Nomegestrol acetate

CAT:
804-HY-105634A-01
Size:
5 mg

For Laboratory Research Only. Not for Clinical or Personal Use.

  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
Nomegestrol acetate - image 1

Nomegestrol acetate

  • Description:

    Nomegestrol acetate is an orally active, highly selective progestogen and a progesterone receptor complete agonist. Nomegestrol acetate inhibits ovulation. Nomegestrol acetate is also effective in inhibiting the proliferation of human endometrial cancer RL95-2 cells in vitro and in vivo. Nomegestrol acetate can be used in cancer (especially endometrial cancer) and contraceptive studies[1][2][3].
  • UNSPSC:

    12352211
  • Hazard Statement:

    H361, H400
  • Target:

    Progesterone Receptor
  • Type:

    Reference compound
  • Related Pathways:

    Vitamin D Related/Nuclear Receptor
  • Applications:

    Neuroscience-Neuromodulation
  • Field of Research:

    Cancer; Endocrinology
  • Assay Protocol:

    https://www.medchemexpress.com/nomegestrol-acetate.html
  • Purity:

    99.73
  • Solubility:

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

    CC([C@@]1(OC(C)=O)CC[C@@]2([H])[C@]3([H])C=C(C)C4=CC(CC[C@]4([H])[C@@]3([H])CC[C@]12C)=O)=O
  • Molecular Formula:

    C23H30O4
  • Molecular Weight:

    370.48
  • Precautions:

    H361, H400
  • References & Citations:

    [1]Mueck AO, et al. Nomegestrol acetate, a novel progestogen for oral contraception. Steroids. 2011 May;76 (6) :531-9.|[2]Ma AY, et al. Nomegestrol Acetate Suppresses Human Endometrial Cancer RL95-2 Cells Proliferation In Vitro and In Vivo Possibly Related to Upregulating Expression of SUFU and Wnt7a. Int J Mol Sci. 2017 Jun 22;18 (7) :1337.|[3]van Diepen HA, et al. Nomegestrol acetate: steroid receptor transactivation profile in Chinese hamster ovary cells and ovulation inhibition in rat and monkey. Contraception. 2011 Aug;84 (2) :199-204.
  • Shipping Conditions:

    Room Temperature
  • Storage Conditions:

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

    Reference compound1
  • Clinical Information:

    Launched
  • CAS Number:

    58652-20-3