research use only

Treprostinil sodium Prostaglandin Receptor agonist

Cat.No.S0325

Treprostinil sodium is a potent agonist of DP1, EP2 and IP receptors with Ki 4.4 nM, 3.6 nM and 32 nM, respectively.
Treprostinil sodium Prostaglandin Receptor agonist Chemical Structure

Chemical Structure

Molecular Weight: 412.49

Quality Control

Batch: S032501 DMSO]82 mg/mL]false]Water]82 mg/mL]false]Ethanol]82 mg/mL]false Purity: 99.52%
99.52

Chemical Information, Storage & Stability

Molecular Weight 412.49 Formula

C23H33NaO5

Storage (From the date of receipt) 3 years -20°C powder
CAS No. 289480-64-4 -- Storage of Stock Solutions

Synonyms UT-15, Remodulin Smiles CCCCCC(CCC1C(CC2C1CC3=C(C2)C(=CC=C3)OCC(=O)[O-])O)O.[Na+]

Solubility

In vitro
Batch:

DMSO : 82 mg/mL ( (198.79 mM) Moisture-absorbing DMSO reduces solubility. Please use fresh DMSO.)

Water : 82 mg/mL

Ethanol : 82 mg/mL

Molarity Calculator

Mass Concentration Volume Molecular Weight

In vivo
Batch:

In vivo Formulation Calculator (Clear solution)

Step 1: Enter information below (Recommended: An additional animal making an allowance for loss during the experiment)

mg/kg g μL

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%DMSO %

Calculation results:

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.

Mechanism of Action

Targets/IC50/Ki
EP2 [1]
(Cell-free assay)
3.6 nM(Ki)
DP1 [1]
(Cell-free assay)
4.4 nM(Ki)
IP [1]
(Cell-free assay)
32 nM(Ki)
References

Clinical Trial Information

(data from https://clinicaltrials.gov, updated on 2024-05-22)

NCT Number Recruitment Conditions Sponsor/Collaborators Start Date Phases
NCT05060315 Active not recruiting
Pulmonary Arterial Hypertension
United Therapeutics
July 5 2023 --
NCT05649722 Recruiting
Pulmonary Hypertension|Interstitial Lung Disease
Insmed Incorporated
May 11 2023 Phase 2|Phase 3
NCT04882774 Withdrawn
Pulmonary Hypertension Due to Left Heart Disease
Mardi Gomberg -Maitland MD MSc|Ohio State University|Allegheny Singer Research Institute (also known as Allegheny Health Network Research Institute)|George Washington University
April 2023 Phase 2
NCT05649748 Recruiting
Pulmonary Arterial Hypertension
Insmed Incorporated
March 7 2023 Phase 2|Phase 3
NCT05176951 Completed
Pulmonary Hypertension
Insmed Incorporated
December 22 2022 Phase 2

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