What is the catalog number for Fenhexamid?

The catalog number for Fenhexamid is HY-118065.

What sizes are available for Fenhexamid?

Fenhexamid is available in the following size(s): 50 mg, 10 mM - 1 mL, 100 mg.

How many pack sizes does Fenhexamid come in?

Fenhexamid is available in 3 different pack sizes.

Is Fenhexamid in stock?

Fenhexamid is currently made to order / not held in immediate stock. Contact us for lead time.

Who manufactures Fenhexamid?

Fenhexamid is manufactured by QuantiMol.

What is the estimated delivery time for Fenhexamid?

Estimated delivery time for Fenhexamid is approximately 15 business day(s), depending on your location.

Where can I find the safety data sheet (SDS/MSDS) for Fenhexamid?

The safety data sheet for Fenhexamid is available here: http://file.medchemexpress.com/batch_PDF/HY-118065/Fenhexamid-SDS-MedChemExpress.pdf.

Fenhexamid

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

Product Specifications

CAS Number

126833-17-8

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.