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Partial agonist and S-15535

Shortcuts: Differences, Similarities, Jaccard Similarity Coefficient, References.

Difference between Partial agonist and S-15535

Partial agonist vs. S-15535

In pharmacology, partial agonists are drugs that bind to and activate a given receptor, but have only partial efficacy at the receptor relative to a full agonist. S-15535 is a phenylpiperazine drug which is a potent and highly selective 5-HT1A receptor ligand that acts as an agonist and antagonist (weak partial agonist) at the presynaptic and postsynaptic 5-HT1A receptors, respectively.

Similarities between Partial agonist and S-15535

Partial agonist and S-15535 have 4 things in common (in Unionpedia): Agonist, Ligand (biochemistry), Receptor (biochemistry), Receptor antagonist.

Agonist

An agonist is a chemical that binds to a receptor and activates the receptor to produce a biological response.

Agonist and Partial agonist · Agonist and S-15535 · See more »

Ligand (biochemistry)

In biochemistry and pharmacology, a ligand is a substance that forms a complex with a biomolecule to serve a biological purpose.

Ligand (biochemistry) and Partial agonist · Ligand (biochemistry) and S-15535 · See more »

Receptor (biochemistry)

In biochemistry and pharmacology, a receptor is a protein molecule that receives chemical signals from outside a cell.

Partial agonist and Receptor (biochemistry) · Receptor (biochemistry) and S-15535 · See more »

Receptor antagonist

A receptor antagonist is a type of receptor ligand or drug that blocks or dampens a biological response by binding to and blocking a receptor rather than activating it like an agonist.

Partial agonist and Receptor antagonist · Receptor antagonist and S-15535 · See more »

The list above answers the following questions

Partial agonist and S-15535 Comparison

Partial agonist has 20 relations, while S-15535 has 12. As they have in common 4, the Jaccard index is 12.50% = 4 / (20 + 12).

References

This article shows the relationship between Partial agonist and S-15535. To access each article from which the information was extracted, please visit:

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