Synthetic growth hormone-releasing hormone

Tesamorelin

Also known as TH9507 · TH-9507 · trans-3-hexenoyl-GHRH(1-44) · tesamorelin acetate

In receptor-level and cell-based systems, tesamorelin is a stabilized analog of growth hormone-releasing hormone that binds the GHRH receptor (GHRHR), a class B G-protein-coupled receptor expressed on anterior pituitary somatotroph cells.

Tesamorelin - HappyTides research vial
ClassSynthetic growth hormone-releasing hormone
Molecular weight5135.9 g/mol (average; ~5136 Da per PubChem CID 16137828)
Molecular formulaC221H366N72O67S
CAS number218949-48-5

The overview

What is Tesamorelin?

In receptor-level and cell-based systems, tesamorelin is a stabilized analog of growth hormone-releasing hormone that binds the GHRH receptor (GHRHR), a class B G-protein-coupled receptor expressed on anterior pituitary somatotroph cells. Receptor engagement couples to the stimulatory G-protein (Gs), activating adenylyl cyclase and raising intracellular cAMP, which activates protein kinase A (PKA). PKA-mediated phosphorylation of transcription factors such as CREB modulates growth-hormone gene transcription and somatotroph secretory-vesicle mobilization, the canonical GHRH signaling cascade. Structurally, tesamorelin retains the full native GHRH(1-44) sequence but carries a trans-3-hexenoyl group on the N-terminal tyrosine; this lipophilic modification confers resistance to dipeptidyl peptidase-4 (DPP-4) cleavage, the principal route of native GHRH inactivation, prolonging the molecule's stability while preserving receptor-binding determinants. Reported in-vitro and pharmacologic characterizations describe GHRHR agonism and downstream cAMP/PKA pathway activation as the defining signaling properties of the molecule.

In the research

Where Tesamorelin shows up

The areas researchers focus on with Tesamorelin - and why it has the science community paying attention.

  • GHRH receptor (GHRHR) class B GPCR binding and agonist pharmacology
  • Gs/adenylyl cyclase/cAMP/PKA signal-transduction studies in somatotroph cell models
  • CREB phosphorylation and growth-hormone gene transcription regulation
  • DPP-4 enzymatic-stability and peptide-degradation kinetics of N-acylated GHRH analogs
  • Structure-activity relationships of N-terminal lipidation on GHRH-family peptides
  • Population/preclinical pharmacokinetic modeling of long-acting GHRH analogs

By the numbers

The facts that matter

PubChem Compound Identifier (CID)16137828
Molecular formulaC221H366N72O67S
Average molecular weight5135.9 g/mol (~5136 Da)
CAS Registry Number (free base)218949-48-5
Peptide backboneFull native human GHRH(1-44) sequence with N-terminal trans-3-hexenoyl modification on Tyr1
Molecular targetGrowth hormone-releasing hormone receptor (GHRHR), a class B GPCR on pituitary somatotrophs
Stabilizing modification rationaleN-terminal hexenoyl acylation confers resistance to DPP-4 cleavage that inactivates native GHRH
Original development codeTH9507 (TH-9507)

To the molecule

Molecular specifications

Molecular formulaC221H366N72O67S
Molecular weight5135.9 g/mol (average; ~5136 Da per PubChem CID 16137828)
CAS number218949-48-5
Amino-acid sequenceTyr-Ala-Asp-Ala-Ile-Phe-Thr-Asn-Ser-Tyr-Arg-Lys-Val-Leu-Gly-Gln-Leu-Ser-Ala-Arg-Lys-Leu-Leu-Gln-Asp-Ile-Met-Ser-Arg-Gln-Gln-Gly-Glu-Ser-Asn-Gln-Glu-Arg-Gly-Ala-Arg-Ala-Arg-Leu-NH2 (one-letter: YADAIFTNSYRKVLGQLSARKLLQDIMSRQQGESNQERGARARL); native human GHRH(1-44) sequence bearing a trans-3-hexenoyl (3-hexenoic acid) group on the alpha-amino group of the N-terminal Tyr1, with C-terminal amidation

Sourced, not claimed

The science behind it

The peer-reviewed studies behind Tesamorelin, linked so you can read them yourself.

  1. Falutz, J., et al. (2010). Effects of tesamorelin on visceral adipose tissue and metabolic parameters. New England Journal of Medicine.
  2. Stanley, T. L., et al. (2014). Effect of tesamorelin on visceral fat and liver fat: a randomized clinical trial. JAMA.

Straight answers

Questions, answered

Is Tesamorelin approved by the FDA?

No. Tesamorelin is not an FDA-approved drug. We supply it as a research-use-only reference compound, identity-verified for purity with a COA on every vial.

What class of compound is Tesamorelin?

Tesamorelin is classified as: Synthetic growth hormone-releasing hormone (GHRH/GRF) analog; N-terminally lipid-modified 44-residue peptide; GHRH receptor (GHRHR) agonist.

What is the molecular weight of Tesamorelin?

The molecular weight of Tesamorelin is 5135.9 g/mol (average; ~5136 Da per PubChem CID 16137828), with a molecular formula of C221H366N72O67S.

What is the CAS number for Tesamorelin?

The CAS Registry Number for Tesamorelin is 218949-48-5.

What is the amino acid sequence of Tesamorelin?

Tesamorelin has the sequence: Tyr-Ala-Asp-Ala-Ile-Phe-Thr-Asn-Ser-Tyr-Arg-Lys-Val-Leu-Gly-Gln-Leu-Ser-Ala-Arg-Lys-Leu-Leu-Gln-Asp-Ile-Met-Ser-Arg-Gln-Gln-Gly-Glu-Ser-Asn-Gln-Glu-Arg-Gly-Ala-Arg-Ala-Arg-Leu-NH2 (one-letter: YADAIFTNSYRKVLGQLSARKLLQDIMSRQQGESNQERGARARL); native human GHRH(1-44) sequence bearing a trans-3-hexenoyl (3-hexenoic acid) group on the alpha-amino group of the N-terminal Tyr1, with C-terminal amidation.

Available now

Get Tesamorelin

Identity-verified, third-party tested, made in the USA, and traceable to its lot - with a scannable COA on every vial. For research use only.

See pricing & order →

Complete the stack

Researchers often pair Tesamorelin with

CJC-1295 No DAC - HappyTides research vial
CJC-1295 No DAC

Both GHRH-analog mechanism - the GH-axis sibling pairing, frequently co-referenced.

MOTS-c - HappyTides research vial
MOTS-c

GH-axis research overlaps mitochondrial-metabolic research in body-composition literature.

NAD+ - HappyTides research vial
NAD+

Metabolic and cellular-energy / longevity research domains sit side by side.