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

Ebopiprant hydrochloride  (Synonyms: OBE022 hydrochloride)

Cat. No.: HY-112284A
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Ebopiprant (OBE022) hydrochloride is an oral and selective prostaglandin F2α (PGF2α) receptor antagonist, with Kis of 1 nM, 26 nM for human and rat FP receptors, respectively.

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

Ebopiprant hydrochloride Chemical Structure

Ebopiprant hydrochloride Chemical Structure

CAS No. : 2005486-32-6

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Other Forms of Ebopiprant hydrochloride:

Ebopiprant hydrochloride Related Antibodies

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Description

Ebopiprant (OBE022) hydrochloride is an oral and selective prostaglandin F2α (PGF2α) receptor antagonist, with Kis of 1 nM, 26 nM for human and rat FP receptors, respectively.

Molecular Weight

636.20

Formula

C30H35ClFN3O5S2
CAS No.
SMILES

O=C(N[C@H](C1=CC=C(F)C=C1)CCOC([C@H](C(C)C)N)=O)[C@H](SCC2)N2S(C(C=C3)=CC=C3C4=CC=CC=C4)(=O)=O.Cl
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Room temperature in continental US; may vary elsewhere.
Storage

Please store the product under the recommended conditions in the Certificate of Analysis.
Purity & Documentation
References
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Ebopiprant hydrochloride Related Classifications

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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.

Keywords:

Ebopiprant2005486-32-6OBE022OBE 022OBE-022Prostaglandin ReceptorInhibitorinhibitorinhibit

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