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Darifenacin (hydrobromide)

Darifenacin (UK-88525) hydrobromide is a selective and orally active M3 muscarinic receptor (M3R) antagonist with a pKi of 8.9. Darifenacin hydrobromide binds >20-fold more specifically to M3R than to other muscarinic receptors. Darifenacin hydrobromide can be used in the study of urinary incontinence and other symptoms of overactive bladder. Darifenacin hydrobromide inhibits tumor growth in colorectal cancer cells and has anti-tumor effects[1][2][3][4][5][6].

Product Specifications

CAS Number

[133099-07-7]

Product Name Alternative

UK-88525 (hydrobromide)

UNSPSC

12352005

Hazard Statement

H315, H319, H335

Target

Akt; mAChR; p38 MAPK

Type

Reference compound

Related Pathways

GPCR/G Protein; MAPK/ERK Pathway; Neuronal Signaling; PI3K/Akt/mTOR

Applications

Cancer-programmed cell death

Field of Research

Cancer; Metabolic Disease; Neurological Disease

Assay Protocol

https://www.medchemexpress.com/Darifenacin-hydrobromide.html

Purity

99.97

Solubility

DMSO : 33.33 mg/mL (ultrasonic)

Smiles

O=C(C(C1=CC=CC=C1)([C@@H]2CCN(CCC3=CC4=C(OCC4)C=C3)C2)C5=CC=CC=C5)N.Br

Molecular Formula

C28H31BrN2O2

Molecular Weight

507.46

Precautions

H315, H319, H335

References & Citations

+

Shipping Conditions

Room Temperature

Storage Conditions

4°C (Powder, sealed storage, away from moisture)

Scientific Category

Reference compound1

Clinical Information

Launched

Isoform

ERK1; ERK2; mAChR3; MMP-1

Citation 01

ACS Omega. 2020 Oct 12;5 (41) :26551-26561.|Eur J Pharmacol. 2011 Aug 1;663 (1-3) :74-9. |J Transl Med. 2025 Jan 23;23 (1) :112.|Br J Pharmacol. 2015 Dec;172 (23) :5619-33. |Oncotarget. 2016 Apr 5;7 (14) :18085-94. |Sci Rep. 2017 Jan 19;7:40802.

Available Sizes

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