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Darifenacin HBr - 10mM in DMSO, high purity , CAS No.133099-07-7(DMSO), Muscarinic acetylcholine receptor M3 antagonist

    Grade & Purity:
  • 10mM in DMSO
In stock
Item Number
D407822
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D407822-1ml
1ml
Available within 8-12 weeks(?)
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$167.90

mAChR Selective Inhibitors | Agonists | Antagonists | Modulators

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Compound libraries (12325)

Basic Description

Synonyms UK-88525 | (S)-3-(Carbamoyldiphenylmethyl)-1-[2-(2,3-dihydrobenzofuran-5-yl)ethyl]pyrrolidine hydrobromide
Specifications & Purity 10mM in DMSO
Biochemical and Physiological Mechanisms Darifenacin HBr (UK-88525) is a selective M3 muscarinic receptor antagonist with pKi of 8.9.
Storage Temp Store at -80°C
Shipped In
Dry ice packs + Cold packs
This product requires cold chain shipping. Ground and other economy services are not available.
Action Type ANTAGONIST
Mechanism of action Muscarinic acetylcholine receptor M3 antagonist
Product Description

Information

Darifenacin HBr (UK-88525) is a selectiveM3 muscarinicreceptor antagonist withpKiof 8.9.
In vitro

Darifenacin exerts non-parallel rightward displacement of the agonist curve and also significant depression of the maximum response (+)-cis-Dioxolane produced concentration-dependent contraction of the isolated bladder of rat. Darifenacin produces a concentration dependent increase in R123 (P-gp probe) accumulation in MDCK cells. Darifenacin stimulates ATPase activity in P-gp membrane in a clear concentration dependent response manner with an estimated ED50 value of 1.6\u2009µM. Darifenacin (100 nM) shows a significantly greater permeability for darifenacin in the basolateral to apical direction resulting in an efflux ratio in BBMEC monolayers of approximately 2.6.

In vivo

Darifenacin produces dose-dependent inhibition of amplitude of volume-induced bladder contractions(VIBCAMP), producing 35% inhibition at dose of 283.3 nmol/kg and maximal inhibition of approximately 50–55%. Darifenacin (0.1 mg/kg i.v.) reduces bladder afferent activity in both Aδ and C fibers in female Sprague-Dawley rats, the decrease in afferent spikes in C fibers may be more pronounced than that in Aδ fibers. Darifenacin (7.5 mg and 15 mg, daily) reduces the number of incontinence episodes per week from baseline by 67.7% and 72.8% respectively compared with 55.9% with placebo in patients with overactive bladder (OAB). Darifenacin (7.5 mg and 15 mg, daily) also shows significantly superior to placebo for improvements in micturition frequency, bladder capacity, frequency of urgency, severity of urgency and number of incontinence episodes leading to a change in clothing or pads in patients with overactive bladder (OAB).
Cell Data

cell lines:

Concentrations:

Incubation Time:

Powder Purity:≥99%

Product Properties

Ki Data M3 mAChR, pKi: 8.9
ALogP 5.048
hba_count 2
HBD Count 1
Rotatable Bond 7

Names and Identifiers

Smiles Br.NC(=O)C(C1CCN(CCC2=CC=C3OCCC3=C2)C1)(C4=CC=CC=C4)C5=CC=CC=C5
Molecular Weight 507.46
Reaxy-Rn 9029066
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=9029066&ln=

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Chemical and Physical Properties

Solubility Solubility (25°C) In vitro DMSO: 59 mg/mL (198.41 mM); Ethanol: 5 mg/mL (16.81 mM); Water: Insoluble;
DMSO(mg / mL) Max Solubility 100
DMSO(mM) Max Solubility 197.06
Water(mg / mL) Max Solubility <1

Solution Calculators

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