration. Cancer Res. 2000, 60 (8|[2]Murakami M, et al. Tyrosine kinase inhibitor PTK/ZK enhances the antitumor effects of interferon-α/5-fluorouracil therapy for hepatocellular carcinoma cells. Ann Surg Oncol. 2011, 18 (2), 589-596.|[3]Wan J, et al. Local recurrence of small cell lung cancer following radiofrequency ablation is induced by HIF-1α expression in the transition zone. Oncol Rep. 2016 Mar;35 (3) :1297-308.
  • Shipping Conditions:

    Room Temperature
  • Storage Conditions:

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

    Reference compound1
  • Clinical Information:

    Phase 3
  • Isoform:

    VEGFR2/KDR/Flk-1
  • Citation 01:

    Drug Metab Pharmacokinet. 2017 Jun;32 (3) :179-188. |Int J Mol Sci. 2024 Nov 15;25 (22) :12277.|J Microbiol Biotechnol. 2015 Aug;25 (8) :1227-33. |J Pharm Anal. 2024 Jan;14 (1) :100-114.|Mutat Res. 2025 Sep 24:831:111916.|Patent. US20170349880A1.|Bioact Mater. 2022 Jan 2:15:131-144.|Br J Pharmacol. 2019 Sep;176 (17) :3143-3160. |Evid Based Complement Alternat Med. 2021 Apr 26:2021:5543259.|JCI Insight. 2024 May 22;9 (10) :e166402.|Kitasato University. Kitasato University. 2017.|Oncol Rep. 2016 Mar;35 (3) :1297-308.|Oxid Med Cell Longev. 2022 Jul 18:2022:2232365.|Sci Transl Med. 2018 Jul 18;10 (450) :eaaq1093.|Ulm University. 2023 Mar 21.
  • CAS Number:

    [212141-54-3]