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Ritodrine hydrochloride

Catalog No. T1433   CAS 23239-51-2
Synonyms: DU21220, Ritodrine HCl, NSC 291565

Ritodrine hydrochloride (NSC 291565) binds to and activates beta-2 adrenergic receptors of myometrial cells in the uterus, which decreases the intensity and frequency of uterine contractions. Ritodrine hydrochloride (NSC 291565) is a phenethylamine derivative with tocolytic activity. Specifically, Ritodrine hydrochloride (NSC 291565) probably activates adenyl cyclase, thereby increasing production of cyclic adenosine monophosphate (cAMP), which in turn enhances the efflux of calcium from vascular smooth muscle cells. A lack of intracellular calcium prevents uterine myometrial contractions. In addition, this agent may directly inactivate myosin light chain kinase, a critical enzyme necessary for the initiation of muscle contractions.

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Ritodrine hydrochloride Chemical Structure
Ritodrine hydrochloride, CAS 23239-51-2
Pack Size Availability Price/USD Quantity
100 mg In stock $ 58.00
200 mg In stock $ 105.00
1 mL * 10 mM (in DMSO) In stock $ 50.00
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Purity: 99.89%
Purity: 99%
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Biological Description
Chemical Properties
Storage & Solubility Information
Description Ritodrine hydrochloride (NSC 291565) binds to and activates beta-2 adrenergic receptors of myometrial cells in the uterus, which decreases the intensity and frequency of uterine contractions. Ritodrine hydrochloride (NSC 291565) is a phenethylamine derivative with tocolytic activity. Specifically, Ritodrine hydrochloride (NSC 291565) probably activates adenyl cyclase, thereby increasing production of cyclic adenosine monophosphate (cAMP), which in turn enhances the efflux of calcium from vascular smooth muscle cells. A lack of intracellular calcium prevents uterine myometrial contractions. In addition, this agent may directly inactivate myosin light chain kinase, a critical enzyme necessary for the initiation of muscle contractions.
Synonyms DU21220, Ritodrine HCl, NSC 291565
Molecular Weight 323.82
Formula C17H21NO3·HCl
CAS No. 23239-51-2

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

Solubility Information

H2O: 200.7 mM

DMSO: 200.7 mM

TargetMolReferences and Literature

1. Tanaka N, et al. J Med Chem. 2001 Apr 26;44(9):1436-45.

Related compound libraries

This product is contained In the following compound libraries:
GPCR Compound Library Anti-Cancer Approved Drug Library Drug Repurposing Compound Library Anti-Neurodegenerative Disease Compound Library Anti-Cancer Drug Library Anti-Cancer Clinical Compound Library Membrane Protein-targeted Compound Library FDA-Approved Drug Library Adrenergic Receptor-Targeted Compound Library FDA-Approved & Pharmacopeia Drug Library

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Keywords

Ritodrine hydrochloride 23239-51-2 GPCR/G Protein Neuroscience Adrenergic Receptor Ritodrine DU21220 Beta Receptor Inhibitor Ritodrine HCl Ritodrine Hydrochloride inhibit NSC-291565 NSC 291565 DU 21220 NSC291565 DU-21220 inhibitor

 

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