Fenhexamid-d10Fenhexamid-d10 - High-quality laboratory reagent available from Gentaur. Catalog: 804-HY-W701943-01.804-HY-W701943-01804-HY-W701943-01Business & Industrial > Science & LaboratoryFenhexamid-d10
Gentaur
EUR12027-02-19

Fenhexamid-d10

CAT:
804-HY-W701943-01
Size:
1 mg
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
Fenhexamid-d10 - image 1

Fenhexamid-d10

  • Description:

    Fenhexamid-d10 is the deuterium labeled Fenhexamid (HY-118065) . Fenhexamid, a botryticide, is a sterol biosynthesis inhibitor. Fenhexamid shows fungicide efficient against the plant pathogenic fungus Botryotinia fuckeliana (Botrytis cinerea) [1].
  • UNSPSC:

    12352005
  • Target:

    Estrogen Receptor/ERR; Fungal; Isotope-Labeled Compounds; PI3K
  • Related Pathways:

    Anti-infection; Others; PI3K/Akt/mTOR; Vitamin D Related/Nuclear Receptor
  • Field of Research:

    Cancer
  • Smiles:

    OC1=CC=C(C(Cl)=C1Cl)NC(C2(C([2H])(C([2H])(C([2H])(C([2H])(C2([2H])[2H])[2H])[2H])[2H])[2H])C)=O
  • Molecular Formula:

    C14H7D10Cl2NO2
  • Molecular Weight:

    312.26
  • References & Citations:

    [1]Debieu D, et al. The hydroxyanilide fenhexamid, a new sterol biosynthesis inhibitor fungicide efficient against the plant pathogenic fungus Botryotinia fuckeliana (Botrytis cinerea) . Pest Manag Sci. 2001 Nov;57 (11) :1060-7.|[2]Go RE, et al., Effect of fenhexamid and cyprodinil on the expression of cell cycle- and metastasis-related genes via an estrogen receptor-dependent pathway in cellular and xenografted ovarian cancer models. Toxicol Appl Pharmacol. 2015 Nov 15;289 (1) :48-57.|[3]Medjakovic S, et al., Effect of nonpersistent pesticides on estrogen receptor, androgen receptor, and aryl hydrocarbon receptor. Environ Toxicol. 2014 Oct;29 (10) :1201-16.|[4]Go RE, et al., A fungicide, fenhexamid, is involved in the migration and angiogenesis in breast cancer cells expressing estrogen receptors. Life Sci. 2022 Sep 15;305:120754.
  • Shipping Conditions:

    Room temperature
  • Scientific Category:

    Isotope-Labeled Compounds
  • Clinical Information:

    No Development Reported
  • CAS Number:

    [1246815-53-1]