ADRA1D receptor antagonist 1 free base

Modify Date: 2024-02-08 18:39:13

ADRA1D receptor antagonist 1 free base Structure
ADRA1D receptor antagonist 1 free base structure
Common Name ADRA1D receptor antagonist 1 free base
CAS Number 1191908-24-3 Molecular Weight 300.74
Density N/A Boiling Point N/A
Molecular Formula C15H13ClN4O Melting Point N/A
MSDS N/A Flash Point N/A

 Use of ADRA1D receptor antagonist 1 free base


ADRA1D receptor antagonist 1 (free base) (compound (R)-9s) is an orally active, potent and selective human α1D-adrenoceptor (α1D-AR) antagonist (Ki=1.6 nM). ADRA1D receptor antagonist 1 (free base) dose-dependently inhibits bladder contraction with an IC30 value of 15 nM. ADRA1D receptor antagonist 1 (free base) can be used in studies of overactive bladder disorders such as urinary urgency, frequency and incontinence.

 Names

Name ADRA1D receptor antagonist 1 free base

 ADRA1D receptor antagonist 1 free base Biological Activity

Description ADRA1D receptor antagonist 1 (free base) (compound (R)-9s) is an orally active, potent and selective human α1D-adrenoceptor (α1D-AR) antagonist (Ki=1.6 nM). ADRA1D receptor antagonist 1 (free base) dose-dependently inhibits bladder contraction with an IC30 value of 15 nM. ADRA1D receptor antagonist 1 (free base) can be used in studies of overactive bladder disorders such as urinary urgency, frequency and incontinence.
Related Catalog
In Vivo ADRA1D receptor antagonist 1 (free base) (10 µg/kg; p.o.; single) inhibits cyclophosphamide-induced urinary frequency in rats[1]. ADRA1D receptor antagonist 1 (free base) (4.4 µg/kg; i.v.; single) inhibits bladder contraction with an IC 30 value of 15 nM in rats[1]. Animal Model: Rats with cyclophosphamide-induced cystitis[1]. Dosage: 10 µg/kg Administration: Oral administration; single Result: Increased voiding intervals. Animal Model: Rats with BOO (bladder outlet obstruction)[1]. Dosage: 4.4 µg/kg Administration: Intravenous injection; single Result: Dose-dependently decreased the non-voiding bladder contractions during urinary storage phase.

 Chemical & Physical Properties

Molecular Formula C15H13ClN4O
Molecular Weight 300.74