Fenhexamid

CAT:
804-HY-118065-01
Size:
50 mg
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
Fenhexamid - image 1

Fenhexamid

  • Description :

    Fenhexamid, a botryticide, is a sterol biosynthesis inhibitor. Fenhexamid shows fungicide efficient against the plant pathogenic fungus Botryotinia fuckeliana (Botrytis cinerea) [1].
  • Product Name Alternative :

    KBR 2738
  • UNSPSC :

    12352005
  • Hazard Statement :

    H411
  • Target :

    Estrogen Receptor/ERR; Fungal; PI3K
  • Type :

    Reference compound
  • Related Pathways :

    Anti-infection; PI3K/Akt/mTOR; Vitamin D Related/Nuclear Receptor
  • Applications :

    COVID-19-immunoregulation
  • Field of Research :

    Cancer; Infection
  • Assay Protocol :

    https://www.medchemexpress.com/fenhexamid.html
  • Concentration :

    10mM
  • Purity :

    99.60
  • Solubility :

    DMSO : 100 mg/mL (ultrasonic)
  • Smiles :

    O=C(NC1=CC=C(C(Cl)=C1Cl)O)C2(CCCCC2)C
  • Molecular Formula :

    C14H17Cl2NO2
  • Molecular Weight :

    302.20
  • Precautions :

    H411
  • 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
  • Storage Conditions :

    4°C (Powder, protect from light)
  • Scientific Category :

    Reference compound1
  • Clinical Information :

    No Development Reported
  • CAS Number :

    [126833-17-8]

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