2. GPCR/G Protein
  3. Prostaglandin Receptor
  4. Vapiprost hydrochloride

Vapiprost hydrochloride is a thromboxane A2 receptor antagonist. Vapiprost inhibits the aggregation and ATP release stimulated with U-46619, collagen or arachidonic acid (AA) at an IC50 of less than 2.1×10-8 M.

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Vapiprost hydrochloride Chemical Structure

Vapiprost hydrochloride Chemical Structure

CAS No. : 87248-13-3

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Vapiprost hydrochloride Related Antibodies

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Description

Vapiprost hydrochloride is a thromboxane A2 receptor antagonist. Vapiprost inhibits the aggregation and ATP release stimulated with U-46619, collagen or arachidonic acid (AA) at an IC50 of less than 2.1×10-8 M[1].

Molecular Weight

514.10

Formula

C30H40ClNO4
CAS No.
SMILES

OC(CC/C=C\CC[C@@H]1[C@](N2CCCCC2)([H])[C@H](C[C@@H]1OCC3=CC=C(C4=CC=CC=C4)C=C3)O)=O.Cl
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Room temperature in continental US; may vary elsewhere.
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Please store the product under the recommended conditions in the Certificate of Analysis.
Purity & Documentation
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Vapiprost hydrochloride Related Classifications

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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.

Keywords:

Vapiprost87248-13-3Prostaglandin Receptorthromboxane A2 receptoraggregationATP releasearachidonic acidcollagenInhibitorinhibitorinhibit

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Vapiprost hydrochloride
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HY-105120A
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