Growth Hormone & Performance
GHRP-1

GHRP-1 is one of the first synthetic growth hormone-releasing peptides, and it works through a different door from growth hormone-releasing hormone: the ghrelin receptor, which is why the two amplify each other when given together and why the whole class exists. It has largely been superseded by later members of its family. Its human record is a single randomised study from 1998 in which a 100-microgram intravenous bolus went to ten women and 58 new mothers, with blood growth hormone read at twenty minutes — one timepoint, one hormone. The one registered trial of it, in dialysis patients, closed in 2007 for lack of enrolment, with three people signed up.
Last updated
Mechanism
Agonist at the growth hormone secretagogue receptor GHS-R1a; acts synergistically with GHRH and opposes somatostatin.
Reported effects
What sources associate with this compound. Reported categories, not outcomes we have graded — each would need its own citation and rung.
- Growth hormone release research
- IGF-1 response research
- Secretagogue pharmacology context
Dosing on file unverified
IV: 1 mcg/kg bolus; IV: 0.05-2.5 mcg/kg infusion; SC: single injection (NCT00381602)
Carried from a source that labels it unverified, and reproduced with that label attached. A record of what is reported, not a recommendation. No citation on this page establishes it.
Half-life, storage & sport
- Elimination half-life
- not on file — No pharmacokinetic value for GHRP-1 has been published. It has never been an approved medicine, so there is no label, and of the 41 PubMed records naming it none states a half-life or a clearance. The three returned by a pharmacokinetics search report growth hormone responses after a bolus, which is the duration of the effect and not the half-life of the peptide.
Literature on file 4
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human RCT
Postpartum hyperprolactinemia and hyporesponsiveness of growth hormone (GH) to GH-releasing peptide graded on: names a randomised controlled trial — the indexed publication type — “Randomized Controlled”
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in vitro
Growth hormone isoforms in newborns and postpartum women graded on: an in-vitro system — read from the indexed abstract — “assay”
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animal in vivo
In vivo effects of the GH-releasing heptapeptide GHRP-1 in lambs graded on: an animal model — “lambs”
Not graded
1 citation whose study design could not be read from the title. Left ungraded rather than guessed at.
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not graded
NCT00381602: A Phase II, Randomized, Cross-Over, Vehicle-Controlled, Double-Blind, Multicenter Study of the Safety, Pharmacodynamics, and Preliminary Efficacy of GHRP-1/AG in Subjects With ESRD on Hemodialysis graded on: NCT00381602 is terminated and has posted no results - a registration, not a reported outcome — “NCT00381602”
Identity
Skeletal formulathe canonical depiction
Drawn by PubChem from CID 10350910, the identifier on this record.
- Molecular weight
- 955.1
- Molecular formula
- C51H62N12O7
- CAS number
- 141925-59-9
- PubChem CID
- 10350910
- InChI key
- NWQWNCILOXTTHF-HLCSKTDOSA-N
- Sequence
- AHXAWFK
- SMILES
- C[C@@H](C(=O)N[C@@H](CC1=CN=CN1)C(=O)N[C@H](CC2=CC3=CC=CC=C3C=C2)C(=O)N[C@@H](C)C(=O)N[C@@H](CC4=CNC5=CC=CC=C54)C(=O)N[C@H](CC6=CC=CC=C6)C(=O)N[C@@H](CCCCN)C(=O)N)N
- InChI
- InChI=1S/C51H62N12O7/c1-30(53)46(65)60-44(26-37-28-55-29-57-37)51(70)63-42(24-33-19-20-34-14-6-7-15-35(34)22-33)48(67)58-31(2)47(66)61-43(25-36-27-56-39-17-9-8-16-38(36)39)50(69)62-41(23-32-12-4-3-5-13-32)49(68)59-40(45(54)64)18-10-11-21-52/h3-9,12-17,19-20,22,27-31,40-44,56H,10-11,18,21,23-26,52-53H2,1-2H3,(H2,54,64)(H,55,57)(H,58,67)(H,59,68)(H,60,65)(H,61,66)(H,62,69)(H,63,70)/t30-,31-,40-,41+,42+,43-,44-/m0/s1
Notes unverified prose
Human studies: 1 mcg/kg IV; 0.05-2.5 mcg/kg IV; NCT00381602 (SC); Human IV studies: 1 mcg/kg bolus; NCT00381602
Not on file 4
All 8 tracked fields hold a value on this record. 4 further absences are named below. A blank field is a bug; a named absence is a finding.
- half-lifeno pharmacokinetic study in any species on file
- clinical outcomethe human studies on file measured GH secretion after a single intravenous bolus; no study on file measured a clinical outcome
- repeat dose safetyNCT00381602 was terminated at 3 enrolled subjects and posted no results; no repeat-dose human safety record on file
- esrd haemodialysis evidencethe only registered trial in this population reported nothing
Each field links to every other record missing the same thing. The full ledger holds 765 gaps across 163 records.