Tirzepatide
GLP-1 / GIP Receptor Dual Agonist
39-amino-acid synthetic peptide with a C20 fatty-diacid moiety. Dual agonist at the GIP and GLP-1 receptors, modulating glucose-dependent insulin secretion, gastric emptying, and satiety signalling.
Mechanism of Action
Tirzepatide is engineered from the native GIP sequence to co-agonise the GIP and GLP-1 receptors. Receptor engagement potentiates glucose-dependent insulin secretion, suppresses glucagon, slows gastric emptying, and reduces energy intake in research models. Its GIP-biased profile distinguishes it from single-incretin GLP-1 agonists.
Research Evidence
DATA = directly reported in cited study · INFERENCE = derived · SPECULATION = hypothesis
Certificate of Analysis
Every Mindtek batch is independently tested before release. We were among the first peptide suppliers in Southeast Asia to implement mandatory third-party HPLC verification — a standard, not an exception.
Research Protocol Reference
For laboratory research use only — not for human or veterinary use.
Frequently Asked Questions
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