Helen Frankenthaler Foundation

Anti-inflammatory research compound

Pectolinarin | Interleukins inhibitor | CAS 28978-02-1 | Selleck

Pectolinarin | Interleukins inhibitor | CAS 28978-02-1 | Selleck

research use only

Cat.No.S9054

Pectolinarin is a major compound in Cirsium setidens with anti-inflammatory activity. This compound inhibits secretion of IL-6 and IL-8, as well as the production of PGE2 and NO. It also induces apoptosis via inactivation of the PI3K/Akt pathway.

Chemical Structure

Molecular Weight: 622.57

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Quality Control

Select batch Batch:Purity: 99.93%

  • Cited in Nature Medicine for its top-tier quality
  • COA
  • SDS
  • Datasheet

99.93

Related Targets
PD-1/PD-L1 CXCR STING AhR Immunology & Inflammation related CD markers Anti-infection Antioxidant COX Histamine Receptor
Other Interleukins Inhibitors
SC144 Ossirene (AS101) Diacerein Ac-YVAD-cmk Apilimod mesylate EC330 Sodium Thiocyanate IQ 3 Raleukin Cp2-SO4

Solubility

In vitro batch selection In vitro

Batch:DMSO : 10 mg/mL (16.06 mM)

(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO.)

ConcentrationVolumeMass 1 mg5 mg10 mg
1 mM1.6062 mL8.0312 mL16.0625 mL
5 mM0.3212 mL1.6062 mL3.2125 mL
10 mM0.1606 mL0.8031 mL1.6062 mL
50 mM
Molarity Calculator
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Dilution Calculator Molecular Weight Calculator

In vivo batch selection In vivo

Batch:

Oral Administration

Homogeneous suspension CMC-NA≥5mg/ml Taking the 1 mL working solution as an example, add 5 mg of this product to 1 ml of CMC-Na solution, mix evenly to obtain a homogeneous suspension with a final concentration of 5 mg/ml.

In vivo Formulation Calculator (Clear solution)

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

Dosage: mg/kg

Average weight of animals: g

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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.)

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Tween 80 percentage % Tween 80

Water (ddH₂O) percentage % ddH 2 O

DMSO percentage % DMSO

+

Corn oil percentage %

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 ddH 2 O, 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 Weight622.57FormulaC 29 H 34 O 15Storage (From the date of receipt)3 years -20°C powder
CAS No.28978-02-1Storage of Stock Solutions1 year -80°C in solvent 1 month -20°C in solvent
SynonymsN/ASmilesCC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(C(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)OC)O)OC)O)O)O)O)O)O

Specificity

NameCitationIL-6IL-1IL-8IL-12IL-10IL-13IL-2Others
SKF-860020++
JTE-607 Dihydrochloride0++++++++++++TNF-alpha
A-7400032++rat P2X7 receptor,human P2X7 receptor
Apilimod mesylate3++++PIKfyve
MD2-TLR4-IN-10++TLR4,TNF-α
Danirixin (GSK1325756)2++CXCR2
Resatorvid (TAK-242)63++++TLR4,NO,TNF-α
Apilimod (STA-5326)18++++PIKfyve

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1. "+" indicates inhibitory effect. Increased inhibition is marked by a higher "+" designation. 2. "✔" indicates inhibitory effect, but without specific value.

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