Ro 0437626

CAT:
804-HY-108673
Size:
1 Each
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
Ro 0437626 - image 1

Ro 0437626

  • Description:

    Ro 0437626 is a selective purinergic (P2X1) receptor antagonist (IC50 = 3 μM), but shows low affinity for P2X2, P2X3 and P2X2/3 receptors (IC50 > 100 μM) [1].
  • UNSPSC:

    12352005
  • Target:

    P2X Receptor
  • Type:

    Reference compound
  • Related Pathways:

    Membrane Transporter/Ion Channel
  • Applications:

    Cancer-programmed cell death
  • Field of Research:

    Cancer
  • Assay Protocol:

    https://www.medchemexpress.com/ro-0437626.html
  • Solubility:

    10 mM in DMSO
  • Smiles:

    O=C(C1=NC2=CC=CC=C2N1)N[C@H](CC3=CSC=N3)C(N[C@@H](CC4CCCCC4)[C@@H](O)[C@H](C5CC5)O)=O
  • Molecular Formula:

    C27H35N5O4S
  • Molecular Weight:

    525.66
  • References & Citations:

    [1]Jaime-Figueroa S, et al. Discovery and synthesis of a novel and selective drug-like P2X (1) antagonist. Bioorg Med Chem Lett. 2005;15 (13) :3292-3295.|[2]Harper MT, et al. Phorbol ester-evoked Ca2+ signaling in human platelets is via autocrine activation of P (2X1) receptors, not a novel non-capacitative Ca2+ entry. J Thromb Haemost. 2010;8 (7) :1604-1613.|[3]King BF, et al. Investigation of the effects of P2 purinoceptor ligands on the micturition reflex in female urethane-anaesthetized rats. Br J Pharmacol. 2004;142 (3) :519-530.
  • Shipping Conditions:

    Room temperature
  • Scientific Category:

    Reference compound1
  • Clinical Information:

    No Development Reported
  • Isoform:

    P2X1 Receptor
  • CAS Number:

    [134362-79-1]