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Art. -Nr.: HY-149590

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IPA

IPA is a specific Sec18/NSF inhibitor. IPA binds to phosphatidic acid competitively, induces conformational rigidification of Sec18/NSF, disrupts its essential flexibility, and blocks SNARE priming and vacuolar membrane fusion. IPA can be used to investigate the activity of Sec18 and SNARE priming kinetics.

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CAS. Nr.: 200348-48-7
Formel: C₂₂H₁₈O₇
Molecular Weight:394.38

Speicherung:

Please store the product under the recommended conditions in the Certificate of Analysis.

IPA Chemical Structure

CAS. Nr.: 200348-48-7

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Use of MCE Products

Strong Fluorescence Signal / Multi-Disciplinary Applications / High Fluorescence Specificity

Biologische Aktivität
- Beschreibung
- In Vitro
Chemical Information
Reinheit & Dokumentation
Verweise
Calculators
Help & FAQs
Classifications
Bioz

Biologische Aktivität

Beschreibung

In Vitro

IPA binds to purified monomeric Saccharomyces cerevisiae Sec18, as well as isolated Sec18 D1, D2 domains and D1-D2 recombinants, with the D1 domain showing the highest binding affinity (IC₅₀=762 nM (Sec18), 220 nM (D1), 641 nM (D2))^[1].
IPA potently and specifically competes with phosphatidic acid for binding to monomeric Saccharomyces cerevisiae Sec18 and its isolated D1 and D2 domains, but exerts no significant inhibitory effect on the binding of phosphatidic acid to other phosphatidic acid-interacting proteins, or on the binding of Sec18 to PI liposomes^[1].
IPA (100 μM) potently inhibits the binding of monomeric Saccharomyces cerevisiae Sec18 to PA liposomes with different membrane curvatures, and exhibits slightly stronger inhibitory effects on liposomes with larger diameters^[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Chemical Information

CAS. Nr. 200348-48-7
Molecular Weight 394.38
Formel C₂₂H₁₈O₇
SMILES

O=C(O)C1C2C=CC(C1C3=C4C=CC(=O)C(O)=C4OC=5C(O)=C(O)C=CC53)C2C
Versand

Room temperature in continental US; may vary elsewhere.
Speicherung

Please store the product under the recommended conditions in the Certificate of Analysis.

Reinheit & Dokumentation

Handling Instructions (2659 KB)

Verweise

[1]. Sparks RP, et al. A small-molecule competitive inhibitor of phosphatidic acid binding by the AAA+ protein NSF/Sec18 blocks the SNARE-priming stage of vacuole fusion. J Biol Chem. 2019;294(46):17168-17185. [Content Brief]

Calculators

Molaritätsrechner

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

Mass Mass

Konzentration Konzentration

Volumen Volumen

Molecular Weight Molecular Weight

Verdünnungsrechner

Konzentration _{(Stammlösung)} × Volumen _{(Stammlösung)} = Konzentration _{(Ziellösung)} × Volumen _{(Ziellösung)}

Konzentration _{(Stammlösung)} Konzentration _{(Stammlösung)}

Volumen _{(Stammlösung)} Volumen _{(Stammlösung)}

Konzentration _{(Ziellösung)} Konzentration _{(Ziellösung)}

Volumen _{(Ziellösung)} Volumen _{(Ziellösung)}

Help & FAQs

How should lyophilized recombinant proteins be reconstituted and stored?

1. Before opening the cap, centrifuge the vial at 13000 rpm for 20-30 seconds. This step will ensure that any lyophilized powder that may have adhered to the cap or walls is collected at the bottom of the vial, minimizing the risk of product loss.

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