Home / Research library / Sermorelin
Sermorelin: molecular data, studies & sources
Sermorelin is catalogued here as a research compound. This profile brings together the molecular source record, selected indexed publications and available supplier comparisons. Evidence for a named substance does not authenticate a commercial product.
Compiled by PeptideTech Editors · Sources checked · Selected bibliography, not a systematic review
Molecular formula, weight & structure
- Molecular formula (MF)
- C149H246N44O42S
- Molecular weight (MW)
- 3357.9 g/mol
- PubChem compound ID
- 16132413
- Record title
- Sermorelin
Values describe the selected PubChem molecular entity. Counterions, salt forms, hydration and sequence changes can alter the supplied material. Confirm the exact identity against the supplier specification.
Source: PubChem CID 16132413 · retrieved 2026-09-21

Chemical identifiers and source data
- IUPAC name
- (3S)-4-[[(2S)-1-[[(2S,3S)-1-[[(2S)-1-[[(2S,3R)-1-[[(2S)-4-amino-1-[[(2S)-1-[[(2S)-1-[[(2S)-1-[[(2S)-6-amino-1-[[(2S)-1-[[(2S)-1-[[2-[[(2S)-5-amino-1-[[(2S)-1-[[(2S)-1-[[(2S)-1-[[(2S)-1-[[(2S)-6-amino-1-[[(2S)-1-[[(2S)-1-[[(2S)-5-amino-1-[[(2S)-1-[[(2S,3S)-1-[[(2S)-1-[[(2S)-1-[[(2S)-1-amino-5-carbamimidamido-1-oxopentan-2-yl]amino]-3-hydroxy-1-oxopropan-2-yl]amino]-4-methylsulfanyl-1-oxobutan-2-yl]amino]-3-methyl-1-oxopentan-2-yl]amino]-3-carboxy-1-oxopropan-2-yl]amino]-1,5-dioxopentan-2-yl]amino]-4-methyl-1-oxopentan-2-yl]amino]-4-methyl-1-oxopentan-2-yl]amino]-1-oxohexan-2-yl]amino]-5-carbamimidamido-1-oxopentan-2-yl]amino]-1-oxopropan-2-yl]amino]-3-hydroxy-1-oxopropan-2-yl]amino]-4-methyl-1-oxopentan-2-yl]amino]-1,5-dioxopentan-2-yl]amino]-2-oxoethyl]amino]-4-methyl-1-oxopentan-2-yl]amino]-3-methyl-1-oxobutan-2-yl]amino]-1-oxohexan-2-yl]amino]-5-carbamimidamido-1-oxopentan-2-yl]amino]-3-(4-hydroxyphenyl)-1-oxopropan-2-yl]amino]-3-hydroxy-1-oxopropan-2-yl]amino]-1,4-dioxobutan-2-yl]amino]-3-hydroxy-1-oxobutan-2-yl]amino]-1-oxo-3-phenylpropan-2-yl]amino]-3-methyl-1-oxopentan-2-yl]amino]-1-oxopropan-2-yl]amino]-3-[[(2S)-2-[[(2S)-2-amino-3-(4-hydroxyphenyl)propanoyl]amino]propanoyl]amino]-4-oxobutanoic acid
- InChIKey
- WGWPRVFKDLAUQJ-MITYVQBRSA-N
- SMILES
- CC[C@H](C)[C@@H](C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC2=CC=C(C=C2)O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC(C)C)C(=O)NCC(=O)N[C@@H](CCC(=O)N)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CO)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(=O)N)C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N)NC(=O)[C@H](C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](CC3=CC=C(C=C3)O)N
Identifiers & sequence
- PubChem CID
- 16132413
- CAS Registry Number
- 86168-78-7via ChemIDplus, EPA DSSTox, FDA GSRS
- FDA UNII
- 89243S03TE
- InChIKey
- WGWPRVFKDLAUQJ-MITYVQBRSA-N
Peptide sequence · 29 residues (one-letter code; X marks a residue without a one-letter code)
YADAIFTNSYRKVLGQLSARKLLQDIMSR
Condensed notation with terminal groups and non-standard residues
H-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-NH2
Source: PubChem Biologic Line Notation. A reference sequence for the record, not an analysis of a supplied batch.
CAS numbers are published only from ChemIDplus, EPA DSSTox or the FDA Global Substance Registration System; UNII codes are confirmed in FDA GSRS by structure, sequence or exact name. Checked 2026-10-07.
Calculated molecular descriptors
| Monoisotopic (exact) mass | 3355.8187 Da |
|---|---|
| Heavy atoms | 236 |
| Hydrogen-bond donors | 52 |
| Hydrogen-bond acceptors | 47 |
| Rotatable bonds | 115 |
| Topological polar surface area | 1446.9 Ų |
| Calculated logP (Crippen) | -14.35 |
| Rings | 3 |
| Stereocenters | 31 |
| Formal charge | 0 |
Computed with RDKit from the published SMILES (Crippen logP, topological polar surface area). Calculated descriptors are not measured properties of a supplied batch.
