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Pharmacology

Dual Agonist

Definition

One molecule that activates two receptors. Tirzepatide is a GLP-1 and GIP agonist; survodutide combines GLP-1 with glucagon-receptor activity. The pairing is a design decision about which pathways to engage at once.

Terms used in this definition

Other entries this definition refers to.

What this means for research sourcing

Mechanistic terms like this describe how research compounds behave in vitro. See the mechanism overviews for compounds Volta stocks.

Related research compounds at Volta Peptides

Compounds referenced in this definition that Volta supplies for in vitro research use, each >99% HPLC-verified with a certificate of analysis.

For in vitro research use only. Not for human consumption.

Related Terms in Pharmacology

Triple Agonist

One molecule that activates three receptors. Retatrutide acts at the GLP-1, GIP and glucagon receptors, and it is the compound that put the class into clinical development.

Binding Affinity

How tightly a molecule holds its receptor, reported as a dissociation constant where a lower number means tighter binding. Affinity alone does not predict the size of a response: that also depends on how well the bound molecule activates the receptor.

EC50

The concentration producing half of a compound's maximum effect in a given assay. It is a potency measure and is only comparable between compounds tested in the same system, which is why cross-paper EC50 comparisons mislead so often.

Potency

How little of a compound is needed to produce a given effect. A more potent molecule works at a lower concentration, which says nothing about whether its maximum achievable effect is larger.

Receptor Selectivity

How far a compound acts on its intended receptor rather than on related ones. Selectivity is the difference between a GHRP that raises growth hormone alone and one that also moves cortisol and prolactin.

Desensitization

A fall in receptor responsiveness under prolonged or repeated stimulation, achieved by internalising receptors or expressing fewer of them. It is one mechanism behind an effect that fades while exposure continues.

Tachyphylaxis

Response falling away rapidly over a few administrations rather than gradually, which separates it from slower desensitization. Reports of it appear with melanocortin agonists and with some growth hormone releasing peptides.

Downregulation

A reduction in the number of receptors a cell presents, in response to sustained stimulation. It is slower than desensitization and is the usual reason a protocol in the literature includes periods without administration.

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