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Propranolol HCl Adrenergic Receptor inhibitor

Cat.No.S4076

Propranolol HCl (AY-64043, ICI-45520, NCS-91523) is a competitive non-selective beta-adrenergic receptors inhibitor.
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Quality Control

Batch: Purity: 99.78%
99.78

Solubility

In vitro
Batch:

DMSO : 59 mg/mL (199.45 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO.)

Water : 6 mg/mL

Ethanol : Insoluble

Molarity Calculator

Mass Concentration Volume Molecular Weight
Dilution Calculator Molecular Weight Calculator

In vivo
Batch:

In vivo Formulation Calculator (Clear solution)

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Working concentration: mg/ml;

Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

Note: 1. Please make sure the liquid is clear before adding the next solvent.
2. Be sure to add the solvent(s) in order. You must ensure that the solution obtained, in the previous addition, is a clear solution before proceeding to add the next solvent. Physical methods such
as vortex, ultrasound or hot water bath can be used to aid dissolving.

Chemical Information, Storage & Stability

Molecular Weight 295.8 Formula

C16H21NO2.HCl

Storage (From the date of receipt)
CAS No. 318-98-9 Download SDF Storage of Stock Solutions

Synonyms AY-64043, ICI-45520, NCS-91523 SMILES CC(C)NCC(COC1=CC=CC2=CC=CC=C21)O.Cl

Read more about storage stability stock solution CAS number SMILES

Mechanism of Action

Targets/IC50/Ki
β-adrenergic receptor
12 nM
In vitro

Propranolol, a non-selective β1 and β2 adrenergic blocker, has no effect on the proliferation of neonatal mouse cardiac fibroblasts (NMCFs).

In vivo

Propranolol, an anti-arrhythmic drugs, consistently reduces the heart rates of adult mice by approximately 10%-20%, whereas isoproterenol has the opposite effect.

References

Applications

Methods Biomarkers Images PMID
Growth inhibition assay Cell viability
S4076-viability1
27582542
Western blot Bax / Bcl-2 / Cyt C / Caspase-9 / Cleaved Caspase-9 / Caspase-3 / Cleaved Caspase-3 B-Raf / p-B-Raf / MEK / p-MEK / ERK / p-ERK / AKT / p-AKT
S4076-WB1
27582542

Clinical Trial Information

(data from https://clinicaltrials.gov, updated on 2026-06-17)

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2022-12-16 PHASE1
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Post-Traumatic Stress Disorder, PTSD
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2026-09 PHASE3
NCT00262470 ACTIVE_NOT_RECRUITING
Tachycardia; Chronic Orthostatic Intolerance
Satish R. Raj
1997-04 PHASE1; PHASE2
NCT06670976 WITHDRAWN
Soft Tissue Sarcoma
Roswell Park Cancer Institute
2026-05-15 PHASE1
NCT04682158 RECRUITING
Esophageal Adenocarcinoma
Roswell Park Cancer Institute
2021-04-01 PHASE2

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