US regulatory status & drug development
Sermorelin (listed as sermorelin acetate) was the active ingredient of GEREF (NDA 019863, approved December 28, 1990; NDA 020443, approved September 26, 1997). Drugs@FDA lists both applications as discontinued (checked October 7, 2026). Research-labelled Sermorelin listings are not GEREF and are not FDA-approved drugs.
| Medicine | Application | Sponsor | First approval | Marketing status |
|---|---|---|---|---|
| GEREFsermorelin acetate | NDA 019863 | EMD SERONO | Discontinued | |
| GEREFsermorelin acetate | NDA 020443 | EMD SERONO INC | Discontinued |
An FDA approval covers a defined medicine, formulation and labelled use. It does not extend to research-labelled material sold under the same compound name. Identity basis: Same active moiety: the approved products list sermorelin acetate; the research record is sermorelin (PubChem CID 16132413).
Source: Drugs@FDA via openFDA (application records; DailyMed label set IDs) · checked . openFDA data are not intended for clinical decisions.
Registered clinical trials
Studies registered on ClinicalTrials.gov that list Sermorelin as an intervention. Studies that only measure the molecule as a biomarker, or use it only as a comparator or background arm for another drug, are excluded. A registration describes a planned or completed protocol; it does not report a result. Active studies are listed first.
No registered study naming this compound was matched. This is a documented gap in registry coverage, not proof that no study exists.
Registry check 2026-10-01 · Run this search on ClinicalTrials.gov
Human intervention studies
Selected studies in which participants received Sermorelin, with their indexed or reviewed study type. Check the original article for the formulation, population and controls. Studies that only measured the molecule, or used it as a comparator, are listed separately below and are not counted as intervention studies.
- Human study · PubMed trial index Compound given to participants
Once daily subcutaneous growth hormone-releasing hormone therapy accelerates growth in growth hormone-deficient children during the first year of therapy. Geref International Study Group.
Thorner M, Rochiccioli P, Colle M et al. · The Journal of clinical endocrinology and metabolism · 1996
PMID 8772599 · DOI: 10.1210/jcem.81.3.8772599
- Human study · PubMed trial index Compound given to participants
A comparative study of growth hormone (GH) and GH-releasing hormone(1-29)-NH2 for stimulation of growth in children with GH deficiency.
Chen RG, Shen YN, Yei J et al. · Acta paediatrica (Oslo, Norway : 1992). Supplement · 1993
PMID 8329830 · DOI: 10.1111/j.1651-2227.1993.tb12834.x
Preclinical research, reviews & other publications
Animal studies, laboratory experiments, reviews and other indexed papers answer different questions. A review is secondary evidence; a case report does not estimate how often an outcome occurs.
- Research publication · design requires review
Sermorelin: a better approach to management of adult-onset growth hormone insufficiency?
Walker RF · Clinical interventions in aging · 2006
PMID 18046908 · DOI: 10.2147/ciia.2006.1.4.307
- Research publication · design requires review
A potentially effective drug for patients with recurrent glioma: sermorelin.
Chang Y, Huang R, Zhai Y et al. · Annals of translational medicine · 2021
PMID 33842627 · DOI: 10.21037/atm-20-6561
- Research publication · design requires review
Sermorelin: a review of its use in the diagnosis and treatment of children with idiopathic growth hormone deficiency.
Prakash A, Goa KL · BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 1999
PMID 18031173 · DOI: 10.2165/00063030-199912020-00007
Sermorelin supplier sources
Scientific sources describe molecules and experiments. The commercial links below identify recorded supplier packages. A publication or chemical database entry does not verify the seller, purity, sterility or contents of a lot. Some links are affiliate links; see our disclosure.
Sermorelin for sale: compare prices, sizes and forms from every tracked supplier →
Reference sources & further reading
- PubChem compound record 16132413 — chemical identity and structure.
- FDA Global Substance Registration System: UNII 89243S03TE — substance identity, names and codes.
- Drugs@FDA: NDA 019863 — US approval record for a medicine with the same active ingredient.
- Drugs@FDA: NDA 020443 — US approval record for a medicine with the same active ingredient.
- Wikipedia: Sermorelin — Background encyclopedia; not a primary clinical source.
The citations above link directly to publication records. Encyclopedia links are background reading and are not used to establish clinical effectiveness.
Search for additional research
These links run searches; their results have not been individually reviewed and can include unrelated compounds.
Research information is not a dosing guide or a recommendation for personal use. Study findings are specific to the formulation, population and methods tested. Read our source and correction policy.
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