Pentoxifylline

Pentoxifylline is a competitive nonselective phosphodiesterase inhibitor which raises intracellular cAMP, activates PKA, inhibits TNF and leukotriene synthesis, and reduces inflammation and innate immunity.

Pentoxifylline Chemical Structure

Pentoxifylline Chemical Structure

CAS: 6493-05-6

Selleck's Pentoxifylline has been cited by 2 publications

Purity & Quality Control

Batch: Purity: 99.82%
99.82

Pentoxifylline Related Products

Signaling Pathway

Choose Selective PDE Inhibitors

Biological Activity

Description Pentoxifylline is a competitive nonselective phosphodiesterase inhibitor which raises intracellular cAMP, activates PKA, inhibits TNF and leukotriene synthesis, and reduces inflammation and innate immunity.
In vitro
In vitro Pentoxifylline exhibits synergism with CDDP in killing MCF-7/E6 cells but does not affect sensitivity of the control cells. Pentoxifylline inhibits G2 checkpoint function to a greater extent in MCF-7/E6 than in the parental cells. [1] Pentoxifylline acts primarily by increasing red blood cell deformability, by reducing blood viscosity and by decreasing the potential for platelet aggregation and thrombus formation. [2] Pentoxifylline is efficacious in suppressing LPS-induced MO-derived TNF at the level of both TNF mRNA accumulation and TNF supernatant bioactivity. Pentoxifylline (10 μM) suppresses the production of both biologically active TNF and TNF mRNA expression by more than 50% in LM cells. [3] Pentoxifylline blocks cachectin/TNF mRNA accumulation but has no effect upon the efficiency of reporter mRNA translation in RAW 264.7 macrophages. Pentoxifylline combined with Dexamethasone causes a greater suppression of cachectin/TNF biosynthesis that can be achieved by either agent alone in RAW 264.7 macrophages. [4]
In Vivo
In vivo Pentoxifylline (500 mg) markedly inhibits increases in the serum levels of TNF and IL-6, as well as the effects on coagulation and fibrinolysis, in chimpanzees. Pentoxifylline (500 mg) along with Endotoxin (4 ng/kg) also has a significant effect on thrombin generation in chimpanzees. [5]
NCT Number Recruitment Conditions Sponsor/Collaborators Start Date Phases
NCT06041932 Not yet recruiting
Liver Cirrhosis
Institute of Liver and Biliary Sciences India
November 1 2023 Not Applicable
NCT05490953 Recruiting
Hodgkin Lymphoma
University of Guadalajara|Hospital Civil de Guadalajara
July 11 2022 Phase 4
NCT05189535 Recruiting
Breast Cancer Female|Peripheral Neuropathy
Ain Shams University
October 3 2021 Phase 2|Phase 3
NCT04152980 Recruiting
Neonatal Late Onset Sepsis
Erasmus Medical Center
January 12 2020 Phase 3
NCT05660694 Completed
Triamcinolone|Pentoxifylline|Vitamin E|Oral Submucosa Fibrosis|Tumor
Altamash Institute of Dental Medicine
January 1 2020 Phase 4

Chemical Information & Solubility

Molecular Weight 278.31 Formula

C13H18N4O3

CAS No. 6493-05-6 SDF Download Pentoxifylline SDF
Smiles CC(=O)CCCCN1C(=O)C2=C(N=CN2C)N(C1=O)C
Storage (From the date of receipt)

In vitro
Batch:

DMSO : 55 mg/mL ( (197.62 mM); Moisture-absorbing DMSO reduces solubility. Please use fresh DMSO.)

Water : 55 mg/mL

Ethanol : 55 mg/mL


Molecular Weight Calculator

In vivo
Batch:

Add solvents to the product individually and in order.


In vivo Formulation Calculator

Preparing Stock Solutions

Molarity Calculator

Mass Concentration Volume Molecular Weight

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

Step 2: Enter the in vivo formulation (This is only the calculator, not formulation. Please contact us first if there is no in vivo formulation at the solubility Section.)

% DMSO % % Tween 80 % ddH2O
%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.

Tech Support

Answers to questions you may have can be found in the inhibitor handling instructions. Topics include how to prepare stock solutions, how to store inhibitors, and issues that need special attention for cell-based assays and animal experiments.

Handling Instructions

Tel: +1-832-582-8158 Ext:3
If you have any other enquiries, please leave a message.

* Indicates a Required Field

Please enter your name.
Please enter your email. Please enter a valid email address.
Please write something to us.
Tags: buy Pentoxifylline | Pentoxifylline ic50 | Pentoxifylline price | Pentoxifylline cost | Pentoxifylline solubility dmso | Pentoxifylline purchase | Pentoxifylline manufacturer | Pentoxifylline research buy | Pentoxifylline order | Pentoxifylline mouse | Pentoxifylline chemical structure | Pentoxifylline mw | Pentoxifylline molecular weight | Pentoxifylline datasheet | Pentoxifylline supplier | Pentoxifylline in vitro | Pentoxifylline cell line | Pentoxifylline concentration | Pentoxifylline nmr