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