1. Metabolic Enzyme/Protease
  2. Cytochrome P450
  3. Ticlopidine (Standard)

Ticlopidine (Standard) 

Cat. No.: HY-100386R Purity: ≥98%
Handling Instructions

Ticlopidine (Standard) is the analytical standard of Ticlopidine. This product is intended for research and analytical applications. Ticlopidine (PCR 5332), an antithrombotic proagent, acts as an allosteric, noncompetitive inhibitor of CD39 with the IC50 of 81.7 μM. Ticlopidine blocks several NTPDase isoenzymes with IC50s of 170 μM and 149 μM for NTPDase2 and NTPDase3, respectively. Ticlopidine is an inhibitor of CYP2C19 human liver cytochrome. Ticlopidine inhibits CYP2C9 and CYP3A4 with IC50s of 26.0 and 32.3 μM, respectively.

For research use only. We do not sell to patients.

Ticlopidine (Standard) Chemical Structure

Ticlopidine (Standard) Chemical Structure

CAS No. : 55142-85-3

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Description
Molecular Weight

263.79

Formula

C14H14ClNS

CAS No.
SMILES

ClC1=CC=CC=C1CN2CCC3=C(C=CS3)C2

Storage

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

Purity & Documentation
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Ticlopidine (Standard) Related Classifications

  • Molarity Calculator

  • Dilution Calculator

The molarity calculator equation

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

Mass   Concentration   Volume   Molecular Weight *
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The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
× = ×
C1   V1   C2   V2
Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Ticlopidine (Standard)
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HY-100386R
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