AV-412

CAT:
804-HY-10346-01
Size:
5 mg
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
AV-412 - image 1

AV-412

  • Description :

    AV-412 (MP412) is an EGFR inhibitor with IC50s of 0.75, 0.5, 0.79, 2.3, 19 nM for EGFR, EGFRL858R, EGFRT790M, EGFRL858R/T790M and ErbB2, respectively.
  • Product Name Alternative :

    MP412
  • UNSPSC :

    12352005
  • Hazard Statement :

    H302, H315, H319, H335
  • Target :

    EGFR
  • Type :

    Reference compound
  • Related Pathways :

    JAK/STAT Signaling; Protein Tyrosine Kinase/RTK
  • Applications :

    Cancer-Kinase/protease
  • Field of Research :

    Cancer
  • Assay Protocol :

    https://www.medchemexpress.com/AV-412.html
  • Concentration :

    10mM
  • Purity :

    99.17
  • Solubility :

    DMSO : ≥ 28 mg/mL
  • Smiles :

    O=S(C1=CC=C(C)C=C1)(O)=O.C=CC(NC2=CC3=C(NC4=CC=C(F)C(Cl)=C4)N=CN=C3C=C2C#CC(N5CCN(C)CC5)(C)C)=O.O=S(C6=CC=C(C)C=C6)(O)=O
  • Molecular Formula :

    C41H44ClFN6O7S2
  • Molecular Weight :

    851.41
  • Precautions :

    H302, H315, H319, H335
  • References & Citations :

    [1]Suzuki T, et al. Pharmacological characterization of MP-412 (AV-412), a dual epidermal growth factor receptorand ErbB2 tyrosine kinase inhibitor. Cancer Sci. 2007 Dec;98 (12) :1977-84.
  • Shipping Conditions :

    Room Temperature
  • Storage Conditions :

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

    Reference compound1
  • Clinical Information :

    Phase 1
  • Isoform :

    EGFR/ErbB1/HER1; ErbB2/HER2
  • Citation 01 :

    Cancer Med. 2024 May;13 (10) :e7083.|Nature. 2025 Nov 26.|Proc Natl Acad Sci U S A. 2019 Feb 19;116 (8) :2996-3005. |Sci Data. 2024 Sep 19;11 (1) :1024.|Science. 2017 Dec 1;358 (6367) :eaan4368.
  • CAS Number :

    [451493-31-5]

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