country

Change Language

EN - English
FR - Français
DE - Deutsch
ES - Español
JA - 日本語
KO - 한국어

Country or Region:

United States

Product Name	Size / Unit Price	Qty

Total: USD 0.00 Checkout

Cat. No.: HY-125589

Copy Link Print Information

5N-Bicalutamide

5N-Bicalutamide is an androgen receptor (AR) antagonist with a K_i of 0.15 nM. 5N-Bicalutamide is a derivative of Bicalutamide (HY-14249). 5N-Bicalutamide reacts with Cys784 in the AR binding pocket via an activated aryl nitrile group to form a reversible thioimidate covalent adduct, which significantly enhances its binding affinity and inhibitory potency. 5N-Bicalutamide is used in prostate cancer-related research.

For research use only. We do not sell to patients.

CAS No.: 1845688-96-1
Formula: C₁₇H₁₃F₄N₃O₄S
Molecular Weight:431.36

Storage:

Please store the product under the recommended conditions in the Certificate of Analysis.

5N-Bicalutamide Chemical Structure

CAS No.: 1845688-96-1

Price

Stock

Quantity

Amount: USD 0.00

* Please select Quantity before adding items.

Use of MCE Products

Strong Fluorescence Signal / Multi-Disciplinary Applications / High Fluorescence Specificity

Biological Activity
- Description
- Cellular Effect
- In Vitro
Chemical Information
Purity & Documentation
References
Calculators
Help & FAQs
Classifications
Bioz

Biological Activity

Description

Cellular Effect

Cell Line	Type	Value	Description	References
HeLa	IC50	0.015 μM	Inhibition of DHT-induced androgen receptor transactivation in HeLa cells expressing AR-LBD fused to Gal4-DBD, assessed via luciferase reporter assay after overnight incubation with 1 nM DHT. Inhibition of DHT-induced androgen receptor transactivation in HeLa cells expressing AR-LBD fused to Gal4-DBD, assessed via luciferase reporter assay after overnight incubation with 1 nM DHT.	28981251

In Vitro

5N-Bicalutamide has a 10-fold higher electrophilicity than bicalutamide, as measured by the calculated free energy of thioimidate formation with methanethiol^[1].
5N-Bicalutamide (100 μM; 1-24 h) reacts rapidly with free cysteine in physiological buffer, forming a thiazoline adduct with 99% conversion after 4 h at 37 °C, pH 7.4^[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Cytotoxicity Assay^[1]

Cell Line:

LNCaP/AR and HeLa cells
Concentration:

3 μM, 10 μM, 30 μM
Incubation Time:

24 h
Result:

Produced no significant cytotoxicity.

Chemical Information

CAS No. 1845688-96-1
Molecular Weight 431.36
Formula C₁₇H₁₃F₄N₃O₄S
SMILES

N#CC1=NC=C(C=C1C(F)(F)F)NC(=O)C(O)(C)CS(=O)(=O)C2=CC=C(F)C=C2
Shipping

Room temperature in continental US; may vary elsewhere.
Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation

Handling Instructions (2659 KB)

References

[1]. de Jesus Cortez F, et al. Development of 5N-Bicalutamide, a High-Affinity Reversible Covalent Antiandrogen. ACS chemical biology. 2017 Dec 15;12(12):2934-2939.

Calculators

Molarity Calculator

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

Mass Mass

Concentration Concentration

Volume Volume

Molecular Weight Molecular Weight

Dilution Calculator

Concentration _(start) × Volume _(start) = Concentration _(final) × Volume _(final)

Concentration _(start) Concentration _(start)

Volume _(start) Volume _(start)

Concentration _(final) Concentration _(final)

Volume _(final) Volume _(final)

Help & FAQs

How should lyophilized recombinant proteins be reconstituted and stored?

1. Before opening the cap, centrifuge the vial at 13000 rpm for 20-30 seconds. This step will ensure that any lyophilized powder that may have adhered to the cap or walls is collected at the bottom of the vial, minimizing the risk of product loss.

Bioz

Keywords

MOQ

Minimum order quantity

100 mg

Get Quote In-stock

Other size

Get Quote