Seco-Duocarmycin SASeco-Duocarmycin SA - High-quality laboratory reagent available from Gentaur. Catalog: 804-HY-129356.804-HY-129356804-HY-129356Business & Industrial > Science & LaboratorySeco-Duocarmycin SA
Gentaur
EUR12027-02-24

Seco-Duocarmycin SA

CAT:
804-HY-129356
Size:
1 Each
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
Seco-Duocarmycin SA - image 1

Seco-Duocarmycin SA

  • Description:

    Seco-Duocarmycin SA is a DNA alkylator. Seco-Duocarmycin SA is an antitumor antibiotic (IC50 = 10 pM) . Seco-Duocarmycin SA can induce a concentration-dependent increase in apoptotic cell death. Seco-Duocarmycin SA can lead to significant cell cycle arrest in S and G2/M phases. Seco-Duocarmycin SA acts as an ADC cytotoxin for antibody-drug conjugates[1][2][3].
  • UNSPSC:

    12352203
  • Target:

    ADC Payload; Antibiotic; Apoptosis; DNA Alkylator/Crosslinker
  • Type:

    ADC Related
  • Related Pathways:

    Antibody-drug Conjugate/ADC Related; Anti-infection; Apoptosis; Cell Cycle/DNA Damage
  • Applications:

    Cancer-programmed cell death
  • Field of Research:

    Cancer
  • Assay Protocol:

    https://www.medchemexpress.com/seco-duocarmycin-sa.html
  • Solubility:

    10 mM in DMSO
  • Smiles:

    O=C(C1=CC2=C3C(N(C(C(N4)=CC5=C4C(OC)=C(OC)C(OC)=C5)=O)CC3CCl)=CC(O)=C2N1)OC
  • Molecular Formula:

    C25H24ClN3O7
  • Molecular Weight:

    513.93
  • References & Citations:

    [1]Lutz F. Tietze, et al. A Concise and Efficient Synthesis of seco-Duocarmycin SA. European Journal of Organic Chemistry 2003 (3), 562-566.|[2]Morcos, A., et al., (2025) . Seco-Duocarmycin SA in Aggressive Glioblastoma Cell Lines. International journal of molecular sciences, 26 (6), 2766.|[3]Tichenor MS, et al. Systematic exploration of the structural features of yatakemycin impacting DNA alkylation and biological activity. J Am Chem Soc. 2007 Sep 5;129 (35) :10858-69.
  • Shipping Conditions:

    Room temperature
  • Scientific Category:

    ADC Related
  • Clinical Information:

    No Development Reported
  • Isoform:

    Duocarmycins
  • CAS Number:

    [144667-38-9]